Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932416K20Rik |
G |
A |
8: 105,524,271 (GRCm39) |
|
noncoding transcript |
Het |
Abcg8 |
A |
T |
17: 84,994,127 (GRCm39) |
E48V |
probably damaging |
Het |
Afap1l2 |
T |
C |
19: 56,911,406 (GRCm39) |
T289A |
probably benign |
Het |
Atf6 |
T |
A |
1: 170,574,758 (GRCm39) |
D560V |
probably damaging |
Het |
Bcl2l14 |
A |
T |
6: 134,404,362 (GRCm39) |
K183N |
probably damaging |
Het |
Carmil3 |
T |
C |
14: 55,730,696 (GRCm39) |
L52P |
probably damaging |
Het |
Cct3 |
T |
A |
3: 88,208,274 (GRCm39) |
N61K |
probably damaging |
Het |
Col18a1 |
A |
G |
10: 77,002,177 (GRCm39) |
V10A |
unknown |
Het |
Col26a1 |
G |
A |
5: 136,876,420 (GRCm39) |
Q67* |
probably null |
Het |
Cyp2d34 |
T |
C |
15: 82,501,341 (GRCm39) |
D329G |
probably null |
Het |
Dchs1 |
T |
A |
7: 105,422,247 (GRCm39) |
I58F |
probably damaging |
Het |
Ddx60 |
T |
C |
8: 62,401,931 (GRCm39) |
L269P |
probably damaging |
Het |
Dis3l2 |
G |
A |
1: 86,806,154 (GRCm39) |
G325D |
probably damaging |
Het |
Dync1h1 |
A |
T |
12: 110,612,707 (GRCm39) |
K2861* |
probably null |
Het |
Ednra |
A |
G |
8: 78,401,696 (GRCm39) |
I198T |
possibly damaging |
Het |
Ep300 |
T |
C |
15: 81,524,115 (GRCm39) |
|
probably benign |
Het |
Fam120a |
G |
A |
13: 49,034,409 (GRCm39) |
P1068S |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,815,084 (GRCm39) |
M3606L |
probably benign |
Het |
Garre1 |
A |
T |
7: 33,953,413 (GRCm39) |
W238R |
probably damaging |
Het |
Gm7713 |
T |
C |
15: 59,866,492 (GRCm39) |
|
noncoding transcript |
Het |
Gprin3 |
A |
T |
6: 59,331,398 (GRCm39) |
V303D |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,570,629 (GRCm39) |
V2178D |
possibly damaging |
Het |
Hoxa11 |
A |
G |
6: 52,222,380 (GRCm39) |
V107A |
possibly damaging |
Het |
Iqub |
C |
A |
6: 24,454,250 (GRCm39) |
M544I |
possibly damaging |
Het |
Itgb4 |
A |
T |
11: 115,879,258 (GRCm39) |
|
probably benign |
Het |
Itpkb |
A |
G |
1: 180,161,818 (GRCm39) |
|
probably benign |
Het |
Kalrn |
A |
T |
16: 33,796,190 (GRCm39) |
V1195E |
probably damaging |
Het |
Kif12 |
C |
A |
4: 63,084,178 (GRCm39) |
R608M |
probably damaging |
Het |
Lcorl |
A |
T |
5: 45,952,709 (GRCm39) |
|
probably null |
Het |
Lrrc24 |
T |
C |
15: 76,606,910 (GRCm39) |
E162G |
probably damaging |
Het |
Med6 |
A |
G |
12: 81,626,418 (GRCm39) |
S119P |
probably damaging |
Het |
Mmab |
A |
C |
5: 114,574,775 (GRCm39) |
L166R |
probably damaging |
Het |
Myef2l |
A |
G |
3: 10,153,566 (GRCm39) |
R112G |
probably damaging |
Het |
Nom1 |
A |
G |
5: 29,651,873 (GRCm39) |
K737R |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,946,970 (GRCm39) |
S4352G |
probably damaging |
Het |
Or10ag60 |
A |
T |
2: 87,438,517 (GRCm39) |
T262S |
probably benign |
Het |
Or2w25 |
T |
A |
11: 59,504,712 (GRCm39) |
D307E |
probably benign |
Het |
Or4k35 |
A |
T |
2: 111,100,057 (GRCm39) |
Y218* |
probably null |
Het |
Or6d12 |
A |
C |
6: 116,492,912 (GRCm39) |
D58A |
possibly damaging |
Het |
Pdzrn3 |
G |
A |
6: 101,149,275 (GRCm39) |
S351L |
probably benign |
Het |
Pdzrn4 |
A |
T |
15: 92,655,562 (GRCm39) |
E485V |
probably damaging |
Het |
Prkdc |
T |
A |
16: 15,597,252 (GRCm39) |
I2804K |
possibly damaging |
Het |
Psg28 |
A |
G |
7: 18,164,640 (GRCm39) |
L24P |
probably damaging |
Het |
Resp18 |
A |
G |
1: 75,250,644 (GRCm39) |
V145A |
possibly damaging |
Het |
Rgl3 |
T |
C |
9: 21,892,908 (GRCm39) |
M259V |
probably benign |
Het |
Rhot2 |
A |
T |
17: 26,058,781 (GRCm39) |
S540T |
probably benign |
Het |
Ring1 |
T |
C |
17: 34,241,282 (GRCm39) |
Y278C |
possibly damaging |
Het |
Rpn2 |
A |
G |
2: 157,137,265 (GRCm39) |
Y216C |
probably damaging |
Het |
Scgb2b18 |
G |
A |
7: 32,873,255 (GRCm39) |
L5F |
unknown |
Het |
Slamf7 |
T |
C |
1: 171,466,838 (GRCm39) |
|
probably null |
Het |
Slc22a12 |
T |
C |
19: 6,590,479 (GRCm39) |
N237S |
possibly damaging |
Het |
Spen |
A |
T |
4: 141,205,495 (GRCm39) |
V1044D |
unknown |
Het |
Stx16 |
G |
A |
2: 173,935,292 (GRCm39) |
G156R |
probably damaging |
Het |
Tars3 |
T |
G |
7: 65,333,873 (GRCm39) |
F632V |
probably damaging |
Het |
Tln1 |
A |
G |
4: 43,545,191 (GRCm39) |
V1008A |
probably benign |
Het |
Tmem145 |
A |
G |
7: 25,015,039 (GRCm39) |
H554R |
probably benign |
Het |
Trank1 |
A |
T |
9: 111,195,744 (GRCm39) |
D1256V |
possibly damaging |
Het |
Trbv19 |
A |
G |
6: 41,155,794 (GRCm39) |
Y55C |
possibly damaging |
Het |
Ttc23l |
C |
T |
15: 10,551,555 (GRCm39) |
C57Y |
probably benign |
Het |
Uap1 |
A |
T |
1: 169,988,949 (GRCm39) |
C158S |
probably benign |
Het |
Zfp353-ps |
T |
A |
8: 42,535,647 (GRCm39) |
|
noncoding transcript |
Het |
Zfp629 |
T |
A |
7: 127,210,307 (GRCm39) |
I501F |
probably damaging |
Het |
Zfp820 |
T |
C |
17: 22,037,702 (GRCm39) |
Y542C |
probably damaging |
Het |
|
Other mutations in Sqor |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Sqor
|
APN |
2 |
122,629,463 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01544:Sqor
|
APN |
2 |
122,634,266 (GRCm39) |
splice site |
probably benign |
|
IGL02499:Sqor
|
APN |
2 |
122,650,007 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02583:Sqor
|
APN |
2 |
122,641,690 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02732:Sqor
|
APN |
2 |
122,641,682 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03137:Sqor
|
APN |
2 |
122,649,991 (GRCm39) |
missense |
probably benign |
|
H8786:Sqor
|
UTSW |
2 |
122,634,288 (GRCm39) |
missense |
probably benign |
0.10 |
R0126:Sqor
|
UTSW |
2 |
122,639,947 (GRCm39) |
unclassified |
probably benign |
|
R0410:Sqor
|
UTSW |
2 |
122,629,442 (GRCm39) |
missense |
probably benign |
|
R0502:Sqor
|
UTSW |
2 |
122,639,970 (GRCm39) |
missense |
probably benign |
0.04 |
R0709:Sqor
|
UTSW |
2 |
122,641,775 (GRCm39) |
missense |
probably benign |
0.38 |
R1486:Sqor
|
UTSW |
2 |
122,649,565 (GRCm39) |
splice site |
probably null |
|
R2001:Sqor
|
UTSW |
2 |
122,640,018 (GRCm39) |
missense |
probably damaging |
0.98 |
R2020:Sqor
|
UTSW |
2 |
122,646,027 (GRCm39) |
critical splice donor site |
probably null |
|
R2039:Sqor
|
UTSW |
2 |
122,634,324 (GRCm39) |
critical splice donor site |
probably null |
|
R2404:Sqor
|
UTSW |
2 |
122,649,943 (GRCm39) |
missense |
probably benign |
|
R4213:Sqor
|
UTSW |
2 |
122,629,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R4909:Sqor
|
UTSW |
2 |
122,627,101 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5630:Sqor
|
UTSW |
2 |
122,651,277 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5659:Sqor
|
UTSW |
2 |
122,629,523 (GRCm39) |
missense |
probably benign |
0.02 |
R5728:Sqor
|
UTSW |
2 |
122,651,320 (GRCm39) |
makesense |
probably null |
|
R6527:Sqor
|
UTSW |
2 |
122,651,206 (GRCm39) |
missense |
probably damaging |
0.98 |
R6657:Sqor
|
UTSW |
2 |
122,649,514 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6843:Sqor
|
UTSW |
2 |
122,651,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R6843:Sqor
|
UTSW |
2 |
122,626,900 (GRCm39) |
missense |
probably benign |
0.00 |
R7193:Sqor
|
UTSW |
2 |
122,645,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Sqor
|
UTSW |
2 |
122,641,730 (GRCm39) |
missense |
probably benign |
|
R7417:Sqor
|
UTSW |
2 |
122,629,450 (GRCm39) |
missense |
probably benign |
0.35 |
R7846:Sqor
|
UTSW |
2 |
122,627,008 (GRCm39) |
missense |
probably benign |
0.37 |
R8913:Sqor
|
UTSW |
2 |
122,641,806 (GRCm39) |
missense |
probably benign |
|
R8939:Sqor
|
UTSW |
2 |
122,649,549 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9007:Sqor
|
UTSW |
2 |
122,649,876 (GRCm39) |
nonsense |
probably null |
|
R9030:Sqor
|
UTSW |
2 |
122,629,514 (GRCm39) |
missense |
probably benign |
0.14 |
R9447:Sqor
|
UTSW |
2 |
122,649,520 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9790:Sqor
|
UTSW |
2 |
122,626,912 (GRCm39) |
missense |
probably benign |
0.00 |
R9791:Sqor
|
UTSW |
2 |
122,626,912 (GRCm39) |
missense |
probably benign |
0.00 |
|