Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330161L09Rik |
T |
C |
12: 103,373,848 (GRCm39) |
|
probably benign |
Het |
Abca2 |
A |
T |
2: 25,327,517 (GRCm39) |
I669F |
possibly damaging |
Het |
Adam9 |
C |
T |
8: 25,472,142 (GRCm39) |
|
probably benign |
Het |
Adprhl1 |
A |
G |
8: 13,298,694 (GRCm39) |
Y79H |
probably damaging |
Het |
Akp3 |
A |
T |
1: 87,054,607 (GRCm39) |
|
probably null |
Het |
Alpk2 |
T |
C |
18: 65,482,845 (GRCm39) |
S388G |
probably benign |
Het |
Amph |
G |
A |
13: 19,300,436 (GRCm39) |
|
probably benign |
Het |
Arr3 |
T |
A |
X: 99,658,247 (GRCm39) |
F269L |
possibly damaging |
Het |
Atp2a2 |
A |
G |
5: 122,597,609 (GRCm39) |
F808S |
probably damaging |
Het |
Baz1a |
T |
A |
12: 54,958,170 (GRCm39) |
N1027I |
probably damaging |
Het |
C2cd4c |
G |
T |
10: 79,448,255 (GRCm39) |
H297Q |
probably damaging |
Het |
Calr3 |
T |
A |
8: 73,181,112 (GRCm39) |
D160V |
probably damaging |
Het |
Cdc42ep1 |
C |
T |
15: 78,731,692 (GRCm39) |
R46C |
probably damaging |
Het |
Cdh23 |
G |
T |
10: 60,141,362 (GRCm39) |
F3127L |
probably damaging |
Het |
Cfhr4 |
T |
A |
1: 139,702,417 (GRCm39) |
|
probably benign |
Het |
Cps1 |
T |
A |
1: 67,216,139 (GRCm39) |
D821E |
probably benign |
Het |
Cyp2e1 |
C |
A |
7: 140,353,547 (GRCm39) |
T328K |
probably damaging |
Het |
Dcp1a |
T |
C |
14: 30,241,327 (GRCm39) |
V379A |
probably benign |
Het |
Dst |
T |
C |
1: 34,208,259 (GRCm39) |
S737P |
probably damaging |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
Eci2 |
A |
G |
13: 35,174,699 (GRCm39) |
|
probably null |
Het |
Ercc6l2 |
A |
G |
13: 63,982,563 (GRCm39) |
T126A |
probably damaging |
Het |
Fgf6 |
T |
C |
6: 126,992,723 (GRCm39) |
S59P |
probably damaging |
Het |
Fmnl2 |
A |
G |
2: 52,995,549 (GRCm39) |
E424G |
probably damaging |
Het |
Gapvd1 |
G |
T |
2: 34,574,329 (GRCm39) |
A1256D |
probably benign |
Het |
Gcfc2 |
C |
A |
6: 81,900,759 (GRCm39) |
D24E |
probably benign |
Het |
Gigyf2 |
A |
G |
1: 87,368,452 (GRCm39) |
H1044R |
probably damaging |
Het |
Gk2 |
T |
C |
5: 97,604,164 (GRCm39) |
I225V |
probably benign |
Het |
Gm3944 |
C |
A |
12: 18,903,895 (GRCm39) |
S8* |
probably null |
Het |
Gnl3l |
A |
G |
X: 149,780,290 (GRCm39) |
S217P |
probably damaging |
Het |
Gpr156 |
A |
G |
16: 37,799,113 (GRCm39) |
D109G |
probably benign |
Het |
Hoxd1 |
A |
T |
2: 74,593,710 (GRCm39) |
T89S |
probably benign |
Het |
Ift172 |
G |
A |
5: 31,443,423 (GRCm39) |
T112M |
probably benign |
Het |
Igkv1-115 |
C |
A |
6: 68,138,613 (GRCm39) |
S72* |
probably null |
Het |
Ildr1 |
A |
G |
16: 36,542,341 (GRCm39) |
E247G |
probably damaging |
Het |
Insr |
A |
G |
8: 3,219,748 (GRCm39) |
S925P |
probably benign |
Het |
Khdrbs3 |
C |
T |
15: 68,896,673 (GRCm39) |
T111I |
probably benign |
Het |
Mageb3 |
A |
G |
2: 121,785,306 (GRCm39) |
|
probably null |
Het |
Mcf2l |
A |
T |
8: 13,051,867 (GRCm39) |
K433N |
probably damaging |
Het |
Mdn1 |
A |
G |
4: 32,700,409 (GRCm39) |
E1456G |
probably damaging |
Het |
Mta1 |
C |
T |
12: 113,095,248 (GRCm39) |
T467I |
probably damaging |
Het |
Mtr |
A |
T |
13: 12,259,487 (GRCm39) |
I196N |
possibly damaging |
Het |
Mtus1 |
G |
T |
8: 41,475,608 (GRCm39) |
P819T |
probably damaging |
Het |
Myh1 |
G |
A |
11: 67,105,446 (GRCm39) |
D1079N |
possibly damaging |
Het |
Nav1 |
C |
T |
1: 135,376,742 (GRCm39) |
R1694Q |
probably damaging |
Het |
Neb |
A |
G |
2: 52,174,275 (GRCm39) |
I1528T |
probably benign |
Het |
Nek1 |
T |
A |
8: 61,577,360 (GRCm39) |
|
probably null |
Het |
Nes |
A |
G |
3: 87,884,618 (GRCm39) |
E915G |
probably benign |
Het |
Nlrp4f |
T |
C |
13: 65,347,167 (GRCm39) |
I30M |
probably benign |
Het |
Nup153 |
A |
G |
13: 46,837,404 (GRCm39) |
S1273P |
probably benign |
Het |
Nup155 |
A |
G |
15: 8,150,951 (GRCm39) |
I334V |
probably benign |
Het |
Or10j2 |
A |
T |
1: 173,097,879 (GRCm39) |
M46L |
probably benign |
Het |
Or1e1f |
A |
G |
11: 73,855,740 (GRCm39) |
Y102C |
probably damaging |
Het |
Or5b3 |
G |
A |
19: 13,388,307 (GRCm39) |
A125T |
probably damaging |
Het |
Or5d41 |
A |
G |
2: 88,054,818 (GRCm39) |
V186A |
possibly damaging |
Het |
Or6d13 |
T |
C |
6: 116,517,611 (GRCm39) |
Y66H |
possibly damaging |
Het |
Or8b46 |
T |
A |
9: 38,450,576 (GRCm39) |
N128K |
probably benign |
Het |
Or8k38 |
G |
T |
2: 86,488,781 (GRCm39) |
T7K |
probably damaging |
Het |
Parn |
G |
A |
16: 13,420,933 (GRCm39) |
S473L |
probably damaging |
Het |
Pcnt |
T |
C |
10: 76,256,360 (GRCm39) |
K627E |
probably damaging |
Het |
Pja2 |
T |
A |
17: 64,597,031 (GRCm39) |
D553V |
probably damaging |
Het |
Prune2 |
T |
C |
19: 17,185,602 (GRCm39) |
F3004L |
probably damaging |
Het |
Rasgrp3 |
T |
C |
17: 75,807,753 (GRCm39) |
|
probably null |
Het |
Rdh13 |
A |
G |
7: 4,448,482 (GRCm39) |
V10A |
probably benign |
Het |
Rimbp2 |
T |
C |
5: 128,850,565 (GRCm39) |
Y906C |
probably damaging |
Het |
Ripor1 |
T |
C |
8: 106,341,344 (GRCm39) |
F59S |
probably damaging |
Het |
Rnf185 |
T |
C |
11: 3,382,393 (GRCm39) |
|
probably benign |
Het |
Runx3 |
T |
C |
4: 134,882,627 (GRCm39) |
V107A |
probably damaging |
Het |
Scn3b |
T |
C |
9: 40,193,741 (GRCm39) |
V156A |
probably benign |
Het |
Serpina3a |
G |
A |
12: 104,082,481 (GRCm39) |
A85T |
probably damaging |
Het |
Slc12a7 |
C |
T |
13: 73,933,274 (GRCm39) |
R111* |
probably null |
Het |
Slc5a5 |
A |
T |
8: 71,342,395 (GRCm39) |
|
probably null |
Het |
Snx13 |
A |
T |
12: 35,188,084 (GRCm39) |
L787F |
probably damaging |
Het |
Spef2 |
A |
T |
15: 9,589,659 (GRCm39) |
M1535K |
probably damaging |
Het |
Sphkap |
T |
G |
1: 83,253,602 (GRCm39) |
K1382N |
probably benign |
Het |
Tagap1 |
A |
G |
17: 7,224,259 (GRCm39) |
S146P |
probably benign |
Het |
Tagln3 |
A |
G |
16: 45,531,957 (GRCm39) |
Y192H |
probably damaging |
Het |
Tbc1d15 |
A |
C |
10: 115,076,819 (GRCm39) |
S22A |
possibly damaging |
Het |
Tbc1d31 |
A |
G |
15: 57,796,040 (GRCm39) |
E211G |
probably benign |
Het |
Tmod3 |
A |
G |
9: 75,416,645 (GRCm39) |
V229A |
probably damaging |
Het |
Ubr2 |
A |
G |
17: 47,274,071 (GRCm39) |
|
probably null |
Het |
Ugt2b36 |
T |
C |
5: 87,240,100 (GRCm39) |
E95G |
probably benign |
Het |
Unc45b |
G |
A |
11: 82,802,515 (GRCm39) |
A4T |
probably benign |
Het |
Usp40 |
A |
G |
1: 87,877,936 (GRCm39) |
I1117T |
probably benign |
Het |
Vcan |
T |
A |
13: 89,841,422 (GRCm39) |
D414V |
probably damaging |
Het |
Xrn1 |
C |
A |
9: 95,921,885 (GRCm39) |
H1433N |
probably benign |
Het |
Zfp353-ps |
T |
A |
8: 42,536,005 (GRCm39) |
|
noncoding transcript |
Het |
Zfp74 |
G |
A |
7: 29,634,443 (GRCm39) |
Q422* |
probably null |
Het |
Zmym3 |
A |
T |
X: 100,450,993 (GRCm39) |
V1208D |
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 |
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 |
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 |
|