Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730596B20Rik |
A |
T |
6: 52,156,260 (GRCm39) |
N109Y |
unknown |
Het |
A430005L14Rik |
C |
T |
4: 154,044,221 (GRCm39) |
R11W |
probably damaging |
Het |
Aadacl2 |
T |
A |
3: 59,932,306 (GRCm39) |
S274T |
probably damaging |
Het |
Ahctf1 |
T |
C |
1: 179,602,898 (GRCm39) |
R887G |
probably benign |
Het |
Aox4 |
G |
T |
1: 58,263,352 (GRCm39) |
R158L |
possibly damaging |
Het |
Atp10a |
T |
C |
7: 58,308,567 (GRCm39) |
I122T |
probably damaging |
Het |
Batf2 |
G |
T |
19: 6,221,405 (GRCm39) |
A72S |
possibly damaging |
Het |
Bltp3a |
G |
T |
17: 28,109,039 (GRCm39) |
R1086L |
probably damaging |
Het |
Cacybp |
A |
G |
1: 160,031,229 (GRCm39) |
Y200H |
probably damaging |
Het |
Cdc40 |
A |
T |
10: 40,743,869 (GRCm39) |
V76D |
probably benign |
Het |
Cdc42ep4 |
T |
C |
11: 113,619,944 (GRCm39) |
D149G |
probably benign |
Het |
Chtop |
A |
G |
3: 90,414,891 (GRCm39) |
V9A |
probably benign |
Het |
Cnot9 |
A |
G |
1: 74,566,165 (GRCm39) |
I185M |
probably damaging |
Het |
Col6a5 |
A |
G |
9: 105,808,438 (GRCm39) |
I870T |
unknown |
Het |
Cr1l |
A |
G |
1: 194,806,006 (GRCm39) |
I159T |
probably benign |
Het |
Cthrc1 |
T |
C |
15: 38,940,495 (GRCm39) |
S33P |
probably benign |
Het |
Dlg2 |
T |
A |
7: 90,381,192 (GRCm39) |
W44R |
probably benign |
Het |
Dlgap4 |
T |
C |
2: 156,590,342 (GRCm39) |
|
probably null |
Het |
Dna2 |
A |
G |
10: 62,790,096 (GRCm39) |
H193R |
possibly damaging |
Het |
Espnl |
T |
A |
1: 91,262,521 (GRCm39) |
F322Y |
probably benign |
Het |
Fam171a1 |
G |
A |
2: 3,224,512 (GRCm39) |
V293I |
probably benign |
Het |
Fam76b |
A |
G |
9: 13,744,308 (GRCm39) |
Y135C |
probably damaging |
Het |
Flvcr2 |
A |
T |
12: 85,793,728 (GRCm39) |
I35F |
probably benign |
Het |
Gm9195 |
T |
A |
14: 72,680,152 (GRCm39) |
Q2219L |
probably benign |
Het |
Gnptg |
T |
C |
17: 25,453,694 (GRCm39) |
T283A |
probably benign |
Het |
Grap2 |
G |
A |
15: 80,532,699 (GRCm39) |
V289M |
probably benign |
Het |
Hk3 |
T |
C |
13: 55,154,710 (GRCm39) |
T767A |
probably benign |
Het |
Hs3st5 |
A |
G |
10: 36,708,833 (GRCm39) |
I123V |
probably benign |
Het |
Il6st |
A |
G |
13: 112,640,566 (GRCm39) |
T781A |
probably damaging |
Het |
Inpp5d |
T |
A |
1: 87,623,102 (GRCm39) |
H398Q |
probably damaging |
Het |
Kcnk1 |
A |
G |
8: 126,722,287 (GRCm39) |
Y30C |
probably damaging |
Het |
Klhl6 |
T |
C |
16: 19,801,633 (GRCm39) |
T41A |
probably benign |
Het |
Krt14 |
G |
A |
11: 100,094,167 (GRCm39) |
H476Y |
possibly damaging |
Het |
Lingo3 |
G |
C |
10: 80,671,625 (GRCm39) |
R102G |
probably benign |
Het |
Map3k9 |
G |
A |
12: 81,771,476 (GRCm39) |
T704M |
probably damaging |
Het |
Mdn1 |
C |
A |
4: 32,762,341 (GRCm39) |
N5088K |
probably benign |
Het |
Mmp9 |
T |
A |
2: 164,790,812 (GRCm39) |
S67T |
probably benign |
Het |
Mrps18c |
A |
G |
5: 100,952,270 (GRCm39) |
E143G |
probably damaging |
Het |
Msantd5f9 |
G |
T |
4: 73,835,808 (GRCm39) |
L219M |
probably benign |
Het |
Muc21 |
A |
T |
17: 35,932,093 (GRCm39) |
S698T |
unknown |
Het |
Nags |
C |
A |
11: 102,038,298 (GRCm39) |
R335S |
possibly damaging |
Het |
Nars1 |
A |
G |
18: 64,637,425 (GRCm39) |
V385A |
possibly damaging |
Het |
Nipal2 |
A |
C |
15: 34,584,809 (GRCm39) |
V253G |
possibly damaging |
Het |
Nos2 |
C |
A |
11: 78,819,405 (GRCm39) |
T39K |
probably benign |
Het |
Or10p1 |
T |
A |
10: 129,443,416 (GRCm39) |
*311Y |
probably null |
Het |
Or10p1 |
T |
A |
10: 129,443,417 (GRCm39) |
*311L |
probably null |
Het |
Or51t4 |
T |
C |
7: 102,598,455 (GRCm39) |
V261A |
probably damaging |
Het |
Or52s19 |
C |
A |
7: 103,007,495 (GRCm39) |
R302L |
possibly damaging |
Het |
Or6c66 |
C |
T |
10: 129,461,634 (GRCm39) |
V99M |
probably benign |
Het |
Or9s15 |
G |
A |
1: 92,524,140 (GRCm39) |
|
probably benign |
Het |
Panx3 |
G |
A |
9: 37,577,913 (GRCm39) |
P106S |
probably benign |
Het |
Pappa2 |
G |
A |
1: 158,590,689 (GRCm39) |
T1655I |
possibly damaging |
Het |
Pcdhb1 |
A |
G |
18: 37,400,044 (GRCm39) |
D665G |
probably damaging |
Het |
Pde2a |
T |
C |
7: 101,157,303 (GRCm39) |
L676P |
probably damaging |
Het |
Pf4 |
A |
G |
5: 90,920,851 (GRCm39) |
T60A |
possibly damaging |
Het |
Pira12 |
C |
T |
7: 3,898,510 (GRCm39) |
V313M |
probably damaging |
Het |
Pld5 |
A |
T |
1: 175,917,442 (GRCm39) |
C164S |
probably benign |
Het |
Psd3 |
A |
T |
8: 68,356,800 (GRCm39) |
M640K |
probably benign |
Het |
Ptf1a |
A |
G |
2: 19,450,676 (GRCm39) |
D2G |
possibly damaging |
Het |
Ptprq |
C |
T |
10: 107,544,591 (GRCm39) |
C313Y |
probably benign |
Het |
Ranbp10 |
A |
G |
8: 106,500,578 (GRCm39) |
S467P |
probably damaging |
Het |
Rap1gap |
C |
T |
4: 137,446,247 (GRCm39) |
T333M |
probably damaging |
Het |
Rfpl4 |
A |
G |
7: 5,118,558 (GRCm39) |
L4P |
probably benign |
Het |
Rgs12 |
A |
G |
5: 35,124,050 (GRCm39) |
N611S |
probably benign |
Het |
Sacs |
C |
A |
14: 61,447,966 (GRCm39) |
N3337K |
possibly damaging |
Het |
Sbno2 |
A |
T |
10: 79,895,924 (GRCm39) |
|
probably null |
Het |
Scrn2 |
T |
A |
11: 96,923,908 (GRCm39) |
V264E |
possibly damaging |
Het |
Serpinb9c |
T |
A |
13: 33,338,390 (GRCm39) |
I198L |
probably benign |
Het |
Shank2 |
T |
C |
7: 143,964,096 (GRCm39) |
F568S |
probably damaging |
Het |
Slc47a1 |
C |
T |
11: 61,268,767 (GRCm39) |
R36Q |
probably benign |
Het |
Slc4a8 |
A |
C |
15: 100,688,908 (GRCm39) |
E406A |
probably damaging |
Het |
Speg |
C |
T |
1: 75,388,091 (GRCm39) |
T1483I |
probably damaging |
Het |
Srbd1 |
A |
G |
17: 86,365,160 (GRCm39) |
V632A |
probably damaging |
Het |
Srd5a2 |
A |
T |
17: 74,328,515 (GRCm39) |
Y188N |
probably damaging |
Het |
Sspo |
A |
T |
6: 48,455,543 (GRCm39) |
|
probably null |
Het |
Ssx2ip |
A |
T |
3: 146,136,703 (GRCm39) |
D317V |
probably benign |
Het |
Tmco3 |
G |
T |
8: 13,370,847 (GRCm39) |
E172* |
probably null |
Het |
Trpc4 |
G |
A |
3: 54,206,519 (GRCm39) |
W573* |
probably null |
Het |
Ttn |
T |
C |
2: 76,580,340 (GRCm39) |
I23518V |
probably benign |
Het |
Tubal3 |
A |
G |
13: 3,983,050 (GRCm39) |
T277A |
possibly damaging |
Het |
Unc5b |
A |
T |
10: 60,610,867 (GRCm39) |
L391H |
probably damaging |
Het |
Vmn2r76 |
A |
G |
7: 85,874,440 (GRCm39) |
F846L |
probably benign |
Het |
Vps13c |
T |
A |
9: 67,790,735 (GRCm39) |
Y338N |
probably damaging |
Het |
Zc3hav1 |
G |
T |
6: 38,309,328 (GRCm39) |
S498* |
probably null |
Het |
Zfand4 |
T |
A |
6: 116,305,337 (GRCm39) |
|
probably null |
Het |
Zfp451 |
A |
T |
1: 33,811,972 (GRCm39) |
|
probably null |
Het |
Zfp607a |
A |
T |
7: 27,578,183 (GRCm39) |
I418F |
probably damaging |
Het |
Zfp612 |
A |
G |
8: 110,816,337 (GRCm39) |
T515A |
probably damaging |
Het |
Zfp708 |
G |
T |
13: 67,219,200 (GRCm39) |
L208I |
possibly 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 |
R0482:Bptf
|
UTSW |
11 |
106,972,088 (GRCm39) |
missense |
probably benign |
0.13 |
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 |
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 |
|