Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700066M21Rik |
A |
T |
1: 57,421,943 (GRCm39) |
Q106H |
probably damaging |
Het |
Acad9 |
T |
C |
3: 36,139,590 (GRCm39) |
C397R |
probably damaging |
Het |
Ankfn1 |
T |
G |
11: 89,282,602 (GRCm39) |
R348S |
probably damaging |
Het |
Ankrd61 |
A |
G |
5: 143,831,336 (GRCm39) |
C28R |
probably benign |
Het |
Ano5 |
C |
T |
7: 51,194,548 (GRCm39) |
R94* |
probably null |
Het |
Apela |
A |
T |
8: 65,489,590 (GRCm39) |
F10I |
unknown |
Het |
Arhgap31 |
T |
C |
16: 38,429,790 (GRCm39) |
S362G |
probably benign |
Het |
Arhgef18 |
C |
A |
8: 3,430,410 (GRCm39) |
H94Q |
probably benign |
Het |
Astn2 |
A |
T |
4: 65,830,834 (GRCm39) |
L585Q |
possibly damaging |
Het |
Atf3 |
G |
T |
1: 190,909,564 (GRCm39) |
A35D |
probably benign |
Het |
Atp10b |
A |
T |
11: 43,093,978 (GRCm39) |
R507S |
possibly damaging |
Het |
Brip1 |
A |
C |
11: 86,080,598 (GRCm39) |
V156G |
probably benign |
Het |
Ccdc27 |
T |
A |
4: 154,111,205 (GRCm39) |
M636L |
probably benign |
Het |
Ceacam5 |
T |
A |
7: 17,493,285 (GRCm39) |
N769K |
possibly damaging |
Het |
Cklf |
C |
T |
8: 104,977,560 (GRCm39) |
|
probably benign |
Het |
Cpeb4 |
G |
A |
11: 31,870,546 (GRCm39) |
V474M |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,673,834 (GRCm39) |
C1091* |
probably null |
Het |
Eef1akmt4 |
T |
A |
16: 20,437,288 (GRCm39) |
I210N |
possibly damaging |
Het |
Fbxo38 |
A |
T |
18: 62,666,587 (GRCm39) |
H195Q |
probably damaging |
Het |
Fbxw14 |
G |
A |
9: 109,105,305 (GRCm39) |
R287* |
probably null |
Het |
Fes |
A |
G |
7: 80,033,619 (GRCm39) |
S211P |
possibly damaging |
Het |
Fry |
G |
T |
5: 150,317,603 (GRCm39) |
R861L |
possibly damaging |
Het |
Galnt12 |
A |
G |
4: 47,113,908 (GRCm39) |
|
probably benign |
Het |
Gm14226 |
G |
A |
2: 154,866,538 (GRCm39) |
W165* |
probably null |
Het |
Gm40460 |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
7: 141,794,171 (GRCm39) |
|
probably benign |
Het |
Gm40460 |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,554 (GRCm39) |
|
probably benign |
Het |
Gprc6a |
A |
G |
10: 51,497,079 (GRCm39) |
V488A |
probably benign |
Het |
Haus8 |
A |
T |
8: 71,705,910 (GRCm39) |
|
probably benign |
Het |
Helb |
A |
T |
10: 119,948,692 (GRCm39) |
C26S |
possibly damaging |
Het |
Icam1 |
A |
T |
9: 20,937,862 (GRCm39) |
I300F |
probably benign |
Het |
Ip6k1 |
A |
G |
9: 107,918,211 (GRCm39) |
N181S |
probably benign |
Het |
Itga2b |
C |
A |
11: 102,351,687 (GRCm39) |
R546L |
possibly damaging |
Het |
Kif27 |
A |
T |
13: 58,476,818 (GRCm39) |
Y611N |
probably damaging |
Het |
Lpcat2 |
A |
G |
8: 93,640,979 (GRCm39) |
I475V |
possibly damaging |
Het |
Lrit2 |
A |
G |
14: 36,794,487 (GRCm39) |
K517R |
probably benign |
Het |
Lrp1b |
A |
T |
2: 40,555,171 (GRCm39) |
I4085N |
|
Het |
Lrrc32 |
T |
A |
7: 98,148,242 (GRCm39) |
S341T |
probably damaging |
Het |
Lrrn2 |
T |
A |
1: 132,866,831 (GRCm39) |
I632K |
possibly damaging |
Het |
Mettl22 |
A |
G |
16: 8,300,178 (GRCm39) |
Q194R |
probably benign |
Het |
Mfhas1 |
T |
A |
8: 36,057,394 (GRCm39) |
V623E |
probably damaging |
Het |
Mitd1 |
T |
C |
1: 37,929,315 (GRCm39) |
D26G |
probably damaging |
Het |
Myo1a |
C |
T |
10: 127,546,043 (GRCm39) |
T222M |
probably benign |
Het |
Naf1 |
A |
G |
8: 67,317,333 (GRCm39) |
K275R |
possibly damaging |
Het |
Nf1 |
T |
C |
11: 79,332,491 (GRCm39) |
L765P |
probably damaging |
Het |
Or12k7 |
G |
T |
2: 36,958,429 (GRCm39) |
M37I |
probably benign |
Het |
Or52a5 |
A |
G |
7: 103,427,063 (GRCm39) |
L163P |
possibly damaging |
Het |
Or5ac16 |
T |
A |
16: 59,022,264 (GRCm39) |
H175L |
possibly damaging |
Het |
Or9r3 |
T |
A |
10: 129,947,808 (GRCm39) |
I284F |
probably damaging |
Het |
Pappa |
A |
G |
4: 65,099,347 (GRCm39) |
H622R |
probably benign |
Het |
Pcdhb4 |
A |
T |
18: 37,442,055 (GRCm39) |
Y455F |
probably damaging |
Het |
Pepd |
A |
G |
7: 34,671,116 (GRCm39) |
Y220C |
probably damaging |
Het |
Pias3 |
T |
C |
3: 96,607,381 (GRCm39) |
I172T |
probably damaging |
Het |
Polq |
T |
A |
16: 36,853,893 (GRCm39) |
H415Q |
probably damaging |
Het |
Pp2d1 |
A |
T |
17: 53,814,897 (GRCm39) |
M609K |
probably benign |
Het |
Ppm1m |
G |
A |
9: 106,076,237 (GRCm39) |
|
probably benign |
Het |
Prss22 |
T |
A |
17: 24,215,662 (GRCm39) |
T87S |
probably benign |
Het |
Ptprf |
C |
A |
4: 118,095,125 (GRCm39) |
V254L |
possibly damaging |
Het |
Ripply3 |
A |
G |
16: 94,136,723 (GRCm39) |
E128G |
possibly damaging |
Het |
Rrm2 |
A |
C |
12: 24,760,470 (GRCm39) |
I185L |
possibly damaging |
Het |
Sbsn |
T |
A |
7: 30,454,227 (GRCm39) |
|
probably benign |
Het |
Sdc3 |
T |
A |
4: 130,546,336 (GRCm39) |
S232T |
probably benign |
Het |
Slx4 |
G |
C |
16: 3,803,458 (GRCm39) |
P1119A |
probably benign |
Het |
Smc5 |
C |
T |
19: 23,221,422 (GRCm39) |
R369Q |
probably damaging |
Het |
Speer4a3 |
A |
G |
5: 26,158,191 (GRCm39) |
S54P |
probably damaging |
Het |
Spns1 |
G |
A |
7: 125,971,593 (GRCm39) |
S319F |
possibly damaging |
Het |
Sptbn4 |
G |
A |
7: 27,106,657 (GRCm39) |
Q924* |
probably null |
Het |
Srsf12 |
T |
C |
4: 33,226,045 (GRCm39) |
S103P |
possibly damaging |
Het |
Tanc1 |
A |
G |
2: 59,621,185 (GRCm39) |
T335A |
possibly damaging |
Het |
Them4 |
C |
T |
3: 94,231,610 (GRCm39) |
T149I |
probably damaging |
Het |
Trpc7 |
T |
C |
13: 56,970,312 (GRCm39) |
Y424C |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,628,364 (GRCm39) |
D14599N |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,698,244 (GRCm39) |
L186H |
|
Het |
Usp17lc |
T |
C |
7: 103,067,524 (GRCm39) |
F273S |
probably benign |
Het |
Vwa5b2 |
T |
C |
16: 20,419,516 (GRCm39) |
S620P |
probably damaging |
Het |
|
Other mutations in Srcap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Srcap
|
APN |
7 |
127,141,885 (GRCm39) |
splice site |
probably benign |
|
IGL00475:Srcap
|
APN |
7 |
127,152,093 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01064:Srcap
|
APN |
7 |
127,159,064 (GRCm39) |
unclassified |
probably benign |
|
IGL01129:Srcap
|
APN |
7 |
127,120,823 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01670:Srcap
|
APN |
7 |
127,127,604 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01861:Srcap
|
APN |
7 |
127,124,457 (GRCm39) |
splice site |
probably benign |
|
IGL02237:Srcap
|
APN |
7 |
127,133,864 (GRCm39) |
splice site |
probably benign |
|
IGL02665:Srcap
|
APN |
7 |
127,140,075 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02688:Srcap
|
APN |
7 |
127,141,625 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02744:Srcap
|
APN |
7 |
127,133,838 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02810:Srcap
|
APN |
7 |
127,120,835 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03184:Srcap
|
APN |
7 |
127,129,674 (GRCm39) |
unclassified |
probably benign |
|
IGL03309:Srcap
|
APN |
7 |
127,129,965 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4453001:Srcap
|
UTSW |
7 |
127,148,492 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1340:Srcap
|
UTSW |
7 |
127,159,910 (GRCm39) |
intron |
probably benign |
|
R1401:Srcap
|
UTSW |
7 |
127,159,124 (GRCm39) |
unclassified |
probably benign |
|
R1455:Srcap
|
UTSW |
7 |
127,129,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R1470:Srcap
|
UTSW |
7 |
127,158,899 (GRCm39) |
unclassified |
probably benign |
|
R1470:Srcap
|
UTSW |
7 |
127,158,899 (GRCm39) |
unclassified |
probably benign |
|
R1761:Srcap
|
UTSW |
7 |
127,134,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Srcap
|
UTSW |
7 |
127,133,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R2483:Srcap
|
UTSW |
7 |
127,141,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R2892:Srcap
|
UTSW |
7 |
127,138,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R2893:Srcap
|
UTSW |
7 |
127,138,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R3623:Srcap
|
UTSW |
7 |
127,141,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R3976:Srcap
|
UTSW |
7 |
127,148,411 (GRCm39) |
missense |
probably benign |
0.18 |
R4001:Srcap
|
UTSW |
7 |
127,131,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R4015:Srcap
|
UTSW |
7 |
127,124,595 (GRCm39) |
missense |
probably benign |
0.27 |
R4581:Srcap
|
UTSW |
7 |
127,157,482 (GRCm39) |
unclassified |
probably benign |
|
R4643:Srcap
|
UTSW |
7 |
127,140,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4644:Srcap
|
UTSW |
7 |
127,151,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R4690:Srcap
|
UTSW |
7 |
127,137,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R4693:Srcap
|
UTSW |
7 |
127,137,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Srcap
|
UTSW |
7 |
127,140,731 (GRCm39) |
missense |
probably benign |
0.13 |
R4728:Srcap
|
UTSW |
7 |
127,140,096 (GRCm39) |
critical splice donor site |
probably null |
|
R4740:Srcap
|
UTSW |
7 |
127,148,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R4752:Srcap
|
UTSW |
7 |
127,158,172 (GRCm39) |
unclassified |
probably benign |
|
R4834:Srcap
|
UTSW |
7 |
127,156,782 (GRCm39) |
critical splice donor site |
probably null |
|
R4837:Srcap
|
UTSW |
7 |
127,158,134 (GRCm39) |
unclassified |
probably benign |
|
R4884:Srcap
|
UTSW |
7 |
127,121,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R4889:Srcap
|
UTSW |
7 |
127,137,719 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5088:Srcap
|
UTSW |
7 |
127,140,833 (GRCm39) |
missense |
probably benign |
0.02 |
R5102:Srcap
|
UTSW |
7 |
127,129,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R5358:Srcap
|
UTSW |
7 |
127,139,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R5372:Srcap
|
UTSW |
7 |
127,156,785 (GRCm39) |
splice site |
probably null |
|
R5397:Srcap
|
UTSW |
7 |
127,152,468 (GRCm39) |
critical splice donor site |
probably null |
|
R5481:Srcap
|
UTSW |
7 |
127,131,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5566:Srcap
|
UTSW |
7 |
127,124,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R5584:Srcap
|
UTSW |
7 |
127,127,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R5693:Srcap
|
UTSW |
7 |
127,118,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R5769:Srcap
|
UTSW |
7 |
127,158,994 (GRCm39) |
unclassified |
probably benign |
|
R5805:Srcap
|
UTSW |
7 |
127,141,211 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5806:Srcap
|
UTSW |
7 |
127,158,335 (GRCm39) |
unclassified |
probably benign |
|
R5921:Srcap
|
UTSW |
7 |
127,158,005 (GRCm39) |
unclassified |
probably benign |
|
R5942:Srcap
|
UTSW |
7 |
127,137,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Srcap
|
UTSW |
7 |
127,137,922 (GRCm39) |
missense |
probably benign |
0.01 |
R6057:Srcap
|
UTSW |
7 |
127,140,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R6113:Srcap
|
UTSW |
7 |
127,159,453 (GRCm39) |
unclassified |
probably benign |
|
R6150:Srcap
|
UTSW |
7 |
127,134,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R6212:Srcap
|
UTSW |
7 |
127,148,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Srcap
|
UTSW |
7 |
127,129,626 (GRCm39) |
unclassified |
probably benign |
|
R6437:Srcap
|
UTSW |
7 |
127,127,722 (GRCm39) |
splice site |
probably null |
|
R6492:Srcap
|
UTSW |
7 |
127,121,317 (GRCm39) |
nonsense |
probably null |
|
R6537:Srcap
|
UTSW |
7 |
127,141,392 (GRCm39) |
missense |
probably damaging |
0.97 |
R6659:Srcap
|
UTSW |
7 |
127,141,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R6713:Srcap
|
UTSW |
7 |
127,134,089 (GRCm39) |
missense |
probably benign |
0.28 |
R6717:Srcap
|
UTSW |
7 |
127,157,482 (GRCm39) |
unclassified |
probably benign |
|
R6941:Srcap
|
UTSW |
7 |
127,141,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R7068:Srcap
|
UTSW |
7 |
127,141,115 (GRCm39) |
missense |
probably benign |
0.00 |
R7097:Srcap
|
UTSW |
7 |
127,138,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R7394:Srcap
|
UTSW |
7 |
127,134,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R7426:Srcap
|
UTSW |
7 |
127,137,689 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7434:Srcap
|
UTSW |
7 |
127,159,414 (GRCm39) |
missense |
unknown |
|
R7559:Srcap
|
UTSW |
7 |
127,129,722 (GRCm39) |
missense |
unknown |
|
R7638:Srcap
|
UTSW |
7 |
127,137,920 (GRCm39) |
missense |
probably benign |
0.39 |
R7677:Srcap
|
UTSW |
7 |
127,158,980 (GRCm39) |
missense |
unknown |
|
R7715:Srcap
|
UTSW |
7 |
127,148,460 (GRCm39) |
missense |
probably damaging |
0.99 |
R7757:Srcap
|
UTSW |
7 |
127,129,966 (GRCm39) |
missense |
probably damaging |
0.99 |
R7811:Srcap
|
UTSW |
7 |
127,141,221 (GRCm39) |
missense |
probably damaging |
0.97 |
R7821:Srcap
|
UTSW |
7 |
127,129,499 (GRCm39) |
unclassified |
probably benign |
|
R7869:Srcap
|
UTSW |
7 |
127,138,366 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7870:Srcap
|
UTSW |
7 |
127,159,730 (GRCm39) |
missense |
unknown |
|
R7941:Srcap
|
UTSW |
7 |
127,157,462 (GRCm39) |
unclassified |
probably benign |
|
R7994:Srcap
|
UTSW |
7 |
127,140,930 (GRCm39) |
missense |
probably benign |
0.00 |
R8035:Srcap
|
UTSW |
7 |
127,141,784 (GRCm39) |
missense |
probably benign |
0.05 |
R8066:Srcap
|
UTSW |
7 |
127,139,484 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8066:Srcap
|
UTSW |
7 |
127,120,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R8168:Srcap
|
UTSW |
7 |
127,141,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R8194:Srcap
|
UTSW |
7 |
127,138,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R8288:Srcap
|
UTSW |
7 |
127,130,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:Srcap
|
UTSW |
7 |
127,124,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R8308:Srcap
|
UTSW |
7 |
127,152,353 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8309:Srcap
|
UTSW |
7 |
127,148,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R8311:Srcap
|
UTSW |
7 |
127,156,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R8321:Srcap
|
UTSW |
7 |
127,140,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8365:Srcap
|
UTSW |
7 |
127,148,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8424:Srcap
|
UTSW |
7 |
127,141,560 (GRCm39) |
missense |
probably benign |
0.00 |
R8817:Srcap
|
UTSW |
7 |
127,152,395 (GRCm39) |
missense |
probably benign |
0.23 |
R8924:Srcap
|
UTSW |
7 |
127,158,204 (GRCm39) |
missense |
unknown |
|
R8933:Srcap
|
UTSW |
7 |
127,151,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R8961:Srcap
|
UTSW |
7 |
127,141,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R9000:Srcap
|
UTSW |
7 |
127,130,943 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9098:Srcap
|
UTSW |
7 |
127,151,816 (GRCm39) |
missense |
probably damaging |
0.99 |
R9124:Srcap
|
UTSW |
7 |
127,159,874 (GRCm39) |
missense |
unknown |
|
R9163:Srcap
|
UTSW |
7 |
127,121,162 (GRCm39) |
missense |
unknown |
|
R9332:Srcap
|
UTSW |
7 |
127,158,812 (GRCm39) |
missense |
unknown |
|
R9389:Srcap
|
UTSW |
7 |
127,141,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R9464:Srcap
|
UTSW |
7 |
127,137,273 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9467:Srcap
|
UTSW |
7 |
127,139,531 (GRCm39) |
missense |
probably damaging |
0.98 |
R9554:Srcap
|
UTSW |
7 |
127,151,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R9596:Srcap
|
UTSW |
7 |
127,131,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R9597:Srcap
|
UTSW |
7 |
127,121,219 (GRCm39) |
missense |
possibly damaging |
0.91 |
X0025:Srcap
|
UTSW |
7 |
127,159,277 (GRCm39) |
unclassified |
probably benign |
|
|