Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
C |
T |
6: 142,602,340 (GRCm39) |
R691Q |
probably benign |
Het |
Ambra1 |
G |
T |
2: 91,655,631 (GRCm39) |
G700W |
probably damaging |
Het |
Atp6v1c1 |
A |
G |
15: 38,683,204 (GRCm39) |
I198V |
probably benign |
Het |
Bptf |
T |
C |
11: 106,946,733 (GRCm39) |
N2353S |
probably benign |
Het |
Cd84 |
A |
T |
1: 171,713,937 (GRCm39) |
T312S |
probably benign |
Het |
Chl1 |
G |
T |
6: 103,692,325 (GRCm39) |
C1064F |
probably damaging |
Het |
Clca4a |
T |
C |
3: 144,666,433 (GRCm39) |
D473G |
probably damaging |
Het |
Dsp |
A |
G |
13: 38,377,593 (GRCm39) |
R1793G |
probably benign |
Het |
Dync1h1 |
A |
G |
12: 110,605,285 (GRCm39) |
N2374S |
probably benign |
Het |
Ecpas |
A |
G |
4: 58,809,718 (GRCm39) |
L1583P |
probably damaging |
Het |
Gm43191 |
A |
T |
3: 116,439,112 (GRCm39) |
I130N |
probably damaging |
Het |
Gm5134 |
T |
G |
10: 75,840,581 (GRCm39) |
L475R |
probably damaging |
Het |
Grm1 |
A |
G |
10: 10,595,783 (GRCm39) |
V615A |
probably benign |
Het |
Inhca |
T |
C |
9: 103,131,975 (GRCm39) |
E504G |
possibly damaging |
Het |
Loxl1 |
T |
A |
9: 58,201,705 (GRCm39) |
Q462L |
possibly damaging |
Het |
Or10j27 |
A |
G |
1: 172,958,098 (GRCm39) |
S229P |
possibly damaging |
Het |
Or5b106 |
G |
A |
19: 13,123,192 (GRCm39) |
T277I |
possibly damaging |
Het |
Or5t17 |
A |
T |
2: 86,833,267 (GRCm39) |
K318M |
probably benign |
Het |
Otud4 |
T |
C |
8: 80,400,390 (GRCm39) |
F1034L |
probably damaging |
Het |
Pakap |
C |
A |
4: 57,856,325 (GRCm39) |
D551E |
probably benign |
Het |
Panx3 |
T |
G |
9: 37,572,771 (GRCm39) |
T260P |
probably benign |
Het |
Ppfia4 |
A |
T |
1: 134,255,824 (GRCm39) |
S194T |
probably benign |
Het |
Rnf135 |
T |
A |
11: 80,080,081 (GRCm39) |
I124N |
probably benign |
Het |
Rpf1 |
T |
C |
3: 146,213,302 (GRCm39) |
N283S |
probably damaging |
Het |
Smg5 |
A |
G |
3: 88,266,951 (GRCm39) |
|
probably benign |
Het |
Stard9 |
A |
G |
2: 120,531,849 (GRCm39) |
E2702G |
probably benign |
Het |
Tbk1 |
A |
T |
10: 121,395,776 (GRCm39) |
M439K |
probably benign |
Het |
Tmem235 |
T |
C |
11: 117,753,132 (GRCm39) |
L85P |
possibly damaging |
Het |
Trhde |
A |
T |
10: 114,424,405 (GRCm39) |
V460E |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,620,608 (GRCm39) |
|
probably benign |
Het |
Vmn1r83 |
A |
G |
7: 12,055,160 (GRCm39) |
F299S |
probably benign |
Het |
|
Other mutations in Nwd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Nwd1
|
APN |
8 |
73,397,705 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01294:Nwd1
|
APN |
8 |
73,438,373 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01298:Nwd1
|
APN |
8 |
73,388,959 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01333:Nwd1
|
APN |
8 |
73,393,439 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02244:Nwd1
|
APN |
8 |
73,434,210 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02579:Nwd1
|
APN |
8 |
73,434,155 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02608:Nwd1
|
APN |
8 |
73,394,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02632:Nwd1
|
APN |
8 |
73,394,082 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02893:Nwd1
|
APN |
8 |
73,394,129 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03010:Nwd1
|
APN |
8 |
73,414,688 (GRCm39) |
splice site |
probably benign |
|
R0017:Nwd1
|
UTSW |
8 |
73,436,053 (GRCm39) |
splice site |
probably benign |
|
R0066:Nwd1
|
UTSW |
8 |
73,438,484 (GRCm39) |
missense |
probably benign |
0.27 |
R0066:Nwd1
|
UTSW |
8 |
73,438,484 (GRCm39) |
missense |
probably benign |
0.27 |
R0505:Nwd1
|
UTSW |
8 |
73,388,965 (GRCm39) |
missense |
probably damaging |
0.96 |
R0511:Nwd1
|
UTSW |
8 |
73,408,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R0612:Nwd1
|
UTSW |
8 |
73,394,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R0681:Nwd1
|
UTSW |
8 |
73,388,965 (GRCm39) |
missense |
probably damaging |
0.96 |
R0763:Nwd1
|
UTSW |
8 |
73,397,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0905:Nwd1
|
UTSW |
8 |
73,436,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R1136:Nwd1
|
UTSW |
8 |
73,424,397 (GRCm39) |
splice site |
probably benign |
|
R1483:Nwd1
|
UTSW |
8 |
73,383,714 (GRCm39) |
missense |
probably damaging |
0.96 |
R1630:Nwd1
|
UTSW |
8 |
73,393,657 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1724:Nwd1
|
UTSW |
8 |
73,438,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Nwd1
|
UTSW |
8 |
73,393,463 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1885:Nwd1
|
UTSW |
8 |
73,431,622 (GRCm39) |
missense |
probably benign |
0.00 |
R1973:Nwd1
|
UTSW |
8 |
73,431,590 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2393:Nwd1
|
UTSW |
8 |
73,389,055 (GRCm39) |
missense |
probably benign |
|
R2926:Nwd1
|
UTSW |
8 |
73,393,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R3706:Nwd1
|
UTSW |
8 |
73,393,744 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3916:Nwd1
|
UTSW |
8 |
73,394,439 (GRCm39) |
nonsense |
probably null |
|
R3917:Nwd1
|
UTSW |
8 |
73,394,439 (GRCm39) |
nonsense |
probably null |
|
R4153:Nwd1
|
UTSW |
8 |
73,408,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R4426:Nwd1
|
UTSW |
8 |
73,393,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R4435:Nwd1
|
UTSW |
8 |
73,414,764 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4522:Nwd1
|
UTSW |
8 |
73,397,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R4622:Nwd1
|
UTSW |
8 |
73,393,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R4659:Nwd1
|
UTSW |
8 |
73,421,949 (GRCm39) |
missense |
probably benign |
0.03 |
R4694:Nwd1
|
UTSW |
8 |
73,393,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Nwd1
|
UTSW |
8 |
73,383,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R4844:Nwd1
|
UTSW |
8 |
73,393,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R4906:Nwd1
|
UTSW |
8 |
73,398,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R5041:Nwd1
|
UTSW |
8 |
73,431,683 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5183:Nwd1
|
UTSW |
8 |
73,397,714 (GRCm39) |
missense |
probably benign |
0.07 |
R5416:Nwd1
|
UTSW |
8 |
73,393,322 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5553:Nwd1
|
UTSW |
8 |
73,431,604 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5670:Nwd1
|
UTSW |
8 |
73,419,745 (GRCm39) |
missense |
probably damaging |
0.97 |
R5699:Nwd1
|
UTSW |
8 |
73,429,602 (GRCm39) |
critical splice donor site |
probably null |
|
R5722:Nwd1
|
UTSW |
8 |
73,401,872 (GRCm39) |
missense |
probably damaging |
0.97 |
R5762:Nwd1
|
UTSW |
8 |
73,397,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R5778:Nwd1
|
UTSW |
8 |
73,419,745 (GRCm39) |
missense |
probably damaging |
0.97 |
R5992:Nwd1
|
UTSW |
8 |
73,380,201 (GRCm39) |
critical splice donor site |
probably null |
|
R6163:Nwd1
|
UTSW |
8 |
73,388,814 (GRCm39) |
missense |
probably damaging |
0.96 |
R6164:Nwd1
|
UTSW |
8 |
73,388,814 (GRCm39) |
missense |
probably damaging |
0.96 |
R6165:Nwd1
|
UTSW |
8 |
73,388,814 (GRCm39) |
missense |
probably damaging |
0.96 |
R6212:Nwd1
|
UTSW |
8 |
73,421,950 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6443:Nwd1
|
UTSW |
8 |
73,388,994 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6865:Nwd1
|
UTSW |
8 |
73,383,690 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6928:Nwd1
|
UTSW |
8 |
73,408,653 (GRCm39) |
missense |
probably benign |
0.27 |
R6944:Nwd1
|
UTSW |
8 |
73,380,162 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6979:Nwd1
|
UTSW |
8 |
73,394,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R7060:Nwd1
|
UTSW |
8 |
73,393,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Nwd1
|
UTSW |
8 |
73,421,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R7265:Nwd1
|
UTSW |
8 |
73,419,556 (GRCm39) |
missense |
probably benign |
0.29 |
R7343:Nwd1
|
UTSW |
8 |
73,438,410 (GRCm39) |
missense |
probably damaging |
0.98 |
R7391:Nwd1
|
UTSW |
8 |
73,389,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R7424:Nwd1
|
UTSW |
8 |
73,401,801 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7438:Nwd1
|
UTSW |
8 |
73,434,458 (GRCm39) |
missense |
probably benign |
0.00 |
R7487:Nwd1
|
UTSW |
8 |
73,393,266 (GRCm39) |
missense |
unknown |
|
R7502:Nwd1
|
UTSW |
8 |
73,434,021 (GRCm39) |
missense |
probably damaging |
0.98 |
R7883:Nwd1
|
UTSW |
8 |
73,393,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R8235:Nwd1
|
UTSW |
8 |
73,438,314 (GRCm39) |
frame shift |
probably null |
|
R8282:Nwd1
|
UTSW |
8 |
73,431,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R8672:Nwd1
|
UTSW |
8 |
73,394,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Nwd1
|
UTSW |
8 |
73,388,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Nwd1
|
UTSW |
8 |
73,394,192 (GRCm39) |
missense |
probably damaging |
0.98 |
R8793:Nwd1
|
UTSW |
8 |
73,419,704 (GRCm39) |
missense |
probably benign |
|
R8890:Nwd1
|
UTSW |
8 |
73,438,484 (GRCm39) |
missense |
probably benign |
0.27 |
R9072:Nwd1
|
UTSW |
8 |
73,422,046 (GRCm39) |
missense |
probably benign |
0.00 |
R9073:Nwd1
|
UTSW |
8 |
73,422,046 (GRCm39) |
missense |
probably benign |
0.00 |
R9257:Nwd1
|
UTSW |
8 |
73,397,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R9582:Nwd1
|
UTSW |
8 |
73,421,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Nwd1
|
UTSW |
8 |
73,401,106 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Nwd1
|
UTSW |
8 |
73,393,884 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1176:Nwd1
|
UTSW |
8 |
73,398,928 (GRCm39) |
missense |
not run |
|
Z1177:Nwd1
|
UTSW |
8 |
73,436,087 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Nwd1
|
UTSW |
8 |
73,422,015 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1177:Nwd1
|
UTSW |
8 |
73,393,256 (GRCm39) |
missense |
probably damaging |
0.97 |
|