Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm1 |
C |
T |
4: 144,246,619 (GRCm39) |
T55I |
probably benign |
Het |
Acod1 |
T |
A |
14: 103,292,418 (GRCm39) |
I314N |
probably damaging |
Het |
Actl11 |
T |
A |
9: 107,806,967 (GRCm39) |
V430E |
probably damaging |
Het |
Adam19 |
A |
C |
11: 46,018,219 (GRCm39) |
D427A |
possibly damaging |
Het |
Adarb2 |
C |
T |
13: 8,802,606 (GRCm39) |
|
probably benign |
Het |
Akap7 |
A |
T |
10: 25,147,450 (GRCm39) |
H93Q |
probably damaging |
Het |
Ankrd36 |
C |
A |
11: 5,578,981 (GRCm39) |
R82S |
possibly damaging |
Het |
Arhgap21 |
A |
T |
2: 20,864,612 (GRCm39) |
|
probably benign |
Het |
Atm |
T |
A |
9: 53,427,644 (GRCm39) |
I489F |
probably benign |
Het |
Carmil1 |
T |
C |
13: 24,323,324 (GRCm39) |
S243G |
probably damaging |
Het |
Cdc42bpg |
T |
C |
19: 6,367,278 (GRCm39) |
V939A |
probably damaging |
Het |
Cel |
A |
C |
2: 28,447,783 (GRCm39) |
L377R |
probably benign |
Het |
Clock |
A |
G |
5: 76,374,832 (GRCm39) |
V779A |
unknown |
Het |
Cluap1 |
G |
A |
16: 3,747,782 (GRCm39) |
|
probably benign |
Het |
Ctif |
A |
T |
18: 75,654,889 (GRCm39) |
H212Q |
probably benign |
Het |
Cyp4a29 |
T |
A |
4: 115,110,129 (GRCm39) |
|
probably benign |
Het |
Cytip |
T |
C |
2: 58,038,258 (GRCm39) |
N101S |
possibly damaging |
Het |
D130043K22Rik |
T |
C |
13: 25,048,798 (GRCm39) |
M434T |
probably benign |
Het |
Ddx47 |
A |
G |
6: 134,994,183 (GRCm39) |
I154V |
possibly damaging |
Het |
Dnah6 |
C |
T |
6: 73,136,098 (GRCm39) |
E1014K |
probably damaging |
Het |
Dnajc27 |
T |
G |
12: 4,156,793 (GRCm39) |
|
probably benign |
Het |
Drc7 |
A |
T |
8: 95,785,756 (GRCm39) |
D204V |
probably damaging |
Het |
Dsc3 |
A |
G |
18: 20,114,298 (GRCm39) |
Y319H |
probably damaging |
Het |
Eml6 |
T |
C |
11: 29,727,441 (GRCm39) |
Q1227R |
probably benign |
Het |
Enpp2 |
A |
T |
15: 54,741,202 (GRCm39) |
D365E |
probably benign |
Het |
Ercc2 |
T |
C |
7: 19,120,633 (GRCm39) |
I199T |
possibly damaging |
Het |
Exd2 |
G |
A |
12: 80,538,014 (GRCm39) |
|
probably benign |
Het |
F2 |
A |
T |
2: 91,463,578 (GRCm39) |
I128N |
probably damaging |
Het |
Fam219b |
T |
C |
9: 57,446,159 (GRCm39) |
L123P |
probably damaging |
Het |
Fasn |
A |
G |
11: 120,710,762 (GRCm39) |
V299A |
possibly damaging |
Het |
Fastkd2 |
T |
C |
1: 63,791,559 (GRCm39) |
V689A |
possibly damaging |
Het |
Fbxw13 |
C |
T |
9: 109,023,789 (GRCm39) |
R85Q |
probably benign |
Het |
Fer1l6 |
A |
G |
15: 58,462,411 (GRCm39) |
Y822C |
probably benign |
Het |
Fhl5 |
T |
C |
4: 25,207,241 (GRCm39) |
T176A |
probably benign |
Het |
Gm20530 |
T |
G |
17: 36,405,118 (GRCm39) |
|
noncoding transcript |
Het |
Gm4787 |
A |
T |
12: 81,425,708 (GRCm39) |
I150N |
probably damaging |
Het |
Grip1 |
G |
A |
10: 119,911,376 (GRCm39) |
S618N |
probably benign |
Het |
Hdac9 |
T |
C |
12: 34,424,110 (GRCm39) |
K454E |
probably damaging |
Het |
Iars2 |
T |
A |
1: 185,019,353 (GRCm39) |
I978F |
possibly damaging |
Het |
Icosl |
A |
G |
10: 77,911,156 (GRCm39) |
Y299C |
probably benign |
Het |
Idi1 |
T |
C |
13: 8,940,393 (GRCm39) |
Y192H |
probably damaging |
Het |
Iqub |
T |
G |
6: 24,454,290 (GRCm39) |
Q531P |
probably damaging |
Het |
Itih4 |
T |
A |
14: 30,612,051 (GRCm39) |
|
probably null |
Het |
Izumo4 |
A |
T |
10: 80,538,770 (GRCm39) |
H71L |
probably damaging |
Het |
Jcad |
A |
T |
18: 4,673,325 (GRCm39) |
E362D |
possibly damaging |
Het |
Kif21a |
G |
T |
15: 90,860,724 (GRCm39) |
|
probably null |
Het |
Kynu |
A |
T |
2: 43,569,893 (GRCm39) |
I392F |
probably damaging |
Het |
Luc7l2 |
A |
G |
6: 38,569,711 (GRCm39) |
E223G |
probably damaging |
Het |
Map3k8 |
A |
C |
18: 4,339,552 (GRCm39) |
L273R |
probably damaging |
Het |
Max |
A |
G |
12: 76,985,361 (GRCm39) |
L119P |
probably benign |
Het |
Mphosph9 |
T |
C |
5: 124,436,892 (GRCm39) |
N484S |
probably benign |
Het |
Mrgprg |
A |
G |
7: 143,318,792 (GRCm39) |
Y107H |
probably damaging |
Het |
Mrps31 |
A |
T |
8: 22,911,354 (GRCm39) |
I199F |
probably benign |
Het |
Mtr |
C |
G |
13: 12,237,040 (GRCm39) |
|
probably null |
Het |
Muc6 |
G |
A |
7: 141,218,313 (GRCm39) |
S2120F |
possibly damaging |
Het |
Nkapd1 |
T |
C |
9: 50,519,222 (GRCm39) |
D130G |
probably damaging |
Het |
Nptx2 |
A |
G |
5: 144,490,460 (GRCm39) |
|
probably benign |
Het |
Nrip1 |
T |
C |
16: 76,089,595 (GRCm39) |
Q654R |
possibly damaging |
Het |
Ocm |
A |
G |
5: 143,961,352 (GRCm39) |
F30L |
probably damaging |
Het |
Oosp1 |
T |
C |
19: 11,668,333 (GRCm39) |
M17V |
probably benign |
Het |
Or14c45 |
C |
T |
7: 86,176,195 (GRCm39) |
P77S |
probably damaging |
Het |
Or4c111 |
G |
A |
2: 88,843,632 (GRCm39) |
R259W |
probably damaging |
Het |
Or4c118 |
A |
C |
2: 88,975,108 (GRCm39) |
Y86* |
probably null |
Het |
Or52ad1 |
G |
T |
7: 102,995,918 (GRCm39) |
D72E |
probably damaging |
Het |
Pax1 |
A |
T |
2: 147,208,067 (GRCm39) |
Y225F |
probably benign |
Het |
Pde4dip |
T |
A |
3: 97,751,028 (GRCm39) |
H62L |
probably benign |
Het |
Pkd1 |
C |
A |
17: 24,804,920 (GRCm39) |
Q3190K |
probably damaging |
Het |
Pkn1 |
A |
C |
8: 84,410,236 (GRCm39) |
|
probably benign |
Het |
Plin5 |
T |
C |
17: 56,422,597 (GRCm39) |
D113G |
probably damaging |
Het |
Ppfia1 |
A |
G |
7: 144,036,082 (GRCm39) |
V1141A |
probably damaging |
Het |
Ppp4r1 |
T |
A |
17: 66,123,001 (GRCm39) |
D334E |
probably benign |
Het |
Ptov1 |
A |
T |
7: 44,512,873 (GRCm39) |
|
probably null |
Het |
Rab22a |
G |
A |
2: 173,503,252 (GRCm39) |
V22M |
probably damaging |
Het |
Rictor |
T |
A |
15: 6,815,852 (GRCm39) |
|
probably null |
Het |
Sart1 |
G |
T |
19: 5,430,559 (GRCm39) |
|
probably benign |
Het |
Scn11a |
G |
A |
9: 119,648,928 (GRCm39) |
A45V |
probably benign |
Het |
Serpina5 |
A |
G |
12: 104,069,459 (GRCm39) |
T224A |
possibly damaging |
Het |
Siglecf |
G |
T |
7: 43,001,825 (GRCm39) |
G212C |
probably damaging |
Het |
Slc38a4 |
A |
T |
15: 96,906,335 (GRCm39) |
M378K |
probably damaging |
Het |
Spata22 |
T |
A |
11: 73,231,275 (GRCm39) |
C176* |
probably null |
Het |
Tmc3 |
G |
A |
7: 83,245,347 (GRCm39) |
E131K |
probably damaging |
Het |
Uvrag |
A |
G |
7: 98,537,180 (GRCm39) |
F672L |
probably benign |
Het |
Vmn1r121 |
A |
G |
7: 20,832,332 (GRCm39) |
V36A |
possibly damaging |
Het |
Vmn1r13 |
A |
T |
6: 57,187,611 (GRCm39) |
M257L |
probably benign |
Het |
Vmn1r58 |
C |
T |
7: 5,413,495 (GRCm39) |
C245Y |
probably damaging |
Het |
Vmn1r86 |
C |
A |
7: 12,836,707 (GRCm39) |
M56I |
probably benign |
Het |
Wdr62 |
T |
C |
7: 29,942,299 (GRCm39) |
Y1051C |
probably benign |
Het |
Xpnpep3 |
A |
G |
15: 81,314,915 (GRCm39) |
D205G |
probably damaging |
Het |
Zdhhc14 |
T |
C |
17: 5,775,611 (GRCm39) |
|
probably benign |
Het |
Zfp607a |
A |
T |
7: 27,578,637 (GRCm39) |
D569V |
possibly damaging |
Het |
Zfp609 |
C |
T |
9: 65,608,470 (GRCm39) |
E1137K |
possibly damaging |
Het |
Zfp871 |
T |
C |
17: 32,993,408 (GRCm39) |
Y589C |
probably damaging |
Het |
Zzef1 |
A |
T |
11: 72,771,450 (GRCm39) |
D1644V |
probably benign |
Het |
|
Other mutations in Trappc10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00329:Trappc10
|
APN |
10 |
78,039,711 (GRCm39) |
splice site |
probably benign |
|
IGL01375:Trappc10
|
APN |
10 |
78,024,733 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01413:Trappc10
|
APN |
10 |
78,033,678 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02413:Trappc10
|
APN |
10 |
78,046,610 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03037:Trappc10
|
APN |
10 |
78,034,869 (GRCm39) |
unclassified |
probably benign |
|
IGL03094:Trappc10
|
APN |
10 |
78,064,754 (GRCm39) |
splice site |
probably benign |
|
IGL03164:Trappc10
|
APN |
10 |
78,056,076 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03351:Trappc10
|
APN |
10 |
78,024,595 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03055:Trappc10
|
UTSW |
10 |
78,050,520 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03098:Trappc10
|
UTSW |
10 |
78,050,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R0605:Trappc10
|
UTSW |
10 |
78,037,331 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1806:Trappc10
|
UTSW |
10 |
78,046,610 (GRCm39) |
missense |
probably damaging |
0.99 |
R1856:Trappc10
|
UTSW |
10 |
78,032,285 (GRCm39) |
missense |
probably benign |
0.00 |
R2045:Trappc10
|
UTSW |
10 |
78,045,313 (GRCm39) |
splice site |
probably benign |
|
R2088:Trappc10
|
UTSW |
10 |
78,032,168 (GRCm39) |
missense |
probably benign |
0.00 |
R2126:Trappc10
|
UTSW |
10 |
78,039,758 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2202:Trappc10
|
UTSW |
10 |
78,034,876 (GRCm39) |
critical splice donor site |
probably null |
|
R2509:Trappc10
|
UTSW |
10 |
78,047,357 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2510:Trappc10
|
UTSW |
10 |
78,047,357 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2511:Trappc10
|
UTSW |
10 |
78,047,357 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2893:Trappc10
|
UTSW |
10 |
78,029,235 (GRCm39) |
missense |
probably benign |
0.00 |
R3744:Trappc10
|
UTSW |
10 |
78,034,924 (GRCm39) |
missense |
probably benign |
0.00 |
R3778:Trappc10
|
UTSW |
10 |
78,036,636 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3876:Trappc10
|
UTSW |
10 |
78,056,020 (GRCm39) |
splice site |
probably null |
|
R3930:Trappc10
|
UTSW |
10 |
78,046,237 (GRCm39) |
missense |
probably benign |
0.03 |
R4078:Trappc10
|
UTSW |
10 |
78,046,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R4111:Trappc10
|
UTSW |
10 |
78,032,264 (GRCm39) |
missense |
probably benign |
0.09 |
R4418:Trappc10
|
UTSW |
10 |
78,053,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R4549:Trappc10
|
UTSW |
10 |
78,067,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R4695:Trappc10
|
UTSW |
10 |
78,033,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R4799:Trappc10
|
UTSW |
10 |
78,037,424 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5022:Trappc10
|
UTSW |
10 |
78,052,994 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5023:Trappc10
|
UTSW |
10 |
78,052,994 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5026:Trappc10
|
UTSW |
10 |
78,040,122 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5057:Trappc10
|
UTSW |
10 |
78,052,994 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5282:Trappc10
|
UTSW |
10 |
78,023,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R5363:Trappc10
|
UTSW |
10 |
78,024,674 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5813:Trappc10
|
UTSW |
10 |
78,058,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R5831:Trappc10
|
UTSW |
10 |
78,045,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Trappc10
|
UTSW |
10 |
78,050,646 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6450:Trappc10
|
UTSW |
10 |
78,045,284 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6520:Trappc10
|
UTSW |
10 |
78,037,287 (GRCm39) |
missense |
probably benign |
0.00 |
R6533:Trappc10
|
UTSW |
10 |
78,024,728 (GRCm39) |
missense |
probably damaging |
0.96 |
R6767:Trappc10
|
UTSW |
10 |
78,029,345 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6798:Trappc10
|
UTSW |
10 |
78,024,665 (GRCm39) |
missense |
probably benign |
0.00 |
R7205:Trappc10
|
UTSW |
10 |
78,046,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R7282:Trappc10
|
UTSW |
10 |
78,043,327 (GRCm39) |
missense |
probably damaging |
0.98 |
R7378:Trappc10
|
UTSW |
10 |
78,029,252 (GRCm39) |
missense |
probably damaging |
0.96 |
R7384:Trappc10
|
UTSW |
10 |
78,045,218 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7770:Trappc10
|
UTSW |
10 |
78,046,679 (GRCm39) |
missense |
probably damaging |
0.96 |
R7829:Trappc10
|
UTSW |
10 |
78,034,909 (GRCm39) |
missense |
probably benign |
|
R7839:Trappc10
|
UTSW |
10 |
78,024,646 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8298:Trappc10
|
UTSW |
10 |
78,038,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R8306:Trappc10
|
UTSW |
10 |
78,036,460 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8814:Trappc10
|
UTSW |
10 |
78,038,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Trappc10
|
UTSW |
10 |
78,043,723 (GRCm39) |
unclassified |
probably benign |
|
R9075:Trappc10
|
UTSW |
10 |
78,040,130 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9112:Trappc10
|
UTSW |
10 |
78,029,201 (GRCm39) |
missense |
probably damaging |
0.99 |
R9182:Trappc10
|
UTSW |
10 |
78,050,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R9444:Trappc10
|
UTSW |
10 |
78,033,612 (GRCm39) |
missense |
probably benign |
0.10 |
R9801:Trappc10
|
UTSW |
10 |
78,045,263 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Trappc10
|
UTSW |
10 |
78,052,987 (GRCm39) |
missense |
probably damaging |
1.00 |
|