Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700067K01Rik |
T |
C |
8: 84,729,637 (GRCm39) |
|
probably benign |
Het |
A530064D06Rik |
G |
A |
17: 48,473,824 (GRCm39) |
T31I |
probably benign |
Het |
Abca17 |
A |
G |
17: 24,500,223 (GRCm39) |
F1323L |
probably benign |
Het |
Abcf3 |
T |
A |
16: 20,369,237 (GRCm39) |
N206K |
probably damaging |
Het |
Adam10 |
A |
G |
9: 70,673,223 (GRCm39) |
|
probably benign |
Het |
Adamtsl3 |
A |
T |
7: 82,172,390 (GRCm39) |
Q451L |
probably damaging |
Het |
Adgrl3 |
T |
A |
5: 81,708,752 (GRCm39) |
I413N |
probably benign |
Het |
Asb18 |
G |
T |
1: 89,920,893 (GRCm39) |
A128E |
probably damaging |
Het |
Atf7ip2 |
T |
C |
16: 10,059,743 (GRCm39) |
S428P |
possibly damaging |
Het |
Atp8b5 |
G |
T |
4: 43,291,672 (GRCm39) |
C15F |
possibly damaging |
Het |
Bahcc1 |
A |
G |
11: 120,178,146 (GRCm39) |
E2235G |
probably damaging |
Het |
Blnk |
G |
T |
19: 40,926,111 (GRCm39) |
S330* |
probably null |
Het |
Bpnt1 |
T |
G |
1: 185,088,808 (GRCm39) |
N319K |
probably benign |
Het |
Brip1 |
G |
A |
11: 86,043,493 (GRCm39) |
T357I |
possibly damaging |
Het |
Cadm1 |
T |
A |
9: 47,725,104 (GRCm39) |
D288E |
probably benign |
Het |
Calcoco2 |
A |
G |
11: 95,998,354 (GRCm39) |
V23A |
probably damaging |
Het |
Cand2 |
G |
A |
6: 115,780,766 (GRCm39) |
E1217K |
probably damaging |
Het |
Ccdc154 |
G |
T |
17: 25,386,259 (GRCm39) |
|
probably benign |
Het |
Cdk12 |
T |
C |
11: 98,120,935 (GRCm39) |
|
probably benign |
Het |
Clec4a3 |
A |
G |
6: 122,930,993 (GRCm39) |
|
probably null |
Het |
Cpne2 |
T |
A |
8: 95,274,970 (GRCm39) |
|
probably benign |
Het |
Cyfip1 |
T |
C |
7: 55,573,710 (GRCm39) |
|
probably null |
Het |
Cyp26c1 |
A |
G |
19: 37,675,009 (GRCm39) |
H110R |
probably damaging |
Het |
Cyp2j13 |
A |
G |
4: 95,959,932 (GRCm39) |
Y75H |
probably damaging |
Het |
Defb43 |
T |
A |
14: 63,249,287 (GRCm39) |
V10D |
probably damaging |
Het |
Dhx36 |
G |
A |
3: 62,401,162 (GRCm39) |
S368L |
possibly damaging |
Het |
Dock6 |
G |
A |
9: 21,715,923 (GRCm39) |
|
probably benign |
Het |
Elp2 |
T |
C |
18: 24,745,499 (GRCm39) |
|
probably benign |
Het |
Emilin3 |
A |
G |
2: 160,750,249 (GRCm39) |
L453P |
probably damaging |
Het |
Eml6 |
A |
T |
11: 29,755,065 (GRCm39) |
D903E |
probably benign |
Het |
Ep300 |
T |
C |
15: 81,500,335 (GRCm39) |
|
probably benign |
Het |
Ep400 |
G |
A |
5: 110,836,062 (GRCm39) |
T1899M |
unknown |
Het |
Fancg |
A |
G |
4: 43,002,998 (GRCm39) |
S620P |
probably benign |
Het |
Fbxo42 |
G |
A |
4: 140,922,550 (GRCm39) |
V239M |
probably damaging |
Het |
Fermt2 |
T |
C |
14: 45,706,776 (GRCm39) |
D340G |
probably benign |
Het |
Filip1 |
A |
T |
9: 79,726,672 (GRCm39) |
V649E |
probably damaging |
Het |
Fut8 |
G |
A |
12: 77,521,791 (GRCm39) |
E477K |
probably damaging |
Het |
Gbp3 |
G |
A |
3: 142,271,151 (GRCm39) |
G185D |
probably benign |
Het |
Gclc |
G |
T |
9: 77,694,080 (GRCm39) |
D345Y |
probably damaging |
Het |
Gfus |
A |
G |
15: 75,800,807 (GRCm39) |
V27A |
possibly damaging |
Het |
Gkn2 |
A |
G |
6: 87,352,800 (GRCm39) |
D43G |
possibly damaging |
Het |
Gnptab |
A |
G |
10: 88,279,166 (GRCm39) |
|
probably benign |
Het |
Greb1l |
C |
T |
18: 10,474,303 (GRCm39) |
T206I |
probably damaging |
Het |
Grk4 |
A |
G |
5: 34,905,611 (GRCm39) |
N452S |
probably benign |
Het |
Hcn2 |
G |
C |
10: 79,570,066 (GRCm39) |
|
probably null |
Het |
Hpn |
T |
C |
7: 30,808,585 (GRCm39) |
K76E |
possibly damaging |
Het |
Hspg2 |
A |
G |
4: 137,280,591 (GRCm39) |
D3268G |
probably damaging |
Het |
Immt |
A |
T |
6: 71,848,541 (GRCm39) |
Q467L |
possibly damaging |
Het |
Kalrn |
T |
C |
16: 33,936,778 (GRCm39) |
S1636G |
probably benign |
Het |
Kcnh8 |
T |
A |
17: 53,285,141 (GRCm39) |
L1037* |
probably null |
Het |
Klhl33 |
T |
C |
14: 51,129,851 (GRCm39) |
T548A |
probably damaging |
Het |
Klri2 |
T |
C |
6: 129,717,171 (GRCm39) |
I71V |
probably benign |
Het |
Lama3 |
T |
C |
18: 12,610,647 (GRCm39) |
I1170T |
possibly damaging |
Het |
Med12l |
A |
G |
3: 59,172,350 (GRCm39) |
Q1702R |
probably damaging |
Het |
Mga |
A |
T |
2: 119,750,391 (GRCm39) |
|
probably null |
Het |
Mis18a |
A |
T |
16: 90,517,561 (GRCm39) |
I172K |
possibly damaging |
Het |
Mrgpre |
T |
C |
7: 143,335,254 (GRCm39) |
D83G |
probably benign |
Het |
Mroh2a |
C |
A |
1: 88,170,142 (GRCm39) |
A685D |
possibly damaging |
Het |
Mrpl39 |
T |
C |
16: 84,531,282 (GRCm39) |
|
probably benign |
Het |
Mrrf |
C |
T |
2: 36,043,710 (GRCm39) |
A149V |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,432,024 (GRCm39) |
M2338K |
possibly damaging |
Het |
Myo18b |
T |
C |
5: 112,840,632 (GRCm39) |
Q2387R |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,964,780 (GRCm39) |
I943T |
probably damaging |
Het |
Ncapd3 |
T |
A |
9: 26,998,773 (GRCm39) |
N1254K |
probably benign |
Het |
Ncoa1 |
A |
T |
12: 4,299,758 (GRCm39) |
|
probably null |
Het |
Ncor2 |
C |
T |
5: 125,126,451 (GRCm39) |
A136T |
probably benign |
Het |
Opa1 |
T |
C |
16: 29,421,025 (GRCm39) |
|
probably benign |
Het |
Or13a25 |
A |
G |
7: 140,247,590 (GRCm39) |
D123G |
probably damaging |
Het |
Or5p59 |
C |
A |
7: 107,703,363 (GRCm39) |
Y282* |
probably null |
Het |
Or8b39 |
T |
A |
9: 37,996,423 (GRCm39) |
M97K |
possibly damaging |
Het |
Or9e1 |
T |
A |
11: 58,732,681 (GRCm39) |
I247N |
possibly damaging |
Het |
Pcdhb4 |
T |
C |
18: 37,440,795 (GRCm39) |
M35T |
probably benign |
Het |
Per3 |
T |
C |
4: 151,113,288 (GRCm39) |
I347V |
probably benign |
Het |
Pex13 |
G |
A |
11: 23,615,831 (GRCm39) |
P5L |
possibly damaging |
Het |
Phkb |
T |
A |
8: 86,602,322 (GRCm39) |
W38R |
probably damaging |
Het |
Plekhf1 |
A |
T |
7: 37,920,826 (GRCm39) |
D247E |
probably benign |
Het |
Plxnb2 |
A |
G |
15: 89,042,184 (GRCm39) |
S1607P |
probably benign |
Het |
Plxnc1 |
T |
A |
10: 94,635,194 (GRCm39) |
H1344L |
possibly damaging |
Het |
Potefam1 |
A |
C |
2: 111,034,482 (GRCm39) |
V350G |
possibly damaging |
Het |
Ptk7 |
T |
G |
17: 46,901,238 (GRCm39) |
N196H |
possibly damaging |
Het |
Rab27a |
G |
T |
9: 72,982,715 (GRCm39) |
D7Y |
probably damaging |
Het |
Rars2 |
T |
A |
4: 34,630,505 (GRCm39) |
C82* |
probably null |
Het |
Rccd1 |
A |
T |
7: 79,969,965 (GRCm39) |
|
probably benign |
Het |
Riiad1 |
T |
C |
3: 94,379,546 (GRCm39) |
I56V |
possibly damaging |
Het |
Rnase4 |
A |
G |
14: 51,342,507 (GRCm39) |
E77G |
probably damaging |
Het |
Rnf126 |
A |
T |
10: 79,597,441 (GRCm39) |
I157N |
possibly damaging |
Het |
Rnf207 |
T |
C |
4: 152,391,925 (GRCm39) |
R623G |
probably benign |
Het |
Rpusd1 |
T |
G |
17: 25,947,498 (GRCm39) |
F62V |
possibly damaging |
Het |
Rxfp1 |
T |
C |
3: 79,570,600 (GRCm39) |
|
probably null |
Het |
Scfd1 |
A |
T |
12: 51,459,411 (GRCm39) |
Q324L |
probably benign |
Het |
Skint3 |
G |
T |
4: 112,112,974 (GRCm39) |
E195* |
probably null |
Het |
Slc7a10 |
A |
T |
7: 34,896,758 (GRCm39) |
T165S |
probably benign |
Het |
Smagp |
A |
G |
15: 100,519,733 (GRCm39) |
I97T |
probably damaging |
Het |
Sostdc1 |
A |
G |
12: 36,367,340 (GRCm39) |
H172R |
probably damaging |
Het |
Spast |
A |
G |
17: 74,646,446 (GRCm39) |
|
probably benign |
Het |
Sspo |
G |
T |
6: 48,467,325 (GRCm39) |
|
probably benign |
Het |
Ston2 |
C |
T |
12: 91,707,240 (GRCm39) |
|
probably null |
Het |
Tas2r103 |
T |
G |
6: 133,013,313 (GRCm39) |
E251A |
probably benign |
Het |
Tbc1d2b |
A |
T |
9: 90,104,558 (GRCm39) |
|
probably benign |
Het |
Telo2 |
G |
A |
17: 25,332,139 (GRCm39) |
P143L |
probably benign |
Het |
Tgfbi |
A |
T |
13: 56,786,539 (GRCm39) |
Y674F |
probably null |
Het |
Tha1 |
T |
A |
11: 117,763,983 (GRCm39) |
|
probably benign |
Het |
Timp4 |
T |
A |
6: 115,226,814 (GRCm39) |
S110C |
probably damaging |
Het |
Tlr6 |
T |
C |
5: 65,111,935 (GRCm39) |
K324R |
probably benign |
Het |
Tnip3 |
A |
G |
6: 65,574,347 (GRCm39) |
E137G |
probably damaging |
Het |
Top6bl |
A |
G |
19: 4,676,216 (GRCm39) |
S639P |
probably damaging |
Het |
Trak1 |
T |
C |
9: 121,278,021 (GRCm39) |
|
probably null |
Het |
Trim47 |
A |
G |
11: 115,999,178 (GRCm39) |
S233P |
probably benign |
Het |
Tspoap1 |
A |
T |
11: 87,653,635 (GRCm39) |
E155V |
probably damaging |
Het |
Uggt1 |
A |
T |
1: 36,194,209 (GRCm39) |
L1343Q |
probably damaging |
Het |
Utp14b |
T |
C |
1: 78,642,452 (GRCm39) |
S117P |
probably benign |
Het |
Vmn1r124 |
A |
T |
7: 20,994,436 (GRCm39) |
V36D |
probably damaging |
Het |
Wdr27 |
T |
C |
17: 15,148,658 (GRCm39) |
T112A |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,065,367 (GRCm39) |
T1630A |
probably benign |
Het |
Zfp352 |
A |
G |
4: 90,112,156 (GRCm39) |
T99A |
probably benign |
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 |
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 |
R2049:Kmt2c
|
UTSW |
5 |
25,490,077 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|