Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310002L09Rik |
A |
T |
4: 73,861,115 (GRCm39) |
W162R |
probably benign |
Het |
4930438A08Rik |
C |
A |
11: 58,184,464 (GRCm39) |
P394H |
probably damaging |
Het |
Aggf1 |
C |
T |
13: 95,508,123 (GRCm39) |
C81Y |
probably benign |
Het |
Agxt2 |
A |
T |
15: 10,378,963 (GRCm39) |
D188V |
probably damaging |
Het |
Angpt2 |
T |
C |
8: 18,748,132 (GRCm39) |
K376R |
probably benign |
Het |
Anxa5 |
A |
G |
3: 36,504,840 (GRCm39) |
S241P |
probably damaging |
Het |
Aox3 |
A |
T |
1: 58,209,018 (GRCm39) |
K850N |
probably damaging |
Het |
Arid5a |
T |
C |
1: 36,358,473 (GRCm39) |
M415T |
probably benign |
Het |
Aspa |
T |
A |
11: 73,199,578 (GRCm39) |
N233I |
probably damaging |
Het |
Atp4b |
C |
T |
8: 13,438,782 (GRCm39) |
R198Q |
probably damaging |
Het |
Atp8b2 |
A |
T |
3: 89,853,528 (GRCm39) |
V719E |
possibly damaging |
Het |
Bltp2 |
C |
A |
11: 78,162,210 (GRCm39) |
L691I |
possibly damaging |
Het |
Cacna1s |
T |
G |
1: 136,033,574 (GRCm39) |
V1017G |
probably damaging |
Het |
Chrna4 |
G |
T |
2: 180,671,235 (GRCm39) |
Q174K |
probably damaging |
Het |
Chrnb1 |
A |
T |
11: 69,677,765 (GRCm39) |
V329D |
probably damaging |
Het |
Chst14 |
T |
C |
2: 118,758,214 (GRCm39) |
L336P |
probably damaging |
Het |
Clec2e |
T |
C |
6: 129,077,772 (GRCm39) |
D22G |
probably benign |
Het |
Csrnp2 |
A |
C |
15: 100,380,263 (GRCm39) |
S343A |
probably benign |
Het |
Dapl1 |
C |
A |
2: 59,315,057 (GRCm39) |
A2E |
probably damaging |
Het |
Dlec1 |
G |
T |
9: 118,950,991 (GRCm39) |
R519L |
probably damaging |
Het |
Dmgdh |
T |
A |
13: 93,845,251 (GRCm39) |
F415I |
possibly damaging |
Het |
Dmgdh |
T |
C |
13: 93,888,834 (GRCm39) |
V824A |
probably damaging |
Het |
Dnah11 |
T |
G |
12: 117,892,191 (GRCm39) |
T3661P |
probably benign |
Het |
Dnah3 |
A |
G |
7: 119,629,254 (GRCm39) |
F1434L |
probably damaging |
Het |
Dnajc11 |
C |
A |
4: 152,062,583 (GRCm39) |
|
probably benign |
Het |
Dot1l |
A |
G |
10: 80,621,929 (GRCm39) |
E527G |
probably damaging |
Het |
Drc7 |
T |
C |
8: 95,801,679 (GRCm39) |
L680P |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,083,844 (GRCm39) |
Y742H |
probably benign |
Het |
Ece1 |
A |
G |
4: 137,688,958 (GRCm39) |
Y665C |
probably damaging |
Het |
Emc1 |
A |
G |
4: 139,081,533 (GRCm39) |
K54E |
possibly damaging |
Het |
Enoph1 |
C |
T |
5: 100,215,760 (GRCm39) |
T247M |
probably damaging |
Het |
Exoc2 |
T |
C |
13: 31,084,812 (GRCm39) |
K383R |
probably benign |
Het |
Fam227b |
A |
T |
2: 125,962,972 (GRCm39) |
H181Q |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,816,017 (GRCm39) |
M3917L |
probably benign |
Het |
Gtf3a |
T |
A |
5: 146,892,338 (GRCm39) |
|
probably benign |
Het |
Hgfac |
T |
A |
5: 35,198,973 (GRCm39) |
C11* |
probably null |
Het |
Hmcn1 |
C |
A |
1: 150,539,660 (GRCm39) |
A2944S |
probably damaging |
Het |
Hps5 |
T |
A |
7: 46,416,521 (GRCm39) |
Y947F |
probably benign |
Het |
Ighv2-5 |
A |
T |
12: 113,649,120 (GRCm39) |
I111K |
probably benign |
Het |
Inpp5e |
A |
T |
2: 26,297,860 (GRCm39) |
L247* |
probably null |
Het |
Kbtbd11 |
T |
C |
8: 15,077,577 (GRCm39) |
S59P |
probably benign |
Het |
Kctd19 |
G |
A |
8: 106,123,082 (GRCm39) |
H111Y |
probably damaging |
Het |
Kif1a |
T |
C |
1: 92,952,370 (GRCm39) |
D1303G |
probably damaging |
Het |
Kif7 |
A |
G |
7: 79,363,842 (GRCm39) |
V22A |
possibly damaging |
Het |
Lrit3 |
A |
T |
3: 129,583,004 (GRCm39) |
C328S |
probably damaging |
Het |
Lrrc37a |
G |
T |
11: 103,388,484 (GRCm39) |
Q2314K |
unknown |
Het |
LTO1 |
G |
T |
7: 144,469,023 (GRCm39) |
V17L |
possibly damaging |
Het |
Lurap1 |
G |
T |
4: 115,994,599 (GRCm39) |
P211T |
possibly damaging |
Het |
Mbd2 |
T |
A |
18: 70,713,874 (GRCm39) |
N5K |
possibly damaging |
Het |
Mbtps1 |
A |
C |
8: 120,242,341 (GRCm39) |
L894V |
probably benign |
Het |
Mefv |
G |
A |
16: 3,525,906 (GRCm39) |
S787F |
possibly damaging |
Het |
Miip |
T |
A |
4: 147,946,792 (GRCm39) |
I289F |
probably damaging |
Het |
Mogat2 |
T |
A |
7: 98,872,720 (GRCm39) |
I155F |
possibly damaging |
Het |
Mpp3 |
C |
A |
11: 101,902,515 (GRCm39) |
|
probably null |
Het |
Mrrf |
A |
G |
2: 36,067,233 (GRCm39) |
K220E |
probably damaging |
Het |
Mtmr6 |
C |
T |
14: 60,535,619 (GRCm39) |
P485L |
probably damaging |
Het |
Mtor |
G |
A |
4: 148,621,892 (GRCm39) |
R1896K |
probably benign |
Het |
Myh3 |
C |
T |
11: 66,978,371 (GRCm39) |
P453S |
probably benign |
Het |
Nebl |
A |
G |
2: 17,455,045 (GRCm39) |
V112A |
probably benign |
Het |
Nmnat2 |
G |
A |
1: 152,950,480 (GRCm39) |
W55* |
probably null |
Het |
Nprl3 |
A |
G |
11: 32,217,432 (GRCm39) |
S37P |
probably damaging |
Het |
Or4a73 |
T |
C |
2: 89,421,445 (GRCm39) |
N5D |
possibly damaging |
Het |
Pcdhga4 |
T |
G |
18: 37,819,383 (GRCm39) |
S311A |
probably benign |
Het |
Pcdhgb6 |
T |
C |
18: 37,876,165 (GRCm39) |
V291A |
probably benign |
Het |
Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
Peg3 |
T |
C |
7: 6,712,570 (GRCm39) |
E884G |
probably damaging |
Het |
Pgpep1 |
G |
A |
8: 71,105,101 (GRCm39) |
T53M |
probably damaging |
Het |
Phf12 |
A |
G |
11: 77,900,341 (GRCm39) |
T146A |
probably benign |
Het |
Polr3k |
C |
G |
2: 181,506,281 (GRCm39) |
N10K |
probably damaging |
Het |
Prickle4 |
C |
A |
17: 48,001,135 (GRCm39) |
G144C |
probably damaging |
Het |
Ptpn6 |
T |
C |
6: 124,709,398 (GRCm39) |
Y25C |
probably damaging |
Het |
Rad1 |
A |
G |
15: 10,488,160 (GRCm39) |
I95V |
probably damaging |
Het |
Rad23b |
A |
G |
4: 55,382,540 (GRCm39) |
T248A |
probably benign |
Het |
Rapgef3 |
T |
C |
15: 97,656,742 (GRCm39) |
D299G |
probably damaging |
Het |
Rcc2 |
T |
G |
4: 140,444,335 (GRCm39) |
V342G |
possibly damaging |
Het |
Rgs3 |
G |
T |
4: 62,544,143 (GRCm39) |
R136L |
probably damaging |
Het |
Scube2 |
A |
T |
7: 109,432,220 (GRCm39) |
C399* |
probably null |
Het |
Serpinb3d |
T |
C |
1: 107,007,452 (GRCm39) |
Y178C |
probably damaging |
Het |
Slc1a7 |
A |
G |
4: 107,869,458 (GRCm39) |
T508A |
probably benign |
Het |
Slc29a4 |
C |
T |
5: 142,705,832 (GRCm39) |
R439C |
probably damaging |
Het |
Sntg2 |
A |
G |
12: 30,362,560 (GRCm39) |
I62T |
probably benign |
Het |
Sowaha |
G |
A |
11: 53,369,914 (GRCm39) |
P274L |
probably damaging |
Het |
Sptan1 |
A |
G |
2: 29,886,794 (GRCm39) |
N869S |
probably benign |
Het |
Stx18 |
C |
A |
5: 38,263,908 (GRCm39) |
A64D |
probably damaging |
Het |
Stxbp5 |
A |
G |
10: 9,646,430 (GRCm39) |
V94A |
probably benign |
Het |
Sult1a1 |
T |
A |
7: 126,275,624 (GRCm39) |
|
probably null |
Het |
Susd1 |
G |
T |
4: 59,379,687 (GRCm39) |
H313Q |
possibly damaging |
Het |
Tdrd9 |
A |
T |
12: 111,951,475 (GRCm39) |
K88N |
probably damaging |
Het |
Tlr5 |
A |
C |
1: 182,801,603 (GRCm39) |
R302S |
possibly damaging |
Het |
Tnr |
C |
T |
1: 159,714,479 (GRCm39) |
T786I |
probably damaging |
Het |
Tprg1l |
A |
G |
4: 154,244,552 (GRCm39) |
S148P |
probably damaging |
Het |
Trpc4ap |
T |
A |
2: 155,512,994 (GRCm39) |
N127I |
probably damaging |
Het |
Tulp2 |
T |
A |
7: 45,139,797 (GRCm39) |
|
probably null |
Het |
Uggt2 |
C |
T |
14: 119,273,381 (GRCm39) |
|
probably null |
Het |
Ulk4 |
T |
A |
9: 121,102,021 (GRCm39) |
Y19F |
probably damaging |
Het |
Upf1 |
T |
C |
8: 70,785,687 (GRCm39) |
Y1053C |
probably damaging |
Het |
Vmn2r106 |
T |
A |
17: 20,487,806 (GRCm39) |
|
probably null |
Het |
Ythdc2 |
T |
A |
18: 44,973,277 (GRCm39) |
F305I |
probably damaging |
Het |
Zfp281 |
T |
C |
1: 136,553,178 (GRCm39) |
F52S |
possibly damaging |
Het |
Zfp292 |
A |
T |
4: 34,809,784 (GRCm39) |
C1087S |
probably damaging |
Het |
Zfp335 |
A |
T |
2: 164,737,018 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vars2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02106:Vars2
|
APN |
17 |
35,975,513 (GRCm39) |
unclassified |
probably benign |
|
IGL02320:Vars2
|
APN |
17 |
35,971,346 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02580:Vars2
|
APN |
17 |
35,971,777 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02691:Vars2
|
APN |
17 |
35,971,140 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03039:Vars2
|
APN |
17 |
35,975,013 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4445001:Vars2
|
UTSW |
17 |
35,977,103 (GRCm39) |
nonsense |
probably null |
|
R0079:Vars2
|
UTSW |
17 |
35,970,048 (GRCm39) |
missense |
probably damaging |
0.99 |
R0152:Vars2
|
UTSW |
17 |
35,970,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R0346:Vars2
|
UTSW |
17 |
35,975,756 (GRCm39) |
unclassified |
probably benign |
|
R0426:Vars2
|
UTSW |
17 |
35,975,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R0584:Vars2
|
UTSW |
17 |
35,977,578 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0589:Vars2
|
UTSW |
17 |
35,970,068 (GRCm39) |
missense |
probably benign |
|
R0882:Vars2
|
UTSW |
17 |
35,968,191 (GRCm39) |
missense |
probably benign |
0.41 |
R1234:Vars2
|
UTSW |
17 |
35,978,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R1263:Vars2
|
UTSW |
17 |
35,972,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R1559:Vars2
|
UTSW |
17 |
35,977,150 (GRCm39) |
unclassified |
probably benign |
|
R1772:Vars2
|
UTSW |
17 |
35,970,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Vars2
|
UTSW |
17 |
35,973,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1913:Vars2
|
UTSW |
17 |
35,977,814 (GRCm39) |
missense |
probably benign |
0.02 |
R1986:Vars2
|
UTSW |
17 |
35,970,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Vars2
|
UTSW |
17 |
35,975,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R3426:Vars2
|
UTSW |
17 |
35,972,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R4539:Vars2
|
UTSW |
17 |
35,977,780 (GRCm39) |
missense |
probably damaging |
0.99 |
R4751:Vars2
|
UTSW |
17 |
35,970,235 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4861:Vars2
|
UTSW |
17 |
35,972,825 (GRCm39) |
missense |
probably benign |
0.00 |
R4861:Vars2
|
UTSW |
17 |
35,972,825 (GRCm39) |
missense |
probably benign |
0.00 |
R5028:Vars2
|
UTSW |
17 |
35,970,365 (GRCm39) |
critical splice donor site |
probably null |
|
R5217:Vars2
|
UTSW |
17 |
35,969,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R5292:Vars2
|
UTSW |
17 |
35,971,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R6211:Vars2
|
UTSW |
17 |
35,976,554 (GRCm39) |
splice site |
probably null |
|
R6213:Vars2
|
UTSW |
17 |
35,971,332 (GRCm39) |
missense |
probably benign |
0.27 |
R6374:Vars2
|
UTSW |
17 |
35,970,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R6746:Vars2
|
UTSW |
17 |
35,971,294 (GRCm39) |
critical splice donor site |
probably null |
|
R6749:Vars2
|
UTSW |
17 |
35,977,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R6957:Vars2
|
UTSW |
17 |
35,977,967 (GRCm39) |
missense |
probably benign |
0.39 |
R7107:Vars2
|
UTSW |
17 |
35,969,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R7428:Vars2
|
UTSW |
17 |
35,977,578 (GRCm39) |
missense |
probably benign |
0.00 |
R7538:Vars2
|
UTSW |
17 |
35,971,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7553:Vars2
|
UTSW |
17 |
35,975,680 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7741:Vars2
|
UTSW |
17 |
35,971,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R7784:Vars2
|
UTSW |
17 |
35,969,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7823:Vars2
|
UTSW |
17 |
35,970,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R7915:Vars2
|
UTSW |
17 |
35,975,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R8201:Vars2
|
UTSW |
17 |
35,969,202 (GRCm39) |
missense |
probably benign |
|
R8955:Vars2
|
UTSW |
17 |
35,972,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R8964:Vars2
|
UTSW |
17 |
35,970,699 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9101:Vars2
|
UTSW |
17 |
35,969,980 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9202:Vars2
|
UTSW |
17 |
35,977,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R9202:Vars2
|
UTSW |
17 |
35,974,444 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9450:Vars2
|
UTSW |
17 |
35,973,027 (GRCm39) |
missense |
probably damaging |
0.98 |
X0021:Vars2
|
UTSW |
17 |
35,969,926 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1176:Vars2
|
UTSW |
17 |
35,975,683 (GRCm39) |
missense |
possibly damaging |
0.55 |
Z1177:Vars2
|
UTSW |
17 |
35,974,364 (GRCm39) |
missense |
probably benign |
0.17 |
|