Other mutations in this stock |
Total: 118 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931414P19Rik |
G |
A |
14: 54,822,444 (GRCm39) |
R8* |
probably null |
Het |
Abhd17a |
A |
G |
10: 80,421,440 (GRCm39) |
|
probably null |
Het |
Acsm1 |
A |
G |
7: 119,255,262 (GRCm39) |
R415G |
probably damaging |
Het |
Acta1 |
G |
T |
8: 124,618,803 (GRCm39) |
T360N |
probably benign |
Het |
Adam6a |
T |
A |
12: 113,508,049 (GRCm39) |
S141T |
probably benign |
Het |
Adgrd1 |
G |
T |
5: 129,192,159 (GRCm39) |
K76N |
probably benign |
Het |
Afdn |
A |
G |
17: 14,030,695 (GRCm39) |
E202G |
probably damaging |
Het |
Agps |
T |
A |
2: 75,689,270 (GRCm39) |
M156K |
probably benign |
Het |
Agxt |
A |
G |
1: 93,065,037 (GRCm39) |
I149V |
probably benign |
Het |
Aoc1l1 |
T |
A |
6: 48,954,689 (GRCm39) |
L609* |
probably null |
Het |
Aqp2 |
A |
G |
15: 99,477,247 (GRCm39) |
T72A |
probably damaging |
Het |
Arhgap18 |
T |
A |
10: 26,725,938 (GRCm39) |
D54E |
probably benign |
Het |
Asb8 |
C |
A |
15: 98,033,950 (GRCm39) |
E202* |
probably null |
Het |
Bmp5 |
A |
G |
9: 75,801,072 (GRCm39) |
I401V |
probably damaging |
Het |
Bscl2 |
T |
C |
19: 8,822,684 (GRCm39) |
|
probably null |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cep112 |
A |
G |
11: 108,497,151 (GRCm39) |
E697G |
probably damaging |
Het |
Cerk |
G |
A |
15: 86,027,009 (GRCm39) |
S167L |
probably benign |
Het |
Chrm3 |
T |
A |
13: 9,928,371 (GRCm39) |
I222F |
probably damaging |
Het |
Clcn6 |
A |
G |
4: 148,108,594 (GRCm39) |
F145S |
possibly damaging |
Het |
Cnksr1 |
A |
G |
4: 133,956,939 (GRCm39) |
Y488H |
probably damaging |
Het |
Cntrl |
CAGAG |
CAG |
2: 35,012,818 (GRCm39) |
|
probably null |
Het |
Commd10 |
A |
T |
18: 47,096,814 (GRCm39) |
T74S |
probably benign |
Het |
Cyp4f39 |
T |
C |
17: 32,701,112 (GRCm39) |
F201L |
probably benign |
Het |
Dennd4a |
A |
G |
9: 64,796,887 (GRCm39) |
T860A |
possibly damaging |
Het |
Dlg5 |
A |
T |
14: 24,204,715 (GRCm39) |
I1253N |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,307,830 (GRCm39) |
M3048K |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 65,935,509 (GRCm39) |
M1970T |
probably damaging |
Het |
Dsc3 |
A |
T |
18: 20,122,737 (GRCm39) |
D62E |
possibly damaging |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Dusp7 |
C |
T |
9: 106,251,096 (GRCm39) |
T407M |
probably damaging |
Het |
Efnb1 |
A |
G |
X: 98,191,123 (GRCm39) |
Y343C |
probably damaging |
Het |
Eif1ad8 |
A |
G |
12: 87,564,046 (GRCm39) |
D127G |
unknown |
Het |
Entpd5 |
A |
G |
12: 84,443,632 (GRCm39) |
I12T |
probably benign |
Het |
Espn |
T |
C |
4: 152,205,714 (GRCm39) |
E408G |
probably damaging |
Het |
Fhip1b |
A |
T |
7: 105,039,046 (GRCm39) |
D64E |
probably damaging |
Het |
Gdpd3 |
A |
G |
7: 126,367,766 (GRCm39) |
T200A |
probably damaging |
Het |
Gli1 |
A |
G |
10: 127,172,596 (GRCm39) |
L182P |
probably damaging |
Het |
Gm5134 |
G |
A |
10: 75,840,718 (GRCm39) |
A521T |
possibly damaging |
Het |
Gprasp1 |
G |
A |
X: 134,702,791 (GRCm39) |
E995K |
possibly damaging |
Het |
H2-M10.1 |
T |
C |
17: 36,636,108 (GRCm39) |
D153G |
possibly damaging |
Het |
Helb |
A |
T |
10: 119,941,926 (GRCm39) |
M254K |
possibly damaging |
Het |
I0C0044D17Rik |
A |
G |
4: 98,708,533 (GRCm39) |
|
probably benign |
Het |
Igfn1 |
AGGG |
AGG |
1: 135,902,590 (GRCm39) |
|
probably benign |
Het |
Igfn1 |
T |
A |
1: 135,898,376 (GRCm39) |
Q730L |
probably benign |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Jmjd1c |
T |
A |
10: 66,993,777 (GRCm39) |
L86* |
probably null |
Het |
Kat5 |
T |
A |
19: 5,655,713 (GRCm39) |
|
probably null |
Het |
Kif14 |
A |
G |
1: 136,414,818 (GRCm39) |
N768S |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,437,905 (GRCm39) |
E1199G |
possibly damaging |
Het |
Klhl29 |
A |
G |
12: 5,187,876 (GRCm39) |
S163P |
probably damaging |
Het |
Krt82 |
T |
A |
15: 101,453,591 (GRCm39) |
Q265L |
probably damaging |
Het |
Macf1 |
C |
T |
4: 123,248,895 (GRCm39) |
C7210Y |
probably damaging |
Het |
Mx2 |
G |
A |
16: 97,339,903 (GRCm39) |
E20K |
probably benign |
Het |
Myom2 |
T |
G |
8: 15,156,379 (GRCm39) |
I742S |
probably damaging |
Het |
Narf |
A |
T |
11: 121,141,195 (GRCm39) |
R310* |
probably null |
Het |
Nktr |
T |
A |
9: 121,570,760 (GRCm39) |
D167E |
probably damaging |
Het |
Nle1 |
A |
G |
11: 82,796,192 (GRCm39) |
W183R |
probably damaging |
Het |
Npas3 |
A |
G |
12: 54,108,871 (GRCm39) |
N425S |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or4a27 |
A |
T |
2: 88,559,089 (GRCm39) |
Y285N |
probably damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or4d5 |
T |
A |
9: 40,012,415 (GRCm39) |
I124L |
probably benign |
Het |
Or6c69 |
A |
G |
10: 129,748,036 (GRCm39) |
V37A |
probably benign |
Het |
Or8g52 |
A |
T |
9: 39,631,411 (GRCm39) |
D296V |
probably damaging |
Het |
Or8s2 |
G |
A |
15: 98,276,277 (GRCm39) |
T238I |
possibly damaging |
Het |
Otol1 |
T |
A |
3: 69,926,169 (GRCm39) |
F115I |
probably benign |
Het |
Parp8 |
T |
A |
13: 117,031,422 (GRCm39) |
D430V |
probably benign |
Het |
Pex7 |
T |
A |
10: 19,770,061 (GRCm39) |
H123L |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,410,909 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
G |
A |
15: 44,445,137 (GRCm39) |
D3670N |
probably damaging |
Het |
Plec |
T |
C |
15: 76,067,374 (GRCm39) |
T1331A |
probably benign |
Het |
Plekha4 |
A |
G |
7: 45,203,222 (GRCm39) |
D704G |
probably benign |
Het |
Plxnb2 |
T |
A |
15: 89,043,205 (GRCm39) |
N1453I |
probably damaging |
Het |
Pms1 |
T |
A |
1: 53,321,147 (GRCm39) |
I29F |
probably damaging |
Het |
Ppp1r1a |
G |
A |
15: 103,439,833 (GRCm39) |
T153I |
probably damaging |
Het |
Pramel12 |
T |
A |
4: 143,143,441 (GRCm39) |
L69Q |
probably damaging |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Ptpre |
A |
G |
7: 135,272,424 (GRCm39) |
|
probably benign |
Het |
Ptprt |
A |
T |
2: 161,376,465 (GRCm39) |
I1312N |
probably damaging |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
Rims1 |
C |
T |
1: 22,635,516 (GRCm39) |
C155Y |
probably damaging |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Slitrk6 |
T |
G |
14: 110,988,226 (GRCm39) |
T494P |
probably benign |
Het |
Sltm |
G |
A |
9: 70,488,583 (GRCm39) |
G578S |
probably benign |
Het |
Smyd5 |
A |
G |
6: 85,421,300 (GRCm39) |
E338G |
probably benign |
Het |
Snx2 |
G |
A |
18: 53,327,516 (GRCm39) |
V81M |
probably damaging |
Het |
Sp2 |
G |
T |
11: 96,852,191 (GRCm39) |
N244K |
probably benign |
Het |
Sspo |
C |
A |
6: 48,437,697 (GRCm39) |
|
probably benign |
Het |
Sspo |
A |
C |
6: 48,440,465 (GRCm39) |
D1568A |
probably benign |
Het |
Ssrp1 |
T |
C |
2: 84,871,771 (GRCm39) |
|
probably benign |
Het |
Syt2 |
ACTCTCTCT |
ACTCTCTCTCT |
1: 134,674,479 (GRCm39) |
|
probably benign |
Het |
Syt7 |
G |
A |
19: 10,416,577 (GRCm39) |
R138Q |
probably benign |
Het |
Taar7f |
T |
C |
10: 23,926,323 (GRCm39) |
Y306H |
possibly damaging |
Het |
Tbccd1 |
T |
C |
16: 22,637,291 (GRCm39) |
|
probably null |
Het |
Tesl1 |
T |
A |
X: 23,773,549 (GRCm39) |
V350E |
probably benign |
Het |
Tex261 |
A |
G |
6: 83,749,241 (GRCm39) |
Y119H |
probably damaging |
Het |
Tmem131l |
T |
G |
3: 83,850,095 (GRCm39) |
E234D |
probably damaging |
Het |
Tnnt2 |
TG |
TGG |
1: 135,774,499 (GRCm39) |
|
probably benign |
Het |
Top6bl |
A |
G |
19: 4,748,633 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Ubap1 |
C |
T |
4: 41,379,257 (GRCm39) |
A157V |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,204,518 (GRCm39) |
T4810M |
probably damaging |
Het |
Uso1 |
G |
A |
5: 92,329,795 (GRCm39) |
G427R |
probably damaging |
Het |
Usp15 |
A |
T |
10: 122,955,042 (GRCm39) |
V912D |
probably damaging |
Het |
Vmn1r20 |
T |
C |
6: 57,408,943 (GRCm39) |
S90P |
probably damaging |
Het |
Vmn1r32 |
T |
C |
6: 66,530,545 (GRCm39) |
K77R |
probably damaging |
Het |
Vmn2r100 |
A |
G |
17: 19,742,312 (GRCm39) |
K229E |
probably benign |
Het |
Vmn2r106 |
A |
G |
17: 20,488,566 (GRCm39) |
V611A |
possibly damaging |
Het |
Xrcc6 |
T |
A |
15: 81,907,178 (GRCm39) |
F167I |
probably damaging |
Het |
Zbtb21 |
G |
T |
16: 97,751,355 (GRCm39) |
P804H |
probably damaging |
Het |
Zdhhc3 |
T |
C |
9: 122,929,602 (GRCm39) |
D11G |
probably damaging |
Het |
Zfhx3 |
A |
G |
8: 109,671,809 (GRCm39) |
T1324A |
probably benign |
Het |
Zfp281 |
GCGGCAGCTCCGGCAGC |
GCGGCAGCTCCGGCAGCTCCGGCAGC |
1: 136,553,091 (GRCm39) |
|
probably benign |
Het |
Zfp608 |
G |
T |
18: 55,028,637 (GRCm39) |
L1259I |
probably damaging |
Het |
|
Other mutations in Kmt2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00436:Kmt2c
|
APN |
5 |
25,486,259 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00694:Kmt2c
|
APN |
5 |
25,498,159 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00780:Kmt2c
|
APN |
5 |
25,516,049 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00811:Kmt2c
|
APN |
5 |
25,579,531 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL00885:Kmt2c
|
APN |
5 |
25,614,169 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL00948:Kmt2c
|
APN |
5 |
25,582,159 (GRCm39) |
missense |
probably benign |
0.08 |
IGL00959:Kmt2c
|
APN |
5 |
25,481,227 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01022:Kmt2c
|
APN |
5 |
25,507,699 (GRCm39) |
unclassified |
probably benign |
|
IGL01146:Kmt2c
|
APN |
5 |
25,513,510 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01154:Kmt2c
|
APN |
5 |
25,489,397 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01434:Kmt2c
|
APN |
5 |
25,614,306 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01464:Kmt2c
|
APN |
5 |
25,557,242 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01525:Kmt2c
|
APN |
5 |
25,534,439 (GRCm39) |
splice site |
probably benign |
|
IGL01530:Kmt2c
|
APN |
5 |
25,518,498 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01550:Kmt2c
|
APN |
5 |
25,486,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01598:Kmt2c
|
APN |
5 |
25,478,664 (GRCm39) |
makesense |
probably null |
|
IGL01598:Kmt2c
|
APN |
5 |
25,559,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01608:Kmt2c
|
APN |
5 |
25,559,809 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01663:Kmt2c
|
APN |
5 |
25,515,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01707:Kmt2c
|
APN |
5 |
25,505,096 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01714:Kmt2c
|
APN |
5 |
25,518,398 (GRCm39) |
missense |
probably benign |
|
IGL01784:Kmt2c
|
APN |
5 |
25,518,524 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01813:Kmt2c
|
APN |
5 |
25,495,802 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01825:Kmt2c
|
APN |
5 |
25,515,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01834:Kmt2c
|
APN |
5 |
25,600,453 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02072:Kmt2c
|
APN |
5 |
25,610,430 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02159:Kmt2c
|
APN |
5 |
25,516,341 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02303:Kmt2c
|
APN |
5 |
25,515,155 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02417:Kmt2c
|
APN |
5 |
25,578,018 (GRCm39) |
missense |
probably benign |
|
IGL02578:Kmt2c
|
APN |
5 |
25,571,198 (GRCm39) |
intron |
probably benign |
|
IGL02811:Kmt2c
|
APN |
5 |
25,520,026 (GRCm39) |
nonsense |
probably null |
|
IGL02943:Kmt2c
|
APN |
5 |
25,495,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03000:Kmt2c
|
APN |
5 |
25,489,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03040:Kmt2c
|
APN |
5 |
25,515,350 (GRCm39) |
missense |
probably benign |
|
IGL03076:Kmt2c
|
APN |
5 |
25,504,149 (GRCm39) |
nonsense |
probably null |
|
IGL03088:Kmt2c
|
APN |
5 |
25,504,802 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03131:Kmt2c
|
APN |
5 |
25,520,359 (GRCm39) |
missense |
probably benign |
0.00 |
FR4304:Kmt2c
|
UTSW |
5 |
25,520,764 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Kmt2c
|
UTSW |
5 |
25,520,761 (GRCm39) |
small insertion |
probably benign |
|
PIT4520001:Kmt2c
|
UTSW |
5 |
25,520,664 (GRCm39) |
missense |
probably benign |
0.12 |
PIT4585001:Kmt2c
|
UTSW |
5 |
25,520,104 (GRCm39) |
missense |
probably benign |
0.21 |
R0313:Kmt2c
|
UTSW |
5 |
25,549,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Kmt2c
|
UTSW |
5 |
25,514,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R0411:Kmt2c
|
UTSW |
5 |
25,580,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0422:Kmt2c
|
UTSW |
5 |
25,520,662 (GRCm39) |
missense |
probably benign |
|
R0453:Kmt2c
|
UTSW |
5 |
25,559,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Kmt2c
|
UTSW |
5 |
25,504,250 (GRCm39) |
missense |
probably benign |
|
R0619:Kmt2c
|
UTSW |
5 |
25,503,914 (GRCm39) |
missense |
probably benign |
0.21 |
R0671:Kmt2c
|
UTSW |
5 |
25,609,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R0736:Kmt2c
|
UTSW |
5 |
25,500,432 (GRCm39) |
missense |
probably benign |
|
R0745:Kmt2c
|
UTSW |
5 |
25,564,696 (GRCm39) |
splice site |
probably null |
|
R0760:Kmt2c
|
UTSW |
5 |
25,558,315 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0784:Kmt2c
|
UTSW |
5 |
25,515,893 (GRCm39) |
missense |
probably benign |
0.00 |
R0882:Kmt2c
|
UTSW |
5 |
25,500,605 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0893:Kmt2c
|
UTSW |
5 |
25,556,268 (GRCm39) |
splice site |
probably benign |
|
R0942:Kmt2c
|
UTSW |
5 |
25,520,301 (GRCm39) |
missense |
probably benign |
0.10 |
R1110:Kmt2c
|
UTSW |
5 |
25,519,360 (GRCm39) |
missense |
probably benign |
0.01 |
R1137:Kmt2c
|
UTSW |
5 |
25,515,981 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1255:Kmt2c
|
UTSW |
5 |
25,556,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R1300:Kmt2c
|
UTSW |
5 |
25,610,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R1497:Kmt2c
|
UTSW |
5 |
25,519,513 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1594:Kmt2c
|
UTSW |
5 |
25,519,876 (GRCm39) |
missense |
probably benign |
0.01 |
R1611:Kmt2c
|
UTSW |
5 |
25,564,309 (GRCm39) |
critical splice donor site |
probably null |
|
R1617:Kmt2c
|
UTSW |
5 |
25,580,925 (GRCm39) |
missense |
probably benign |
0.01 |
R1720:Kmt2c
|
UTSW |
5 |
25,504,182 (GRCm39) |
missense |
probably benign |
0.05 |
R1723:Kmt2c
|
UTSW |
5 |
25,520,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1724:Kmt2c
|
UTSW |
5 |
25,520,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1726:Kmt2c
|
UTSW |
5 |
25,520,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1736:Kmt2c
|
UTSW |
5 |
25,495,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Kmt2c
|
UTSW |
5 |
25,577,972 (GRCm39) |
missense |
probably benign |
0.02 |
R1809:Kmt2c
|
UTSW |
5 |
25,489,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R1845:Kmt2c
|
UTSW |
5 |
25,578,434 (GRCm39) |
missense |
probably benign |
0.45 |
R1895:Kmt2c
|
UTSW |
5 |
25,520,152 (GRCm39) |
missense |
probably benign |
0.34 |
R1946:Kmt2c
|
UTSW |
5 |
25,520,152 (GRCm39) |
missense |
probably benign |
0.34 |
R1989:Kmt2c
|
UTSW |
5 |
25,703,542 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2039:Kmt2c
|
UTSW |
5 |
25,534,038 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2079:Kmt2c
|
UTSW |
5 |
25,557,278 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2080:Kmt2c
|
UTSW |
5 |
25,559,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R2107:Kmt2c
|
UTSW |
5 |
25,514,822 (GRCm39) |
missense |
probably benign |
0.01 |
R2186:Kmt2c
|
UTSW |
5 |
25,492,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R2395:Kmt2c
|
UTSW |
5 |
25,520,150 (GRCm39) |
missense |
probably benign |
|
R2983:Kmt2c
|
UTSW |
5 |
25,520,755 (GRCm39) |
small deletion |
probably benign |
|
R3109:Kmt2c
|
UTSW |
5 |
25,480,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R3500:Kmt2c
|
UTSW |
5 |
25,504,477 (GRCm39) |
missense |
probably benign |
0.02 |
R3738:Kmt2c
|
UTSW |
5 |
25,610,381 (GRCm39) |
missense |
probably benign |
0.41 |
R3809:Kmt2c
|
UTSW |
5 |
25,614,136 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4088:Kmt2c
|
UTSW |
5 |
25,492,711 (GRCm39) |
missense |
probably benign |
|
R4107:Kmt2c
|
UTSW |
5 |
25,503,918 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4212:Kmt2c
|
UTSW |
5 |
25,552,357 (GRCm39) |
critical splice donor site |
probably null |
|
R4376:Kmt2c
|
UTSW |
5 |
25,520,324 (GRCm39) |
missense |
probably benign |
0.00 |
R4377:Kmt2c
|
UTSW |
5 |
25,520,324 (GRCm39) |
missense |
probably benign |
0.00 |
R4383:Kmt2c
|
UTSW |
5 |
25,556,060 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4435:Kmt2c
|
UTSW |
5 |
25,519,875 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4456:Kmt2c
|
UTSW |
5 |
25,515,210 (GRCm39) |
missense |
probably benign |
|
R4461:Kmt2c
|
UTSW |
5 |
25,504,874 (GRCm39) |
missense |
probably benign |
0.00 |
R4519:Kmt2c
|
UTSW |
5 |
25,568,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R4550:Kmt2c
|
UTSW |
5 |
25,505,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R4557:Kmt2c
|
UTSW |
5 |
25,505,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Kmt2c
|
UTSW |
5 |
25,559,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R4671:Kmt2c
|
UTSW |
5 |
25,571,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4704:Kmt2c
|
UTSW |
5 |
25,519,025 (GRCm39) |
nonsense |
probably null |
|
R4781:Kmt2c
|
UTSW |
5 |
25,648,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R4844:Kmt2c
|
UTSW |
5 |
25,520,111 (GRCm39) |
missense |
probably benign |
|
R4855:Kmt2c
|
UTSW |
5 |
25,519,555 (GRCm39) |
missense |
probably benign |
0.00 |
R4919:Kmt2c
|
UTSW |
5 |
25,519,393 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4971:Kmt2c
|
UTSW |
5 |
25,515,870 (GRCm39) |
missense |
probably benign |
0.00 |
R4983:Kmt2c
|
UTSW |
5 |
25,500,509 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5012:Kmt2c
|
UTSW |
5 |
25,504,710 (GRCm39) |
nonsense |
probably null |
|
R5033:Kmt2c
|
UTSW |
5 |
25,519,706 (GRCm39) |
missense |
probably benign |
0.03 |
R5093:Kmt2c
|
UTSW |
5 |
25,614,205 (GRCm39) |
missense |
probably benign |
0.17 |
R5125:Kmt2c
|
UTSW |
5 |
25,489,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R5231:Kmt2c
|
UTSW |
5 |
25,520,471 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5254:Kmt2c
|
UTSW |
5 |
25,519,592 (GRCm39) |
missense |
probably benign |
0.01 |
R5396:Kmt2c
|
UTSW |
5 |
25,499,732 (GRCm39) |
splice site |
probably null |
|
R5415:Kmt2c
|
UTSW |
5 |
25,519,699 (GRCm39) |
missense |
probably benign |
0.21 |
R5523:Kmt2c
|
UTSW |
5 |
25,504,337 (GRCm39) |
missense |
probably benign |
0.00 |
R5554:Kmt2c
|
UTSW |
5 |
25,499,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R5701:Kmt2c
|
UTSW |
5 |
25,519,015 (GRCm39) |
missense |
probably benign |
0.16 |
R5762:Kmt2c
|
UTSW |
5 |
25,515,455 (GRCm39) |
missense |
probably benign |
0.01 |
R5819:Kmt2c
|
UTSW |
5 |
25,614,130 (GRCm39) |
critical splice donor site |
probably null |
|
R5838:Kmt2c
|
UTSW |
5 |
25,489,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R5912:Kmt2c
|
UTSW |
5 |
25,552,467 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5951:Kmt2c
|
UTSW |
5 |
25,535,801 (GRCm39) |
missense |
probably benign |
0.15 |
R5988:Kmt2c
|
UTSW |
5 |
25,516,118 (GRCm39) |
missense |
probably benign |
0.02 |
R5999:Kmt2c
|
UTSW |
5 |
25,489,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R6104:Kmt2c
|
UTSW |
5 |
25,504,127 (GRCm39) |
missense |
probably benign |
|
R6254:Kmt2c
|
UTSW |
5 |
25,554,872 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6311:Kmt2c
|
UTSW |
5 |
25,648,816 (GRCm39) |
critical splice donor site |
probably null |
|
R6329:Kmt2c
|
UTSW |
5 |
25,520,600 (GRCm39) |
missense |
probably benign |
0.01 |
R6347:Kmt2c
|
UTSW |
5 |
25,515,833 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6364:Kmt2c
|
UTSW |
5 |
25,514,634 (GRCm39) |
missense |
probably null |
0.99 |
R6379:Kmt2c
|
UTSW |
5 |
25,564,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R6588:Kmt2c
|
UTSW |
5 |
25,528,787 (GRCm39) |
missense |
probably damaging |
0.99 |
R6628:Kmt2c
|
UTSW |
5 |
25,503,926 (GRCm39) |
missense |
probably benign |
|
R6733:Kmt2c
|
UTSW |
5 |
25,614,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R6787:Kmt2c
|
UTSW |
5 |
25,480,737 (GRCm39) |
splice site |
probably null |
|
R6816:Kmt2c
|
UTSW |
5 |
25,610,530 (GRCm39) |
splice site |
probably null |
|
R6862:Kmt2c
|
UTSW |
5 |
25,515,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R7150:Kmt2c
|
UTSW |
5 |
25,505,360 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7220:Kmt2c
|
UTSW |
5 |
25,549,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Kmt2c
|
UTSW |
5 |
25,514,805 (GRCm39) |
missense |
probably benign |
0.00 |
R7250:Kmt2c
|
UTSW |
5 |
25,504,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Kmt2c
|
UTSW |
5 |
25,600,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R7465:Kmt2c
|
UTSW |
5 |
25,507,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Kmt2c
|
UTSW |
5 |
25,513,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R7491:Kmt2c
|
UTSW |
5 |
25,489,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R7549:Kmt2c
|
UTSW |
5 |
25,619,968 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7637:Kmt2c
|
UTSW |
5 |
25,520,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R7652:Kmt2c
|
UTSW |
5 |
25,520,717 (GRCm39) |
missense |
probably benign |
0.01 |
R7714:Kmt2c
|
UTSW |
5 |
25,580,364 (GRCm39) |
missense |
probably benign |
|
R7838:Kmt2c
|
UTSW |
5 |
25,499,697 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7891:Kmt2c
|
UTSW |
5 |
25,505,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7892:Kmt2c
|
UTSW |
5 |
25,504,814 (GRCm39) |
missense |
probably benign |
0.18 |
R7895:Kmt2c
|
UTSW |
5 |
25,578,174 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7960:Kmt2c
|
UTSW |
5 |
25,520,194 (GRCm39) |
missense |
probably benign |
0.01 |
R7974:Kmt2c
|
UTSW |
5 |
25,505,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R7978:Kmt2c
|
UTSW |
5 |
25,564,676 (GRCm39) |
missense |
probably benign |
0.00 |
R8011:Kmt2c
|
UTSW |
5 |
25,556,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R8021:Kmt2c
|
UTSW |
5 |
25,492,117 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8022:Kmt2c
|
UTSW |
5 |
25,486,678 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8079:Kmt2c
|
UTSW |
5 |
25,507,730 (GRCm39) |
missense |
probably damaging |
0.98 |
R8087:Kmt2c
|
UTSW |
5 |
25,534,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8109:Kmt2c
|
UTSW |
5 |
25,486,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R8161:Kmt2c
|
UTSW |
5 |
25,579,562 (GRCm39) |
missense |
probably benign |
0.00 |
R8169:Kmt2c
|
UTSW |
5 |
25,559,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R8206:Kmt2c
|
UTSW |
5 |
25,519,537 (GRCm39) |
missense |
probably damaging |
0.98 |
R8218:Kmt2c
|
UTSW |
5 |
25,488,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R8223:Kmt2c
|
UTSW |
5 |
25,529,216 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8260:Kmt2c
|
UTSW |
5 |
25,610,514 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8330:Kmt2c
|
UTSW |
5 |
25,509,692 (GRCm39) |
missense |
probably null |
1.00 |
R8355:Kmt2c
|
UTSW |
5 |
25,559,499 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8455:Kmt2c
|
UTSW |
5 |
25,559,499 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8508:Kmt2c
|
UTSW |
5 |
25,519,120 (GRCm39) |
missense |
probably benign |
0.34 |
R8885:Kmt2c
|
UTSW |
5 |
25,520,077 (GRCm39) |
missense |
probably benign |
0.34 |
R8907:Kmt2c
|
UTSW |
5 |
25,514,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Kmt2c
|
UTSW |
5 |
25,503,885 (GRCm39) |
missense |
probably benign |
|
R8969:Kmt2c
|
UTSW |
5 |
25,519,387 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9019:Kmt2c
|
UTSW |
5 |
25,488,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Kmt2c
|
UTSW |
5 |
25,524,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R9074:Kmt2c
|
UTSW |
5 |
25,489,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R9125:Kmt2c
|
UTSW |
5 |
25,489,194 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9130:Kmt2c
|
UTSW |
5 |
25,516,102 (GRCm39) |
missense |
probably benign |
0.01 |
R9171:Kmt2c
|
UTSW |
5 |
25,486,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R9235:Kmt2c
|
UTSW |
5 |
25,504,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Kmt2c
|
UTSW |
5 |
25,554,860 (GRCm39) |
missense |
probably benign |
0.34 |
R9288:Kmt2c
|
UTSW |
5 |
25,497,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R9336:Kmt2c
|
UTSW |
5 |
25,614,165 (GRCm39) |
missense |
probably benign |
0.06 |
R9443:Kmt2c
|
UTSW |
5 |
25,515,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R9481:Kmt2c
|
UTSW |
5 |
25,497,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R9481:Kmt2c
|
UTSW |
5 |
25,554,860 (GRCm39) |
missense |
probably benign |
0.34 |
R9526:Kmt2c
|
UTSW |
5 |
25,486,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R9653:Kmt2c
|
UTSW |
5 |
25,507,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R9729:Kmt2c
|
UTSW |
5 |
25,489,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R9731:Kmt2c
|
UTSW |
5 |
25,577,956 (GRCm39) |
missense |
probably benign |
0.18 |
R9784:Kmt2c
|
UTSW |
5 |
25,549,959 (GRCm39) |
missense |
probably damaging |
1.00 |
RF001:Kmt2c
|
UTSW |
5 |
25,520,773 (GRCm39) |
small insertion |
probably benign |
|
RF006:Kmt2c
|
UTSW |
5 |
25,520,770 (GRCm39) |
small insertion |
probably benign |
|
RF011:Kmt2c
|
UTSW |
5 |
25,543,457 (GRCm39) |
missense |
probably damaging |
1.00 |
RF041:Kmt2c
|
UTSW |
5 |
25,520,773 (GRCm39) |
small insertion |
probably benign |
|
RF047:Kmt2c
|
UTSW |
5 |
25,520,758 (GRCm39) |
small insertion |
probably benign |
|
RF051:Kmt2c
|
UTSW |
5 |
25,518,477 (GRCm39) |
unclassified |
probably benign |
|
RF055:Kmt2c
|
UTSW |
5 |
25,520,770 (GRCm39) |
small insertion |
probably benign |
|
RF059:Kmt2c
|
UTSW |
5 |
25,518,477 (GRCm39) |
unclassified |
probably benign |
|
RF063:Kmt2c
|
UTSW |
5 |
25,520,762 (GRCm39) |
small insertion |
probably benign |
|
X0024:Kmt2c
|
UTSW |
5 |
25,610,483 (GRCm39) |
missense |
probably benign |
0.26 |
X0027:Kmt2c
|
UTSW |
5 |
25,535,885 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1176:Kmt2c
|
UTSW |
5 |
25,559,411 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Kmt2c
|
UTSW |
5 |
25,571,195 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Kmt2c
|
UTSW |
5 |
25,505,001 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Kmt2c
|
UTSW |
5 |
25,500,395 (GRCm39) |
critical splice donor site |
probably null |
|
|