Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933405L10Rik |
C |
T |
8: 106,435,606 (GRCm39) |
T88M |
probably damaging |
Het |
9430038I01Rik |
A |
G |
7: 136,978,795 (GRCm39) |
|
probably benign |
Het |
Adgra3 |
A |
C |
5: 50,118,834 (GRCm39) |
S905A |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,692,652 (GRCm39) |
Y1618H |
probably damaging |
Het |
Anapc15-ps |
T |
C |
10: 95,509,176 (GRCm39) |
T26A |
probably benign |
Het |
Ankrd13d |
T |
C |
19: 4,321,623 (GRCm39) |
K360E |
probably damaging |
Het |
Anks1b |
T |
A |
10: 90,348,751 (GRCm39) |
|
probably null |
Het |
Apob |
T |
C |
12: 8,057,602 (GRCm39) |
F2028S |
possibly damaging |
Het |
Arap3 |
G |
A |
18: 38,108,636 (GRCm39) |
R1265W |
probably damaging |
Het |
Arhgef37 |
A |
G |
18: 61,651,121 (GRCm39) |
Y135H |
probably damaging |
Het |
Armh3 |
A |
C |
19: 45,963,691 (GRCm39) |
S42R |
probably benign |
Het |
Atp1a1 |
T |
C |
3: 101,489,333 (GRCm39) |
T760A |
probably benign |
Het |
Cdc42bpb |
T |
A |
12: 111,289,255 (GRCm39) |
M497L |
probably benign |
Het |
Ces5a |
C |
T |
8: 94,240,859 (GRCm39) |
V413M |
probably damaging |
Het |
Chd5 |
A |
T |
4: 152,470,263 (GRCm39) |
Y1903F |
probably damaging |
Het |
Chmp7 |
G |
T |
14: 69,957,248 (GRCm39) |
D303E |
probably benign |
Het |
Chrnb4 |
A |
T |
9: 54,942,102 (GRCm39) |
Y391N |
possibly damaging |
Het |
Crtc1 |
T |
C |
8: 70,840,802 (GRCm39) |
T475A |
probably benign |
Het |
Cyp2c69 |
A |
G |
19: 39,865,972 (GRCm39) |
I207T |
probably benign |
Het |
Dcp1a |
A |
G |
14: 30,240,940 (GRCm39) |
E250G |
probably damaging |
Het |
Ddx20 |
T |
C |
3: 105,586,398 (GRCm39) |
Q649R |
probably benign |
Het |
Defb12 |
T |
A |
8: 19,162,754 (GRCm39) |
K59N |
probably damaging |
Het |
Dpy19l3 |
A |
T |
7: 35,429,185 (GRCm39) |
I85N |
probably damaging |
Het |
Duox2 |
C |
T |
2: 122,122,739 (GRCm39) |
|
probably null |
Het |
Ebi3 |
T |
A |
17: 56,263,679 (GRCm39) |
Y197N |
probably damaging |
Het |
Emc1 |
G |
A |
4: 139,102,823 (GRCm39) |
R994Q |
probably benign |
Het |
Ercc6 |
G |
T |
14: 32,268,777 (GRCm39) |
M530I |
probably damaging |
Het |
Evl |
T |
A |
12: 108,619,255 (GRCm39) |
D70E |
probably damaging |
Het |
Fbln2 |
A |
G |
6: 91,242,757 (GRCm39) |
N819S |
probably damaging |
Het |
Foxk2 |
A |
G |
11: 121,176,363 (GRCm39) |
I170V |
probably benign |
Het |
Gfm1 |
T |
C |
3: 67,342,943 (GRCm39) |
V159A |
probably damaging |
Het |
Gm10837 |
A |
G |
14: 122,728,177 (GRCm39) |
T18A |
unknown |
Het |
Gm12887 |
A |
T |
4: 121,479,227 (GRCm39) |
V25E |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,435,243 (GRCm39) |
H985R |
possibly damaging |
Het |
Hsfy2 |
A |
G |
1: 56,675,791 (GRCm39) |
Y249H |
possibly damaging |
Het |
Hspg2 |
T |
C |
4: 137,272,878 (GRCm39) |
V2639A |
probably damaging |
Het |
Igf2r |
A |
G |
17: 12,923,157 (GRCm39) |
|
probably null |
Het |
Invs |
T |
A |
4: 48,422,035 (GRCm39) |
I889N |
probably damaging |
Het |
Kcnq1 |
A |
T |
7: 142,736,857 (GRCm39) |
M209L |
probably benign |
Het |
Klra7 |
A |
G |
6: 130,206,957 (GRCm39) |
I48T |
possibly damaging |
Het |
Krt26 |
CTAGTA |
CTA |
11: 99,224,352 (GRCm39) |
|
probably benign |
Het |
Lrif1 |
T |
A |
3: 106,640,127 (GRCm39) |
V404D |
probably damaging |
Het |
Lrriq1 |
T |
A |
10: 103,063,034 (GRCm39) |
|
probably null |
Het |
Lypd6 |
T |
A |
2: 50,078,774 (GRCm39) |
I90N |
possibly damaging |
Het |
Mbp |
A |
G |
18: 82,602,247 (GRCm39) |
D174G |
probably damaging |
Het |
Megf9 |
G |
T |
4: 70,453,022 (GRCm39) |
P13Q |
probably damaging |
Het |
Myo15b |
A |
T |
11: 115,760,412 (GRCm39) |
T1155S |
probably benign |
Het |
Nherf2 |
C |
T |
17: 24,860,693 (GRCm39) |
S150N |
possibly damaging |
Het |
Nlrp6 |
T |
A |
7: 140,503,006 (GRCm39) |
C371S |
probably damaging |
Het |
Nosip |
T |
A |
7: 44,726,733 (GRCm39) |
|
probably null |
Het |
Nox3 |
G |
T |
17: 3,720,153 (GRCm39) |
P344H |
probably damaging |
Het |
Nup210l |
T |
C |
3: 90,079,393 (GRCm39) |
V959A |
probably damaging |
Het |
Or10d1 |
A |
G |
9: 39,484,031 (GRCm39) |
Y175H |
possibly damaging |
Het |
Or2b2b |
C |
A |
13: 21,858,842 (GRCm39) |
V91L |
probably benign |
Het |
Or2k2 |
T |
C |
4: 58,785,384 (GRCm39) |
I113V |
probably benign |
Het |
Or5b119 |
A |
G |
19: 13,457,295 (GRCm39) |
I89T |
probably benign |
Het |
Or5k8 |
T |
A |
16: 58,644,440 (GRCm39) |
I211F |
probably damaging |
Het |
Osbpl3 |
A |
C |
6: 50,347,123 (GRCm39) |
S25A |
probably damaging |
Het |
Otog |
G |
A |
7: 45,895,707 (GRCm39) |
C107Y |
probably damaging |
Het |
Pax7 |
G |
A |
4: 139,511,802 (GRCm39) |
R260C |
probably damaging |
Het |
Pbrm1 |
A |
T |
14: 30,760,914 (GRCm39) |
I224F |
probably damaging |
Het |
Pcdh1 |
T |
A |
18: 38,325,278 (GRCm39) |
|
probably null |
Het |
Pcnx1 |
T |
C |
12: 82,027,709 (GRCm39) |
L1585P |
probably damaging |
Het |
Pde4c |
C |
T |
8: 71,200,599 (GRCm39) |
H362Y |
probably damaging |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Pgm1 |
A |
T |
4: 99,818,675 (GRCm39) |
Q90L |
probably damaging |
Het |
Phlpp1 |
A |
G |
1: 106,271,235 (GRCm39) |
H814R |
probably benign |
Het |
Pknox2 |
A |
T |
9: 36,866,127 (GRCm39) |
M5K |
possibly damaging |
Het |
Pole |
G |
A |
5: 110,478,701 (GRCm39) |
|
probably null |
Het |
Polr1b |
A |
G |
2: 128,944,886 (GRCm39) |
I61V |
probably benign |
Het |
Prelp |
T |
C |
1: 133,842,495 (GRCm39) |
K217E |
probably damaging |
Het |
Prkce |
C |
T |
17: 86,782,974 (GRCm39) |
Q202* |
probably null |
Het |
Psmd2 |
T |
G |
16: 20,475,332 (GRCm39) |
M370R |
probably benign |
Het |
Rimklb |
A |
T |
6: 122,440,968 (GRCm39) |
H68Q |
probably damaging |
Het |
Rnasel |
A |
G |
1: 153,630,420 (GRCm39) |
D312G |
possibly damaging |
Het |
Rxrg |
A |
T |
1: 167,426,321 (GRCm39) |
M1L |
probably benign |
Het |
Scrn1 |
A |
G |
6: 54,499,826 (GRCm39) |
F220L |
possibly damaging |
Het |
Scyl3 |
A |
G |
1: 163,778,244 (GRCm39) |
S461G |
probably benign |
Het |
Serpina1c |
T |
A |
12: 103,861,282 (GRCm39) |
T411S |
probably benign |
Het |
Serpinb6d |
C |
T |
13: 33,855,364 (GRCm39) |
P346L |
probably benign |
Het |
Shld2 |
A |
G |
14: 33,989,760 (GRCm39) |
I382T |
probably benign |
Het |
Spg21 |
G |
T |
9: 65,372,618 (GRCm39) |
V17F |
probably damaging |
Het |
Spink5 |
A |
T |
18: 44,132,958 (GRCm39) |
M525L |
probably benign |
Het |
Sun2 |
T |
C |
15: 79,621,764 (GRCm39) |
T155A |
probably benign |
Het |
Tchh |
T |
A |
3: 93,354,087 (GRCm39) |
F1176I |
unknown |
Het |
Tex15 |
T |
A |
8: 34,066,682 (GRCm39) |
D2037E |
probably benign |
Het |
Tfdp2 |
T |
C |
9: 96,199,857 (GRCm39) |
C392R |
possibly damaging |
Het |
Tmem30c |
T |
C |
16: 57,097,143 (GRCm39) |
N139S |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,021,568 (GRCm39) |
|
probably null |
Het |
Trim66 |
T |
C |
7: 109,075,046 (GRCm39) |
E405G |
probably damaging |
Het |
Trpc4 |
T |
A |
3: 54,187,415 (GRCm39) |
F456I |
probably benign |
Het |
Tspo2 |
T |
C |
17: 48,755,818 (GRCm39) |
D108G |
possibly damaging |
Het |
Tyk2 |
A |
T |
9: 21,032,850 (GRCm39) |
C304* |
probably null |
Het |
Vgll4 |
A |
T |
6: 114,839,756 (GRCm39) |
S185T |
probably benign |
Het |
Vmn2r94 |
A |
C |
17: 18,464,732 (GRCm39) |
S519R |
probably benign |
Het |
Vmn2r96 |
T |
G |
17: 18,818,183 (GRCm39) |
S587A |
probably benign |
Het |
Vps4b |
C |
A |
1: 106,706,712 (GRCm39) |
A287S |
possibly damaging |
Het |
Yeats2 |
C |
T |
16: 20,048,314 (GRCm39) |
P1332S |
probably benign |
Het |
Zfp462 |
T |
G |
4: 55,010,010 (GRCm39) |
S659A |
possibly damaging |
Het |
Zfp507 |
C |
T |
7: 35,493,150 (GRCm39) |
R631Q |
probably damaging |
Het |
Zfp764l1 |
A |
C |
7: 126,990,660 (GRCm39) |
D442E |
probably benign |
Het |
Zswim5 |
G |
T |
4: 116,734,896 (GRCm39) |
E80D |
unknown |
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 |
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 |
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 |
|