Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700020N01Rik |
A |
G |
10: 21,593,438 (GRCm38) |
D17G |
probably damaging |
Het |
Abi3bp |
A |
G |
16: 56,532,953 (GRCm38) |
T82A |
possibly damaging |
Het |
Adgre4 |
A |
C |
17: 55,792,035 (GRCm38) |
E180D |
probably benign |
Het |
Ankrd28 |
G |
A |
14: 31,743,450 (GRCm38) |
|
probably benign |
Het |
Aoc3 |
A |
G |
11: 101,336,447 (GRCm38) |
D382G |
possibly damaging |
Het |
Apob |
C |
A |
12: 8,010,742 (GRCm38) |
R3075S |
probably benign |
Het |
Aqr |
A |
G |
2: 114,140,977 (GRCm38) |
F459S |
probably damaging |
Het |
Bcr |
T |
C |
10: 75,131,643 (GRCm38) |
W570R |
probably damaging |
Het |
Bloc1s5 |
C |
T |
13: 38,603,919 (GRCm38) |
R163K |
probably benign |
Het |
Bod1 |
A |
T |
11: 31,669,267 (GRCm38) |
N101K |
possibly damaging |
Het |
Bysl |
A |
T |
17: 47,602,471 (GRCm38) |
S296T |
probably benign |
Het |
Chl1 |
G |
A |
6: 103,708,542 (GRCm38) |
|
probably null |
Het |
Clstn1 |
G |
A |
4: 149,646,855 (GRCm38) |
A885T |
probably benign |
Het |
Cyp3a25 |
G |
T |
5: 145,998,546 (GRCm38) |
P87T |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,657,192 (GRCm38) |
V3633A |
probably damaging |
Het |
Elp4 |
C |
A |
2: 105,792,277 (GRCm38) |
C241F |
possibly damaging |
Het |
Fat4 |
T |
A |
3: 39,001,178 (GRCm38) |
F4182Y |
probably benign |
Het |
Gabbr2 |
G |
A |
4: 46,787,521 (GRCm38) |
H381Y |
possibly damaging |
Het |
Gm10577 |
G |
T |
4: 101,020,318 (GRCm38) |
|
probably benign |
Het |
Gm884 |
T |
C |
11: 103,616,888 (GRCm38) |
|
probably benign |
Het |
Gm9955 |
G |
T |
18: 24,709,257 (GRCm38) |
|
probably benign |
Het |
Gstm5 |
T |
A |
3: 107,897,319 (GRCm38) |
I73N |
probably damaging |
Het |
Gypa |
T |
A |
8: 80,496,702 (GRCm38) |
|
probably benign |
Het |
Hectd2 |
T |
A |
19: 36,569,431 (GRCm38) |
V64D |
probably damaging |
Het |
Igkv10-95 |
T |
A |
6: 68,680,559 (GRCm38) |
Y20N |
probably benign |
Het |
Il15 |
T |
C |
8: 82,337,559 (GRCm38) |
|
probably benign |
Het |
Iqca |
C |
A |
1: 90,142,731 (GRCm38) |
G133V |
probably null |
Het |
Kiz |
C |
A |
2: 146,856,058 (GRCm38) |
|
probably benign |
Het |
Lcmt2 |
C |
A |
2: 121,139,240 (GRCm38) |
S234I |
probably benign |
Het |
Lilra5 |
A |
G |
7: 4,241,957 (GRCm38) |
|
probably benign |
Het |
Lin37 |
T |
C |
7: 30,555,874 (GRCm38) |
E187G |
probably damaging |
Het |
Mcmdc2 |
T |
A |
1: 9,911,814 (GRCm38) |
|
probably null |
Het |
Mctp1 |
T |
C |
13: 76,825,799 (GRCm38) |
|
probably null |
Het |
Mdp1 |
C |
A |
14: 55,659,269 (GRCm38) |
G112* |
probably null |
Het |
Mmp15 |
T |
C |
8: 95,372,134 (GRCm38) |
Y530H |
possibly damaging |
Het |
Mtss1l |
T |
C |
8: 110,727,397 (GRCm38) |
|
probably null |
Het |
Muc5ac |
T |
C |
7: 141,807,709 (GRCm38) |
S1586P |
probably benign |
Het |
Nap1l5 |
A |
T |
6: 58,906,772 (GRCm38) |
C66S |
possibly damaging |
Het |
Ninl |
G |
T |
2: 150,939,855 (GRCm38) |
Q1237K |
possibly damaging |
Het |
Olfr1160 |
T |
C |
2: 88,006,418 (GRCm38) |
E111G |
probably damaging |
Het |
Olfr495 |
A |
T |
7: 108,395,263 (GRCm38) |
T48S |
possibly damaging |
Het |
Orc6 |
T |
G |
8: 85,301,154 (GRCm38) |
S37R |
possibly damaging |
Het |
Papss1 |
A |
C |
3: 131,583,093 (GRCm38) |
N119H |
possibly damaging |
Het |
Phf13 |
A |
T |
4: 151,991,612 (GRCm38) |
F278I |
probably damaging |
Het |
Pole2 |
C |
A |
12: 69,211,413 (GRCm38) |
A239S |
probably damaging |
Het |
Ppt2 |
T |
C |
17: 34,626,572 (GRCm38) |
D75G |
probably damaging |
Het |
Psd2 |
A |
G |
18: 36,002,991 (GRCm38) |
D443G |
possibly damaging |
Het |
Psen1 |
C |
A |
12: 83,714,820 (GRCm38) |
S132* |
probably null |
Het |
Psme4 |
A |
G |
11: 30,878,415 (GRCm38) |
T1812A |
probably damaging |
Het |
Rasgrf1 |
T |
C |
9: 89,915,482 (GRCm38) |
|
probably benign |
Het |
Reep3 |
A |
G |
10: 67,021,739 (GRCm38) |
|
probably benign |
Het |
Rexo4 |
A |
T |
2: 26,958,574 (GRCm38) |
|
probably benign |
Het |
Rnf6 |
A |
C |
5: 146,211,658 (GRCm38) |
S183R |
probably damaging |
Het |
Scai |
A |
T |
2: 39,103,737 (GRCm38) |
M297K |
probably damaging |
Het |
Scn9a |
A |
T |
2: 66,483,499 (GRCm38) |
S1947R |
probably benign |
Het |
Sema6c |
T |
C |
3: 95,172,710 (GRCm38) |
C772R |
possibly damaging |
Het |
Skint7 |
T |
C |
4: 111,980,345 (GRCm38) |
S107P |
possibly damaging |
Het |
Slc24a3 |
A |
G |
2: 145,606,795 (GRCm38) |
N420D |
probably benign |
Het |
Smc1b |
T |
C |
15: 85,070,820 (GRCm38) |
D1077G |
possibly damaging |
Het |
Smg7 |
G |
A |
1: 152,866,648 (GRCm38) |
P82L |
probably damaging |
Het |
Sp3 |
A |
C |
2: 72,970,998 (GRCm38) |
F268V |
probably damaging |
Het |
Srms |
T |
C |
2: 181,212,633 (GRCm38) |
D47G |
probably benign |
Het |
Ss18 |
A |
C |
18: 14,651,181 (GRCm38) |
M150R |
probably damaging |
Het |
Taf5 |
G |
A |
19: 47,074,854 (GRCm38) |
R281Q |
probably benign |
Het |
Tars |
T |
C |
15: 11,385,173 (GRCm38) |
K644R |
probably benign |
Het |
Tctex1d1 |
T |
C |
4: 103,002,538 (GRCm38) |
Y96H |
probably damaging |
Het |
Tinag |
C |
A |
9: 76,952,003 (GRCm38) |
W441L |
probably damaging |
Het |
Tmtc1 |
T |
C |
6: 148,411,240 (GRCm38) |
S244G |
probably benign |
Het |
Tpr |
T |
C |
1: 150,433,725 (GRCm38) |
V1670A |
possibly damaging |
Het |
Trpv3 |
A |
G |
11: 73,296,814 (GRCm38) |
|
probably benign |
Het |
Uhrf1 |
G |
T |
17: 56,310,742 (GRCm38) |
V155L |
probably damaging |
Het |
Ush2a |
G |
A |
1: 188,400,278 (GRCm38) |
C899Y |
probably damaging |
Het |
Vmn2r115 |
G |
A |
17: 23,359,275 (GRCm38) |
R574H |
probably benign |
Het |
Vmn2r63 |
T |
C |
7: 42,928,010 (GRCm38) |
D368G |
probably benign |
Het |
Wbp11 |
A |
G |
6: 136,814,638 (GRCm38) |
|
probably benign |
Het |
Zcwpw1 |
A |
G |
5: 137,799,592 (GRCm38) |
D145G |
probably benign |
Het |
Zfp607a |
G |
A |
7: 27,878,476 (GRCm38) |
V324I |
probably damaging |
Het |
Zfp618 |
A |
G |
4: 63,133,774 (GRCm38) |
I931V |
probably benign |
Het |
Zfp821 |
T |
C |
8: 109,724,542 (GRCm38) |
V389A |
possibly damaging |
Het |
Zfp976 |
T |
A |
7: 42,613,717 (GRCm38) |
H232L |
probably damaging |
Het |
|
Other mutations in Vps13a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00465:Vps13a
|
APN |
19 |
16,752,175 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL00537:Vps13a
|
APN |
19 |
16,680,045 (GRCm38) |
missense |
probably benign |
0.03 |
IGL00562:Vps13a
|
APN |
19 |
16,734,714 (GRCm38) |
critical splice donor site |
probably null |
|
IGL00563:Vps13a
|
APN |
19 |
16,734,714 (GRCm38) |
critical splice donor site |
probably null |
|
IGL00579:Vps13a
|
APN |
19 |
16,707,362 (GRCm38) |
missense |
probably benign |
0.29 |
IGL00662:Vps13a
|
APN |
19 |
16,704,540 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL00667:Vps13a
|
APN |
19 |
16,759,676 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01102:Vps13a
|
APN |
19 |
16,651,417 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01139:Vps13a
|
APN |
19 |
16,640,625 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01142:Vps13a
|
APN |
19 |
16,687,115 (GRCm38) |
missense |
possibly damaging |
0.86 |
IGL01361:Vps13a
|
APN |
19 |
16,743,007 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01386:Vps13a
|
APN |
19 |
16,701,152 (GRCm38) |
missense |
possibly damaging |
0.87 |
IGL01593:Vps13a
|
APN |
19 |
16,762,181 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01700:Vps13a
|
APN |
19 |
16,744,857 (GRCm38) |
nonsense |
probably null |
|
IGL01767:Vps13a
|
APN |
19 |
16,663,894 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01782:Vps13a
|
APN |
19 |
16,754,337 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01808:Vps13a
|
APN |
19 |
16,710,286 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01812:Vps13a
|
APN |
19 |
16,715,060 (GRCm38) |
missense |
probably benign |
|
IGL01829:Vps13a
|
APN |
19 |
16,619,443 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01893:Vps13a
|
APN |
19 |
16,663,775 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02222:Vps13a
|
APN |
19 |
16,682,175 (GRCm38) |
missense |
probably benign |
0.06 |
IGL02295:Vps13a
|
APN |
19 |
16,715,042 (GRCm38) |
splice site |
probably benign |
|
IGL02465:Vps13a
|
APN |
19 |
16,710,941 (GRCm38) |
missense |
probably benign |
0.11 |
IGL02492:Vps13a
|
APN |
19 |
16,647,637 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02581:Vps13a
|
APN |
19 |
16,655,322 (GRCm38) |
missense |
probably benign |
0.41 |
IGL02633:Vps13a
|
APN |
19 |
16,720,408 (GRCm38) |
missense |
possibly damaging |
0.82 |
IGL02641:Vps13a
|
APN |
19 |
16,698,821 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02659:Vps13a
|
APN |
19 |
16,652,699 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02827:Vps13a
|
APN |
19 |
16,641,634 (GRCm38) |
missense |
possibly damaging |
0.91 |
IGL02943:Vps13a
|
APN |
19 |
16,663,886 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03057:Vps13a
|
APN |
19 |
16,668,694 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03077:Vps13a
|
APN |
19 |
16,710,882 (GRCm38) |
missense |
probably benign |
|
IGL03184:Vps13a
|
APN |
19 |
16,654,370 (GRCm38) |
missense |
probably benign |
0.00 |
eggs
|
UTSW |
19 |
16,701,165 (GRCm38) |
missense |
probably damaging |
1.00 |
excambio
|
UTSW |
19 |
16,745,947 (GRCm38) |
splice site |
probably null |
|
Faster
|
UTSW |
19 |
16,619,485 (GRCm38) |
missense |
probably damaging |
1.00 |
Ham
|
UTSW |
19 |
16,677,969 (GRCm38) |
missense |
probably benign |
0.08 |
interchange
|
UTSW |
19 |
16,668,690 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4377001:Vps13a
|
UTSW |
19 |
16,740,901 (GRCm38) |
missense |
probably damaging |
1.00 |
R0045:Vps13a
|
UTSW |
19 |
16,640,810 (GRCm38) |
nonsense |
probably null |
|
R0045:Vps13a
|
UTSW |
19 |
16,640,810 (GRCm38) |
nonsense |
probably null |
|
R0048:Vps13a
|
UTSW |
19 |
16,676,140 (GRCm38) |
missense |
probably damaging |
1.00 |
R0062:Vps13a
|
UTSW |
19 |
16,668,690 (GRCm38) |
missense |
probably damaging |
1.00 |
R0062:Vps13a
|
UTSW |
19 |
16,668,690 (GRCm38) |
missense |
probably damaging |
1.00 |
R0107:Vps13a
|
UTSW |
19 |
16,691,824 (GRCm38) |
missense |
probably benign |
0.03 |
R0135:Vps13a
|
UTSW |
19 |
16,780,765 (GRCm38) |
missense |
probably damaging |
1.00 |
R0138:Vps13a
|
UTSW |
19 |
16,660,499 (GRCm38) |
missense |
possibly damaging |
0.95 |
R0346:Vps13a
|
UTSW |
19 |
16,677,969 (GRCm38) |
missense |
probably benign |
0.08 |
R0359:Vps13a
|
UTSW |
19 |
16,641,577 (GRCm38) |
missense |
probably damaging |
0.99 |
R0530:Vps13a
|
UTSW |
19 |
16,655,206 (GRCm38) |
splice site |
probably benign |
|
R0541:Vps13a
|
UTSW |
19 |
16,704,577 (GRCm38) |
missense |
probably benign |
0.00 |
R0614:Vps13a
|
UTSW |
19 |
16,652,694 (GRCm38) |
missense |
probably damaging |
1.00 |
R0801:Vps13a
|
UTSW |
19 |
16,686,656 (GRCm38) |
splice site |
probably benign |
|
R0835:Vps13a
|
UTSW |
19 |
16,734,882 (GRCm38) |
splice site |
probably null |
|
R0848:Vps13a
|
UTSW |
19 |
16,698,897 (GRCm38) |
missense |
probably damaging |
1.00 |
R1114:Vps13a
|
UTSW |
19 |
16,750,151 (GRCm38) |
missense |
probably benign |
0.41 |
R1205:Vps13a
|
UTSW |
19 |
16,640,541 (GRCm38) |
missense |
probably damaging |
1.00 |
R1365:Vps13a
|
UTSW |
19 |
16,619,446 (GRCm38) |
missense |
probably damaging |
1.00 |
R1445:Vps13a
|
UTSW |
19 |
16,701,238 (GRCm38) |
nonsense |
probably null |
|
R1451:Vps13a
|
UTSW |
19 |
16,710,864 (GRCm38) |
missense |
probably benign |
0.01 |
R1479:Vps13a
|
UTSW |
19 |
16,750,114 (GRCm38) |
splice site |
probably benign |
|
R1533:Vps13a
|
UTSW |
19 |
16,701,130 (GRCm38) |
nonsense |
probably null |
|
R1600:Vps13a
|
UTSW |
19 |
16,666,272 (GRCm38) |
missense |
probably benign |
0.01 |
R1870:Vps13a
|
UTSW |
19 |
16,759,952 (GRCm38) |
missense |
probably damaging |
1.00 |
R1871:Vps13a
|
UTSW |
19 |
16,664,664 (GRCm38) |
missense |
probably benign |
0.01 |
R1959:Vps13a
|
UTSW |
19 |
16,677,938 (GRCm38) |
missense |
possibly damaging |
0.49 |
R1960:Vps13a
|
UTSW |
19 |
16,725,631 (GRCm38) |
missense |
probably damaging |
1.00 |
R1993:Vps13a
|
UTSW |
19 |
16,722,458 (GRCm38) |
missense |
probably benign |
0.07 |
R2257:Vps13a
|
UTSW |
19 |
16,682,174 (GRCm38) |
missense |
possibly damaging |
0.85 |
R2276:Vps13a
|
UTSW |
19 |
16,710,426 (GRCm38) |
missense |
possibly damaging |
0.47 |
R2326:Vps13a
|
UTSW |
19 |
16,743,057 (GRCm38) |
missense |
possibly damaging |
0.71 |
R2338:Vps13a
|
UTSW |
19 |
16,720,453 (GRCm38) |
missense |
probably damaging |
1.00 |
R2359:Vps13a
|
UTSW |
19 |
16,652,679 (GRCm38) |
splice site |
probably benign |
|
R2421:Vps13a
|
UTSW |
19 |
16,759,671 (GRCm38) |
missense |
probably benign |
|
R2847:Vps13a
|
UTSW |
19 |
16,703,599 (GRCm38) |
missense |
probably damaging |
0.98 |
R3081:Vps13a
|
UTSW |
19 |
16,664,737 (GRCm38) |
missense |
probably benign |
0.02 |
R3522:Vps13a
|
UTSW |
19 |
16,766,493 (GRCm38) |
splice site |
probably benign |
|
R3613:Vps13a
|
UTSW |
19 |
16,685,402 (GRCm38) |
missense |
probably damaging |
1.00 |
R3797:Vps13a
|
UTSW |
19 |
16,745,947 (GRCm38) |
splice site |
probably null |
|
R3874:Vps13a
|
UTSW |
19 |
16,744,953 (GRCm38) |
missense |
probably benign |
0.01 |
R4032:Vps13a
|
UTSW |
19 |
16,616,899 (GRCm38) |
missense |
probably damaging |
1.00 |
R4111:Vps13a
|
UTSW |
19 |
16,640,628 (GRCm38) |
missense |
probably damaging |
1.00 |
R4383:Vps13a
|
UTSW |
19 |
16,701,165 (GRCm38) |
missense |
probably damaging |
1.00 |
R4504:Vps13a
|
UTSW |
19 |
16,695,502 (GRCm38) |
missense |
possibly damaging |
0.93 |
R4578:Vps13a
|
UTSW |
19 |
16,682,110 (GRCm38) |
missense |
probably damaging |
0.98 |
R4587:Vps13a
|
UTSW |
19 |
16,640,039 (GRCm38) |
missense |
probably damaging |
1.00 |
R4588:Vps13a
|
UTSW |
19 |
16,640,039 (GRCm38) |
missense |
probably damaging |
1.00 |
R4605:Vps13a
|
UTSW |
19 |
16,640,039 (GRCm38) |
missense |
probably damaging |
1.00 |
R4714:Vps13a
|
UTSW |
19 |
16,749,856 (GRCm38) |
missense |
probably benign |
0.01 |
R4756:Vps13a
|
UTSW |
19 |
16,655,216 (GRCm38) |
missense |
probably benign |
0.01 |
R4831:Vps13a
|
UTSW |
19 |
16,677,992 (GRCm38) |
missense |
probably benign |
0.04 |
R5068:Vps13a
|
UTSW |
19 |
16,746,058 (GRCm38) |
missense |
probably benign |
0.01 |
R5070:Vps13a
|
UTSW |
19 |
16,654,484 (GRCm38) |
missense |
probably benign |
|
R5082:Vps13a
|
UTSW |
19 |
16,744,893 (GRCm38) |
missense |
probably damaging |
1.00 |
R5182:Vps13a
|
UTSW |
19 |
16,695,499 (GRCm38) |
missense |
possibly damaging |
0.81 |
R5189:Vps13a
|
UTSW |
19 |
16,685,315 (GRCm38) |
missense |
probably damaging |
1.00 |
R5283:Vps13a
|
UTSW |
19 |
16,677,970 (GRCm38) |
missense |
probably damaging |
0.96 |
R5294:Vps13a
|
UTSW |
19 |
16,641,667 (GRCm38) |
missense |
probably damaging |
1.00 |
R5304:Vps13a
|
UTSW |
19 |
16,710,387 (GRCm38) |
missense |
possibly damaging |
0.78 |
R5554:Vps13a
|
UTSW |
19 |
16,722,411 (GRCm38) |
missense |
probably damaging |
1.00 |
R5592:Vps13a
|
UTSW |
19 |
16,725,571 (GRCm38) |
missense |
probably damaging |
1.00 |
R5611:Vps13a
|
UTSW |
19 |
16,725,572 (GRCm38) |
missense |
probably damaging |
1.00 |
R5665:Vps13a
|
UTSW |
19 |
16,668,690 (GRCm38) |
missense |
probably damaging |
1.00 |
R5671:Vps13a
|
UTSW |
19 |
16,715,100 (GRCm38) |
missense |
probably benign |
0.03 |
R5684:Vps13a
|
UTSW |
19 |
16,699,045 (GRCm38) |
missense |
probably benign |
0.00 |
R5767:Vps13a
|
UTSW |
19 |
16,664,564 (GRCm38) |
missense |
probably damaging |
1.00 |
R5810:Vps13a
|
UTSW |
19 |
16,666,324 (GRCm38) |
missense |
probably benign |
0.00 |
R5866:Vps13a
|
UTSW |
19 |
16,680,023 (GRCm38) |
missense |
probably benign |
0.04 |
R5886:Vps13a
|
UTSW |
19 |
16,664,562 (GRCm38) |
missense |
probably benign |
0.01 |
R5933:Vps13a
|
UTSW |
19 |
16,660,530 (GRCm38) |
missense |
probably benign |
0.34 |
R5965:Vps13a
|
UTSW |
19 |
16,619,028 (GRCm38) |
splice site |
probably null |
|
R6259:Vps13a
|
UTSW |
19 |
16,687,170 (GRCm38) |
nonsense |
probably null |
|
R6346:Vps13a
|
UTSW |
19 |
16,682,214 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6459:Vps13a
|
UTSW |
19 |
16,664,018 (GRCm38) |
missense |
possibly damaging |
0.56 |
R6485:Vps13a
|
UTSW |
19 |
16,680,050 (GRCm38) |
missense |
probably damaging |
0.99 |
R6520:Vps13a
|
UTSW |
19 |
16,725,579 (GRCm38) |
missense |
probably damaging |
1.00 |
R6644:Vps13a
|
UTSW |
19 |
16,744,919 (GRCm38) |
missense |
possibly damaging |
0.90 |
R6932:Vps13a
|
UTSW |
19 |
16,678,075 (GRCm38) |
missense |
probably benign |
0.01 |
R6934:Vps13a
|
UTSW |
19 |
16,676,194 (GRCm38) |
missense |
probably damaging |
1.00 |
R6951:Vps13a
|
UTSW |
19 |
16,723,740 (GRCm38) |
missense |
probably benign |
0.00 |
R7027:Vps13a
|
UTSW |
19 |
16,664,664 (GRCm38) |
missense |
probably benign |
0.01 |
R7126:Vps13a
|
UTSW |
19 |
16,710,879 (GRCm38) |
missense |
probably benign |
|
R7206:Vps13a
|
UTSW |
19 |
16,754,298 (GRCm38) |
missense |
probably damaging |
1.00 |
R7248:Vps13a
|
UTSW |
19 |
16,678,042 (GRCm38) |
missense |
probably benign |
0.25 |
R7252:Vps13a
|
UTSW |
19 |
16,661,064 (GRCm38) |
missense |
probably benign |
0.00 |
R7255:Vps13a
|
UTSW |
19 |
16,654,339 (GRCm38) |
critical splice donor site |
probably null |
|
R7382:Vps13a
|
UTSW |
19 |
16,619,485 (GRCm38) |
missense |
probably damaging |
1.00 |
R7422:Vps13a
|
UTSW |
19 |
16,750,173 (GRCm38) |
missense |
probably damaging |
1.00 |
R7425:Vps13a
|
UTSW |
19 |
16,723,702 (GRCm38) |
missense |
probably benign |
0.13 |
R7523:Vps13a
|
UTSW |
19 |
16,703,789 (GRCm38) |
missense |
probably benign |
|
R7586:Vps13a
|
UTSW |
19 |
16,647,598 (GRCm38) |
missense |
probably benign |
0.08 |
R7587:Vps13a
|
UTSW |
19 |
16,703,789 (GRCm38) |
missense |
probably benign |
0.00 |
R7593:Vps13a
|
UTSW |
19 |
16,725,663 (GRCm38) |
missense |
probably damaging |
1.00 |
R7637:Vps13a
|
UTSW |
19 |
16,750,149 (GRCm38) |
missense |
probably benign |
0.02 |
R7763:Vps13a
|
UTSW |
19 |
16,746,000 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7813:Vps13a
|
UTSW |
19 |
16,651,456 (GRCm38) |
missense |
possibly damaging |
0.81 |
R7815:Vps13a
|
UTSW |
19 |
16,725,572 (GRCm38) |
missense |
probably damaging |
1.00 |
R7861:Vps13a
|
UTSW |
19 |
16,655,304 (GRCm38) |
missense |
probably damaging |
1.00 |
R7909:Vps13a
|
UTSW |
19 |
16,720,430 (GRCm38) |
nonsense |
probably null |
|
R7939:Vps13a
|
UTSW |
19 |
16,740,791 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8108:Vps13a
|
UTSW |
19 |
16,640,787 (GRCm38) |
missense |
probably damaging |
1.00 |
R8123:Vps13a
|
UTSW |
19 |
16,647,702 (GRCm38) |
missense |
probably benign |
0.01 |
R8134:Vps13a
|
UTSW |
19 |
16,654,354 (GRCm38) |
missense |
possibly damaging |
0.71 |
R8168:Vps13a
|
UTSW |
19 |
16,749,548 (GRCm38) |
missense |
probably benign |
0.09 |
R8272:Vps13a
|
UTSW |
19 |
16,749,845 (GRCm38) |
critical splice donor site |
probably null |
|
R8293:Vps13a
|
UTSW |
19 |
16,668,605 (GRCm38) |
missense |
possibly damaging |
0.81 |
R8303:Vps13a
|
UTSW |
19 |
16,616,906 (GRCm38) |
missense |
probably benign |
0.00 |
R8383:Vps13a
|
UTSW |
19 |
16,723,705 (GRCm38) |
missense |
possibly damaging |
0.83 |
R8386:Vps13a
|
UTSW |
19 |
16,701,119 (GRCm38) |
critical splice donor site |
probably null |
|
R8433:Vps13a
|
UTSW |
19 |
16,741,236 (GRCm38) |
missense |
possibly damaging |
0.56 |
R8436:Vps13a
|
UTSW |
19 |
16,740,793 (GRCm38) |
missense |
probably benign |
0.10 |
R8450:Vps13a
|
UTSW |
19 |
16,654,507 (GRCm38) |
splice site |
probably null |
|
R8476:Vps13a
|
UTSW |
19 |
16,722,457 (GRCm38) |
missense |
possibly damaging |
0.60 |
R8501:Vps13a
|
UTSW |
19 |
16,682,120 (GRCm38) |
missense |
probably benign |
0.39 |
R8552:Vps13a
|
UTSW |
19 |
16,754,320 (GRCm38) |
missense |
probably damaging |
0.99 |
R8680:Vps13a
|
UTSW |
19 |
16,645,906 (GRCm38) |
missense |
possibly damaging |
0.84 |
R8784:Vps13a
|
UTSW |
19 |
16,664,789 (GRCm38) |
missense |
probably damaging |
1.00 |
R8871:Vps13a
|
UTSW |
19 |
16,663,822 (GRCm38) |
missense |
probably damaging |
1.00 |
R8945:Vps13a
|
UTSW |
19 |
16,664,750 (GRCm38) |
missense |
probably damaging |
1.00 |
R8948:Vps13a
|
UTSW |
19 |
16,745,976 (GRCm38) |
missense |
probably damaging |
0.99 |
R8950:Vps13a
|
UTSW |
19 |
16,745,976 (GRCm38) |
missense |
probably damaging |
0.99 |
R8960:Vps13a
|
UTSW |
19 |
16,705,883 (GRCm38) |
missense |
possibly damaging |
0.67 |
R9189:Vps13a
|
UTSW |
19 |
16,686,597 (GRCm38) |
missense |
probably benign |
|
R9366:Vps13a
|
UTSW |
19 |
16,695,530 (GRCm38) |
missense |
probably damaging |
1.00 |
R9505:Vps13a
|
UTSW |
19 |
16,742,544 (GRCm38) |
missense |
possibly damaging |
0.94 |
R9601:Vps13a
|
UTSW |
19 |
16,645,973 (GRCm38) |
missense |
possibly damaging |
0.84 |
R9735:Vps13a
|
UTSW |
19 |
16,723,747 (GRCm38) |
missense |
probably damaging |
1.00 |
R9776:Vps13a
|
UTSW |
19 |
16,759,594 (GRCm38) |
missense |
probably benign |
|
R9796:Vps13a
|
UTSW |
19 |
16,654,464 (GRCm38) |
missense |
probably benign |
0.01 |
X0061:Vps13a
|
UTSW |
19 |
16,645,868 (GRCm38) |
missense |
probably benign |
0.40 |
X0066:Vps13a
|
UTSW |
19 |
16,742,553 (GRCm38) |
missense |
probably benign |
0.33 |
Z1177:Vps13a
|
UTSW |
19 |
16,699,113 (GRCm38) |
critical splice acceptor site |
probably null |
|
Z31818:Vps13a
|
UTSW |
19 |
16,780,754 (GRCm38) |
missense |
possibly damaging |
0.94 |
|