Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810408A11Rik |
C |
T |
11: 69,791,403 (GRCm39) |
V59I |
possibly damaging |
Het |
4930544M13Rik |
T |
G |
13: 114,744,183 (GRCm39) |
|
noncoding transcript |
Het |
Abca13 |
A |
T |
11: 9,492,077 (GRCm39) |
K4373* |
probably null |
Het |
Abtb2 |
A |
T |
2: 103,513,820 (GRCm39) |
T410S |
probably benign |
Het |
Adamts13 |
T |
C |
2: 26,873,142 (GRCm39) |
|
probably null |
Het |
Ahnak2 |
C |
G |
12: 112,742,183 (GRCm39) |
D630H |
probably damaging |
Het |
Aox3 |
T |
C |
1: 58,191,725 (GRCm39) |
S426P |
probably damaging |
Het |
Atxn10 |
C |
T |
15: 85,271,260 (GRCm39) |
S266F |
probably benign |
Het |
B4galnt4 |
G |
T |
7: 140,647,634 (GRCm39) |
M407I |
probably damaging |
Het |
B4galnt4 |
T |
A |
7: 140,644,470 (GRCm39) |
|
probably null |
Het |
Bclaf1 |
T |
A |
10: 20,197,872 (GRCm39) |
|
probably benign |
Het |
C4b |
C |
T |
17: 34,955,864 (GRCm39) |
|
probably null |
Het |
Cdc42bpg |
T |
C |
19: 6,361,365 (GRCm39) |
F297S |
probably damaging |
Het |
Cdh10 |
A |
T |
15: 19,013,664 (GRCm39) |
T755S |
probably benign |
Het |
Ceacam12 |
T |
A |
7: 17,811,305 (GRCm39) |
|
probably null |
Het |
Cfap65 |
C |
A |
1: 74,956,454 (GRCm39) |
V1042F |
possibly damaging |
Het |
Cfap77 |
T |
C |
2: 28,875,844 (GRCm39) |
I89V |
probably benign |
Het |
Cfh |
T |
C |
1: 140,014,125 (GRCm39) |
D688G |
probably benign |
Het |
Clip1 |
C |
G |
5: 123,721,664 (GRCm39) |
A1182P |
probably damaging |
Het |
Cyp2b10 |
T |
A |
7: 25,614,921 (GRCm39) |
Y309* |
probably null |
Het |
Dcaf5 |
T |
C |
12: 80,385,858 (GRCm39) |
E756G |
probably benign |
Het |
Dctn1 |
A |
T |
6: 83,176,753 (GRCm39) |
Q1231L |
possibly damaging |
Het |
Dennd1c |
T |
A |
17: 57,373,428 (GRCm39) |
R682* |
probably null |
Het |
Eml6 |
C |
A |
11: 29,727,052 (GRCm39) |
E1319* |
probably null |
Het |
Erap1 |
T |
C |
13: 74,838,766 (GRCm39) |
I904T |
probably damaging |
Het |
Eri1 |
A |
T |
8: 35,943,673 (GRCm39) |
I207N |
possibly damaging |
Het |
Farp1 |
G |
A |
14: 121,514,469 (GRCm39) |
A933T |
probably damaging |
Het |
Fcna |
T |
A |
2: 25,515,353 (GRCm39) |
Q210L |
probably benign |
Het |
Fhad1 |
A |
T |
4: 141,643,378 (GRCm39) |
|
probably null |
Het |
Fut8 |
T |
G |
12: 77,440,603 (GRCm39) |
Y197D |
probably damaging |
Het |
Garem1 |
G |
A |
18: 21,262,825 (GRCm39) |
T663I |
probably benign |
Het |
Gfm2 |
T |
C |
13: 97,301,546 (GRCm39) |
S450P |
probably damaging |
Het |
Gstk1 |
T |
G |
6: 42,222,938 (GRCm39) |
|
probably benign |
Het |
Helz2 |
C |
T |
2: 180,879,210 (GRCm39) |
A803T |
probably damaging |
Het |
Igsf9 |
T |
A |
1: 172,319,455 (GRCm39) |
I280N |
probably damaging |
Het |
Klhl10 |
A |
G |
11: 100,336,669 (GRCm39) |
K219E |
probably benign |
Het |
L3mbtl4 |
T |
A |
17: 68,768,558 (GRCm39) |
V222D |
probably damaging |
Het |
Lrrc9 |
A |
T |
12: 72,546,453 (GRCm39) |
N1214Y |
probably damaging |
Het |
Ltbp2 |
C |
T |
12: 84,840,414 (GRCm39) |
E1051K |
possibly damaging |
Het |
Mettl17 |
T |
C |
14: 52,122,440 (GRCm39) |
F13S |
probably benign |
Het |
Mettl24 |
C |
A |
10: 40,559,413 (GRCm39) |
A21D |
possibly damaging |
Het |
Mfsd6l |
T |
A |
11: 68,447,331 (GRCm39) |
C61S |
probably benign |
Het |
Mob4 |
T |
G |
1: 55,191,899 (GRCm39) |
D204E |
probably benign |
Het |
Mtus1 |
C |
G |
8: 41,536,189 (GRCm39) |
R509T |
probably damaging |
Het |
Nlrp4a |
T |
A |
7: 26,149,844 (GRCm39) |
F484I |
possibly damaging |
Het |
Nsrp1 |
T |
C |
11: 76,941,444 (GRCm39) |
N88S |
probably benign |
Het |
Odad2 |
G |
T |
18: 7,222,564 (GRCm39) |
H568Q |
possibly damaging |
Het |
Or10d5 |
C |
T |
9: 39,861,408 (GRCm39) |
V220I |
probably benign |
Het |
Or2g25 |
T |
A |
17: 37,970,969 (GRCm39) |
H85L |
probably benign |
Het |
Or51b6b |
T |
C |
7: 103,309,678 (GRCm39) |
T260A |
probably benign |
Het |
Or6c2 |
T |
A |
10: 129,362,449 (GRCm39) |
Y118N |
probably damaging |
Het |
Parg |
A |
G |
14: 31,924,408 (GRCm39) |
N69S |
probably benign |
Het |
Pcdh9 |
A |
C |
14: 94,125,377 (GRCm39) |
N264K |
probably damaging |
Het |
Pcdhb22 |
G |
T |
18: 37,653,615 (GRCm39) |
L694F |
probably damaging |
Het |
Pcnt |
T |
C |
10: 76,248,335 (GRCm39) |
E928G |
probably damaging |
Het |
Pdzk1 |
G |
A |
3: 96,775,751 (GRCm39) |
G373D |
probably benign |
Het |
Pea15a |
A |
G |
1: 172,026,740 (GRCm39) |
I89T |
probably damaging |
Het |
Phc1 |
T |
A |
6: 122,313,964 (GRCm39) |
|
probably benign |
Het |
Pikfyve |
T |
A |
1: 65,235,900 (GRCm39) |
C191S |
probably damaging |
Het |
Pitpnm1 |
T |
A |
19: 4,158,130 (GRCm39) |
D573E |
probably damaging |
Het |
Pld5 |
A |
G |
1: 176,102,450 (GRCm39) |
|
probably benign |
Het |
Plscr2 |
A |
T |
9: 92,173,130 (GRCm39) |
N89I |
possibly damaging |
Het |
Pm20d2 |
A |
C |
4: 33,179,293 (GRCm39) |
N315K |
probably damaging |
Het |
Pnpla1 |
T |
A |
17: 29,097,518 (GRCm39) |
M228K |
probably benign |
Het |
Prim2 |
T |
C |
1: 33,709,217 (GRCm39) |
|
probably benign |
Het |
Ralgapa2 |
A |
G |
2: 146,246,987 (GRCm39) |
|
probably benign |
Het |
Rgs22 |
G |
T |
15: 36,050,294 (GRCm39) |
H719N |
probably benign |
Het |
Ror2 |
C |
T |
13: 53,272,880 (GRCm39) |
D250N |
probably damaging |
Het |
Saal1 |
A |
G |
7: 46,349,071 (GRCm39) |
V281A |
probably benign |
Het |
Selenof |
A |
T |
3: 144,296,411 (GRCm39) |
K94N |
probably damaging |
Het |
Slamf9 |
T |
A |
1: 172,304,831 (GRCm39) |
C148* |
probably null |
Het |
Slc4a7 |
T |
C |
14: 14,772,699 (GRCm38) |
|
probably null |
Het |
Slco1a5 |
A |
G |
6: 142,180,431 (GRCm39) |
I657T |
probably benign |
Het |
St3gal2 |
A |
T |
8: 111,684,480 (GRCm39) |
H46L |
probably benign |
Het |
Sucnr1 |
T |
G |
3: 59,994,069 (GRCm39) |
M199R |
probably damaging |
Het |
Taok1 |
T |
A |
11: 77,444,500 (GRCm39) |
E525V |
probably null |
Het |
Tbc1d10c |
T |
A |
19: 4,235,445 (GRCm39) |
E298V |
probably damaging |
Het |
Tll2 |
T |
A |
19: 41,118,951 (GRCm39) |
H259L |
probably damaging |
Het |
Tpcn1 |
A |
T |
5: 120,691,554 (GRCm39) |
F300Y |
probably damaging |
Het |
Uba6 |
T |
A |
5: 86,279,197 (GRCm39) |
I642L |
probably benign |
Het |
Ubqln5 |
T |
A |
7: 103,778,829 (GRCm39) |
|
probably benign |
Het |
Vmn1r27 |
A |
T |
6: 58,192,827 (GRCm39) |
L9Q |
possibly damaging |
Het |
Vmn2r100 |
C |
T |
17: 19,741,672 (GRCm39) |
T128I |
probably benign |
Het |
Vmn2r109 |
C |
T |
17: 20,761,494 (GRCm39) |
G621D |
probably benign |
Het |
Vmn2r49 |
C |
T |
7: 9,720,352 (GRCm39) |
D380N |
probably benign |
Het |
Wbp2 |
G |
T |
11: 115,971,463 (GRCm39) |
Y147* |
probably null |
Het |
Wdr46 |
T |
A |
17: 34,160,810 (GRCm39) |
N191K |
probably benign |
Het |
Wdr46 |
T |
C |
17: 34,168,373 (GRCm39) |
|
probably benign |
Het |
Wnt2 |
A |
C |
6: 18,023,285 (GRCm39) |
F121L |
probably benign |
Het |
Xpnpep1 |
T |
A |
19: 53,003,053 (GRCm39) |
D100V |
probably benign |
Het |
Xpo4 |
T |
C |
14: 57,827,559 (GRCm39) |
Y879C |
probably damaging |
Het |
Zswim4 |
A |
T |
8: 84,938,948 (GRCm39) |
V978D |
probably damaging |
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 |
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 |
|