Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930003A15Rik |
T |
G |
16: 19,702,530 (GRCm39) |
|
noncoding transcript |
Het |
Abca5 |
T |
C |
11: 110,210,658 (GRCm39) |
T174A |
probably benign |
Het |
Abcg3 |
G |
A |
5: 105,114,680 (GRCm39) |
S279L |
probably benign |
Het |
Acap3 |
T |
C |
4: 155,981,369 (GRCm39) |
L85P |
probably damaging |
Het |
Adgrl3 |
A |
G |
5: 81,660,101 (GRCm39) |
K290R |
probably damaging |
Het |
Ankhd1 |
A |
G |
18: 36,780,674 (GRCm39) |
T1909A |
probably benign |
Het |
Asap1 |
T |
C |
15: 63,982,808 (GRCm39) |
D832G |
probably damaging |
Het |
Atp6v0a2 |
T |
A |
5: 124,795,552 (GRCm39) |
L702Q |
possibly damaging |
Het |
Bsn |
A |
G |
9: 107,990,430 (GRCm39) |
V1774A |
probably damaging |
Het |
Cd209e |
T |
C |
8: 3,903,248 (GRCm39) |
E48G |
probably benign |
Het |
Cdadc1 |
T |
C |
14: 59,805,493 (GRCm39) |
|
probably null |
Het |
Cfap65 |
C |
CA |
1: 74,956,432 (GRCm39) |
|
probably null |
Het |
Cln3 |
A |
C |
7: 126,181,971 (GRCm39) |
S30R |
probably benign |
Het |
Cluap1 |
C |
T |
16: 3,751,636 (GRCm39) |
R332W |
probably damaging |
Het |
Crb1 |
A |
T |
1: 139,265,163 (GRCm39) |
V85E |
probably benign |
Het |
Crocc |
G |
A |
4: 140,760,265 (GRCm39) |
R789W |
probably damaging |
Het |
Cwh43 |
A |
G |
5: 73,572,397 (GRCm39) |
I212V |
probably benign |
Het |
Cyp2t4 |
C |
A |
7: 26,857,585 (GRCm39) |
F391L |
probably benign |
Het |
Dhx35 |
G |
T |
2: 158,673,781 (GRCm39) |
R404L |
probably damaging |
Het |
Disp1 |
A |
G |
1: 182,869,942 (GRCm39) |
L826S |
probably damaging |
Het |
Dync2h1 |
T |
A |
9: 7,122,772 (GRCm39) |
E2061D |
probably damaging |
Het |
Ep300 |
T |
A |
15: 81,524,648 (GRCm39) |
Y1393N |
unknown |
Het |
Fap |
C |
T |
2: 62,354,551 (GRCm39) |
G446D |
possibly damaging |
Het |
Fat3 |
A |
G |
9: 16,288,347 (GRCm39) |
I392T |
probably benign |
Het |
Fpr-rs4 |
CAGGAA |
CA |
17: 18,242,596 (GRCm39) |
|
probably null |
Het |
Glipr1l1 |
T |
C |
10: 111,896,381 (GRCm39) |
V56A |
probably damaging |
Het |
Grsf1 |
A |
G |
5: 88,820,517 (GRCm39) |
V7A |
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,509,410 (GRCm39) |
A3646V |
probably damaging |
Het |
Ipo9 |
A |
T |
1: 135,322,023 (GRCm39) |
I569N |
probably damaging |
Het |
Irs1 |
G |
T |
1: 82,267,763 (GRCm39) |
P151Q |
probably damaging |
Het |
Kalrn |
T |
C |
16: 34,128,094 (GRCm39) |
D491G |
possibly damaging |
Het |
Kctd7 |
T |
C |
5: 130,181,207 (GRCm39) |
L210P |
probably damaging |
Het |
Lifr |
C |
A |
15: 7,211,338 (GRCm39) |
D625E |
possibly damaging |
Het |
Lrguk |
T |
C |
6: 34,020,454 (GRCm39) |
V201A |
probably benign |
Het |
Mark1 |
A |
G |
1: 184,651,770 (GRCm39) |
V135A |
probably damaging |
Het |
Mical2 |
T |
A |
7: 111,870,722 (GRCm39) |
D70E |
possibly damaging |
Het |
Mrc1 |
T |
C |
2: 14,275,000 (GRCm39) |
Y434H |
probably damaging |
Het |
Myh10 |
C |
A |
11: 68,695,540 (GRCm39) |
Q1556K |
probably damaging |
Het |
Nav1 |
G |
A |
1: 135,382,174 (GRCm39) |
T1400I |
probably null |
Het |
Or1j11 |
A |
G |
2: 36,311,950 (GRCm39) |
D180G |
probably damaging |
Het |
Or2a7 |
A |
G |
6: 43,151,435 (GRCm39) |
K172E |
probably benign |
Het |
Or4b13 |
A |
C |
2: 90,082,597 (GRCm39) |
V245G |
probably damaging |
Het |
Or4f4b |
T |
C |
2: 111,313,961 (GRCm39) |
V62A |
probably damaging |
Het |
Or4p7 |
T |
A |
2: 88,221,663 (GRCm39) |
I24N |
probably benign |
Het |
Or5d43 |
T |
C |
2: 88,104,584 (GRCm39) |
K270E |
probably damaging |
Het |
Or5e1 |
G |
A |
7: 108,354,430 (GRCm39) |
M122I |
possibly damaging |
Het |
Osmr |
T |
A |
15: 6,881,943 (GRCm39) |
Q67L |
probably damaging |
Het |
Pan2 |
T |
G |
10: 128,149,506 (GRCm39) |
V522G |
possibly damaging |
Het |
Pard3 |
T |
G |
8: 128,103,366 (GRCm39) |
|
probably null |
Het |
Pcdhgc5 |
G |
T |
18: 37,953,166 (GRCm39) |
A147S |
possibly damaging |
Het |
Polr3d |
GCCCCC |
GCCCC |
14: 70,680,487 (GRCm39) |
|
probably null |
Het |
Prdm4 |
G |
A |
10: 85,729,215 (GRCm39) |
R731* |
probably null |
Het |
Prdx6b |
T |
A |
2: 80,123,507 (GRCm39) |
D105E |
probably damaging |
Het |
Prss3b |
A |
G |
6: 41,012,396 (GRCm39) |
F6S |
probably benign |
Het |
Rab42 |
A |
G |
4: 132,029,790 (GRCm39) |
L144P |
probably damaging |
Het |
Ralbp1 |
T |
A |
17: 66,171,661 (GRCm39) |
K104M |
probably damaging |
Het |
Resf1 |
T |
A |
6: 149,230,320 (GRCm39) |
I1122K |
probably benign |
Het |
Rrp12 |
A |
G |
19: 41,881,038 (GRCm39) |
V131A |
probably damaging |
Het |
Sbno1 |
C |
T |
5: 124,525,597 (GRCm39) |
|
probably null |
Het |
Sbno2 |
A |
T |
10: 79,898,527 (GRCm39) |
I645N |
probably damaging |
Het |
Scfd2 |
T |
C |
5: 74,367,028 (GRCm39) |
K624R |
probably benign |
Het |
Sgk2 |
C |
A |
2: 162,841,099 (GRCm39) |
|
probably null |
Het |
Sirt4 |
A |
G |
5: 115,617,760 (GRCm39) |
S299P |
probably benign |
Het |
Skic3 |
T |
C |
13: 76,321,473 (GRCm39) |
S1322P |
possibly damaging |
Het |
Slit2 |
C |
T |
5: 48,461,567 (GRCm39) |
A1521V |
probably benign |
Het |
Socs7 |
T |
G |
11: 97,263,933 (GRCm39) |
V275G |
possibly damaging |
Het |
Spink11 |
G |
A |
18: 44,323,554 (GRCm39) |
P102S |
probably benign |
Het |
Tacc3 |
A |
G |
5: 33,828,748 (GRCm39) |
N534D |
probably damaging |
Het |
Tas2r115 |
T |
C |
6: 132,714,309 (GRCm39) |
Y214C |
probably damaging |
Het |
Tcaf1 |
A |
T |
6: 42,650,454 (GRCm39) |
M875K |
probably benign |
Het |
Ttc22 |
T |
A |
4: 106,479,869 (GRCm39) |
L41Q |
possibly damaging |
Het |
Vasn |
T |
A |
16: 4,467,659 (GRCm39) |
C535* |
probably null |
Het |
Vcan |
T |
A |
13: 89,837,856 (GRCm39) |
I2563F |
probably damaging |
Het |
Vmn2r63 |
T |
G |
7: 42,576,297 (GRCm39) |
Q505H |
probably damaging |
Het |
Vmn2r65 |
T |
G |
7: 84,592,781 (GRCm39) |
Q475H |
probably damaging |
Het |
Zbtb43 |
T |
C |
2: 33,344,532 (GRCm39) |
Y231C |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,810,266 (GRCm39) |
V931A |
probably benign |
Het |
|
Other mutations in Pcsk9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02140:Pcsk9
|
APN |
4 |
106,311,843 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02709:Pcsk9
|
APN |
4 |
106,304,886 (GRCm39) |
splice site |
probably benign |
|
IGL02804:Pcsk9
|
APN |
4 |
106,314,161 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02850:Pcsk9
|
APN |
4 |
106,316,062 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03009:Pcsk9
|
APN |
4 |
106,311,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03294:Pcsk9
|
APN |
4 |
106,303,967 (GRCm39) |
missense |
probably benign |
|
R0271:Pcsk9
|
UTSW |
4 |
106,306,246 (GRCm39) |
splice site |
probably benign |
|
R0321:Pcsk9
|
UTSW |
4 |
106,301,891 (GRCm39) |
missense |
probably benign |
|
R0413:Pcsk9
|
UTSW |
4 |
106,311,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R0426:Pcsk9
|
UTSW |
4 |
106,307,274 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0783:Pcsk9
|
UTSW |
4 |
106,307,314 (GRCm39) |
missense |
probably benign |
0.00 |
R4056:Pcsk9
|
UTSW |
4 |
106,301,899 (GRCm39) |
missense |
probably benign |
0.02 |
R4438:Pcsk9
|
UTSW |
4 |
106,316,156 (GRCm39) |
missense |
probably benign |
0.00 |
R4683:Pcsk9
|
UTSW |
4 |
106,316,092 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4739:Pcsk9
|
UTSW |
4 |
106,304,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Pcsk9
|
UTSW |
4 |
106,304,766 (GRCm39) |
missense |
probably benign |
0.43 |
R4802:Pcsk9
|
UTSW |
4 |
106,304,766 (GRCm39) |
missense |
probably benign |
0.43 |
R5249:Pcsk9
|
UTSW |
4 |
106,320,950 (GRCm39) |
missense |
probably benign |
0.01 |
R5307:Pcsk9
|
UTSW |
4 |
106,304,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Pcsk9
|
UTSW |
4 |
106,320,988 (GRCm39) |
missense |
probably benign |
0.00 |
R5653:Pcsk9
|
UTSW |
4 |
106,316,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R5827:Pcsk9
|
UTSW |
4 |
106,306,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Pcsk9
|
UTSW |
4 |
106,311,469 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6019:Pcsk9
|
UTSW |
4 |
106,314,073 (GRCm39) |
missense |
probably benign |
0.02 |
R6393:Pcsk9
|
UTSW |
4 |
106,304,793 (GRCm39) |
missense |
probably benign |
0.00 |
R7472:Pcsk9
|
UTSW |
4 |
106,316,094 (GRCm39) |
missense |
probably benign |
0.08 |
R7614:Pcsk9
|
UTSW |
4 |
106,304,763 (GRCm39) |
missense |
probably benign |
0.34 |
R7807:Pcsk9
|
UTSW |
4 |
106,321,092 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8036:Pcsk9
|
UTSW |
4 |
106,311,536 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8735:Pcsk9
|
UTSW |
4 |
106,311,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R9258:Pcsk9
|
UTSW |
4 |
106,316,047 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9404:Pcsk9
|
UTSW |
4 |
106,311,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R9684:Pcsk9
|
UTSW |
4 |
106,307,386 (GRCm39) |
missense |
probably benign |
0.29 |
Z1176:Pcsk9
|
UTSW |
4 |
106,316,138 (GRCm39) |
missense |
probably damaging |
0.96 |
|