Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,242,134 (GRCm39) |
E1332D |
probably benign |
Het |
Abca5 |
C |
A |
11: 110,220,043 (GRCm39) |
V8L |
probably benign |
Het |
Abcc8 |
C |
T |
7: 45,773,339 (GRCm39) |
E797K |
probably benign |
Het |
Acd |
C |
A |
8: 106,425,039 (GRCm39) |
|
probably null |
Het |
Adam34l |
A |
T |
8: 44,078,132 (GRCm39) |
Y697* |
probably null |
Het |
Adamts12 |
T |
C |
15: 11,311,240 (GRCm39) |
S1166P |
probably benign |
Het |
Alox12b |
T |
C |
11: 69,049,199 (GRCm39) |
Y83H |
possibly damaging |
Het |
Antxr2 |
A |
T |
5: 98,178,297 (GRCm39) |
S38T |
probably damaging |
Het |
Aox1 |
A |
G |
1: 58,115,262 (GRCm39) |
E749G |
probably damaging |
Het |
Arpc1a |
T |
A |
5: 145,043,901 (GRCm39) |
C344S |
possibly damaging |
Het |
Bcan |
T |
C |
3: 87,902,908 (GRCm39) |
Y290C |
probably damaging |
Het |
Bod1l |
G |
A |
5: 41,991,018 (GRCm39) |
S179F |
possibly damaging |
Het |
Catsper3 |
A |
C |
13: 55,953,561 (GRCm39) |
D224A |
probably damaging |
Het |
Ccar2 |
A |
G |
14: 70,377,946 (GRCm39) |
S680P |
probably damaging |
Het |
Ccdc18 |
A |
G |
5: 108,368,703 (GRCm39) |
H1275R |
possibly damaging |
Het |
Ccdc40 |
T |
C |
11: 119,150,730 (GRCm39) |
M1011T |
possibly damaging |
Het |
Cfap46 |
T |
A |
7: 139,263,386 (GRCm39) |
D17V |
probably damaging |
Het |
Csn1s2a |
T |
C |
5: 87,926,058 (GRCm39) |
F45L |
probably benign |
Het |
Cwf19l2 |
T |
G |
9: 3,458,802 (GRCm39) |
N750K |
possibly damaging |
Het |
Cyb5r4 |
A |
G |
9: 86,922,462 (GRCm39) |
D157G |
probably benign |
Het |
D130040H23Rik |
T |
A |
8: 69,755,354 (GRCm39) |
I253N |
probably benign |
Het |
Dennd4a |
C |
T |
9: 64,804,516 (GRCm39) |
A1285V |
probably benign |
Het |
Dlat |
A |
G |
9: 50,548,874 (GRCm39) |
S561P |
probably damaging |
Het |
Dlgap2 |
T |
A |
8: 14,823,347 (GRCm39) |
V522E |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,331,859 (GRCm39) |
Y2148* |
probably null |
Het |
Dnase2a |
T |
C |
8: 85,635,392 (GRCm39) |
|
probably benign |
Het |
Elapor2 |
A |
G |
5: 9,468,007 (GRCm39) |
E225G |
probably damaging |
Het |
Fam83f |
T |
C |
15: 80,574,113 (GRCm39) |
|
probably benign |
Het |
Firrm |
G |
A |
1: 163,792,363 (GRCm39) |
L545F |
probably damaging |
Het |
Foxi1 |
A |
T |
11: 34,157,937 (GRCm39) |
N29K |
possibly damaging |
Het |
Galk2 |
T |
C |
2: 125,817,183 (GRCm39) |
L324P |
probably benign |
Het |
Gdpd4 |
G |
A |
7: 97,622,162 (GRCm39) |
V214I |
probably benign |
Het |
Gfra3 |
C |
T |
18: 34,844,373 (GRCm39) |
A56T |
probably damaging |
Het |
Glyctk |
A |
G |
9: 106,032,547 (GRCm39) |
S489P |
probably damaging |
Het |
Izumo4 |
A |
T |
10: 80,539,569 (GRCm39) |
I135F |
probably damaging |
Het |
Krt87 |
T |
A |
15: 101,385,071 (GRCm39) |
T342S |
probably benign |
Het |
L1td1 |
T |
A |
4: 98,625,714 (GRCm39) |
D636E |
possibly damaging |
Het |
Letm2 |
A |
G |
8: 26,086,460 (GRCm39) |
|
probably benign |
Het |
Lpin1 |
A |
G |
12: 16,591,744 (GRCm39) |
F828L |
probably damaging |
Het |
Lrrc37 |
T |
C |
11: 103,511,431 (GRCm39) |
D179G |
unknown |
Het |
Mdn1 |
T |
A |
4: 32,763,339 (GRCm39) |
D5146E |
probably damaging |
Het |
Megf10 |
T |
A |
18: 57,324,257 (GRCm39) |
Y99* |
probably null |
Het |
Men1 |
A |
G |
19: 6,387,660 (GRCm39) |
D285G |
probably damaging |
Het |
Mertk |
T |
G |
2: 128,643,116 (GRCm39) |
D838E |
probably benign |
Het |
Mta1 |
T |
C |
12: 113,091,694 (GRCm39) |
S266P |
possibly damaging |
Het |
Mta3 |
G |
A |
17: 84,089,397 (GRCm39) |
V320M |
probably damaging |
Het |
Nlrp9c |
G |
A |
7: 26,084,245 (GRCm39) |
Q445* |
probably null |
Het |
Or2m12 |
A |
T |
16: 19,105,357 (GRCm39) |
N45K |
probably damaging |
Het |
Or51e1 |
T |
C |
7: 102,358,961 (GRCm39) |
I165T |
possibly damaging |
Het |
Or8b38 |
A |
T |
9: 37,972,646 (GRCm39) |
K10I |
probably benign |
Het |
Or8d6 |
T |
G |
9: 39,854,117 (GRCm39) |
I187R |
probably damaging |
Het |
Pbrm1 |
T |
A |
14: 30,828,132 (GRCm39) |
L1320I |
probably damaging |
Het |
Pdzd2 |
G |
T |
15: 12,457,972 (GRCm39) |
T297K |
probably damaging |
Het |
Pfas |
T |
C |
11: 68,882,795 (GRCm39) |
D782G |
probably damaging |
Het |
Pik3c3 |
T |
C |
18: 30,426,185 (GRCm39) |
|
probably null |
Het |
Pira2 |
T |
C |
7: 3,847,452 (GRCm39) |
N79S |
probably damaging |
Het |
Pkdrej |
G |
T |
15: 85,700,632 (GRCm39) |
T1768K |
probably damaging |
Het |
Plcb3 |
T |
C |
19: 6,940,353 (GRCm39) |
I439V |
probably benign |
Het |
Pold4 |
T |
A |
19: 4,282,593 (GRCm39) |
Y58* |
probably null |
Het |
Ppef2 |
T |
G |
5: 92,398,371 (GRCm39) |
Q49P |
probably damaging |
Het |
Ralgapa1 |
T |
A |
12: 55,723,817 (GRCm39) |
I2026F |
possibly damaging |
Het |
Rest |
T |
A |
5: 77,416,209 (GRCm39) |
V141E |
possibly damaging |
Het |
Rnf139 |
T |
C |
15: 58,771,202 (GRCm39) |
V409A |
probably benign |
Het |
Rnpc3 |
T |
C |
3: 113,404,704 (GRCm39) |
|
probably benign |
Het |
S100a10 |
A |
T |
3: 93,468,377 (GRCm39) |
E36V |
probably benign |
Het |
S1pr3 |
A |
C |
13: 51,573,952 (GRCm39) |
K378Q |
probably benign |
Het |
Scaper |
T |
A |
9: 55,593,222 (GRCm39) |
I472F |
probably damaging |
Het |
Sgcg |
G |
A |
14: 61,477,896 (GRCm39) |
|
probably benign |
Het |
Shank1 |
A |
T |
7: 43,991,539 (GRCm39) |
R69* |
probably null |
Het |
Shoc1 |
G |
A |
4: 59,054,142 (GRCm39) |
|
probably benign |
Het |
Siglecf |
A |
G |
7: 43,004,967 (GRCm39) |
N399S |
probably benign |
Het |
Slc25a54 |
T |
A |
3: 108,987,932 (GRCm39) |
Y24* |
probably null |
Het |
Slc29a4 |
T |
C |
5: 142,707,243 (GRCm39) |
*529R |
probably null |
Het |
Slc41a2 |
G |
A |
10: 83,137,029 (GRCm39) |
Q293* |
probably null |
Het |
Slc4a7 |
T |
C |
14: 14,737,509 (GRCm38) |
|
probably null |
Het |
Slfn9 |
G |
T |
11: 82,872,402 (GRCm39) |
T778N |
probably benign |
Het |
Ssr2 |
T |
C |
3: 88,483,949 (GRCm39) |
|
probably benign |
Het |
Tecrl |
T |
A |
5: 83,502,706 (GRCm39) |
T33S |
probably benign |
Het |
Tnfrsf9 |
T |
A |
4: 151,018,804 (GRCm39) |
C158* |
probably null |
Het |
Tradd |
T |
C |
8: 105,985,792 (GRCm39) |
E253G |
possibly damaging |
Het |
Usp34 |
A |
G |
11: 23,314,479 (GRCm39) |
H807R |
probably benign |
Het |
Vmn2r129 |
G |
T |
4: 156,686,692 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r27 |
T |
C |
6: 124,201,170 (GRCm39) |
I262M |
probably benign |
Het |
Vwf |
C |
T |
6: 125,619,902 (GRCm39) |
R1527C |
probably damaging |
Het |
Wwc1 |
C |
T |
11: 35,752,772 (GRCm39) |
G763D |
probably damaging |
Het |
Zfp526 |
T |
G |
7: 24,924,594 (GRCm39) |
D284E |
possibly damaging |
Het |
Zfp646 |
T |
C |
7: 127,483,021 (GRCm39) |
F1733L |
possibly damaging |
Het |
Zfp90 |
A |
G |
8: 107,145,755 (GRCm39) |
H29R |
probably benign |
Het |
Zkscan4 |
A |
G |
13: 21,668,104 (GRCm39) |
E185G |
probably benign |
Het |
|
Other mutations in Vps13a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00465:Vps13a
|
APN |
19 |
16,729,539 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00537:Vps13a
|
APN |
19 |
16,657,409 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00562:Vps13a
|
APN |
19 |
16,712,078 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00563:Vps13a
|
APN |
19 |
16,712,078 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00579:Vps13a
|
APN |
19 |
16,684,726 (GRCm39) |
missense |
probably benign |
0.29 |
IGL00662:Vps13a
|
APN |
19 |
16,681,904 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00667:Vps13a
|
APN |
19 |
16,737,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01102:Vps13a
|
APN |
19 |
16,628,781 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01139:Vps13a
|
APN |
19 |
16,617,989 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01142:Vps13a
|
APN |
19 |
16,664,479 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01361:Vps13a
|
APN |
19 |
16,720,371 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01386:Vps13a
|
APN |
19 |
16,678,516 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01593:Vps13a
|
APN |
19 |
16,739,545 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01700:Vps13a
|
APN |
19 |
16,722,221 (GRCm39) |
nonsense |
probably null |
|
IGL01767:Vps13a
|
APN |
19 |
16,641,258 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01782:Vps13a
|
APN |
19 |
16,731,701 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01808:Vps13a
|
APN |
19 |
16,687,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01812:Vps13a
|
APN |
19 |
16,692,424 (GRCm39) |
missense |
probably benign |
|
IGL01829:Vps13a
|
APN |
19 |
16,596,807 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01893:Vps13a
|
APN |
19 |
16,641,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02222:Vps13a
|
APN |
19 |
16,659,539 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02295:Vps13a
|
APN |
19 |
16,692,406 (GRCm39) |
splice site |
probably benign |
|
IGL02465:Vps13a
|
APN |
19 |
16,688,305 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02492:Vps13a
|
APN |
19 |
16,625,001 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02581:Vps13a
|
APN |
19 |
16,632,686 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02633:Vps13a
|
APN |
19 |
16,697,772 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02641:Vps13a
|
APN |
19 |
16,676,185 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02659:Vps13a
|
APN |
19 |
16,630,063 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02827:Vps13a
|
APN |
19 |
16,618,998 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02943:Vps13a
|
APN |
19 |
16,641,250 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03057:Vps13a
|
APN |
19 |
16,646,058 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03077:Vps13a
|
APN |
19 |
16,688,246 (GRCm39) |
missense |
probably benign |
|
IGL03184:Vps13a
|
APN |
19 |
16,631,734 (GRCm39) |
missense |
probably benign |
0.00 |
eggs
|
UTSW |
19 |
16,678,529 (GRCm39) |
missense |
probably damaging |
1.00 |
excambio
|
UTSW |
19 |
16,723,311 (GRCm39) |
splice site |
probably null |
|
Faster
|
UTSW |
19 |
16,596,849 (GRCm39) |
missense |
probably damaging |
1.00 |
Ham
|
UTSW |
19 |
16,655,333 (GRCm39) |
missense |
probably benign |
0.08 |
interchange
|
UTSW |
19 |
16,646,054 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4377001:Vps13a
|
UTSW |
19 |
16,718,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0045:Vps13a
|
UTSW |
19 |
16,618,174 (GRCm39) |
nonsense |
probably null |
|
R0045:Vps13a
|
UTSW |
19 |
16,618,174 (GRCm39) |
nonsense |
probably null |
|
R0048:Vps13a
|
UTSW |
19 |
16,653,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R0062:Vps13a
|
UTSW |
19 |
16,646,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R0062:Vps13a
|
UTSW |
19 |
16,646,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Vps13a
|
UTSW |
19 |
16,669,188 (GRCm39) |
missense |
probably benign |
0.03 |
R0135:Vps13a
|
UTSW |
19 |
16,758,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Vps13a
|
UTSW |
19 |
16,637,863 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0346:Vps13a
|
UTSW |
19 |
16,655,333 (GRCm39) |
missense |
probably benign |
0.08 |
R0359:Vps13a
|
UTSW |
19 |
16,618,941 (GRCm39) |
missense |
probably damaging |
0.99 |
R0530:Vps13a
|
UTSW |
19 |
16,632,570 (GRCm39) |
splice site |
probably benign |
|
R0541:Vps13a
|
UTSW |
19 |
16,681,941 (GRCm39) |
missense |
probably benign |
0.00 |
R0614:Vps13a
|
UTSW |
19 |
16,630,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R0685:Vps13a
|
UTSW |
19 |
16,758,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R0801:Vps13a
|
UTSW |
19 |
16,664,020 (GRCm39) |
splice site |
probably benign |
|
R0835:Vps13a
|
UTSW |
19 |
16,712,246 (GRCm39) |
splice site |
probably null |
|
R0848:Vps13a
|
UTSW |
19 |
16,676,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R1114:Vps13a
|
UTSW |
19 |
16,727,515 (GRCm39) |
missense |
probably benign |
0.41 |
R1205:Vps13a
|
UTSW |
19 |
16,617,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R1365:Vps13a
|
UTSW |
19 |
16,596,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Vps13a
|
UTSW |
19 |
16,678,602 (GRCm39) |
nonsense |
probably null |
|
R1451:Vps13a
|
UTSW |
19 |
16,688,228 (GRCm39) |
missense |
probably benign |
0.01 |
R1479:Vps13a
|
UTSW |
19 |
16,727,478 (GRCm39) |
splice site |
probably benign |
|
R1533:Vps13a
|
UTSW |
19 |
16,678,494 (GRCm39) |
nonsense |
probably null |
|
R1600:Vps13a
|
UTSW |
19 |
16,643,636 (GRCm39) |
missense |
probably benign |
0.01 |
R1871:Vps13a
|
UTSW |
19 |
16,642,028 (GRCm39) |
missense |
probably benign |
0.01 |
R1959:Vps13a
|
UTSW |
19 |
16,655,302 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1960:Vps13a
|
UTSW |
19 |
16,702,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Vps13a
|
UTSW |
19 |
16,699,822 (GRCm39) |
missense |
probably benign |
0.07 |
R2257:Vps13a
|
UTSW |
19 |
16,659,538 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2276:Vps13a
|
UTSW |
19 |
16,687,790 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2326:Vps13a
|
UTSW |
19 |
16,720,421 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2338:Vps13a
|
UTSW |
19 |
16,697,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R2359:Vps13a
|
UTSW |
19 |
16,630,043 (GRCm39) |
splice site |
probably benign |
|
R2421:Vps13a
|
UTSW |
19 |
16,737,035 (GRCm39) |
missense |
probably benign |
|
R2847:Vps13a
|
UTSW |
19 |
16,680,963 (GRCm39) |
missense |
probably damaging |
0.98 |
R3081:Vps13a
|
UTSW |
19 |
16,642,101 (GRCm39) |
missense |
probably benign |
0.02 |
R3522:Vps13a
|
UTSW |
19 |
16,743,857 (GRCm39) |
splice site |
probably benign |
|
R3613:Vps13a
|
UTSW |
19 |
16,662,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R3797:Vps13a
|
UTSW |
19 |
16,723,311 (GRCm39) |
splice site |
probably null |
|
R3874:Vps13a
|
UTSW |
19 |
16,722,317 (GRCm39) |
missense |
probably benign |
0.01 |
R4032:Vps13a
|
UTSW |
19 |
16,594,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R4111:Vps13a
|
UTSW |
19 |
16,617,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R4383:Vps13a
|
UTSW |
19 |
16,678,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R4504:Vps13a
|
UTSW |
19 |
16,672,866 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4578:Vps13a
|
UTSW |
19 |
16,659,474 (GRCm39) |
missense |
probably damaging |
0.98 |
R4587:Vps13a
|
UTSW |
19 |
16,617,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R4588:Vps13a
|
UTSW |
19 |
16,617,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R4605:Vps13a
|
UTSW |
19 |
16,617,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R4714:Vps13a
|
UTSW |
19 |
16,727,220 (GRCm39) |
missense |
probably benign |
0.01 |
R4756:Vps13a
|
UTSW |
19 |
16,632,580 (GRCm39) |
missense |
probably benign |
0.01 |
R4831:Vps13a
|
UTSW |
19 |
16,655,356 (GRCm39) |
missense |
probably benign |
0.04 |
R5068:Vps13a
|
UTSW |
19 |
16,723,422 (GRCm39) |
missense |
probably benign |
0.01 |
R5070:Vps13a
|
UTSW |
19 |
16,631,848 (GRCm39) |
missense |
probably benign |
|
R5082:Vps13a
|
UTSW |
19 |
16,722,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R5182:Vps13a
|
UTSW |
19 |
16,672,863 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5189:Vps13a
|
UTSW |
19 |
16,662,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R5283:Vps13a
|
UTSW |
19 |
16,655,334 (GRCm39) |
missense |
probably damaging |
0.96 |
R5294:Vps13a
|
UTSW |
19 |
16,619,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R5304:Vps13a
|
UTSW |
19 |
16,687,751 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5554:Vps13a
|
UTSW |
19 |
16,699,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R5592:Vps13a
|
UTSW |
19 |
16,702,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R5611:Vps13a
|
UTSW |
19 |
16,702,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R5665:Vps13a
|
UTSW |
19 |
16,646,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Vps13a
|
UTSW |
19 |
16,692,464 (GRCm39) |
missense |
probably benign |
0.03 |
R5684:Vps13a
|
UTSW |
19 |
16,676,409 (GRCm39) |
missense |
probably benign |
0.00 |
R5767:Vps13a
|
UTSW |
19 |
16,641,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R5810:Vps13a
|
UTSW |
19 |
16,643,688 (GRCm39) |
missense |
probably benign |
0.00 |
R5866:Vps13a
|
UTSW |
19 |
16,657,387 (GRCm39) |
missense |
probably benign |
0.04 |
R5886:Vps13a
|
UTSW |
19 |
16,641,926 (GRCm39) |
missense |
probably benign |
0.01 |
R5933:Vps13a
|
UTSW |
19 |
16,637,894 (GRCm39) |
missense |
probably benign |
0.34 |
R5965:Vps13a
|
UTSW |
19 |
16,596,392 (GRCm39) |
splice site |
probably null |
|
R6259:Vps13a
|
UTSW |
19 |
16,664,534 (GRCm39) |
nonsense |
probably null |
|
R6346:Vps13a
|
UTSW |
19 |
16,659,578 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6459:Vps13a
|
UTSW |
19 |
16,641,382 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6485:Vps13a
|
UTSW |
19 |
16,657,414 (GRCm39) |
missense |
probably damaging |
0.99 |
R6520:Vps13a
|
UTSW |
19 |
16,702,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R6644:Vps13a
|
UTSW |
19 |
16,722,283 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6932:Vps13a
|
UTSW |
19 |
16,655,439 (GRCm39) |
missense |
probably benign |
0.01 |
R6934:Vps13a
|
UTSW |
19 |
16,653,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R6951:Vps13a
|
UTSW |
19 |
16,701,104 (GRCm39) |
missense |
probably benign |
0.00 |
R7027:Vps13a
|
UTSW |
19 |
16,642,028 (GRCm39) |
missense |
probably benign |
0.01 |
R7126:Vps13a
|
UTSW |
19 |
16,688,243 (GRCm39) |
missense |
probably benign |
|
R7206:Vps13a
|
UTSW |
19 |
16,731,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R7248:Vps13a
|
UTSW |
19 |
16,655,406 (GRCm39) |
missense |
probably benign |
0.25 |
R7252:Vps13a
|
UTSW |
19 |
16,638,428 (GRCm39) |
missense |
probably benign |
0.00 |
R7255:Vps13a
|
UTSW |
19 |
16,631,703 (GRCm39) |
critical splice donor site |
probably null |
|
R7382:Vps13a
|
UTSW |
19 |
16,596,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Vps13a
|
UTSW |
19 |
16,727,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R7425:Vps13a
|
UTSW |
19 |
16,701,066 (GRCm39) |
missense |
probably benign |
0.13 |
R7523:Vps13a
|
UTSW |
19 |
16,681,153 (GRCm39) |
missense |
probably benign |
|
R7586:Vps13a
|
UTSW |
19 |
16,624,962 (GRCm39) |
missense |
probably benign |
0.08 |
R7587:Vps13a
|
UTSW |
19 |
16,681,153 (GRCm39) |
missense |
probably benign |
0.00 |
R7593:Vps13a
|
UTSW |
19 |
16,703,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R7637:Vps13a
|
UTSW |
19 |
16,727,513 (GRCm39) |
missense |
probably benign |
0.02 |
R7763:Vps13a
|
UTSW |
19 |
16,723,364 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7813:Vps13a
|
UTSW |
19 |
16,628,820 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7815:Vps13a
|
UTSW |
19 |
16,702,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R7861:Vps13a
|
UTSW |
19 |
16,632,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R7909:Vps13a
|
UTSW |
19 |
16,697,794 (GRCm39) |
nonsense |
probably null |
|
R7939:Vps13a
|
UTSW |
19 |
16,718,155 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8108:Vps13a
|
UTSW |
19 |
16,618,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R8123:Vps13a
|
UTSW |
19 |
16,625,066 (GRCm39) |
missense |
probably benign |
0.01 |
R8134:Vps13a
|
UTSW |
19 |
16,631,718 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8168:Vps13a
|
UTSW |
19 |
16,726,912 (GRCm39) |
missense |
probably benign |
0.09 |
R8272:Vps13a
|
UTSW |
19 |
16,727,209 (GRCm39) |
critical splice donor site |
probably null |
|
R8293:Vps13a
|
UTSW |
19 |
16,645,969 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8303:Vps13a
|
UTSW |
19 |
16,594,270 (GRCm39) |
missense |
probably benign |
0.00 |
R8383:Vps13a
|
UTSW |
19 |
16,701,069 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8386:Vps13a
|
UTSW |
19 |
16,678,483 (GRCm39) |
critical splice donor site |
probably null |
|
R8433:Vps13a
|
UTSW |
19 |
16,718,600 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8436:Vps13a
|
UTSW |
19 |
16,718,157 (GRCm39) |
missense |
probably benign |
0.10 |
R8450:Vps13a
|
UTSW |
19 |
16,631,871 (GRCm39) |
splice site |
probably null |
|
R8476:Vps13a
|
UTSW |
19 |
16,699,821 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8501:Vps13a
|
UTSW |
19 |
16,659,484 (GRCm39) |
missense |
probably benign |
0.39 |
R8552:Vps13a
|
UTSW |
19 |
16,731,684 (GRCm39) |
missense |
probably damaging |
0.99 |
R8680:Vps13a
|
UTSW |
19 |
16,623,270 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8784:Vps13a
|
UTSW |
19 |
16,642,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Vps13a
|
UTSW |
19 |
16,641,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R8945:Vps13a
|
UTSW |
19 |
16,642,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R8948:Vps13a
|
UTSW |
19 |
16,723,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R8950:Vps13a
|
UTSW |
19 |
16,723,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R8960:Vps13a
|
UTSW |
19 |
16,683,247 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9189:Vps13a
|
UTSW |
19 |
16,663,961 (GRCm39) |
missense |
probably benign |
|
R9366:Vps13a
|
UTSW |
19 |
16,672,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R9505:Vps13a
|
UTSW |
19 |
16,719,908 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9601:Vps13a
|
UTSW |
19 |
16,623,337 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9735:Vps13a
|
UTSW |
19 |
16,701,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R9776:Vps13a
|
UTSW |
19 |
16,736,958 (GRCm39) |
missense |
probably benign |
|
R9796:Vps13a
|
UTSW |
19 |
16,631,828 (GRCm39) |
missense |
probably benign |
0.01 |
X0061:Vps13a
|
UTSW |
19 |
16,623,232 (GRCm39) |
missense |
probably benign |
0.40 |
X0066:Vps13a
|
UTSW |
19 |
16,719,917 (GRCm39) |
missense |
probably benign |
0.33 |
Z1177:Vps13a
|
UTSW |
19 |
16,676,477 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z31818:Vps13a
|
UTSW |
19 |
16,758,118 (GRCm39) |
missense |
possibly damaging |
0.94 |
|