Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
C |
T |
7: 27,278,198 (GRCm39) |
Q156* |
probably null |
Het |
2700097O09Rik |
A |
G |
12: 55,092,727 (GRCm39) |
I264T |
probably benign |
Het |
Arid3a |
G |
T |
10: 79,786,718 (GRCm39) |
M488I |
possibly damaging |
Het |
Auts2 |
A |
G |
5: 131,494,961 (GRCm39) |
F331S |
probably damaging |
Het |
Axdnd1 |
T |
C |
1: 156,158,532 (GRCm39) |
|
probably null |
Het |
Bpifb5 |
C |
A |
2: 154,066,876 (GRCm39) |
S43* |
probably null |
Het |
Carhsp1 |
A |
G |
16: 8,478,869 (GRCm39) |
V128A |
probably benign |
Het |
Ccdc141 |
A |
G |
2: 76,962,641 (GRCm39) |
V101A |
probably damaging |
Het |
Cdk6 |
C |
G |
5: 3,523,152 (GRCm39) |
L191V |
probably damaging |
Het |
Cgnl1 |
T |
G |
9: 71,632,416 (GRCm39) |
K312Q |
possibly damaging |
Het |
Col6a1 |
T |
C |
10: 76,557,277 (GRCm39) |
E225G |
probably damaging |
Het |
Copg1 |
T |
A |
6: 87,879,322 (GRCm39) |
L456Q |
probably damaging |
Het |
Ctif |
T |
A |
18: 75,570,279 (GRCm39) |
D540V |
possibly damaging |
Het |
Cyfip1 |
T |
C |
7: 55,569,241 (GRCm39) |
I917T |
probably benign |
Het |
Cyth1 |
T |
C |
11: 118,103,477 (GRCm39) |
D9G |
probably benign |
Het |
Dnajb1 |
T |
C |
8: 84,336,884 (GRCm39) |
I118T |
probably damaging |
Het |
Ebna1bp2 |
T |
A |
4: 118,480,575 (GRCm39) |
Y139* |
probably null |
Het |
Efcab3 |
A |
G |
11: 104,584,248 (GRCm39) |
T100A |
probably benign |
Het |
Fam162a |
A |
T |
16: 35,870,302 (GRCm39) |
V59E |
probably damaging |
Het |
Fhad1 |
CGG |
CG |
4: 141,645,602 (GRCm39) |
|
probably null |
Het |
Fmo6 |
C |
G |
1: 162,753,877 (GRCm39) |
R112T |
probably benign |
Het |
Gm17087 |
T |
A |
17: 8,785,304 (GRCm39) |
D133V |
probably benign |
Het |
Gm42669 |
A |
G |
5: 107,656,142 (GRCm39) |
I802V |
probably benign |
Het |
Gp2 |
T |
C |
7: 119,050,868 (GRCm39) |
N288D |
probably damaging |
Het |
Gstm7 |
C |
T |
3: 107,834,278 (GRCm39) |
D196N |
probably benign |
Het |
Hsph1 |
A |
T |
5: 149,553,865 (GRCm39) |
V201D |
probably damaging |
Het |
Il20ra |
T |
C |
10: 19,588,458 (GRCm39) |
L26P |
unknown |
Het |
Itpr1 |
T |
A |
6: 108,408,459 (GRCm39) |
|
probably null |
Het |
Kcns3 |
A |
T |
12: 11,141,688 (GRCm39) |
I337N |
probably damaging |
Het |
Kdm4d |
A |
G |
9: 14,375,475 (GRCm39) |
Y128H |
probably damaging |
Het |
Kirrel2 |
A |
G |
7: 30,153,999 (GRCm39) |
I200T |
probably benign |
Het |
Klhdc10 |
T |
A |
6: 30,450,502 (GRCm39) |
I294N |
probably damaging |
Het |
Marchf8 |
C |
G |
6: 116,380,504 (GRCm39) |
C118W |
probably damaging |
Het |
Marchf8 |
T |
G |
6: 116,380,505 (GRCm39) |
C119G |
probably damaging |
Het |
Mrpl38 |
G |
T |
11: 116,025,741 (GRCm39) |
P195Q |
probably damaging |
Het |
Ms4a4d |
A |
T |
19: 11,525,947 (GRCm39) |
Q27L |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,569,532 (GRCm39) |
T996S |
unknown |
Het |
Mug1 |
C |
T |
6: 121,838,084 (GRCm39) |
A438V |
probably benign |
Het |
Mup7 |
T |
A |
4: 60,069,866 (GRCm39) |
I33F |
probably damaging |
Het |
Ndufa5 |
C |
T |
6: 24,519,190 (GRCm39) |
|
probably null |
Het |
Or2b7 |
A |
G |
13: 21,740,108 (GRCm39) |
F28S |
probably benign |
Het |
Or2l5 |
A |
T |
16: 19,334,206 (GRCm39) |
F60Y |
probably benign |
Het |
Or5w17 |
T |
C |
2: 87,584,215 (GRCm39) |
I41V |
probably benign |
Het |
Or5w1b |
A |
T |
2: 87,476,320 (GRCm39) |
L49Q |
probably damaging |
Het |
Or7e177 |
T |
A |
9: 20,211,959 (GRCm39) |
C154* |
probably null |
Het |
Parp9 |
T |
A |
16: 35,780,433 (GRCm39) |
|
probably null |
Het |
Pate8 |
C |
A |
9: 36,493,854 (GRCm39) |
W26C |
unknown |
Het |
Pbx1 |
T |
A |
1: 168,258,949 (GRCm39) |
D42V |
probably damaging |
Het |
Pde4dip |
G |
T |
3: 97,622,738 (GRCm39) |
N1490K |
possibly damaging |
Het |
Pdzd2 |
T |
C |
15: 12,372,647 (GRCm39) |
N2496S |
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,373,061 (GRCm39) |
M2358T |
probably benign |
Het |
Pglyrp2 |
C |
A |
17: 32,634,904 (GRCm39) |
C486F |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,114,931 (GRCm39) |
|
probably benign |
Het |
Pknox2 |
T |
A |
9: 36,820,963 (GRCm39) |
T300S |
probably damaging |
Het |
Plekhm3 |
A |
G |
1: 64,922,429 (GRCm39) |
I582T |
probably damaging |
Het |
Prtg |
T |
C |
9: 72,799,267 (GRCm39) |
Y766H |
possibly damaging |
Het |
Prxl2a |
T |
C |
14: 40,724,451 (GRCm39) |
E71G |
probably benign |
Het |
Rabgap1 |
A |
G |
2: 37,450,575 (GRCm39) |
E901G |
probably benign |
Het |
Rabgap1l |
A |
T |
1: 160,169,642 (GRCm39) |
N60K |
probably damaging |
Het |
Rnf150 |
C |
T |
8: 83,769,292 (GRCm39) |
T359I |
probably benign |
Het |
Rps6ka2 |
C |
T |
17: 7,523,331 (GRCm39) |
H236Y |
probably benign |
Het |
Rrp1b |
T |
A |
17: 32,268,401 (GRCm39) |
L120Q |
probably damaging |
Het |
Scn7a |
C |
A |
2: 66,572,303 (GRCm39) |
G223C |
probably null |
Het |
Sema6a |
T |
A |
18: 47,431,284 (GRCm39) |
N138I |
probably damaging |
Het |
Septin5 |
T |
A |
16: 18,443,659 (GRCm39) |
I97F |
probably damaging |
Het |
Shcbp1 |
T |
A |
8: 4,804,234 (GRCm39) |
E225D |
probably damaging |
Het |
Slc25a19 |
A |
G |
11: 115,511,792 (GRCm39) |
C124R |
probably damaging |
Het |
Slc37a2 |
C |
T |
9: 37,145,183 (GRCm39) |
A428T |
probably damaging |
Het |
Slc5a12 |
A |
G |
2: 110,474,709 (GRCm39) |
I538V |
probably benign |
Het |
Slco4c1 |
A |
T |
1: 96,751,506 (GRCm39) |
|
probably null |
Het |
Smarcad1 |
T |
C |
6: 65,029,654 (GRCm39) |
S81P |
probably damaging |
Het |
Smyd1 |
T |
C |
6: 71,215,611 (GRCm39) |
D116G |
probably damaging |
Het |
Themis |
T |
C |
10: 28,665,703 (GRCm39) |
Y589H |
probably benign |
Het |
Trim30d |
T |
C |
7: 104,132,543 (GRCm39) |
K248R |
probably benign |
Het |
Tspan12 |
C |
T |
6: 21,772,918 (GRCm39) |
M210I |
probably benign |
Het |
Vmn2r11 |
T |
C |
5: 109,201,289 (GRCm39) |
Y405C |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 102,042,775 (GRCm39) |
|
probably null |
Het |
Wiz |
C |
A |
17: 32,580,840 (GRCm39) |
A83S |
probably damaging |
Het |
Zfp1002 |
A |
T |
2: 150,097,182 (GRCm39) |
C82* |
probably null |
Het |
Zmym6 |
T |
A |
4: 127,017,337 (GRCm39) |
Y947* |
probably null |
Het |
|
Other mutations in Map1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00419:Map1a
|
APN |
2 |
121,129,508 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00826:Map1a
|
APN |
2 |
121,132,757 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01476:Map1a
|
APN |
2 |
121,135,688 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02029:Map1a
|
APN |
2 |
121,133,779 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02100:Map1a
|
APN |
2 |
121,133,327 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02136:Map1a
|
APN |
2 |
121,130,693 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02146:Map1a
|
APN |
2 |
121,129,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02264:Map1a
|
APN |
2 |
121,137,794 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02456:Map1a
|
APN |
2 |
121,129,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02485:Map1a
|
APN |
2 |
121,129,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02535:Map1a
|
APN |
2 |
121,132,658 (GRCm39) |
nonsense |
probably null |
|
IGL02628:Map1a
|
APN |
2 |
121,130,585 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02721:Map1a
|
APN |
2 |
121,134,518 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03273:Map1a
|
APN |
2 |
121,130,719 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03281:Map1a
|
APN |
2 |
121,135,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02991:Map1a
|
UTSW |
2 |
121,132,091 (GRCm39) |
missense |
probably damaging |
0.99 |
R0096:Map1a
|
UTSW |
2 |
121,131,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Map1a
|
UTSW |
2 |
121,131,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R0218:Map1a
|
UTSW |
2 |
121,135,906 (GRCm39) |
missense |
probably benign |
0.00 |
R0363:Map1a
|
UTSW |
2 |
121,132,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0450:Map1a
|
UTSW |
2 |
121,136,255 (GRCm39) |
missense |
probably benign |
0.27 |
R0469:Map1a
|
UTSW |
2 |
121,136,255 (GRCm39) |
missense |
probably benign |
0.27 |
R0477:Map1a
|
UTSW |
2 |
121,132,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Map1a
|
UTSW |
2 |
121,133,422 (GRCm39) |
missense |
probably benign |
0.03 |
R0510:Map1a
|
UTSW |
2 |
121,136,255 (GRCm39) |
missense |
probably benign |
0.27 |
R0521:Map1a
|
UTSW |
2 |
121,136,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Map1a
|
UTSW |
2 |
121,129,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R0619:Map1a
|
UTSW |
2 |
121,135,736 (GRCm39) |
missense |
probably damaging |
0.96 |
R0633:Map1a
|
UTSW |
2 |
121,138,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Map1a
|
UTSW |
2 |
121,133,264 (GRCm39) |
missense |
probably benign |
0.04 |
R0893:Map1a
|
UTSW |
2 |
121,131,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R0960:Map1a
|
UTSW |
2 |
121,132,124 (GRCm39) |
missense |
probably benign |
0.16 |
R1115:Map1a
|
UTSW |
2 |
121,137,859 (GRCm39) |
splice site |
probably null |
|
R1166:Map1a
|
UTSW |
2 |
121,130,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R1326:Map1a
|
UTSW |
2 |
121,136,671 (GRCm39) |
nonsense |
probably null |
|
R1331:Map1a
|
UTSW |
2 |
121,136,701 (GRCm39) |
nonsense |
probably null |
|
R1395:Map1a
|
UTSW |
2 |
121,134,406 (GRCm39) |
missense |
probably benign |
0.26 |
R1489:Map1a
|
UTSW |
2 |
121,130,918 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1573:Map1a
|
UTSW |
2 |
121,134,607 (GRCm39) |
missense |
probably benign |
0.37 |
R1596:Map1a
|
UTSW |
2 |
121,120,246 (GRCm39) |
missense |
probably benign |
0.00 |
R1662:Map1a
|
UTSW |
2 |
121,136,889 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1675:Map1a
|
UTSW |
2 |
121,133,136 (GRCm39) |
nonsense |
probably null |
|
R1919:Map1a
|
UTSW |
2 |
121,137,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Map1a
|
UTSW |
2 |
121,129,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R2126:Map1a
|
UTSW |
2 |
121,129,122 (GRCm39) |
missense |
probably damaging |
0.96 |
R2143:Map1a
|
UTSW |
2 |
121,132,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Map1a
|
UTSW |
2 |
121,138,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R2249:Map1a
|
UTSW |
2 |
121,130,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R2254:Map1a
|
UTSW |
2 |
121,134,272 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2255:Map1a
|
UTSW |
2 |
121,134,272 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3834:Map1a
|
UTSW |
2 |
121,137,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R4011:Map1a
|
UTSW |
2 |
121,130,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R4346:Map1a
|
UTSW |
2 |
121,131,806 (GRCm39) |
missense |
probably benign |
0.13 |
R4842:Map1a
|
UTSW |
2 |
121,132,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4933:Map1a
|
UTSW |
2 |
121,136,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R4978:Map1a
|
UTSW |
2 |
121,131,623 (GRCm39) |
missense |
probably benign |
0.00 |
R4988:Map1a
|
UTSW |
2 |
121,133,531 (GRCm39) |
missense |
probably benign |
0.34 |
R5026:Map1a
|
UTSW |
2 |
121,138,019 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5086:Map1a
|
UTSW |
2 |
121,134,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R5155:Map1a
|
UTSW |
2 |
121,132,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R5232:Map1a
|
UTSW |
2 |
121,132,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R5311:Map1a
|
UTSW |
2 |
121,132,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R5401:Map1a
|
UTSW |
2 |
121,130,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R5465:Map1a
|
UTSW |
2 |
121,136,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R5526:Map1a
|
UTSW |
2 |
121,136,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Map1a
|
UTSW |
2 |
121,136,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Map1a
|
UTSW |
2 |
121,135,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R5817:Map1a
|
UTSW |
2 |
121,129,391 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5855:Map1a
|
UTSW |
2 |
121,134,155 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5917:Map1a
|
UTSW |
2 |
121,135,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R5974:Map1a
|
UTSW |
2 |
121,134,857 (GRCm39) |
missense |
probably benign |
0.20 |
R5987:Map1a
|
UTSW |
2 |
121,134,776 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6151:Map1a
|
UTSW |
2 |
121,120,304 (GRCm39) |
missense |
probably benign |
0.12 |
R6406:Map1a
|
UTSW |
2 |
121,131,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7099:Map1a
|
UTSW |
2 |
121,130,998 (GRCm39) |
missense |
probably benign |
0.04 |
R7211:Map1a
|
UTSW |
2 |
121,135,124 (GRCm39) |
missense |
probably benign |
0.02 |
R7230:Map1a
|
UTSW |
2 |
121,131,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R7305:Map1a
|
UTSW |
2 |
121,129,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7382:Map1a
|
UTSW |
2 |
121,121,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R7524:Map1a
|
UTSW |
2 |
121,120,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Map1a
|
UTSW |
2 |
121,130,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R7767:Map1a
|
UTSW |
2 |
121,132,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R7883:Map1a
|
UTSW |
2 |
121,135,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Map1a
|
UTSW |
2 |
121,135,657 (GRCm39) |
missense |
probably benign |
0.00 |
R7993:Map1a
|
UTSW |
2 |
121,135,057 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8270:Map1a
|
UTSW |
2 |
121,129,501 (GRCm39) |
missense |
probably damaging |
0.99 |
R8365:Map1a
|
UTSW |
2 |
121,138,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R8428:Map1a
|
UTSW |
2 |
121,135,418 (GRCm39) |
missense |
probably benign |
0.42 |
R8490:Map1a
|
UTSW |
2 |
121,135,045 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8678:Map1a
|
UTSW |
2 |
121,137,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R8798:Map1a
|
UTSW |
2 |
121,132,768 (GRCm39) |
missense |
probably benign |
0.20 |
R8857:Map1a
|
UTSW |
2 |
121,138,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R8878:Map1a
|
UTSW |
2 |
121,138,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R8909:Map1a
|
UTSW |
2 |
121,129,391 (GRCm39) |
missense |
probably damaging |
0.99 |
R8917:Map1a
|
UTSW |
2 |
121,131,791 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8947:Map1a
|
UTSW |
2 |
121,135,450 (GRCm39) |
missense |
probably benign |
0.27 |
R9069:Map1a
|
UTSW |
2 |
121,134,145 (GRCm39) |
missense |
probably benign |
0.15 |
R9198:Map1a
|
UTSW |
2 |
121,133,854 (GRCm39) |
missense |
probably benign |
0.00 |
R9253:Map1a
|
UTSW |
2 |
121,132,823 (GRCm39) |
missense |
probably benign |
0.00 |
R9290:Map1a
|
UTSW |
2 |
121,131,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R9300:Map1a
|
UTSW |
2 |
121,133,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R9589:Map1a
|
UTSW |
2 |
121,136,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R9680:Map1a
|
UTSW |
2 |
121,132,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R9792:Map1a
|
UTSW |
2 |
121,121,304 (GRCm39) |
critical splice donor site |
probably null |
|
R9793:Map1a
|
UTSW |
2 |
121,121,304 (GRCm39) |
critical splice donor site |
probably null |
|
R9795:Map1a
|
UTSW |
2 |
121,121,304 (GRCm39) |
critical splice donor site |
probably null |
|
RF003:Map1a
|
UTSW |
2 |
121,136,777 (GRCm39) |
small insertion |
probably benign |
|
RF007:Map1a
|
UTSW |
2 |
121,136,789 (GRCm39) |
small insertion |
probably benign |
|
RF009:Map1a
|
UTSW |
2 |
121,136,782 (GRCm39) |
small insertion |
probably benign |
|
RF010:Map1a
|
UTSW |
2 |
121,136,799 (GRCm39) |
small insertion |
probably benign |
|
RF014:Map1a
|
UTSW |
2 |
121,136,776 (GRCm39) |
small insertion |
probably benign |
|
RF017:Map1a
|
UTSW |
2 |
121,136,789 (GRCm39) |
small insertion |
probably benign |
|
RF024:Map1a
|
UTSW |
2 |
121,136,788 (GRCm39) |
small insertion |
probably benign |
|
RF025:Map1a
|
UTSW |
2 |
121,136,775 (GRCm39) |
small insertion |
probably benign |
|
RF030:Map1a
|
UTSW |
2 |
121,136,798 (GRCm39) |
small insertion |
probably benign |
|
RF030:Map1a
|
UTSW |
2 |
121,136,792 (GRCm39) |
small insertion |
probably benign |
|
RF033:Map1a
|
UTSW |
2 |
121,136,780 (GRCm39) |
small insertion |
probably benign |
|
RF034:Map1a
|
UTSW |
2 |
121,136,788 (GRCm39) |
small insertion |
probably benign |
|
RF034:Map1a
|
UTSW |
2 |
121,136,785 (GRCm39) |
small insertion |
probably benign |
|
RF035:Map1a
|
UTSW |
2 |
121,136,782 (GRCm39) |
small insertion |
probably benign |
|
RF037:Map1a
|
UTSW |
2 |
121,136,775 (GRCm39) |
small insertion |
probably benign |
|
RF039:Map1a
|
UTSW |
2 |
121,136,785 (GRCm39) |
small insertion |
probably benign |
|
RF042:Map1a
|
UTSW |
2 |
121,136,768 (GRCm39) |
small insertion |
probably benign |
|
RF044:Map1a
|
UTSW |
2 |
121,136,774 (GRCm39) |
small insertion |
probably benign |
|
RF045:Map1a
|
UTSW |
2 |
121,136,774 (GRCm39) |
small insertion |
probably benign |
|
RF051:Map1a
|
UTSW |
2 |
121,136,777 (GRCm39) |
small insertion |
probably benign |
|
RF052:Map1a
|
UTSW |
2 |
121,136,776 (GRCm39) |
small insertion |
probably benign |
|
RF053:Map1a
|
UTSW |
2 |
121,136,771 (GRCm39) |
small insertion |
probably benign |
|
RF060:Map1a
|
UTSW |
2 |
121,136,799 (GRCm39) |
small insertion |
probably benign |
|
RF061:Map1a
|
UTSW |
2 |
121,136,768 (GRCm39) |
small insertion |
probably benign |
|
Z1176:Map1a
|
UTSW |
2 |
121,133,719 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Map1a
|
UTSW |
2 |
121,135,760 (GRCm39) |
missense |
probably damaging |
0.99 |
|