Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
T |
C |
5: 138,561,107 (GRCm39) |
E185G |
probably damaging |
Het |
3425401B19Rik |
A |
G |
14: 32,384,508 (GRCm39) |
S486P |
probably benign |
Het |
A630023A22Rik |
T |
C |
14: 33,774,707 (GRCm39) |
|
probably benign |
Het |
Abca1 |
T |
C |
4: 53,069,881 (GRCm39) |
N1271S |
probably benign |
Het |
AI597479 |
C |
T |
1: 43,150,280 (GRCm39) |
A130V |
probably benign |
Het |
Angptl4 |
A |
G |
17: 33,999,498 (GRCm39) |
|
probably null |
Het |
Arhgef25 |
T |
A |
10: 127,021,004 (GRCm39) |
N294I |
probably damaging |
Het |
Atp2b1 |
T |
C |
10: 98,850,421 (GRCm39) |
V848A |
probably damaging |
Het |
Bard1 |
T |
C |
1: 71,114,031 (GRCm39) |
T317A |
probably benign |
Het |
C1rl |
T |
C |
6: 124,470,781 (GRCm39) |
W30R |
probably benign |
Het |
Cchcr1 |
A |
G |
17: 35,837,317 (GRCm39) |
E379G |
probably damaging |
Het |
Cfap36 |
G |
T |
11: 29,197,122 (GRCm39) |
A3E |
probably damaging |
Het |
Cilp |
G |
A |
9: 65,186,997 (GRCm39) |
G1031S |
probably damaging |
Het |
Clca4a |
A |
G |
3: 144,676,489 (GRCm39) |
Y64H |
probably damaging |
Het |
Cops5 |
A |
G |
1: 10,102,562 (GRCm39) |
|
probably null |
Het |
Cracr2a |
G |
T |
6: 127,585,564 (GRCm39) |
E121* |
probably null |
Het |
D630044L22Rik |
A |
C |
17: 26,180,951 (GRCm39) |
D733E |
probably damaging |
Het |
Dlc1 |
A |
T |
8: 37,060,535 (GRCm39) |
C514S |
probably damaging |
Het |
Dmwd |
G |
T |
7: 18,810,610 (GRCm39) |
R139L |
probably benign |
Het |
Dnah17 |
A |
T |
11: 117,958,357 (GRCm39) |
S2709T |
probably benign |
Het |
Dnmt3a |
T |
C |
12: 3,922,859 (GRCm39) |
I154T |
probably benign |
Het |
Dpp7 |
T |
C |
2: 25,244,490 (GRCm39) |
N297S |
possibly damaging |
Het |
Ern2 |
A |
T |
7: 121,783,168 (GRCm39) |
V34D |
possibly damaging |
Het |
Erp27 |
A |
G |
6: 136,885,227 (GRCm39) |
|
probably benign |
Het |
F2 |
T |
C |
2: 91,458,787 (GRCm39) |
T508A |
probably benign |
Het |
Fam181b |
A |
G |
7: 92,729,634 (GRCm39) |
T136A |
probably benign |
Het |
Fam227b |
C |
A |
2: 125,942,874 (GRCm39) |
V308L |
probably benign |
Het |
Fbxw20 |
A |
T |
9: 109,050,442 (GRCm39) |
H394Q |
probably damaging |
Het |
G530012D18Rik |
CAGAGAGA |
CAGAGAGAGA |
1: 85,504,945 (GRCm39) |
|
probably null |
Het |
Glt8d1 |
T |
G |
14: 30,731,693 (GRCm39) |
S111A |
probably benign |
Het |
Gm11146 |
A |
T |
16: 77,391,969 (GRCm39) |
|
probably benign |
Het |
Grip1 |
C |
T |
10: 119,885,416 (GRCm39) |
|
probably benign |
Het |
H2-Q2 |
A |
T |
17: 35,564,247 (GRCm39) |
T334S |
probably benign |
Het |
Hcrtr1 |
A |
G |
4: 130,024,680 (GRCm39) |
V402A |
probably benign |
Het |
Hmcn2 |
C |
A |
2: 31,268,294 (GRCm39) |
A1130D |
probably benign |
Het |
Hsd17b2 |
T |
C |
8: 118,428,913 (GRCm39) |
L60P |
possibly damaging |
Het |
Htr1f |
A |
T |
16: 64,746,398 (GRCm39) |
I298N |
probably damaging |
Het |
Ighmbp2 |
G |
T |
19: 3,315,095 (GRCm39) |
A775D |
probably benign |
Het |
Kcnn3 |
A |
G |
3: 89,428,682 (GRCm39) |
T303A |
probably damaging |
Het |
Kiz |
C |
A |
2: 146,733,203 (GRCm39) |
Q460K |
probably benign |
Het |
Krt75 |
C |
T |
15: 101,481,196 (GRCm39) |
V193I |
probably benign |
Het |
Lsp1 |
G |
A |
7: 142,043,144 (GRCm39) |
|
probably null |
Het |
Mfsd12 |
A |
G |
10: 81,196,063 (GRCm39) |
H146R |
probably damaging |
Het |
Mmp23 |
T |
C |
4: 155,736,444 (GRCm39) |
K199R |
possibly damaging |
Het |
Naip2 |
A |
G |
13: 100,315,880 (GRCm39) |
V300A |
probably benign |
Het |
Nbeal1 |
C |
T |
1: 60,350,216 (GRCm39) |
L2422F |
probably damaging |
Het |
Nbeal2 |
G |
T |
9: 110,464,375 (GRCm39) |
D1094E |
possibly damaging |
Het |
Nckap5 |
T |
C |
1: 125,954,635 (GRCm39) |
E639G |
probably damaging |
Het |
Nr4a3 |
A |
G |
4: 48,067,771 (GRCm39) |
I456V |
possibly damaging |
Het |
Or2t43 |
A |
G |
11: 58,457,673 (GRCm39) |
F166S |
probably damaging |
Het |
Parp9 |
G |
T |
16: 35,773,984 (GRCm39) |
V86L |
probably damaging |
Het |
Phactr1 |
A |
G |
13: 43,231,416 (GRCm39) |
N386S |
probably damaging |
Het |
Pold2 |
A |
T |
11: 5,823,516 (GRCm39) |
Y304* |
probably null |
Het |
Pou5f2 |
A |
G |
13: 78,173,940 (GRCm39) |
Y294C |
probably benign |
Het |
Rars1 |
A |
G |
11: 35,717,410 (GRCm39) |
|
probably benign |
Het |
Rbm12b1 |
A |
G |
4: 12,145,606 (GRCm39) |
E526G |
probably benign |
Het |
Sacs |
T |
C |
14: 61,451,498 (GRCm39) |
Y4515H |
probably damaging |
Het |
Sdk2 |
C |
A |
11: 113,741,780 (GRCm39) |
R813L |
probably damaging |
Het |
Six5 |
T |
C |
7: 18,829,154 (GRCm39) |
V198A |
possibly damaging |
Het |
Slco1a7 |
A |
T |
6: 141,671,181 (GRCm39) |
H430Q |
probably benign |
Het |
Spata31e2 |
A |
T |
1: 26,724,813 (GRCm39) |
N122K |
possibly damaging |
Het |
Spn |
A |
G |
7: 126,736,388 (GRCm39) |
S40P |
probably damaging |
Het |
Ssr1 |
A |
G |
13: 38,171,761 (GRCm39) |
|
probably benign |
Het |
Tlr6 |
C |
A |
5: 65,111,269 (GRCm39) |
C546F |
probably damaging |
Het |
Top1 |
T |
A |
2: 160,544,748 (GRCm39) |
|
probably benign |
Het |
Trhr2 |
A |
G |
8: 123,085,532 (GRCm39) |
S151P |
probably damaging |
Het |
Tubb2b |
T |
G |
13: 34,311,708 (GRCm39) |
K362Q |
probably benign |
Het |
Unc13c |
T |
C |
9: 73,643,832 (GRCm39) |
T1211A |
probably damaging |
Het |
Vmn1r15 |
T |
C |
6: 57,235,729 (GRCm39) |
V199A |
possibly damaging |
Het |
Vnn1 |
A |
G |
10: 23,776,475 (GRCm39) |
|
probably benign |
Het |
Vps41 |
T |
A |
13: 19,038,786 (GRCm39) |
N737K |
possibly damaging |
Het |
Vps50 |
T |
A |
6: 3,522,265 (GRCm39) |
N144K |
probably benign |
Het |
Zc3h7a |
A |
T |
16: 10,955,340 (GRCm39) |
N911K |
probably benign |
Het |
Zkscan7 |
T |
A |
9: 122,718,002 (GRCm39) |
S132R |
probably damaging |
Het |
|
Other mutations in Cstf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01658:Cstf1
|
APN |
2 |
172,214,993 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02306:Cstf1
|
APN |
2 |
172,214,891 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02553:Cstf1
|
APN |
2 |
172,219,774 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02756:Cstf1
|
APN |
2 |
172,217,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Cstf1
|
UTSW |
2 |
172,214,976 (GRCm39) |
missense |
probably benign |
0.04 |
R0066:Cstf1
|
UTSW |
2 |
172,214,976 (GRCm39) |
missense |
probably benign |
0.04 |
R0244:Cstf1
|
UTSW |
2 |
172,219,630 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1448:Cstf1
|
UTSW |
2 |
172,217,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R1770:Cstf1
|
UTSW |
2 |
172,214,983 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2146:Cstf1
|
UTSW |
2 |
172,217,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R3119:Cstf1
|
UTSW |
2 |
172,214,990 (GRCm39) |
missense |
possibly damaging |
0.75 |
R3701:Cstf1
|
UTSW |
2 |
172,222,312 (GRCm39) |
missense |
probably benign |
0.00 |
R4816:Cstf1
|
UTSW |
2 |
172,214,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R4893:Cstf1
|
UTSW |
2 |
172,222,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R4991:Cstf1
|
UTSW |
2 |
172,219,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Cstf1
|
UTSW |
2 |
172,219,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R5743:Cstf1
|
UTSW |
2 |
172,219,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R6386:Cstf1
|
UTSW |
2 |
172,219,816 (GRCm39) |
missense |
probably damaging |
0.97 |
R7314:Cstf1
|
UTSW |
2 |
172,214,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R7843:Cstf1
|
UTSW |
2 |
172,219,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R8212:Cstf1
|
UTSW |
2 |
172,219,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R8930:Cstf1
|
UTSW |
2 |
172,217,623 (GRCm39) |
missense |
probably benign |
|
R8932:Cstf1
|
UTSW |
2 |
172,217,623 (GRCm39) |
missense |
probably benign |
|
R9089:Cstf1
|
UTSW |
2 |
172,217,807 (GRCm39) |
missense |
|
|
R9240:Cstf1
|
UTSW |
2 |
172,217,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R9545:Cstf1
|
UTSW |
2 |
172,212,885 (GRCm39) |
intron |
probably benign |
|
R9610:Cstf1
|
UTSW |
2 |
172,214,984 (GRCm39) |
missense |
probably benign |
0.33 |
R9611:Cstf1
|
UTSW |
2 |
172,214,984 (GRCm39) |
missense |
probably benign |
0.33 |
X0026:Cstf1
|
UTSW |
2 |
172,217,780 (GRCm39) |
missense |
probably damaging |
1.00 |
|