Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
C |
T |
17: 24,500,370 (GRCm39) |
V1274M |
probably damaging |
Het |
Abca4 |
A |
G |
3: 121,967,556 (GRCm39) |
H2202R |
possibly damaging |
Het |
Ablim3 |
A |
G |
18: 61,953,463 (GRCm39) |
L350P |
probably benign |
Het |
Adamts17 |
C |
T |
7: 66,654,117 (GRCm39) |
T449I |
probably damaging |
Het |
Ankrd39 |
T |
A |
1: 36,586,241 (GRCm39) |
D9V |
probably benign |
Het |
Arhgef7 |
T |
C |
8: 11,835,819 (GRCm39) |
V192A |
probably damaging |
Het |
Art4 |
C |
T |
6: 136,834,269 (GRCm39) |
|
probably benign |
Het |
Atg4a-ps |
A |
T |
3: 103,553,254 (GRCm39) |
V29E |
possibly damaging |
Het |
Ccdc180 |
A |
T |
4: 45,949,466 (GRCm39) |
K1574* |
probably null |
Het |
Cfap54 |
T |
G |
10: 92,846,882 (GRCm39) |
T1028P |
probably damaging |
Het |
Clip2 |
C |
T |
5: 134,532,254 (GRCm39) |
R517H |
possibly damaging |
Het |
Col5a1 |
A |
G |
2: 27,914,665 (GRCm39) |
T94A |
probably benign |
Het |
Cpne1 |
T |
A |
2: 155,918,210 (GRCm39) |
|
probably null |
Het |
Csnk2a1-ps3 |
A |
T |
1: 156,352,213 (GRCm39) |
Y138F |
probably benign |
Het |
Cyp2f2 |
T |
A |
7: 26,830,667 (GRCm39) |
M346K |
possibly damaging |
Het |
D130040H23Rik |
AAGAATATATTCTACAGAATATA |
AAGAATATA |
8: 69,755,748 (GRCm39) |
|
probably null |
Het |
Ddi2 |
T |
A |
4: 141,419,590 (GRCm39) |
I387F |
probably benign |
Het |
Dsg1b |
A |
G |
18: 20,523,282 (GRCm39) |
N103S |
probably damaging |
Het |
Duxf3 |
GCCC |
GCC |
10: 58,066,944 (GRCm39) |
|
probably null |
Het |
Dysf |
A |
G |
6: 84,156,666 (GRCm39) |
I1464V |
probably benign |
Het |
Epha2 |
A |
G |
4: 141,044,012 (GRCm39) |
Y314C |
possibly damaging |
Het |
Etl4 |
A |
G |
2: 20,782,964 (GRCm39) |
E675G |
probably damaging |
Het |
Fam114a1 |
A |
C |
5: 65,188,733 (GRCm39) |
I488L |
probably benign |
Het |
Fbxo31 |
G |
A |
8: 122,281,136 (GRCm39) |
R337C |
probably damaging |
Het |
Fn1 |
A |
C |
1: 71,647,149 (GRCm39) |
I1547S |
probably null |
Het |
Garre1 |
A |
T |
7: 33,956,770 (GRCm39) |
|
probably null |
Het |
Get1 |
T |
A |
16: 95,954,244 (GRCm39) |
|
probably benign |
Het |
Gm14305 |
T |
A |
2: 176,413,045 (GRCm39) |
Y312* |
probably null |
Het |
Golm2 |
T |
A |
2: 121,756,096 (GRCm39) |
L375Q |
probably damaging |
Het |
Gpihbp1 |
A |
G |
15: 75,469,641 (GRCm39) |
T119A |
possibly damaging |
Het |
Harbi1 |
T |
G |
2: 91,542,980 (GRCm39) |
V147G |
probably damaging |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,899 (GRCm39) |
Y186C |
probably damaging |
Het |
Ighv13-2 |
C |
A |
12: 114,321,494 (GRCm39) |
A82S |
probably benign |
Het |
Krtap4-2 |
C |
T |
11: 99,525,801 (GRCm39) |
G17D |
unknown |
Het |
Ly6a |
A |
T |
15: 74,867,333 (GRCm39) |
|
probably benign |
Het |
Mad1l1 |
C |
T |
5: 140,288,741 (GRCm39) |
E203K |
probably damaging |
Het |
Mapk14 |
C |
A |
17: 28,934,413 (GRCm39) |
D101E |
probably benign |
Het |
Meis3 |
G |
T |
7: 15,917,764 (GRCm39) |
G306W |
probably damaging |
Het |
Mixl1 |
T |
C |
1: 180,524,402 (GRCm39) |
D59G |
probably benign |
Het |
Nav2 |
G |
A |
7: 49,254,293 (GRCm39) |
V2364M |
probably damaging |
Het |
Nell1 |
T |
C |
7: 50,506,150 (GRCm39) |
S786P |
possibly damaging |
Het |
Or13a25 |
T |
G |
7: 140,247,813 (GRCm39) |
N197K |
probably damaging |
Het |
Or51e2 |
C |
A |
7: 102,391,473 (GRCm39) |
V246L |
possibly damaging |
Het |
Or51g1 |
A |
G |
7: 102,633,687 (GRCm39) |
L228P |
probably damaging |
Het |
Or5b107 |
T |
G |
19: 13,143,310 (GRCm39) |
S311A |
probably benign |
Het |
Pcdhgb8 |
A |
T |
18: 37,896,052 (GRCm39) |
D374V |
probably damaging |
Het |
Phactr2 |
A |
G |
10: 13,129,386 (GRCm39) |
I294T |
probably benign |
Het |
Plekha4 |
C |
T |
7: 45,190,492 (GRCm39) |
A400V |
probably damaging |
Het |
Pramel21 |
T |
C |
4: 143,341,760 (GRCm39) |
F63S |
probably damaging |
Het |
Pramel4 |
C |
A |
4: 143,794,928 (GRCm39) |
D441E |
probably benign |
Het |
Prr12 |
G |
A |
7: 44,695,267 (GRCm39) |
P1400S |
unknown |
Het |
Prss3b |
T |
A |
6: 41,010,038 (GRCm39) |
N99Y |
possibly damaging |
Het |
Rbm6 |
G |
A |
9: 107,669,089 (GRCm39) |
Q608* |
probably null |
Het |
Scamp1 |
T |
A |
13: 94,369,598 (GRCm39) |
I76F |
probably benign |
Het |
Sez6 |
G |
A |
11: 77,865,121 (GRCm39) |
E623K |
possibly damaging |
Het |
Sirt1 |
A |
T |
10: 63,158,077 (GRCm39) |
S446T |
probably damaging |
Het |
Slc25a54 |
A |
G |
3: 109,019,404 (GRCm39) |
K336R |
probably benign |
Het |
Spag17 |
G |
T |
3: 99,912,092 (GRCm39) |
V321F |
possibly damaging |
Het |
Sstr1 |
A |
G |
12: 58,259,620 (GRCm39) |
Y81C |
probably damaging |
Het |
St8sia4 |
T |
C |
1: 95,519,525 (GRCm39) |
K321R |
probably damaging |
Het |
Stac3 |
T |
C |
10: 127,343,584 (GRCm39) |
F242S |
probably damaging |
Het |
Tanc2 |
T |
G |
11: 105,758,104 (GRCm39) |
S622A |
probably benign |
Het |
Tcf4 |
G |
A |
18: 69,598,464 (GRCm39) |
D106N |
possibly damaging |
Het |
Tfrc |
T |
A |
16: 32,433,571 (GRCm39) |
I75N |
possibly damaging |
Het |
Tigd2 |
G |
A |
6: 59,187,509 (GRCm39) |
W125* |
probably null |
Het |
Tjp1 |
T |
C |
7: 64,952,745 (GRCm39) |
T1530A |
possibly damaging |
Het |
Tmem132a |
T |
A |
19: 10,844,412 (GRCm39) |
H62L |
probably benign |
Het |
Tmem89 |
T |
C |
9: 108,743,729 (GRCm39) |
S10P |
unknown |
Het |
Trrap |
C |
T |
5: 144,733,961 (GRCm39) |
P938L |
probably damaging |
Het |
Unc80 |
C |
A |
1: 66,545,912 (GRCm39) |
P488T |
probably damaging |
Het |
Uri1 |
C |
A |
7: 37,662,873 (GRCm39) |
G374C |
probably damaging |
Het |
Utp20 |
T |
C |
10: 88,611,180 (GRCm39) |
N1379S |
probably damaging |
Het |
Vcan |
G |
T |
13: 89,852,644 (GRCm39) |
T772K |
probably benign |
Het |
Zbtb37 |
A |
T |
1: 160,847,941 (GRCm39) |
Y355* |
probably null |
Het |
Zfp3 |
A |
G |
11: 70,662,405 (GRCm39) |
I121M |
probably benign |
Het |
Zfp629 |
A |
T |
7: 127,209,547 (GRCm39) |
L754Q |
probably damaging |
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 |
R7014:Itpr1
|
UTSW |
6 |
108,408,459 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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 |
|