Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
C |
T |
7: 27,278,198 (GRCm39) |
Q156* |
probably null |
Het |
2700097O09Rik |
A |
G |
12: 55,092,727 (GRCm39) |
I264T |
probably benign |
Het |
Arid3a |
G |
T |
10: 79,786,718 (GRCm39) |
M488I |
possibly damaging |
Het |
Auts2 |
A |
G |
5: 131,494,961 (GRCm39) |
F331S |
probably damaging |
Het |
Axdnd1 |
T |
C |
1: 156,158,532 (GRCm39) |
|
probably null |
Het |
Bpifb5 |
C |
A |
2: 154,066,876 (GRCm39) |
S43* |
probably null |
Het |
Carhsp1 |
A |
G |
16: 8,478,869 (GRCm39) |
V128A |
probably benign |
Het |
Ccdc141 |
A |
G |
2: 76,962,641 (GRCm39) |
V101A |
probably damaging |
Het |
Cdk6 |
C |
G |
5: 3,523,152 (GRCm39) |
L191V |
probably damaging |
Het |
Cgnl1 |
T |
G |
9: 71,632,416 (GRCm39) |
K312Q |
possibly damaging |
Het |
Col6a1 |
T |
C |
10: 76,557,277 (GRCm39) |
E225G |
probably damaging |
Het |
Copg1 |
T |
A |
6: 87,879,322 (GRCm39) |
L456Q |
probably damaging |
Het |
Ctif |
T |
A |
18: 75,570,279 (GRCm39) |
D540V |
possibly damaging |
Het |
Cyfip1 |
T |
C |
7: 55,569,241 (GRCm39) |
I917T |
probably benign |
Het |
Cyth1 |
T |
C |
11: 118,103,477 (GRCm39) |
D9G |
probably benign |
Het |
Dnajb1 |
T |
C |
8: 84,336,884 (GRCm39) |
I118T |
probably damaging |
Het |
Ebna1bp2 |
T |
A |
4: 118,480,575 (GRCm39) |
Y139* |
probably null |
Het |
Efcab3 |
A |
G |
11: 104,584,248 (GRCm39) |
T100A |
probably benign |
Het |
Fam162a |
A |
T |
16: 35,870,302 (GRCm39) |
V59E |
probably damaging |
Het |
Fhad1 |
CGG |
CG |
4: 141,645,602 (GRCm39) |
|
probably null |
Het |
Fmo6 |
C |
G |
1: 162,753,877 (GRCm39) |
R112T |
probably benign |
Het |
Gm17087 |
T |
A |
17: 8,785,304 (GRCm39) |
D133V |
probably benign |
Het |
Gm42669 |
A |
G |
5: 107,656,142 (GRCm39) |
I802V |
probably benign |
Het |
Gp2 |
T |
C |
7: 119,050,868 (GRCm39) |
N288D |
probably damaging |
Het |
Gstm7 |
C |
T |
3: 107,834,278 (GRCm39) |
D196N |
probably benign |
Het |
Hsph1 |
A |
T |
5: 149,553,865 (GRCm39) |
V201D |
probably damaging |
Het |
Il20ra |
T |
C |
10: 19,588,458 (GRCm39) |
L26P |
unknown |
Het |
Kcns3 |
A |
T |
12: 11,141,688 (GRCm39) |
I337N |
probably damaging |
Het |
Kdm4d |
A |
G |
9: 14,375,475 (GRCm39) |
Y128H |
probably damaging |
Het |
Kirrel2 |
A |
G |
7: 30,153,999 (GRCm39) |
I200T |
probably benign |
Het |
Klhdc10 |
T |
A |
6: 30,450,502 (GRCm39) |
I294N |
probably damaging |
Het |
Map1a |
A |
C |
2: 121,130,720 (GRCm39) |
N512T |
probably damaging |
Het |
Marchf8 |
C |
G |
6: 116,380,504 (GRCm39) |
C118W |
probably damaging |
Het |
Marchf8 |
T |
G |
6: 116,380,505 (GRCm39) |
C119G |
probably damaging |
Het |
Mrpl38 |
G |
T |
11: 116,025,741 (GRCm39) |
P195Q |
probably damaging |
Het |
Ms4a4d |
A |
T |
19: 11,525,947 (GRCm39) |
Q27L |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,569,532 (GRCm39) |
T996S |
unknown |
Het |
Mug1 |
C |
T |
6: 121,838,084 (GRCm39) |
A438V |
probably benign |
Het |
Mup7 |
T |
A |
4: 60,069,866 (GRCm39) |
I33F |
probably damaging |
Het |
Ndufa5 |
C |
T |
6: 24,519,190 (GRCm39) |
|
probably null |
Het |
Or2b7 |
A |
G |
13: 21,740,108 (GRCm39) |
F28S |
probably benign |
Het |
Or2l5 |
A |
T |
16: 19,334,206 (GRCm39) |
F60Y |
probably benign |
Het |
Or5w17 |
T |
C |
2: 87,584,215 (GRCm39) |
I41V |
probably benign |
Het |
Or5w1b |
A |
T |
2: 87,476,320 (GRCm39) |
L49Q |
probably damaging |
Het |
Or7e177 |
T |
A |
9: 20,211,959 (GRCm39) |
C154* |
probably null |
Het |
Parp9 |
T |
A |
16: 35,780,433 (GRCm39) |
|
probably null |
Het |
Pate8 |
C |
A |
9: 36,493,854 (GRCm39) |
W26C |
unknown |
Het |
Pbx1 |
T |
A |
1: 168,258,949 (GRCm39) |
D42V |
probably damaging |
Het |
Pde4dip |
G |
T |
3: 97,622,738 (GRCm39) |
N1490K |
possibly damaging |
Het |
Pdzd2 |
T |
C |
15: 12,372,647 (GRCm39) |
N2496S |
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,373,061 (GRCm39) |
M2358T |
probably benign |
Het |
Pglyrp2 |
C |
A |
17: 32,634,904 (GRCm39) |
C486F |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,114,931 (GRCm39) |
|
probably benign |
Het |
Pknox2 |
T |
A |
9: 36,820,963 (GRCm39) |
T300S |
probably damaging |
Het |
Plekhm3 |
A |
G |
1: 64,922,429 (GRCm39) |
I582T |
probably damaging |
Het |
Prtg |
T |
C |
9: 72,799,267 (GRCm39) |
Y766H |
possibly damaging |
Het |
Prxl2a |
T |
C |
14: 40,724,451 (GRCm39) |
E71G |
probably benign |
Het |
Rabgap1 |
A |
G |
2: 37,450,575 (GRCm39) |
E901G |
probably benign |
Het |
Rabgap1l |
A |
T |
1: 160,169,642 (GRCm39) |
N60K |
probably damaging |
Het |
Rnf150 |
C |
T |
8: 83,769,292 (GRCm39) |
T359I |
probably benign |
Het |
Rps6ka2 |
C |
T |
17: 7,523,331 (GRCm39) |
H236Y |
probably benign |
Het |
Rrp1b |
T |
A |
17: 32,268,401 (GRCm39) |
L120Q |
probably damaging |
Het |
Scn7a |
C |
A |
2: 66,572,303 (GRCm39) |
G223C |
probably null |
Het |
Sema6a |
T |
A |
18: 47,431,284 (GRCm39) |
N138I |
probably damaging |
Het |
Septin5 |
T |
A |
16: 18,443,659 (GRCm39) |
I97F |
probably damaging |
Het |
Shcbp1 |
T |
A |
8: 4,804,234 (GRCm39) |
E225D |
probably damaging |
Het |
Slc25a19 |
A |
G |
11: 115,511,792 (GRCm39) |
C124R |
probably damaging |
Het |
Slc37a2 |
C |
T |
9: 37,145,183 (GRCm39) |
A428T |
probably damaging |
Het |
Slc5a12 |
A |
G |
2: 110,474,709 (GRCm39) |
I538V |
probably benign |
Het |
Slco4c1 |
A |
T |
1: 96,751,506 (GRCm39) |
|
probably null |
Het |
Smarcad1 |
T |
C |
6: 65,029,654 (GRCm39) |
S81P |
probably damaging |
Het |
Smyd1 |
T |
C |
6: 71,215,611 (GRCm39) |
D116G |
probably damaging |
Het |
Themis |
T |
C |
10: 28,665,703 (GRCm39) |
Y589H |
probably benign |
Het |
Trim30d |
T |
C |
7: 104,132,543 (GRCm39) |
K248R |
probably benign |
Het |
Tspan12 |
C |
T |
6: 21,772,918 (GRCm39) |
M210I |
probably benign |
Het |
Vmn2r11 |
T |
C |
5: 109,201,289 (GRCm39) |
Y405C |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 102,042,775 (GRCm39) |
|
probably null |
Het |
Wiz |
C |
A |
17: 32,580,840 (GRCm39) |
A83S |
probably damaging |
Het |
Zfp1002 |
A |
T |
2: 150,097,182 (GRCm39) |
C82* |
probably null |
Het |
Zmym6 |
T |
A |
4: 127,017,337 (GRCm39) |
Y947* |
probably null |
Het |
|
Other mutations in Itpr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00979:Itpr1
|
APN |
6 |
108,448,081 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01073:Itpr1
|
APN |
6 |
108,390,781 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01105:Itpr1
|
APN |
6 |
108,358,294 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01296:Itpr1
|
APN |
6 |
108,376,322 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01325:Itpr1
|
APN |
6 |
108,358,169 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01418:Itpr1
|
APN |
6 |
108,316,585 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01464:Itpr1
|
APN |
6 |
108,363,688 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01467:Itpr1
|
APN |
6 |
108,465,457 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01645:Itpr1
|
APN |
6 |
108,450,560 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01672:Itpr1
|
APN |
6 |
108,357,993 (GRCm39) |
nonsense |
probably null |
|
IGL01969:Itpr1
|
APN |
6 |
108,354,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02164:Itpr1
|
APN |
6 |
108,366,444 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02206:Itpr1
|
APN |
6 |
108,526,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02232:Itpr1
|
APN |
6 |
108,394,884 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02297:Itpr1
|
APN |
6 |
108,316,478 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02434:Itpr1
|
APN |
6 |
108,466,883 (GRCm39) |
splice site |
probably null |
|
IGL02568:Itpr1
|
APN |
6 |
108,316,515 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02992:Itpr1
|
APN |
6 |
108,358,276 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03109:Itpr1
|
APN |
6 |
108,394,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03130:Itpr1
|
APN |
6 |
108,500,362 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03333:Itpr1
|
APN |
6 |
108,357,871 (GRCm39) |
unclassified |
probably benign |
|
aboriginal
|
UTSW |
6 |
108,492,908 (GRCm39) |
missense |
probably benign |
|
approximation
|
UTSW |
6 |
108,371,802 (GRCm39) |
missense |
probably benign |
|
estimate
|
UTSW |
6 |
108,366,514 (GRCm39) |
missense |
probably null |
1.00 |
icarus
|
UTSW |
6 |
108,387,861 (GRCm39) |
missense |
probably damaging |
1.00 |
marsupialized
|
UTSW |
6 |
108,371,034 (GRCm39) |
splice site |
probably null |
|
primordial
|
UTSW |
6 |
108,495,716 (GRCm39) |
missense |
probably benign |
0.06 |
roo
|
UTSW |
6 |
108,387,828 (GRCm39) |
missense |
probably benign |
0.00 |
wallaby
|
UTSW |
6 |
108,366,348 (GRCm39) |
missense |
probably damaging |
1.00 |
P0005:Itpr1
|
UTSW |
6 |
108,358,218 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4366001:Itpr1
|
UTSW |
6 |
108,470,718 (GRCm39) |
nonsense |
probably null |
|
R0019:Itpr1
|
UTSW |
6 |
108,331,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R0128:Itpr1
|
UTSW |
6 |
108,448,170 (GRCm39) |
splice site |
probably benign |
|
R0129:Itpr1
|
UTSW |
6 |
108,326,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R0135:Itpr1
|
UTSW |
6 |
108,465,443 (GRCm39) |
splice site |
probably benign |
|
R0244:Itpr1
|
UTSW |
6 |
108,450,550 (GRCm39) |
missense |
probably benign |
0.00 |
R0391:Itpr1
|
UTSW |
6 |
108,355,128 (GRCm39) |
missense |
probably benign |
0.22 |
R0543:Itpr1
|
UTSW |
6 |
108,492,709 (GRCm39) |
splice site |
probably benign |
|
R0647:Itpr1
|
UTSW |
6 |
108,360,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Itpr1
|
UTSW |
6 |
108,387,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R0971:Itpr1
|
UTSW |
6 |
108,326,590 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1083:Itpr1
|
UTSW |
6 |
108,487,657 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1277:Itpr1
|
UTSW |
6 |
108,316,582 (GRCm39) |
missense |
probably benign |
0.22 |
R1403:Itpr1
|
UTSW |
6 |
108,366,514 (GRCm39) |
missense |
probably null |
1.00 |
R1403:Itpr1
|
UTSW |
6 |
108,366,514 (GRCm39) |
missense |
probably null |
1.00 |
R1404:Itpr1
|
UTSW |
6 |
108,363,609 (GRCm39) |
missense |
probably benign |
0.04 |
R1404:Itpr1
|
UTSW |
6 |
108,363,609 (GRCm39) |
missense |
probably benign |
0.04 |
R1605:Itpr1
|
UTSW |
6 |
108,326,620 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1661:Itpr1
|
UTSW |
6 |
108,459,858 (GRCm39) |
missense |
probably benign |
0.38 |
R1852:Itpr1
|
UTSW |
6 |
108,363,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Itpr1
|
UTSW |
6 |
108,470,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R2012:Itpr1
|
UTSW |
6 |
108,417,497 (GRCm39) |
missense |
probably benign |
0.02 |
R2027:Itpr1
|
UTSW |
6 |
108,363,814 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2111:Itpr1
|
UTSW |
6 |
108,355,270 (GRCm39) |
unclassified |
probably benign |
|
R2166:Itpr1
|
UTSW |
6 |
108,365,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R2272:Itpr1
|
UTSW |
6 |
108,470,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R2484:Itpr1
|
UTSW |
6 |
108,346,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R3115:Itpr1
|
UTSW |
6 |
108,383,070 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3751:Itpr1
|
UTSW |
6 |
108,326,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R3798:Itpr1
|
UTSW |
6 |
108,358,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R3930:Itpr1
|
UTSW |
6 |
108,371,802 (GRCm39) |
missense |
probably benign |
|
R4081:Itpr1
|
UTSW |
6 |
108,368,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R4119:Itpr1
|
UTSW |
6 |
108,371,316 (GRCm39) |
missense |
probably benign |
|
R4406:Itpr1
|
UTSW |
6 |
108,331,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R4506:Itpr1
|
UTSW |
6 |
108,409,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R4616:Itpr1
|
UTSW |
6 |
108,458,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R4655:Itpr1
|
UTSW |
6 |
108,458,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R4661:Itpr1
|
UTSW |
6 |
108,387,892 (GRCm39) |
critical splice donor site |
probably null |
|
R4760:Itpr1
|
UTSW |
6 |
108,326,593 (GRCm39) |
missense |
probably benign |
0.29 |
R4836:Itpr1
|
UTSW |
6 |
108,366,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R4857:Itpr1
|
UTSW |
6 |
108,387,828 (GRCm39) |
missense |
probably benign |
0.00 |
R4876:Itpr1
|
UTSW |
6 |
108,459,867 (GRCm39) |
missense |
probably damaging |
0.97 |
R4939:Itpr1
|
UTSW |
6 |
108,417,519 (GRCm39) |
nonsense |
probably null |
|
R5076:Itpr1
|
UTSW |
6 |
108,382,490 (GRCm39) |
splice site |
probably null |
|
R5088:Itpr1
|
UTSW |
6 |
108,366,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R5248:Itpr1
|
UTSW |
6 |
108,519,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R5290:Itpr1
|
UTSW |
6 |
108,383,106 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5308:Itpr1
|
UTSW |
6 |
108,333,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Itpr1
|
UTSW |
6 |
108,370,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R5368:Itpr1
|
UTSW |
6 |
108,364,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R5369:Itpr1
|
UTSW |
6 |
108,496,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R5419:Itpr1
|
UTSW |
6 |
108,470,755 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5615:Itpr1
|
UTSW |
6 |
108,465,561 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5779:Itpr1
|
UTSW |
6 |
108,329,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R5781:Itpr1
|
UTSW |
6 |
108,487,699 (GRCm39) |
missense |
probably benign |
0.23 |
R5869:Itpr1
|
UTSW |
6 |
108,450,490 (GRCm39) |
missense |
probably benign |
0.30 |
R5903:Itpr1
|
UTSW |
6 |
108,466,758 (GRCm39) |
intron |
probably benign |
|
R5929:Itpr1
|
UTSW |
6 |
108,400,297 (GRCm39) |
missense |
probably benign |
|
R5956:Itpr1
|
UTSW |
6 |
108,482,988 (GRCm39) |
missense |
probably benign |
0.25 |
R6160:Itpr1
|
UTSW |
6 |
108,495,716 (GRCm39) |
missense |
probably benign |
0.06 |
R6163:Itpr1
|
UTSW |
6 |
108,365,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Itpr1
|
UTSW |
6 |
108,346,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R6237:Itpr1
|
UTSW |
6 |
108,355,164 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6398:Itpr1
|
UTSW |
6 |
108,482,864 (GRCm39) |
missense |
probably damaging |
0.96 |
R6455:Itpr1
|
UTSW |
6 |
108,394,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R6522:Itpr1
|
UTSW |
6 |
108,365,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Itpr1
|
UTSW |
6 |
108,340,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R6650:Itpr1
|
UTSW |
6 |
108,371,034 (GRCm39) |
splice site |
probably null |
|
R6806:Itpr1
|
UTSW |
6 |
108,492,908 (GRCm39) |
missense |
probably benign |
|
R6838:Itpr1
|
UTSW |
6 |
108,448,152 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6841:Itpr1
|
UTSW |
6 |
108,365,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R6896:Itpr1
|
UTSW |
6 |
108,458,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R7076:Itpr1
|
UTSW |
6 |
108,365,257 (GRCm39) |
missense |
probably benign |
|
R7116:Itpr1
|
UTSW |
6 |
108,458,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R7152:Itpr1
|
UTSW |
6 |
108,371,368 (GRCm39) |
critical splice donor site |
probably null |
|
R7161:Itpr1
|
UTSW |
6 |
108,363,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R7166:Itpr1
|
UTSW |
6 |
108,355,151 (GRCm39) |
missense |
probably benign |
0.06 |
R7241:Itpr1
|
UTSW |
6 |
108,494,581 (GRCm39) |
critical splice donor site |
probably null |
|
R7301:Itpr1
|
UTSW |
6 |
108,518,985 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7330:Itpr1
|
UTSW |
6 |
108,415,292 (GRCm39) |
missense |
probably benign |
0.28 |
R7449:Itpr1
|
UTSW |
6 |
108,366,345 (GRCm39) |
missense |
probably damaging |
0.98 |
R7472:Itpr1
|
UTSW |
6 |
108,380,357 (GRCm39) |
missense |
probably benign |
0.05 |
R7502:Itpr1
|
UTSW |
6 |
108,360,639 (GRCm39) |
missense |
probably benign |
0.00 |
R7779:Itpr1
|
UTSW |
6 |
108,500,309 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7828:Itpr1
|
UTSW |
6 |
108,459,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R7854:Itpr1
|
UTSW |
6 |
108,364,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Itpr1
|
UTSW |
6 |
108,500,366 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7998:Itpr1
|
UTSW |
6 |
108,394,909 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8039:Itpr1
|
UTSW |
6 |
108,363,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R8136:Itpr1
|
UTSW |
6 |
108,415,321 (GRCm39) |
missense |
probably benign |
0.18 |
R8200:Itpr1
|
UTSW |
6 |
108,371,826 (GRCm39) |
missense |
probably benign |
0.00 |
R8242:Itpr1
|
UTSW |
6 |
108,363,658 (GRCm39) |
missense |
probably benign |
0.44 |
R8322:Itpr1
|
UTSW |
6 |
108,365,190 (GRCm39) |
missense |
probably benign |
0.05 |
R8377:Itpr1
|
UTSW |
6 |
108,487,699 (GRCm39) |
missense |
probably benign |
0.00 |
R8412:Itpr1
|
UTSW |
6 |
108,340,581 (GRCm39) |
missense |
probably benign |
0.07 |
R8443:Itpr1
|
UTSW |
6 |
108,496,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R8669:Itpr1
|
UTSW |
6 |
108,370,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R8697:Itpr1
|
UTSW |
6 |
108,500,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R8744:Itpr1
|
UTSW |
6 |
108,354,763 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8870:Itpr1
|
UTSW |
6 |
108,365,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R8921:Itpr1
|
UTSW |
6 |
108,355,159 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8961:Itpr1
|
UTSW |
6 |
108,470,666 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9095:Itpr1
|
UTSW |
6 |
108,364,352 (GRCm39) |
missense |
probably benign |
0.02 |
R9205:Itpr1
|
UTSW |
6 |
108,466,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R9282:Itpr1
|
UTSW |
6 |
108,370,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9323:Itpr1
|
UTSW |
6 |
108,328,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R9376:Itpr1
|
UTSW |
6 |
108,326,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R9392:Itpr1
|
UTSW |
6 |
108,390,837 (GRCm39) |
missense |
probably benign |
|
R9428:Itpr1
|
UTSW |
6 |
108,378,308 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9621:Itpr1
|
UTSW |
6 |
108,393,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Itpr1
|
UTSW |
6 |
108,382,481 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9646:Itpr1
|
UTSW |
6 |
108,371,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R9695:Itpr1
|
UTSW |
6 |
108,378,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R9710:Itpr1
|
UTSW |
6 |
108,382,481 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9721:Itpr1
|
UTSW |
6 |
108,383,063 (GRCm39) |
missense |
probably damaging |
0.96 |
R9780:Itpr1
|
UTSW |
6 |
108,487,795 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Itpr1
|
UTSW |
6 |
108,476,110 (GRCm39) |
missense |
probably damaging |
1.00 |
|