Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
A |
G |
16: 14,261,319 (GRCm39) |
E699G |
probably damaging |
Het |
Ap4e1 |
T |
A |
2: 126,906,899 (GRCm39) |
V1053D |
possibly damaging |
Het |
Apobec1 |
T |
A |
6: 122,558,456 (GRCm39) |
I100F |
probably damaging |
Het |
Atp6v1g3 |
G |
T |
1: 138,211,480 (GRCm39) |
K53N |
probably damaging |
Het |
Bag3 |
C |
T |
7: 128,147,830 (GRCm39) |
R482W |
probably damaging |
Het |
Brme1 |
C |
T |
8: 84,894,114 (GRCm39) |
T427I |
probably damaging |
Het |
Cacna1i |
A |
G |
15: 80,279,279 (GRCm39) |
T2007A |
possibly damaging |
Het |
Cd44 |
T |
C |
2: 102,731,687 (GRCm39) |
D2G |
probably damaging |
Het |
Cdadc1 |
T |
A |
14: 59,827,372 (GRCm39) |
I100F |
possibly damaging |
Het |
Cdh16 |
A |
G |
8: 105,344,677 (GRCm39) |
F485L |
probably damaging |
Het |
Cdhr5 |
T |
A |
7: 140,849,110 (GRCm39) |
K817* |
probably null |
Het |
Cfap46 |
G |
T |
7: 139,258,493 (GRCm39) |
P260Q |
probably damaging |
Het |
Clec11a |
C |
T |
7: 43,955,832 (GRCm39) |
E72K |
possibly damaging |
Het |
Cnr2 |
C |
A |
4: 135,644,076 (GRCm39) |
N51K |
probably damaging |
Het |
Col3a1 |
T |
A |
1: 45,370,872 (GRCm39) |
|
probably benign |
Het |
Cxcr1 |
G |
A |
1: 74,230,987 (GRCm39) |
T345M |
probably damaging |
Het |
Cyp2s1 |
T |
C |
7: 25,515,744 (GRCm39) |
|
probably null |
Het |
Dalrd3 |
C |
T |
9: 108,449,489 (GRCm39) |
T474M |
probably damaging |
Het |
Ddit4 |
C |
T |
10: 59,787,327 (GRCm39) |
S3N |
probably benign |
Het |
Ddx41 |
T |
C |
13: 55,683,708 (GRCm39) |
K108E |
possibly damaging |
Het |
Dnaaf10 |
A |
G |
11: 17,177,263 (GRCm39) |
N207S |
possibly damaging |
Het |
Ece2 |
A |
T |
16: 20,462,477 (GRCm39) |
H732L |
probably benign |
Het |
Etv3 |
T |
G |
3: 87,443,322 (GRCm39) |
L302R |
possibly damaging |
Het |
Fam135b |
A |
G |
15: 71,333,985 (GRCm39) |
S1070P |
probably damaging |
Het |
Fhip1b |
A |
T |
7: 105,039,089 (GRCm39) |
I50N |
probably damaging |
Het |
Gm11567 |
T |
A |
11: 99,770,437 (GRCm39) |
I125N |
unknown |
Het |
Grm3 |
A |
G |
5: 9,620,536 (GRCm39) |
L236P |
probably benign |
Het |
Hip1 |
T |
A |
5: 135,461,939 (GRCm39) |
R97* |
probably null |
Het |
Hoxa5 |
T |
C |
6: 52,181,197 (GRCm39) |
Y45C |
probably damaging |
Het |
Ighg1 |
T |
A |
12: 113,292,654 (GRCm39) |
H305L |
probably damaging |
Het |
Inpp5b |
T |
A |
4: 124,676,229 (GRCm39) |
C362S |
probably benign |
Het |
Kif1c |
A |
G |
11: 70,599,273 (GRCm39) |
K391E |
probably benign |
Het |
Klf9 |
T |
C |
19: 23,119,246 (GRCm39) |
V43A |
probably benign |
Het |
Krt28 |
T |
A |
11: 99,265,320 (GRCm39) |
I116F |
probably damaging |
Het |
Lct |
A |
T |
1: 128,222,969 (GRCm39) |
D1439E |
probably damaging |
Het |
Liph |
G |
A |
16: 21,784,745 (GRCm39) |
T284M |
possibly damaging |
Het |
Lrrc75b |
T |
C |
10: 75,393,055 (GRCm39) |
K98R |
possibly damaging |
Het |
Lypd4 |
T |
C |
7: 24,564,604 (GRCm39) |
Q178R |
probably benign |
Het |
Map3k21 |
C |
T |
8: 126,665,563 (GRCm39) |
T584I |
probably benign |
Het |
Map3k6 |
T |
C |
4: 132,972,855 (GRCm39) |
V338A |
probably damaging |
Het |
Mapk8ip3 |
A |
T |
17: 25,122,285 (GRCm39) |
V699E |
possibly damaging |
Het |
Mtarc1 |
A |
C |
1: 184,543,116 (GRCm39) |
S71A |
probably damaging |
Het |
Nckap1l |
T |
C |
15: 103,363,452 (GRCm39) |
S53P |
probably benign |
Het |
Nt5e |
T |
C |
9: 88,209,740 (GRCm39) |
M1T |
probably null |
Het |
Nudt22 |
T |
C |
19: 6,972,896 (GRCm39) |
H64R |
probably damaging |
Het |
Or1o11 |
A |
T |
17: 37,756,663 (GRCm39) |
T84S |
probably damaging |
Het |
Or2t44 |
A |
T |
11: 58,677,654 (GRCm39) |
Y198F |
probably damaging |
Het |
Or2w3 |
T |
C |
11: 58,557,225 (GRCm39) |
I280T |
possibly damaging |
Het |
Or52b1 |
A |
T |
7: 104,978,772 (GRCm39) |
V209D |
probably damaging |
Het |
Or5ac16 |
A |
G |
16: 59,022,369 (GRCm39) |
L140P |
probably damaging |
Het |
Or8k17 |
T |
C |
2: 86,066,276 (GRCm39) |
N294S |
probably damaging |
Het |
Otogl |
T |
C |
10: 107,722,413 (GRCm39) |
I314V |
probably benign |
Het |
Pan2 |
G |
T |
10: 128,143,969 (GRCm39) |
E106D |
probably benign |
Het |
Papss1 |
T |
A |
3: 131,337,565 (GRCm39) |
Y554* |
probably null |
Het |
Pcnx1 |
T |
C |
12: 81,941,803 (GRCm39) |
V67A |
possibly damaging |
Het |
Pdpk1 |
A |
C |
17: 24,325,829 (GRCm39) |
Y122* |
probably null |
Het |
Pkd1l1 |
A |
T |
11: 8,829,202 (GRCm39) |
N1463K |
probably damaging |
Het |
Ptgfrn |
C |
A |
3: 100,950,678 (GRCm39) |
M878I |
probably damaging |
Het |
Ranbp3 |
G |
A |
17: 57,017,703 (GRCm39) |
G453E |
probably benign |
Het |
Rapgef2 |
T |
C |
3: 79,002,157 (GRCm39) |
D261G |
probably damaging |
Het |
Reep2 |
A |
G |
18: 34,979,271 (GRCm39) |
S199G |
probably benign |
Het |
Rnpep |
G |
A |
1: 135,205,259 (GRCm39) |
T202I |
probably damaging |
Het |
Sass6 |
T |
A |
3: 116,401,145 (GRCm39) |
|
probably null |
Het |
Sema3e |
A |
G |
5: 14,212,257 (GRCm39) |
D111G |
probably damaging |
Het |
Slc29a4 |
A |
G |
5: 142,697,727 (GRCm39) |
E60G |
probably damaging |
Het |
Spata31g1 |
T |
C |
4: 42,971,831 (GRCm39) |
L388P |
possibly damaging |
Het |
Spata31h1 |
T |
A |
10: 82,120,317 (GRCm39) |
Q4231L |
probably damaging |
Het |
Sptlc3 |
T |
C |
2: 139,388,328 (GRCm39) |
Y107H |
probably damaging |
Het |
Stx6 |
T |
C |
1: 155,073,925 (GRCm39) |
I245T |
probably benign |
Het |
Syne2 |
T |
C |
12: 75,965,306 (GRCm39) |
S774P |
probably damaging |
Het |
Tbc1d16 |
T |
A |
11: 119,049,617 (GRCm39) |
Q293L |
probably damaging |
Het |
Tbc1d30 |
T |
C |
10: 121,132,692 (GRCm39) |
D224G |
probably damaging |
Het |
Tbc1d32 |
T |
A |
10: 56,026,973 (GRCm39) |
N759Y |
possibly damaging |
Het |
Tdrd12 |
G |
T |
7: 35,210,725 (GRCm39) |
A166E |
probably damaging |
Het |
Tex14 |
A |
G |
11: 87,405,046 (GRCm39) |
R653G |
probably benign |
Het |
Them6 |
A |
T |
15: 74,593,654 (GRCm39) |
R171W |
probably null |
Het |
Tln2 |
T |
C |
9: 67,203,640 (GRCm39) |
T489A |
probably benign |
Het |
Tmem87a |
A |
G |
2: 120,234,427 (GRCm39) |
F39L |
probably benign |
Het |
Toporsl |
T |
A |
4: 52,611,515 (GRCm39) |
C469* |
probably null |
Het |
Tpr |
T |
C |
1: 150,299,569 (GRCm39) |
S1147P |
probably damaging |
Het |
Trp53bp1 |
T |
C |
2: 121,067,143 (GRCm39) |
M528V |
probably benign |
Het |
Trpm6 |
T |
A |
19: 18,807,571 (GRCm39) |
C1039S |
probably damaging |
Het |
Ttc16 |
T |
A |
2: 32,665,348 (GRCm39) |
S5C |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,617,412 (GRCm39) |
Y14607C |
probably damaging |
Het |
Usp6nl |
T |
C |
2: 6,435,275 (GRCm39) |
F345L |
probably damaging |
Het |
Vmn1r205 |
C |
T |
13: 22,776,206 (GRCm39) |
G299R |
probably benign |
Het |
Vmn2r74 |
G |
A |
7: 85,606,588 (GRCm39) |
H253Y |
probably benign |
Het |
Vps13d |
A |
T |
4: 144,896,872 (GRCm39) |
D343E |
possibly damaging |
Het |
Vwf |
A |
G |
6: 125,580,381 (GRCm39) |
E543G |
|
Het |
Zfat |
A |
T |
15: 68,052,765 (GRCm39) |
V343E |
probably damaging |
Het |
Zfp316 |
T |
C |
5: 143,249,846 (GRCm39) |
E139G |
unknown |
Het |
Zfp943 |
T |
A |
17: 22,211,813 (GRCm39) |
C300S |
probably damaging |
Het |
Zkscan16 |
A |
G |
4: 58,957,748 (GRCm39) |
K677E |
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 |
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 |
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 |
|