Other mutations in this stock |
Total: 145 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921517D22Rik |
T |
C |
13: 59,839,406 (GRCm39) |
D13G |
probably benign |
Het |
4930442H23Rik |
C |
T |
10: 81,018,978 (GRCm39) |
|
probably benign |
Het |
Adamts13 |
T |
A |
2: 26,873,054 (GRCm39) |
S341T |
probably damaging |
Het |
Adamts2 |
A |
G |
11: 50,683,549 (GRCm39) |
I944V |
probably benign |
Het |
Adcy3 |
A |
G |
12: 4,256,542 (GRCm39) |
T783A |
probably benign |
Het |
Ago3 |
A |
T |
4: 126,262,296 (GRCm39) |
M418K |
probably benign |
Het |
Alpk1 |
G |
T |
3: 127,481,241 (GRCm39) |
N175K |
possibly damaging |
Het |
Als2 |
A |
G |
1: 59,254,472 (GRCm39) |
V295A |
probably benign |
Het |
Anapc13 |
T |
C |
9: 102,507,020 (GRCm39) |
I11T |
probably benign |
Het |
Ankrd12 |
T |
A |
17: 66,289,994 (GRCm39) |
N1813I |
probably damaging |
Het |
Anks1b |
A |
T |
10: 90,750,612 (GRCm39) |
I176F |
probably null |
Het |
Ap3d1 |
TTCTCTCTCTCTCTCTCT |
TTCTCTCTCTCTCTCT |
10: 80,548,612 (GRCm39) |
|
probably null |
Het |
Arhgap32 |
T |
C |
9: 32,172,076 (GRCm39) |
C1619R |
probably damaging |
Het |
Arhgap32 |
A |
G |
9: 32,040,949 (GRCm39) |
D67G |
probably damaging |
Het |
Atp1a4 |
A |
T |
1: 172,081,677 (GRCm39) |
Y158* |
probably null |
Het |
Atp8b5 |
A |
T |
4: 43,356,980 (GRCm39) |
D576V |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,617,590 (GRCm39) |
I122V |
probably damaging |
Het |
B430203G13Rik |
A |
T |
12: 17,974,520 (GRCm39) |
|
noncoding transcript |
Het |
Baz1b |
T |
G |
5: 135,246,267 (GRCm39) |
L572R |
possibly damaging |
Het |
Ccn3 |
A |
T |
15: 54,615,603 (GRCm39) |
|
probably null |
Het |
Ccnd2 |
T |
C |
6: 127,125,761 (GRCm39) |
T92A |
possibly damaging |
Het |
Ccndbp1 |
A |
T |
2: 120,839,003 (GRCm39) |
T5S |
probably benign |
Het |
Ccr2 |
G |
A |
9: 123,906,409 (GRCm39) |
V230I |
probably benign |
Het |
Cct4 |
T |
A |
11: 22,952,866 (GRCm39) |
V514E |
probably damaging |
Het |
Cep152 |
A |
G |
2: 125,428,249 (GRCm39) |
|
probably null |
Het |
Cflar |
C |
T |
1: 58,791,726 (GRCm39) |
T343M |
probably benign |
Het |
Chrm5 |
A |
C |
2: 112,309,930 (GRCm39) |
N395K |
probably benign |
Het |
Chrna10 |
G |
A |
7: 101,762,426 (GRCm39) |
P255S |
possibly damaging |
Het |
Chrna6 |
T |
A |
8: 27,897,134 (GRCm39) |
I248F |
probably damaging |
Het |
Clip1 |
T |
C |
5: 123,717,356 (GRCm39) |
D1387G |
probably damaging |
Het |
Clstn3 |
T |
C |
6: 124,414,331 (GRCm39) |
|
probably null |
Het |
Cntnap5a |
C |
T |
1: 116,029,295 (GRCm39) |
R250W |
probably benign |
Het |
Col12a1 |
C |
A |
9: 79,585,776 (GRCm39) |
V1228F |
possibly damaging |
Het |
Cxcr5 |
T |
C |
9: 44,424,638 (GRCm39) |
T340A |
probably benign |
Het |
Cyp2a4 |
G |
A |
7: 26,012,300 (GRCm39) |
R361K |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 30,985,436 (GRCm39) |
K3818N |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,567,047 (GRCm39) |
K2393M |
probably benign |
Het |
Dpy19l1 |
A |
T |
9: 24,336,119 (GRCm39) |
L529Q |
probably damaging |
Het |
Eif4g2 |
C |
T |
7: 110,676,003 (GRCm39) |
R399H |
probably damaging |
Het |
Elapor1 |
A |
T |
3: 108,365,543 (GRCm39) |
|
probably benign |
Het |
Fam76a |
A |
T |
4: 132,629,428 (GRCm39) |
|
probably null |
Het |
Fam76a |
A |
G |
4: 132,643,501 (GRCm39) |
Y78H |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,166,839 (GRCm39) |
C2026S |
probably damaging |
Het |
Fbxo4 |
T |
C |
15: 3,998,523 (GRCm39) |
T312A |
probably benign |
Het |
Fbxw26 |
A |
G |
9: 109,553,868 (GRCm39) |
V257A |
possibly damaging |
Het |
Fhip1a |
G |
T |
3: 85,595,877 (GRCm39) |
T115K |
probably damaging |
Het |
Flnb |
A |
T |
14: 7,905,701 (GRCm38) |
E1150D |
probably benign |
Het |
Fndc3c1 |
A |
T |
X: 105,481,308 (GRCm39) |
S661R |
possibly damaging |
Het |
Gba2 |
A |
C |
4: 43,568,315 (GRCm39) |
L684R |
probably damaging |
Het |
Gbf1 |
G |
T |
19: 46,256,834 (GRCm39) |
C812F |
possibly damaging |
Het |
Glt8d2 |
A |
T |
10: 82,496,583 (GRCm39) |
D158E |
probably damaging |
Het |
Golga2 |
T |
A |
2: 32,187,168 (GRCm39) |
N89K |
probably damaging |
Het |
Got1 |
A |
G |
19: 43,491,376 (GRCm39) |
I358T |
possibly damaging |
Het |
Gpx6 |
C |
T |
13: 21,496,434 (GRCm39) |
Q3* |
probably null |
Het |
Grin1 |
T |
A |
2: 25,182,393 (GRCm39) |
H956L |
possibly damaging |
Het |
Grin2d |
A |
G |
7: 45,506,205 (GRCm39) |
V562A |
probably damaging |
Het |
Grm6 |
A |
G |
11: 50,748,104 (GRCm39) |
I405V |
probably benign |
Het |
Hcar2 |
C |
G |
5: 124,002,513 (GRCm39) |
G330A |
probably benign |
Het |
Hcfc1 |
T |
C |
X: 73,009,552 (GRCm39) |
K20E |
probably damaging |
Het |
Iars1 |
T |
A |
13: 49,878,139 (GRCm39) |
Y888N |
probably damaging |
Het |
Ifi206 |
A |
T |
1: 173,308,432 (GRCm39) |
H521Q |
probably benign |
Het |
Impg1 |
A |
G |
9: 80,305,732 (GRCm39) |
S112P |
probably benign |
Het |
Incenp |
C |
A |
19: 9,855,054 (GRCm39) |
R619M |
unknown |
Het |
Incenp |
T |
A |
19: 9,855,055 (GRCm39) |
R619W |
unknown |
Het |
Kat2b |
A |
G |
17: 53,960,231 (GRCm39) |
E513G |
possibly damaging |
Het |
Kbtbd12 |
G |
T |
6: 88,595,003 (GRCm39) |
L276I |
probably damaging |
Het |
Kctd9 |
T |
A |
14: 67,971,613 (GRCm39) |
D229E |
probably damaging |
Het |
Kdm1b |
C |
T |
13: 47,216,553 (GRCm39) |
R308W |
probably damaging |
Het |
Kif2b |
G |
A |
11: 91,467,254 (GRCm39) |
P343L |
probably benign |
Het |
Kntc1 |
T |
G |
5: 123,954,825 (GRCm39) |
M2081R |
possibly damaging |
Het |
Lamc1 |
T |
C |
1: 153,107,486 (GRCm39) |
N1231S |
probably damaging |
Het |
Lclat1 |
T |
A |
17: 73,547,065 (GRCm39) |
Y327* |
probably null |
Het |
Lgals3bp |
G |
A |
11: 118,284,340 (GRCm39) |
T413I |
probably damaging |
Het |
Lin54 |
A |
G |
5: 100,607,597 (GRCm39) |
I250T |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,394,002 (GRCm39) |
N2621S |
probably benign |
Het |
Lrrtm3 |
T |
A |
10: 63,923,781 (GRCm39) |
H462L |
probably benign |
Het |
Lysmd1 |
A |
G |
3: 95,042,297 (GRCm39) |
Y57C |
probably damaging |
Het |
Mccc1 |
C |
A |
3: 36,030,022 (GRCm39) |
M429I |
probably damaging |
Het |
Metrnl |
A |
G |
11: 121,598,750 (GRCm39) |
E40G |
probably benign |
Het |
Mios |
T |
A |
6: 8,222,464 (GRCm39) |
M466K |
probably benign |
Het |
Mrgpra1 |
A |
G |
7: 46,985,218 (GRCm39) |
S154P |
probably damaging |
Het |
Mrpl24 |
T |
C |
3: 87,829,357 (GRCm39) |
|
probably null |
Het |
Myo1f |
A |
G |
17: 33,817,165 (GRCm39) |
N736S |
possibly damaging |
Het |
Myo1h |
A |
G |
5: 114,498,660 (GRCm39) |
I919V |
possibly damaging |
Het |
Nampt |
T |
C |
12: 32,898,713 (GRCm39) |
L443P |
possibly damaging |
Het |
Ndufaf2 |
C |
G |
13: 108,189,314 (GRCm39) |
A145P |
probably damaging |
Het |
Nek10 |
A |
T |
14: 14,855,714 (GRCm38) |
T403S |
probably benign |
Het |
Nme8 |
C |
A |
13: 19,842,100 (GRCm39) |
V219L |
probably damaging |
Het |
Nps |
T |
A |
7: 134,870,517 (GRCm39) |
L13Q |
probably damaging |
Het |
Nutm1 |
G |
A |
2: 112,079,281 (GRCm39) |
A878V |
probably benign |
Het |
Ogdh |
T |
C |
11: 6,299,875 (GRCm39) |
F794L |
probably damaging |
Het |
Or14a259 |
C |
A |
7: 86,012,943 (GRCm39) |
G201C |
probably damaging |
Het |
Or14c39 |
T |
C |
7: 86,343,736 (GRCm39) |
L24P |
probably damaging |
Het |
Or2t35 |
A |
C |
14: 14,407,729 (GRCm38) |
Y167S |
possibly damaging |
Het |
Or4f56 |
A |
T |
2: 111,703,395 (GRCm39) |
D268E |
possibly damaging |
Het |
Or5a3 |
A |
T |
19: 12,400,341 (GRCm39) |
I223F |
probably damaging |
Het |
Or5g29 |
A |
G |
2: 85,421,282 (GRCm39) |
T133A |
probably benign |
Het |
Pik3cg |
T |
C |
12: 32,255,198 (GRCm39) |
E263G |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,307,005 (GRCm39) |
T1798A |
probably benign |
Het |
Poldip3 |
T |
C |
15: 83,015,702 (GRCm39) |
Y305C |
probably damaging |
Het |
Prkdc |
T |
C |
16: 15,466,840 (GRCm39) |
I107T |
probably benign |
Het |
Prmt2 |
A |
G |
10: 76,062,055 (GRCm39) |
I50T |
probably damaging |
Het |
Ptprd |
T |
C |
4: 76,058,790 (GRCm39) |
T168A |
probably benign |
Het |
Pudp |
A |
G |
18: 50,701,136 (GRCm39) |
V199A |
probably damaging |
Het |
Rab3c |
T |
C |
13: 110,198,434 (GRCm39) |
E198G |
probably benign |
Het |
Rasl12 |
A |
G |
9: 65,320,730 (GRCm39) |
Y156C |
probably damaging |
Het |
Rbm12 |
T |
C |
2: 155,938,484 (GRCm39) |
D596G |
possibly damaging |
Het |
Rbm6 |
T |
C |
9: 107,664,551 (GRCm39) |
E694G |
probably benign |
Het |
Rif1 |
T |
C |
2: 52,002,759 (GRCm39) |
V2071A |
probably damaging |
Het |
Ripply2 |
A |
T |
9: 86,901,849 (GRCm39) |
N125I |
probably damaging |
Het |
Rps6kc1 |
A |
T |
1: 190,482,385 (GRCm39) |
H284Q |
probably benign |
Het |
Scara3 |
A |
T |
14: 66,190,950 (GRCm39) |
M1K |
probably null |
Het |
Sfswap |
A |
G |
5: 129,590,147 (GRCm39) |
T215A |
probably damaging |
Het |
Shroom2 |
A |
C |
X: 151,443,903 (GRCm39) |
F421V |
probably benign |
Het |
Sipa1l3 |
A |
G |
7: 29,077,066 (GRCm39) |
V902A |
probably damaging |
Het |
Slamf8 |
G |
T |
1: 172,411,781 (GRCm39) |
P238Q |
probably damaging |
Het |
Slc44a3 |
T |
C |
3: 121,320,723 (GRCm39) |
T93A |
possibly damaging |
Het |
Slc5a7 |
A |
T |
17: 54,585,728 (GRCm39) |
I363N |
probably damaging |
Het |
Slc66a1 |
G |
T |
4: 139,027,312 (GRCm39) |
H343Q |
probably benign |
Het |
Slc7a2 |
T |
A |
8: 41,364,095 (GRCm39) |
M436K |
probably benign |
Het |
Spindoc |
A |
G |
19: 7,351,456 (GRCm39) |
S223P |
probably benign |
Het |
Stk11ip |
T |
C |
1: 75,506,925 (GRCm39) |
F669L |
possibly damaging |
Het |
Sun3 |
G |
A |
11: 8,988,266 (GRCm39) |
L19F |
probably benign |
Het |
Sycp1 |
C |
A |
3: 102,760,805 (GRCm39) |
A703S |
possibly damaging |
Het |
Tas2r139 |
T |
G |
6: 42,118,218 (GRCm39) |
F117V |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,936,467 (GRCm39) |
Y1527C |
probably damaging |
Het |
Tenm4 |
A |
C |
7: 96,423,253 (GRCm39) |
K683Q |
probably damaging |
Het |
Tfeb |
T |
A |
17: 48,099,152 (GRCm39) |
|
probably null |
Het |
Tmco4 |
T |
C |
4: 138,725,350 (GRCm39) |
S121P |
probably damaging |
Het |
Tmprss11d |
C |
T |
5: 86,454,140 (GRCm39) |
V222M |
probably damaging |
Het |
Tnks1bp1 |
T |
C |
2: 84,893,378 (GRCm39) |
W440R |
probably damaging |
Het |
Trp53bp2 |
A |
G |
1: 182,276,562 (GRCm39) |
T848A |
probably benign |
Het |
Tssk1 |
G |
A |
16: 17,712,926 (GRCm39) |
R237H |
probably benign |
Het |
Ttll4 |
A |
T |
1: 74,718,166 (GRCm39) |
T6S |
possibly damaging |
Het |
Ttn |
G |
T |
2: 76,552,141 (GRCm39) |
Y29419* |
probably null |
Het |
Ttn |
A |
G |
2: 76,599,947 (GRCm39) |
Y19076H |
probably damaging |
Het |
Ubr3 |
T |
A |
2: 69,789,947 (GRCm39) |
V867D |
probably damaging |
Het |
Usp29 |
A |
G |
7: 6,964,390 (GRCm39) |
T78A |
probably damaging |
Het |
Utrn |
T |
G |
10: 12,530,489 (GRCm39) |
Q2108P |
probably benign |
Het |
Vmn1r61 |
A |
T |
7: 5,614,124 (GRCm39) |
Y63* |
probably null |
Het |
Vmn1r61 |
A |
T |
7: 5,614,126 (GRCm39) |
Y63N |
probably benign |
Het |
Vmn1r85 |
A |
T |
7: 12,818,788 (GRCm39) |
W119R |
probably damaging |
Het |
Zbtb21 |
A |
C |
16: 97,751,655 (GRCm39) |
V190G |
possibly damaging |
Het |
Zfp157 |
C |
A |
5: 138,443,051 (GRCm39) |
T14N |
probably damaging |
Het |
Zfp942 |
A |
T |
17: 22,148,400 (GRCm39) |
H76Q |
probably damaging |
Het |
|
Other mutations in Vcan |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00434:Vcan
|
APN |
13 |
89,852,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00502:Vcan
|
APN |
13 |
89,840,438 (GRCm39) |
missense |
probably benign |
|
IGL00504:Vcan
|
APN |
13 |
89,839,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL00566:Vcan
|
APN |
13 |
89,837,098 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00701:Vcan
|
APN |
13 |
89,851,845 (GRCm39) |
missense |
probably benign |
|
IGL00743:Vcan
|
APN |
13 |
89,873,425 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00962:Vcan
|
APN |
13 |
89,810,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01085:Vcan
|
APN |
13 |
89,828,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01317:Vcan
|
APN |
13 |
89,839,787 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01349:Vcan
|
APN |
13 |
89,852,062 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01391:Vcan
|
APN |
13 |
89,852,288 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01644:Vcan
|
APN |
13 |
89,836,794 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01657:Vcan
|
APN |
13 |
89,838,705 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01707:Vcan
|
APN |
13 |
89,837,864 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01764:Vcan
|
APN |
13 |
89,873,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01920:Vcan
|
APN |
13 |
89,837,324 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01989:Vcan
|
APN |
13 |
89,837,478 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01999:Vcan
|
APN |
13 |
89,832,557 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02083:Vcan
|
APN |
13 |
89,873,684 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02160:Vcan
|
APN |
13 |
89,832,612 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02217:Vcan
|
APN |
13 |
89,851,196 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02522:Vcan
|
APN |
13 |
89,852,968 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02527:Vcan
|
APN |
13 |
89,838,776 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02926:Vcan
|
APN |
13 |
89,836,742 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03061:Vcan
|
APN |
13 |
89,851,394 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03331:Vcan
|
APN |
13 |
89,810,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03352:Vcan
|
APN |
13 |
89,853,125 (GRCm39) |
missense |
probably benign |
0.00 |
R0041:Vcan
|
UTSW |
13 |
89,810,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R0102:Vcan
|
UTSW |
13 |
89,851,787 (GRCm39) |
missense |
probably benign |
0.01 |
R0102:Vcan
|
UTSW |
13 |
89,851,787 (GRCm39) |
missense |
probably benign |
0.01 |
R0109:Vcan
|
UTSW |
13 |
89,826,192 (GRCm39) |
critical splice donor site |
probably null |
|
R0139:Vcan
|
UTSW |
13 |
89,839,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0295:Vcan
|
UTSW |
13 |
89,860,310 (GRCm39) |
missense |
probably benign |
0.06 |
R0375:Vcan
|
UTSW |
13 |
89,839,394 (GRCm39) |
missense |
probably damaging |
0.99 |
R0379:Vcan
|
UTSW |
13 |
89,851,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R0457:Vcan
|
UTSW |
13 |
89,851,318 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0482:Vcan
|
UTSW |
13 |
89,826,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R0485:Vcan
|
UTSW |
13 |
89,852,779 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0532:Vcan
|
UTSW |
13 |
89,851,891 (GRCm39) |
missense |
probably damaging |
0.99 |
R0561:Vcan
|
UTSW |
13 |
89,879,583 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0561:Vcan
|
UTSW |
13 |
89,860,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R0636:Vcan
|
UTSW |
13 |
89,860,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0636:Vcan
|
UTSW |
13 |
89,852,825 (GRCm39) |
missense |
probably damaging |
0.99 |
R0680:Vcan
|
UTSW |
13 |
89,827,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R0849:Vcan
|
UTSW |
13 |
89,853,072 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1006:Vcan
|
UTSW |
13 |
89,833,196 (GRCm39) |
critical splice donor site |
probably null |
|
R1104:Vcan
|
UTSW |
13 |
89,840,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R1118:Vcan
|
UTSW |
13 |
89,853,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R1137:Vcan
|
UTSW |
13 |
89,852,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R1199:Vcan
|
UTSW |
13 |
89,827,913 (GRCm39) |
splice site |
probably null |
|
R1219:Vcan
|
UTSW |
13 |
89,828,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R1296:Vcan
|
UTSW |
13 |
89,805,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R1332:Vcan
|
UTSW |
13 |
89,841,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R1336:Vcan
|
UTSW |
13 |
89,841,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R1403:Vcan
|
UTSW |
13 |
89,836,603 (GRCm39) |
missense |
probably benign |
0.00 |
R1403:Vcan
|
UTSW |
13 |
89,836,603 (GRCm39) |
missense |
probably benign |
0.00 |
R1546:Vcan
|
UTSW |
13 |
89,841,075 (GRCm39) |
missense |
probably damaging |
0.99 |
R1604:Vcan
|
UTSW |
13 |
89,837,780 (GRCm39) |
missense |
probably benign |
0.42 |
R1616:Vcan
|
UTSW |
13 |
89,853,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R1636:Vcan
|
UTSW |
13 |
89,851,786 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1654:Vcan
|
UTSW |
13 |
89,810,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R1680:Vcan
|
UTSW |
13 |
89,851,666 (GRCm39) |
missense |
probably benign |
0.19 |
R1694:Vcan
|
UTSW |
13 |
89,836,602 (GRCm39) |
missense |
probably damaging |
0.98 |
R1712:Vcan
|
UTSW |
13 |
89,869,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R1754:Vcan
|
UTSW |
13 |
89,852,854 (GRCm39) |
missense |
probably benign |
0.01 |
R1756:Vcan
|
UTSW |
13 |
89,839,800 (GRCm39) |
missense |
probably benign |
0.05 |
R1824:Vcan
|
UTSW |
13 |
89,853,331 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1852:Vcan
|
UTSW |
13 |
89,853,511 (GRCm39) |
missense |
probably damaging |
0.99 |
R1868:Vcan
|
UTSW |
13 |
89,838,990 (GRCm39) |
missense |
probably benign |
0.12 |
R1920:Vcan
|
UTSW |
13 |
89,841,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R1932:Vcan
|
UTSW |
13 |
89,853,653 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1934:Vcan
|
UTSW |
13 |
89,851,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1942:Vcan
|
UTSW |
13 |
89,851,543 (GRCm39) |
missense |
probably benign |
0.01 |
R1964:Vcan
|
UTSW |
13 |
89,840,861 (GRCm39) |
missense |
probably benign |
0.02 |
R1970:Vcan
|
UTSW |
13 |
89,837,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Vcan
|
UTSW |
13 |
89,839,104 (GRCm39) |
missense |
probably benign |
0.00 |
R2110:Vcan
|
UTSW |
13 |
89,841,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Vcan
|
UTSW |
13 |
89,841,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Vcan
|
UTSW |
13 |
89,841,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R2136:Vcan
|
UTSW |
13 |
89,837,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R2158:Vcan
|
UTSW |
13 |
89,851,648 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2376:Vcan
|
UTSW |
13 |
89,851,529 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2385:Vcan
|
UTSW |
13 |
89,837,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R2443:Vcan
|
UTSW |
13 |
89,852,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R2876:Vcan
|
UTSW |
13 |
89,852,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R3607:Vcan
|
UTSW |
13 |
89,851,420 (GRCm39) |
missense |
probably damaging |
0.98 |
R4042:Vcan
|
UTSW |
13 |
89,840,662 (GRCm39) |
missense |
probably benign |
0.35 |
R4043:Vcan
|
UTSW |
13 |
89,840,662 (GRCm39) |
missense |
probably benign |
0.35 |
R4044:Vcan
|
UTSW |
13 |
89,840,662 (GRCm39) |
missense |
probably benign |
0.35 |
R4065:Vcan
|
UTSW |
13 |
89,828,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4161:Vcan
|
UTSW |
13 |
89,833,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R4178:Vcan
|
UTSW |
13 |
89,873,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R4290:Vcan
|
UTSW |
13 |
89,873,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R4530:Vcan
|
UTSW |
13 |
89,852,147 (GRCm39) |
missense |
probably damaging |
0.97 |
R4666:Vcan
|
UTSW |
13 |
89,828,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R4870:Vcan
|
UTSW |
13 |
89,852,858 (GRCm39) |
missense |
probably benign |
0.01 |
R4973:Vcan
|
UTSW |
13 |
89,836,961 (GRCm39) |
missense |
probably benign |
0.30 |
R5037:Vcan
|
UTSW |
13 |
89,852,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R5104:Vcan
|
UTSW |
13 |
89,805,591 (GRCm39) |
intron |
probably benign |
|
R5124:Vcan
|
UTSW |
13 |
89,873,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R5129:Vcan
|
UTSW |
13 |
89,838,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R5198:Vcan
|
UTSW |
13 |
89,838,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R5240:Vcan
|
UTSW |
13 |
89,840,651 (GRCm39) |
missense |
probably benign |
0.08 |
R5254:Vcan
|
UTSW |
13 |
89,839,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R5280:Vcan
|
UTSW |
13 |
89,838,405 (GRCm39) |
missense |
probably benign |
0.00 |
R5522:Vcan
|
UTSW |
13 |
89,839,929 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5557:Vcan
|
UTSW |
13 |
89,851,231 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5568:Vcan
|
UTSW |
13 |
89,836,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R5578:Vcan
|
UTSW |
13 |
89,839,622 (GRCm39) |
missense |
probably benign |
0.01 |
R5627:Vcan
|
UTSW |
13 |
89,839,254 (GRCm39) |
frame shift |
probably null |
|
R5687:Vcan
|
UTSW |
13 |
89,826,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R5752:Vcan
|
UTSW |
13 |
89,828,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R5879:Vcan
|
UTSW |
13 |
89,852,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R5941:Vcan
|
UTSW |
13 |
89,840,810 (GRCm39) |
missense |
probably damaging |
0.98 |
R6113:Vcan
|
UTSW |
13 |
89,805,655 (GRCm39) |
nonsense |
probably null |
|
R6135:Vcan
|
UTSW |
13 |
89,838,045 (GRCm39) |
missense |
probably benign |
0.36 |
R6252:Vcan
|
UTSW |
13 |
89,839,339 (GRCm39) |
nonsense |
probably null |
|
R6280:Vcan
|
UTSW |
13 |
89,873,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Vcan
|
UTSW |
13 |
89,839,716 (GRCm39) |
missense |
probably benign |
0.22 |
R6327:Vcan
|
UTSW |
13 |
89,852,951 (GRCm39) |
missense |
probably damaging |
0.99 |
R6460:Vcan
|
UTSW |
13 |
89,838,806 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6669:Vcan
|
UTSW |
13 |
89,852,850 (GRCm39) |
missense |
probably benign |
0.21 |
R6744:Vcan
|
UTSW |
13 |
89,853,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R6819:Vcan
|
UTSW |
13 |
89,853,244 (GRCm39) |
missense |
probably benign |
0.00 |
R6880:Vcan
|
UTSW |
13 |
89,860,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R6956:Vcan
|
UTSW |
13 |
89,837,550 (GRCm39) |
missense |
probably damaging |
0.99 |
R6971:Vcan
|
UTSW |
13 |
89,826,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R6985:Vcan
|
UTSW |
13 |
89,828,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R6994:Vcan
|
UTSW |
13 |
89,841,526 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6997:Vcan
|
UTSW |
13 |
89,838,737 (GRCm39) |
missense |
probably damaging |
0.98 |
R7029:Vcan
|
UTSW |
13 |
89,838,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R7066:Vcan
|
UTSW |
13 |
89,853,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R7156:Vcan
|
UTSW |
13 |
89,837,229 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7171:Vcan
|
UTSW |
13 |
89,873,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R7176:Vcan
|
UTSW |
13 |
89,837,055 (GRCm39) |
missense |
probably benign |
0.01 |
R7229:Vcan
|
UTSW |
13 |
89,853,389 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7250:Vcan
|
UTSW |
13 |
89,879,576 (GRCm39) |
critical splice donor site |
probably null |
|
R7250:Vcan
|
UTSW |
13 |
89,869,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R7262:Vcan
|
UTSW |
13 |
89,853,280 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7289:Vcan
|
UTSW |
13 |
89,840,852 (GRCm39) |
nonsense |
probably null |
|
R7299:Vcan
|
UTSW |
13 |
89,853,385 (GRCm39) |
missense |
probably benign |
|
R7301:Vcan
|
UTSW |
13 |
89,853,385 (GRCm39) |
missense |
probably benign |
|
R7425:Vcan
|
UTSW |
13 |
89,837,951 (GRCm39) |
missense |
probably damaging |
0.99 |
R7514:Vcan
|
UTSW |
13 |
89,852,237 (GRCm39) |
missense |
probably damaging |
0.97 |
R7579:Vcan
|
UTSW |
13 |
89,840,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7618:Vcan
|
UTSW |
13 |
89,840,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R7655:Vcan
|
UTSW |
13 |
89,833,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R7656:Vcan
|
UTSW |
13 |
89,833,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R7676:Vcan
|
UTSW |
13 |
89,839,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R7719:Vcan
|
UTSW |
13 |
89,852,738 (GRCm39) |
missense |
probably damaging |
0.98 |
R7753:Vcan
|
UTSW |
13 |
89,837,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R7762:Vcan
|
UTSW |
13 |
89,841,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R7778:Vcan
|
UTSW |
13 |
89,836,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R7824:Vcan
|
UTSW |
13 |
89,836,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R7995:Vcan
|
UTSW |
13 |
89,839,977 (GRCm39) |
missense |
probably benign |
|
R7998:Vcan
|
UTSW |
13 |
89,852,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R8033:Vcan
|
UTSW |
13 |
89,852,479 (GRCm39) |
missense |
probably benign |
0.04 |
R8061:Vcan
|
UTSW |
13 |
89,805,409 (GRCm39) |
missense |
probably benign |
0.45 |
R8103:Vcan
|
UTSW |
13 |
89,851,439 (GRCm39) |
nonsense |
probably null |
|
R8103:Vcan
|
UTSW |
13 |
89,805,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Vcan
|
UTSW |
13 |
89,852,373 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8162:Vcan
|
UTSW |
13 |
89,853,106 (GRCm39) |
nonsense |
probably null |
|
R8166:Vcan
|
UTSW |
13 |
89,840,855 (GRCm39) |
missense |
probably benign |
0.02 |
R8274:Vcan
|
UTSW |
13 |
89,853,089 (GRCm39) |
missense |
probably benign |
0.02 |
R8284:Vcan
|
UTSW |
13 |
89,852,454 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8417:Vcan
|
UTSW |
13 |
89,836,862 (GRCm39) |
missense |
probably benign |
0.19 |
R8696:Vcan
|
UTSW |
13 |
89,839,217 (GRCm39) |
missense |
probably benign |
0.00 |
R8738:Vcan
|
UTSW |
13 |
89,840,439 (GRCm39) |
missense |
probably benign |
0.17 |
R8792:Vcan
|
UTSW |
13 |
89,840,230 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8887:Vcan
|
UTSW |
13 |
89,853,026 (GRCm39) |
missense |
probably benign |
|
R9049:Vcan
|
UTSW |
13 |
89,826,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R9074:Vcan
|
UTSW |
13 |
89,839,146 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9095:Vcan
|
UTSW |
13 |
89,852,644 (GRCm39) |
missense |
probably benign |
0.32 |
R9172:Vcan
|
UTSW |
13 |
89,828,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R9199:Vcan
|
UTSW |
13 |
89,838,615 (GRCm39) |
nonsense |
probably null |
|
R9259:Vcan
|
UTSW |
13 |
89,838,989 (GRCm39) |
missense |
probably damaging |
0.99 |
R9455:Vcan
|
UTSW |
13 |
89,837,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R9476:Vcan
|
UTSW |
13 |
89,851,531 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9477:Vcan
|
UTSW |
13 |
89,841,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R9555:Vcan
|
UTSW |
13 |
89,839,659 (GRCm39) |
missense |
|
|
R9579:Vcan
|
UTSW |
13 |
89,837,713 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9606:Vcan
|
UTSW |
13 |
89,853,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R9645:Vcan
|
UTSW |
13 |
89,841,081 (GRCm39) |
missense |
probably benign |
0.00 |
R9659:Vcan
|
UTSW |
13 |
89,839,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R9766:Vcan
|
UTSW |
13 |
89,839,247 (GRCm39) |
missense |
probably benign |
0.00 |
R9778:Vcan
|
UTSW |
13 |
89,837,930 (GRCm39) |
missense |
probably damaging |
1.00 |
X0058:Vcan
|
UTSW |
13 |
89,840,612 (GRCm39) |
missense |
probably benign |
0.21 |
X0065:Vcan
|
UTSW |
13 |
89,853,868 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Vcan
|
UTSW |
13 |
89,840,690 (GRCm39) |
missense |
probably benign |
0.10 |
Z1177:Vcan
|
UTSW |
13 |
89,852,192 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Vcan
|
UTSW |
13 |
89,851,907 (GRCm39) |
nonsense |
probably null |
|
Z1177:Vcan
|
UTSW |
13 |
89,851,643 (GRCm39) |
missense |
probably benign |
0.00 |
|