Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ccdc136 |
A |
T |
6: 29,417,122 (GRCm39) |
S648C |
probably damaging |
Het |
Ccna2 |
A |
G |
3: 36,625,152 (GRCm39) |
|
probably benign |
Het |
Cdc23 |
C |
A |
18: 34,784,742 (GRCm39) |
V7L |
unknown |
Het |
Cenpf |
T |
C |
1: 189,416,043 (GRCm39) |
E94G |
probably damaging |
Het |
Clic1 |
G |
A |
17: 35,274,235 (GRCm39) |
V139I |
probably benign |
Het |
Coasy |
A |
G |
11: 100,975,648 (GRCm39) |
E327G |
probably damaging |
Het |
Col6a5 |
C |
T |
9: 105,805,337 (GRCm39) |
E1190K |
unknown |
Het |
Cyp2c70 |
A |
G |
19: 40,172,441 (GRCm39) |
V67A |
possibly damaging |
Het |
Dglucy |
A |
G |
12: 100,801,500 (GRCm39) |
S52G |
probably benign |
Het |
Dync1h1 |
A |
G |
12: 110,607,341 (GRCm39) |
N2644S |
probably benign |
Het |
Eif4g2 |
A |
T |
7: 110,676,239 (GRCm39) |
N347K |
probably benign |
Het |
Epha10 |
T |
C |
4: 124,809,178 (GRCm39) |
|
probably benign |
Het |
Epm2aip1 |
T |
C |
9: 111,101,218 (GRCm39) |
F64L |
probably benign |
Het |
Eri2 |
G |
A |
7: 119,384,897 (GRCm39) |
L535F |
probably benign |
Het |
Garin5b |
T |
G |
7: 4,761,575 (GRCm39) |
K379T |
possibly damaging |
Het |
Gm17430 |
T |
C |
18: 9,726,561 (GRCm39) |
E37G |
probably benign |
Het |
Heatr5b |
T |
A |
17: 79,131,939 (GRCm39) |
Q388L |
probably benign |
Het |
Htr1f |
A |
G |
16: 64,746,291 (GRCm39) |
W334R |
probably damaging |
Het |
Icam4 |
A |
T |
9: 20,940,937 (GRCm39) |
C717* |
probably null |
Het |
Iqgap1 |
A |
C |
7: 80,383,848 (GRCm39) |
L1072W |
probably damaging |
Het |
Kbtbd11 |
G |
T |
8: 15,077,886 (GRCm39) |
A162S |
probably benign |
Het |
Kif13b |
T |
G |
14: 64,996,038 (GRCm39) |
Y941* |
probably null |
Het |
Kndc1 |
T |
C |
7: 139,490,371 (GRCm39) |
V291A |
possibly damaging |
Het |
Lrrn3 |
A |
T |
12: 41,503,594 (GRCm39) |
I241N |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,349,312 (GRCm39) |
S2387P |
probably damaging |
Het |
Msh5 |
A |
G |
17: 35,251,369 (GRCm39) |
L451S |
possibly damaging |
Het |
Mthfd1 |
T |
G |
12: 76,340,914 (GRCm39) |
F258V |
probably damaging |
Het |
Ncstn |
C |
T |
1: 171,896,193 (GRCm39) |
R495H |
probably damaging |
Het |
Or4k2 |
T |
G |
14: 50,423,745 (GRCm39) |
T310P |
probably benign |
Het |
Pkd1l3 |
T |
A |
8: 110,392,268 (GRCm39) |
I1954N |
probably damaging |
Het |
Ppox |
C |
A |
1: 171,105,169 (GRCm39) |
V340L |
probably damaging |
Het |
Prkag1 |
T |
C |
15: 98,713,768 (GRCm39) |
T21A |
possibly damaging |
Het |
Pygo1 |
C |
A |
9: 72,852,199 (GRCm39) |
H129N |
probably damaging |
Het |
Rad9a |
A |
T |
19: 4,247,173 (GRCm39) |
C271S |
probably benign |
Het |
Raph1 |
T |
C |
1: 60,535,381 (GRCm39) |
|
probably null |
Het |
Reln |
A |
G |
5: 22,153,510 (GRCm39) |
F2265L |
probably damaging |
Het |
Shc4 |
A |
G |
2: 125,471,647 (GRCm39) |
I304T |
probably damaging |
Het |
Slc35f3 |
T |
A |
8: 127,116,011 (GRCm39) |
L313M |
probably damaging |
Het |
Spata31g1 |
T |
A |
4: 42,972,195 (GRCm39) |
H509Q |
probably benign |
Het |
Spef1l |
A |
T |
7: 139,558,587 (GRCm39) |
S3R |
possibly damaging |
Het |
Sycp2l |
T |
A |
13: 41,283,337 (GRCm39) |
M191K |
possibly damaging |
Het |
Tmem132c |
C |
A |
5: 127,630,199 (GRCm39) |
Q579K |
probably benign |
Het |
Trbj2-5 |
A |
G |
6: 41,520,394 (GRCm39) |
|
probably benign |
Het |
Ttc38 |
A |
G |
15: 85,728,741 (GRCm39) |
E231G |
probably benign |
Het |
Utp20 |
A |
G |
10: 88,611,192 (GRCm39) |
V1375A |
probably benign |
Het |
Vcan |
T |
A |
13: 89,852,096 (GRCm39) |
T955S |
probably damaging |
Het |
Vmn1r89 |
T |
C |
7: 12,953,314 (GRCm39) |
C17R |
possibly damaging |
Het |
Wnk1 |
A |
G |
6: 119,942,696 (GRCm39) |
|
probably benign |
Het |
Zfp667 |
T |
G |
7: 6,308,949 (GRCm39) |
I539S |
possibly damaging |
Het |
Zfp738 |
T |
A |
13: 67,818,320 (GRCm39) |
H557L |
probably damaging |
Het |
|
Other mutations in Btaf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Btaf1
|
APN |
19 |
36,987,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00535:Btaf1
|
APN |
19 |
36,974,935 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00574:Btaf1
|
APN |
19 |
36,947,330 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00969:Btaf1
|
APN |
19 |
36,988,652 (GRCm39) |
splice site |
probably benign |
|
IGL01325:Btaf1
|
APN |
19 |
36,982,049 (GRCm39) |
splice site |
probably benign |
|
IGL01399:Btaf1
|
APN |
19 |
36,977,570 (GRCm39) |
nonsense |
probably null |
|
IGL02024:Btaf1
|
APN |
19 |
36,969,826 (GRCm39) |
splice site |
probably benign |
|
IGL02471:Btaf1
|
APN |
19 |
36,977,592 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02664:Btaf1
|
APN |
19 |
36,955,828 (GRCm39) |
splice site |
probably benign |
|
IGL02898:Btaf1
|
APN |
19 |
36,946,468 (GRCm39) |
missense |
probably benign |
|
IGL02995:Btaf1
|
APN |
19 |
36,958,535 (GRCm39) |
splice site |
probably benign |
|
IGL03023:Btaf1
|
APN |
19 |
36,987,415 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03188:Btaf1
|
APN |
19 |
36,926,508 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03353:Btaf1
|
APN |
19 |
36,969,900 (GRCm39) |
missense |
probably damaging |
1.00 |
freudenberg
|
UTSW |
19 |
36,965,573 (GRCm39) |
critical splice donor site |
probably null |
|
Galanos
|
UTSW |
19 |
36,926,502 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Btaf1
|
UTSW |
19 |
36,987,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Btaf1
|
UTSW |
19 |
36,935,773 (GRCm39) |
missense |
probably benign |
|
R0048:Btaf1
|
UTSW |
19 |
36,980,924 (GRCm39) |
missense |
probably benign |
0.01 |
R0117:Btaf1
|
UTSW |
19 |
36,947,368 (GRCm39) |
missense |
probably benign |
0.06 |
R0207:Btaf1
|
UTSW |
19 |
36,987,048 (GRCm39) |
nonsense |
probably null |
|
R0310:Btaf1
|
UTSW |
19 |
36,981,934 (GRCm39) |
missense |
probably damaging |
0.96 |
R0377:Btaf1
|
UTSW |
19 |
36,966,402 (GRCm39) |
missense |
probably benign |
|
R0419:Btaf1
|
UTSW |
19 |
36,922,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R0440:Btaf1
|
UTSW |
19 |
36,964,053 (GRCm39) |
missense |
probably damaging |
0.99 |
R0532:Btaf1
|
UTSW |
19 |
36,928,586 (GRCm39) |
splice site |
probably benign |
|
R0612:Btaf1
|
UTSW |
19 |
36,946,537 (GRCm39) |
missense |
probably damaging |
0.99 |
R0731:Btaf1
|
UTSW |
19 |
36,974,895 (GRCm39) |
splice site |
probably null |
|
R0780:Btaf1
|
UTSW |
19 |
36,966,322 (GRCm39) |
missense |
probably damaging |
0.99 |
R0919:Btaf1
|
UTSW |
19 |
36,968,143 (GRCm39) |
missense |
probably benign |
0.03 |
R1104:Btaf1
|
UTSW |
19 |
36,982,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R1263:Btaf1
|
UTSW |
19 |
36,933,924 (GRCm39) |
missense |
probably benign |
0.10 |
R1325:Btaf1
|
UTSW |
19 |
36,946,562 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1447:Btaf1
|
UTSW |
19 |
36,969,854 (GRCm39) |
missense |
probably benign |
0.00 |
R1554:Btaf1
|
UTSW |
19 |
36,973,998 (GRCm39) |
missense |
probably benign |
0.02 |
R1649:Btaf1
|
UTSW |
19 |
36,959,122 (GRCm39) |
missense |
probably benign |
|
R1715:Btaf1
|
UTSW |
19 |
36,946,521 (GRCm39) |
missense |
probably damaging |
0.99 |
R1733:Btaf1
|
UTSW |
19 |
36,972,362 (GRCm39) |
missense |
probably benign |
|
R1764:Btaf1
|
UTSW |
19 |
36,928,518 (GRCm39) |
missense |
probably benign |
0.12 |
R1874:Btaf1
|
UTSW |
19 |
36,957,983 (GRCm39) |
missense |
probably benign |
|
R1911:Btaf1
|
UTSW |
19 |
36,964,030 (GRCm39) |
missense |
probably benign |
|
R1933:Btaf1
|
UTSW |
19 |
36,950,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Btaf1
|
UTSW |
19 |
36,928,548 (GRCm39) |
missense |
probably benign |
0.09 |
R2483:Btaf1
|
UTSW |
19 |
36,958,486 (GRCm39) |
missense |
probably benign |
0.02 |
R2510:Btaf1
|
UTSW |
19 |
36,979,845 (GRCm39) |
missense |
probably benign |
0.08 |
R3623:Btaf1
|
UTSW |
19 |
36,958,486 (GRCm39) |
missense |
probably benign |
0.02 |
R3624:Btaf1
|
UTSW |
19 |
36,958,486 (GRCm39) |
missense |
probably benign |
0.02 |
R3801:Btaf1
|
UTSW |
19 |
36,966,373 (GRCm39) |
missense |
probably benign |
0.00 |
R3801:Btaf1
|
UTSW |
19 |
36,963,948 (GRCm39) |
missense |
probably benign |
|
R3802:Btaf1
|
UTSW |
19 |
36,966,373 (GRCm39) |
missense |
probably benign |
0.00 |
R3802:Btaf1
|
UTSW |
19 |
36,963,948 (GRCm39) |
missense |
probably benign |
|
R3803:Btaf1
|
UTSW |
19 |
36,966,373 (GRCm39) |
missense |
probably benign |
0.00 |
R3803:Btaf1
|
UTSW |
19 |
36,963,948 (GRCm39) |
missense |
probably benign |
|
R4077:Btaf1
|
UTSW |
19 |
36,963,879 (GRCm39) |
missense |
probably benign |
0.00 |
R4079:Btaf1
|
UTSW |
19 |
36,963,879 (GRCm39) |
missense |
probably benign |
0.00 |
R4133:Btaf1
|
UTSW |
19 |
36,939,138 (GRCm39) |
missense |
probably benign |
0.00 |
R4673:Btaf1
|
UTSW |
19 |
36,955,772 (GRCm39) |
missense |
probably benign |
0.00 |
R4731:Btaf1
|
UTSW |
19 |
36,958,478 (GRCm39) |
missense |
probably benign |
0.03 |
R4796:Btaf1
|
UTSW |
19 |
36,933,828 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4824:Btaf1
|
UTSW |
19 |
36,958,448 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4835:Btaf1
|
UTSW |
19 |
36,979,858 (GRCm39) |
missense |
probably benign |
0.00 |
R4837:Btaf1
|
UTSW |
19 |
36,944,185 (GRCm39) |
missense |
probably benign |
|
R4925:Btaf1
|
UTSW |
19 |
36,988,733 (GRCm39) |
missense |
probably benign |
|
R4968:Btaf1
|
UTSW |
19 |
36,947,351 (GRCm39) |
missense |
probably null |
0.71 |
R4976:Btaf1
|
UTSW |
19 |
36,963,979 (GRCm39) |
missense |
probably benign |
|
R5001:Btaf1
|
UTSW |
19 |
36,964,052 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5039:Btaf1
|
UTSW |
19 |
36,968,162 (GRCm39) |
missense |
probably benign |
|
R5211:Btaf1
|
UTSW |
19 |
36,973,962 (GRCm39) |
missense |
probably benign |
0.32 |
R5422:Btaf1
|
UTSW |
19 |
36,928,507 (GRCm39) |
missense |
probably benign |
0.09 |
R5429:Btaf1
|
UTSW |
19 |
36,972,257 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5530:Btaf1
|
UTSW |
19 |
36,968,175 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5582:Btaf1
|
UTSW |
19 |
36,965,573 (GRCm39) |
critical splice donor site |
probably null |
|
R5654:Btaf1
|
UTSW |
19 |
36,961,015 (GRCm39) |
missense |
probably benign |
0.35 |
R5744:Btaf1
|
UTSW |
19 |
36,981,890 (GRCm39) |
missense |
probably benign |
0.02 |
R6082:Btaf1
|
UTSW |
19 |
36,960,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R6243:Btaf1
|
UTSW |
19 |
36,958,520 (GRCm39) |
missense |
probably benign |
0.02 |
R6291:Btaf1
|
UTSW |
19 |
36,950,408 (GRCm39) |
missense |
probably benign |
0.00 |
R6502:Btaf1
|
UTSW |
19 |
36,961,017 (GRCm39) |
missense |
probably benign |
|
R7034:Btaf1
|
UTSW |
19 |
36,981,869 (GRCm39) |
missense |
probably benign |
|
R7036:Btaf1
|
UTSW |
19 |
36,981,869 (GRCm39) |
missense |
probably benign |
|
R7085:Btaf1
|
UTSW |
19 |
36,950,318 (GRCm39) |
missense |
probably benign |
|
R7097:Btaf1
|
UTSW |
19 |
36,926,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R7248:Btaf1
|
UTSW |
19 |
36,922,714 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7386:Btaf1
|
UTSW |
19 |
36,935,782 (GRCm39) |
missense |
probably benign |
0.02 |
R7402:Btaf1
|
UTSW |
19 |
36,980,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7452:Btaf1
|
UTSW |
19 |
36,946,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7493:Btaf1
|
UTSW |
19 |
36,987,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Btaf1
|
UTSW |
19 |
36,955,803 (GRCm39) |
missense |
probably benign |
0.30 |
R7888:Btaf1
|
UTSW |
19 |
36,943,036 (GRCm39) |
missense |
probably benign |
0.10 |
R7944:Btaf1
|
UTSW |
19 |
36,926,565 (GRCm39) |
missense |
probably benign |
|
R8062:Btaf1
|
UTSW |
19 |
36,969,865 (GRCm39) |
missense |
probably benign |
0.00 |
R8559:Btaf1
|
UTSW |
19 |
36,964,273 (GRCm39) |
missense |
probably benign |
0.00 |
R8793:Btaf1
|
UTSW |
19 |
36,958,429 (GRCm39) |
missense |
probably benign |
0.21 |
R8855:Btaf1
|
UTSW |
19 |
36,935,901 (GRCm39) |
missense |
probably benign |
|
R8866:Btaf1
|
UTSW |
19 |
36,935,901 (GRCm39) |
missense |
probably benign |
|
R9016:Btaf1
|
UTSW |
19 |
36,971,705 (GRCm39) |
missense |
probably benign |
0.00 |
R9028:Btaf1
|
UTSW |
19 |
36,946,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R9109:Btaf1
|
UTSW |
19 |
36,964,114 (GRCm39) |
missense |
probably benign |
|
R9172:Btaf1
|
UTSW |
19 |
36,977,630 (GRCm39) |
missense |
probably damaging |
0.98 |
R9298:Btaf1
|
UTSW |
19 |
36,964,114 (GRCm39) |
missense |
probably benign |
|
R9717:Btaf1
|
UTSW |
19 |
36,922,646 (GRCm39) |
missense |
probably benign |
0.28 |
W0251:Btaf1
|
UTSW |
19 |
36,980,904 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Btaf1
|
UTSW |
19 |
36,926,496 (GRCm39) |
nonsense |
probably null |
|
Z1088:Btaf1
|
UTSW |
19 |
36,964,018 (GRCm39) |
missense |
probably damaging |
0.99 |
|