Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
T |
13: 81,545,570 (GRCm39) |
V5572I |
probably benign |
Het |
Agap1 |
C |
T |
1: 89,770,818 (GRCm39) |
T656I |
probably damaging |
Het |
Als2cl |
C |
T |
9: 110,716,432 (GRCm39) |
R247W |
probably damaging |
Het |
Ankfy1 |
A |
T |
11: 72,603,071 (GRCm39) |
R33S |
probably benign |
Het |
Ano5 |
T |
C |
7: 51,235,079 (GRCm39) |
F671L |
probably damaging |
Het |
Arhgap26 |
A |
G |
18: 39,283,145 (GRCm39) |
M361V |
probably damaging |
Het |
Bckdk |
A |
G |
7: 127,505,145 (GRCm39) |
E175G |
probably damaging |
Het |
Btn2a2 |
T |
A |
13: 23,670,398 (GRCm39) |
I112F |
probably damaging |
Het |
Cln8 |
T |
A |
8: 14,946,621 (GRCm39) |
W212R |
probably damaging |
Het |
Cnbd1 |
T |
C |
4: 18,886,119 (GRCm39) |
E300G |
probably benign |
Het |
Cnksr3 |
T |
C |
10: 7,092,993 (GRCm39) |
I173V |
probably benign |
Het |
Cntn2 |
T |
A |
1: 132,451,170 (GRCm39) |
D484V |
probably damaging |
Het |
Cyp4a14 |
C |
A |
4: 115,348,607 (GRCm39) |
G319V |
probably damaging |
Het |
Cyp4f37 |
G |
A |
17: 32,848,957 (GRCm39) |
R275Q |
possibly damaging |
Het |
Def8 |
C |
T |
8: 124,186,809 (GRCm39) |
|
probably benign |
Het |
Dnaaf4 |
T |
C |
9: 72,879,280 (GRCm39) |
V356A |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,868,855 (GRCm39) |
|
probably null |
Het |
Dock6 |
A |
G |
9: 21,735,712 (GRCm39) |
V1012A |
probably benign |
Het |
Dus3l |
T |
A |
17: 57,076,579 (GRCm39) |
N586K |
probably damaging |
Het |
Dyrk2 |
T |
A |
10: 118,696,173 (GRCm39) |
I362F |
probably damaging |
Het |
Eeig2 |
A |
T |
3: 108,887,468 (GRCm39) |
S265R |
probably benign |
Het |
Erc2 |
T |
A |
14: 27,498,815 (GRCm39) |
D230E |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,497,073 (GRCm39) |
H4186R |
probably benign |
Het |
Fbxo44 |
A |
G |
4: 148,241,052 (GRCm39) |
F179S |
probably damaging |
Het |
Fech |
A |
G |
18: 64,611,720 (GRCm39) |
|
probably null |
Het |
Fer1l5 |
T |
A |
1: 36,424,254 (GRCm39) |
C289* |
probably null |
Het |
Fhl5 |
T |
A |
4: 25,214,756 (GRCm39) |
D7V |
probably benign |
Het |
Flvcr1 |
G |
T |
1: 190,741,748 (GRCm39) |
T514K |
probably damaging |
Het |
Fmo1 |
A |
T |
1: 162,667,185 (GRCm39) |
|
probably null |
Het |
Gabra6 |
G |
A |
11: 42,198,268 (GRCm39) |
T384M |
probably benign |
Het |
Gli3 |
A |
G |
13: 15,723,210 (GRCm39) |
Y117C |
probably damaging |
Het |
Gnao1 |
A |
G |
8: 94,622,873 (GRCm39) |
D59G |
probably benign |
Het |
Gria2 |
T |
C |
3: 80,614,556 (GRCm39) |
I495V |
possibly damaging |
Het |
Hnf1b |
C |
A |
11: 83,754,811 (GRCm39) |
H161Q |
probably benign |
Het |
Itga8 |
T |
A |
2: 12,235,019 (GRCm39) |
D413V |
possibly damaging |
Het |
Itpr3 |
A |
T |
17: 27,329,895 (GRCm39) |
Q1563L |
possibly damaging |
Het |
Kctd16 |
A |
G |
18: 40,663,882 (GRCm39) |
N337S |
probably benign |
Het |
Klra4 |
C |
T |
6: 130,030,016 (GRCm39) |
V190M |
possibly damaging |
Het |
Krtap4-9 |
T |
A |
11: 99,676,462 (GRCm39) |
|
probably benign |
Het |
L3mbtl1 |
GGCCG |
GG |
2: 162,809,256 (GRCm39) |
|
probably benign |
Het |
Mchr1 |
T |
C |
15: 81,122,044 (GRCm39) |
F265L |
probably damaging |
Het |
Megf8 |
T |
A |
7: 25,025,866 (GRCm39) |
Y83* |
probably null |
Het |
Mettl18 |
A |
G |
1: 163,824,746 (GRCm39) |
M356V |
probably null |
Het |
Mrm1 |
G |
A |
11: 84,710,018 (GRCm39) |
R61W |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,570,523 (GRCm39) |
T528S |
probably benign |
Het |
Myef2 |
A |
T |
2: 124,937,651 (GRCm39) |
L530* |
probably null |
Het |
Nhlrc4 |
T |
C |
17: 26,162,693 (GRCm39) |
E18G |
probably benign |
Het |
Nisch |
C |
T |
14: 30,895,102 (GRCm39) |
V1065I |
probably benign |
Het |
Nlgn2 |
C |
T |
11: 69,724,975 (GRCm39) |
R97H |
probably damaging |
Het |
Nos2 |
T |
C |
11: 78,828,741 (GRCm39) |
L321S |
probably damaging |
Het |
Oaz3 |
T |
C |
3: 94,343,717 (GRCm39) |
M49V |
possibly damaging |
Het |
Olfm5 |
A |
G |
7: 103,803,362 (GRCm39) |
V367A |
probably damaging |
Het |
Omd |
C |
T |
13: 49,743,112 (GRCm39) |
P54L |
possibly damaging |
Het |
Or10ak12 |
C |
T |
4: 118,666,575 (GRCm39) |
R162H |
probably benign |
Het |
Or11g26 |
C |
A |
14: 50,753,249 (GRCm39) |
A196D |
probably benign |
Het |
Or2g7 |
C |
A |
17: 38,378,641 (GRCm39) |
A193D |
probably benign |
Het |
Or51f23 |
A |
T |
7: 102,453,481 (GRCm39) |
R265S |
probably damaging |
Het |
Or7d10 |
A |
G |
9: 19,832,206 (GRCm39) |
K234E |
probably damaging |
Het |
Pard3b |
T |
A |
1: 61,807,289 (GRCm39) |
|
probably benign |
Het |
Pcdhb18 |
A |
C |
18: 37,624,988 (GRCm39) |
I773L |
possibly damaging |
Het |
Pde11a |
T |
C |
2: 75,970,175 (GRCm39) |
|
probably null |
Het |
Pfkfb4 |
A |
C |
9: 108,859,462 (GRCm39) |
|
probably benign |
Het |
Phb2 |
T |
G |
6: 124,692,612 (GRCm39) |
I260S |
probably damaging |
Het |
Pkd1l1 |
G |
A |
11: 8,908,969 (GRCm39) |
T345I |
unknown |
Het |
Pla2g6 |
T |
C |
15: 79,187,728 (GRCm39) |
|
probably benign |
Het |
Pou4f2 |
G |
A |
8: 79,163,020 (GRCm39) |
S5F |
unknown |
Het |
Ppp1r9a |
A |
T |
6: 5,157,002 (GRCm39) |
|
probably null |
Het |
Pramel5 |
A |
G |
4: 143,999,553 (GRCm39) |
I178T |
probably benign |
Het |
Prom2 |
C |
T |
2: 127,372,053 (GRCm39) |
W745* |
probably null |
Het |
Pros1 |
T |
A |
16: 62,748,424 (GRCm39) |
N632K |
probably damaging |
Het |
Rab4b |
A |
G |
7: 26,873,927 (GRCm39) |
I117T |
probably benign |
Het |
Rbm25 |
T |
A |
12: 83,724,640 (GRCm39) |
H796Q |
possibly damaging |
Het |
Rnf151 |
A |
T |
17: 24,937,004 (GRCm39) |
|
probably null |
Het |
Rps6ka1 |
A |
T |
4: 133,598,882 (GRCm39) |
L97I |
probably damaging |
Het |
Scart1 |
C |
T |
7: 139,810,359 (GRCm39) |
P984S |
probably benign |
Het |
Semp2l2a |
T |
A |
8: 13,887,263 (GRCm39) |
D276V |
probably benign |
Het |
Sergef |
T |
A |
7: 46,092,888 (GRCm39) |
T374S |
probably benign |
Het |
Sh3rf3 |
G |
T |
10: 58,966,808 (GRCm39) |
G717C |
probably damaging |
Het |
Slc29a4 |
C |
T |
5: 142,707,157 (GRCm39) |
T500I |
possibly damaging |
Het |
Smc1b |
T |
A |
15: 84,970,322 (GRCm39) |
D977V |
probably damaging |
Het |
Spata31d1d |
C |
T |
13: 59,874,829 (GRCm39) |
C902Y |
probably benign |
Het |
St14 |
A |
T |
9: 31,015,056 (GRCm39) |
V314D |
probably damaging |
Het |
Stat3 |
A |
T |
11: 100,784,496 (GRCm39) |
I602N |
possibly damaging |
Het |
Stx4a |
T |
A |
7: 127,445,661 (GRCm39) |
I189N |
probably damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,215 (GRCm39) |
S338P |
probably benign |
Het |
Tcirg1 |
T |
A |
19: 3,952,424 (GRCm39) |
T315S |
possibly damaging |
Het |
Tenm4 |
A |
T |
7: 96,503,926 (GRCm39) |
N1295I |
probably damaging |
Het |
Tm7sf3 |
T |
C |
6: 146,505,409 (GRCm39) |
K516E |
possibly damaging |
Het |
Tmem198b |
T |
C |
10: 128,637,323 (GRCm39) |
E272G |
possibly damaging |
Het |
Tnip3 |
A |
G |
6: 65,582,937 (GRCm39) |
Q237R |
probably damaging |
Het |
Trim15 |
C |
T |
17: 37,173,252 (GRCm39) |
|
probably null |
Het |
Trim30a |
T |
A |
7: 104,070,657 (GRCm39) |
N252I |
possibly damaging |
Het |
Ttc39a |
A |
G |
4: 109,288,075 (GRCm39) |
E227G |
probably benign |
Het |
Ttll13 |
A |
G |
7: 79,902,914 (GRCm39) |
E194G |
probably damaging |
Het |
Upf1 |
G |
A |
8: 70,796,912 (GRCm39) |
T107I |
probably benign |
Het |
Vac14 |
A |
G |
8: 111,436,981 (GRCm39) |
I565V |
probably damaging |
Het |
Zcchc14 |
A |
T |
8: 122,338,097 (GRCm39) |
|
probably benign |
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 |
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 |
|