Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34l |
A |
T |
8: 44,078,954 (GRCm39) |
C423* |
probably null |
Het |
Akr1cl |
T |
A |
1: 65,053,857 (GRCm39) |
Y271F |
probably benign |
Het |
Asnsd1 |
A |
G |
1: 53,386,386 (GRCm39) |
S414P |
possibly damaging |
Het |
Atp12a |
T |
A |
14: 56,602,739 (GRCm39) |
M1K |
probably null |
Het |
Atp4b |
A |
C |
8: 13,437,477 (GRCm39) |
N225K |
possibly damaging |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Cactin |
C |
T |
10: 81,158,727 (GRCm39) |
T231I |
possibly damaging |
Het |
Casp8ap2 |
T |
C |
4: 32,644,560 (GRCm39) |
V1211A |
probably benign |
Het |
Ccdc180 |
C |
A |
4: 45,944,418 (GRCm39) |
H1423N |
probably benign |
Het |
Cfap251 |
G |
A |
5: 123,411,853 (GRCm39) |
G495D |
probably benign |
Het |
Chst8 |
A |
G |
7: 34,374,589 (GRCm39) |
Y417H |
possibly damaging |
Het |
Clcn6 |
A |
G |
4: 148,095,109 (GRCm39) |
|
probably null |
Het |
Clec5a |
A |
T |
6: 40,562,128 (GRCm39) |
V12E |
probably damaging |
Het |
Crebbp |
C |
T |
16: 3,903,683 (GRCm39) |
R1852H |
probably damaging |
Het |
Cyp2c40 |
T |
A |
19: 39,801,224 (GRCm39) |
|
probably benign |
Het |
Dip2c |
T |
C |
13: 9,601,836 (GRCm39) |
L265P |
probably damaging |
Het |
Dnah3 |
A |
G |
7: 119,550,465 (GRCm39) |
Y3274H |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,004,405 (GRCm39) |
T3853S |
probably benign |
Het |
Dnttip2 |
T |
C |
3: 122,069,870 (GRCm39) |
S362P |
probably damaging |
Het |
Dst |
G |
A |
1: 34,205,372 (GRCm39) |
V1025I |
possibly damaging |
Het |
Dym |
T |
C |
18: 75,213,321 (GRCm39) |
V181A |
probably benign |
Het |
Dynlt4 |
A |
G |
4: 116,985,504 (GRCm39) |
E109G |
possibly damaging |
Het |
Elk3 |
T |
A |
10: 93,101,539 (GRCm39) |
I71F |
probably damaging |
Het |
Epb41l4a |
C |
T |
18: 34,054,893 (GRCm39) |
S65N |
probably benign |
Het |
Erap1 |
T |
A |
13: 74,814,627 (GRCm39) |
V451E |
probably benign |
Het |
F830045P16Rik |
T |
A |
2: 129,314,585 (GRCm39) |
I231F |
probably damaging |
Het |
Fahd1 |
T |
C |
17: 25,068,814 (GRCm39) |
I88V |
probably benign |
Het |
Fam120b |
C |
T |
17: 15,644,638 (GRCm39) |
T744I |
possibly damaging |
Het |
Fam83f |
T |
G |
15: 80,576,468 (GRCm39) |
V373G |
possibly damaging |
Het |
Frem1 |
G |
T |
4: 82,831,795 (GRCm39) |
T1988K |
probably benign |
Het |
Gdap1l1 |
A |
T |
2: 163,289,517 (GRCm39) |
T161S |
probably benign |
Het |
Gm6309 |
C |
T |
5: 146,105,121 (GRCm39) |
G264D |
probably benign |
Het |
Hsd11b1 |
T |
C |
1: 192,922,686 (GRCm39) |
T124A |
probably benign |
Het |
Ino80b |
A |
G |
6: 83,101,353 (GRCm39) |
M119T |
probably damaging |
Het |
Kif3a |
G |
A |
11: 53,461,408 (GRCm39) |
V17M |
probably damaging |
Het |
Krt40 |
T |
A |
11: 99,430,818 (GRCm39) |
E285D |
probably damaging |
Het |
Lair1 |
C |
G |
7: 4,066,063 (GRCm39) |
|
probably null |
Het |
Lvrn |
A |
G |
18: 46,999,503 (GRCm39) |
T290A |
possibly damaging |
Het |
Macf1 |
G |
T |
4: 123,366,523 (GRCm39) |
A2746E |
probably damaging |
Het |
Matn4 |
A |
G |
2: 164,242,573 (GRCm39) |
V175A |
probably damaging |
Het |
Mok |
A |
T |
12: 110,778,257 (GRCm39) |
D216E |
probably benign |
Het |
Muc15 |
A |
T |
2: 110,561,821 (GRCm39) |
T86S |
probably benign |
Het |
Myo16 |
A |
G |
8: 10,322,633 (GRCm39) |
K21R |
probably benign |
Het |
Ncl |
A |
G |
1: 86,284,677 (GRCm39) |
|
probably null |
Het |
Nfrkb |
C |
T |
9: 31,322,546 (GRCm39) |
T872I |
probably benign |
Het |
Nhlrc2 |
A |
T |
19: 56,585,710 (GRCm39) |
E648D |
probably benign |
Het |
Nlrp9c |
A |
T |
7: 26,084,221 (GRCm39) |
Y453N |
probably damaging |
Het |
Notch4 |
T |
C |
17: 34,806,502 (GRCm39) |
L1813P |
probably damaging |
Het |
Nrg3 |
T |
A |
14: 38,098,309 (GRCm39) |
D515V |
probably damaging |
Het |
Nsd1 |
T |
C |
13: 55,361,092 (GRCm39) |
V20A |
probably damaging |
Het |
Opn4 |
T |
A |
14: 34,319,028 (GRCm39) |
T186S |
probably benign |
Het |
Or9k2 |
T |
C |
10: 129,999,049 (GRCm39) |
M49V |
probably benign |
Het |
Pcdh15 |
T |
G |
10: 74,467,025 (GRCm39) |
S1684A |
possibly damaging |
Het |
Phf11a |
T |
A |
14: 59,532,363 (GRCm39) |
E24V |
possibly damaging |
Het |
Pigg |
A |
T |
5: 108,460,788 (GRCm39) |
|
probably benign |
Het |
Plscr2 |
A |
G |
9: 92,177,647 (GRCm39) |
D136G |
probably damaging |
Het |
Ppp3r2 |
T |
C |
4: 49,681,723 (GRCm39) |
I76V |
probably benign |
Het |
Prdm6 |
A |
G |
18: 53,598,031 (GRCm39) |
|
probably benign |
Het |
Prex1 |
A |
G |
2: 166,417,534 (GRCm39) |
W1188R |
possibly damaging |
Het |
Prmt2 |
T |
A |
10: 76,061,292 (GRCm39) |
R65* |
probably null |
Het |
Prom1 |
G |
T |
5: 44,187,068 (GRCm39) |
D396E |
probably benign |
Het |
Ptcd3 |
C |
T |
6: 71,862,537 (GRCm39) |
C466Y |
probably damaging |
Het |
Ptk2 |
A |
G |
15: 73,114,255 (GRCm39) |
V701A |
possibly damaging |
Het |
Rab36 |
T |
C |
10: 74,888,306 (GRCm39) |
I250T |
probably benign |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Scn11a |
G |
T |
9: 119,640,274 (GRCm39) |
A207E |
possibly damaging |
Het |
Serpinb3d |
A |
G |
1: 107,006,182 (GRCm39) |
V302A |
probably benign |
Het |
Slc22a16 |
T |
C |
10: 40,467,873 (GRCm39) |
Y469H |
probably damaging |
Het |
Smo |
A |
G |
6: 29,754,715 (GRCm39) |
N262D |
possibly damaging |
Het |
Spata31e5 |
A |
T |
1: 28,817,234 (GRCm39) |
V266D |
probably damaging |
Het |
Sptan1 |
C |
T |
2: 29,897,573 (GRCm39) |
A1212V |
probably damaging |
Het |
Ssr1 |
C |
T |
13: 38,173,525 (GRCm39) |
A79T |
probably damaging |
Het |
Tiam1 |
T |
A |
16: 89,674,075 (GRCm39) |
T479S |
probably benign |
Het |
Tm9sf3 |
A |
G |
19: 41,227,231 (GRCm39) |
F280S |
probably damaging |
Het |
Tmem72 |
T |
C |
6: 116,673,800 (GRCm39) |
H106R |
probably damaging |
Het |
Tnr |
A |
G |
1: 159,679,592 (GRCm39) |
I189V |
probably benign |
Het |
Tpbpa |
T |
A |
13: 61,088,036 (GRCm39) |
N50I |
probably benign |
Het |
Tshz1 |
T |
A |
18: 84,031,987 (GRCm39) |
Y807F |
probably damaging |
Het |
Tspo2 |
C |
T |
17: 48,755,750 (GRCm39) |
A131T |
possibly damaging |
Het |
Usp16 |
T |
C |
16: 87,270,014 (GRCm39) |
L322P |
probably damaging |
Het |
Vmn1r185 |
A |
G |
7: 26,310,935 (GRCm39) |
V190A |
possibly damaging |
Het |
Vmn1r34 |
T |
C |
6: 66,614,385 (GRCm39) |
K118E |
possibly damaging |
Het |
Vmn1r68 |
A |
G |
7: 10,261,918 (GRCm39) |
L60P |
probably damaging |
Het |
Vmn2r-ps158 |
A |
G |
7: 42,673,454 (GRCm39) |
N171D |
probably benign |
Het |
Vps51 |
T |
C |
19: 6,121,612 (GRCm39) |
E162G |
probably benign |
Het |
Yy1 |
CGGG |
CGGGGGG |
12: 108,759,916 (GRCm39) |
|
probably benign |
Het |
Zdhhc4 |
C |
T |
5: 143,307,538 (GRCm39) |
R161H |
probably damaging |
Het |
Zfp456 |
A |
T |
13: 67,514,616 (GRCm39) |
C363* |
probably null |
Het |
Zfp541 |
T |
A |
7: 15,816,110 (GRCm39) |
S866T |
probably damaging |
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 |
|
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 |
R2276:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
|