Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
G |
5: 109,884,067 (GRCm39) |
F597S |
probably benign |
Het |
Aasdh |
C |
A |
5: 77,036,501 (GRCm39) |
E347* |
probably null |
Het |
Abca16 |
G |
T |
7: 120,126,309 (GRCm39) |
C1155F |
probably damaging |
Het |
Adam26a |
T |
C |
8: 44,021,918 (GRCm39) |
D524G |
probably damaging |
Het |
Adamts20 |
G |
C |
15: 94,277,656 (GRCm39) |
H269D |
probably benign |
Het |
Akap9 |
T |
A |
5: 4,100,145 (GRCm39) |
|
probably null |
Het |
Akt3 |
T |
C |
1: 176,877,693 (GRCm39) |
I358M |
possibly damaging |
Het |
Aldh9a1 |
G |
T |
1: 167,189,376 (GRCm39) |
A375S |
probably damaging |
Het |
Alg2 |
A |
G |
4: 47,473,974 (GRCm39) |
S105P |
probably benign |
Het |
Amph |
A |
G |
13: 19,288,515 (GRCm39) |
T335A |
probably damaging |
Het |
Ank2 |
C |
T |
3: 126,756,050 (GRCm39) |
V1056M |
probably damaging |
Het |
Apoh |
A |
G |
11: 108,298,204 (GRCm39) |
D168G |
probably benign |
Het |
Arfgef3 |
C |
T |
10: 18,465,454 (GRCm39) |
A2130T |
probably damaging |
Het |
Arhgap30 |
A |
G |
1: 171,230,897 (GRCm39) |
D218G |
probably benign |
Het |
Atp11b |
T |
G |
3: 35,861,157 (GRCm39) |
|
probably null |
Het |
B4galnt2 |
A |
G |
11: 95,759,255 (GRCm39) |
V343A |
probably damaging |
Het |
Barhl1 |
T |
C |
2: 28,799,785 (GRCm39) |
Y280C |
probably damaging |
Het |
Bcar1 |
A |
T |
8: 112,447,669 (GRCm39) |
Y103N |
probably damaging |
Het |
Bid |
A |
G |
6: 120,872,707 (GRCm39) |
I150T |
probably benign |
Het |
Ccdc171 |
T |
C |
4: 83,467,876 (GRCm39) |
S74P |
probably damaging |
Het |
Ccni |
A |
T |
5: 93,336,113 (GRCm39) |
|
probably null |
Het |
Cct8l1 |
A |
G |
5: 25,721,891 (GRCm39) |
E202G |
probably benign |
Het |
Cd200r3 |
A |
G |
16: 44,774,622 (GRCm39) |
K212E |
probably benign |
Het |
Cdh19 |
A |
G |
1: 110,817,694 (GRCm39) |
S683P |
probably damaging |
Het |
Ces2b |
A |
T |
8: 105,559,413 (GRCm39) |
H93L |
probably benign |
Het |
Cimip2b |
T |
A |
4: 43,427,514 (GRCm39) |
Q270L |
possibly damaging |
Het |
Clec4a1 |
G |
A |
6: 122,907,654 (GRCm39) |
C114Y |
probably damaging |
Het |
Dcc |
G |
T |
18: 71,675,320 (GRCm39) |
S636* |
probably null |
Het |
Dcdc2c |
T |
C |
12: 28,580,472 (GRCm39) |
D187G |
possibly damaging |
Het |
Dgkb |
G |
T |
12: 38,164,657 (GRCm39) |
E150* |
probably null |
Het |
Dhx30 |
A |
G |
9: 109,915,029 (GRCm39) |
L884P |
probably damaging |
Het |
Dmwd |
T |
G |
7: 18,815,228 (GRCm39) |
|
probably null |
Het |
Dnah17 |
T |
A |
11: 117,932,980 (GRCm39) |
N3593Y |
probably damaging |
Het |
Dnm2 |
G |
A |
9: 21,392,633 (GRCm39) |
S447N |
probably benign |
Het |
Elk4 |
G |
A |
1: 131,945,419 (GRCm39) |
G99D |
probably damaging |
Het |
Entpd1 |
A |
T |
19: 40,727,965 (GRCm39) |
|
probably benign |
Het |
Fam114a1 |
T |
A |
5: 65,137,070 (GRCm39) |
D4E |
probably damaging |
Het |
Fbln2 |
A |
G |
6: 91,241,681 (GRCm39) |
D754G |
probably damaging |
Het |
Fhip2a |
T |
C |
19: 57,367,069 (GRCm39) |
V204A |
probably benign |
Het |
Foxred2 |
T |
C |
15: 77,840,035 (GRCm39) |
N85S |
probably damaging |
Het |
Fut9 |
A |
G |
4: 25,799,591 (GRCm39) |
|
probably benign |
Het |
Gm1818 |
G |
A |
12: 48,606,607 (GRCm39) |
|
noncoding transcript |
Het |
Gm4894 |
C |
A |
9: 49,190,000 (GRCm39) |
Q92K |
unknown |
Het |
Gpx2 |
T |
C |
12: 76,839,574 (GRCm39) |
I141M |
probably benign |
Het |
Gusb |
T |
C |
5: 130,024,326 (GRCm39) |
T476A |
probably damaging |
Het |
Hmmr |
G |
A |
11: 40,612,667 (GRCm39) |
T180I |
possibly damaging |
Het |
Itgbl1 |
T |
C |
14: 124,210,780 (GRCm39) |
Y493H |
probably benign |
Het |
Klhdc9 |
G |
T |
1: 171,187,951 (GRCm39) |
C93* |
probably null |
Het |
Ldaf1 |
T |
C |
7: 119,715,535 (GRCm39) |
S120P |
probably damaging |
Het |
Lpar3 |
A |
G |
3: 145,990,506 (GRCm39) |
K275E |
probably damaging |
Het |
Lrp1b |
A |
G |
2: 40,692,897 (GRCm39) |
|
probably null |
Het |
Lrrc63 |
C |
T |
14: 75,322,389 (GRCm39) |
G572S |
probably damaging |
Het |
Mapk11 |
A |
T |
15: 89,030,685 (GRCm39) |
D98E |
probably benign |
Het |
Mgat4f |
T |
A |
1: 134,317,714 (GRCm39) |
M162K |
probably benign |
Het |
Net1 |
G |
A |
13: 3,934,905 (GRCm39) |
R374W |
probably damaging |
Het |
Nlrp4g |
T |
A |
9: 124,354,005 (GRCm38) |
|
noncoding transcript |
Het |
Nrap |
T |
A |
19: 56,335,652 (GRCm39) |
Y923F |
probably damaging |
Het |
Or13a20 |
T |
A |
7: 140,232,534 (GRCm39) |
M214K |
probably benign |
Het |
Or4c108 |
T |
A |
2: 88,803,834 (GRCm39) |
I134F |
probably damaging |
Het |
Or6c215 |
A |
T |
10: 129,637,932 (GRCm39) |
V154E |
probably benign |
Het |
Plxnc1 |
A |
G |
10: 94,677,335 (GRCm39) |
V964A |
probably damaging |
Het |
Pmfbp1 |
A |
G |
8: 110,262,498 (GRCm39) |
I731V |
probably benign |
Het |
Polq |
T |
A |
16: 36,848,274 (GRCm39) |
S294T |
probably benign |
Het |
Pomgnt2 |
T |
C |
9: 121,811,620 (GRCm39) |
D387G |
probably benign |
Het |
Pramel25 |
T |
C |
4: 143,520,407 (GRCm39) |
V53A |
possibly damaging |
Het |
Prmt2 |
G |
A |
10: 76,056,842 (GRCm39) |
T227I |
probably damaging |
Het |
Psmd1 |
T |
A |
1: 86,010,947 (GRCm39) |
F341I |
probably damaging |
Het |
Ptpn23 |
T |
C |
9: 110,221,806 (GRCm39) |
M127V |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,017,238 (GRCm39) |
F483L |
probably damaging |
Het |
Rab35 |
A |
C |
5: 115,778,147 (GRCm39) |
I38L |
probably damaging |
Het |
Rapgef6 |
A |
G |
11: 54,548,143 (GRCm39) |
T486A |
probably damaging |
Het |
Rgl3 |
A |
T |
9: 21,899,004 (GRCm39) |
C68* |
probably null |
Het |
Rilpl1 |
T |
C |
5: 124,653,594 (GRCm39) |
E189G |
possibly damaging |
Het |
Rnf217 |
T |
C |
10: 31,393,520 (GRCm39) |
I354V |
probably benign |
Het |
Rspo3 |
T |
C |
10: 29,382,524 (GRCm39) |
D50G |
probably damaging |
Het |
Sbno1 |
A |
G |
5: 124,512,672 (GRCm39) |
S1366P |
possibly damaging |
Het |
Sema3c |
A |
G |
5: 17,899,684 (GRCm39) |
D392G |
probably benign |
Het |
Serpinb9e |
A |
T |
13: 33,436,935 (GRCm39) |
Y85F |
probably benign |
Het |
Shprh |
C |
T |
10: 11,032,863 (GRCm39) |
T283I |
probably benign |
Het |
Sipa1l1 |
T |
C |
12: 82,388,103 (GRCm39) |
S110P |
probably benign |
Het |
Slc16a12 |
T |
A |
19: 34,652,643 (GRCm39) |
I168F |
probably damaging |
Het |
Slc23a3 |
A |
G |
1: 75,109,268 (GRCm39) |
S221P |
probably damaging |
Het |
Slc35b3 |
A |
T |
13: 39,116,887 (GRCm39) |
I366K |
possibly damaging |
Het |
Slc44a5 |
T |
C |
3: 153,949,252 (GRCm39) |
|
probably null |
Het |
Slc5a12 |
A |
T |
2: 110,450,753 (GRCm39) |
D316V |
probably damaging |
Het |
Ssr3 |
A |
G |
3: 65,299,874 (GRCm39) |
S29P |
probably damaging |
Het |
Taf2 |
G |
A |
15: 54,890,619 (GRCm39) |
Q1055* |
probably null |
Het |
Them6 |
A |
T |
15: 74,593,367 (GRCm39) |
D75V |
probably damaging |
Het |
Tom1l2 |
A |
G |
11: 60,149,744 (GRCm39) |
S239P |
probably damaging |
Het |
Tspear |
A |
G |
10: 77,710,877 (GRCm39) |
T500A |
probably damaging |
Het |
Tubgcp6 |
G |
A |
15: 88,985,752 (GRCm39) |
A1487V |
probably damaging |
Het |
Uba7 |
G |
A |
9: 107,856,190 (GRCm39) |
V522I |
possibly damaging |
Het |
Virma |
C |
A |
4: 11,521,147 (GRCm39) |
C901* |
probably null |
Het |
Vmn1r172 |
A |
T |
7: 23,359,312 (GRCm39) |
I66F |
possibly damaging |
Het |
Vmn2r82 |
A |
T |
10: 79,215,010 (GRCm39) |
Y331F |
probably benign |
Het |
Wdr55 |
G |
A |
18: 36,895,451 (GRCm39) |
V143I |
probably benign |
Het |
Zbtb49 |
A |
T |
5: 38,371,307 (GRCm39) |
D191E |
possibly damaging |
Het |
Zfhx4 |
A |
G |
3: 5,307,071 (GRCm39) |
H99R |
probably damaging |
Het |
Zfp1005 |
C |
T |
2: 150,110,680 (GRCm39) |
H457Y |
unknown |
Het |
Zfp560 |
C |
T |
9: 20,259,263 (GRCm39) |
C533Y |
probably damaging |
Het |
Zfp646 |
C |
T |
7: 127,478,354 (GRCm39) |
A177V |
probably benign |
Het |
Zfp653 |
C |
T |
9: 21,967,074 (GRCm39) |
E604K |
probably damaging |
Het |
|
Other mutations in Ascc3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Ascc3
|
APN |
10 |
50,590,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00690:Ascc3
|
APN |
10 |
50,576,039 (GRCm39) |
nonsense |
probably null |
|
IGL00897:Ascc3
|
APN |
10 |
50,604,187 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01077:Ascc3
|
APN |
10 |
50,525,413 (GRCm39) |
splice site |
probably benign |
|
IGL01124:Ascc3
|
APN |
10 |
50,608,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01555:Ascc3
|
APN |
10 |
50,626,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02019:Ascc3
|
APN |
10 |
50,566,235 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02161:Ascc3
|
APN |
10 |
50,726,623 (GRCm39) |
nonsense |
probably null |
|
IGL02247:Ascc3
|
APN |
10 |
50,526,686 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02318:Ascc3
|
APN |
10 |
50,604,250 (GRCm39) |
nonsense |
probably null |
|
IGL02428:Ascc3
|
APN |
10 |
50,721,791 (GRCm39) |
nonsense |
probably null |
|
IGL02432:Ascc3
|
APN |
10 |
50,576,589 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02449:Ascc3
|
APN |
10 |
50,576,695 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02640:Ascc3
|
APN |
10 |
50,643,470 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02673:Ascc3
|
APN |
10 |
50,536,769 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03144:Ascc3
|
APN |
10 |
50,643,539 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03161:Ascc3
|
APN |
10 |
50,494,168 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03218:Ascc3
|
APN |
10 |
50,699,949 (GRCm39) |
missense |
possibly damaging |
0.89 |
algorithm
|
UTSW |
10 |
50,594,472 (GRCm39) |
missense |
probably damaging |
0.97 |
heuristic
|
UTSW |
10 |
50,718,289 (GRCm39) |
missense |
probably damaging |
0.99 |
network
|
UTSW |
10 |
50,630,175 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0045:Ascc3
|
UTSW |
10 |
50,594,498 (GRCm39) |
nonsense |
probably null |
|
R0045:Ascc3
|
UTSW |
10 |
50,594,498 (GRCm39) |
nonsense |
probably null |
|
R0131:Ascc3
|
UTSW |
10 |
50,611,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R0131:Ascc3
|
UTSW |
10 |
50,611,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R0132:Ascc3
|
UTSW |
10 |
50,611,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R0149:Ascc3
|
UTSW |
10 |
50,484,089 (GRCm39) |
missense |
probably benign |
0.31 |
R0165:Ascc3
|
UTSW |
10 |
50,718,223 (GRCm39) |
splice site |
probably null |
|
R0255:Ascc3
|
UTSW |
10 |
50,521,154 (GRCm39) |
missense |
probably benign |
0.00 |
R0310:Ascc3
|
UTSW |
10 |
50,625,022 (GRCm39) |
missense |
probably benign |
0.02 |
R0314:Ascc3
|
UTSW |
10 |
50,514,095 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0362:Ascc3
|
UTSW |
10 |
50,625,051 (GRCm39) |
splice site |
probably benign |
|
R0418:Ascc3
|
UTSW |
10 |
50,625,022 (GRCm39) |
missense |
probably benign |
0.02 |
R0419:Ascc3
|
UTSW |
10 |
50,625,022 (GRCm39) |
missense |
probably benign |
0.02 |
R0421:Ascc3
|
UTSW |
10 |
50,625,022 (GRCm39) |
missense |
probably benign |
0.02 |
R0480:Ascc3
|
UTSW |
10 |
50,611,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:Ascc3
|
UTSW |
10 |
50,721,762 (GRCm39) |
missense |
probably benign |
0.17 |
R0833:Ascc3
|
UTSW |
10 |
50,721,762 (GRCm39) |
missense |
probably benign |
0.17 |
R1231:Ascc3
|
UTSW |
10 |
50,699,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Ascc3
|
UTSW |
10 |
50,518,615 (GRCm39) |
splice site |
probably benign |
|
R1302:Ascc3
|
UTSW |
10 |
50,480,890 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R1751:Ascc3
|
UTSW |
10 |
50,594,472 (GRCm39) |
missense |
probably damaging |
0.97 |
R1767:Ascc3
|
UTSW |
10 |
50,594,472 (GRCm39) |
missense |
probably damaging |
0.97 |
R1769:Ascc3
|
UTSW |
10 |
50,576,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Ascc3
|
UTSW |
10 |
50,566,257 (GRCm39) |
missense |
probably benign |
0.00 |
R1855:Ascc3
|
UTSW |
10 |
50,494,018 (GRCm39) |
missense |
probably benign |
0.01 |
R1953:Ascc3
|
UTSW |
10 |
50,721,726 (GRCm39) |
missense |
probably benign |
|
R1976:Ascc3
|
UTSW |
10 |
50,525,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R2004:Ascc3
|
UTSW |
10 |
50,493,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Ascc3
|
UTSW |
10 |
50,525,908 (GRCm39) |
missense |
probably damaging |
0.99 |
R2017:Ascc3
|
UTSW |
10 |
50,566,307 (GRCm39) |
missense |
probably benign |
0.00 |
R2040:Ascc3
|
UTSW |
10 |
50,604,227 (GRCm39) |
missense |
probably benign |
|
R2043:Ascc3
|
UTSW |
10 |
50,576,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Ascc3
|
UTSW |
10 |
50,597,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R2226:Ascc3
|
UTSW |
10 |
50,630,148 (GRCm39) |
missense |
probably benign |
0.07 |
R2310:Ascc3
|
UTSW |
10 |
50,624,988 (GRCm39) |
missense |
probably benign |
0.15 |
R2405:Ascc3
|
UTSW |
10 |
50,607,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R2424:Ascc3
|
UTSW |
10 |
50,494,297 (GRCm39) |
missense |
probably benign |
0.14 |
R3410:Ascc3
|
UTSW |
10 |
50,576,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R3617:Ascc3
|
UTSW |
10 |
50,494,281 (GRCm39) |
missense |
probably benign |
0.00 |
R3771:Ascc3
|
UTSW |
10 |
50,596,814 (GRCm39) |
splice site |
probably benign |
|
R3783:Ascc3
|
UTSW |
10 |
50,604,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R3891:Ascc3
|
UTSW |
10 |
50,718,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R3892:Ascc3
|
UTSW |
10 |
50,718,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R4435:Ascc3
|
UTSW |
10 |
50,597,981 (GRCm39) |
missense |
probably benign |
0.14 |
R4509:Ascc3
|
UTSW |
10 |
50,718,339 (GRCm39) |
missense |
probably benign |
0.00 |
R4520:Ascc3
|
UTSW |
10 |
50,536,766 (GRCm39) |
missense |
probably benign |
|
R4521:Ascc3
|
UTSW |
10 |
50,536,766 (GRCm39) |
missense |
probably benign |
|
R4522:Ascc3
|
UTSW |
10 |
50,536,766 (GRCm39) |
missense |
probably benign |
|
R4524:Ascc3
|
UTSW |
10 |
50,536,766 (GRCm39) |
missense |
probably benign |
|
R4581:Ascc3
|
UTSW |
10 |
50,587,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Ascc3
|
UTSW |
10 |
50,596,760 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4704:Ascc3
|
UTSW |
10 |
50,535,110 (GRCm39) |
missense |
probably benign |
0.02 |
R4768:Ascc3
|
UTSW |
10 |
50,576,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Ascc3
|
UTSW |
10 |
50,589,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4906:Ascc3
|
UTSW |
10 |
50,625,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5001:Ascc3
|
UTSW |
10 |
50,699,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Ascc3
|
UTSW |
10 |
50,514,059 (GRCm39) |
missense |
probably damaging |
0.99 |
R5263:Ascc3
|
UTSW |
10 |
50,592,757 (GRCm39) |
missense |
probably benign |
0.00 |
R5302:Ascc3
|
UTSW |
10 |
50,583,873 (GRCm39) |
missense |
probably benign |
0.09 |
R5436:Ascc3
|
UTSW |
10 |
50,535,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R5455:Ascc3
|
UTSW |
10 |
50,725,679 (GRCm39) |
missense |
probably benign |
0.06 |
R5474:Ascc3
|
UTSW |
10 |
50,725,634 (GRCm39) |
missense |
probably benign |
0.25 |
R5744:Ascc3
|
UTSW |
10 |
50,586,977 (GRCm39) |
missense |
probably benign |
|
R5781:Ascc3
|
UTSW |
10 |
50,514,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R5850:Ascc3
|
UTSW |
10 |
50,587,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R5867:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R5868:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R5869:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R6031:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R6031:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R6032:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R6032:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R6109:Ascc3
|
UTSW |
10 |
50,525,343 (GRCm39) |
missense |
probably benign |
0.37 |
R6122:Ascc3
|
UTSW |
10 |
50,494,021 (GRCm39) |
missense |
probably benign |
|
R6128:Ascc3
|
UTSW |
10 |
50,526,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R6351:Ascc3
|
UTSW |
10 |
50,596,769 (GRCm39) |
missense |
probably damaging |
0.99 |
R6368:Ascc3
|
UTSW |
10 |
50,576,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6369:Ascc3
|
UTSW |
10 |
50,576,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6409:Ascc3
|
UTSW |
10 |
50,721,676 (GRCm39) |
missense |
probably benign |
0.09 |
R6472:Ascc3
|
UTSW |
10 |
50,596,783 (GRCm39) |
missense |
probably benign |
0.03 |
R6474:Ascc3
|
UTSW |
10 |
50,624,932 (GRCm39) |
missense |
probably benign |
0.01 |
R6480:Ascc3
|
UTSW |
10 |
50,587,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R6553:Ascc3
|
UTSW |
10 |
50,718,273 (GRCm39) |
missense |
probably benign |
0.05 |
R6572:Ascc3
|
UTSW |
10 |
50,566,343 (GRCm39) |
nonsense |
probably null |
|
R6585:Ascc3
|
UTSW |
10 |
50,718,273 (GRCm39) |
missense |
probably benign |
0.05 |
R6656:Ascc3
|
UTSW |
10 |
50,526,021 (GRCm39) |
nonsense |
probably null |
|
R6669:Ascc3
|
UTSW |
10 |
50,716,469 (GRCm39) |
missense |
probably benign |
|
R6675:Ascc3
|
UTSW |
10 |
50,626,659 (GRCm39) |
nonsense |
probably null |
|
R6790:Ascc3
|
UTSW |
10 |
50,521,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R6856:Ascc3
|
UTSW |
10 |
50,625,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R6862:Ascc3
|
UTSW |
10 |
50,725,742 (GRCm39) |
missense |
probably null |
0.51 |
R6919:Ascc3
|
UTSW |
10 |
50,521,849 (GRCm39) |
nonsense |
probably null |
|
R6936:Ascc3
|
UTSW |
10 |
50,606,057 (GRCm39) |
missense |
probably damaging |
0.98 |
R6953:Ascc3
|
UTSW |
10 |
50,521,762 (GRCm39) |
missense |
probably benign |
0.00 |
R6957:Ascc3
|
UTSW |
10 |
50,604,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Ascc3
|
UTSW |
10 |
50,592,725 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7050:Ascc3
|
UTSW |
10 |
50,716,446 (GRCm39) |
missense |
probably benign |
0.43 |
R7358:Ascc3
|
UTSW |
10 |
50,590,448 (GRCm39) |
nonsense |
probably null |
|
R7479:Ascc3
|
UTSW |
10 |
50,525,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R7538:Ascc3
|
UTSW |
10 |
50,721,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R7838:Ascc3
|
UTSW |
10 |
50,604,393 (GRCm39) |
missense |
probably benign |
0.04 |
R8021:Ascc3
|
UTSW |
10 |
50,607,744 (GRCm39) |
missense |
probably benign |
0.02 |
R8134:Ascc3
|
UTSW |
10 |
50,643,554 (GRCm39) |
missense |
probably benign |
0.02 |
R8252:Ascc3
|
UTSW |
10 |
50,518,706 (GRCm39) |
missense |
probably benign |
|
R8348:Ascc3
|
UTSW |
10 |
50,494,173 (GRCm39) |
missense |
probably benign |
|
R8351:Ascc3
|
UTSW |
10 |
50,725,693 (GRCm39) |
missense |
probably benign |
|
R8356:Ascc3
|
UTSW |
10 |
50,526,003 (GRCm39) |
missense |
probably benign |
0.38 |
R8362:Ascc3
|
UTSW |
10 |
50,518,692 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8395:Ascc3
|
UTSW |
10 |
50,525,400 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8448:Ascc3
|
UTSW |
10 |
50,494,173 (GRCm39) |
missense |
probably benign |
|
R8957:Ascc3
|
UTSW |
10 |
50,576,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Ascc3
|
UTSW |
10 |
50,718,276 (GRCm39) |
missense |
probably benign |
|
R9133:Ascc3
|
UTSW |
10 |
50,630,175 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9200:Ascc3
|
UTSW |
10 |
50,521,787 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9328:Ascc3
|
UTSW |
10 |
50,535,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Ascc3
|
UTSW |
10 |
50,608,858 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9412:Ascc3
|
UTSW |
10 |
50,525,230 (GRCm39) |
missense |
probably benign |
0.00 |
R9576:Ascc3
|
UTSW |
10 |
50,494,254 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9796:Ascc3
|
UTSW |
10 |
50,608,801 (GRCm39) |
nonsense |
probably null |
|
X0021:Ascc3
|
UTSW |
10 |
50,576,686 (GRCm39) |
missense |
possibly damaging |
0.88 |
X0025:Ascc3
|
UTSW |
10 |
50,526,692 (GRCm39) |
missense |
probably benign |
0.00 |
X0026:Ascc3
|
UTSW |
10 |
50,608,574 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ascc3
|
UTSW |
10 |
50,594,517 (GRCm39) |
missense |
probably benign |
|
|