Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4gnt |
C |
A |
9: 99,502,613 (GRCm39) |
P258T |
probably damaging |
Het |
Adamts1 |
C |
A |
16: 85,593,579 (GRCm39) |
G719* |
probably null |
Het |
Ano5 |
G |
T |
7: 51,194,599 (GRCm39) |
D111Y |
probably damaging |
Het |
Arvcf |
T |
C |
16: 18,221,699 (GRCm39) |
V714A |
possibly damaging |
Het |
AU021092 |
T |
A |
16: 5,038,253 (GRCm39) |
S85C |
probably damaging |
Het |
Capn5 |
T |
C |
7: 97,773,195 (GRCm39) |
D603G |
probably benign |
Het |
Cbr1 |
T |
A |
16: 93,406,692 (GRCm39) |
V136E |
probably damaging |
Het |
Ccdc27 |
T |
C |
4: 154,126,184 (GRCm39) |
M102V |
unknown |
Het |
Ccr1 |
T |
C |
9: 123,763,765 (GRCm39) |
Y255C |
probably damaging |
Het |
Cdr1 |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
X: 60,228,130 (GRCm39) |
|
probably benign |
Het |
Cep112 |
A |
G |
11: 108,410,722 (GRCm39) |
T553A |
probably benign |
Het |
Cntnap1 |
T |
C |
11: 101,068,131 (GRCm39) |
F48L |
probably benign |
Het |
Cyb5r3 |
T |
C |
15: 83,046,064 (GRCm39) |
D84G |
probably damaging |
Het |
Ddx47 |
T |
C |
6: 134,992,803 (GRCm39) |
I154T |
probably benign |
Het |
Dennd2b |
G |
A |
7: 109,130,337 (GRCm39) |
A888V |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,185,624 (GRCm39) |
L99P |
probably benign |
Het |
Dzank1 |
A |
G |
2: 144,325,293 (GRCm39) |
I558T |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,148,421 (GRCm39) |
D2609G |
possibly damaging |
Het |
Fhl5 |
C |
A |
4: 25,211,194 (GRCm39) |
C166F |
probably damaging |
Het |
Fndc1 |
A |
G |
17: 7,969,206 (GRCm39) |
L1553P |
probably damaging |
Het |
Frem1 |
G |
A |
4: 82,890,374 (GRCm39) |
T1035I |
probably benign |
Het |
Gm3099 |
A |
G |
14: 15,346,517 (GRCm39) |
M128V |
probably benign |
Het |
Gpaa1 |
C |
T |
15: 76,218,940 (GRCm39) |
T594I |
probably benign |
Het |
Hck |
C |
T |
2: 152,966,191 (GRCm39) |
T55M |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,471,123 (GRCm39) |
|
probably null |
Het |
Ica1l |
C |
T |
1: 60,054,995 (GRCm39) |
|
probably null |
Het |
Ilf3 |
T |
C |
9: 21,314,662 (GRCm39) |
Y765H |
unknown |
Het |
Mast4 |
G |
A |
13: 102,941,226 (GRCm39) |
T277M |
probably damaging |
Het |
Mfsd6 |
T |
C |
1: 52,748,056 (GRCm39) |
T270A |
probably benign |
Het |
Mib1 |
G |
A |
18: 10,775,541 (GRCm39) |
D498N |
probably benign |
Het |
Naaladl1 |
A |
T |
19: 6,164,663 (GRCm39) |
T576S |
possibly damaging |
Het |
Ncoa6 |
A |
T |
2: 155,247,577 (GRCm39) |
I1909N |
probably benign |
Het |
Negr1 |
A |
G |
3: 156,565,235 (GRCm39) |
D107G |
probably benign |
Het |
Nlrc4 |
A |
G |
17: 74,734,114 (GRCm39) |
M933T |
probably benign |
Het |
Nmnat3 |
T |
G |
9: 98,292,306 (GRCm39) |
F184V |
probably benign |
Het |
Or4b12 |
A |
T |
2: 90,096,639 (GRCm39) |
V45E |
probably damaging |
Het |
Or5p81 |
T |
C |
7: 108,266,743 (GRCm39) |
V40A |
possibly damaging |
Het |
Or6c76 |
C |
T |
10: 129,612,142 (GRCm39) |
R120C |
probably benign |
Het |
Or7a42 |
C |
A |
10: 78,791,676 (GRCm39) |
F212L |
probably benign |
Het |
Pfkfb4 |
T |
C |
9: 108,828,222 (GRCm39) |
Y86H |
probably benign |
Het |
Pgm5 |
T |
G |
19: 24,801,693 (GRCm39) |
Q178H |
probably damaging |
Het |
Phrf1 |
C |
T |
7: 140,838,725 (GRCm39) |
T640M |
unknown |
Het |
Pramel34 |
A |
C |
5: 93,784,147 (GRCm39) |
L439R |
probably damaging |
Het |
Psg18 |
T |
G |
7: 18,083,241 (GRCm39) |
T305P |
probably benign |
Het |
Skil |
T |
A |
3: 31,152,381 (GRCm39) |
V301D |
probably damaging |
Het |
Slc36a1 |
C |
A |
11: 55,109,895 (GRCm39) |
P68T |
probably damaging |
Het |
Smim6 |
T |
C |
11: 115,804,371 (GRCm39) |
F53L |
probably benign |
Het |
Tpgs2 |
G |
A |
18: 25,301,652 (GRCm39) |
T5M |
possibly damaging |
Het |
Trrap |
T |
A |
5: 144,765,410 (GRCm39) |
V2523D |
probably benign |
Het |
Usp9y |
A |
T |
Y: 1,432,197 (GRCm39) |
D429E |
probably damaging |
Het |
Vmn1r125 |
A |
G |
7: 21,006,818 (GRCm39) |
T239A |
probably benign |
Het |
Vmn1r168 |
T |
C |
7: 23,240,421 (GRCm39) |
F93L |
probably damaging |
Het |
Vmn1r88 |
A |
G |
7: 12,912,403 (GRCm39) |
N253S |
possibly damaging |
Het |
Zfp644 |
C |
T |
5: 106,784,343 (GRCm39) |
A735T |
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 |
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 |
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 |
|