Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
G |
10: 78,902,925 (GRCm39) |
T464P |
probably damaging |
Het |
Abca16 |
A |
G |
7: 120,126,950 (GRCm39) |
I1214V |
probably benign |
Het |
Arap2 |
A |
G |
5: 62,833,860 (GRCm39) |
F869S |
probably damaging |
Het |
Astn2 |
G |
T |
4: 65,910,540 (GRCm39) |
H431N |
possibly damaging |
Het |
Bap1 |
A |
G |
14: 30,977,608 (GRCm39) |
T308A |
probably benign |
Het |
Bcr |
G |
A |
10: 74,966,868 (GRCm39) |
E492K |
possibly damaging |
Het |
Bltp3b |
A |
G |
10: 89,641,979 (GRCm39) |
D1050G |
probably benign |
Het |
Camta1 |
A |
G |
4: 151,229,501 (GRCm39) |
F444L |
probably damaging |
Het |
Dnmt1 |
A |
T |
9: 20,827,110 (GRCm39) |
Y877* |
probably null |
Het |
Fam13b |
A |
G |
18: 34,630,500 (GRCm39) |
V86A |
possibly damaging |
Het |
Gm11562 |
T |
A |
11: 99,510,817 (GRCm39) |
R128W |
unknown |
Het |
Krt86 |
A |
G |
15: 101,371,714 (GRCm39) |
I95V |
probably benign |
Het |
Mroh2b |
A |
G |
15: 4,942,284 (GRCm39) |
T349A |
possibly damaging |
Het |
Ms4a7 |
A |
T |
19: 11,310,605 (GRCm39) |
L38Q |
probably damaging |
Het |
Myo1h |
T |
C |
5: 114,468,221 (GRCm39) |
S339P |
probably damaging |
Het |
Nf2 |
T |
C |
11: 4,749,944 (GRCm39) |
I46V |
probably benign |
Het |
Nr1h4 |
T |
C |
10: 89,290,792 (GRCm39) |
D416G |
probably benign |
Het |
Oga |
G |
A |
19: 45,755,915 (GRCm39) |
A576V |
probably benign |
Het |
Or11l3 |
T |
C |
11: 58,516,284 (GRCm39) |
E196G |
probably damaging |
Het |
Or4p18 |
A |
G |
2: 88,232,639 (GRCm39) |
M213T |
probably benign |
Het |
Pde1c |
C |
G |
6: 56,419,020 (GRCm39) |
E87Q |
possibly damaging |
Het |
Peg10 |
T |
TCCA |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Pga5 |
A |
T |
19: 10,646,779 (GRCm39) |
D317E |
probably benign |
Het |
Pira2 |
T |
A |
7: 3,844,067 (GRCm39) |
K568N |
probably damaging |
Het |
Ppp2cb |
A |
G |
8: 34,109,161 (GRCm39) |
D290G |
probably benign |
Het |
Sall4 |
T |
C |
2: 168,596,990 (GRCm39) |
K617E |
probably damaging |
Het |
Slc7a14 |
G |
A |
3: 31,277,728 (GRCm39) |
P626S |
possibly damaging |
Het |
Speer4b |
A |
T |
5: 27,702,076 (GRCm39) |
L228* |
probably null |
Het |
Spns2 |
T |
C |
11: 72,380,447 (GRCm39) |
T59A |
probably benign |
Het |
Tbc1d5 |
A |
T |
17: 51,275,260 (GRCm39) |
N78K |
probably benign |
Het |
Tmem63a |
T |
C |
1: 180,788,686 (GRCm39) |
V341A |
probably benign |
Het |
Trpt1 |
A |
G |
19: 6,975,683 (GRCm39) |
T146A |
probably benign |
Het |
Tyrp1 |
T |
C |
4: 80,753,674 (GRCm39) |
C122R |
probably damaging |
Het |
Uchl1 |
A |
G |
5: 66,839,818 (GRCm39) |
E120G |
possibly damaging |
Het |
Ucn3 |
C |
T |
13: 3,991,295 (GRCm39) |
R119Q |
possibly damaging |
Het |
Vmn2r2 |
T |
G |
3: 64,024,608 (GRCm39) |
I658L |
probably benign |
Het |
Vmn2r96 |
T |
A |
17: 18,804,082 (GRCm39) |
V444E |
probably benign |
Het |
Wdr54 |
A |
C |
6: 83,132,629 (GRCm39) |
|
probably null |
Het |
Xcr1 |
A |
G |
9: 123,685,300 (GRCm39) |
L154P |
probably benign |
Het |
Zbtb26 |
T |
C |
2: 37,326,557 (GRCm39) |
K160E |
probably benign |
Het |
Zfp157 |
T |
G |
5: 138,454,772 (GRCm39) |
Y323* |
probably null |
Het |
Zfp850 |
A |
T |
7: 27,689,801 (GRCm39) |
F136I |
probably benign |
Het |
|
Other mutations in Chd7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00422:Chd7
|
APN |
4 |
8,859,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00510:Chd7
|
APN |
4 |
8,801,404 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00741:Chd7
|
APN |
4 |
8,839,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00796:Chd7
|
APN |
4 |
8,847,271 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00907:Chd7
|
APN |
4 |
8,840,435 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00930:Chd7
|
APN |
4 |
8,805,181 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01542:Chd7
|
APN |
4 |
8,859,285 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01602:Chd7
|
APN |
4 |
8,833,834 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01605:Chd7
|
APN |
4 |
8,833,834 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01670:Chd7
|
APN |
4 |
8,827,033 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02434:Chd7
|
APN |
4 |
8,752,145 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02531:Chd7
|
APN |
4 |
8,854,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02626:Chd7
|
APN |
4 |
8,826,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Chd7
|
APN |
4 |
8,751,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02972:Chd7
|
APN |
4 |
8,855,174 (GRCm39) |
missense |
probably benign |
0.30 |
IGL03329:Chd7
|
APN |
4 |
8,841,108 (GRCm39) |
missense |
probably damaging |
1.00 |
Fili
|
UTSW |
4 |
8,839,523 (GRCm39) |
missense |
probably damaging |
1.00 |
D4043:Chd7
|
UTSW |
4 |
8,862,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02991:Chd7
|
UTSW |
4 |
8,828,398 (GRCm39) |
missense |
possibly damaging |
0.91 |
PIT4466001:Chd7
|
UTSW |
4 |
8,753,101 (GRCm39) |
missense |
unknown |
|
PIT4472001:Chd7
|
UTSW |
4 |
8,753,101 (GRCm39) |
missense |
unknown |
|
R0157:Chd7
|
UTSW |
4 |
8,833,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R0179:Chd7
|
UTSW |
4 |
8,862,516 (GRCm39) |
missense |
probably benign |
0.22 |
R0240:Chd7
|
UTSW |
4 |
8,852,670 (GRCm39) |
unclassified |
probably benign |
|
R0388:Chd7
|
UTSW |
4 |
8,854,560 (GRCm39) |
missense |
probably benign |
0.27 |
R0462:Chd7
|
UTSW |
4 |
8,850,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R0512:Chd7
|
UTSW |
4 |
8,805,139 (GRCm39) |
intron |
probably benign |
|
R0657:Chd7
|
UTSW |
4 |
8,753,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R0799:Chd7
|
UTSW |
4 |
8,801,310 (GRCm39) |
intron |
probably benign |
|
R0885:Chd7
|
UTSW |
4 |
8,866,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R1056:Chd7
|
UTSW |
4 |
8,822,402 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1086:Chd7
|
UTSW |
4 |
8,866,458 (GRCm39) |
missense |
probably benign |
0.04 |
R1353:Chd7
|
UTSW |
4 |
8,839,556 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Chd7
|
UTSW |
4 |
8,840,561 (GRCm39) |
splice site |
probably null |
|
R1466:Chd7
|
UTSW |
4 |
8,840,561 (GRCm39) |
splice site |
probably null |
|
R1605:Chd7
|
UTSW |
4 |
8,844,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R1693:Chd7
|
UTSW |
4 |
8,864,307 (GRCm39) |
critical splice donor site |
probably null |
|
R1695:Chd7
|
UTSW |
4 |
8,833,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Chd7
|
UTSW |
4 |
8,847,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R1964:Chd7
|
UTSW |
4 |
8,865,978 (GRCm39) |
missense |
probably damaging |
0.96 |
R2020:Chd7
|
UTSW |
4 |
8,855,226 (GRCm39) |
missense |
probably benign |
0.00 |
R2134:Chd7
|
UTSW |
4 |
8,753,147 (GRCm39) |
missense |
probably damaging |
0.99 |
R2171:Chd7
|
UTSW |
4 |
8,752,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R2271:Chd7
|
UTSW |
4 |
8,785,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R2300:Chd7
|
UTSW |
4 |
8,855,241 (GRCm39) |
missense |
probably benign |
0.02 |
R2355:Chd7
|
UTSW |
4 |
8,801,350 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3153:Chd7
|
UTSW |
4 |
8,855,174 (GRCm39) |
missense |
probably benign |
0.30 |
R3430:Chd7
|
UTSW |
4 |
8,844,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R3746:Chd7
|
UTSW |
4 |
8,752,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R4118:Chd7
|
UTSW |
4 |
8,865,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R4119:Chd7
|
UTSW |
4 |
8,785,658 (GRCm39) |
intron |
probably benign |
|
R4332:Chd7
|
UTSW |
4 |
8,854,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R4402:Chd7
|
UTSW |
4 |
8,866,353 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4571:Chd7
|
UTSW |
4 |
8,866,217 (GRCm39) |
missense |
probably benign |
0.09 |
R4722:Chd7
|
UTSW |
4 |
8,822,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4821:Chd7
|
UTSW |
4 |
8,844,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R4894:Chd7
|
UTSW |
4 |
8,838,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R5205:Chd7
|
UTSW |
4 |
8,752,509 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5344:Chd7
|
UTSW |
4 |
8,844,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R5484:Chd7
|
UTSW |
4 |
8,828,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R5578:Chd7
|
UTSW |
4 |
8,847,149 (GRCm39) |
missense |
probably benign |
0.09 |
R5583:Chd7
|
UTSW |
4 |
8,752,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R5888:Chd7
|
UTSW |
4 |
8,866,382 (GRCm39) |
missense |
probably damaging |
0.98 |
R5905:Chd7
|
UTSW |
4 |
8,840,553 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6091:Chd7
|
UTSW |
4 |
8,751,875 (GRCm39) |
missense |
probably damaging |
0.99 |
R6126:Chd7
|
UTSW |
4 |
8,826,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R6399:Chd7
|
UTSW |
4 |
8,828,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R6751:Chd7
|
UTSW |
4 |
8,833,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R6810:Chd7
|
UTSW |
4 |
8,839,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Chd7
|
UTSW |
4 |
8,811,501 (GRCm39) |
splice site |
probably null |
|
R6952:Chd7
|
UTSW |
4 |
8,856,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R6986:Chd7
|
UTSW |
4 |
8,859,285 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7139:Chd7
|
UTSW |
4 |
8,865,865 (GRCm39) |
missense |
probably benign |
0.00 |
R7288:Chd7
|
UTSW |
4 |
8,847,093 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7355:Chd7
|
UTSW |
4 |
8,752,196 (GRCm39) |
missense |
unknown |
|
R7452:Chd7
|
UTSW |
4 |
8,854,731 (GRCm39) |
missense |
probably benign |
0.03 |
R7471:Chd7
|
UTSW |
4 |
8,859,197 (GRCm39) |
missense |
probably damaging |
0.96 |
R7588:Chd7
|
UTSW |
4 |
8,864,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Chd7
|
UTSW |
4 |
8,805,234 (GRCm39) |
missense |
probably benign |
0.00 |
R7744:Chd7
|
UTSW |
4 |
8,862,485 (GRCm39) |
splice site |
probably null |
|
R7842:Chd7
|
UTSW |
4 |
8,854,115 (GRCm39) |
missense |
probably benign |
0.01 |
R7883:Chd7
|
UTSW |
4 |
8,826,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R7934:Chd7
|
UTSW |
4 |
8,854,121 (GRCm39) |
missense |
probably benign |
0.00 |
R7983:Chd7
|
UTSW |
4 |
8,844,609 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7983:Chd7
|
UTSW |
4 |
8,752,628 (GRCm39) |
missense |
unknown |
|
R8022:Chd7
|
UTSW |
4 |
8,751,605 (GRCm39) |
missense |
unknown |
|
R8161:Chd7
|
UTSW |
4 |
8,855,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Chd7
|
UTSW |
4 |
8,839,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R8278:Chd7
|
UTSW |
4 |
8,862,485 (GRCm39) |
splice site |
probably null |
|
R8358:Chd7
|
UTSW |
4 |
8,839,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R8464:Chd7
|
UTSW |
4 |
8,811,465 (GRCm39) |
missense |
probably benign |
0.06 |
R8483:Chd7
|
UTSW |
4 |
8,822,412 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8507:Chd7
|
UTSW |
4 |
8,858,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8535:Chd7
|
UTSW |
4 |
8,859,211 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8695:Chd7
|
UTSW |
4 |
8,850,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R8700:Chd7
|
UTSW |
4 |
8,833,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Chd7
|
UTSW |
4 |
8,866,069 (GRCm39) |
missense |
probably benign |
0.31 |
R8774:Chd7
|
UTSW |
4 |
8,854,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774-TAIL:Chd7
|
UTSW |
4 |
8,854,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R8796:Chd7
|
UTSW |
4 |
8,838,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R8992:Chd7
|
UTSW |
4 |
8,839,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R9018:Chd7
|
UTSW |
4 |
8,847,083 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9122:Chd7
|
UTSW |
4 |
8,840,510 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9131:Chd7
|
UTSW |
4 |
8,785,642 (GRCm39) |
missense |
|
|
R9182:Chd7
|
UTSW |
4 |
8,838,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R9227:Chd7
|
UTSW |
4 |
8,805,272 (GRCm39) |
missense |
probably benign |
0.03 |
R9254:Chd7
|
UTSW |
4 |
8,752,210 (GRCm39) |
missense |
unknown |
|
R9379:Chd7
|
UTSW |
4 |
8,752,210 (GRCm39) |
missense |
unknown |
|
R9388:Chd7
|
UTSW |
4 |
8,865,756 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9455:Chd7
|
UTSW |
4 |
8,752,061 (GRCm39) |
missense |
unknown |
|
R9531:Chd7
|
UTSW |
4 |
8,858,489 (GRCm39) |
missense |
|
|
R9577:Chd7
|
UTSW |
4 |
8,752,964 (GRCm39) |
missense |
unknown |
|
R9634:Chd7
|
UTSW |
4 |
8,832,499 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Chd7
|
UTSW |
4 |
8,844,313 (GRCm39) |
missense |
probably damaging |
1.00 |
|