Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930519P11Rik |
T |
C |
2: 154,454,897 (GRCm39) |
N154S |
unknown |
Het |
Ank3 |
C |
T |
10: 69,828,311 (GRCm39) |
H2327Y |
|
Het |
Ano6 |
A |
G |
15: 95,818,172 (GRCm39) |
Y305C |
probably damaging |
Het |
Apc2 |
A |
G |
10: 80,151,170 (GRCm39) |
T2075A |
possibly damaging |
Het |
Arl6 |
A |
G |
16: 59,443,455 (GRCm39) |
V93A |
possibly damaging |
Het |
Bcas3 |
T |
C |
11: 85,474,763 (GRCm39) |
S790P |
probably damaging |
Het |
Bcl9l |
C |
A |
9: 44,416,448 (GRCm39) |
H211N |
probably benign |
Het |
Card9 |
T |
G |
2: 26,249,496 (GRCm39) |
I22L |
possibly damaging |
Het |
Catsperg1 |
C |
A |
7: 28,884,637 (GRCm39) |
G933V |
probably damaging |
Het |
Catsperg2 |
T |
A |
7: 29,404,750 (GRCm39) |
H771L |
possibly damaging |
Het |
Ccdc66 |
T |
C |
14: 27,215,229 (GRCm39) |
N281S |
possibly damaging |
Het |
Cfap54 |
A |
T |
10: 92,612,072 (GRCm39) |
L3162H |
probably damaging |
Het |
Clca4a |
A |
G |
3: 144,663,934 (GRCm39) |
L503P |
probably benign |
Het |
Cpn1 |
T |
C |
19: 43,962,470 (GRCm39) |
N160D |
probably damaging |
Het |
Ctsh |
T |
A |
9: 89,949,154 (GRCm39) |
I206K |
probably benign |
Het |
Cyb561d1 |
G |
A |
3: 108,106,679 (GRCm39) |
T180M |
probably damaging |
Het |
Dapk1 |
A |
T |
13: 60,909,599 (GRCm39) |
D1404V |
probably damaging |
Het |
Dip2c |
G |
T |
13: 9,556,684 (GRCm39) |
R76L |
probably benign |
Het |
Dnah7c |
T |
C |
1: 46,719,898 (GRCm39) |
I2783T |
probably damaging |
Het |
E130308A19Rik |
T |
C |
4: 59,690,333 (GRCm39) |
Y56H |
probably damaging |
Het |
Efemp2 |
G |
T |
19: 5,530,285 (GRCm39) |
A310S |
probably benign |
Het |
Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
Faap24 |
G |
A |
7: 35,092,279 (GRCm39) |
Q213* |
probably null |
Het |
Fam181b |
G |
A |
7: 92,729,943 (GRCm39) |
G239S |
possibly damaging |
Het |
Fancm |
T |
C |
12: 65,148,394 (GRCm39) |
W670R |
probably damaging |
Het |
Fcgbpl1 |
T |
A |
7: 27,853,944 (GRCm39) |
L1636* |
probably null |
Het |
Fmnl1 |
T |
C |
11: 103,081,224 (GRCm39) |
Y357H |
probably damaging |
Het |
Fryl |
A |
T |
5: 73,279,653 (GRCm39) |
V215E |
probably damaging |
Het |
Fscn2 |
C |
A |
11: 120,253,335 (GRCm39) |
N267K |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,816,571 (GRCm39) |
Y4101* |
probably null |
Het |
Gcn1 |
G |
A |
5: 115,728,352 (GRCm39) |
V738I |
probably benign |
Het |
Gdf9 |
C |
T |
11: 53,328,366 (GRCm39) |
R441C |
probably damaging |
Het |
Gipc3 |
C |
T |
10: 81,177,455 (GRCm39) |
G79E |
probably damaging |
Het |
Gzmf |
T |
A |
14: 56,443,391 (GRCm39) |
I196L |
probably benign |
Het |
Hectd1 |
A |
T |
12: 51,806,080 (GRCm39) |
V1852E |
probably damaging |
Het |
Hip1r |
A |
T |
5: 124,134,007 (GRCm39) |
Q256L |
probably benign |
Het |
Hmgxb4 |
T |
C |
8: 75,746,890 (GRCm39) |
S405P |
probably damaging |
Het |
Il9r |
T |
A |
11: 32,142,671 (GRCm39) |
H294L |
probably benign |
Het |
Kif12 |
G |
A |
4: 63,086,931 (GRCm39) |
T331I |
probably damaging |
Het |
Krtap8-1 |
A |
T |
16: 89,284,794 (GRCm39) |
M1K |
probably null |
Het |
Lamc2 |
A |
T |
1: 153,015,495 (GRCm39) |
C613S |
probably damaging |
Het |
Lgr4 |
T |
A |
2: 109,831,314 (GRCm39) |
N314K |
probably benign |
Het |
Lpcat2 |
T |
C |
8: 93,635,894 (GRCm39) |
I432T |
probably benign |
Het |
Mfhas1 |
T |
C |
8: 36,056,146 (GRCm39) |
V207A |
probably benign |
Het |
Msh3 |
T |
G |
13: 92,485,806 (GRCm39) |
T173P |
probably benign |
Het |
Mup15 |
T |
A |
4: 61,356,505 (GRCm39) |
M87L |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,965,365 (GRCm39) |
V1138A |
probably benign |
Het |
Noc2l |
T |
C |
4: 156,326,179 (GRCm39) |
V422A |
probably benign |
Het |
Notch3 |
C |
T |
17: 32,377,936 (GRCm39) |
G74D |
probably damaging |
Het |
Ocstamp |
T |
A |
2: 165,240,081 (GRCm39) |
K35I |
probably benign |
Het |
Or12k7 |
T |
C |
2: 36,958,400 (GRCm39) |
F28L |
possibly damaging |
Het |
Or52w1 |
A |
G |
7: 105,017,968 (GRCm39) |
H145R |
probably benign |
Het |
Or5p58 |
A |
G |
7: 107,694,342 (GRCm39) |
V145A |
probably benign |
Het |
Or9a2 |
T |
G |
6: 41,748,961 (GRCm39) |
T91P |
probably benign |
Het |
Plekhh2 |
T |
A |
17: 84,829,216 (GRCm39) |
V29D |
probably damaging |
Het |
Pof1b |
A |
G |
X: 111,554,042 (GRCm39) |
I544T |
probably benign |
Het |
Rad54l2 |
C |
T |
9: 106,590,677 (GRCm39) |
R483H |
probably damaging |
Het |
Rapgef6 |
T |
A |
11: 54,567,189 (GRCm39) |
D1128E |
possibly damaging |
Het |
Rhbdl2 |
T |
A |
4: 123,708,049 (GRCm39) |
I86N |
possibly damaging |
Het |
Rims1 |
C |
A |
1: 22,498,740 (GRCm39) |
R68L |
|
Het |
Rnf157 |
A |
G |
11: 116,253,199 (GRCm39) |
F70L |
possibly damaging |
Het |
Rtp3 |
C |
T |
9: 110,815,009 (GRCm39) |
C452Y |
unknown |
Het |
S100a14 |
A |
T |
3: 90,435,069 (GRCm39) |
K27* |
probably null |
Het |
Scai |
C |
T |
2: 38,996,948 (GRCm39) |
G282D |
possibly damaging |
Het |
Sclt1 |
A |
T |
3: 41,672,195 (GRCm39) |
I132N |
probably benign |
Het |
Serpinf1 |
T |
A |
11: 75,308,811 (GRCm39) |
Q2L |
possibly damaging |
Het |
Skor2 |
T |
A |
18: 76,948,681 (GRCm39) |
V801E |
probably benign |
Het |
Slc16a10 |
C |
G |
10: 39,913,255 (GRCm39) |
E484D |
probably benign |
Het |
Slc1a5 |
T |
A |
7: 16,531,463 (GRCm39) |
D489E |
probably damaging |
Het |
Slx4 |
C |
T |
16: 3,808,650 (GRCm39) |
R430H |
probably benign |
Het |
Teddm1b |
A |
T |
1: 153,750,679 (GRCm39) |
I163F |
probably damaging |
Het |
Tmem171 |
A |
T |
13: 98,828,744 (GRCm39) |
C135* |
probably null |
Het |
Tmem82 |
C |
T |
4: 141,342,284 (GRCm39) |
R306H |
possibly damaging |
Het |
Tmem94 |
T |
A |
11: 115,681,781 (GRCm39) |
|
probably null |
Het |
Trpm2 |
A |
C |
10: 77,759,848 (GRCm39) |
L1096R |
probably damaging |
Het |
Trrap |
T |
A |
5: 144,730,859 (GRCm39) |
L780Q |
probably damaging |
Het |
Txlnb |
A |
G |
10: 17,718,732 (GRCm39) |
D521G |
probably benign |
Het |
Usp7 |
T |
C |
16: 8,534,390 (GRCm39) |
D59G |
probably benign |
Het |
Vcan |
G |
A |
13: 89,873,710 (GRCm39) |
T48I |
probably damaging |
Het |
Vmn1r45 |
A |
G |
6: 89,910,316 (GRCm39) |
L218P |
probably damaging |
Het |
Wdr25 |
A |
T |
12: 108,990,922 (GRCm39) |
T370S |
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 |
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 |
R7162:Bptf
|
UTSW |
11 |
106,934,457 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
|