Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
T |
C |
2: 35,244,461 (GRCm39) |
E297G |
probably damaging |
Het |
Astn1 |
C |
T |
1: 158,427,950 (GRCm39) |
P707L |
possibly damaging |
Het |
Cep290 |
T |
C |
10: 100,334,936 (GRCm39) |
S319P |
possibly damaging |
Het |
Chrna4 |
A |
C |
2: 180,670,451 (GRCm39) |
L435W |
probably damaging |
Het |
Cilp |
C |
A |
9: 65,187,625 (GRCm39) |
A1240D |
possibly damaging |
Het |
Col17a1 |
A |
G |
19: 47,637,511 (GRCm39) |
F1249S |
possibly damaging |
Het |
Creb3l3 |
T |
C |
10: 80,928,367 (GRCm39) |
|
probably benign |
Het |
Cyp4f40 |
C |
A |
17: 32,894,731 (GRCm39) |
T432N |
probably benign |
Het |
Dsg1c |
T |
G |
18: 20,416,658 (GRCm39) |
I853R |
possibly damaging |
Het |
Ebna1bp2 |
T |
A |
4: 118,478,620 (GRCm39) |
D34E |
probably damaging |
Het |
Edc4 |
C |
T |
8: 106,614,654 (GRCm39) |
T112I |
possibly damaging |
Het |
Enpep |
T |
A |
3: 129,106,227 (GRCm39) |
Y333F |
probably damaging |
Het |
Exoc6 |
A |
G |
19: 37,570,693 (GRCm39) |
H291R |
probably damaging |
Het |
Fbln5 |
G |
T |
12: 101,731,485 (GRCm39) |
N236K |
probably damaging |
Het |
Fndc8 |
A |
T |
11: 82,789,555 (GRCm39) |
T238S |
probably damaging |
Het |
Frem3 |
T |
C |
8: 81,340,917 (GRCm39) |
V1070A |
probably damaging |
Het |
Gabra4 |
A |
T |
5: 71,729,234 (GRCm39) |
N515K |
possibly damaging |
Het |
Gemin5 |
A |
G |
11: 58,013,181 (GRCm39) |
V1422A |
possibly damaging |
Het |
Gm10118 |
A |
G |
10: 63,762,890 (GRCm39) |
|
probably benign |
Het |
Grm5 |
A |
G |
7: 87,252,281 (GRCm39) |
D177G |
probably damaging |
Het |
Gtf2h4 |
G |
A |
17: 35,981,792 (GRCm39) |
P147L |
possibly damaging |
Het |
Hgsnat |
T |
C |
8: 26,453,395 (GRCm39) |
D265G |
probably damaging |
Het |
Hsd17b4 |
T |
A |
18: 50,310,276 (GRCm39) |
L513Q |
probably damaging |
Het |
Hsd17b7 |
A |
T |
1: 169,783,487 (GRCm39) |
M307K |
probably benign |
Het |
Hspa5 |
T |
C |
2: 34,664,629 (GRCm39) |
V361A |
probably damaging |
Het |
Iqgap2 |
A |
G |
13: 95,768,550 (GRCm39) |
V1450A |
probably benign |
Het |
Itprid2 |
T |
A |
2: 79,488,072 (GRCm39) |
D718E |
probably damaging |
Het |
Lama5 |
T |
C |
2: 179,835,467 (GRCm39) |
|
probably benign |
Het |
Manba |
G |
T |
3: 135,230,359 (GRCm39) |
G311* |
probably null |
Het |
Mettl24 |
T |
A |
10: 40,622,486 (GRCm39) |
V236E |
probably benign |
Het |
Myh3 |
A |
G |
11: 66,977,201 (GRCm39) |
D310G |
probably damaging |
Het |
Ncoa4 |
A |
T |
14: 31,888,616 (GRCm39) |
|
probably benign |
Het |
Nop56 |
G |
T |
2: 130,117,902 (GRCm39) |
R126L |
probably damaging |
Het |
Nos3 |
C |
A |
5: 24,573,775 (GRCm39) |
|
probably benign |
Het |
Or13c7b |
T |
C |
4: 43,820,492 (GRCm39) |
M290V |
possibly damaging |
Het |
Pcdhga3 |
T |
A |
18: 37,809,662 (GRCm39) |
V705D |
probably damaging |
Het |
Prom2 |
C |
T |
2: 127,371,331 (GRCm39) |
A776T |
possibly damaging |
Het |
Prss48 |
A |
G |
3: 85,905,492 (GRCm39) |
I127T |
probably damaging |
Het |
Rtca |
T |
C |
3: 116,293,232 (GRCm39) |
Y193C |
possibly damaging |
Het |
Samd9l |
T |
C |
6: 3,376,460 (GRCm39) |
Y267C |
probably damaging |
Het |
Scube3 |
A |
G |
17: 28,379,887 (GRCm39) |
R272G |
possibly damaging |
Het |
Sprr1a |
G |
T |
3: 92,391,951 (GRCm39) |
H17N |
probably benign |
Het |
Stard3 |
G |
C |
11: 98,266,361 (GRCm39) |
Q120H |
probably benign |
Het |
Supt6 |
A |
G |
11: 78,103,574 (GRCm39) |
I1377T |
probably damaging |
Het |
Svop |
A |
T |
5: 114,203,692 (GRCm39) |
S30T |
probably benign |
Het |
Syne2 |
T |
A |
12: 76,119,026 (GRCm39) |
L5882* |
probably null |
Het |
Tanc2 |
G |
T |
11: 105,812,633 (GRCm39) |
R1359L |
probably benign |
Het |
Tmc7 |
A |
C |
7: 118,165,549 (GRCm39) |
L55R |
probably benign |
Het |
Trappc11 |
G |
A |
8: 47,972,613 (GRCm39) |
A320V |
probably benign |
Het |
Ttll8 |
G |
C |
15: 88,818,142 (GRCm39) |
P178A |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,560,993 (GRCm39) |
E20809G |
probably damaging |
Het |
Tubb2a |
A |
T |
13: 34,259,451 (GRCm39) |
V113E |
possibly damaging |
Het |
Ube2d1 |
A |
T |
10: 71,095,699 (GRCm39) |
|
probably benign |
Het |
Usp48 |
T |
C |
4: 137,343,723 (GRCm39) |
V452A |
probably benign |
Het |
Vldlr |
T |
A |
19: 27,217,064 (GRCm39) |
I39N |
probably damaging |
Het |
Wbp1l |
C |
T |
19: 46,642,619 (GRCm39) |
R191* |
probably null |
Het |
Zyg11b |
C |
T |
4: 108,094,577 (GRCm39) |
W669* |
probably null |
Het |
|
Other mutations in Itpr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00715:Itpr3
|
APN |
17 |
27,302,603 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00980:Itpr3
|
APN |
17 |
27,329,930 (GRCm39) |
missense |
probably benign |
|
IGL01151:Itpr3
|
APN |
17 |
27,310,503 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01289:Itpr3
|
APN |
17 |
27,318,739 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01403:Itpr3
|
APN |
17 |
27,337,569 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01666:Itpr3
|
APN |
17 |
27,336,152 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01897:Itpr3
|
APN |
17 |
27,330,236 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02003:Itpr3
|
APN |
17 |
27,340,449 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02012:Itpr3
|
APN |
17 |
27,323,069 (GRCm39) |
missense |
probably benign |
|
IGL02063:Itpr3
|
APN |
17 |
27,338,997 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02146:Itpr3
|
APN |
17 |
27,336,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02158:Itpr3
|
APN |
17 |
27,317,416 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02177:Itpr3
|
APN |
17 |
27,318,588 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02247:Itpr3
|
APN |
17 |
27,317,153 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02606:Itpr3
|
APN |
17 |
27,333,486 (GRCm39) |
splice site |
probably benign |
|
IGL02651:Itpr3
|
APN |
17 |
27,325,372 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02902:Itpr3
|
APN |
17 |
27,323,530 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03001:Itpr3
|
APN |
17 |
27,308,586 (GRCm39) |
splice site |
probably benign |
|
IGL03004:Itpr3
|
APN |
17 |
27,316,952 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03065:Itpr3
|
APN |
17 |
27,310,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03117:Itpr3
|
APN |
17 |
27,338,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03181:Itpr3
|
APN |
17 |
27,330,242 (GRCm39) |
missense |
probably benign |
|
IGL03404:Itpr3
|
APN |
17 |
27,310,492 (GRCm39) |
missense |
probably damaging |
1.00 |
Allure
|
UTSW |
17 |
27,326,277 (GRCm39) |
missense |
probably damaging |
1.00 |
alopecia
|
UTSW |
17 |
27,314,452 (GRCm39) |
missense |
probably damaging |
0.98 |
Beauty
|
UTSW |
17 |
27,325,316 (GRCm39) |
missense |
probably damaging |
1.00 |
Opuesto
|
UTSW |
17 |
27,306,566 (GRCm39) |
missense |
probably damaging |
1.00 |
Paradox
|
UTSW |
17 |
27,317,145 (GRCm39) |
missense |
probably damaging |
1.00 |
Pulchritude
|
UTSW |
17 |
27,305,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R0010:Itpr3
|
UTSW |
17 |
27,339,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Itpr3
|
UTSW |
17 |
27,317,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Itpr3
|
UTSW |
17 |
27,323,034 (GRCm39) |
splice site |
probably benign |
|
R0068:Itpr3
|
UTSW |
17 |
27,323,034 (GRCm39) |
splice site |
probably benign |
|
R0104:Itpr3
|
UTSW |
17 |
27,314,966 (GRCm39) |
missense |
probably benign |
0.01 |
R0195:Itpr3
|
UTSW |
17 |
27,333,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R0212:Itpr3
|
UTSW |
17 |
27,308,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Itpr3
|
UTSW |
17 |
27,332,793 (GRCm39) |
missense |
probably benign |
|
R0485:Itpr3
|
UTSW |
17 |
27,330,903 (GRCm39) |
missense |
probably damaging |
0.98 |
R0501:Itpr3
|
UTSW |
17 |
27,326,263 (GRCm39) |
missense |
probably benign |
0.09 |
R0781:Itpr3
|
UTSW |
17 |
27,329,529 (GRCm39) |
missense |
probably benign |
0.00 |
R0890:Itpr3
|
UTSW |
17 |
27,307,985 (GRCm39) |
nonsense |
probably null |
|
R1028:Itpr3
|
UTSW |
17 |
27,310,343 (GRCm39) |
missense |
probably benign |
0.04 |
R1144:Itpr3
|
UTSW |
17 |
27,333,897 (GRCm39) |
missense |
probably benign |
0.01 |
R1347:Itpr3
|
UTSW |
17 |
27,330,535 (GRCm39) |
missense |
probably benign |
0.02 |
R1347:Itpr3
|
UTSW |
17 |
27,330,535 (GRCm39) |
missense |
probably benign |
0.02 |
R1458:Itpr3
|
UTSW |
17 |
27,337,346 (GRCm39) |
missense |
probably benign |
0.01 |
R1463:Itpr3
|
UTSW |
17 |
27,336,128 (GRCm39) |
splice site |
probably benign |
|
R1472:Itpr3
|
UTSW |
17 |
27,333,199 (GRCm39) |
missense |
probably benign |
0.09 |
R1529:Itpr3
|
UTSW |
17 |
27,324,459 (GRCm39) |
splice site |
probably null |
|
R1533:Itpr3
|
UTSW |
17 |
27,314,534 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1537:Itpr3
|
UTSW |
17 |
27,333,121 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1618:Itpr3
|
UTSW |
17 |
27,335,581 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1672:Itpr3
|
UTSW |
17 |
27,307,987 (GRCm39) |
missense |
probably benign |
|
R1726:Itpr3
|
UTSW |
17 |
27,330,664 (GRCm39) |
missense |
probably damaging |
0.96 |
R1865:Itpr3
|
UTSW |
17 |
27,338,997 (GRCm39) |
missense |
probably benign |
0.01 |
R1940:Itpr3
|
UTSW |
17 |
27,330,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R2023:Itpr3
|
UTSW |
17 |
27,321,785 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2063:Itpr3
|
UTSW |
17 |
27,317,050 (GRCm39) |
missense |
probably benign |
0.19 |
R2064:Itpr3
|
UTSW |
17 |
27,317,050 (GRCm39) |
missense |
probably benign |
0.19 |
R2065:Itpr3
|
UTSW |
17 |
27,317,050 (GRCm39) |
missense |
probably benign |
0.19 |
R2067:Itpr3
|
UTSW |
17 |
27,317,050 (GRCm39) |
missense |
probably benign |
0.19 |
R2068:Itpr3
|
UTSW |
17 |
27,317,050 (GRCm39) |
missense |
probably benign |
0.19 |
R2219:Itpr3
|
UTSW |
17 |
27,334,027 (GRCm39) |
missense |
probably benign |
|
R2248:Itpr3
|
UTSW |
17 |
27,334,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R2291:Itpr3
|
UTSW |
17 |
27,332,553 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2320:Itpr3
|
UTSW |
17 |
27,314,889 (GRCm39) |
missense |
probably benign |
|
R2864:Itpr3
|
UTSW |
17 |
27,310,525 (GRCm39) |
missense |
probably benign |
0.01 |
R2865:Itpr3
|
UTSW |
17 |
27,310,525 (GRCm39) |
missense |
probably benign |
0.01 |
R3778:Itpr3
|
UTSW |
17 |
27,314,446 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3881:Itpr3
|
UTSW |
17 |
27,332,814 (GRCm39) |
missense |
probably benign |
0.01 |
R3979:Itpr3
|
UTSW |
17 |
27,310,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R3979:Itpr3
|
UTSW |
17 |
27,304,105 (GRCm39) |
missense |
probably benign |
0.23 |
R4224:Itpr3
|
UTSW |
17 |
27,326,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R4259:Itpr3
|
UTSW |
17 |
27,325,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R4321:Itpr3
|
UTSW |
17 |
27,330,948 (GRCm39) |
missense |
probably benign |
0.00 |
R4466:Itpr3
|
UTSW |
17 |
27,325,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R4493:Itpr3
|
UTSW |
17 |
27,323,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R4597:Itpr3
|
UTSW |
17 |
27,312,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Itpr3
|
UTSW |
17 |
27,304,121 (GRCm39) |
missense |
probably benign |
0.30 |
R4921:Itpr3
|
UTSW |
17 |
27,316,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Itpr3
|
UTSW |
17 |
27,302,582 (GRCm39) |
missense |
probably damaging |
0.96 |
R5063:Itpr3
|
UTSW |
17 |
27,308,885 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5079:Itpr3
|
UTSW |
17 |
27,317,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R5303:Itpr3
|
UTSW |
17 |
27,335,663 (GRCm39) |
missense |
probably benign |
0.38 |
R5518:Itpr3
|
UTSW |
17 |
27,306,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R5521:Itpr3
|
UTSW |
17 |
27,326,308 (GRCm39) |
missense |
probably benign |
0.09 |
R5566:Itpr3
|
UTSW |
17 |
27,334,926 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5567:Itpr3
|
UTSW |
17 |
27,322,880 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5579:Itpr3
|
UTSW |
17 |
27,332,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R5610:Itpr3
|
UTSW |
17 |
27,337,540 (GRCm39) |
missense |
probably benign |
0.42 |
R5658:Itpr3
|
UTSW |
17 |
27,326,852 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5856:Itpr3
|
UTSW |
17 |
27,325,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Itpr3
|
UTSW |
17 |
27,305,950 (GRCm39) |
missense |
probably benign |
0.02 |
R5878:Itpr3
|
UTSW |
17 |
27,329,836 (GRCm39) |
missense |
probably benign |
0.01 |
R5907:Itpr3
|
UTSW |
17 |
27,336,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R5930:Itpr3
|
UTSW |
17 |
27,329,895 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5987:Itpr3
|
UTSW |
17 |
27,323,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Itpr3
|
UTSW |
17 |
27,317,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R6195:Itpr3
|
UTSW |
17 |
27,305,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R6213:Itpr3
|
UTSW |
17 |
27,330,174 (GRCm39) |
missense |
probably benign |
0.03 |
R6233:Itpr3
|
UTSW |
17 |
27,305,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R6376:Itpr3
|
UTSW |
17 |
27,314,449 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6514:Itpr3
|
UTSW |
17 |
27,310,344 (GRCm39) |
missense |
probably benign |
|
R6515:Itpr3
|
UTSW |
17 |
27,310,344 (GRCm39) |
missense |
probably benign |
|
R6516:Itpr3
|
UTSW |
17 |
27,310,344 (GRCm39) |
missense |
probably benign |
|
R6955:Itpr3
|
UTSW |
17 |
27,340,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R7002:Itpr3
|
UTSW |
17 |
27,329,554 (GRCm39) |
missense |
probably benign |
0.00 |
R7064:Itpr3
|
UTSW |
17 |
27,308,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R7257:Itpr3
|
UTSW |
17 |
27,337,535 (GRCm39) |
missense |
probably benign |
0.00 |
R7349:Itpr3
|
UTSW |
17 |
27,326,786 (GRCm39) |
splice site |
probably null |
|
R7469:Itpr3
|
UTSW |
17 |
27,340,028 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7493:Itpr3
|
UTSW |
17 |
27,313,774 (GRCm39) |
missense |
probably benign |
0.09 |
R7510:Itpr3
|
UTSW |
17 |
27,308,013 (GRCm39) |
missense |
probably damaging |
0.97 |
R7565:Itpr3
|
UTSW |
17 |
27,329,862 (GRCm39) |
missense |
probably benign |
0.01 |
R7616:Itpr3
|
UTSW |
17 |
27,307,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R7728:Itpr3
|
UTSW |
17 |
27,317,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R7779:Itpr3
|
UTSW |
17 |
27,315,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R7788:Itpr3
|
UTSW |
17 |
27,337,571 (GRCm39) |
nonsense |
probably null |
|
R7871:Itpr3
|
UTSW |
17 |
27,336,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R7889:Itpr3
|
UTSW |
17 |
27,335,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R7966:Itpr3
|
UTSW |
17 |
27,331,002 (GRCm39) |
critical splice donor site |
probably null |
|
R8065:Itpr3
|
UTSW |
17 |
27,329,836 (GRCm39) |
missense |
probably benign |
0.01 |
R8067:Itpr3
|
UTSW |
17 |
27,329,836 (GRCm39) |
missense |
probably benign |
0.01 |
R8230:Itpr3
|
UTSW |
17 |
27,326,711 (GRCm39) |
critical splice donor site |
probably null |
|
R8263:Itpr3
|
UTSW |
17 |
27,334,887 (GRCm39) |
nonsense |
probably null |
|
R8264:Itpr3
|
UTSW |
17 |
27,323,086 (GRCm39) |
synonymous |
silent |
|
R8269:Itpr3
|
UTSW |
17 |
27,312,258 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8271:Itpr3
|
UTSW |
17 |
27,306,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R8316:Itpr3
|
UTSW |
17 |
27,325,199 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8354:Itpr3
|
UTSW |
17 |
27,334,893 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8413:Itpr3
|
UTSW |
17 |
27,330,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R8437:Itpr3
|
UTSW |
17 |
27,326,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R8676:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8679:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8846:Itpr3
|
UTSW |
17 |
27,330,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R8884:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8885:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8886:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8887:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8888:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8891:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8896:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8975:Itpr3
|
UTSW |
17 |
27,335,628 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9025:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9026:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9063:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9087:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9088:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9089:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9090:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9091:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9200:Itpr3
|
UTSW |
17 |
27,326,636 (GRCm39) |
missense |
probably damaging |
0.99 |
R9270:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9271:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9294:Itpr3
|
UTSW |
17 |
27,330,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R9389:Itpr3
|
UTSW |
17 |
27,314,899 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9433:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9434:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9443:Itpr3
|
UTSW |
17 |
27,324,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R9472:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9474:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9475:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9476:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9477:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9507:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9508:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9511:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9694:Itpr3
|
UTSW |
17 |
27,334,927 (GRCm39) |
missense |
probably damaging |
0.99 |
R9789:Itpr3
|
UTSW |
17 |
27,308,915 (GRCm39) |
missense |
probably benign |
0.15 |
V7732:Itpr3
|
UTSW |
17 |
27,330,000 (GRCm39) |
splice site |
probably null |
|
V7732:Itpr3
|
UTSW |
17 |
27,329,998 (GRCm39) |
splice site |
probably benign |
|
Z1088:Itpr3
|
UTSW |
17 |
27,332,502 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1177:Itpr3
|
UTSW |
17 |
27,338,961 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Itpr3
|
UTSW |
17 |
27,333,903 (GRCm39) |
missense |
probably damaging |
1.00 |
Z31818:Itpr3
|
UTSW |
17 |
27,314,452 (GRCm39) |
missense |
probably damaging |
0.98 |
|