Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ambn |
A |
C |
5: 88,612,343 (GRCm39) |
D188A |
probably damaging |
Het |
Arfgef1 |
T |
C |
1: 10,270,054 (GRCm39) |
E365G |
probably benign |
Het |
Arhgef10 |
C |
T |
8: 14,980,198 (GRCm39) |
A146V |
probably benign |
Het |
AW554918 |
C |
T |
18: 25,423,001 (GRCm39) |
Q151* |
probably null |
Het |
Chd6 |
T |
C |
2: 160,802,183 (GRCm39) |
D2217G |
probably damaging |
Het |
Cntn5 |
T |
A |
9: 9,984,115 (GRCm39) |
E166V |
probably damaging |
Het |
Cyp4f15 |
T |
C |
17: 32,918,926 (GRCm39) |
S319P |
possibly damaging |
Het |
Dna2 |
G |
A |
10: 62,792,821 (GRCm39) |
V279I |
possibly damaging |
Het |
Edrf1 |
A |
G |
7: 133,258,220 (GRCm39) |
|
probably benign |
Het |
Fmo3 |
A |
T |
1: 162,786,052 (GRCm39) |
F313I |
probably damaging |
Het |
Kcnj10 |
A |
G |
1: 172,197,221 (GRCm39) |
D245G |
possibly damaging |
Het |
Lrsam1 |
T |
C |
2: 32,818,661 (GRCm39) |
|
probably null |
Het |
Mfn1 |
A |
T |
3: 32,628,439 (GRCm39) |
H690L |
probably benign |
Het |
Nlrp4a |
T |
G |
7: 26,159,240 (GRCm39) |
|
probably benign |
Het |
Or2t44 |
T |
A |
11: 58,677,606 (GRCm39) |
L182* |
probably null |
Het |
Or4d10b |
A |
G |
19: 12,036,811 (GRCm39) |
F102L |
probably damaging |
Het |
Or4k45 |
T |
A |
2: 111,394,888 (GRCm39) |
R300S |
possibly damaging |
Het |
Or51f5 |
T |
A |
7: 102,424,505 (GRCm39) |
I258N |
probably damaging |
Het |
Or52n2c |
T |
C |
7: 104,574,075 (GRCm39) |
T299A |
probably damaging |
Het |
Or8g35 |
G |
A |
9: 39,381,542 (GRCm39) |
T160I |
probably benign |
Het |
Plcxd3 |
G |
A |
15: 4,604,285 (GRCm39) |
V298I |
possibly damaging |
Het |
Prrc2b |
C |
T |
2: 32,084,441 (GRCm39) |
S302F |
probably damaging |
Het |
Serpine2 |
A |
T |
1: 79,779,272 (GRCm39) |
F149I |
probably damaging |
Het |
Slc24a5 |
T |
C |
2: 124,930,154 (GRCm39) |
L485P |
probably damaging |
Het |
Spg11 |
T |
A |
2: 121,889,988 (GRCm39) |
H2118L |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Stxbp1 |
T |
C |
2: 32,709,913 (GRCm39) |
D60G |
probably damaging |
Het |
Themis2 |
T |
A |
4: 132,510,795 (GRCm39) |
E582D |
probably benign |
Het |
Tmem131 |
T |
G |
1: 36,832,232 (GRCm39) |
I1802L |
probably benign |
Het |
Tnrc6a |
A |
G |
7: 122,770,696 (GRCm39) |
K829E |
probably damaging |
Het |
Usp8 |
T |
C |
2: 126,575,943 (GRCm39) |
M213T |
probably damaging |
Het |
Wnk2 |
A |
G |
13: 49,248,920 (GRCm39) |
V377A |
probably damaging |
Het |
Wwox |
T |
G |
8: 116,078,443 (GRCm39) |
Y375D |
probably damaging |
Het |
|
Other mutations in Msh2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01405:Msh2
|
APN |
17 |
87,985,663 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01602:Msh2
|
APN |
17 |
88,003,917 (GRCm39) |
unclassified |
probably benign |
|
IGL01605:Msh2
|
APN |
17 |
88,003,917 (GRCm39) |
unclassified |
probably benign |
|
IGL01775:Msh2
|
APN |
17 |
87,990,074 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02243:Msh2
|
APN |
17 |
87,985,796 (GRCm39) |
splice site |
probably benign |
|
IGL02524:Msh2
|
APN |
17 |
87,985,785 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02730:Msh2
|
APN |
17 |
88,014,643 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03049:Msh2
|
APN |
17 |
88,015,937 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03282:Msh2
|
APN |
17 |
87,996,430 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03286:Msh2
|
APN |
17 |
87,990,095 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0011:Msh2
|
UTSW |
17 |
87,987,521 (GRCm39) |
intron |
probably benign |
|
R0363:Msh2
|
UTSW |
17 |
88,024,904 (GRCm39) |
missense |
probably benign |
0.30 |
R0520:Msh2
|
UTSW |
17 |
88,024,972 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0633:Msh2
|
UTSW |
17 |
87,980,238 (GRCm39) |
splice site |
probably null |
|
R0862:Msh2
|
UTSW |
17 |
87,987,480 (GRCm39) |
missense |
probably benign |
|
R0864:Msh2
|
UTSW |
17 |
87,987,480 (GRCm39) |
missense |
probably benign |
|
R1146:Msh2
|
UTSW |
17 |
87,987,488 (GRCm39) |
missense |
probably benign |
0.00 |
R1146:Msh2
|
UTSW |
17 |
87,987,488 (GRCm39) |
missense |
probably benign |
0.00 |
R1264:Msh2
|
UTSW |
17 |
88,014,607 (GRCm39) |
splice site |
probably null |
|
R1459:Msh2
|
UTSW |
17 |
87,985,771 (GRCm39) |
missense |
probably benign |
0.01 |
R1572:Msh2
|
UTSW |
17 |
88,026,080 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1592:Msh2
|
UTSW |
17 |
87,987,441 (GRCm39) |
splice site |
probably null |
|
R1647:Msh2
|
UTSW |
17 |
87,980,064 (GRCm39) |
missense |
probably benign |
|
R1984:Msh2
|
UTSW |
17 |
88,026,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R2298:Msh2
|
UTSW |
17 |
88,015,930 (GRCm39) |
missense |
probably damaging |
0.99 |
R2871:Msh2
|
UTSW |
17 |
87,993,012 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2871:Msh2
|
UTSW |
17 |
87,993,012 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4383:Msh2
|
UTSW |
17 |
87,996,566 (GRCm39) |
missense |
probably benign |
0.00 |
R4411:Msh2
|
UTSW |
17 |
88,025,032 (GRCm39) |
missense |
probably damaging |
0.97 |
R4589:Msh2
|
UTSW |
17 |
87,987,460 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4598:Msh2
|
UTSW |
17 |
88,016,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4599:Msh2
|
UTSW |
17 |
88,016,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4712:Msh2
|
UTSW |
17 |
87,985,813 (GRCm39) |
intron |
probably benign |
|
R4714:Msh2
|
UTSW |
17 |
88,026,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Msh2
|
UTSW |
17 |
88,030,841 (GRCm39) |
missense |
probably benign |
|
R4842:Msh2
|
UTSW |
17 |
88,030,841 (GRCm39) |
missense |
probably benign |
|
R4859:Msh2
|
UTSW |
17 |
88,026,187 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5007:Msh2
|
UTSW |
17 |
88,030,841 (GRCm39) |
missense |
probably benign |
|
R5008:Msh2
|
UTSW |
17 |
88,030,841 (GRCm39) |
missense |
probably benign |
|
R5010:Msh2
|
UTSW |
17 |
88,030,841 (GRCm39) |
missense |
probably benign |
|
R5014:Msh2
|
UTSW |
17 |
88,025,004 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5048:Msh2
|
UTSW |
17 |
87,980,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Msh2
|
UTSW |
17 |
88,030,841 (GRCm39) |
missense |
probably benign |
|
R5162:Msh2
|
UTSW |
17 |
88,030,841 (GRCm39) |
missense |
probably benign |
|
R5163:Msh2
|
UTSW |
17 |
88,030,841 (GRCm39) |
missense |
probably benign |
|
R5183:Msh2
|
UTSW |
17 |
88,030,841 (GRCm39) |
missense |
probably benign |
|
R5184:Msh2
|
UTSW |
17 |
88,030,841 (GRCm39) |
missense |
probably benign |
|
R5597:Msh2
|
UTSW |
17 |
88,030,789 (GRCm39) |
missense |
probably benign |
0.04 |
R5655:Msh2
|
UTSW |
17 |
88,026,871 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5973:Msh2
|
UTSW |
17 |
88,016,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R6191:Msh2
|
UTSW |
17 |
88,030,900 (GRCm39) |
missense |
probably benign |
0.03 |
R6632:Msh2
|
UTSW |
17 |
88,020,094 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7260:Msh2
|
UTSW |
17 |
88,025,047 (GRCm39) |
missense |
probably damaging |
0.97 |
R7358:Msh2
|
UTSW |
17 |
88,024,957 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9197:Msh2
|
UTSW |
17 |
88,026,943 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9227:Msh2
|
UTSW |
17 |
88,026,717 (GRCm39) |
missense |
probably benign |
0.10 |
R9230:Msh2
|
UTSW |
17 |
88,026,717 (GRCm39) |
missense |
probably benign |
0.10 |
R9459:Msh2
|
UTSW |
17 |
87,985,758 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9799:Msh2
|
UTSW |
17 |
88,024,933 (GRCm39) |
missense |
probably damaging |
1.00 |
X0058:Msh2
|
UTSW |
17 |
87,987,362 (GRCm39) |
missense |
probably damaging |
1.00 |
|