Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap11 |
T |
A |
14: 78,747,477 (GRCm39) |
I1637L |
possibly damaging |
Het |
Ankrd27 |
T |
C |
7: 35,315,265 (GRCm39) |
|
probably benign |
Het |
Anxa3 |
T |
C |
5: 96,978,349 (GRCm39) |
|
probably null |
Het |
Arfgef2 |
G |
C |
2: 166,707,679 (GRCm39) |
G1025A |
probably benign |
Het |
Arhgap21 |
T |
C |
2: 20,868,037 (GRCm39) |
I829V |
possibly damaging |
Het |
Arhgap42 |
T |
C |
9: 9,035,512 (GRCm39) |
M277V |
probably benign |
Het |
Cep112 |
A |
T |
11: 108,746,671 (GRCm39) |
R176S |
probably damaging |
Het |
Cnga1 |
C |
T |
5: 72,776,404 (GRCm39) |
V20I |
possibly damaging |
Het |
Cpped1 |
A |
C |
16: 11,712,745 (GRCm39) |
|
probably null |
Het |
Cr2 |
T |
C |
1: 194,839,676 (GRCm39) |
R960G |
possibly damaging |
Het |
Dbf4 |
T |
C |
5: 8,471,333 (GRCm39) |
N36S |
possibly damaging |
Het |
Dnah6 |
G |
A |
6: 73,090,564 (GRCm39) |
S2210L |
probably benign |
Het |
Dnajb12 |
C |
T |
10: 59,728,799 (GRCm39) |
T229I |
probably benign |
Het |
Dnajc28 |
G |
A |
16: 91,413,755 (GRCm39) |
T187M |
probably damaging |
Het |
Epb41l2 |
T |
C |
10: 25,364,842 (GRCm39) |
|
probably benign |
Het |
Fam178b |
A |
G |
1: 36,671,539 (GRCm39) |
L194P |
probably damaging |
Het |
Fam50b |
C |
T |
13: 34,930,823 (GRCm39) |
Q100* |
probably null |
Het |
Gimap9 |
A |
G |
6: 48,654,812 (GRCm39) |
H133R |
probably benign |
Het |
Gpbp1 |
A |
T |
13: 111,603,512 (GRCm39) |
|
probably null |
Het |
Gpr89 |
A |
G |
3: 96,804,743 (GRCm39) |
Y38H |
probably damaging |
Het |
Gsdmc3 |
T |
A |
15: 63,732,105 (GRCm39) |
Y307F |
probably benign |
Het |
H4c16 |
T |
A |
6: 136,781,299 (GRCm39) |
I27F |
probably damaging |
Het |
Hip1 |
C |
T |
5: 135,485,900 (GRCm39) |
R101K |
probably damaging |
Het |
Hsf4 |
G |
A |
8: 105,996,628 (GRCm39) |
D18N |
probably null |
Het |
Igfn1 |
T |
C |
1: 135,892,479 (GRCm39) |
K2214E |
probably damaging |
Het |
Itgal |
A |
T |
7: 126,927,919 (GRCm39) |
E1038V |
probably null |
Het |
Kank2 |
C |
A |
9: 21,681,080 (GRCm39) |
M816I |
probably damaging |
Het |
Kctd15 |
T |
C |
7: 34,344,366 (GRCm39) |
D95G |
possibly damaging |
Het |
Kif1a |
A |
T |
1: 92,996,199 (GRCm39) |
|
probably benign |
Het |
Lgi4 |
T |
G |
7: 30,760,037 (GRCm39) |
L78V |
probably damaging |
Het |
Lrrc7 |
A |
G |
3: 157,885,429 (GRCm39) |
F432L |
probably damaging |
Het |
Madd |
A |
T |
2: 90,974,028 (GRCm39) |
C1419S |
possibly damaging |
Het |
Nisch |
T |
C |
14: 30,898,803 (GRCm39) |
|
probably benign |
Het |
Or2h1b |
A |
T |
17: 37,462,145 (GRCm39) |
C239* |
probably null |
Het |
Osbpl2 |
G |
A |
2: 179,790,319 (GRCm39) |
G198S |
possibly damaging |
Het |
Pclo |
T |
A |
5: 14,764,287 (GRCm39) |
D4253E |
unknown |
Het |
Phactr1 |
A |
T |
13: 43,231,265 (GRCm39) |
S244C |
possibly damaging |
Het |
Pja2 |
T |
C |
17: 64,599,865 (GRCm39) |
S478G |
probably damaging |
Het |
Prex1 |
A |
T |
2: 166,419,875 (GRCm39) |
I79N |
probably benign |
Het |
Ptpn4 |
T |
C |
1: 119,612,321 (GRCm39) |
D24G |
probably damaging |
Het |
Rars2 |
T |
C |
4: 34,656,835 (GRCm39) |
S495P |
probably damaging |
Het |
Rhebl1 |
A |
T |
15: 98,776,167 (GRCm39) |
D162E |
probably benign |
Het |
Rhou |
T |
C |
8: 124,382,258 (GRCm39) |
V100A |
probably damaging |
Het |
Rpn2 |
A |
G |
2: 157,152,208 (GRCm39) |
T394A |
possibly damaging |
Het |
Ryr3 |
A |
T |
2: 112,479,664 (GRCm39) |
M4386K |
possibly damaging |
Het |
Scmh1 |
G |
T |
4: 120,340,869 (GRCm39) |
C185F |
probably damaging |
Het |
Sema3d |
A |
T |
5: 12,592,549 (GRCm39) |
Q326L |
possibly damaging |
Het |
Sis |
T |
A |
3: 72,821,934 (GRCm39) |
K1376* |
probably null |
Het |
Slc25a29 |
T |
C |
12: 108,792,852 (GRCm39) |
E242G |
probably benign |
Het |
Slc26a5 |
A |
G |
5: 22,028,545 (GRCm39) |
V304A |
probably benign |
Het |
Slc39a7 |
C |
T |
17: 34,250,241 (GRCm39) |
|
probably benign |
Het |
Slco1a4 |
A |
G |
6: 141,761,308 (GRCm39) |
V435A |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 75,974,240 (GRCm39) |
E1146G |
possibly damaging |
Het |
Tgm5 |
T |
A |
2: 120,879,304 (GRCm39) |
|
probably benign |
Het |
Tgm7 |
A |
G |
2: 120,929,045 (GRCm39) |
S284P |
probably damaging |
Het |
Tmem132d |
G |
A |
5: 127,872,987 (GRCm39) |
R541W |
probably damaging |
Het |
Tmem170 |
C |
A |
8: 112,596,349 (GRCm39) |
V59L |
probably benign |
Het |
Tpbgl |
G |
T |
7: 99,275,233 (GRCm39) |
A208E |
possibly damaging |
Het |
Ttc23l |
A |
G |
15: 10,523,678 (GRCm39) |
I347T |
possibly damaging |
Het |
Ulk1 |
T |
C |
5: 110,936,028 (GRCm39) |
E827G |
probably benign |
Het |
Vps13a |
A |
G |
19: 16,687,790 (GRCm39) |
V886A |
possibly damaging |
Het |
Wrn |
A |
T |
8: 33,814,584 (GRCm39) |
C44S |
probably benign |
Het |
Zscan22 |
T |
A |
7: 12,640,750 (GRCm39) |
C331* |
probably null |
Het |
|
Other mutations in Chd9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00420:Chd9
|
APN |
8 |
91,752,020 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL00547:Chd9
|
APN |
8 |
91,732,426 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00589:Chd9
|
APN |
8 |
91,742,474 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00640:Chd9
|
APN |
8 |
91,712,760 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00663:Chd9
|
APN |
8 |
91,710,118 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00852:Chd9
|
APN |
8 |
91,699,835 (GRCm39) |
missense |
probably benign |
0.29 |
IGL00908:Chd9
|
APN |
8 |
91,723,508 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00911:Chd9
|
APN |
8 |
91,778,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01068:Chd9
|
APN |
8 |
91,768,744 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01668:Chd9
|
APN |
8 |
91,753,404 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01873:Chd9
|
APN |
8 |
91,660,395 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01969:Chd9
|
APN |
8 |
91,760,138 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02105:Chd9
|
APN |
8 |
91,659,116 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02153:Chd9
|
APN |
8 |
91,683,122 (GRCm39) |
nonsense |
probably null |
|
IGL02164:Chd9
|
APN |
8 |
91,659,849 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02725:Chd9
|
APN |
8 |
91,778,312 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02755:Chd9
|
APN |
8 |
91,760,210 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02892:Chd9
|
APN |
8 |
91,703,543 (GRCm39) |
splice site |
probably benign |
|
IGL02897:Chd9
|
APN |
8 |
91,660,496 (GRCm39) |
splice site |
probably benign |
|
IGL03005:Chd9
|
APN |
8 |
91,738,075 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03062:Chd9
|
APN |
8 |
91,741,895 (GRCm39) |
splice site |
probably benign |
|
IGL03140:Chd9
|
APN |
8 |
91,768,856 (GRCm39) |
missense |
possibly damaging |
0.91 |
hovel
|
UTSW |
8 |
91,741,832 (GRCm39) |
missense |
probably benign |
0.19 |
shack
|
UTSW |
8 |
91,659,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R0056:Chd9
|
UTSW |
8 |
91,660,165 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0157:Chd9
|
UTSW |
8 |
91,735,464 (GRCm39) |
splice site |
probably null |
|
R0238:Chd9
|
UTSW |
8 |
91,659,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Chd9
|
UTSW |
8 |
91,659,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R0432:Chd9
|
UTSW |
8 |
91,721,078 (GRCm39) |
splice site |
probably benign |
|
R0454:Chd9
|
UTSW |
8 |
91,699,859 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0573:Chd9
|
UTSW |
8 |
91,725,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R0580:Chd9
|
UTSW |
8 |
91,721,191 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0604:Chd9
|
UTSW |
8 |
91,763,170 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0662:Chd9
|
UTSW |
8 |
91,704,304 (GRCm39) |
missense |
probably damaging |
0.99 |
R0825:Chd9
|
UTSW |
8 |
91,777,825 (GRCm39) |
missense |
probably benign |
0.06 |
R0945:Chd9
|
UTSW |
8 |
91,659,630 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0964:Chd9
|
UTSW |
8 |
91,741,832 (GRCm39) |
missense |
probably benign |
0.19 |
R0967:Chd9
|
UTSW |
8 |
91,716,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R1015:Chd9
|
UTSW |
8 |
91,659,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R1066:Chd9
|
UTSW |
8 |
91,712,764 (GRCm39) |
nonsense |
probably null |
|
R1244:Chd9
|
UTSW |
8 |
91,749,557 (GRCm39) |
missense |
probably damaging |
0.99 |
R1505:Chd9
|
UTSW |
8 |
91,733,123 (GRCm39) |
splice site |
probably null |
|
R1570:Chd9
|
UTSW |
8 |
91,763,170 (GRCm39) |
missense |
probably benign |
0.03 |
R1591:Chd9
|
UTSW |
8 |
91,710,166 (GRCm39) |
missense |
probably damaging |
0.97 |
R1624:Chd9
|
UTSW |
8 |
91,725,163 (GRCm39) |
missense |
probably benign |
0.17 |
R1626:Chd9
|
UTSW |
8 |
91,721,224 (GRCm39) |
missense |
probably benign |
0.00 |
R1632:Chd9
|
UTSW |
8 |
91,683,335 (GRCm39) |
nonsense |
probably null |
|
R1649:Chd9
|
UTSW |
8 |
91,659,229 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1664:Chd9
|
UTSW |
8 |
91,749,418 (GRCm39) |
splice site |
probably null |
|
R1668:Chd9
|
UTSW |
8 |
91,767,814 (GRCm39) |
missense |
probably damaging |
0.99 |
R1681:Chd9
|
UTSW |
8 |
91,699,763 (GRCm39) |
missense |
probably damaging |
0.98 |
R1695:Chd9
|
UTSW |
8 |
91,728,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R1714:Chd9
|
UTSW |
8 |
91,760,853 (GRCm39) |
utr 3 prime |
probably benign |
|
R1746:Chd9
|
UTSW |
8 |
91,737,326 (GRCm39) |
missense |
probably benign |
0.01 |
R1843:Chd9
|
UTSW |
8 |
91,737,422 (GRCm39) |
missense |
probably benign |
0.19 |
R1844:Chd9
|
UTSW |
8 |
91,683,323 (GRCm39) |
nonsense |
probably null |
|
R1941:Chd9
|
UTSW |
8 |
91,703,697 (GRCm39) |
critical splice donor site |
probably null |
|
R2022:Chd9
|
UTSW |
8 |
91,761,682 (GRCm39) |
missense |
probably benign |
0.17 |
R2027:Chd9
|
UTSW |
8 |
91,634,619 (GRCm39) |
unclassified |
probably benign |
|
R2098:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2099:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2100:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2101:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2224:Chd9
|
UTSW |
8 |
91,737,913 (GRCm39) |
missense |
probably benign |
0.04 |
R2278:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2316:Chd9
|
UTSW |
8 |
91,777,756 (GRCm39) |
missense |
probably damaging |
0.99 |
R2507:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2508:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2988:Chd9
|
UTSW |
8 |
91,757,088 (GRCm39) |
splice site |
probably null |
|
R3418:Chd9
|
UTSW |
8 |
91,763,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R3817:Chd9
|
UTSW |
8 |
91,710,893 (GRCm39) |
splice site |
probably benign |
|
R3923:Chd9
|
UTSW |
8 |
91,660,147 (GRCm39) |
missense |
probably benign |
0.16 |
R4001:Chd9
|
UTSW |
8 |
91,683,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R4003:Chd9
|
UTSW |
8 |
91,683,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R4006:Chd9
|
UTSW |
8 |
91,660,188 (GRCm39) |
missense |
probably benign |
0.12 |
R4013:Chd9
|
UTSW |
8 |
91,699,797 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4067:Chd9
|
UTSW |
8 |
91,750,202 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4108:Chd9
|
UTSW |
8 |
91,737,304 (GRCm39) |
missense |
probably benign |
0.04 |
R4125:Chd9
|
UTSW |
8 |
91,777,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R4126:Chd9
|
UTSW |
8 |
91,777,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R4452:Chd9
|
UTSW |
8 |
91,704,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R4463:Chd9
|
UTSW |
8 |
91,705,627 (GRCm39) |
missense |
probably benign |
0.01 |
R4478:Chd9
|
UTSW |
8 |
91,760,659 (GRCm39) |
utr 3 prime |
probably benign |
|
R4587:Chd9
|
UTSW |
8 |
91,763,134 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4628:Chd9
|
UTSW |
8 |
91,710,091 (GRCm39) |
missense |
probably benign |
0.05 |
R4667:Chd9
|
UTSW |
8 |
91,760,428 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4908:Chd9
|
UTSW |
8 |
91,741,877 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4912:Chd9
|
UTSW |
8 |
91,760,858 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4977:Chd9
|
UTSW |
8 |
91,760,336 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5016:Chd9
|
UTSW |
8 |
91,733,254 (GRCm39) |
nonsense |
probably null |
|
R5083:Chd9
|
UTSW |
8 |
91,711,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Chd9
|
UTSW |
8 |
91,704,147 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5090:Chd9
|
UTSW |
8 |
91,753,462 (GRCm39) |
nonsense |
probably null |
|
R5307:Chd9
|
UTSW |
8 |
91,723,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Chd9
|
UTSW |
8 |
91,778,132 (GRCm39) |
missense |
probably benign |
0.09 |
R5559:Chd9
|
UTSW |
8 |
91,742,553 (GRCm39) |
critical splice donor site |
probably null |
|
R5638:Chd9
|
UTSW |
8 |
91,738,078 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5640:Chd9
|
UTSW |
8 |
91,763,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R5793:Chd9
|
UTSW |
8 |
91,728,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R5827:Chd9
|
UTSW |
8 |
91,716,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5834:Chd9
|
UTSW |
8 |
91,723,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5875:Chd9
|
UTSW |
8 |
91,778,464 (GRCm39) |
missense |
probably damaging |
0.99 |
R6002:Chd9
|
UTSW |
8 |
91,705,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Chd9
|
UTSW |
8 |
91,761,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R6185:Chd9
|
UTSW |
8 |
91,775,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R6246:Chd9
|
UTSW |
8 |
91,659,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R6292:Chd9
|
UTSW |
8 |
91,659,550 (GRCm39) |
missense |
probably benign |
0.05 |
R6305:Chd9
|
UTSW |
8 |
91,757,174 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6348:Chd9
|
UTSW |
8 |
91,737,903 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6438:Chd9
|
UTSW |
8 |
91,725,149 (GRCm39) |
missense |
probably benign |
0.02 |
R6470:Chd9
|
UTSW |
8 |
91,659,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Chd9
|
UTSW |
8 |
91,778,182 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6902:Chd9
|
UTSW |
8 |
91,769,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R6908:Chd9
|
UTSW |
8 |
91,683,044 (GRCm39) |
missense |
probably benign |
0.02 |
R6929:Chd9
|
UTSW |
8 |
91,769,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R6969:Chd9
|
UTSW |
8 |
91,705,542 (GRCm39) |
missense |
probably benign |
0.34 |
R7043:Chd9
|
UTSW |
8 |
91,760,843 (GRCm39) |
utr 3 prime |
probably benign |
|
R7094:Chd9
|
UTSW |
8 |
91,716,189 (GRCm39) |
missense |
unknown |
|
R7126:Chd9
|
UTSW |
8 |
91,741,853 (GRCm39) |
missense |
unknown |
|
R7182:Chd9
|
UTSW |
8 |
91,733,250 (GRCm39) |
missense |
unknown |
|
R7219:Chd9
|
UTSW |
8 |
91,728,394 (GRCm39) |
missense |
unknown |
|
R7260:Chd9
|
UTSW |
8 |
91,721,171 (GRCm39) |
missense |
unknown |
|
R7293:Chd9
|
UTSW |
8 |
91,760,707 (GRCm39) |
missense |
unknown |
|
R7303:Chd9
|
UTSW |
8 |
91,778,532 (GRCm39) |
missense |
unknown |
|
R7358:Chd9
|
UTSW |
8 |
91,760,846 (GRCm39) |
missense |
unknown |
|
R7358:Chd9
|
UTSW |
8 |
91,710,115 (GRCm39) |
missense |
unknown |
|
R7451:Chd9
|
UTSW |
8 |
91,760,446 (GRCm39) |
missense |
probably benign |
0.27 |
R7451:Chd9
|
UTSW |
8 |
91,760,418 (GRCm39) |
frame shift |
probably null |
|
R7456:Chd9
|
UTSW |
8 |
91,659,153 (GRCm39) |
nonsense |
probably null |
|
R7481:Chd9
|
UTSW |
8 |
91,683,066 (GRCm39) |
missense |
unknown |
|
R7532:Chd9
|
UTSW |
8 |
91,721,193 (GRCm39) |
missense |
unknown |
|
R7570:Chd9
|
UTSW |
8 |
91,721,208 (GRCm39) |
missense |
unknown |
|
R7611:Chd9
|
UTSW |
8 |
91,763,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R7673:Chd9
|
UTSW |
8 |
91,778,325 (GRCm39) |
missense |
probably damaging |
0.96 |
R7723:Chd9
|
UTSW |
8 |
91,741,837 (GRCm39) |
missense |
unknown |
|
R7739:Chd9
|
UTSW |
8 |
91,761,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R7759:Chd9
|
UTSW |
8 |
91,704,178 (GRCm39) |
critical splice donor site |
probably null |
|
R7916:Chd9
|
UTSW |
8 |
91,761,684 (GRCm39) |
nonsense |
probably null |
|
R7921:Chd9
|
UTSW |
8 |
91,768,909 (GRCm39) |
critical splice donor site |
probably null |
|
R7957:Chd9
|
UTSW |
8 |
91,778,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R7972:Chd9
|
UTSW |
8 |
91,732,395 (GRCm39) |
missense |
unknown |
|
R8108:Chd9
|
UTSW |
8 |
91,659,852 (GRCm39) |
missense |
unknown |
|
R8115:Chd9
|
UTSW |
8 |
91,762,960 (GRCm39) |
missense |
probably damaging |
0.99 |
R8165:Chd9
|
UTSW |
8 |
91,767,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Chd9
|
UTSW |
8 |
91,752,015 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8186:Chd9
|
UTSW |
8 |
91,725,233 (GRCm39) |
missense |
unknown |
|
R8208:Chd9
|
UTSW |
8 |
91,763,891 (GRCm39) |
splice site |
probably null |
|
R8256:Chd9
|
UTSW |
8 |
91,660,129 (GRCm39) |
missense |
unknown |
|
R8281:Chd9
|
UTSW |
8 |
91,763,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R8504:Chd9
|
UTSW |
8 |
91,723,472 (GRCm39) |
missense |
unknown |
|
R8836:Chd9
|
UTSW |
8 |
91,767,812 (GRCm39) |
missense |
probably damaging |
0.99 |
R8892:Chd9
|
UTSW |
8 |
91,660,468 (GRCm39) |
missense |
unknown |
|
R8985:Chd9
|
UTSW |
8 |
91,721,101 (GRCm39) |
missense |
unknown |
|
R9029:Chd9
|
UTSW |
8 |
91,683,198 (GRCm39) |
missense |
unknown |
|
R9030:Chd9
|
UTSW |
8 |
91,683,198 (GRCm39) |
missense |
unknown |
|
R9038:Chd9
|
UTSW |
8 |
91,716,233 (GRCm39) |
missense |
unknown |
|
R9081:Chd9
|
UTSW |
8 |
91,704,144 (GRCm39) |
nonsense |
probably null |
|
R9134:Chd9
|
UTSW |
8 |
91,659,754 (GRCm39) |
missense |
unknown |
|
R9205:Chd9
|
UTSW |
8 |
91,757,270 (GRCm39) |
missense |
probably benign |
0.01 |
R9309:Chd9
|
UTSW |
8 |
91,733,319 (GRCm39) |
missense |
unknown |
|
R9375:Chd9
|
UTSW |
8 |
91,725,335 (GRCm39) |
critical splice donor site |
probably null |
|
R9449:Chd9
|
UTSW |
8 |
91,659,174 (GRCm39) |
missense |
unknown |
|
R9547:Chd9
|
UTSW |
8 |
91,683,186 (GRCm39) |
missense |
unknown |
|
R9573:Chd9
|
UTSW |
8 |
91,704,302 (GRCm39) |
missense |
unknown |
|
R9576:Chd9
|
UTSW |
8 |
91,659,294 (GRCm39) |
missense |
unknown |
|
R9601:Chd9
|
UTSW |
8 |
91,732,360 (GRCm39) |
nonsense |
probably null |
|
R9613:Chd9
|
UTSW |
8 |
91,683,150 (GRCm39) |
nonsense |
probably null |
|
R9639:Chd9
|
UTSW |
8 |
91,760,840 (GRCm39) |
missense |
probably null |
|
R9718:Chd9
|
UTSW |
8 |
91,712,801 (GRCm39) |
missense |
unknown |
|
R9746:Chd9
|
UTSW |
8 |
91,738,063 (GRCm39) |
missense |
unknown |
|
R9762:Chd9
|
UTSW |
8 |
91,712,741 (GRCm39) |
missense |
unknown |
|
R9764:Chd9
|
UTSW |
8 |
91,721,220 (GRCm39) |
missense |
unknown |
|
R9790:Chd9
|
UTSW |
8 |
91,760,417 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9791:Chd9
|
UTSW |
8 |
91,760,417 (GRCm39) |
missense |
possibly damaging |
0.82 |
RF007:Chd9
|
UTSW |
8 |
91,760,578 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0065:Chd9
|
UTSW |
8 |
91,763,200 (GRCm39) |
missense |
probably damaging |
1.00 |
|