Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,135,081 (GRCm39) |
I235V |
probably benign |
Het |
Acsm4 |
T |
C |
7: 119,297,801 (GRCm39) |
I146T |
probably benign |
Het |
Adgrv1 |
T |
C |
13: 81,676,984 (GRCm39) |
N1949S |
probably benign |
Het |
Afdn |
T |
C |
17: 14,066,798 (GRCm39) |
V630A |
probably damaging |
Het |
Amfr |
A |
G |
8: 94,712,027 (GRCm39) |
V301A |
possibly damaging |
Het |
Anapc16 |
T |
C |
10: 59,832,279 (GRCm39) |
M45V |
probably benign |
Het |
Ankrd12 |
T |
C |
17: 66,290,375 (GRCm39) |
E1686G |
possibly damaging |
Het |
Ap2m1 |
T |
G |
16: 20,359,979 (GRCm39) |
H193Q |
probably damaging |
Het |
Aplnr |
T |
C |
2: 84,967,805 (GRCm39) |
W277R |
possibly damaging |
Het |
Atp8b4 |
T |
A |
2: 126,220,664 (GRCm39) |
D578V |
probably benign |
Het |
Ccr1 |
T |
A |
9: 123,763,999 (GRCm39) |
E177V |
probably benign |
Het |
Cecr2 |
A |
G |
6: 120,739,092 (GRCm39) |
E1245G |
probably damaging |
Het |
Cep162 |
A |
T |
9: 87,103,255 (GRCm39) |
C638S |
probably benign |
Het |
Ces1b |
A |
T |
8: 93,794,705 (GRCm39) |
I298N |
probably benign |
Het |
Cfap47 |
C |
T |
X: 78,553,507 (GRCm39) |
V323I |
possibly damaging |
Het |
Chdh |
T |
A |
14: 29,753,391 (GRCm39) |
L100Q |
probably damaging |
Het |
Chrnd |
T |
C |
1: 87,120,312 (GRCm39) |
I156T |
probably damaging |
Het |
Clpx |
G |
A |
9: 65,234,170 (GRCm39) |
R605Q |
probably null |
Het |
Cnga1 |
T |
A |
5: 72,769,526 (GRCm39) |
K135* |
probably null |
Het |
Col6a4 |
A |
T |
9: 105,940,144 (GRCm39) |
V1262E |
probably benign |
Het |
Cracr2b |
T |
C |
7: 141,043,481 (GRCm39) |
L53P |
probably damaging |
Het |
Crhr1 |
T |
C |
11: 104,065,220 (GRCm39) |
S372P |
possibly damaging |
Het |
Cyp11b2 |
T |
A |
15: 74,723,624 (GRCm39) |
|
probably null |
Het |
Cyp21a1 |
T |
A |
17: 35,021,184 (GRCm39) |
D373V |
probably damaging |
Het |
D6Ertd527e |
C |
G |
6: 87,088,506 (GRCm39) |
T223S |
unknown |
Het |
Ddah1 |
A |
T |
3: 145,594,966 (GRCm39) |
Y242F |
probably benign |
Het |
Dlgap3 |
A |
G |
4: 127,088,719 (GRCm39) |
D105G |
possibly damaging |
Het |
Dtl |
A |
G |
1: 191,301,829 (GRCm39) |
V76A |
probably damaging |
Het |
Dzank1 |
A |
G |
2: 144,333,751 (GRCm39) |
S361P |
probably benign |
Het |
Ehd3 |
T |
A |
17: 74,127,538 (GRCm39) |
I157N |
probably damaging |
Het |
Elk4 |
T |
C |
1: 131,945,568 (GRCm39) |
F149L |
probably damaging |
Het |
Eme2 |
G |
A |
17: 25,111,892 (GRCm39) |
S263F |
probably damaging |
Het |
Fam83a |
A |
G |
15: 57,849,899 (GRCm39) |
R148G |
probably damaging |
Het |
Farp2 |
C |
A |
1: 93,547,873 (GRCm39) |
|
probably null |
Het |
Fbxw25 |
T |
A |
9: 109,483,709 (GRCm39) |
I168F |
possibly damaging |
Het |
Fermt1 |
T |
C |
2: 132,757,978 (GRCm39) |
D479G |
probably damaging |
Het |
Fgf17 |
C |
A |
14: 70,874,210 (GRCm39) |
R193L |
probably damaging |
Het |
Foxred2 |
T |
G |
15: 77,832,721 (GRCm39) |
|
probably null |
Het |
Gad1 |
T |
C |
2: 70,404,467 (GRCm39) |
V119A |
possibly damaging |
Het |
Gas2l3 |
A |
G |
10: 89,250,215 (GRCm39) |
V301A |
possibly damaging |
Het |
Gimap8 |
G |
A |
6: 48,633,587 (GRCm39) |
V469I |
probably benign |
Het |
Gja1 |
A |
T |
10: 56,264,065 (GRCm39) |
E141D |
probably benign |
Het |
Glod4 |
C |
T |
11: 76,112,829 (GRCm39) |
W268* |
probably null |
Het |
Guf1 |
C |
T |
5: 69,720,505 (GRCm39) |
H309Y |
probably benign |
Het |
Hax1 |
A |
G |
3: 89,903,156 (GRCm39) |
V215A |
probably damaging |
Het |
Heatr9 |
T |
C |
11: 83,409,651 (GRCm39) |
D107G |
probably benign |
Het |
Hephl1 |
T |
A |
9: 14,988,050 (GRCm39) |
Y686F |
probably benign |
Het |
Hk3 |
T |
C |
13: 55,154,843 (GRCm39) |
|
probably null |
Het |
Ikbkb |
G |
T |
8: 23,155,633 (GRCm39) |
Q620K |
possibly damaging |
Het |
Il18rap |
C |
T |
1: 40,570,682 (GRCm39) |
A208V |
probably benign |
Het |
Kif26b |
T |
C |
1: 178,743,209 (GRCm39) |
S1102P |
probably benign |
Het |
Kif5b |
A |
T |
18: 6,226,383 (GRCm39) |
D147E |
probably damaging |
Het |
Klhl3 |
T |
C |
13: 58,178,247 (GRCm39) |
T348A |
probably damaging |
Het |
Krt10 |
T |
C |
11: 99,276,746 (GRCm39) |
|
probably benign |
Het |
Lama3 |
A |
T |
18: 12,610,427 (GRCm39) |
H1124L |
probably benign |
Het |
Lin7a |
A |
T |
10: 107,247,983 (GRCm39) |
Q96L |
unknown |
Het |
Ly6c2 |
T |
G |
15: 74,982,438 (GRCm39) |
I37L |
probably benign |
Het |
Mov10l1 |
A |
G |
15: 88,895,589 (GRCm39) |
Y585C |
possibly damaging |
Het |
Msr1 |
G |
A |
8: 40,042,334 (GRCm39) |
Q414* |
probably null |
Het |
Myh13 |
T |
C |
11: 67,261,776 (GRCm39) |
C1900R |
possibly damaging |
Het |
Obscn |
T |
A |
11: 59,024,679 (GRCm39) |
N454Y |
probably damaging |
Het |
Olfml2b |
T |
G |
1: 170,508,731 (GRCm39) |
Y530D |
probably damaging |
Het |
Or1ad1 |
T |
C |
11: 50,876,194 (GRCm39) |
F222S |
probably damaging |
Het |
Or4c11 |
T |
A |
2: 88,695,697 (GRCm39) |
F249L |
probably benign |
Het |
Or52s1b |
T |
A |
7: 102,822,574 (GRCm39) |
H90L |
probably benign |
Het |
Or5b24 |
A |
T |
19: 12,912,503 (GRCm39) |
T134S |
probably benign |
Het |
Or7e174 |
T |
A |
9: 20,012,878 (GRCm39) |
N274K |
probably benign |
Het |
Or8j3b |
A |
G |
2: 86,205,265 (GRCm39) |
F164L |
probably damaging |
Het |
Pde10a |
T |
G |
17: 9,172,574 (GRCm39) |
V648G |
probably damaging |
Het |
Pde7b |
T |
A |
10: 20,294,547 (GRCm39) |
H258L |
probably damaging |
Het |
Pik3cb |
A |
G |
9: 98,946,080 (GRCm39) |
V582A |
possibly damaging |
Het |
Plxnb1 |
T |
C |
9: 108,930,091 (GRCm39) |
S316P |
probably benign |
Het |
Pmpca |
C |
T |
2: 26,282,530 (GRCm39) |
T246I |
probably damaging |
Het |
Reep3 |
A |
T |
10: 66,898,788 (GRCm39) |
V32D |
possibly damaging |
Het |
Rfx4 |
A |
G |
10: 84,699,149 (GRCm39) |
M252V |
probably damaging |
Het |
Rnf168 |
C |
A |
16: 32,117,781 (GRCm39) |
D447E |
probably damaging |
Het |
Rnf31 |
T |
C |
14: 55,834,221 (GRCm39) |
V518A |
probably damaging |
Het |
Rnpc3 |
A |
T |
3: 113,407,433 (GRCm39) |
L340* |
probably null |
Het |
Scn2a |
A |
G |
2: 65,519,085 (GRCm39) |
E437G |
probably damaging |
Het |
Scnn1b |
C |
A |
7: 121,501,711 (GRCm39) |
N175K |
possibly damaging |
Het |
Slc39a11 |
T |
A |
11: 113,138,550 (GRCm39) |
I344F |
probably benign |
Het |
Slc9a2 |
T |
A |
1: 40,758,178 (GRCm39) |
L239Q |
probably damaging |
Het |
Smg5 |
T |
C |
3: 88,262,978 (GRCm39) |
F794L |
probably damaging |
Het |
Smim13 |
C |
T |
13: 41,426,168 (GRCm39) |
S68L |
possibly damaging |
Het |
Sos2 |
A |
T |
12: 69,661,432 (GRCm39) |
Y680N |
probably damaging |
Het |
Spag6 |
T |
A |
2: 18,739,057 (GRCm39) |
M329K |
possibly damaging |
Het |
Spire2 |
G |
A |
8: 124,088,105 (GRCm39) |
|
probably null |
Het |
Tdrd9 |
T |
A |
12: 112,011,238 (GRCm39) |
V1149D |
probably benign |
Het |
Tns3 |
T |
A |
11: 8,468,261 (GRCm39) |
Y321F |
probably benign |
Het |
Top3b |
T |
C |
16: 16,698,493 (GRCm39) |
V112A |
probably benign |
Het |
Trafd1 |
G |
A |
5: 121,517,715 (GRCm39) |
T26I |
probably damaging |
Het |
Ttc28 |
G |
A |
5: 111,373,543 (GRCm39) |
S962N |
probably damaging |
Het |
Vmn2r78 |
T |
C |
7: 86,564,615 (GRCm39) |
L20S |
unknown |
Het |
Vmn2r82 |
A |
T |
10: 79,214,545 (GRCm39) |
D176V |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,923,458 (GRCm39) |
F3778L |
probably damaging |
Het |
Vwa3b |
T |
C |
1: 37,090,962 (GRCm39) |
|
probably null |
Het |
Vwc2 |
C |
T |
11: 11,104,262 (GRCm39) |
P265S |
probably damaging |
Het |
Zbtb9 |
T |
A |
17: 27,193,612 (GRCm39) |
I339N |
probably damaging |
Het |
Zfp335 |
T |
C |
2: 164,740,161 (GRCm39) |
T764A |
probably benign |
Het |
Zfp366 |
T |
A |
13: 99,383,063 (GRCm39) |
V742D |
probably damaging |
Het |
Zfp709 |
A |
T |
8: 72,644,506 (GRCm39) |
Y645F |
probably damaging |
Het |
Zmym2 |
T |
A |
14: 57,150,548 (GRCm39) |
C424S |
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 |
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 |
|
R7272:Aspm
|
UTSW |
1 |
139,386,066 (GRCm39) |
missense |
probably benign |
0.14 |
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 |
|