Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
G |
5: 8,871,322 (GRCm39) |
I292S |
possibly damaging |
Het |
Abcc4 |
T |
C |
14: 118,763,694 (GRCm39) |
N1047S |
probably benign |
Het |
Abcc8 |
G |
T |
7: 45,766,847 (GRCm39) |
|
probably null |
Het |
Akap9 |
T |
A |
5: 4,088,520 (GRCm39) |
|
probably null |
Het |
Alox5 |
T |
A |
6: 116,392,424 (GRCm39) |
I366F |
probably damaging |
Het |
Amn |
A |
G |
12: 111,242,526 (GRCm39) |
N447S |
probably damaging |
Het |
Ankrd22 |
A |
T |
19: 34,143,174 (GRCm39) |
M1K |
probably null |
Het |
Asic1 |
G |
T |
15: 99,569,765 (GRCm39) |
G29C |
probably damaging |
Het |
Atxn7l1 |
A |
G |
12: 33,395,976 (GRCm39) |
N235S |
probably benign |
Het |
AY358078 |
T |
A |
14: 52,063,519 (GRCm39) |
D388E |
probably damaging |
Het |
Bod1l |
A |
G |
5: 41,974,679 (GRCm39) |
S2212P |
probably damaging |
Het |
Cacna1e |
T |
A |
1: 154,353,563 (GRCm39) |
Q423L |
probably damaging |
Het |
Calu |
T |
C |
6: 29,366,974 (GRCm39) |
I62T |
possibly damaging |
Het |
Cars2 |
A |
G |
8: 11,564,515 (GRCm39) |
V75A |
probably benign |
Het |
Catsperb |
T |
A |
12: 101,569,026 (GRCm39) |
N899K |
possibly damaging |
Het |
Ccdc50 |
T |
A |
16: 27,228,089 (GRCm39) |
C86* |
probably null |
Het |
Cdh5 |
G |
T |
8: 104,864,447 (GRCm39) |
L469F |
probably damaging |
Het |
Clrn3 |
A |
T |
7: 135,115,848 (GRCm39) |
D167E |
probably benign |
Het |
Csmd1 |
A |
T |
8: 16,396,698 (GRCm39) |
C411S |
probably damaging |
Het |
Dchs1 |
A |
T |
7: 105,411,755 (GRCm39) |
S1454T |
probably benign |
Het |
Ddx20 |
G |
A |
3: 105,586,660 (GRCm39) |
Q562* |
probably null |
Het |
Dgkg |
T |
G |
16: 22,419,344 (GRCm39) |
Y52S |
probably damaging |
Het |
Dhx58 |
T |
C |
11: 100,594,316 (GRCm39) |
|
probably null |
Het |
Dpp6 |
A |
T |
5: 27,604,004 (GRCm39) |
I145L |
probably benign |
Het |
Efna2 |
A |
T |
10: 80,022,711 (GRCm39) |
Y85F |
possibly damaging |
Het |
Eif3a |
C |
T |
19: 60,769,954 (GRCm39) |
V127I |
probably benign |
Het |
Exph5 |
A |
T |
9: 53,284,935 (GRCm39) |
H672L |
possibly damaging |
Het |
Fam131b |
T |
C |
6: 42,297,818 (GRCm39) |
T112A |
possibly damaging |
Het |
Fcgr1 |
A |
T |
3: 96,193,184 (GRCm39) |
V271E |
probably damaging |
Het |
Fgfr4 |
A |
G |
13: 55,313,715 (GRCm39) |
D508G |
probably damaging |
Het |
Fndc3b |
A |
G |
3: 27,473,549 (GRCm39) |
M1172T |
probably benign |
Het |
Fryl |
G |
T |
5: 73,265,836 (GRCm39) |
T495K |
probably damaging |
Het |
Garin5b |
A |
T |
7: 4,761,017 (GRCm39) |
V565E |
probably damaging |
Het |
Gm5134 |
A |
T |
10: 75,802,227 (GRCm39) |
I93F |
probably damaging |
Het |
Gpbar1 |
G |
A |
1: 74,318,603 (GRCm39) |
G282D |
possibly damaging |
Het |
Gria2 |
G |
A |
3: 80,709,664 (GRCm39) |
L10F |
probably benign |
Het |
Grm7 |
T |
C |
6: 111,184,769 (GRCm39) |
Y367H |
probably benign |
Het |
H1f9 |
T |
A |
11: 94,858,858 (GRCm39) |
V51E |
probably damaging |
Het |
Hivep1 |
G |
A |
13: 42,310,969 (GRCm39) |
A1070T |
probably benign |
Het |
Il33 |
A |
G |
19: 29,934,304 (GRCm39) |
D155G |
possibly damaging |
Het |
Kdm6b |
T |
C |
11: 69,297,129 (GRCm39) |
S408G |
probably null |
Het |
Kntc1 |
A |
G |
5: 123,948,874 (GRCm39) |
|
probably null |
Het |
Kntc1 |
G |
A |
5: 123,897,162 (GRCm39) |
|
probably null |
Het |
Ltbp2 |
T |
G |
12: 84,855,220 (GRCm39) |
|
probably null |
Het |
Mapk8ip3 |
G |
T |
17: 25,133,562 (GRCm39) |
L83I |
probably damaging |
Het |
Meltf |
C |
A |
16: 31,711,440 (GRCm39) |
Y554* |
probably null |
Het |
Mov10 |
A |
C |
3: 104,706,735 (GRCm39) |
F725C |
probably damaging |
Het |
Ms4a6d |
A |
C |
19: 11,567,523 (GRCm39) |
L18R |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,298,515 (GRCm39) |
N507S |
probably benign |
Het |
Nodal |
A |
G |
10: 61,254,113 (GRCm39) |
Q12R |
probably benign |
Het |
Npy6r |
T |
C |
18: 44,409,575 (GRCm39) |
L332P |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,227,181 (GRCm39) |
K272R |
possibly damaging |
Het |
Obox2 |
G |
T |
7: 15,131,174 (GRCm39) |
K93N |
probably benign |
Het |
Or10j27 |
C |
T |
1: 172,958,418 (GRCm39) |
R122H |
possibly damaging |
Het |
Or51a6 |
G |
T |
7: 102,603,953 (GRCm39) |
P285Q |
probably damaging |
Het |
Or5b112 |
A |
G |
19: 13,319,178 (GRCm39) |
T19A |
possibly damaging |
Het |
Or5w13 |
C |
T |
2: 87,523,777 (GRCm39) |
V150M |
probably benign |
Het |
Pcdh12 |
T |
A |
18: 38,415,196 (GRCm39) |
D643V |
possibly damaging |
Het |
Pcsk2 |
A |
G |
2: 143,529,539 (GRCm39) |
D112G |
probably benign |
Het |
Pms1 |
A |
G |
1: 53,234,174 (GRCm39) |
S781P |
probably benign |
Het |
Prtg |
A |
G |
9: 72,752,178 (GRCm39) |
D188G |
probably benign |
Het |
Psg21 |
A |
T |
7: 18,388,695 (GRCm39) |
N132K |
probably benign |
Het |
Psip1 |
A |
G |
4: 83,400,769 (GRCm39) |
V25A |
probably damaging |
Het |
Psmd13 |
T |
A |
7: 140,478,107 (GRCm39) |
I319N |
probably damaging |
Het |
Ptges2 |
A |
G |
2: 32,290,104 (GRCm39) |
T173A |
probably benign |
Het |
Ptprm |
G |
A |
17: 67,054,155 (GRCm39) |
R975W |
probably damaging |
Het |
Rdh1 |
A |
G |
10: 127,601,214 (GRCm39) |
D254G |
probably benign |
Het |
Rnf138 |
T |
G |
18: 21,157,540 (GRCm39) |
N212K |
probably damaging |
Het |
Serpine2 |
A |
G |
1: 79,799,159 (GRCm39) |
S32P |
probably damaging |
Het |
Serpini1 |
G |
T |
3: 75,521,971 (GRCm39) |
W154L |
probably damaging |
Het |
Sf3a1 |
C |
A |
11: 4,129,177 (GRCm39) |
Q713K |
possibly damaging |
Het |
Sgo2b |
A |
T |
8: 64,379,867 (GRCm39) |
H988Q |
probably benign |
Het |
Sin3a |
T |
C |
9: 57,008,483 (GRCm39) |
F468L |
probably damaging |
Het |
Slamf6 |
A |
T |
1: 171,761,776 (GRCm39) |
I66F |
possibly damaging |
Het |
Slc22a28 |
A |
T |
19: 8,094,488 (GRCm39) |
C178S |
possibly damaging |
Het |
Slc35a1 |
A |
C |
4: 34,675,181 (GRCm39) |
V119G |
probably damaging |
Het |
Slc39a12 |
A |
T |
2: 14,439,030 (GRCm39) |
H428L |
probably damaging |
Het |
Speer2 |
A |
G |
16: 69,654,965 (GRCm39) |
S167P |
probably benign |
Het |
Sphkap |
G |
A |
1: 83,255,236 (GRCm39) |
R838* |
probably null |
Het |
Spsb2 |
T |
C |
6: 124,786,329 (GRCm39) |
|
probably null |
Het |
Stam2 |
A |
T |
2: 52,593,168 (GRCm39) |
Y341* |
probably null |
Het |
Sv2b |
G |
A |
7: 74,856,089 (GRCm39) |
A67V |
probably benign |
Het |
Svep1 |
A |
G |
4: 58,064,170 (GRCm39) |
|
probably null |
Het |
Syt15 |
A |
T |
14: 33,944,969 (GRCm39) |
Q172L |
probably benign |
Het |
T |
G |
A |
17: 8,660,634 (GRCm39) |
S415N |
probably benign |
Het |
Tep1 |
A |
G |
14: 51,061,641 (GRCm39) |
F2625S |
possibly damaging |
Het |
Tex14 |
T |
C |
11: 87,427,581 (GRCm39) |
V11A |
possibly damaging |
Het |
Tiam2 |
A |
T |
17: 3,465,401 (GRCm39) |
R377* |
probably null |
Het |
Tirap |
A |
G |
9: 35,102,312 (GRCm39) |
|
probably null |
Het |
Tm4sf20 |
T |
C |
1: 82,737,938 (GRCm39) |
T118A |
probably benign |
Het |
Trank1 |
A |
T |
9: 111,207,900 (GRCm39) |
Q1715L |
probably benign |
Het |
Trpm2 |
C |
T |
10: 77,783,823 (GRCm39) |
V217M |
probably damaging |
Het |
Ubap1l |
G |
A |
9: 65,279,078 (GRCm39) |
E126K |
possibly damaging |
Het |
Urgcp |
G |
T |
11: 5,666,526 (GRCm39) |
P604Q |
probably damaging |
Het |
Vmn1r63 |
A |
G |
7: 5,806,254 (GRCm39) |
V126A |
probably benign |
Het |
Vmn2r90 |
T |
C |
17: 17,933,525 (GRCm39) |
C362R |
probably damaging |
Het |
Vmn2r96 |
A |
G |
17: 18,804,138 (GRCm39) |
I271V |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,883,138 (GRCm39) |
T3562A |
probably damaging |
Het |
Wdr91 |
T |
A |
6: 34,869,297 (GRCm39) |
H409L |
probably damaging |
Het |
Wnt7a |
T |
A |
6: 91,342,938 (GRCm39) |
T315S |
possibly damaging |
Het |
Zfp616 |
A |
G |
11: 73,975,795 (GRCm39) |
H688R |
probably benign |
Het |
Zfp763 |
A |
T |
17: 33,237,413 (GRCm39) |
H577Q |
probably damaging |
Het |
Zfp808 |
G |
A |
13: 62,320,721 (GRCm39) |
S650N |
probably benign |
Het |
Zfp977 |
A |
T |
7: 42,229,409 (GRCm39) |
M372K |
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 |
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 |
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 |
|