Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
A |
G |
1: 130,670,428 (GRCm39) |
S217G |
probably benign |
Het |
Adrb3 |
C |
A |
8: 27,717,591 (GRCm39) |
R286L |
probably damaging |
Het |
Akap11 |
T |
A |
14: 78,749,306 (GRCm39) |
D1027V |
probably benign |
Het |
Ank3 |
A |
T |
10: 69,733,913 (GRCm39) |
I726F |
probably damaging |
Het |
Ankmy2 |
T |
A |
12: 36,215,930 (GRCm39) |
D43E |
possibly damaging |
Het |
Ankrd34b |
A |
G |
13: 92,576,064 (GRCm39) |
D432G |
probably damaging |
Het |
Ano3 |
A |
C |
2: 110,715,217 (GRCm39) |
S74A |
probably benign |
Het |
B4galnt4 |
T |
A |
7: 140,650,439 (GRCm39) |
S769T |
probably damaging |
Het |
Bicral |
T |
A |
17: 47,136,104 (GRCm39) |
T369S |
probably benign |
Het |
Blm |
A |
G |
7: 80,147,166 (GRCm39) |
L738P |
probably damaging |
Het |
Bpifb3 |
A |
G |
2: 153,767,760 (GRCm39) |
T278A |
probably benign |
Het |
Bpifb5 |
A |
G |
2: 154,069,122 (GRCm39) |
|
probably benign |
Het |
Brd8 |
G |
C |
18: 34,743,527 (GRCm39) |
P266R |
probably damaging |
Het |
Btaf1 |
A |
T |
19: 36,957,983 (GRCm39) |
M587L |
probably benign |
Het |
Casz1 |
C |
G |
4: 149,027,668 (GRCm39) |
T1015S |
probably damaging |
Het |
Cdh23 |
A |
G |
10: 60,272,597 (GRCm39) |
I524T |
possibly damaging |
Het |
Celsr3 |
T |
C |
9: 108,713,037 (GRCm39) |
V1825A |
probably benign |
Het |
Cenpf |
A |
G |
1: 189,416,013 (GRCm39) |
L104P |
probably damaging |
Het |
Clasp1 |
G |
T |
1: 118,528,315 (GRCm39) |
|
probably null |
Het |
Coprs |
A |
G |
8: 13,935,112 (GRCm39) |
W148R |
probably damaging |
Het |
Cpne1 |
A |
G |
2: 155,920,302 (GRCm39) |
S168P |
probably damaging |
Het |
Cpxm2 |
T |
C |
7: 131,661,563 (GRCm39) |
Y408C |
probably damaging |
Het |
Ctnna3 |
A |
G |
10: 63,339,886 (GRCm39) |
E24G |
possibly damaging |
Het |
Cubn |
T |
A |
2: 13,327,813 (GRCm39) |
S2671C |
probably damaging |
Het |
Cyp4f39 |
T |
A |
17: 32,702,298 (GRCm39) |
F265Y |
probably damaging |
Het |
Dgkq |
C |
A |
5: 108,808,461 (GRCm39) |
R34L |
probably benign |
Het |
Dnajc7 |
C |
T |
11: 100,490,139 (GRCm39) |
|
probably benign |
Het |
Eml6 |
T |
G |
11: 29,781,136 (GRCm39) |
D632A |
probably damaging |
Het |
Fbxl18 |
G |
A |
5: 142,871,978 (GRCm39) |
A419V |
probably damaging |
Het |
Fbxw22 |
A |
T |
9: 109,214,179 (GRCm39) |
C212* |
probably null |
Het |
Ffar2 |
A |
G |
7: 30,518,839 (GRCm39) |
|
probably null |
Het |
Fga |
A |
T |
3: 82,940,028 (GRCm39) |
T561S |
probably damaging |
Het |
Gal3st1 |
A |
G |
11: 3,948,231 (GRCm39) |
Y146C |
probably damaging |
Het |
Gapvd1 |
A |
T |
2: 34,596,033 (GRCm39) |
H788Q |
probably damaging |
Het |
Gimap7 |
G |
A |
6: 48,700,449 (GRCm39) |
V12I |
possibly damaging |
Het |
Gli2 |
C |
A |
1: 118,929,779 (GRCm39) |
A43S |
possibly damaging |
Het |
Gm15446 |
T |
C |
5: 110,090,419 (GRCm39) |
F224L |
probably damaging |
Het |
Gm21738 |
C |
T |
14: 19,418,824 (GRCm38) |
V35I |
possibly damaging |
Het |
Grhl1 |
T |
C |
12: 24,636,155 (GRCm39) |
|
probably benign |
Het |
Grk6 |
T |
C |
13: 55,598,086 (GRCm39) |
Y53H |
probably damaging |
Het |
Hcar1 |
C |
T |
5: 124,017,328 (GRCm39) |
R121K |
probably damaging |
Het |
Hmcn1 |
A |
C |
1: 150,596,446 (GRCm39) |
S1797A |
probably damaging |
Het |
Hsd17b7 |
A |
T |
1: 169,783,562 (GRCm39) |
L282Q |
possibly damaging |
Het |
Irs1 |
TTCTCTGAGTGGCCACAGCGTCT |
TTCT |
1: 82,267,574 (GRCm39) |
|
probably null |
Het |
Kif1b |
C |
T |
4: 149,272,089 (GRCm39) |
V1571I |
probably benign |
Het |
Lpl |
T |
A |
8: 69,349,271 (GRCm39) |
C266S |
probably damaging |
Het |
Mag |
G |
A |
7: 30,608,476 (GRCm39) |
H213Y |
probably benign |
Het |
Mansc4 |
T |
G |
6: 146,976,688 (GRCm39) |
R309S |
probably benign |
Het |
Mlh3 |
A |
G |
12: 85,284,287 (GRCm39) |
|
probably null |
Het |
Mndal |
G |
A |
1: 173,687,933 (GRCm39) |
|
probably benign |
Het |
Mrgpra2b |
T |
A |
7: 47,113,742 (GRCm39) |
E330V |
probably damaging |
Het |
Myh3 |
A |
G |
11: 66,984,005 (GRCm39) |
I990V |
probably benign |
Het |
Myoz2 |
A |
T |
3: 122,819,765 (GRCm39) |
S65T |
probably damaging |
Het |
Naa16 |
T |
C |
14: 79,593,183 (GRCm39) |
E463G |
possibly damaging |
Het |
Nadsyn1 |
A |
G |
7: 143,351,581 (GRCm39) |
F684S |
probably damaging |
Het |
Notch1 |
T |
C |
2: 26,371,591 (GRCm39) |
E286G |
possibly damaging |
Het |
Nynrin |
A |
T |
14: 56,100,950 (GRCm39) |
I247L |
probably benign |
Het |
Oprm1 |
A |
G |
10: 6,739,035 (GRCm39) |
H54R |
probably benign |
Het |
Or10g6 |
T |
A |
9: 39,934,151 (GRCm39) |
I154N |
possibly damaging |
Het |
Or2n1d |
C |
T |
17: 38,646,860 (GRCm39) |
P271S |
probably damaging |
Het |
Or51a43 |
T |
C |
7: 103,717,336 (GRCm39) |
I301V |
probably null |
Het |
P4hb |
C |
T |
11: 120,452,992 (GRCm39) |
D483N |
probably benign |
Het |
Pak1 |
T |
C |
7: 97,520,787 (GRCm39) |
S149P |
probably benign |
Het |
Pars2 |
T |
C |
4: 106,510,913 (GRCm39) |
F232L |
possibly damaging |
Het |
Pih1d2 |
A |
G |
9: 50,532,245 (GRCm39) |
M88V |
possibly damaging |
Het |
Pms1 |
A |
T |
1: 53,246,392 (GRCm39) |
N382K |
probably benign |
Het |
Pnliprp2 |
G |
T |
19: 58,751,821 (GRCm39) |
V189L |
probably benign |
Het |
Pole |
G |
A |
5: 110,471,530 (GRCm39) |
V1425M |
possibly damaging |
Het |
Pot1b |
T |
A |
17: 55,961,805 (GRCm39) |
Q591L |
probably benign |
Het |
Ppp1r9a |
C |
T |
6: 4,906,348 (GRCm39) |
T301M |
possibly damaging |
Het |
Psg21 |
T |
C |
7: 18,384,741 (GRCm39) |
E335G |
probably benign |
Het |
Ptpru |
T |
A |
4: 131,497,066 (GRCm39) |
M1416L |
probably benign |
Het |
Pxn |
T |
C |
5: 115,683,049 (GRCm39) |
V117A |
probably damaging |
Het |
Qsox1 |
C |
T |
1: 155,688,385 (GRCm39) |
R54H |
possibly damaging |
Het |
Rad1 |
A |
G |
15: 10,488,092 (GRCm39) |
E42G |
probably damaging |
Het |
Rpp14 |
A |
G |
14: 8,090,145 (GRCm38) |
Y23C |
probably benign |
Het |
Sdk2 |
C |
T |
11: 113,725,782 (GRCm39) |
V1156I |
probably benign |
Het |
Serpina3j |
G |
T |
12: 104,285,958 (GRCm39) |
R371L |
probably benign |
Het |
Serpinb9d |
T |
A |
13: 33,381,946 (GRCm39) |
|
probably null |
Het |
Sirt5 |
C |
T |
13: 43,524,267 (GRCm39) |
S13F |
possibly damaging |
Het |
Slc6a7 |
T |
A |
18: 61,134,470 (GRCm39) |
|
probably benign |
Het |
Slx4 |
A |
G |
16: 3,804,712 (GRCm39) |
S701P |
probably benign |
Het |
Snx29 |
A |
G |
16: 11,185,545 (GRCm39) |
T43A |
probably benign |
Het |
Speg |
T |
C |
1: 75,400,550 (GRCm39) |
V2570A |
probably benign |
Het |
Srrm4 |
T |
A |
5: 116,591,565 (GRCm39) |
|
probably benign |
Het |
Stk32a |
A |
G |
18: 43,394,381 (GRCm39) |
Y110C |
probably damaging |
Het |
Tbc1d31 |
G |
A |
15: 57,779,506 (GRCm39) |
G73E |
probably benign |
Het |
Thsd7a |
A |
T |
6: 12,555,434 (GRCm39) |
I150N |
possibly damaging |
Het |
Tjp1 |
A |
T |
7: 64,969,001 (GRCm39) |
D699E |
probably damaging |
Het |
Tmem143 |
A |
G |
7: 45,565,988 (GRCm39) |
D437G |
possibly damaging |
Het |
Tmem45a2 |
A |
G |
16: 56,867,447 (GRCm39) |
Y85H |
possibly damaging |
Het |
Tmem45b |
T |
A |
9: 31,340,383 (GRCm39) |
T7S |
probably damaging |
Het |
Tut4 |
T |
A |
4: 108,407,922 (GRCm39) |
V1397D |
probably damaging |
Het |
Ube4b |
A |
G |
4: 149,432,428 (GRCm39) |
L832P |
probably damaging |
Het |
Ugp2 |
G |
T |
11: 21,279,048 (GRCm39) |
F379L |
probably damaging |
Het |
Ugt3a1 |
A |
T |
15: 9,365,437 (GRCm39) |
D350V |
probably damaging |
Het |
Vmn2r8 |
T |
A |
5: 108,950,284 (GRCm39) |
T188S |
possibly damaging |
Het |
Vwa7 |
C |
G |
17: 35,236,088 (GRCm39) |
P14R |
probably benign |
Het |
Vwc2 |
C |
A |
11: 11,211,495 (GRCm39) |
T317K |
probably damaging |
Het |
Vwf |
A |
T |
6: 125,605,335 (GRCm39) |
Q906L |
probably benign |
Het |
Wdr49 |
A |
G |
3: 75,336,654 (GRCm39) |
V351A |
probably damaging |
Het |
Wdr7 |
A |
G |
18: 63,861,575 (GRCm39) |
S196G |
probably benign |
Het |
Xkr6 |
C |
A |
14: 64,035,745 (GRCm39) |
A26E |
unknown |
Het |
Zfp955b |
T |
C |
17: 33,524,427 (GRCm39) |
I47V |
probably benign |
Het |
|
Other mutations in Fry |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00327:Fry
|
APN |
5 |
150,263,869 (GRCm39) |
nonsense |
probably null |
|
IGL00328:Fry
|
APN |
5 |
150,263,869 (GRCm39) |
nonsense |
probably null |
|
IGL00841:Fry
|
APN |
5 |
150,346,189 (GRCm39) |
missense |
probably benign |
|
IGL00938:Fry
|
APN |
5 |
150,293,645 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01015:Fry
|
APN |
5 |
150,346,252 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01401:Fry
|
APN |
5 |
150,362,253 (GRCm39) |
missense |
probably benign |
|
IGL01616:Fry
|
APN |
5 |
150,323,064 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01616:Fry
|
APN |
5 |
150,362,276 (GRCm39) |
splice site |
probably null |
|
IGL01748:Fry
|
APN |
5 |
150,269,116 (GRCm39) |
splice site |
probably benign |
|
IGL01965:Fry
|
APN |
5 |
150,305,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02030:Fry
|
APN |
5 |
150,395,083 (GRCm39) |
splice site |
probably benign |
|
IGL02079:Fry
|
APN |
5 |
150,323,089 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02087:Fry
|
APN |
5 |
150,327,059 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02113:Fry
|
APN |
5 |
150,323,070 (GRCm39) |
missense |
probably benign |
|
IGL02209:Fry
|
APN |
5 |
150,360,491 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02250:Fry
|
APN |
5 |
150,326,899 (GRCm39) |
splice site |
probably benign |
|
IGL02265:Fry
|
APN |
5 |
150,360,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02486:Fry
|
APN |
5 |
150,414,642 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02552:Fry
|
APN |
5 |
150,304,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02881:Fry
|
APN |
5 |
150,282,516 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03008:Fry
|
APN |
5 |
150,269,021 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03140:Fry
|
APN |
5 |
150,419,166 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03171:Fry
|
APN |
5 |
150,304,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03389:Fry
|
APN |
5 |
150,317,696 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03404:Fry
|
APN |
5 |
150,249,633 (GRCm39) |
missense |
probably damaging |
1.00 |
Brook
|
UTSW |
5 |
150,249,597 (GRCm39) |
missense |
probably damaging |
1.00 |
haydn
|
UTSW |
5 |
150,341,929 (GRCm39) |
missense |
possibly damaging |
0.94 |
miracle
|
UTSW |
5 |
150,360,624 (GRCm39) |
missense |
probably damaging |
0.99 |
quickening
|
UTSW |
5 |
150,358,241 (GRCm39) |
missense |
probably damaging |
1.00 |
seasons
|
UTSW |
5 |
150,389,902 (GRCm39) |
missense |
probably benign |
0.06 |
Vivaldi
|
UTSW |
5 |
150,317,603 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0023:Fry
|
UTSW |
5 |
150,374,563 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0024:Fry
|
UTSW |
5 |
150,304,268 (GRCm39) |
missense |
probably benign |
0.03 |
R0030:Fry
|
UTSW |
5 |
150,296,034 (GRCm39) |
nonsense |
probably null |
|
R0053:Fry
|
UTSW |
5 |
150,384,842 (GRCm39) |
splice site |
probably benign |
|
R0089:Fry
|
UTSW |
5 |
150,263,892 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0212:Fry
|
UTSW |
5 |
150,419,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R0241:Fry
|
UTSW |
5 |
150,183,811 (GRCm39) |
intron |
probably benign |
|
R0265:Fry
|
UTSW |
5 |
150,358,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R0317:Fry
|
UTSW |
5 |
150,394,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R0532:Fry
|
UTSW |
5 |
150,402,226 (GRCm39) |
splice site |
probably benign |
|
R0532:Fry
|
UTSW |
5 |
150,357,172 (GRCm39) |
unclassified |
probably benign |
|
R0599:Fry
|
UTSW |
5 |
150,360,624 (GRCm39) |
missense |
probably damaging |
0.99 |
R0631:Fry
|
UTSW |
5 |
150,419,817 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0723:Fry
|
UTSW |
5 |
150,419,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Fry
|
UTSW |
5 |
150,326,897 (GRCm39) |
splice site |
probably benign |
|
R0790:Fry
|
UTSW |
5 |
150,389,902 (GRCm39) |
missense |
probably benign |
0.06 |
R0928:Fry
|
UTSW |
5 |
150,360,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R1104:Fry
|
UTSW |
5 |
150,419,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1144:Fry
|
UTSW |
5 |
150,341,929 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1172:Fry
|
UTSW |
5 |
150,404,959 (GRCm39) |
nonsense |
probably null |
|
R1312:Fry
|
UTSW |
5 |
150,326,897 (GRCm39) |
splice site |
probably benign |
|
R1347:Fry
|
UTSW |
5 |
150,419,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R1347:Fry
|
UTSW |
5 |
150,419,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R1437:Fry
|
UTSW |
5 |
150,233,890 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1458:Fry
|
UTSW |
5 |
150,304,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Fry
|
UTSW |
5 |
150,328,431 (GRCm39) |
missense |
probably benign |
0.13 |
R1692:Fry
|
UTSW |
5 |
150,293,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Fry
|
UTSW |
5 |
150,360,174 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1875:Fry
|
UTSW |
5 |
150,249,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R1881:Fry
|
UTSW |
5 |
150,401,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R1884:Fry
|
UTSW |
5 |
150,326,985 (GRCm39) |
missense |
probably benign |
0.00 |
R1929:Fry
|
UTSW |
5 |
150,324,389 (GRCm39) |
missense |
probably null |
0.02 |
R2066:Fry
|
UTSW |
5 |
150,293,584 (GRCm39) |
splice site |
probably benign |
|
R2270:Fry
|
UTSW |
5 |
150,324,389 (GRCm39) |
missense |
probably null |
0.02 |
R2356:Fry
|
UTSW |
5 |
150,394,897 (GRCm39) |
missense |
probably benign |
|
R3720:Fry
|
UTSW |
5 |
150,378,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Fry
|
UTSW |
5 |
150,321,663 (GRCm39) |
missense |
probably damaging |
0.96 |
R3824:Fry
|
UTSW |
5 |
150,419,884 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3902:Fry
|
UTSW |
5 |
150,269,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Fry
|
UTSW |
5 |
150,336,814 (GRCm39) |
missense |
probably benign |
|
R4250:Fry
|
UTSW |
5 |
150,233,825 (GRCm39) |
missense |
probably damaging |
0.99 |
R4332:Fry
|
UTSW |
5 |
150,305,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R4495:Fry
|
UTSW |
5 |
150,233,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Fry
|
UTSW |
5 |
150,309,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R4682:Fry
|
UTSW |
5 |
150,346,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Fry
|
UTSW |
5 |
150,309,472 (GRCm39) |
missense |
|
|
R4733:Fry
|
UTSW |
5 |
150,309,472 (GRCm39) |
missense |
|
|
R4755:Fry
|
UTSW |
5 |
150,321,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R4788:Fry
|
UTSW |
5 |
150,323,101 (GRCm39) |
missense |
probably benign |
0.00 |
R4803:Fry
|
UTSW |
5 |
150,322,998 (GRCm39) |
missense |
probably benign |
0.31 |
R4858:Fry
|
UTSW |
5 |
150,325,108 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4872:Fry
|
UTSW |
5 |
150,317,704 (GRCm39) |
critical splice donor site |
probably null |
|
R4902:Fry
|
UTSW |
5 |
150,419,168 (GRCm39) |
missense |
probably benign |
0.43 |
R4915:Fry
|
UTSW |
5 |
150,402,328 (GRCm39) |
missense |
probably benign |
0.30 |
R4938:Fry
|
UTSW |
5 |
150,401,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4983:Fry
|
UTSW |
5 |
150,321,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Fry
|
UTSW |
5 |
150,357,069 (GRCm39) |
missense |
probably benign |
0.16 |
R5040:Fry
|
UTSW |
5 |
150,312,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R5145:Fry
|
UTSW |
5 |
150,293,689 (GRCm39) |
missense |
probably damaging |
0.98 |
R5170:Fry
|
UTSW |
5 |
150,353,319 (GRCm39) |
missense |
probably benign |
0.03 |
R5233:Fry
|
UTSW |
5 |
150,393,185 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5428:Fry
|
UTSW |
5 |
150,328,824 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5468:Fry
|
UTSW |
5 |
150,323,053 (GRCm39) |
missense |
probably benign |
0.44 |
R5481:Fry
|
UTSW |
5 |
150,183,784 (GRCm39) |
missense |
probably benign |
0.01 |
R5494:Fry
|
UTSW |
5 |
150,314,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R5538:Fry
|
UTSW |
5 |
150,419,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R5638:Fry
|
UTSW |
5 |
150,282,546 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5645:Fry
|
UTSW |
5 |
150,304,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5716:Fry
|
UTSW |
5 |
150,293,686 (GRCm39) |
nonsense |
probably null |
|
R5812:Fry
|
UTSW |
5 |
150,323,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R5813:Fry
|
UTSW |
5 |
150,323,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R5873:Fry
|
UTSW |
5 |
150,302,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Fry
|
UTSW |
5 |
150,314,265 (GRCm39) |
intron |
probably benign |
|
R6037:Fry
|
UTSW |
5 |
150,351,644 (GRCm39) |
missense |
probably benign |
0.03 |
R6037:Fry
|
UTSW |
5 |
150,351,644 (GRCm39) |
missense |
probably benign |
0.03 |
R6158:Fry
|
UTSW |
5 |
150,378,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Fry
|
UTSW |
5 |
150,377,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R6481:Fry
|
UTSW |
5 |
150,309,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R6562:Fry
|
UTSW |
5 |
150,249,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R6676:Fry
|
UTSW |
5 |
150,304,387 (GRCm39) |
missense |
probably benign |
0.22 |
R6717:Fry
|
UTSW |
5 |
150,419,777 (GRCm39) |
missense |
probably benign |
0.00 |
R6828:Fry
|
UTSW |
5 |
150,389,911 (GRCm39) |
splice site |
probably null |
|
R6874:Fry
|
UTSW |
5 |
150,360,768 (GRCm39) |
missense |
probably benign |
0.00 |
R6930:Fry
|
UTSW |
5 |
150,351,695 (GRCm39) |
missense |
probably benign |
0.00 |
R6963:Fry
|
UTSW |
5 |
150,381,309 (GRCm39) |
missense |
probably benign |
0.17 |
R6965:Fry
|
UTSW |
5 |
150,339,685 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7051:Fry
|
UTSW |
5 |
150,318,634 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7085:Fry
|
UTSW |
5 |
150,362,214 (GRCm39) |
missense |
probably benign |
0.02 |
R7108:Fry
|
UTSW |
5 |
150,414,555 (GRCm39) |
missense |
|
|
R7108:Fry
|
UTSW |
5 |
150,319,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R7115:Fry
|
UTSW |
5 |
150,309,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7116:Fry
|
UTSW |
5 |
150,319,334 (GRCm39) |
critical splice donor site |
probably null |
|
R7197:Fry
|
UTSW |
5 |
150,393,232 (GRCm39) |
missense |
|
|
R7256:Fry
|
UTSW |
5 |
150,390,251 (GRCm39) |
missense |
|
|
R7318:Fry
|
UTSW |
5 |
150,360,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R7323:Fry
|
UTSW |
5 |
150,419,814 (GRCm39) |
missense |
|
|
R7358:Fry
|
UTSW |
5 |
150,339,788 (GRCm39) |
missense |
probably benign |
|
R7361:Fry
|
UTSW |
5 |
150,360,312 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7395:Fry
|
UTSW |
5 |
150,304,348 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7487:Fry
|
UTSW |
5 |
150,338,039 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7491:Fry
|
UTSW |
5 |
150,389,791 (GRCm39) |
missense |
|
|
R7574:Fry
|
UTSW |
5 |
150,304,359 (GRCm39) |
missense |
probably benign |
0.00 |
R7582:Fry
|
UTSW |
5 |
150,419,847 (GRCm39) |
missense |
|
|
R7586:Fry
|
UTSW |
5 |
150,349,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7650:Fry
|
UTSW |
5 |
150,336,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Fry
|
UTSW |
5 |
150,328,792 (GRCm39) |
missense |
probably damaging |
0.98 |
R7700:Fry
|
UTSW |
5 |
150,328,792 (GRCm39) |
missense |
probably damaging |
0.98 |
R7972:Fry
|
UTSW |
5 |
150,233,861 (GRCm39) |
missense |
probably benign |
0.05 |
R8058:Fry
|
UTSW |
5 |
150,419,232 (GRCm39) |
missense |
|
|
R8070:Fry
|
UTSW |
5 |
150,401,472 (GRCm39) |
missense |
|
|
R8159:Fry
|
UTSW |
5 |
150,322,998 (GRCm39) |
missense |
probably benign |
0.31 |
R8202:Fry
|
UTSW |
5 |
150,355,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R8261:Fry
|
UTSW |
5 |
150,369,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R8279:Fry
|
UTSW |
5 |
150,419,726 (GRCm39) |
missense |
|
|
R8338:Fry
|
UTSW |
5 |
150,282,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R8370:Fry
|
UTSW |
5 |
150,319,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R8673:Fry
|
UTSW |
5 |
150,318,576 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8786:Fry
|
UTSW |
5 |
150,317,501 (GRCm39) |
missense |
probably benign |
0.00 |
R8815:Fry
|
UTSW |
5 |
150,317,603 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8847:Fry
|
UTSW |
5 |
150,309,472 (GRCm39) |
missense |
|
|
R9023:Fry
|
UTSW |
5 |
150,360,768 (GRCm39) |
missense |
probably benign |
0.00 |
R9025:Fry
|
UTSW |
5 |
150,219,273 (GRCm39) |
intron |
probably benign |
|
R9125:Fry
|
UTSW |
5 |
150,269,525 (GRCm39) |
missense |
probably damaging |
0.97 |
R9172:Fry
|
UTSW |
5 |
150,336,793 (GRCm39) |
missense |
probably benign |
|
R9262:Fry
|
UTSW |
5 |
150,305,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R9263:Fry
|
UTSW |
5 |
150,322,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R9293:Fry
|
UTSW |
5 |
150,419,297 (GRCm39) |
missense |
|
|
R9368:Fry
|
UTSW |
5 |
150,401,403 (GRCm39) |
missense |
|
|
R9401:Fry
|
UTSW |
5 |
150,302,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Fry
|
UTSW |
5 |
150,360,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Fry
|
UTSW |
5 |
150,357,161 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9420:Fry
|
UTSW |
5 |
150,356,994 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9557:Fry
|
UTSW |
5 |
150,389,781 (GRCm39) |
missense |
|
|
R9647:Fry
|
UTSW |
5 |
150,292,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9650:Fry
|
UTSW |
5 |
150,369,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Fry
|
UTSW |
5 |
150,362,251 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9664:Fry
|
UTSW |
5 |
150,282,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R9668:Fry
|
UTSW |
5 |
150,282,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R9732:Fry
|
UTSW |
5 |
150,328,758 (GRCm39) |
missense |
probably benign |
0.00 |
R9773:Fry
|
UTSW |
5 |
150,322,728 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fry
|
UTSW |
5 |
150,233,902 (GRCm39) |
missense |
possibly damaging |
0.80 |
|