Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
A |
G |
3: 124,212,977 (GRCm39) |
S105P |
probably damaging |
Het |
9930111J21Rik2 |
T |
A |
11: 48,910,119 (GRCm39) |
K771N |
possibly damaging |
Het |
Abcc2 |
A |
G |
19: 43,818,318 (GRCm39) |
E1268G |
probably damaging |
Het |
Adamts4 |
T |
C |
1: 171,084,244 (GRCm39) |
F574L |
possibly damaging |
Het |
Adamts9 |
A |
G |
6: 92,773,375 (GRCm39) |
V1165A |
probably benign |
Het |
Agap2 |
A |
T |
10: 126,918,913 (GRCm39) |
K430* |
probably null |
Het |
Amn |
G |
T |
12: 111,241,431 (GRCm39) |
G232V |
probably damaging |
Het |
Ank3 |
A |
G |
10: 69,703,258 (GRCm39) |
E297G |
probably damaging |
Het |
Arhgap45 |
T |
C |
10: 79,856,530 (GRCm39) |
L26P |
probably damaging |
Het |
Atp10b |
C |
A |
11: 43,063,595 (GRCm39) |
Q177K |
probably benign |
Het |
Bbs10 |
A |
T |
10: 111,135,118 (GRCm39) |
D77V |
probably damaging |
Het |
Bltp2 |
A |
T |
11: 78,165,438 (GRCm39) |
H1318L |
probably damaging |
Het |
Bpifa1 |
T |
A |
2: 153,986,256 (GRCm39) |
L127Q |
probably damaging |
Het |
Brinp2 |
T |
C |
1: 158,074,348 (GRCm39) |
N591S |
probably damaging |
Het |
C2cd2 |
A |
C |
16: 97,671,471 (GRCm39) |
V476G |
probably damaging |
Het |
C7 |
T |
A |
15: 5,041,494 (GRCm39) |
T471S |
possibly damaging |
Het |
Cacna1b |
A |
T |
2: 24,538,998 (GRCm39) |
Y1488N |
probably damaging |
Het |
Cadps2 |
A |
G |
6: 23,323,379 (GRCm39) |
F1001L |
probably damaging |
Het |
Ccdc188 |
T |
C |
16: 18,036,707 (GRCm39) |
S216P |
probably damaging |
Het |
Ccdc24 |
A |
G |
4: 117,729,213 (GRCm39) |
L88P |
probably damaging |
Het |
Dab1 |
T |
C |
4: 104,470,412 (GRCm39) |
I65T |
probably damaging |
Het |
Dock4 |
A |
T |
12: 40,780,062 (GRCm39) |
D621V |
probably damaging |
Het |
Drd5 |
A |
T |
5: 38,477,456 (GRCm39) |
M150L |
probably damaging |
Het |
Eef2k |
T |
A |
7: 120,472,569 (GRCm39) |
M94K |
possibly damaging |
Het |
Epg5 |
A |
G |
18: 78,025,521 (GRCm39) |
|
probably null |
Het |
Epsti1 |
T |
C |
14: 78,169,673 (GRCm39) |
|
probably null |
Het |
Ern2 |
T |
A |
7: 121,770,752 (GRCm39) |
D754V |
probably benign |
Het |
Fbxo6 |
A |
G |
4: 148,230,552 (GRCm39) |
Y237H |
probably damaging |
Het |
Fbxw24 |
A |
G |
9: 109,436,124 (GRCm39) |
S303P |
probably damaging |
Het |
Fpr-rs3 |
A |
T |
17: 20,844,103 (GRCm39) |
|
probably null |
Het |
Gab1 |
G |
T |
8: 81,493,010 (GRCm39) |
T679K |
probably damaging |
Het |
Gbp9 |
C |
A |
5: 105,253,590 (GRCm39) |
V42F |
probably damaging |
Het |
Gbp9 |
A |
T |
5: 105,253,652 (GRCm39) |
V21E |
probably damaging |
Het |
Gm20821 |
A |
G |
Y: 9,783,927 (GRCm39) |
Q183R |
probably benign |
Het |
Gpatch11 |
A |
T |
17: 79,151,266 (GRCm39) |
I226F |
probably benign |
Het |
Hephl1 |
T |
G |
9: 14,965,848 (GRCm39) |
E1035A |
probably damaging |
Het |
Hspa4l |
T |
C |
3: 40,714,833 (GRCm39) |
V156A |
probably damaging |
Het |
Ifna13 |
A |
G |
4: 88,562,588 (GRCm39) |
V12A |
probably benign |
Het |
Il24 |
G |
A |
1: 130,810,268 (GRCm39) |
T196I |
probably benign |
Het |
Irgm2 |
A |
G |
11: 58,110,384 (GRCm39) |
D37G |
probably benign |
Het |
Irs1 |
A |
G |
1: 82,266,486 (GRCm39) |
S577P |
probably damaging |
Het |
Kif21b |
G |
A |
1: 136,075,284 (GRCm39) |
D166N |
probably damaging |
Het |
Krtap4-16 |
T |
C |
11: 99,742,322 (GRCm39) |
Q26R |
unknown |
Het |
Lig1 |
T |
A |
7: 13,043,067 (GRCm39) |
Y837* |
probably null |
Het |
Lrrc69 |
T |
C |
4: 14,708,669 (GRCm39) |
E225G |
possibly damaging |
Het |
Map3k20 |
C |
T |
2: 72,271,638 (GRCm39) |
Q589* |
probably null |
Het |
Masp1 |
T |
G |
16: 23,302,211 (GRCm39) |
M347L |
probably benign |
Het |
Mgat3 |
A |
T |
15: 80,096,390 (GRCm39) |
I406F |
probably benign |
Het |
Mmp1b |
T |
G |
9: 7,368,577 (GRCm39) |
D425A |
probably benign |
Het |
Mss51 |
T |
C |
14: 20,533,259 (GRCm39) |
H404R |
probably benign |
Het |
Myo15b |
A |
T |
11: 115,773,701 (GRCm39) |
H1911L |
probably benign |
Het |
Nedd4l |
A |
G |
18: 65,276,874 (GRCm39) |
D102G |
probably damaging |
Het |
Niban3 |
T |
A |
8: 72,056,404 (GRCm39) |
I368N |
possibly damaging |
Het |
Npc2 |
T |
C |
12: 84,807,523 (GRCm39) |
K112E |
probably benign |
Het |
Nuggc |
T |
A |
14: 65,879,370 (GRCm39) |
V694E |
probably damaging |
Het |
Olfm1 |
T |
G |
2: 28,104,718 (GRCm39) |
V157G |
probably benign |
Het |
Or10h28 |
T |
C |
17: 33,488,489 (GRCm39) |
S264P |
probably benign |
Het |
Or5p55 |
T |
C |
7: 107,566,877 (GRCm39) |
V91A |
probably benign |
Het |
Otogl |
T |
A |
10: 107,630,051 (GRCm39) |
|
probably null |
Het |
Ovgp1 |
G |
A |
3: 105,882,251 (GRCm39) |
C38Y |
probably damaging |
Het |
Pisd |
A |
T |
5: 32,894,672 (GRCm39) |
S344T |
probably damaging |
Het |
Psme4 |
T |
C |
11: 30,780,352 (GRCm39) |
V840A |
probably benign |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Rims2 |
T |
A |
15: 39,208,710 (GRCm39) |
M171K |
probably damaging |
Het |
Rin2 |
T |
A |
2: 145,720,860 (GRCm39) |
M731K |
probably damaging |
Het |
Scgb1b19 |
T |
C |
7: 32,987,108 (GRCm39) |
|
probably null |
Het |
Serpina10 |
A |
G |
12: 103,594,514 (GRCm39) |
I235T |
possibly damaging |
Het |
Setbp1 |
T |
A |
18: 78,901,759 (GRCm39) |
E636V |
probably damaging |
Het |
Sh3d21 |
C |
T |
4: 126,056,290 (GRCm39) |
E101K |
probably damaging |
Het |
Ski |
T |
G |
4: 155,306,148 (GRCm39) |
D225A |
probably damaging |
Het |
Slc28a2b |
A |
G |
2: 122,357,910 (GRCm39) |
T655A |
probably benign |
Het |
Slc29a3 |
T |
C |
10: 60,559,593 (GRCm39) |
Y187C |
probably damaging |
Het |
Sort1 |
T |
A |
3: 108,253,043 (GRCm39) |
D494E |
possibly damaging |
Het |
Sphkap |
A |
T |
1: 83,255,643 (GRCm39) |
L702Q |
probably damaging |
Het |
Srr |
A |
G |
11: 74,799,545 (GRCm39) |
I285T |
probably damaging |
Het |
Stam2 |
T |
C |
2: 52,599,638 (GRCm39) |
T257A |
possibly damaging |
Het |
Suds3 |
A |
T |
5: 117,246,417 (GRCm39) |
N112K |
probably damaging |
Het |
Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
Tesk2 |
T |
C |
4: 116,608,390 (GRCm39) |
L104P |
probably damaging |
Het |
Tie1 |
C |
T |
4: 118,336,160 (GRCm39) |
R702H |
probably benign |
Het |
Tpo |
G |
T |
12: 30,169,465 (GRCm39) |
A90E |
probably damaging |
Het |
Trim30a |
T |
C |
7: 104,060,672 (GRCm39) |
D368G |
probably damaging |
Het |
Ugt2a2 |
A |
T |
5: 87,608,438 (GRCm39) |
M633K |
possibly damaging |
Het |
Vars2 |
A |
G |
17: 35,970,953 (GRCm39) |
W626R |
probably damaging |
Het |
Vmn2r10 |
A |
T |
5: 109,154,120 (GRCm39) |
Y61* |
probably null |
Het |
Vmn2r95 |
T |
C |
17: 18,671,805 (GRCm39) |
V514A |
probably benign |
Het |
Zfp365 |
A |
T |
10: 67,745,686 (GRCm39) |
C31S |
probably damaging |
Het |
Zfp397 |
A |
T |
18: 24,093,108 (GRCm39) |
I198F |
possibly damaging |
Het |
Zfp407 |
C |
T |
18: 84,577,898 (GRCm39) |
A1072T |
probably benign |
Het |
Zfp593 |
T |
C |
4: 133,972,206 (GRCm39) |
E100G |
possibly damaging |
Het |
|
Other mutations in Vwa5a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Vwa5a
|
APN |
9 |
38,649,110 (GRCm39) |
splice site |
probably null |
|
IGL00966:Vwa5a
|
APN |
9 |
38,634,675 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01597:Vwa5a
|
APN |
9 |
38,645,161 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01950:Vwa5a
|
APN |
9 |
38,638,266 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02008:Vwa5a
|
APN |
9 |
38,649,072 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02326:Vwa5a
|
APN |
9 |
38,649,252 (GRCm39) |
missense |
probably benign |
|
IGL02378:Vwa5a
|
APN |
9 |
38,645,266 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02442:Vwa5a
|
APN |
9 |
38,646,080 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02458:Vwa5a
|
APN |
9 |
38,638,259 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02570:Vwa5a
|
APN |
9 |
38,646,167 (GRCm39) |
unclassified |
probably benign |
|
IGL03068:Vwa5a
|
APN |
9 |
38,646,143 (GRCm39) |
missense |
probably benign |
0.45 |
R0126:Vwa5a
|
UTSW |
9 |
38,649,103 (GRCm39) |
splice site |
probably null |
|
R0325:Vwa5a
|
UTSW |
9 |
38,639,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Vwa5a
|
UTSW |
9 |
38,635,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R0928:Vwa5a
|
UTSW |
9 |
38,639,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R1334:Vwa5a
|
UTSW |
9 |
38,646,037 (GRCm39) |
missense |
probably benign |
0.01 |
R1446:Vwa5a
|
UTSW |
9 |
38,645,264 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1708:Vwa5a
|
UTSW |
9 |
38,639,128 (GRCm39) |
missense |
probably benign |
|
R2024:Vwa5a
|
UTSW |
9 |
38,647,357 (GRCm39) |
missense |
probably damaging |
0.98 |
R2230:Vwa5a
|
UTSW |
9 |
38,645,174 (GRCm39) |
missense |
probably null |
1.00 |
R2252:Vwa5a
|
UTSW |
9 |
38,639,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R2278:Vwa5a
|
UTSW |
9 |
38,634,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R3912:Vwa5a
|
UTSW |
9 |
38,646,039 (GRCm39) |
missense |
probably damaging |
0.97 |
R3913:Vwa5a
|
UTSW |
9 |
38,646,039 (GRCm39) |
missense |
probably damaging |
0.97 |
R4172:Vwa5a
|
UTSW |
9 |
38,635,166 (GRCm39) |
missense |
probably damaging |
0.98 |
R4244:Vwa5a
|
UTSW |
9 |
38,649,112 (GRCm39) |
splice site |
probably benign |
|
R4510:Vwa5a
|
UTSW |
9 |
38,633,853 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4511:Vwa5a
|
UTSW |
9 |
38,633,853 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4549:Vwa5a
|
UTSW |
9 |
38,649,221 (GRCm39) |
missense |
probably benign |
0.09 |
R4591:Vwa5a
|
UTSW |
9 |
38,646,916 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4639:Vwa5a
|
UTSW |
9 |
38,638,410 (GRCm39) |
critical splice donor site |
probably null |
|
R4811:Vwa5a
|
UTSW |
9 |
38,647,249 (GRCm39) |
missense |
probably benign |
0.00 |
R4911:Vwa5a
|
UTSW |
9 |
38,649,268 (GRCm39) |
missense |
probably benign |
0.03 |
R4936:Vwa5a
|
UTSW |
9 |
38,647,494 (GRCm39) |
missense |
probably benign |
0.00 |
R4989:Vwa5a
|
UTSW |
9 |
38,633,926 (GRCm39) |
missense |
probably benign |
0.40 |
R5370:Vwa5a
|
UTSW |
9 |
38,652,512 (GRCm39) |
missense |
probably benign |
0.02 |
R5596:Vwa5a
|
UTSW |
9 |
38,633,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R5914:Vwa5a
|
UTSW |
9 |
38,653,038 (GRCm39) |
missense |
probably benign |
0.00 |
R6207:Vwa5a
|
UTSW |
9 |
38,633,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R6486:Vwa5a
|
UTSW |
9 |
38,645,174 (GRCm39) |
missense |
probably null |
1.00 |
R7666:Vwa5a
|
UTSW |
9 |
38,645,259 (GRCm39) |
missense |
probably benign |
0.06 |
R7683:Vwa5a
|
UTSW |
9 |
38,646,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Vwa5a
|
UTSW |
9 |
38,652,458 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7839:Vwa5a
|
UTSW |
9 |
38,634,799 (GRCm39) |
missense |
probably damaging |
0.98 |
R7996:Vwa5a
|
UTSW |
9 |
38,639,124 (GRCm39) |
nonsense |
probably null |
|
R8024:Vwa5a
|
UTSW |
9 |
38,647,316 (GRCm39) |
nonsense |
probably null |
|
R8491:Vwa5a
|
UTSW |
9 |
38,652,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R9572:Vwa5a
|
UTSW |
9 |
38,649,239 (GRCm39) |
missense |
probably benign |
0.10 |
X0022:Vwa5a
|
UTSW |
9 |
38,647,258 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Vwa5a
|
UTSW |
9 |
38,634,547 (GRCm39) |
critical splice donor site |
probably null |
|
|