Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700026F02Rik |
A |
G |
8: 71,495,689 (GRCm39) |
|
noncoding transcript |
Het |
Adam29 |
T |
C |
8: 56,324,732 (GRCm39) |
H574R |
probably damaging |
Het |
Arap1 |
C |
A |
7: 101,049,490 (GRCm39) |
T984K |
probably damaging |
Het |
Ccdc146 |
A |
T |
5: 21,521,837 (GRCm39) |
S396T |
probably benign |
Het |
Col6a3 |
T |
C |
1: 90,700,770 (GRCm39) |
K2587E |
unknown |
Het |
Cyp3a44 |
A |
G |
5: 145,727,496 (GRCm39) |
S278P |
probably damaging |
Het |
Daw1 |
T |
G |
1: 83,159,965 (GRCm39) |
|
probably benign |
Het |
Dnah17 |
T |
C |
11: 117,943,502 (GRCm39) |
K3200R |
probably benign |
Het |
Efhd2 |
A |
G |
4: 141,601,913 (GRCm39) |
F89S |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,856,642 (GRCm39) |
|
probably benign |
Het |
Ggps1 |
T |
C |
13: 14,228,979 (GRCm39) |
D68G |
probably damaging |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm3604 |
A |
T |
13: 62,517,954 (GRCm39) |
C134S |
probably damaging |
Het |
Gpaa1 |
A |
G |
15: 76,217,198 (GRCm39) |
T178A |
probably benign |
Het |
Lama3 |
A |
G |
18: 12,657,820 (GRCm39) |
N312S |
possibly damaging |
Het |
Npepps |
T |
C |
11: 97,126,948 (GRCm39) |
I437M |
probably damaging |
Het |
Or10q12 |
A |
G |
19: 13,746,534 (GRCm39) |
D276G |
probably benign |
Het |
Or11i1 |
C |
T |
3: 106,729,342 (GRCm39) |
D178N |
probably benign |
Het |
Rcor1 |
C |
A |
12: 111,070,193 (GRCm39) |
T330K |
possibly damaging |
Het |
Sbno2 |
A |
G |
10: 79,896,226 (GRCm39) |
|
probably null |
Het |
Sema3g |
A |
G |
14: 30,945,624 (GRCm39) |
E478G |
probably damaging |
Het |
Smg9 |
A |
G |
7: 24,115,949 (GRCm39) |
D280G |
probably damaging |
Het |
Smtnl1 |
A |
T |
2: 84,641,741 (GRCm39) |
*460R |
probably null |
Het |
Syde1 |
A |
G |
10: 78,424,753 (GRCm39) |
C360R |
possibly damaging |
Het |
Szt2 |
A |
G |
4: 118,256,268 (GRCm39) |
V197A |
possibly damaging |
Het |
Tnrc6c |
T |
C |
11: 117,646,274 (GRCm39) |
V1405A |
possibly damaging |
Het |
Ttbk1 |
A |
G |
17: 46,757,989 (GRCm39) |
S882P |
probably damaging |
Het |
Tubgcp4 |
T |
A |
2: 121,006,269 (GRCm39) |
H116Q |
possibly damaging |
Het |
Vmn1r192 |
T |
A |
13: 22,371,750 (GRCm39) |
N157Y |
probably damaging |
Het |
Vmn1r60 |
C |
T |
7: 5,547,228 (GRCm39) |
V291M |
probably benign |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Xpo5 |
C |
T |
17: 46,553,133 (GRCm39) |
P1184L |
possibly damaging |
Het |
Zfp946 |
T |
G |
17: 22,673,684 (GRCm39) |
I146S |
probably benign |
Het |
|
Other mutations in Gm21738 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Gm21738
|
APN |
14 |
19,418,885 (GRCm38) |
missense |
probably benign |
|
IGL01010:Gm21738
|
APN |
14 |
19,417,361 (GRCm38) |
missense |
probably benign |
0.03 |
IGL01018:Gm21738
|
APN |
14 |
19,418,856 (GRCm38) |
missense |
probably benign |
0.39 |
IGL01865:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01873:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01877:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01878:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01879:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01880:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01882:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01883:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01884:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01885:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01886:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01888:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01891:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01892:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01893:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01894:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01895:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01896:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01898:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01899:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01900:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01901:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01902:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01903:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01904:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01905:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01906:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01908:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01909:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01910:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01911:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01912:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01913:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01914:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01915:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01916:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01917:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01918:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01919:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01922:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01923:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01924:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01925:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01926:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01932:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01940:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01949:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
PIT4131001:Gm21738
|
UTSW |
14 |
19,417,330 (GRCm38) |
missense |
probably benign |
0.00 |
PIT4142001:Gm21738
|
UTSW |
14 |
19,417,330 (GRCm38) |
missense |
probably benign |
0.00 |
R0831:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R0831:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R0976:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1029:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R1146:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1231:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1231:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R1402:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1402:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R1638:Gm21738
|
UTSW |
14 |
19,418,908 (GRCm38) |
missense |
probably benign |
|
R1874:Gm21738
|
UTSW |
14 |
19,418,824 (GRCm38) |
missense |
possibly damaging |
0.64 |
R4392:Gm21738
|
UTSW |
14 |
19,417,178 (GRCm38) |
missense |
probably benign |
|
R4393:Gm21738
|
UTSW |
14 |
19,417,178 (GRCm38) |
missense |
probably benign |
|
R5049:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R5257:Gm21738
|
UTSW |
14 |
19,415,942 (GRCm38) |
missense |
probably benign |
|
R6756:Gm21738
|
UTSW |
14 |
19,418,824 (GRCm38) |
missense |
possibly damaging |
0.64 |
R6915:Gm21738
|
UTSW |
14 |
19,415,933 (GRCm38) |
missense |
probably benign |
|
V5622:Gm21738
|
UTSW |
14 |
19,417,180 (GRCm38) |
missense |
probably damaging |
1.00 |
|