Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
C |
1: 71,297,257 (GRCm39) |
L2411R |
probably damaging |
Het |
Als2 |
A |
G |
1: 59,245,746 (GRCm39) |
W577R |
probably damaging |
Het |
Aox1 |
C |
A |
1: 58,346,518 (GRCm39) |
R551S |
probably benign |
Het |
Areg |
A |
T |
5: 91,294,577 (GRCm39) |
H245L |
possibly damaging |
Het |
Arhgap35 |
T |
C |
7: 16,297,392 (GRCm39) |
T558A |
possibly damaging |
Het |
Arhgef28 |
A |
T |
13: 98,073,368 (GRCm39) |
C1322* |
probably null |
Het |
Arhgef38 |
T |
C |
3: 132,912,719 (GRCm39) |
R107G |
possibly damaging |
Het |
Atf7ip |
T |
A |
6: 136,548,500 (GRCm39) |
F695L |
probably damaging |
Het |
AW209491 |
C |
T |
13: 14,812,365 (GRCm39) |
A406V |
probably benign |
Het |
Bche |
T |
G |
3: 73,556,011 (GRCm39) |
Q549P |
possibly damaging |
Het |
Blnk |
A |
G |
19: 40,917,733 (GRCm39) |
F417L |
possibly damaging |
Het |
Bloc1s1 |
T |
G |
10: 128,759,255 (GRCm39) |
K17T |
probably damaging |
Het |
C330018D20Rik |
G |
T |
18: 57,090,968 (GRCm39) |
T65K |
probably damaging |
Het |
Ccdc168 |
A |
T |
1: 44,096,417 (GRCm39) |
N1560K |
probably benign |
Het |
Cers1 |
T |
A |
8: 70,774,228 (GRCm39) |
S162T |
possibly damaging |
Het |
Cgn |
T |
C |
3: 94,686,832 (GRCm39) |
K157E |
probably benign |
Het |
Cldn7 |
G |
A |
11: 69,858,494 (GRCm39) |
R196Q |
probably benign |
Het |
Clrn2 |
C |
A |
5: 45,611,369 (GRCm39) |
Q73K |
probably benign |
Het |
Cmss1 |
A |
G |
16: 57,122,608 (GRCm39) |
V262A |
probably benign |
Het |
Cpb2 |
T |
A |
14: 75,498,128 (GRCm39) |
V97E |
probably damaging |
Het |
Ctnnd2 |
G |
A |
15: 30,683,387 (GRCm39) |
V463I |
probably benign |
Het |
Cyp7a1 |
A |
T |
4: 6,268,476 (GRCm39) |
S416R |
probably benign |
Het |
Dip2b |
C |
T |
15: 100,087,960 (GRCm39) |
R965C |
probably damaging |
Het |
Dkk3 |
T |
C |
7: 111,749,865 (GRCm39) |
T102A |
probably benign |
Het |
Dmap1 |
C |
A |
4: 117,538,039 (GRCm39) |
|
probably null |
Het |
Dnah12 |
C |
A |
14: 26,608,828 (GRCm39) |
D3872E |
possibly damaging |
Het |
Dnah7b |
A |
G |
1: 46,158,558 (GRCm39) |
|
probably null |
Het |
Dnai1 |
C |
T |
4: 41,632,391 (GRCm39) |
T575I |
probably benign |
Het |
Dsg1a |
T |
A |
18: 20,464,599 (GRCm39) |
Y365N |
probably damaging |
Het |
Dusp11 |
T |
A |
6: 85,936,215 (GRCm39) |
K18* |
probably null |
Het |
E2f2 |
A |
T |
4: 135,900,245 (GRCm39) |
T52S |
probably benign |
Het |
Elavl4 |
A |
G |
4: 110,147,841 (GRCm39) |
L13S |
probably benign |
Het |
Epor |
T |
C |
9: 21,873,572 (GRCm39) |
D59G |
possibly damaging |
Het |
Eral1 |
A |
G |
11: 77,971,059 (GRCm39) |
C43R |
possibly damaging |
Het |
Fam135b |
A |
G |
15: 71,362,697 (GRCm39) |
V228A |
probably benign |
Het |
Gba1 |
T |
C |
3: 89,113,129 (GRCm39) |
S187P |
probably damaging |
Het |
Gcc2 |
G |
T |
10: 58,091,669 (GRCm39) |
|
probably benign |
Het |
Gdap2 |
C |
A |
3: 100,109,572 (GRCm39) |
|
probably benign |
Het |
Gm10271 |
A |
T |
10: 116,808,497 (GRCm39) |
F6L |
probably damaging |
Het |
Gm10801 |
C |
CGTG |
2: 98,494,152 (GRCm39) |
|
probably null |
Het |
Gpr160 |
T |
C |
3: 30,950,612 (GRCm39) |
L228P |
probably benign |
Het |
Gsdmc2 |
A |
C |
15: 63,702,715 (GRCm39) |
V184G |
probably benign |
Het |
Gtf2e2 |
A |
T |
8: 34,266,080 (GRCm39) |
K252M |
probably damaging |
Het |
Gtf2e2 |
G |
T |
8: 34,266,081 (GRCm39) |
K252N |
probably benign |
Het |
Gys1 |
T |
C |
7: 45,087,529 (GRCm39) |
Y102H |
probably benign |
Het |
H4c2 |
A |
G |
13: 23,941,209 (GRCm39) |
D69G |
probably damaging |
Het |
Ifit3b |
A |
C |
19: 34,589,598 (GRCm39) |
D258A |
probably damaging |
Het |
Kcng4 |
A |
T |
8: 120,353,098 (GRCm39) |
F271I |
probably damaging |
Het |
Klhdc2 |
C |
T |
12: 69,350,387 (GRCm39) |
S144L |
possibly damaging |
Het |
Lhcgr |
A |
G |
17: 89,063,006 (GRCm39) |
F222S |
probably damaging |
Het |
Lrp5 |
C |
G |
19: 3,678,299 (GRCm39) |
G519R |
probably damaging |
Het |
Magel2 |
T |
C |
7: 62,028,515 (GRCm39) |
V473A |
probably benign |
Het |
Map1a |
T |
C |
2: 121,134,776 (GRCm39) |
V1864A |
possibly damaging |
Het |
Mast4 |
T |
A |
13: 102,895,242 (GRCm39) |
Q760H |
probably damaging |
Het |
Mertk |
A |
G |
2: 128,613,294 (GRCm39) |
N437D |
probably benign |
Het |
Mettl18 |
G |
A |
1: 163,824,344 (GRCm39) |
V222I |
probably benign |
Het |
Mical2 |
C |
T |
7: 111,934,155 (GRCm39) |
T782M |
probably benign |
Het |
Mocos |
T |
A |
18: 24,819,750 (GRCm39) |
V664E |
probably damaging |
Het |
Neb |
G |
T |
2: 52,185,306 (GRCm39) |
N975K |
probably benign |
Het |
Nectin3 |
A |
T |
16: 46,284,508 (GRCm39) |
S59T |
probably benign |
Het |
Nelfb |
A |
T |
2: 25,093,900 (GRCm39) |
M11K |
probably damaging |
Het |
Nrp1 |
A |
G |
8: 129,202,650 (GRCm39) |
N545S |
probably damaging |
Het |
Or10ak11 |
T |
C |
4: 118,687,478 (GRCm39) |
D53G |
probably damaging |
Het |
Or2g1 |
T |
A |
17: 38,107,248 (GRCm39) |
N304K |
probably benign |
Het |
Or51b4 |
T |
A |
7: 103,530,907 (GRCm39) |
D181V |
probably damaging |
Het |
Or5b117 |
A |
T |
19: 13,431,324 (GRCm39) |
S186T |
possibly damaging |
Het |
Or5p67 |
T |
A |
7: 107,922,254 (GRCm39) |
T210S |
probably benign |
Het |
Or6c70 |
A |
T |
10: 129,710,390 (GRCm39) |
F79I |
probably damaging |
Het |
Or8g53 |
T |
C |
9: 39,683,836 (GRCm39) |
T87A |
probably benign |
Het |
P3h1 |
A |
G |
4: 119,103,862 (GRCm39) |
H587R |
probably damaging |
Het |
Paqr4 |
A |
G |
17: 23,958,832 (GRCm39) |
|
probably null |
Het |
Pde12 |
A |
G |
14: 26,390,253 (GRCm39) |
V152A |
probably benign |
Het |
Ppip5k1 |
C |
A |
2: 121,180,972 (GRCm39) |
E45* |
probably null |
Het |
Ptch2 |
C |
T |
4: 116,967,254 (GRCm39) |
A677V |
probably benign |
Het |
Rgs12 |
A |
G |
5: 35,177,689 (GRCm39) |
N93S |
probably damaging |
Het |
Rif1 |
C |
G |
2: 51,985,856 (GRCm39) |
L614V |
probably damaging |
Het |
Rnf32 |
T |
C |
5: 29,408,145 (GRCm39) |
S125P |
probably damaging |
Het |
Robo4 |
A |
G |
9: 37,322,696 (GRCm39) |
I850V |
probably damaging |
Het |
Scap |
T |
A |
9: 110,210,219 (GRCm39) |
I876N |
probably damaging |
Het |
Sin3a |
A |
G |
9: 57,034,484 (GRCm39) |
D1219G |
possibly damaging |
Het |
Skint5 |
T |
C |
4: 113,743,005 (GRCm39) |
E354G |
unknown |
Het |
Spart |
A |
G |
3: 55,033,962 (GRCm39) |
D396G |
probably benign |
Het |
Spindoc |
G |
A |
19: 7,351,024 (GRCm39) |
S311L |
probably benign |
Het |
Spta1 |
G |
T |
1: 174,050,894 (GRCm39) |
R1791L |
probably damaging |
Het |
Tbck |
T |
C |
3: 132,507,278 (GRCm39) |
I750T |
possibly damaging |
Het |
Tmem191 |
T |
C |
16: 17,094,334 (GRCm39) |
|
probably null |
Het |
Trgv1 |
A |
T |
13: 19,524,474 (GRCm39) |
Y66F |
probably benign |
Het |
Vmn2r125 |
A |
G |
4: 156,702,292 (GRCm39) |
Y26C |
probably damaging |
Het |
Zbtb17 |
T |
C |
4: 141,192,128 (GRCm39) |
C358R |
possibly damaging |
Het |
Zfp180 |
G |
A |
7: 23,804,859 (GRCm39) |
G426E |
probably damaging |
Het |
Zfp445 |
A |
G |
9: 122,682,951 (GRCm39) |
V330A |
probably benign |
Het |
Zfp595 |
A |
G |
13: 67,465,688 (GRCm39) |
C192R |
probably damaging |
Het |
Zkscan4 |
A |
G |
13: 21,668,623 (GRCm39) |
H387R |
probably damaging |
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 |
R5889:Itpr3
|
UTSW |
17 |
27,334,039 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
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 |
|