Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
T |
C |
17: 9,207,255 (GRCm39) |
|
probably null |
Het |
Abca13 |
G |
A |
11: 9,278,207 (GRCm39) |
G3129D |
possibly damaging |
Het |
Acnat2 |
T |
C |
4: 49,383,534 (GRCm39) |
I6M |
probably benign |
Het |
Adcy4 |
T |
A |
14: 56,012,029 (GRCm39) |
|
probably null |
Het |
Agrn |
A |
G |
4: 156,258,012 (GRCm39) |
S1117P |
probably damaging |
Het |
Anks1b |
A |
G |
10: 90,195,057 (GRCm39) |
N545S |
probably benign |
Het |
Antxr1 |
C |
T |
6: 87,246,220 (GRCm39) |
|
probably null |
Het |
Arhgef17 |
T |
C |
7: 100,529,828 (GRCm39) |
K476E |
probably damaging |
Het |
Cacna1s |
C |
T |
1: 136,041,132 (GRCm39) |
T1286I |
probably benign |
Het |
Ccdc174 |
T |
A |
6: 91,872,247 (GRCm39) |
M292K |
probably benign |
Het |
Cdk5rap2 |
G |
A |
4: 70,328,506 (GRCm39) |
|
probably benign |
Het |
Celsr3 |
T |
A |
9: 108,706,272 (GRCm39) |
Y918* |
probably null |
Het |
Cep250 |
T |
C |
2: 155,806,894 (GRCm39) |
|
probably benign |
Het |
Ces2h |
A |
G |
8: 105,746,903 (GRCm39) |
D513G |
possibly damaging |
Het |
Clec2l |
A |
G |
6: 38,640,327 (GRCm39) |
T53A |
probably benign |
Het |
Cntnap2 |
C |
T |
6: 45,692,750 (GRCm39) |
S77L |
probably benign |
Het |
Cped1 |
A |
T |
6: 22,016,957 (GRCm39) |
H102L |
probably benign |
Het |
Crim1 |
T |
A |
17: 78,680,008 (GRCm39) |
D916E |
probably benign |
Het |
Csmd1 |
T |
A |
8: 16,283,115 (GRCm39) |
I614F |
probably damaging |
Het |
Csnk1g1 |
G |
A |
9: 65,917,751 (GRCm39) |
E37K |
probably damaging |
Het |
Ctnnbl1 |
T |
A |
2: 157,713,110 (GRCm39) |
|
probably null |
Het |
Cuzd1 |
A |
T |
7: 130,911,601 (GRCm39) |
|
probably benign |
Het |
Cyp4f16 |
T |
A |
17: 32,769,525 (GRCm39) |
V433D |
probably damaging |
Het |
Ddi1 |
A |
G |
9: 6,266,144 (GRCm39) |
L75P |
probably damaging |
Het |
Ddias |
G |
A |
7: 92,508,736 (GRCm39) |
A393V |
probably benign |
Het |
Dgka |
A |
T |
10: 128,569,990 (GRCm39) |
Y123* |
probably null |
Het |
Dlgap1 |
T |
C |
17: 70,823,185 (GRCm39) |
C57R |
probably benign |
Het |
Dysf |
T |
A |
6: 84,129,387 (GRCm39) |
V1458D |
probably benign |
Het |
Eif2ak4 |
T |
A |
2: 118,292,828 (GRCm39) |
Y1230N |
probably damaging |
Het |
Fbxl7 |
A |
T |
15: 26,543,632 (GRCm39) |
S338R |
probably benign |
Het |
Fgf23 |
A |
T |
6: 127,050,122 (GRCm39) |
T44S |
probably damaging |
Het |
Fhip1b |
G |
A |
7: 105,033,419 (GRCm39) |
P599L |
possibly damaging |
Het |
Folh1 |
A |
T |
7: 86,395,309 (GRCm39) |
|
probably benign |
Het |
Gpsm2 |
A |
T |
3: 108,609,710 (GRCm39) |
|
probably benign |
Het |
H2bc13 |
A |
G |
13: 21,900,295 (GRCm39) |
|
probably benign |
Het |
Hdac2 |
T |
A |
10: 36,865,130 (GRCm39) |
|
probably benign |
Het |
Il31ra |
G |
T |
13: 112,664,015 (GRCm39) |
T446N |
possibly damaging |
Het |
Irf5 |
T |
A |
6: 29,535,369 (GRCm39) |
L199H |
probably benign |
Het |
Kif18a |
T |
A |
2: 109,118,188 (GRCm39) |
M1K |
probably null |
Het |
Kif4-ps |
A |
C |
12: 101,114,921 (GRCm39) |
I1017L |
probably benign |
Het |
Klhl2 |
C |
T |
8: 65,211,164 (GRCm39) |
V295M |
probably benign |
Het |
Krt75 |
A |
T |
15: 101,478,746 (GRCm39) |
M296K |
probably benign |
Het |
Krt81 |
C |
A |
15: 101,361,508 (GRCm39) |
R24L |
possibly damaging |
Het |
Lgr4 |
T |
C |
2: 109,838,437 (GRCm39) |
S439P |
probably damaging |
Het |
Lhfpl2 |
C |
A |
13: 94,311,118 (GRCm39) |
N129K |
probably damaging |
Het |
Lnx2 |
A |
G |
5: 146,955,771 (GRCm39) |
V675A |
probably damaging |
Het |
Med13 |
T |
C |
11: 86,175,977 (GRCm39) |
T1673A |
probably benign |
Het |
Mif |
A |
G |
10: 75,695,974 (GRCm39) |
V10A |
possibly damaging |
Het |
Mki67 |
A |
T |
7: 135,301,158 (GRCm39) |
I1292N |
possibly damaging |
Het |
Mylip |
C |
A |
13: 45,558,059 (GRCm39) |
N89K |
probably benign |
Het |
Myo19 |
G |
T |
11: 84,800,245 (GRCm39) |
D877Y |
probably benign |
Het |
Nckap5 |
A |
G |
1: 125,954,102 (GRCm39) |
S753P |
possibly damaging |
Het |
Nlrc3 |
T |
C |
16: 3,783,056 (GRCm39) |
T118A |
possibly damaging |
Het |
Nptx2 |
T |
C |
5: 144,490,269 (GRCm39) |
Y233H |
probably damaging |
Het |
Nsl1 |
T |
A |
1: 190,795,237 (GRCm39) |
M1K |
probably null |
Het |
Ntsr1 |
T |
A |
2: 180,142,849 (GRCm39) |
S213R |
possibly damaging |
Het |
Or4c120 |
A |
T |
2: 89,000,975 (GRCm39) |
F194I |
probably benign |
Het |
Or4c58 |
A |
G |
2: 89,674,513 (GRCm39) |
V268A |
probably benign |
Het |
Or52n5 |
T |
A |
7: 104,588,021 (GRCm39) |
F96Y |
possibly damaging |
Het |
Pde4d |
G |
A |
13: 110,073,244 (GRCm39) |
V347I |
probably benign |
Het |
Pik3r4 |
T |
A |
9: 105,546,244 (GRCm39) |
S865T |
probably benign |
Het |
Ppp2r2d |
A |
G |
7: 138,472,160 (GRCm39) |
R136G |
probably benign |
Het |
Proser2 |
A |
C |
2: 6,118,721 (GRCm39) |
S41A |
probably damaging |
Het |
Proz |
A |
T |
8: 13,123,460 (GRCm39) |
K244* |
probably null |
Het |
Prpf38b |
A |
T |
3: 108,812,586 (GRCm39) |
L209H |
probably damaging |
Het |
R3hdm1 |
C |
A |
1: 128,112,254 (GRCm39) |
A390E |
probably benign |
Het |
Rb1cc1 |
A |
C |
1: 6,310,547 (GRCm39) |
D315A |
probably damaging |
Het |
Rnf141 |
G |
A |
7: 110,436,345 (GRCm39) |
R28* |
probably null |
Het |
Rps6kc1 |
A |
T |
1: 190,531,627 (GRCm39) |
S792T |
probably benign |
Het |
Rxrg |
A |
G |
1: 167,458,606 (GRCm39) |
D233G |
possibly damaging |
Het |
Sh2d7 |
A |
G |
9: 54,448,321 (GRCm39) |
N114S |
probably benign |
Het |
Slc25a38 |
T |
C |
9: 119,949,899 (GRCm39) |
V205A |
probably benign |
Het |
Slc4a10 |
T |
C |
2: 62,127,361 (GRCm39) |
|
probably benign |
Het |
Spred1 |
T |
A |
2: 116,983,459 (GRCm39) |
|
probably null |
Het |
Stt3b |
A |
G |
9: 115,077,635 (GRCm39) |
S706P |
probably benign |
Het |
Tcerg1 |
C |
A |
18: 42,697,305 (GRCm39) |
|
probably benign |
Het |
Tent5a |
T |
C |
9: 85,207,108 (GRCm39) |
Y230C |
probably damaging |
Het |
Thsd4 |
A |
T |
9: 59,910,261 (GRCm39) |
I109N |
probably damaging |
Het |
Ticrr |
C |
A |
7: 79,344,236 (GRCm39) |
P1367Q |
probably damaging |
Het |
Trpv1 |
A |
G |
11: 73,130,255 (GRCm39) |
D146G |
probably damaging |
Het |
Tubd1 |
T |
G |
11: 86,448,602 (GRCm39) |
V305G |
possibly damaging |
Het |
Tubgcp4 |
T |
C |
2: 121,005,855 (GRCm39) |
L81P |
probably benign |
Het |
Ubxn2b |
T |
A |
4: 6,196,404 (GRCm39) |
|
probably null |
Het |
Usp36 |
A |
T |
11: 118,156,020 (GRCm39) |
S586T |
probably benign |
Het |
Vcan |
T |
A |
13: 89,826,264 (GRCm39) |
D2220V |
probably damaging |
Het |
Vmn1r173 |
T |
A |
7: 23,402,216 (GRCm39) |
N150K |
probably damaging |
Het |
Vmn1r70 |
G |
A |
7: 10,368,204 (GRCm39) |
A231T |
probably damaging |
Het |
Vmn2r97 |
A |
G |
17: 19,167,930 (GRCm39) |
D728G |
probably damaging |
Het |
Zbtb40 |
T |
C |
4: 136,710,539 (GRCm39) |
E1200G |
probably damaging |
Het |
Zfp365 |
A |
T |
10: 67,733,436 (GRCm39) |
V252D |
probably damaging |
Het |
|
Other mutations in Bptf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00553:Bptf
|
APN |
11 |
106,946,105 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00664:Bptf
|
APN |
11 |
106,968,491 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00705:Bptf
|
APN |
11 |
106,986,534 (GRCm39) |
splice site |
probably benign |
|
IGL00796:Bptf
|
APN |
11 |
106,945,376 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00834:Bptf
|
APN |
11 |
106,964,754 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01155:Bptf
|
APN |
11 |
106,971,553 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01314:Bptf
|
APN |
11 |
106,945,679 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01371:Bptf
|
APN |
11 |
106,946,733 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01567:Bptf
|
APN |
11 |
106,949,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01794:Bptf
|
APN |
11 |
106,944,047 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02108:Bptf
|
APN |
11 |
106,965,814 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02367:Bptf
|
APN |
11 |
106,964,178 (GRCm39) |
missense |
probably benign |
|
IGL02437:Bptf
|
APN |
11 |
106,965,521 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02589:Bptf
|
APN |
11 |
107,002,357 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02897:Bptf
|
APN |
11 |
106,937,947 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02935:Bptf
|
APN |
11 |
106,971,625 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02954:Bptf
|
APN |
11 |
106,945,575 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02982:Bptf
|
APN |
11 |
106,967,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03109:Bptf
|
APN |
11 |
106,952,527 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL03265:Bptf
|
APN |
11 |
106,945,454 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03403:Bptf
|
APN |
11 |
106,990,559 (GRCm39) |
missense |
possibly damaging |
0.51 |
Anodyne
|
UTSW |
11 |
106,934,457 (GRCm39) |
critical splice donor site |
probably null |
|
Arroyo
|
UTSW |
11 |
106,933,516 (GRCm39) |
missense |
probably benign |
0.32 |
mojado
|
UTSW |
11 |
106,935,466 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03097:Bptf
|
UTSW |
11 |
106,968,506 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4486001:Bptf
|
UTSW |
11 |
106,945,614 (GRCm39) |
missense |
probably damaging |
0.98 |
R0066:Bptf
|
UTSW |
11 |
106,952,962 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0157:Bptf
|
UTSW |
11 |
106,965,484 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0320:Bptf
|
UTSW |
11 |
106,963,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R0328:Bptf
|
UTSW |
11 |
106,937,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R0402:Bptf
|
UTSW |
11 |
106,964,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R0574:Bptf
|
UTSW |
11 |
106,967,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R0598:Bptf
|
UTSW |
11 |
106,963,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R0599:Bptf
|
UTSW |
11 |
106,959,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Bptf
|
UTSW |
11 |
106,952,518 (GRCm39) |
missense |
probably benign |
0.04 |
R0744:Bptf
|
UTSW |
11 |
107,001,638 (GRCm39) |
critical splice donor site |
probably null |
|
R0836:Bptf
|
UTSW |
11 |
107,001,638 (GRCm39) |
critical splice donor site |
probably null |
|
R0885:Bptf
|
UTSW |
11 |
106,934,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R1070:Bptf
|
UTSW |
11 |
106,945,881 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1252:Bptf
|
UTSW |
11 |
106,964,077 (GRCm39) |
missense |
probably benign |
0.00 |
R1370:Bptf
|
UTSW |
11 |
106,937,920 (GRCm39) |
missense |
probably damaging |
0.99 |
R1428:Bptf
|
UTSW |
11 |
106,963,873 (GRCm39) |
missense |
probably damaging |
0.99 |
R1467:Bptf
|
UTSW |
11 |
106,945,881 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1467:Bptf
|
UTSW |
11 |
106,945,881 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1742:Bptf
|
UTSW |
11 |
107,001,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1816:Bptf
|
UTSW |
11 |
106,951,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Bptf
|
UTSW |
11 |
106,964,127 (GRCm39) |
missense |
probably benign |
0.00 |
R1989:Bptf
|
UTSW |
11 |
106,965,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R2253:Bptf
|
UTSW |
11 |
107,002,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R2392:Bptf
|
UTSW |
11 |
106,963,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R2431:Bptf
|
UTSW |
11 |
106,938,066 (GRCm39) |
missense |
possibly damaging |
0.48 |
R3022:Bptf
|
UTSW |
11 |
107,002,463 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3161:Bptf
|
UTSW |
11 |
106,965,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R3686:Bptf
|
UTSW |
11 |
106,965,024 (GRCm39) |
missense |
probably benign |
0.25 |
R3687:Bptf
|
UTSW |
11 |
106,965,024 (GRCm39) |
missense |
probably benign |
0.25 |
R3688:Bptf
|
UTSW |
11 |
106,965,024 (GRCm39) |
missense |
probably benign |
0.25 |
R3787:Bptf
|
UTSW |
11 |
106,964,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3834:Bptf
|
UTSW |
11 |
106,964,683 (GRCm39) |
missense |
probably benign |
0.05 |
R3885:Bptf
|
UTSW |
11 |
106,965,339 (GRCm39) |
missense |
probably damaging |
0.97 |
R4090:Bptf
|
UTSW |
11 |
106,972,349 (GRCm39) |
missense |
probably damaging |
0.99 |
R4398:Bptf
|
UTSW |
11 |
107,001,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Bptf
|
UTSW |
11 |
106,965,300 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4514:Bptf
|
UTSW |
11 |
106,968,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R4565:Bptf
|
UTSW |
11 |
106,963,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R4715:Bptf
|
UTSW |
11 |
106,938,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R4748:Bptf
|
UTSW |
11 |
106,986,706 (GRCm39) |
missense |
probably damaging |
0.96 |
R4764:Bptf
|
UTSW |
11 |
106,934,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Bptf
|
UTSW |
11 |
106,965,474 (GRCm39) |
missense |
probably benign |
0.39 |
R4901:Bptf
|
UTSW |
11 |
107,001,686 (GRCm39) |
nonsense |
probably null |
|
R4995:Bptf
|
UTSW |
11 |
106,945,391 (GRCm39) |
missense |
probably damaging |
0.98 |
R5057:Bptf
|
UTSW |
11 |
106,973,354 (GRCm39) |
missense |
probably damaging |
0.98 |
R5120:Bptf
|
UTSW |
11 |
106,964,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R5320:Bptf
|
UTSW |
11 |
106,972,193 (GRCm39) |
nonsense |
probably null |
|
R5329:Bptf
|
UTSW |
11 |
106,964,121 (GRCm39) |
missense |
probably benign |
0.06 |
R5418:Bptf
|
UTSW |
11 |
107,002,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R5461:Bptf
|
UTSW |
11 |
106,952,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R5664:Bptf
|
UTSW |
11 |
106,964,525 (GRCm39) |
missense |
probably benign |
0.01 |
R5718:Bptf
|
UTSW |
11 |
107,002,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R5774:Bptf
|
UTSW |
11 |
107,001,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R5851:Bptf
|
UTSW |
11 |
107,001,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R5930:Bptf
|
UTSW |
11 |
106,964,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R5949:Bptf
|
UTSW |
11 |
107,001,915 (GRCm39) |
missense |
probably damaging |
0.99 |
R5975:Bptf
|
UTSW |
11 |
106,926,690 (GRCm39) |
utr 3 prime |
probably benign |
|
R6027:Bptf
|
UTSW |
11 |
106,965,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R6128:Bptf
|
UTSW |
11 |
106,965,516 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6337:Bptf
|
UTSW |
11 |
106,949,605 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6407:Bptf
|
UTSW |
11 |
107,001,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R6470:Bptf
|
UTSW |
11 |
106,963,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R6487:Bptf
|
UTSW |
11 |
106,968,552 (GRCm39) |
missense |
probably damaging |
0.99 |
R6501:Bptf
|
UTSW |
11 |
106,968,509 (GRCm39) |
missense |
probably null |
1.00 |
R6755:Bptf
|
UTSW |
11 |
106,938,082 (GRCm39) |
missense |
probably benign |
0.27 |
R6861:Bptf
|
UTSW |
11 |
106,953,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R6866:Bptf
|
UTSW |
11 |
106,964,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6879:Bptf
|
UTSW |
11 |
106,933,516 (GRCm39) |
missense |
probably benign |
0.32 |
R6927:Bptf
|
UTSW |
11 |
106,945,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R6944:Bptf
|
UTSW |
11 |
106,971,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R7082:Bptf
|
UTSW |
11 |
106,977,573 (GRCm39) |
missense |
probably benign |
0.00 |
R7136:Bptf
|
UTSW |
11 |
106,990,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R7162:Bptf
|
UTSW |
11 |
106,934,457 (GRCm39) |
critical splice donor site |
probably null |
|
R7171:Bptf
|
UTSW |
11 |
107,022,233 (GRCm39) |
missense |
unknown |
|
R7193:Bptf
|
UTSW |
11 |
106,945,635 (GRCm39) |
nonsense |
probably null |
|
R7210:Bptf
|
UTSW |
11 |
106,945,290 (GRCm39) |
nonsense |
probably null |
|
R7221:Bptf
|
UTSW |
11 |
106,945,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R7316:Bptf
|
UTSW |
11 |
107,001,740 (GRCm39) |
nonsense |
probably null |
|
R7316:Bptf
|
UTSW |
11 |
106,963,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Bptf
|
UTSW |
11 |
106,951,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R7454:Bptf
|
UTSW |
11 |
106,935,466 (GRCm39) |
missense |
probably benign |
0.03 |
R7657:Bptf
|
UTSW |
11 |
106,965,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R7718:Bptf
|
UTSW |
11 |
106,972,282 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7827:Bptf
|
UTSW |
11 |
106,938,013 (GRCm39) |
missense |
probably benign |
0.01 |
R7844:Bptf
|
UTSW |
11 |
106,964,887 (GRCm39) |
missense |
probably damaging |
0.97 |
R7992:Bptf
|
UTSW |
11 |
107,001,709 (GRCm39) |
missense |
probably benign |
0.00 |
R8001:Bptf
|
UTSW |
11 |
106,938,166 (GRCm39) |
nonsense |
probably null |
|
R8037:Bptf
|
UTSW |
11 |
106,946,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Bptf
|
UTSW |
11 |
106,927,417 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8235:Bptf
|
UTSW |
11 |
106,967,458 (GRCm39) |
missense |
probably benign |
0.04 |
R8308:Bptf
|
UTSW |
11 |
106,943,815 (GRCm39) |
missense |
probably damaging |
0.99 |
R8409:Bptf
|
UTSW |
11 |
106,953,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8464:Bptf
|
UTSW |
11 |
107,022,168 (GRCm39) |
missense |
probably benign |
0.01 |
R8477:Bptf
|
UTSW |
11 |
106,943,679 (GRCm39) |
missense |
probably damaging |
0.98 |
R8482:Bptf
|
UTSW |
11 |
106,934,524 (GRCm39) |
missense |
probably benign |
0.19 |
R8515:Bptf
|
UTSW |
11 |
106,946,064 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8519:Bptf
|
UTSW |
11 |
106,952,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Bptf
|
UTSW |
11 |
106,964,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Bptf
|
UTSW |
11 |
106,964,139 (GRCm39) |
missense |
probably damaging |
0.99 |
R8722:Bptf
|
UTSW |
11 |
107,022,295 (GRCm39) |
missense |
unknown |
|
R8732:Bptf
|
UTSW |
11 |
106,931,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R8783:Bptf
|
UTSW |
11 |
107,022,357 (GRCm39) |
missense |
unknown |
|
R8828:Bptf
|
UTSW |
11 |
106,945,836 (GRCm39) |
missense |
probably damaging |
0.98 |
R9004:Bptf
|
UTSW |
11 |
106,945,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R9010:Bptf
|
UTSW |
11 |
106,964,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Bptf
|
UTSW |
11 |
106,963,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Bptf
|
UTSW |
11 |
106,959,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Bptf
|
UTSW |
11 |
106,946,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R9345:Bptf
|
UTSW |
11 |
106,971,588 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9393:Bptf
|
UTSW |
11 |
106,965,134 (GRCm39) |
missense |
probably benign |
0.00 |
R9451:Bptf
|
UTSW |
11 |
106,935,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R9561:Bptf
|
UTSW |
11 |
106,964,954 (GRCm39) |
nonsense |
probably null |
|
R9632:Bptf
|
UTSW |
11 |
106,952,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R9648:Bptf
|
UTSW |
11 |
106,943,720 (GRCm39) |
missense |
probably damaging |
0.99 |
R9650:Bptf
|
UTSW |
11 |
106,935,412 (GRCm39) |
missense |
probably benign |
0.15 |
R9658:Bptf
|
UTSW |
11 |
107,002,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R9775:Bptf
|
UTSW |
11 |
106,934,502 (GRCm39) |
missense |
probably benign |
0.04 |
R9776:Bptf
|
UTSW |
11 |
106,969,396 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Bptf
|
UTSW |
11 |
106,965,408 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Bptf
|
UTSW |
11 |
106,949,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|