Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam7 |
A |
G |
14: 68,763,773 (GRCm39) |
C126R |
probably damaging |
Het |
Agpat5 |
G |
A |
8: 18,928,043 (GRCm39) |
V203I |
possibly damaging |
Het |
Ankrd12 |
T |
A |
17: 66,293,904 (GRCm39) |
R510* |
probably null |
Het |
Anxa6 |
C |
T |
11: 54,904,696 (GRCm39) |
A22T |
probably benign |
Het |
Barx2 |
A |
T |
9: 31,770,309 (GRCm39) |
L73Q |
probably damaging |
Het |
BC024139 |
T |
C |
15: 76,004,333 (GRCm39) |
K702R |
possibly damaging |
Het |
Cc2d1a |
T |
C |
8: 84,861,605 (GRCm39) |
K739R |
probably benign |
Het |
Cdk12 |
A |
G |
11: 98,141,111 (GRCm39) |
T1451A |
unknown |
Het |
Cp |
A |
G |
3: 20,025,193 (GRCm39) |
Y384C |
probably damaging |
Het |
Dnah14 |
T |
A |
1: 181,468,979 (GRCm39) |
W1270R |
probably benign |
Het |
Dyrk2 |
G |
T |
10: 118,696,567 (GRCm39) |
S230R |
probably damaging |
Het |
Epn3 |
A |
T |
11: 94,384,602 (GRCm39) |
S290R |
probably damaging |
Het |
Fas |
C |
T |
19: 34,304,626 (GRCm39) |
R296C |
probably benign |
Het |
Fmnl1 |
A |
T |
11: 103,084,859 (GRCm39) |
N659I |
unknown |
Het |
Gas8 |
T |
C |
8: 124,257,777 (GRCm39) |
|
probably null |
Het |
Gpr156 |
A |
G |
16: 37,768,598 (GRCm39) |
T40A |
probably benign |
Het |
Hey1 |
G |
C |
3: 8,729,836 (GRCm39) |
A207G |
probably benign |
Het |
Htr3b |
C |
A |
9: 48,876,177 (GRCm39) |
|
probably benign |
Het |
Itgal |
C |
T |
7: 126,928,607 (GRCm39) |
T1044I |
probably benign |
Het |
Itprid2 |
A |
G |
2: 79,475,208 (GRCm39) |
Q389R |
probably benign |
Het |
Kcnip4 |
T |
G |
5: 48,639,997 (GRCm39) |
D38A |
possibly damaging |
Het |
Kcnma1 |
G |
T |
14: 23,641,706 (GRCm39) |
Q216K |
probably benign |
Het |
Kdsr |
T |
A |
1: 106,671,400 (GRCm39) |
E203V |
probably null |
Het |
Lrp1b |
T |
C |
2: 41,298,387 (GRCm39) |
E999G |
|
Het |
Malt1 |
T |
A |
18: 65,603,594 (GRCm39) |
W577R |
probably damaging |
Het |
Mroh2b |
A |
C |
15: 4,978,572 (GRCm39) |
T1373P |
probably damaging |
Het |
Mymk |
A |
G |
2: 26,952,712 (GRCm39) |
|
probably null |
Het |
Myo1f |
T |
A |
17: 33,816,992 (GRCm39) |
H707Q |
probably benign |
Het |
Ncam2 |
C |
A |
16: 81,309,867 (GRCm39) |
H452Q |
possibly damaging |
Het |
Ndrg4 |
A |
G |
8: 96,404,975 (GRCm39) |
M1V |
probably null |
Het |
Nps |
C |
T |
7: 134,874,079 (GRCm39) |
S83L |
probably damaging |
Het |
Nup155 |
T |
A |
15: 8,177,044 (GRCm39) |
Y1040* |
probably null |
Het |
Or1j15 |
T |
C |
2: 36,459,443 (GRCm39) |
Y278H |
probably damaging |
Het |
Or2ak4 |
C |
T |
11: 58,648,985 (GRCm39) |
Q165* |
probably null |
Het |
Or4f7 |
T |
C |
2: 111,645,051 (GRCm39) |
T7A |
probably benign |
Het |
Or5h22 |
C |
T |
16: 58,895,243 (GRCm39) |
V67M |
possibly damaging |
Het |
Pak1ip1 |
G |
A |
13: 41,162,770 (GRCm39) |
R191Q |
probably benign |
Het |
Pcdh17 |
G |
A |
14: 84,683,384 (GRCm39) |
|
probably benign |
Het |
Pcdhgc5 |
G |
T |
18: 37,952,945 (GRCm39) |
R73L |
probably benign |
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Plat |
G |
T |
8: 23,262,248 (GRCm39) |
G91W |
probably damaging |
Het |
Plscr4 |
C |
T |
9: 92,372,843 (GRCm39) |
R322* |
probably null |
Het |
Plxnd1 |
A |
T |
6: 115,943,866 (GRCm39) |
N1144K |
probably damaging |
Het |
Ppp1r1b |
G |
T |
11: 98,246,310 (GRCm39) |
E133D |
probably damaging |
Het |
Ptpn13 |
A |
G |
5: 103,705,815 (GRCm39) |
E1396G |
probably damaging |
Het |
Reps1 |
T |
C |
10: 17,970,218 (GRCm39) |
S272P |
probably damaging |
Het |
Ric8b |
T |
C |
10: 84,816,039 (GRCm39) |
V430A |
probably damaging |
Het |
Septin10 |
A |
T |
10: 59,012,825 (GRCm39) |
N264K |
possibly damaging |
Het |
Sgms1 |
A |
T |
19: 32,137,109 (GRCm39) |
F152L |
probably benign |
Het |
Snapc1 |
C |
A |
12: 74,011,506 (GRCm39) |
F57L |
probably damaging |
Het |
Spidr |
A |
G |
16: 15,786,540 (GRCm39) |
L401P |
probably damaging |
Het |
Spn |
C |
T |
7: 126,735,728 (GRCm39) |
V260M |
probably damaging |
Het |
Sptan1 |
G |
A |
2: 29,916,596 (GRCm39) |
A2095T |
probably damaging |
Het |
Tbc1d15 |
A |
G |
10: 115,038,407 (GRCm39) |
|
probably null |
Het |
Thsd7b |
T |
A |
1: 129,605,790 (GRCm39) |
F510L |
probably benign |
Het |
Trpm5 |
T |
A |
7: 142,632,050 (GRCm39) |
I920F |
probably damaging |
Het |
Tspear |
C |
A |
10: 77,710,898 (GRCm39) |
H507N |
probably benign |
Het |
Vmn2r108 |
T |
A |
17: 20,683,195 (GRCm39) |
K670* |
probably null |
Het |
Vmn2r75 |
A |
T |
7: 85,797,685 (GRCm39) |
C709* |
probably null |
Het |
Wdfy3 |
G |
T |
5: 102,020,767 (GRCm39) |
S2494R |
probably benign |
Het |
Zfp456 |
A |
T |
13: 67,515,108 (GRCm39) |
F199L |
probably damaging |
Het |
Zfp830 |
A |
G |
11: 82,655,529 (GRCm39) |
Q111R |
probably benign |
Het |
Znrf1 |
G |
A |
8: 112,263,842 (GRCm39) |
A24T |
probably damaging |
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 |
R6990:Chd7
|
UTSW |
4 |
8,844,525 (GRCm39) |
missense |
probably benign |
0.28 |
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 |
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 |
|