Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adsl |
T |
A |
15: 80,847,901 (GRCm39) |
M278K |
probably damaging |
Het |
Ago1 |
T |
C |
4: 126,347,397 (GRCm39) |
I147V |
probably benign |
Het |
Ank1 |
T |
C |
8: 23,578,634 (GRCm39) |
L261P |
probably damaging |
Het |
Ank2 |
T |
C |
3: 126,740,997 (GRCm39) |
|
probably benign |
Het |
Ap1b1 |
T |
C |
11: 4,968,020 (GRCm39) |
V177A |
possibly damaging |
Het |
Arhgap21 |
A |
G |
2: 20,853,645 (GRCm39) |
S1906P |
probably benign |
Het |
Asb1 |
A |
G |
1: 91,482,533 (GRCm39) |
Y214C |
probably benign |
Het |
BC049715 |
C |
T |
6: 136,817,429 (GRCm39) |
T223M |
probably damaging |
Het |
C1ra |
T |
A |
6: 124,496,688 (GRCm39) |
C375S |
probably damaging |
Het |
Cdh26 |
C |
T |
2: 178,083,210 (GRCm39) |
R26* |
probably null |
Het |
Chordc1 |
A |
G |
9: 18,224,131 (GRCm39) |
M304V |
probably benign |
Het |
Cpne8 |
T |
C |
15: 90,532,771 (GRCm39) |
|
probably benign |
Het |
Cracd |
A |
G |
5: 77,004,971 (GRCm39) |
E444G |
unknown |
Het |
Csf1 |
T |
C |
3: 107,656,026 (GRCm39) |
E335G |
possibly damaging |
Het |
Ctnnd2 |
C |
T |
15: 30,683,493 (GRCm39) |
P498L |
possibly damaging |
Het |
Cyp4f18 |
C |
T |
8: 72,756,276 (GRCm39) |
R100H |
probably benign |
Het |
Dnaaf2 |
G |
A |
12: 69,244,060 (GRCm39) |
R334C |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Dock10 |
A |
G |
1: 80,529,189 (GRCm39) |
S1071P |
possibly damaging |
Het |
Dtnb |
T |
C |
12: 3,682,942 (GRCm39) |
V7A |
probably benign |
Het |
Eif1 |
T |
C |
11: 100,211,552 (GRCm39) |
I62T |
probably damaging |
Het |
Fbxo44 |
T |
A |
4: 148,240,669 (GRCm39) |
T145S |
probably benign |
Het |
G530012D18Rik |
G |
C |
1: 85,504,941 (GRCm39) |
|
probably benign |
Het |
Gabbr2 |
A |
T |
4: 46,724,342 (GRCm39) |
M17K |
probably damaging |
Het |
Gm5860 |
T |
A |
4: 81,984,173 (GRCm39) |
|
noncoding transcript |
Het |
Gm7964 |
T |
A |
7: 83,406,560 (GRCm39) |
F439Y |
possibly damaging |
Het |
Gpbp1l1 |
C |
A |
4: 116,445,789 (GRCm39) |
T297N |
probably benign |
Het |
Greb1 |
C |
T |
12: 16,758,023 (GRCm39) |
|
probably benign |
Het |
Gvin3 |
A |
T |
7: 106,197,234 (GRCm39) |
|
noncoding transcript |
Het |
Hkdc1 |
T |
C |
10: 62,231,053 (GRCm39) |
|
probably benign |
Het |
Ighv16-1 |
T |
A |
12: 114,032,510 (GRCm39) |
L97F |
probably benign |
Het |
Il21r |
A |
G |
7: 125,232,027 (GRCm39) |
D485G |
probably damaging |
Het |
Inpp5d |
A |
G |
1: 87,633,686 (GRCm39) |
H441R |
probably damaging |
Het |
Iqgap2 |
G |
T |
13: 95,772,088 (GRCm39) |
R1364S |
probably benign |
Het |
Krtap20-2 |
G |
T |
16: 89,002,806 (GRCm39) |
C2F |
unknown |
Het |
Man2c1 |
T |
A |
9: 57,038,924 (GRCm39) |
D111E |
probably damaging |
Het |
Mdc1 |
T |
A |
17: 36,159,522 (GRCm39) |
V634E |
probably benign |
Het |
Mgam2-ps |
A |
G |
6: 40,800,547 (GRCm39) |
|
noncoding transcript |
Het |
Mllt3 |
T |
A |
4: 87,707,535 (GRCm39) |
N68Y |
probably damaging |
Het |
Mrps18a |
T |
A |
17: 46,436,621 (GRCm39) |
D143E |
probably benign |
Het |
Myl12a |
T |
C |
17: 71,301,611 (GRCm39) |
D172G |
possibly damaging |
Het |
Notch3 |
T |
C |
17: 32,362,308 (GRCm39) |
N1439S |
probably benign |
Het |
Npepps |
T |
C |
11: 97,108,625 (GRCm39) |
M764V |
probably benign |
Het |
Or8d2b |
T |
C |
9: 38,789,087 (GRCm39) |
L205P |
probably damaging |
Het |
Paxbp1 |
A |
T |
16: 90,812,104 (GRCm39) |
|
probably benign |
Het |
Pcdhb7 |
A |
T |
18: 37,476,162 (GRCm39) |
T433S |
possibly damaging |
Het |
Pcdhb8 |
A |
T |
18: 37,489,159 (GRCm39) |
Y279F |
probably damaging |
Het |
Pim3 |
T |
C |
15: 88,748,606 (GRCm39) |
L235P |
probably damaging |
Het |
Plekha4 |
C |
T |
7: 45,203,082 (GRCm39) |
S685F |
possibly damaging |
Het |
Plekhg1 |
C |
A |
10: 3,853,649 (GRCm39) |
H167Q |
probably damaging |
Het |
Plekhn1 |
G |
C |
4: 156,306,881 (GRCm39) |
P503A |
probably benign |
Het |
Sar1a |
T |
C |
10: 61,527,125 (GRCm39) |
L181P |
probably damaging |
Het |
Sec22a |
G |
T |
16: 35,168,112 (GRCm39) |
S133* |
probably null |
Het |
Sipa1l3 |
G |
A |
7: 29,048,000 (GRCm39) |
S247F |
probably damaging |
Het |
Slc31a1 |
T |
C |
4: 62,306,190 (GRCm39) |
S103P |
probably damaging |
Het |
Spag6 |
A |
C |
2: 18,747,688 (GRCm39) |
|
probably benign |
Het |
Stab1 |
T |
A |
14: 30,865,581 (GRCm39) |
D1769V |
probably damaging |
Het |
Stab1 |
G |
A |
14: 30,881,261 (GRCm39) |
L590F |
probably damaging |
Het |
Syde2 |
CAGTT |
CAGTTAGTT |
3: 145,707,163 (GRCm39) |
|
probably null |
Het |
Tbc1d2b |
A |
G |
9: 90,109,510 (GRCm39) |
L322P |
probably benign |
Het |
Tdrp |
T |
C |
8: 14,024,590 (GRCm39) |
E18G |
possibly damaging |
Het |
Tlr3 |
T |
A |
8: 45,855,862 (GRCm39) |
N106I |
probably damaging |
Het |
Tmem104 |
T |
A |
11: 115,092,227 (GRCm39) |
I112N |
probably damaging |
Het |
Tmem14c |
C |
T |
13: 41,174,598 (GRCm39) |
T69I |
probably benign |
Het |
Tmprss11g |
G |
A |
5: 86,644,377 (GRCm39) |
P156S |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,700,947 (GRCm39) |
|
probably benign |
Het |
Vmn1r45 |
A |
T |
6: 89,910,082 (GRCm39) |
I296N |
probably benign |
Het |
Vmn2r1 |
T |
A |
3: 63,997,418 (GRCm39) |
V358D |
probably benign |
Het |
Zc3h7b |
T |
C |
15: 81,677,375 (GRCm39) |
L892P |
probably damaging |
Het |
Zfp366 |
A |
G |
13: 99,365,451 (GRCm39) |
Q204R |
probably benign |
Het |
Zfp598 |
C |
A |
17: 24,899,872 (GRCm39) |
|
probably benign |
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 |
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 |
R7014:Map1a
|
UTSW |
2 |
121,130,720 (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 |
|