Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aarsd1 |
T |
C |
11: 101,301,986 (GRCm39) |
I196V |
probably benign |
Het |
Aass |
T |
A |
6: 23,075,855 (GRCm39) |
K761* |
probably null |
Het |
Abca13 |
A |
G |
11: 9,242,306 (GRCm39) |
T1390A |
possibly damaging |
Het |
Abhd16a |
T |
C |
17: 35,315,582 (GRCm39) |
|
probably null |
Het |
Acad11 |
C |
T |
9: 103,972,764 (GRCm39) |
Q486* |
probably null |
Het |
Actl9 |
T |
C |
17: 33,652,909 (GRCm39) |
L323P |
probably benign |
Het |
Adam12 |
T |
A |
7: 133,518,191 (GRCm39) |
I650F |
possibly damaging |
Het |
Adgre4 |
A |
T |
17: 56,091,971 (GRCm39) |
D77V |
probably damaging |
Het |
Ankrd26 |
A |
G |
6: 118,483,446 (GRCm39) |
F1586S |
possibly damaging |
Het |
Anpep |
T |
C |
7: 79,489,213 (GRCm39) |
T320A |
probably benign |
Het |
Arl15 |
T |
A |
13: 114,104,261 (GRCm39) |
C133S |
probably benign |
Het |
Atf4 |
T |
A |
15: 80,141,618 (GRCm39) |
I336K |
probably damaging |
Het |
Atp7b |
A |
T |
8: 22,490,137 (GRCm39) |
S1044T |
probably benign |
Het |
Atp8b4 |
A |
G |
2: 126,256,213 (GRCm39) |
F249L |
probably damaging |
Het |
AU021092 |
G |
T |
16: 5,030,057 (GRCm39) |
N319K |
probably benign |
Het |
Bbs4 |
A |
G |
9: 59,230,802 (GRCm39) |
V440A |
probably benign |
Het |
Bpifb4 |
G |
T |
2: 153,792,305 (GRCm39) |
G450C |
probably damaging |
Het |
Cadm1 |
G |
A |
9: 47,730,120 (GRCm39) |
|
probably benign |
Het |
Ccser2 |
G |
A |
14: 36,660,654 (GRCm39) |
L500F |
probably damaging |
Het |
Cd22 |
T |
A |
7: 30,575,578 (GRCm39) |
I155F |
probably damaging |
Het |
Cdkl4 |
A |
T |
17: 80,851,081 (GRCm39) |
V207E |
probably damaging |
Het |
Cfap251 |
A |
G |
5: 123,460,676 (GRCm39) |
K1213E |
probably benign |
Het |
Cfap65 |
T |
C |
1: 74,958,067 (GRCm39) |
D947G |
probably damaging |
Het |
Cntn6 |
T |
C |
6: 104,781,321 (GRCm39) |
V397A |
probably benign |
Het |
Cpox |
T |
A |
16: 58,498,332 (GRCm39) |
Y388* |
probably null |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dda1 |
T |
A |
8: 71,926,454 (GRCm39) |
Y58N |
probably damaging |
Het |
Dennd4a |
C |
T |
9: 64,804,639 (GRCm39) |
T1326I |
possibly damaging |
Het |
Eps8l2 |
A |
T |
7: 140,937,173 (GRCm39) |
I338F |
probably damaging |
Het |
Fbxo42 |
A |
G |
4: 140,927,120 (GRCm39) |
T467A |
probably benign |
Het |
Flt4 |
T |
C |
11: 49,517,635 (GRCm39) |
F319S |
possibly damaging |
Het |
Fmn1 |
A |
T |
2: 113,414,416 (GRCm39) |
Y895F |
possibly damaging |
Het |
Gm6887 |
C |
A |
7: 42,114,517 (GRCm39) |
|
noncoding transcript |
Het |
Grid2 |
A |
G |
6: 64,642,899 (GRCm39) |
D887G |
probably benign |
Het |
Grm6 |
C |
T |
11: 50,753,837 (GRCm39) |
P714S |
probably damaging |
Het |
Gsto2 |
A |
G |
19: 47,873,095 (GRCm39) |
I157V |
probably benign |
Het |
Il15ra |
A |
G |
2: 11,723,156 (GRCm39) |
|
probably null |
Het |
Impg1 |
A |
G |
9: 80,221,682 (GRCm39) |
F713L |
probably benign |
Het |
Jag1 |
T |
A |
2: 136,936,376 (GRCm39) |
T373S |
probably benign |
Het |
Kcnh3 |
T |
A |
15: 99,139,826 (GRCm39) |
L904Q |
probably benign |
Het |
Kctd19 |
C |
A |
8: 106,117,061 (GRCm39) |
G356V |
possibly damaging |
Het |
Kdm5b |
T |
A |
1: 134,533,750 (GRCm39) |
|
probably benign |
Het |
Kif1a |
T |
C |
1: 93,006,557 (GRCm39) |
I37V |
probably damaging |
Het |
Lama5 |
G |
A |
2: 179,833,489 (GRCm39) |
R1508C |
probably damaging |
Het |
Lamb1 |
T |
A |
12: 31,316,847 (GRCm39) |
C65* |
probably null |
Het |
Lingo1 |
A |
G |
9: 56,527,542 (GRCm39) |
F349S |
probably damaging |
Het |
Loxl4 |
G |
A |
19: 42,596,052 (GRCm39) |
H147Y |
probably benign |
Het |
Lrrn4cl |
T |
A |
19: 8,829,419 (GRCm39) |
N132K |
probably damaging |
Het |
Med17 |
A |
T |
9: 15,181,656 (GRCm39) |
H31Q |
probably damaging |
Het |
Med23 |
A |
T |
10: 24,769,546 (GRCm39) |
L476F |
probably damaging |
Het |
Mgst1 |
A |
T |
6: 138,127,836 (GRCm39) |
D66V |
probably damaging |
Het |
Mroh2a |
T |
C |
1: 88,162,334 (GRCm39) |
|
probably null |
Het |
Mroh2a |
A |
C |
1: 88,169,340 (GRCm39) |
I672L |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,576,220 (GRCm39) |
|
probably benign |
Het |
Myo18a |
C |
T |
11: 77,708,491 (GRCm39) |
T30M |
probably damaging |
Het |
Ncapg2 |
G |
T |
12: 116,404,238 (GRCm39) |
R903L |
probably benign |
Het |
Nme1 |
A |
G |
11: 93,856,734 (GRCm39) |
I9T |
probably damaging |
Het |
Nmt2 |
T |
A |
2: 3,323,678 (GRCm39) |
I357N |
probably benign |
Het |
Nphp4 |
T |
C |
4: 152,581,116 (GRCm39) |
F100S |
probably damaging |
Het |
Oca2 |
C |
A |
7: 55,904,750 (GRCm39) |
T72K |
probably benign |
Het |
Or52e4 |
A |
T |
7: 104,706,086 (GRCm39) |
D211V |
probably damaging |
Het |
Or52e7 |
A |
T |
7: 104,684,798 (GRCm39) |
D131V |
probably damaging |
Het |
Or52z15 |
G |
A |
7: 103,332,269 (GRCm39) |
V105M |
probably damaging |
Het |
Or7h8 |
T |
C |
9: 20,123,921 (GRCm39) |
I92T |
probably damaging |
Het |
Or9s15 |
C |
A |
1: 92,525,160 (GRCm39) |
D306E |
probably benign |
Het |
Plce1 |
A |
T |
19: 38,713,451 (GRCm39) |
T1240S |
probably benign |
Het |
Plch1 |
A |
T |
3: 63,606,917 (GRCm39) |
|
probably null |
Het |
Plxna4 |
T |
C |
6: 32,493,623 (GRCm39) |
D331G |
probably damaging |
Het |
Ppp1r3a |
T |
C |
6: 14,718,992 (GRCm39) |
T641A |
probably benign |
Het |
Rab32 |
A |
G |
10: 10,426,598 (GRCm39) |
L116P |
probably benign |
Het |
Recql4 |
C |
T |
15: 76,592,785 (GRCm39) |
C302Y |
probably damaging |
Het |
Rorc |
G |
C |
3: 94,299,017 (GRCm39) |
E391Q |
probably null |
Het |
Saa4 |
A |
T |
7: 46,381,051 (GRCm39) |
F24I |
possibly damaging |
Het |
Sall1 |
T |
A |
8: 89,757,788 (GRCm39) |
K772M |
probably damaging |
Het |
Sdk1 |
T |
G |
5: 142,170,986 (GRCm39) |
L1950V |
probably damaging |
Het |
Sil1 |
T |
C |
18: 35,399,949 (GRCm39) |
E352G |
probably benign |
Het |
Slc26a3 |
C |
T |
12: 31,497,773 (GRCm39) |
P59L |
probably damaging |
Het |
Smco2 |
T |
C |
6: 146,763,440 (GRCm39) |
|
probably benign |
Het |
Sppl3 |
A |
G |
5: 115,241,372 (GRCm39) |
|
probably null |
Het |
St6gal2 |
T |
A |
17: 55,803,345 (GRCm39) |
V360D |
probably damaging |
Het |
Stard9 |
G |
A |
2: 120,536,194 (GRCm39) |
R345Q |
possibly damaging |
Het |
Susd4 |
T |
A |
1: 182,719,626 (GRCm39) |
Y414N |
probably damaging |
Het |
Tenm4 |
T |
C |
7: 96,544,556 (GRCm39) |
Y2191H |
probably damaging |
Het |
Tln2 |
A |
G |
9: 67,253,809 (GRCm39) |
V754A |
probably benign |
Het |
Tmem132c |
T |
A |
5: 127,641,560 (GRCm39) |
|
probably benign |
Het |
Tnn |
A |
T |
1: 159,975,338 (GRCm39) |
S30T |
possibly damaging |
Het |
Trpd52l3 |
G |
T |
19: 29,981,895 (GRCm39) |
V217F |
probably damaging |
Het |
Trpm1 |
G |
T |
7: 63,893,248 (GRCm39) |
L1033F |
probably damaging |
Het |
Tulp2 |
A |
G |
7: 45,167,348 (GRCm39) |
E182G |
probably damaging |
Het |
Ubr4 |
A |
G |
4: 139,198,647 (GRCm39) |
K4490R |
possibly damaging |
Het |
Usp17la |
A |
T |
7: 104,509,856 (GRCm39) |
R154* |
probably null |
Het |
Vmn2r17 |
T |
G |
5: 109,575,849 (GRCm39) |
M240R |
probably damaging |
Het |
Vmn2r22 |
T |
A |
6: 123,627,428 (GRCm39) |
N56I |
probably benign |
Het |
Zdhhc21 |
A |
T |
4: 82,738,571 (GRCm39) |
I206N |
possibly damaging |
Het |
Zfp148 |
T |
A |
16: 33,277,278 (GRCm39) |
D122E |
probably benign |
Het |
Zfp804a |
A |
T |
2: 82,086,926 (GRCm39) |
S252C |
probably damaging |
Het |
Zgrf1 |
C |
T |
3: 127,392,353 (GRCm39) |
T1291I |
probably benign |
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 |
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 |
R4937:Ascc3
|
UTSW |
10 |
50,699,894 (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 |
|
|