Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
T |
A |
11: 58,771,885 (GRCm39) |
C456S |
probably damaging |
Het |
4930524J08Rik |
T |
C |
5: 100,127,068 (GRCm39) |
|
probably benign |
Het |
Adam28 |
T |
G |
14: 68,864,326 (GRCm39) |
R492S |
probably damaging |
Het |
Adarb2 |
G |
A |
13: 8,807,313 (GRCm39) |
A705T |
possibly damaging |
Het |
Adprhl1 |
T |
C |
8: 13,272,873 (GRCm39) |
D1295G |
probably benign |
Het |
Aldh3b3 |
A |
G |
19: 4,016,476 (GRCm39) |
I365V |
probably benign |
Het |
Aldh8a1 |
T |
C |
10: 21,264,996 (GRCm39) |
F208L |
possibly damaging |
Het |
Ap3b1 |
G |
A |
13: 94,664,673 (GRCm39) |
V871I |
unknown |
Het |
Apol7e |
A |
T |
15: 77,598,552 (GRCm39) |
R6* |
probably null |
Het |
Arfgap3 |
T |
C |
15: 83,191,150 (GRCm39) |
E456G |
probably damaging |
Het |
Arhgef1 |
T |
C |
7: 24,615,461 (GRCm39) |
L285P |
probably benign |
Het |
Arhgef7 |
T |
A |
8: 11,850,861 (GRCm39) |
C315S |
probably benign |
Het |
Atp9a |
A |
T |
2: 168,490,513 (GRCm39) |
L829Q |
probably damaging |
Het |
Babam2 |
T |
A |
5: 31,888,393 (GRCm39) |
|
probably null |
Het |
Bptf |
C |
T |
11: 106,951,384 (GRCm39) |
R2185H |
probably damaging |
Het |
Brd9 |
A |
C |
13: 74,102,697 (GRCm39) |
M473L |
probably benign |
Het |
C7 |
T |
C |
15: 5,041,538 (GRCm39) |
H456R |
probably benign |
Het |
Cabp7 |
C |
A |
11: 4,688,856 (GRCm39) |
A205S |
probably damaging |
Het |
Catsperb |
A |
G |
12: 101,554,293 (GRCm39) |
I662M |
probably damaging |
Het |
Ccl21a |
T |
C |
4: 42,773,906 (GRCm39) |
M5V |
probably benign |
Het |
Cdyl |
G |
T |
13: 36,042,177 (GRCm39) |
R405L |
possibly damaging |
Het |
Cep89 |
T |
C |
7: 35,127,672 (GRCm39) |
L538P |
probably damaging |
Het |
Cercam |
A |
G |
2: 29,762,892 (GRCm39) |
M209V |
possibly damaging |
Het |
Chfr |
T |
A |
5: 110,310,571 (GRCm39) |
|
probably null |
Het |
Cntnap5c |
T |
A |
17: 58,717,226 (GRCm39) |
Y1269* |
probably null |
Het |
Col6a2 |
G |
T |
10: 76,439,170 (GRCm39) |
C833* |
probably null |
Het |
Cpeb3 |
T |
A |
19: 37,151,900 (GRCm39) |
I159F |
probably benign |
Het |
Cplx2 |
G |
A |
13: 54,526,663 (GRCm39) |
E24K |
possibly damaging |
Het |
Ctsb |
A |
G |
14: 63,379,752 (GRCm39) |
T332A |
probably benign |
Het |
Cyp2j12 |
T |
A |
4: 96,029,222 (GRCm39) |
T20S |
probably benign |
Het |
Dcst2 |
T |
A |
3: 89,273,993 (GRCm39) |
H181Q |
probably damaging |
Het |
Dnm1l |
T |
C |
16: 16,136,338 (GRCm39) |
I411V |
probably benign |
Het |
Dock5 |
T |
A |
14: 68,046,479 (GRCm39) |
I768F |
probably benign |
Het |
Ecel1 |
A |
G |
1: 87,077,334 (GRCm39) |
Y625H |
probably damaging |
Het |
Efl1 |
T |
G |
7: 82,330,587 (GRCm39) |
S253R |
probably damaging |
Het |
Elmod1 |
T |
A |
9: 53,820,127 (GRCm39) |
D287V |
probably damaging |
Het |
Fam171a2 |
T |
C |
11: 102,329,491 (GRCm39) |
S423G |
probably benign |
Het |
Fbxo8 |
A |
T |
8: 57,022,317 (GRCm39) |
|
probably null |
Het |
Flnc |
G |
T |
6: 29,455,470 (GRCm39) |
G2040W |
probably damaging |
Het |
Fras1 |
C |
T |
5: 96,821,458 (GRCm39) |
A1405V |
probably benign |
Het |
Frem3 |
A |
C |
8: 81,342,392 (GRCm39) |
I1562L |
probably benign |
Het |
Fxr1 |
C |
T |
3: 34,103,369 (GRCm39) |
A233V |
probably damaging |
Het |
H1f9 |
A |
G |
11: 94,859,184 (GRCm39) |
R160G |
possibly damaging |
Het |
Helb |
A |
G |
10: 119,944,799 (GRCm39) |
F246L |
probably damaging |
Het |
Hoxb6 |
G |
T |
11: 96,183,510 (GRCm39) |
|
probably benign |
Het |
Hspa2 |
A |
G |
12: 76,452,884 (GRCm39) |
E526G |
probably damaging |
Het |
Hyal5 |
A |
T |
6: 24,875,983 (GRCm39) |
|
probably benign |
Het |
Ints6 |
A |
T |
14: 62,942,224 (GRCm39) |
V503E |
probably benign |
Het |
Ints9 |
C |
T |
14: 65,269,747 (GRCm39) |
T479I |
possibly damaging |
Het |
Jag1 |
C |
T |
2: 136,926,975 (GRCm39) |
R928H |
probably benign |
Het |
Lman2 |
A |
T |
13: 55,499,338 (GRCm39) |
I179N |
probably damaging |
Het |
Lta |
T |
C |
17: 35,422,805 (GRCm39) |
S173G |
probably benign |
Het |
Mki67 |
G |
A |
7: 135,300,099 (GRCm39) |
P1645L |
probably damaging |
Het |
Mrc2 |
A |
T |
11: 105,183,609 (GRCm39) |
|
probably benign |
Het |
Muc4 |
T |
A |
16: 32,754,689 (GRCm38) |
M1521K |
probably benign |
Het |
Mucl3 |
T |
A |
17: 35,949,312 (GRCm39) |
T96S |
probably benign |
Het |
Mylk3 |
T |
G |
8: 86,081,873 (GRCm39) |
D438A |
probably benign |
Het |
Myo7a |
T |
A |
7: 97,700,833 (GRCm39) |
|
probably null |
Het |
Nsmce4a |
G |
T |
7: 130,135,547 (GRCm39) |
Q342K |
probably benign |
Het |
Or10ac1 |
A |
G |
6: 42,515,053 (GRCm39) |
I301T |
possibly damaging |
Het |
Or4c124 |
T |
A |
2: 89,156,423 (GRCm39) |
I34F |
probably benign |
Het |
Or5p60 |
A |
G |
7: 107,724,068 (GRCm39) |
L134P |
probably damaging |
Het |
Or6c65 |
A |
T |
10: 129,604,136 (GRCm39) |
Y257F |
possibly damaging |
Het |
Osbpl6 |
T |
A |
2: 76,423,730 (GRCm39) |
F864L |
probably damaging |
Het |
Pla2g4a |
A |
G |
1: 149,808,438 (GRCm39) |
S2P |
probably benign |
Het |
Plce1 |
T |
C |
19: 38,640,329 (GRCm39) |
L525P |
probably damaging |
Het |
Por |
A |
T |
5: 135,763,773 (GRCm39) |
M667L |
probably benign |
Het |
Psma4 |
T |
C |
9: 54,862,166 (GRCm39) |
Y97H |
probably benign |
Het |
Qtrt1 |
A |
T |
9: 21,323,753 (GRCm39) |
H126L |
probably benign |
Het |
Rab3a |
A |
T |
8: 71,209,170 (GRCm39) |
Y102F |
possibly damaging |
Het |
Rnf212 |
T |
A |
5: 108,879,555 (GRCm39) |
H87L |
probably benign |
Het |
Rnf216 |
A |
G |
5: 143,076,591 (GRCm39) |
S98P |
probably benign |
Het |
Ryr1 |
G |
T |
7: 28,785,295 (GRCm39) |
R1806S |
probably benign |
Het |
Scgb1b3 |
A |
T |
7: 31,075,262 (GRCm39) |
L37F |
probably benign |
Het |
Sds |
T |
C |
5: 120,617,254 (GRCm39) |
S37P |
probably damaging |
Het |
Senp6 |
A |
G |
9: 80,021,159 (GRCm39) |
R280G |
probably damaging |
Het |
She |
T |
A |
3: 89,761,864 (GRCm39) |
I441K |
possibly damaging |
Het |
Slc6a20b |
A |
G |
9: 123,436,682 (GRCm39) |
S244P |
possibly damaging |
Het |
Slc9a3 |
A |
T |
13: 74,299,004 (GRCm39) |
Y141F |
probably damaging |
Het |
Slco6c1 |
A |
T |
1: 97,009,207 (GRCm39) |
H426Q |
probably benign |
Het |
Smc2 |
C |
A |
4: 52,440,301 (GRCm39) |
Q16K |
probably benign |
Het |
Sphkap |
A |
C |
1: 83,241,547 (GRCm39) |
V1535G |
probably benign |
Het |
Stard9 |
C |
A |
2: 120,532,633 (GRCm39) |
N2963K |
probably benign |
Het |
Sycp2 |
C |
T |
2: 178,035,944 (GRCm39) |
A248T |
probably damaging |
Het |
Taar8a |
T |
C |
10: 23,952,762 (GRCm39) |
L122P |
probably damaging |
Het |
Tab1 |
T |
A |
15: 80,044,445 (GRCm39) |
V491E |
probably benign |
Het |
Tanc1 |
T |
C |
2: 59,636,688 (GRCm39) |
M857T |
probably benign |
Het |
Tcirg1 |
C |
A |
19: 3,949,008 (GRCm39) |
R427L |
possibly damaging |
Het |
Tmem109 |
A |
C |
19: 10,849,124 (GRCm39) |
*244G |
probably null |
Het |
Tox2 |
A |
G |
2: 163,163,435 (GRCm39) |
Y136C |
|
Het |
Tubb1 |
T |
C |
2: 174,298,825 (GRCm39) |
V169A |
possibly damaging |
Het |
Ubr3 |
T |
C |
2: 69,783,886 (GRCm39) |
|
probably null |
Het |
Vmn1r225 |
T |
A |
17: 20,723,059 (GRCm39) |
F167I |
probably benign |
Het |
Vmn2r65 |
A |
C |
7: 84,595,569 (GRCm39) |
W372G |
probably damaging |
Het |
Vsnl1 |
G |
T |
12: 11,376,439 (GRCm39) |
Q149K |
probably benign |
Het |
Wdr35 |
A |
G |
12: 9,054,105 (GRCm39) |
N466S |
probably benign |
Het |
Ywhae |
T |
A |
11: 75,650,169 (GRCm39) |
S210R |
probably damaging |
Het |
Zfp28 |
T |
A |
7: 6,397,748 (GRCm39) |
S728T |
probably damaging |
Het |
Zfpm1 |
A |
G |
8: 123,063,698 (GRCm39) |
D919G |
unknown |
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 |
R1870:Vps13a
|
UTSW |
19 |
16,737,316 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|