Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700036A12Rik |
A |
G |
9: 60,677,043 (GRCm39) |
|
noncoding transcript |
Het |
A430110L20Rik |
T |
A |
1: 181,055,423 (GRCm39) |
|
noncoding transcript |
Het |
Abce1 |
T |
C |
8: 80,433,864 (GRCm39) |
K63R |
possibly damaging |
Het |
Acp6 |
A |
G |
3: 97,081,104 (GRCm39) |
|
probably benign |
Het |
Adamts13 |
T |
A |
2: 26,878,366 (GRCm39) |
L579Q |
probably damaging |
Het |
Adamtsl3 |
T |
A |
7: 82,172,528 (GRCm39) |
M497K |
probably damaging |
Het |
Adgrb2 |
T |
A |
4: 129,908,384 (GRCm39) |
M1042K |
possibly damaging |
Het |
Akap12 |
A |
T |
10: 4,303,693 (GRCm39) |
S168C |
probably damaging |
Het |
Akap3 |
A |
T |
6: 126,842,517 (GRCm39) |
M379L |
probably damaging |
Het |
Aldh6a1 |
C |
T |
12: 84,486,437 (GRCm39) |
M135I |
probably null |
Het |
Arhgef12 |
A |
G |
9: 42,900,294 (GRCm39) |
S860P |
probably damaging |
Het |
Atp11b |
A |
C |
3: 35,843,707 (GRCm39) |
T185P |
probably damaging |
Het |
Bcas1 |
T |
C |
2: 170,229,871 (GRCm39) |
D243G |
probably damaging |
Het |
Cdhr2 |
T |
A |
13: 54,865,685 (GRCm39) |
S228T |
probably damaging |
Het |
Cic |
T |
C |
7: 24,979,162 (GRCm39) |
|
probably benign |
Het |
Cimap1d |
A |
T |
10: 79,481,392 (GRCm39) |
|
probably benign |
Het |
Cmya5 |
T |
A |
13: 93,201,835 (GRCm39) |
I3376L |
probably benign |
Het |
Ctrc |
C |
A |
4: 141,573,535 (GRCm39) |
|
probably null |
Het |
Dchs1 |
G |
T |
7: 105,404,451 (GRCm39) |
P2697Q |
probably damaging |
Het |
Dmbt1 |
A |
G |
7: 130,646,217 (GRCm39) |
|
probably benign |
Het |
Drd2 |
G |
A |
9: 49,313,512 (GRCm39) |
R227H |
probably damaging |
Het |
Dscc1 |
C |
A |
15: 54,950,160 (GRCm39) |
C195F |
probably damaging |
Het |
Dzip1 |
T |
A |
14: 119,160,125 (GRCm39) |
M28L |
probably benign |
Het |
Edar |
A |
T |
10: 58,443,188 (GRCm39) |
S313T |
probably benign |
Het |
Eef1e1 |
C |
A |
13: 38,840,099 (GRCm39) |
A69S |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,143,849 (GRCm39) |
V2760A |
probably benign |
Het |
Fez1 |
GACAAACA |
GACA |
9: 36,781,845 (GRCm39) |
|
probably null |
Het |
Fgl1 |
C |
G |
8: 41,663,496 (GRCm39) |
A11P |
possibly damaging |
Het |
Fras1 |
T |
C |
5: 96,748,592 (GRCm39) |
V689A |
probably benign |
Het |
Fry |
T |
A |
5: 150,304,324 (GRCm39) |
D571E |
probably damaging |
Het |
Gm11232 |
T |
A |
4: 71,675,450 (GRCm39) |
R104* |
probably null |
Het |
Gm1527 |
A |
G |
3: 28,972,199 (GRCm39) |
I439V |
possibly damaging |
Het |
Gm4922 |
C |
A |
10: 18,659,640 (GRCm39) |
G361* |
probably null |
Het |
Gm7052 |
T |
A |
17: 22,259,447 (GRCm39) |
|
probably benign |
Het |
Gpatch8 |
A |
T |
11: 102,372,055 (GRCm39) |
S494R |
unknown |
Het |
Gria2 |
A |
T |
3: 80,639,352 (GRCm39) |
V220E |
possibly damaging |
Het |
Grik4 |
G |
A |
9: 42,432,418 (GRCm39) |
H860Y |
probably benign |
Het |
Gtpbp1 |
A |
C |
15: 79,591,930 (GRCm39) |
S93R |
probably damaging |
Het |
Gucy2g |
C |
A |
19: 55,203,468 (GRCm39) |
|
probably benign |
Het |
H2ac8 |
C |
A |
13: 23,755,221 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,485,451 (GRCm39) |
R4384C |
probably damaging |
Het |
Hspa12b |
G |
C |
2: 130,987,112 (GRCm39) |
A678P |
probably damaging |
Het |
Igsf21 |
T |
A |
4: 139,755,435 (GRCm39) |
N407Y |
probably damaging |
Het |
Insig2 |
A |
G |
1: 121,234,885 (GRCm39) |
Y174H |
probably benign |
Het |
Kalrn |
A |
T |
16: 33,994,857 (GRCm39) |
I1322N |
probably damaging |
Het |
Klk1b24 |
T |
A |
7: 43,840,890 (GRCm39) |
M106K |
possibly damaging |
Het |
Krt81 |
G |
T |
15: 101,358,198 (GRCm39) |
Q352K |
probably benign |
Het |
Lca5l |
A |
T |
16: 95,961,059 (GRCm39) |
S468T |
possibly damaging |
Het |
Lvrn |
T |
C |
18: 47,015,452 (GRCm39) |
|
probably benign |
Het |
Mcpt1 |
T |
A |
14: 56,256,621 (GRCm39) |
|
probably benign |
Het |
Med13l |
T |
C |
5: 118,876,524 (GRCm39) |
M900T |
probably benign |
Het |
Med16 |
A |
G |
10: 79,743,312 (GRCm39) |
|
probably benign |
Het |
Megf6 |
G |
T |
4: 154,261,578 (GRCm39) |
V68L |
probably benign |
Het |
Mep1a |
T |
C |
17: 43,802,563 (GRCm39) |
H154R |
probably damaging |
Het |
Mrc2 |
A |
T |
11: 105,228,598 (GRCm39) |
D659V |
probably benign |
Het |
Mroh8 |
T |
A |
2: 157,063,224 (GRCm39) |
E799V |
probably damaging |
Het |
Mrpl21 |
A |
G |
19: 3,334,808 (GRCm39) |
Y50C |
possibly damaging |
Het |
Msl1 |
A |
G |
11: 98,694,808 (GRCm39) |
|
probably benign |
Het |
Myo1a |
C |
A |
10: 127,555,806 (GRCm39) |
Q932K |
probably benign |
Het |
Nav3 |
A |
C |
10: 109,555,905 (GRCm39) |
S1675R |
probably damaging |
Het |
Neurl2 |
A |
G |
2: 164,674,666 (GRCm39) |
V232A |
possibly damaging |
Het |
Nfatc1 |
T |
A |
18: 80,708,482 (GRCm39) |
|
probably benign |
Het |
Or2w4 |
C |
T |
13: 21,795,992 (GRCm39) |
C49Y |
probably benign |
Het |
Or5k8 |
T |
A |
16: 58,645,039 (GRCm39) |
E11V |
probably null |
Het |
P4hb |
A |
G |
11: 120,453,381 (GRCm39) |
|
probably benign |
Het |
Papss1 |
T |
G |
3: 131,311,615 (GRCm39) |
I281S |
probably damaging |
Het |
Pde10a |
A |
T |
17: 9,183,540 (GRCm39) |
D832V |
probably damaging |
Het |
Pfkfb2 |
A |
T |
1: 130,635,927 (GRCm39) |
Y35N |
possibly damaging |
Het |
Phaf1 |
T |
C |
8: 105,973,188 (GRCm39) |
|
probably null |
Het |
Phf20l1 |
T |
A |
15: 66,476,662 (GRCm39) |
F253Y |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,379,511 (GRCm39) |
V1046I |
probably benign |
Het |
Plin3 |
C |
T |
17: 56,591,337 (GRCm39) |
A148T |
probably benign |
Het |
Ppp1r8 |
T |
C |
4: 132,567,942 (GRCm39) |
|
probably benign |
Het |
Ppp2r3d |
A |
G |
9: 101,088,511 (GRCm39) |
L604P |
probably damaging |
Het |
Prdm5 |
T |
C |
6: 65,860,585 (GRCm39) |
V239A |
probably damaging |
Het |
Prickle1 |
A |
G |
15: 93,398,519 (GRCm39) |
S770P |
probably damaging |
Het |
Prl2c5 |
T |
A |
13: 13,365,310 (GRCm39) |
I155N |
probably benign |
Het |
Prom1 |
T |
C |
5: 44,190,274 (GRCm39) |
|
probably benign |
Het |
Psg25 |
C |
T |
7: 18,263,512 (GRCm39) |
G104R |
probably damaging |
Het |
Rbm19 |
T |
C |
5: 120,282,094 (GRCm39) |
V817A |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,741,908 (GRCm39) |
Y2091F |
probably damaging |
Het |
Slc16a4 |
A |
G |
3: 107,208,248 (GRCm39) |
T253A |
probably benign |
Het |
Smg7 |
A |
T |
1: 152,731,594 (GRCm39) |
|
probably null |
Het |
Spink5 |
C |
A |
18: 44,140,786 (GRCm39) |
H662N |
probably benign |
Het |
Taf2 |
A |
T |
15: 54,923,311 (GRCm39) |
M322K |
probably damaging |
Het |
Tmc2 |
T |
C |
2: 130,090,682 (GRCm39) |
F676S |
probably damaging |
Het |
Tmem177 |
A |
G |
1: 119,837,915 (GRCm39) |
S255P |
possibly damaging |
Het |
Trim46 |
A |
T |
3: 89,142,375 (GRCm39) |
|
probably null |
Het |
Tubb1 |
T |
A |
2: 174,292,596 (GRCm39) |
|
probably null |
Het |
Upf1 |
T |
C |
8: 70,796,904 (GRCm39) |
T110A |
probably benign |
Het |
Vmn2r9 |
T |
A |
5: 108,996,850 (GRCm39) |
I140L |
probably benign |
Het |
Zfp638 |
T |
A |
6: 83,921,638 (GRCm39) |
H588Q |
probably damaging |
Het |
Zfp780b |
T |
A |
7: 27,664,252 (GRCm39) |
N101I |
probably damaging |
Het |
Zpld2 |
T |
C |
4: 133,924,144 (GRCm39) |
D467G |
probably benign |
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 |
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 |
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 |
|