Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd44 |
C |
T |
1: 54,696,779 (GRCm39) |
G654S |
possibly damaging |
Het |
Ark2c |
A |
T |
18: 77,556,055 (GRCm39) |
V167E |
probably damaging |
Het |
Arl14ep |
C |
T |
2: 106,797,458 (GRCm39) |
A180T |
probably benign |
Het |
Btbd9 |
A |
C |
17: 30,736,124 (GRCm39) |
S330A |
probably damaging |
Het |
Cep78 |
T |
C |
19: 15,962,102 (GRCm39) |
D48G |
probably damaging |
Het |
Col4a4 |
C |
T |
1: 82,501,681 (GRCm39) |
|
probably benign |
Het |
Ctdsp1 |
C |
T |
1: 74,433,175 (GRCm39) |
|
probably benign |
Het |
Gapvd1 |
G |
A |
2: 34,594,203 (GRCm39) |
P949L |
probably damaging |
Het |
Gas6 |
T |
C |
8: 13,518,359 (GRCm39) |
T492A |
possibly damaging |
Het |
Igbp1b |
A |
T |
6: 138,634,601 (GRCm39) |
V281D |
probably benign |
Het |
Mapk8ip3 |
G |
A |
17: 25,122,254 (GRCm39) |
|
probably benign |
Het |
Mmachc |
A |
G |
4: 116,560,907 (GRCm39) |
F196S |
probably damaging |
Het |
Or52z13 |
T |
A |
7: 103,246,937 (GRCm39) |
I138N |
probably damaging |
Het |
Pah |
A |
T |
10: 87,417,789 (GRCm39) |
T427S |
probably benign |
Het |
Pcdh7 |
C |
A |
5: 57,877,045 (GRCm39) |
P200Q |
probably benign |
Het |
Pde3a |
C |
A |
6: 141,404,870 (GRCm39) |
P365Q |
probably null |
Het |
Pkm |
A |
G |
9: 59,576,244 (GRCm39) |
T143A |
possibly damaging |
Het |
Plppr4 |
A |
G |
3: 117,129,222 (GRCm39) |
S82P |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,777,260 (GRCm39) |
E299G |
possibly damaging |
Het |
Sdk2 |
G |
A |
11: 113,729,320 (GRCm39) |
P1086S |
probably damaging |
Het |
Spats1 |
G |
A |
17: 45,772,166 (GRCm39) |
R81C |
probably benign |
Het |
Spmap2l |
T |
A |
5: 77,195,002 (GRCm39) |
F59I |
probably damaging |
Het |
Tbc1d2 |
T |
C |
4: 46,649,778 (GRCm39) |
N86S |
possibly damaging |
Het |
Vezt |
T |
A |
10: 93,832,811 (GRCm39) |
Y10F |
probably benign |
Het |
Vmn1r174 |
C |
A |
7: 23,453,583 (GRCm39) |
P83H |
probably damaging |
Het |
Vmn1r218 |
C |
T |
13: 23,321,001 (GRCm39) |
T36I |
probably damaging |
Het |
Zmym4 |
A |
T |
4: 126,794,462 (GRCm39) |
N889K |
possibly damaging |
Het |
|
Other mutations in Met |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00533:Met
|
APN |
6 |
17,534,936 (GRCm39) |
unclassified |
probably benign |
|
IGL01066:Met
|
APN |
6 |
17,535,104 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01344:Met
|
APN |
6 |
17,547,031 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01413:Met
|
APN |
6 |
17,558,895 (GRCm39) |
splice site |
probably benign |
|
IGL01608:Met
|
APN |
6 |
17,558,729 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01613:Met
|
APN |
6 |
17,540,576 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01820:Met
|
APN |
6 |
17,534,230 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01843:Met
|
APN |
6 |
17,491,700 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02027:Met
|
APN |
6 |
17,563,726 (GRCm39) |
splice site |
probably benign |
|
IGL02243:Met
|
APN |
6 |
17,549,093 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02373:Met
|
APN |
6 |
17,491,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02616:Met
|
APN |
6 |
17,553,346 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02702:Met
|
APN |
6 |
17,534,142 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02704:Met
|
APN |
6 |
17,491,256 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02714:Met
|
APN |
6 |
17,491,851 (GRCm39) |
nonsense |
probably null |
|
IGL02936:Met
|
APN |
6 |
17,553,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02943:Met
|
APN |
6 |
17,535,928 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03057:Met
|
APN |
6 |
17,558,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03124:Met
|
APN |
6 |
17,492,077 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03171:Met
|
APN |
6 |
17,562,272 (GRCm39) |
splice site |
probably benign |
|
IGL03266:Met
|
APN |
6 |
17,540,537 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03285:Met
|
APN |
6 |
17,553,336 (GRCm39) |
missense |
probably damaging |
0.98 |
R0453:Met
|
UTSW |
6 |
17,534,197 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0543:Met
|
UTSW |
6 |
17,491,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Met
|
UTSW |
6 |
17,555,631 (GRCm39) |
splice site |
probably null |
|
R0652:Met
|
UTSW |
6 |
17,491,709 (GRCm39) |
missense |
probably benign |
0.00 |
R0941:Met
|
UTSW |
6 |
17,491,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R1142:Met
|
UTSW |
6 |
17,527,182 (GRCm39) |
nonsense |
probably null |
|
R1553:Met
|
UTSW |
6 |
17,491,460 (GRCm39) |
missense |
probably benign |
0.01 |
R1569:Met
|
UTSW |
6 |
17,531,503 (GRCm39) |
nonsense |
probably null |
|
R1744:Met
|
UTSW |
6 |
17,540,645 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2224:Met
|
UTSW |
6 |
17,563,721 (GRCm39) |
splice site |
probably null |
|
R2308:Met
|
UTSW |
6 |
17,491,741 (GRCm39) |
missense |
probably benign |
0.00 |
R2369:Met
|
UTSW |
6 |
17,531,527 (GRCm39) |
missense |
probably benign |
0.04 |
R2393:Met
|
UTSW |
6 |
17,534,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R2419:Met
|
UTSW |
6 |
17,535,829 (GRCm39) |
splice site |
probably benign |
|
R2483:Met
|
UTSW |
6 |
17,549,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R2511:Met
|
UTSW |
6 |
17,491,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R3622:Met
|
UTSW |
6 |
17,549,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R3623:Met
|
UTSW |
6 |
17,549,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R3624:Met
|
UTSW |
6 |
17,549,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4050:Met
|
UTSW |
6 |
17,533,983 (GRCm39) |
missense |
probably benign |
|
R4051:Met
|
UTSW |
6 |
17,548,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4159:Met
|
UTSW |
6 |
17,562,271 (GRCm39) |
splice site |
probably null |
|
R4208:Met
|
UTSW |
6 |
17,548,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4622:Met
|
UTSW |
6 |
17,513,383 (GRCm39) |
missense |
probably benign |
0.19 |
R4672:Met
|
UTSW |
6 |
17,571,803 (GRCm39) |
missense |
probably benign |
0.33 |
R4737:Met
|
UTSW |
6 |
17,491,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R4738:Met
|
UTSW |
6 |
17,491,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Met
|
UTSW |
6 |
17,491,412 (GRCm39) |
missense |
probably damaging |
0.97 |
R4846:Met
|
UTSW |
6 |
17,491,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R4855:Met
|
UTSW |
6 |
17,558,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R4878:Met
|
UTSW |
6 |
17,549,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R4902:Met
|
UTSW |
6 |
17,546,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5208:Met
|
UTSW |
6 |
17,526,422 (GRCm39) |
nonsense |
probably null |
|
R5355:Met
|
UTSW |
6 |
17,491,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R5415:Met
|
UTSW |
6 |
17,527,084 (GRCm39) |
missense |
probably benign |
0.01 |
R5556:Met
|
UTSW |
6 |
17,534,175 (GRCm39) |
missense |
probably benign |
0.04 |
R5590:Met
|
UTSW |
6 |
17,548,781 (GRCm39) |
missense |
probably benign |
0.00 |
R5683:Met
|
UTSW |
6 |
17,571,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Met
|
UTSW |
6 |
17,562,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R5891:Met
|
UTSW |
6 |
17,491,538 (GRCm39) |
missense |
probably benign |
0.02 |
R5895:Met
|
UTSW |
6 |
17,531,581 (GRCm39) |
missense |
probably benign |
0.02 |
R6063:Met
|
UTSW |
6 |
17,491,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R6262:Met
|
UTSW |
6 |
17,553,403 (GRCm39) |
missense |
probably benign |
0.00 |
R6362:Met
|
UTSW |
6 |
17,558,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Met
|
UTSW |
6 |
17,571,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R6966:Met
|
UTSW |
6 |
17,531,531 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6989:Met
|
UTSW |
6 |
17,535,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R6989:Met
|
UTSW |
6 |
17,535,927 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7017:Met
|
UTSW |
6 |
17,491,286 (GRCm39) |
nonsense |
probably null |
|
R7037:Met
|
UTSW |
6 |
17,547,127 (GRCm39) |
intron |
probably benign |
|
R7141:Met
|
UTSW |
6 |
17,527,154 (GRCm39) |
missense |
probably benign |
0.01 |
R7242:Met
|
UTSW |
6 |
17,491,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R7282:Met
|
UTSW |
6 |
17,547,011 (GRCm39) |
nonsense |
probably null |
|
R7624:Met
|
UTSW |
6 |
17,558,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R7770:Met
|
UTSW |
6 |
17,491,406 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7797:Met
|
UTSW |
6 |
17,533,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8082:Met
|
UTSW |
6 |
17,492,312 (GRCm39) |
missense |
probably damaging |
0.98 |
R8109:Met
|
UTSW |
6 |
17,562,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R8162:Met
|
UTSW |
6 |
17,547,061 (GRCm39) |
missense |
probably damaging |
0.98 |
R8315:Met
|
UTSW |
6 |
17,533,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R8325:Met
|
UTSW |
6 |
17,571,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R8348:Met
|
UTSW |
6 |
17,571,799 (GRCm39) |
missense |
probably benign |
0.00 |
R8354:Met
|
UTSW |
6 |
17,491,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8448:Met
|
UTSW |
6 |
17,571,799 (GRCm39) |
missense |
probably benign |
0.00 |
R8454:Met
|
UTSW |
6 |
17,491,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8465:Met
|
UTSW |
6 |
17,571,809 (GRCm39) |
missense |
probably benign |
0.04 |
R8479:Met
|
UTSW |
6 |
17,491,746 (GRCm39) |
splice site |
probably null |
|
R8737:Met
|
UTSW |
6 |
17,540,510 (GRCm39) |
missense |
probably benign |
0.00 |
R8903:Met
|
UTSW |
6 |
17,549,137 (GRCm39) |
missense |
probably benign |
0.19 |
R8964:Met
|
UTSW |
6 |
17,527,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R8998:Met
|
UTSW |
6 |
17,491,534 (GRCm39) |
missense |
probably benign |
0.43 |
R9088:Met
|
UTSW |
6 |
17,548,715 (GRCm39) |
nonsense |
probably null |
|
R9369:Met
|
UTSW |
6 |
17,492,228 (GRCm39) |
missense |
probably benign |
|
R9394:Met
|
UTSW |
6 |
17,513,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R9530:Met
|
UTSW |
6 |
17,558,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Met
|
UTSW |
6 |
17,531,425 (GRCm39) |
missense |
probably benign |
|
R9759:Met
|
UTSW |
6 |
17,555,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|