Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
T |
C |
13: 77,471,655 (GRCm39) |
I1020T |
probably benign |
Het |
2310057N15Rik |
A |
T |
16: 88,570,523 (GRCm39) |
Y172* |
probably null |
Het |
4930558K02Rik |
T |
A |
1: 161,770,092 (GRCm39) |
Y139F |
possibly damaging |
Het |
A830018L16Rik |
T |
G |
1: 11,658,695 (GRCm39) |
M202R |
probably damaging |
Het |
Abca12 |
T |
C |
1: 71,287,591 (GRCm39) |
E2450G |
probably damaging |
Het |
Ank2 |
C |
T |
3: 126,736,782 (GRCm39) |
R3034H |
unknown |
Het |
Anxa9 |
A |
G |
3: 95,213,184 (GRCm39) |
I54T |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,961,941 (GRCm39) |
|
probably null |
Het |
Bcar3 |
A |
T |
3: 122,302,045 (GRCm39) |
I247F |
possibly damaging |
Het |
Cep350 |
A |
G |
1: 155,829,334 (GRCm39) |
V130A |
probably damaging |
Het |
Cep89 |
A |
T |
7: 35,137,888 (GRCm39) |
R757S |
probably benign |
Het |
Cryga |
A |
T |
1: 65,142,381 (GRCm39) |
I4N |
probably damaging |
Het |
Cyp2d26 |
T |
A |
15: 82,676,764 (GRCm39) |
Y194F |
probably benign |
Het |
Edn2 |
G |
A |
4: 120,019,143 (GRCm39) |
R44H |
probably damaging |
Het |
Ep400 |
G |
A |
5: 110,903,511 (GRCm39) |
Q363* |
probably null |
Het |
Gpr33 |
T |
C |
12: 52,070,848 (GRCm39) |
T64A |
probably damaging |
Het |
Ice2 |
T |
A |
9: 69,324,365 (GRCm39) |
S763T |
possibly damaging |
Het |
Itgad |
C |
A |
7: 127,804,245 (GRCm39) |
F1169L |
probably damaging |
Het |
Kcnv1 |
A |
G |
15: 44,976,576 (GRCm39) |
L237P |
probably benign |
Het |
Kctd18 |
T |
C |
1: 57,995,710 (GRCm39) |
E356G |
probably damaging |
Het |
Krt33a |
C |
T |
11: 99,902,837 (GRCm39) |
R329Q |
probably damaging |
Het |
Lama2 |
C |
A |
10: 27,000,552 (GRCm39) |
G1657C |
probably damaging |
Het |
Marchf3 |
T |
G |
18: 56,895,593 (GRCm39) |
R217S |
probably benign |
Het |
Mmel1 |
A |
T |
4: 154,978,547 (GRCm39) |
T660S |
probably damaging |
Het |
Ms4a7 |
T |
A |
19: 11,310,642 (GRCm39) |
K59* |
probably null |
Het |
Mss51 |
G |
A |
14: 20,534,981 (GRCm39) |
T263I |
probably damaging |
Het |
Ncaph2 |
A |
G |
15: 89,248,385 (GRCm39) |
M199V |
probably benign |
Het |
Ndufa4 |
G |
A |
6: 11,905,209 (GRCm39) |
Q62* |
probably null |
Het |
Nectin4 |
A |
G |
1: 171,214,212 (GRCm39) |
T456A |
probably damaging |
Het |
Nek1 |
T |
C |
8: 61,578,120 (GRCm39) |
M1214T |
probably benign |
Het |
Nsf |
T |
A |
11: 103,718,064 (GRCm39) |
L710F |
probably damaging |
Het |
Nynrin |
G |
T |
14: 56,107,872 (GRCm39) |
G993V |
probably damaging |
Het |
Or1e31 |
T |
A |
11: 73,689,695 (GRCm39) |
D296V |
probably damaging |
Het |
Pbk |
T |
A |
14: 66,052,621 (GRCm39) |
Y155N |
probably damaging |
Het |
Plec |
T |
C |
15: 76,059,153 (GRCm39) |
I3595V |
possibly damaging |
Het |
Pom121 |
G |
A |
5: 135,409,941 (GRCm39) |
T1072I |
unknown |
Het |
Sdc1 |
T |
A |
12: 8,840,554 (GRCm39) |
H106Q |
probably benign |
Het |
Slc44a3 |
T |
C |
3: 121,254,764 (GRCm39) |
D618G |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,401,878 (GRCm39) |
D755G |
possibly damaging |
Het |
Slfn9 |
T |
C |
11: 82,872,387 (GRCm39) |
Y783C |
probably benign |
Het |
Sorl1 |
C |
T |
9: 41,975,006 (GRCm39) |
|
probably null |
Het |
Spindoc |
C |
T |
19: 7,360,085 (GRCm39) |
E28K |
possibly damaging |
Het |
Sptbn1 |
T |
C |
11: 30,064,859 (GRCm39) |
D1880G |
possibly damaging |
Het |
Sspn |
T |
A |
6: 145,907,200 (GRCm39) |
D210E |
probably benign |
Het |
Stx12 |
A |
T |
4: 132,584,687 (GRCm39) |
I219K |
possibly damaging |
Het |
Syne2 |
T |
C |
12: 76,095,417 (GRCm39) |
V508A |
probably benign |
Het |
Tkt |
G |
T |
14: 30,287,564 (GRCm39) |
R186L |
probably damaging |
Het |
Trmt10a |
T |
A |
3: 137,860,527 (GRCm39) |
M241K |
probably damaging |
Het |
Vgll2 |
C |
A |
10: 51,903,758 (GRCm39) |
A207E |
possibly damaging |
Het |
Vmn1r114 |
A |
G |
7: 20,545,543 (GRCm39) |
F190S |
probably damaging |
Het |
Xpot |
C |
T |
10: 121,453,094 (GRCm39) |
|
probably null |
Het |
Yrdc |
G |
A |
4: 124,744,820 (GRCm39) |
A85T |
probably benign |
Het |
Zfp385c |
C |
T |
11: 100,520,865 (GRCm39) |
R265K |
possibly damaging |
Het |
Zgrf1 |
A |
T |
3: 127,392,409 (GRCm39) |
I1310F |
probably damaging |
Het |
|
Other mutations in Aspm |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00489:Aspm
|
APN |
1 |
139,406,429 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00594:Aspm
|
APN |
1 |
139,415,160 (GRCm39) |
splice site |
probably benign |
|
IGL00808:Aspm
|
APN |
1 |
139,389,214 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00897:Aspm
|
APN |
1 |
139,405,145 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01024:Aspm
|
APN |
1 |
139,405,862 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01410:Aspm
|
APN |
1 |
139,410,182 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01588:Aspm
|
APN |
1 |
139,405,900 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01610:Aspm
|
APN |
1 |
139,417,408 (GRCm39) |
nonsense |
probably null |
|
IGL01633:Aspm
|
APN |
1 |
139,408,574 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01982:Aspm
|
APN |
1 |
139,419,326 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02429:Aspm
|
APN |
1 |
139,407,548 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02468:Aspm
|
APN |
1 |
139,408,688 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02519:Aspm
|
APN |
1 |
139,389,665 (GRCm39) |
splice site |
probably benign |
|
IGL02526:Aspm
|
APN |
1 |
139,417,457 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02716:Aspm
|
APN |
1 |
139,407,425 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02876:Aspm
|
APN |
1 |
139,401,391 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02953:Aspm
|
APN |
1 |
139,385,157 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03275:Aspm
|
APN |
1 |
139,415,033 (GRCm39) |
missense |
probably damaging |
1.00 |
Stemware
|
UTSW |
1 |
139,405,197 (GRCm39) |
nonsense |
probably null |
|
3-1:Aspm
|
UTSW |
1 |
139,385,279 (GRCm39) |
missense |
probably benign |
|
R0016:Aspm
|
UTSW |
1 |
139,407,282 (GRCm39) |
missense |
probably benign |
0.01 |
R0016:Aspm
|
UTSW |
1 |
139,407,282 (GRCm39) |
missense |
probably benign |
0.01 |
R0106:Aspm
|
UTSW |
1 |
139,404,614 (GRCm39) |
missense |
probably benign |
0.02 |
R0106:Aspm
|
UTSW |
1 |
139,404,614 (GRCm39) |
missense |
probably benign |
0.02 |
R0140:Aspm
|
UTSW |
1 |
139,408,379 (GRCm39) |
missense |
probably benign |
0.00 |
R0195:Aspm
|
UTSW |
1 |
139,406,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R0217:Aspm
|
UTSW |
1 |
139,385,618 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0276:Aspm
|
UTSW |
1 |
139,406,209 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0309:Aspm
|
UTSW |
1 |
139,410,249 (GRCm39) |
splice site |
probably benign |
|
R0466:Aspm
|
UTSW |
1 |
139,405,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R0520:Aspm
|
UTSW |
1 |
139,406,558 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0615:Aspm
|
UTSW |
1 |
139,415,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Aspm
|
UTSW |
1 |
139,419,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R0660:Aspm
|
UTSW |
1 |
139,385,502 (GRCm39) |
missense |
probably benign |
0.03 |
R0751:Aspm
|
UTSW |
1 |
139,384,636 (GRCm39) |
splice site |
probably benign |
|
R0830:Aspm
|
UTSW |
1 |
139,401,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R1109:Aspm
|
UTSW |
1 |
139,384,496 (GRCm39) |
missense |
probably damaging |
0.99 |
R1114:Aspm
|
UTSW |
1 |
139,389,662 (GRCm39) |
splice site |
probably benign |
|
R1130:Aspm
|
UTSW |
1 |
139,405,572 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1298:Aspm
|
UTSW |
1 |
139,385,157 (GRCm39) |
missense |
probably benign |
0.01 |
R1386:Aspm
|
UTSW |
1 |
139,385,361 (GRCm39) |
missense |
probably benign |
0.03 |
R1386:Aspm
|
UTSW |
1 |
139,406,710 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1557:Aspm
|
UTSW |
1 |
139,396,406 (GRCm39) |
missense |
probably benign |
0.01 |
R1625:Aspm
|
UTSW |
1 |
139,408,777 (GRCm39) |
missense |
probably benign |
0.01 |
R1728:Aspm
|
UTSW |
1 |
139,401,312 (GRCm39) |
missense |
probably benign |
|
R1729:Aspm
|
UTSW |
1 |
139,401,312 (GRCm39) |
missense |
probably benign |
|
R1730:Aspm
|
UTSW |
1 |
139,401,312 (GRCm39) |
missense |
probably benign |
|
R1733:Aspm
|
UTSW |
1 |
139,384,855 (GRCm39) |
missense |
probably benign |
0.27 |
R1739:Aspm
|
UTSW |
1 |
139,401,312 (GRCm39) |
missense |
probably benign |
|
R1762:Aspm
|
UTSW |
1 |
139,401,312 (GRCm39) |
missense |
probably benign |
|
R1783:Aspm
|
UTSW |
1 |
139,401,312 (GRCm39) |
missense |
probably benign |
|
R1784:Aspm
|
UTSW |
1 |
139,401,312 (GRCm39) |
missense |
probably benign |
|
R1785:Aspm
|
UTSW |
1 |
139,401,312 (GRCm39) |
missense |
probably benign |
|
R1793:Aspm
|
UTSW |
1 |
139,385,079 (GRCm39) |
missense |
probably benign |
0.00 |
R1893:Aspm
|
UTSW |
1 |
139,407,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Aspm
|
UTSW |
1 |
139,405,832 (GRCm39) |
missense |
probably benign |
0.06 |
R2103:Aspm
|
UTSW |
1 |
139,419,403 (GRCm39) |
missense |
probably damaging |
0.99 |
R2128:Aspm
|
UTSW |
1 |
139,385,373 (GRCm39) |
missense |
probably benign |
0.14 |
R2129:Aspm
|
UTSW |
1 |
139,385,373 (GRCm39) |
missense |
probably benign |
0.14 |
R2239:Aspm
|
UTSW |
1 |
139,384,584 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2352:Aspm
|
UTSW |
1 |
139,385,300 (GRCm39) |
missense |
probably benign |
0.02 |
R2353:Aspm
|
UTSW |
1 |
139,405,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R2380:Aspm
|
UTSW |
1 |
139,407,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R2413:Aspm
|
UTSW |
1 |
139,405,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R2421:Aspm
|
UTSW |
1 |
139,416,225 (GRCm39) |
missense |
possibly damaging |
0.49 |
R3607:Aspm
|
UTSW |
1 |
139,408,406 (GRCm39) |
missense |
probably benign |
0.13 |
R3711:Aspm
|
UTSW |
1 |
139,385,838 (GRCm39) |
missense |
probably benign |
0.17 |
R3718:Aspm
|
UTSW |
1 |
139,418,165 (GRCm39) |
missense |
probably benign |
0.31 |
R3718:Aspm
|
UTSW |
1 |
139,408,627 (GRCm39) |
missense |
probably benign |
0.09 |
R3741:Aspm
|
UTSW |
1 |
139,406,357 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3788:Aspm
|
UTSW |
1 |
139,390,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R3838:Aspm
|
UTSW |
1 |
139,405,792 (GRCm39) |
missense |
probably benign |
0.24 |
R3839:Aspm
|
UTSW |
1 |
139,405,792 (GRCm39) |
missense |
probably benign |
0.24 |
R3849:Aspm
|
UTSW |
1 |
139,386,024 (GRCm39) |
missense |
probably benign |
0.21 |
R4075:Aspm
|
UTSW |
1 |
139,402,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R4080:Aspm
|
UTSW |
1 |
139,398,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R4463:Aspm
|
UTSW |
1 |
139,382,748 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4537:Aspm
|
UTSW |
1 |
139,402,041 (GRCm39) |
missense |
probably benign |
0.01 |
R4547:Aspm
|
UTSW |
1 |
139,405,925 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4573:Aspm
|
UTSW |
1 |
139,407,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R4680:Aspm
|
UTSW |
1 |
139,408,409 (GRCm39) |
missense |
probably benign |
0.05 |
R4807:Aspm
|
UTSW |
1 |
139,405,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R4840:Aspm
|
UTSW |
1 |
139,398,269 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4854:Aspm
|
UTSW |
1 |
139,405,810 (GRCm39) |
nonsense |
probably null |
|
R4859:Aspm
|
UTSW |
1 |
139,397,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R4893:Aspm
|
UTSW |
1 |
139,417,577 (GRCm39) |
critical splice donor site |
probably null |
|
R4910:Aspm
|
UTSW |
1 |
139,419,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Aspm
|
UTSW |
1 |
139,399,472 (GRCm39) |
missense |
probably benign |
0.00 |
R4974:Aspm
|
UTSW |
1 |
139,405,748 (GRCm39) |
missense |
probably benign |
0.03 |
R4981:Aspm
|
UTSW |
1 |
139,398,498 (GRCm39) |
splice site |
probably null |
|
R5082:Aspm
|
UTSW |
1 |
139,406,414 (GRCm39) |
nonsense |
probably null |
|
R5223:Aspm
|
UTSW |
1 |
139,406,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R5268:Aspm
|
UTSW |
1 |
139,392,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R5371:Aspm
|
UTSW |
1 |
139,398,279 (GRCm39) |
nonsense |
probably null |
|
R5377:Aspm
|
UTSW |
1 |
139,398,133 (GRCm39) |
splice site |
probably null |
|
R5377:Aspm
|
UTSW |
1 |
139,385,221 (GRCm39) |
missense |
probably damaging |
0.96 |
R5481:Aspm
|
UTSW |
1 |
139,384,799 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5513:Aspm
|
UTSW |
1 |
139,410,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R5578:Aspm
|
UTSW |
1 |
139,398,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R5649:Aspm
|
UTSW |
1 |
139,407,407 (GRCm39) |
missense |
probably benign |
|
R5685:Aspm
|
UTSW |
1 |
139,415,026 (GRCm39) |
missense |
probably benign |
0.10 |
R5695:Aspm
|
UTSW |
1 |
139,407,407 (GRCm39) |
missense |
probably benign |
|
R5766:Aspm
|
UTSW |
1 |
139,406,740 (GRCm39) |
missense |
probably damaging |
0.99 |
R5964:Aspm
|
UTSW |
1 |
139,382,965 (GRCm39) |
intron |
probably benign |
|
R5993:Aspm
|
UTSW |
1 |
139,407,269 (GRCm39) |
missense |
probably benign |
0.28 |
R6027:Aspm
|
UTSW |
1 |
139,390,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Aspm
|
UTSW |
1 |
139,408,728 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6102:Aspm
|
UTSW |
1 |
139,405,197 (GRCm39) |
nonsense |
probably null |
|
R6188:Aspm
|
UTSW |
1 |
139,406,977 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6257:Aspm
|
UTSW |
1 |
139,409,791 (GRCm39) |
splice site |
probably null |
|
R6433:Aspm
|
UTSW |
1 |
139,401,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R6682:Aspm
|
UTSW |
1 |
139,385,460 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6763:Aspm
|
UTSW |
1 |
139,398,255 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6798:Aspm
|
UTSW |
1 |
139,396,423 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6815:Aspm
|
UTSW |
1 |
139,407,880 (GRCm39) |
missense |
probably benign |
0.04 |
R6854:Aspm
|
UTSW |
1 |
139,390,920 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6928:Aspm
|
UTSW |
1 |
139,407,944 (GRCm39) |
nonsense |
probably null |
|
R6943:Aspm
|
UTSW |
1 |
139,408,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R6979:Aspm
|
UTSW |
1 |
139,408,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R6998:Aspm
|
UTSW |
1 |
139,397,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R7126:Aspm
|
UTSW |
1 |
139,408,541 (GRCm39) |
missense |
probably benign |
0.27 |
R7237:Aspm
|
UTSW |
1 |
139,405,667 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7240:Aspm
|
UTSW |
1 |
139,406,389 (GRCm39) |
nonsense |
probably null |
|
R7427:Aspm
|
UTSW |
1 |
139,385,354 (GRCm39) |
missense |
probably benign |
0.01 |
R7519:Aspm
|
UTSW |
1 |
139,418,074 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7776:Aspm
|
UTSW |
1 |
139,407,584 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7875:Aspm
|
UTSW |
1 |
139,382,872 (GRCm39) |
missense |
probably benign |
0.02 |
R7883:Aspm
|
UTSW |
1 |
139,406,405 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7964:Aspm
|
UTSW |
1 |
139,408,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Aspm
|
UTSW |
1 |
139,385,202 (GRCm39) |
missense |
probably benign |
0.03 |
R8029:Aspm
|
UTSW |
1 |
139,399,370 (GRCm39) |
missense |
probably benign |
0.00 |
R8233:Aspm
|
UTSW |
1 |
139,385,042 (GRCm39) |
missense |
probably benign |
0.28 |
R8277:Aspm
|
UTSW |
1 |
139,382,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R8345:Aspm
|
UTSW |
1 |
139,392,011 (GRCm39) |
nonsense |
probably null |
|
R8491:Aspm
|
UTSW |
1 |
139,385,433 (GRCm39) |
missense |
probably damaging |
0.98 |
R8511:Aspm
|
UTSW |
1 |
139,385,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R8557:Aspm
|
UTSW |
1 |
139,384,494 (GRCm39) |
missense |
probably benign |
0.01 |
R8927:Aspm
|
UTSW |
1 |
139,418,125 (GRCm39) |
nonsense |
probably null |
|
R8928:Aspm
|
UTSW |
1 |
139,418,125 (GRCm39) |
nonsense |
probably null |
|
R8950:Aspm
|
UTSW |
1 |
139,406,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R9033:Aspm
|
UTSW |
1 |
139,405,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Aspm
|
UTSW |
1 |
139,421,436 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9133:Aspm
|
UTSW |
1 |
139,419,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R9160:Aspm
|
UTSW |
1 |
139,417,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R9179:Aspm
|
UTSW |
1 |
139,404,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R9265:Aspm
|
UTSW |
1 |
139,389,182 (GRCm39) |
missense |
probably benign |
0.24 |
R9400:Aspm
|
UTSW |
1 |
139,407,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R9419:Aspm
|
UTSW |
1 |
139,384,923 (GRCm39) |
missense |
probably benign |
0.29 |
R9454:Aspm
|
UTSW |
1 |
139,408,732 (GRCm39) |
missense |
probably benign |
0.00 |
R9517:Aspm
|
UTSW |
1 |
139,407,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R9524:Aspm
|
UTSW |
1 |
139,408,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R9544:Aspm
|
UTSW |
1 |
139,385,523 (GRCm39) |
missense |
probably benign |
0.01 |
R9640:Aspm
|
UTSW |
1 |
139,408,010 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9698:Aspm
|
UTSW |
1 |
139,389,646 (GRCm39) |
missense |
probably benign |
0.28 |
R9790:Aspm
|
UTSW |
1 |
139,408,375 (GRCm39) |
missense |
probably damaging |
0.98 |
R9791:Aspm
|
UTSW |
1 |
139,408,375 (GRCm39) |
missense |
probably damaging |
0.98 |
R9794:Aspm
|
UTSW |
1 |
139,406,480 (GRCm39) |
missense |
probably damaging |
0.99 |
X0063:Aspm
|
UTSW |
1 |
139,385,828 (GRCm39) |
missense |
probably benign |
0.01 |
|