Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akp3 |
C |
T |
1: 87,055,471 (GRCm39) |
T506I |
unknown |
Het |
Ank1 |
T |
C |
8: 23,622,370 (GRCm39) |
W1640R |
possibly damaging |
Het |
Atp2a2 |
A |
G |
5: 122,627,387 (GRCm39) |
M126T |
probably benign |
Het |
Brat1 |
T |
C |
5: 140,696,004 (GRCm39) |
V125A |
probably benign |
Het |
Cables1 |
T |
C |
18: 12,059,423 (GRCm39) |
|
probably null |
Het |
Cabp5 |
A |
T |
7: 13,135,260 (GRCm39) |
M67L |
probably damaging |
Het |
Cacna1b |
A |
C |
2: 24,590,034 (GRCm39) |
I558S |
probably benign |
Het |
Ccdc166 |
A |
G |
15: 75,853,044 (GRCm39) |
S308P |
probably benign |
Het |
Cfap57 |
C |
T |
4: 118,472,128 (GRCm39) |
V84I |
probably benign |
Het |
Cfhr2 |
A |
G |
1: 139,741,264 (GRCm39) |
V237A |
probably benign |
Het |
Clybl |
C |
A |
14: 122,608,732 (GRCm39) |
S108* |
probably null |
Het |
Cubn |
A |
G |
2: 13,347,309 (GRCm39) |
Y2070H |
probably damaging |
Het |
Cyp8b1 |
A |
G |
9: 121,744,777 (GRCm39) |
F185S |
probably damaging |
Het |
Dennd2c |
T |
A |
3: 103,063,423 (GRCm39) |
V620D |
probably damaging |
Het |
Dis3l2 |
T |
C |
1: 86,971,752 (GRCm39) |
F597L |
possibly damaging |
Het |
Eif3f |
G |
A |
7: 108,539,938 (GRCm39) |
R282H |
probably benign |
Het |
Ell |
C |
A |
8: 71,031,559 (GRCm39) |
R86S |
possibly damaging |
Het |
Eppk1 |
A |
G |
15: 75,990,809 (GRCm39) |
V2024A |
possibly damaging |
Het |
Exoc6 |
T |
C |
19: 37,565,566 (GRCm39) |
I214T |
probably damaging |
Het |
Faim2 |
A |
G |
15: 99,419,048 (GRCm39) |
|
probably null |
Het |
Gli1 |
A |
G |
10: 127,168,306 (GRCm39) |
S516P |
probably benign |
Het |
Gm18596 |
A |
T |
10: 77,578,034 (GRCm39) |
S147T |
unknown |
Het |
Gm19965 |
A |
G |
1: 116,750,095 (GRCm39) |
Y592C |
unknown |
Het |
Gng12 |
T |
C |
6: 66,994,285 (GRCm39) |
S36P |
unknown |
Het |
Gramd2b |
G |
A |
18: 56,618,529 (GRCm39) |
|
probably null |
Het |
Hmcn1 |
T |
A |
1: 150,624,744 (GRCm39) |
T1054S |
probably benign |
Het |
Ifngr1 |
A |
G |
10: 19,485,101 (GRCm39) |
T367A |
probably benign |
Het |
Il21r |
G |
T |
7: 125,231,483 (GRCm39) |
V304L |
probably benign |
Het |
Ino80d |
G |
A |
1: 63,104,894 (GRCm39) |
T394M |
probably damaging |
Het |
Itfg2 |
C |
T |
6: 128,387,546 (GRCm39) |
V380M |
probably damaging |
Het |
Kcna5 |
C |
T |
6: 126,510,806 (GRCm39) |
V441I |
possibly damaging |
Het |
Kcp |
T |
A |
6: 29,497,199 (GRCm39) |
|
probably null |
Het |
Kdf1 |
C |
T |
4: 133,257,229 (GRCm39) |
T375I |
unknown |
Het |
Klk1b1 |
A |
T |
7: 43,618,671 (GRCm39) |
D16V |
probably damaging |
Het |
Krtap5-4 |
A |
C |
7: 141,857,335 (GRCm39) |
T2P |
unknown |
Het |
Lamtor1 |
A |
G |
7: 101,555,243 (GRCm39) |
D13G |
probably benign |
Het |
Lrp10 |
T |
C |
14: 54,703,163 (GRCm39) |
V72A |
possibly damaging |
Het |
Lrrc1 |
C |
A |
9: 77,339,472 (GRCm39) |
A503S |
probably benign |
Het |
Mylk |
A |
T |
16: 34,742,899 (GRCm39) |
D1137V |
probably damaging |
Het |
Myo5b |
C |
G |
18: 74,828,498 (GRCm39) |
L717V |
probably benign |
Het |
Myoz3 |
T |
A |
18: 60,709,485 (GRCm39) |
R225S |
probably damaging |
Het |
Myrf |
A |
G |
19: 10,196,010 (GRCm39) |
F335L |
possibly damaging |
Het |
Nfib |
A |
C |
4: 82,268,677 (GRCm39) |
S292A |
probably damaging |
Het |
Notch3 |
G |
T |
17: 32,365,423 (GRCm39) |
H1096Q |
probably damaging |
Het |
Nt5c1a |
A |
G |
4: 123,107,898 (GRCm39) |
R194G |
probably benign |
Het |
Or10d3 |
A |
G |
9: 39,461,525 (GRCm39) |
I214T |
probably damaging |
Het |
Or5a1 |
A |
G |
19: 12,097,501 (GRCm39) |
F192L |
possibly damaging |
Het |
Parp4 |
A |
G |
14: 56,886,333 (GRCm39) |
E1804G |
unknown |
Het |
Pcdhac2 |
A |
T |
18: 37,278,840 (GRCm39) |
I607L |
probably benign |
Het |
Pcdhb5 |
A |
G |
18: 37,454,739 (GRCm39) |
D373G |
probably benign |
Het |
Pcf11 |
A |
T |
7: 92,313,221 (GRCm39) |
V154E |
probably damaging |
Het |
Pdia3 |
T |
G |
2: 121,260,002 (GRCm39) |
D180E |
probably benign |
Het |
Piezo2 |
C |
A |
18: 63,257,780 (GRCm39) |
V313F |
possibly damaging |
Het |
Pik3ap1 |
C |
A |
19: 41,309,965 (GRCm39) |
A452S |
probably benign |
Het |
Plb1 |
A |
G |
5: 32,507,007 (GRCm39) |
K1194R |
probably benign |
Het |
Pld3 |
A |
C |
7: 27,231,899 (GRCm39) |
W431G |
probably damaging |
Het |
Plekha3 |
T |
C |
2: 76,523,110 (GRCm39) |
|
probably null |
Het |
Ppm1f |
G |
T |
16: 16,732,057 (GRCm39) |
R169L |
probably damaging |
Het |
Ppp2r3d |
A |
G |
9: 124,439,673 (GRCm38) |
V60A |
|
Het |
Prop1 |
T |
A |
11: 50,842,881 (GRCm39) |
D102V |
probably damaging |
Het |
Rbm27 |
G |
A |
18: 42,447,092 (GRCm39) |
G446R |
unknown |
Het |
Rc3h2 |
C |
A |
2: 37,299,617 (GRCm39) |
V138L |
possibly damaging |
Het |
Rorc |
G |
A |
3: 94,284,915 (GRCm39) |
|
probably null |
Het |
Sardh |
A |
G |
2: 27,087,702 (GRCm39) |
V723A |
possibly damaging |
Het |
Sart3 |
A |
G |
5: 113,900,896 (GRCm39) |
Y181H |
probably damaging |
Het |
Sbpl |
A |
T |
17: 24,172,439 (GRCm39) |
M160K |
possibly damaging |
Het |
Sh3gl3 |
A |
G |
7: 81,933,350 (GRCm39) |
S238G |
probably benign |
Het |
Slc22a30 |
A |
G |
19: 8,314,081 (GRCm39) |
|
probably null |
Het |
Slc3a1 |
A |
T |
17: 85,371,442 (GRCm39) |
R665* |
probably null |
Het |
Stk32a |
C |
A |
18: 43,430,649 (GRCm39) |
Y186* |
probably null |
Het |
Stxbp6 |
T |
C |
12: 44,949,663 (GRCm39) |
N89D |
probably benign |
Het |
Svep1 |
A |
G |
4: 58,070,262 (GRCm39) |
F2508S |
possibly damaging |
Het |
Tas1r1 |
A |
G |
4: 152,116,695 (GRCm39) |
V313A |
possibly damaging |
Het |
Tmem81 |
T |
C |
1: 132,435,355 (GRCm39) |
Y54H |
probably damaging |
Het |
Tmtc1 |
T |
C |
6: 148,172,985 (GRCm39) |
N582S |
probably damaging |
Het |
Top2b |
T |
C |
14: 16,416,653 (GRCm38) |
S1138P |
probably benign |
Het |
Trim24 |
T |
A |
6: 37,942,456 (GRCm39) |
N989K |
possibly damaging |
Het |
Trim72 |
T |
A |
7: 127,606,821 (GRCm39) |
M145K |
probably benign |
Het |
Ttll9 |
T |
A |
2: 152,831,523 (GRCm39) |
S154T |
probably damaging |
Het |
Tusc3 |
T |
C |
8: 39,593,741 (GRCm39) |
V286A |
probably benign |
Het |
Vat1l |
C |
A |
8: 114,963,518 (GRCm39) |
H185N |
probably damaging |
Het |
Vmn1r209 |
A |
T |
13: 22,990,128 (GRCm39) |
D187E |
probably damaging |
Het |
Vmn2r87 |
T |
C |
10: 130,313,416 (GRCm39) |
N450S |
probably benign |
Het |
Wdr7 |
T |
A |
18: 63,857,210 (GRCm39) |
D95E |
possibly damaging |
Het |
Zfp937 |
C |
T |
2: 150,081,439 (GRCm39) |
H490Y |
probably benign |
Het |
Zfp974 |
A |
T |
7: 27,610,944 (GRCm39) |
H260Q |
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 |
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 |
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 |
|