Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700025B11Rik |
C |
T |
15: 77,443,189 (GRCm39) |
V17I |
unknown |
Het |
Acad8 |
T |
A |
9: 26,889,726 (GRCm39) |
K323* |
probably null |
Het |
Adam18 |
A |
T |
8: 25,137,824 (GRCm39) |
C339S |
probably damaging |
Het |
Anxa7 |
A |
G |
14: 20,510,263 (GRCm39) |
F396L |
probably damaging |
Het |
Ap2m1 |
T |
A |
16: 20,358,201 (GRCm39) |
V73D |
probably damaging |
Het |
Asic2 |
A |
T |
11: 80,862,340 (GRCm39) |
I270N |
probably damaging |
Het |
Atrn |
T |
G |
2: 130,828,664 (GRCm39) |
C1070G |
probably damaging |
Het |
Bag6 |
A |
G |
17: 35,361,921 (GRCm39) |
N517S |
unknown |
Het |
Bhmt1b |
A |
G |
18: 87,775,590 (GRCm39) |
D371G |
possibly damaging |
Het |
Bltp3b |
A |
T |
10: 89,644,503 (GRCm39) |
Q1181L |
probably benign |
Het |
Cavin1 |
A |
C |
11: 100,861,284 (GRCm39) |
D3E |
probably benign |
Het |
Cc2d2b |
T |
C |
19: 40,779,751 (GRCm39) |
L571P |
unknown |
Het |
Ccbe1 |
A |
T |
18: 66,216,199 (GRCm39) |
C175S |
probably damaging |
Het |
Cd19 |
A |
G |
7: 126,013,995 (GRCm39) |
L5P |
unknown |
Het |
Cd46 |
A |
G |
1: 194,724,314 (GRCm39) |
S362P |
possibly damaging |
Het |
Celf5 |
A |
G |
10: 81,303,863 (GRCm39) |
S198P |
probably damaging |
Het |
Cep170b |
A |
G |
12: 112,704,359 (GRCm39) |
R706G |
possibly damaging |
Het |
Cpsf6 |
A |
C |
10: 117,197,727 (GRCm39) |
W253G |
unknown |
Het |
Cyp27a1 |
G |
A |
1: 74,776,507 (GRCm39) |
G481D |
probably damaging |
Het |
Ddr1 |
C |
T |
17: 36,002,039 (GRCm39) |
D218N |
possibly damaging |
Het |
Dhx34 |
A |
T |
7: 15,932,801 (GRCm39) |
V1046D |
probably damaging |
Het |
Dhx9 |
A |
T |
1: 153,341,423 (GRCm39) |
D608E |
probably benign |
Het |
Dnajc6 |
C |
A |
4: 101,496,569 (GRCm39) |
A912E |
probably damaging |
Het |
Ehmt1 |
T |
C |
2: 24,694,794 (GRCm39) |
D1051G |
probably damaging |
Het |
Fam217b |
C |
A |
2: 178,062,996 (GRCm39) |
A320E |
probably benign |
Het |
Farsa |
T |
A |
8: 85,590,689 (GRCm39) |
I169N |
probably benign |
Het |
Fbn2 |
A |
G |
18: 58,170,142 (GRCm39) |
C2210R |
probably damaging |
Het |
Fbxo3 |
T |
A |
2: 103,880,642 (GRCm39) |
S251T |
probably benign |
Het |
Fer1l6 |
C |
T |
15: 58,462,384 (GRCm39) |
T813I |
probably benign |
Het |
Ftl1-ps1 |
A |
T |
13: 74,555,114 (GRCm39) |
E131V |
probably damaging |
Het |
Gins3 |
T |
A |
8: 96,364,499 (GRCm39) |
I83N |
probably damaging |
Het |
Gja3 |
T |
C |
14: 57,273,350 (GRCm39) |
T341A |
probably benign |
Het |
Gja5 |
A |
G |
3: 96,958,174 (GRCm39) |
Y77C |
probably damaging |
Het |
Gm7247 |
A |
G |
14: 51,602,808 (GRCm39) |
K48R |
probably damaging |
Het |
Gsx2 |
C |
A |
5: 75,236,621 (GRCm39) |
S67* |
probably null |
Het |
H2-Q5 |
T |
A |
17: 35,616,089 (GRCm39) |
L217Q |
|
Het |
Impg2 |
T |
A |
16: 56,087,467 (GRCm39) |
C1095* |
probably null |
Het |
Itga7 |
G |
T |
10: 128,776,801 (GRCm39) |
W222L |
probably damaging |
Het |
Kdm2b |
T |
A |
5: 123,059,512 (GRCm39) |
D530V |
possibly damaging |
Het |
Klhdc8a |
A |
T |
1: 132,230,344 (GRCm39) |
D153V |
probably damaging |
Het |
Lin28a |
C |
T |
4: 133,733,619 (GRCm39) |
G143S |
probably damaging |
Het |
Memo1 |
A |
G |
17: 74,509,338 (GRCm39) |
L227S |
probably damaging |
Het |
Mettl27 |
T |
A |
5: 134,964,657 (GRCm39) |
V138E |
probably damaging |
Het |
Mov10 |
G |
T |
3: 104,708,328 (GRCm39) |
L474I |
probably damaging |
Het |
Nat10 |
T |
C |
2: 103,557,098 (GRCm39) |
N852S |
probably benign |
Het |
Nfkbie |
T |
C |
17: 45,870,153 (GRCm39) |
V166A |
possibly damaging |
Het |
Nktr |
T |
C |
9: 121,575,599 (GRCm39) |
M369T |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,258,149 (GRCm39) |
N589I |
probably benign |
Het |
Nrn1 |
G |
A |
13: 36,914,577 (GRCm39) |
R8C |
probably benign |
Het |
Nrsn1 |
A |
G |
13: 25,437,451 (GRCm39) |
I159T |
probably damaging |
Het |
Or1e29 |
A |
G |
11: 73,667,503 (GRCm39) |
S217P |
possibly damaging |
Het |
Or2h15 |
C |
T |
17: 38,441,324 (GRCm39) |
G253D |
probably benign |
Het |
Or5p61 |
A |
T |
7: 107,758,164 (GRCm39) |
D305E |
probably benign |
Het |
Or6c88 |
G |
A |
10: 129,406,584 (GRCm39) |
G20D |
probably benign |
Het |
Osbp |
T |
A |
19: 11,956,031 (GRCm39) |
D385E |
probably benign |
Het |
Pan3 |
T |
A |
5: 147,463,802 (GRCm39) |
N547K |
probably damaging |
Het |
Pip4p2 |
T |
A |
4: 14,892,464 (GRCm39) |
D109E |
probably damaging |
Het |
Pum1 |
C |
A |
4: 130,499,292 (GRCm39) |
T1036K |
probably damaging |
Het |
Rad54l2 |
C |
A |
9: 106,590,671 (GRCm39) |
R485L |
probably damaging |
Het |
Rps26 |
A |
T |
10: 128,461,087 (GRCm39) |
F101I |
unknown |
Het |
Sdsl |
T |
C |
5: 120,598,702 (GRCm39) |
N138S |
probably benign |
Het |
Slc28a2b |
C |
A |
2: 122,353,013 (GRCm39) |
R453S |
probably benign |
Het |
Slc39a6 |
A |
T |
18: 24,717,084 (GRCm39) |
H649Q |
probably damaging |
Het |
Snip1 |
T |
A |
4: 124,965,273 (GRCm39) |
F226Y |
probably benign |
Het |
Srrd |
T |
C |
5: 112,485,322 (GRCm39) |
T334A |
unknown |
Het |
St14 |
C |
T |
9: 31,011,448 (GRCm39) |
D448N |
possibly damaging |
Het |
Tmem270 |
T |
A |
5: 134,930,538 (GRCm39) |
Q241L |
probably benign |
Het |
Tubb4b |
T |
C |
2: 25,114,180 (GRCm39) |
D41G |
probably benign |
Het |
Usf3 |
T |
C |
16: 44,040,368 (GRCm39) |
M1616T |
possibly damaging |
Het |
Vmn2r95 |
A |
T |
17: 18,672,245 (GRCm39) |
I733F |
possibly damaging |
Het |
Zfp976 |
A |
T |
7: 42,262,684 (GRCm39) |
C385* |
probably null |
Het |
|
Other mutations in Chd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00478:Chd3
|
APN |
11 |
69,247,888 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00551:Chd3
|
APN |
11 |
69,237,455 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00661:Chd3
|
APN |
11 |
69,248,209 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00698:Chd3
|
APN |
11 |
69,240,697 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01075:Chd3
|
APN |
11 |
69,250,791 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01309:Chd3
|
APN |
11 |
69,248,557 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01317:Chd3
|
APN |
11 |
69,244,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01374:Chd3
|
APN |
11 |
69,250,806 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01444:Chd3
|
APN |
11 |
69,239,568 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01617:Chd3
|
APN |
11 |
69,249,060 (GRCm39) |
unclassified |
probably benign |
|
IGL01635:Chd3
|
APN |
11 |
69,252,076 (GRCm39) |
splice site |
probably benign |
|
IGL01942:Chd3
|
APN |
11 |
69,240,931 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01962:Chd3
|
APN |
11 |
69,248,319 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01981:Chd3
|
APN |
11 |
69,251,501 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02022:Chd3
|
APN |
11 |
69,251,886 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02098:Chd3
|
APN |
11 |
69,250,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02218:Chd3
|
APN |
11 |
69,242,920 (GRCm39) |
unclassified |
probably benign |
|
IGL02415:Chd3
|
APN |
11 |
69,239,739 (GRCm39) |
splice site |
probably benign |
|
IGL02648:Chd3
|
APN |
11 |
69,242,976 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Chd3
|
APN |
11 |
69,251,874 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03030:Chd3
|
APN |
11 |
69,245,230 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03102:Chd3
|
APN |
11 |
69,252,022 (GRCm39) |
nonsense |
probably null |
|
IGL03168:Chd3
|
APN |
11 |
69,239,741 (GRCm39) |
splice site |
probably benign |
|
IGL03327:Chd3
|
APN |
11 |
69,241,012 (GRCm39) |
missense |
probably damaging |
1.00 |
burg
|
UTSW |
11 |
69,247,380 (GRCm39) |
missense |
probably damaging |
1.00 |
castello
|
UTSW |
11 |
69,246,648 (GRCm39) |
critical splice acceptor site |
probably benign |
|
feste
|
UTSW |
11 |
69,245,252 (GRCm39) |
nonsense |
probably null |
|
Fortress
|
UTSW |
11 |
69,254,876 (GRCm39) |
nonsense |
probably null |
|
moat
|
UTSW |
11 |
69,250,011 (GRCm39) |
missense |
probably damaging |
0.98 |
Redoubt
|
UTSW |
11 |
69,244,727 (GRCm39) |
unclassified |
probably benign |
|
schloss
|
UTSW |
11 |
69,252,886 (GRCm39) |
nonsense |
probably null |
|
siege
|
UTSW |
11 |
69,247,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Chd3
|
UTSW |
11 |
69,240,732 (GRCm39) |
missense |
probably damaging |
0.99 |
R0009:Chd3
|
UTSW |
11 |
69,240,732 (GRCm39) |
missense |
probably damaging |
0.99 |
R0056:Chd3
|
UTSW |
11 |
69,250,739 (GRCm39) |
unclassified |
probably benign |
|
R0129:Chd3
|
UTSW |
11 |
69,239,327 (GRCm39) |
nonsense |
probably null |
|
R0130:Chd3
|
UTSW |
11 |
69,250,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Chd3
|
UTSW |
11 |
69,247,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0330:Chd3
|
UTSW |
11 |
69,247,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R0449:Chd3
|
UTSW |
11 |
69,248,367 (GRCm39) |
missense |
probably damaging |
0.98 |
R0502:Chd3
|
UTSW |
11 |
69,244,931 (GRCm39) |
missense |
probably damaging |
0.98 |
R0540:Chd3
|
UTSW |
11 |
69,235,184 (GRCm39) |
missense |
probably damaging |
0.98 |
R0571:Chd3
|
UTSW |
11 |
69,252,495 (GRCm39) |
critical splice donor site |
probably null |
|
R0607:Chd3
|
UTSW |
11 |
69,235,184 (GRCm39) |
missense |
probably damaging |
0.98 |
R0616:Chd3
|
UTSW |
11 |
69,236,313 (GRCm39) |
missense |
probably damaging |
0.96 |
R0630:Chd3
|
UTSW |
11 |
69,238,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R1436:Chd3
|
UTSW |
11 |
69,248,400 (GRCm39) |
splice site |
probably null |
|
R1484:Chd3
|
UTSW |
11 |
69,250,725 (GRCm39) |
missense |
probably benign |
0.17 |
R1741:Chd3
|
UTSW |
11 |
69,246,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R1748:Chd3
|
UTSW |
11 |
69,255,523 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1751:Chd3
|
UTSW |
11 |
69,244,727 (GRCm39) |
unclassified |
probably benign |
|
R1833:Chd3
|
UTSW |
11 |
69,244,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R2012:Chd3
|
UTSW |
11 |
69,239,878 (GRCm39) |
missense |
probably benign |
0.01 |
R2101:Chd3
|
UTSW |
11 |
69,239,877 (GRCm39) |
missense |
probably benign |
|
R2147:Chd3
|
UTSW |
11 |
69,239,854 (GRCm39) |
missense |
probably benign |
0.00 |
R2513:Chd3
|
UTSW |
11 |
69,251,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R2877:Chd3
|
UTSW |
11 |
69,251,998 (GRCm39) |
nonsense |
probably null |
|
R2879:Chd3
|
UTSW |
11 |
69,254,924 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2880:Chd3
|
UTSW |
11 |
69,242,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R2881:Chd3
|
UTSW |
11 |
69,242,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R2973:Chd3
|
UTSW |
11 |
69,251,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R3611:Chd3
|
UTSW |
11 |
69,252,973 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3743:Chd3
|
UTSW |
11 |
69,254,876 (GRCm39) |
nonsense |
probably null |
|
R3845:Chd3
|
UTSW |
11 |
69,237,585 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3889:Chd3
|
UTSW |
11 |
69,250,011 (GRCm39) |
missense |
probably damaging |
0.98 |
R4007:Chd3
|
UTSW |
11 |
69,239,827 (GRCm39) |
missense |
probably benign |
|
R4115:Chd3
|
UTSW |
11 |
69,248,343 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4515:Chd3
|
UTSW |
11 |
69,240,703 (GRCm39) |
missense |
probably benign |
0.00 |
R4612:Chd3
|
UTSW |
11 |
69,244,035 (GRCm39) |
nonsense |
probably null |
|
R4622:Chd3
|
UTSW |
11 |
69,239,834 (GRCm39) |
missense |
probably damaging |
0.98 |
R4634:Chd3
|
UTSW |
11 |
69,253,013 (GRCm39) |
unclassified |
probably benign |
|
R4635:Chd3
|
UTSW |
11 |
69,253,013 (GRCm39) |
unclassified |
probably benign |
|
R4859:Chd3
|
UTSW |
11 |
69,250,722 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4930:Chd3
|
UTSW |
11 |
69,245,034 (GRCm39) |
unclassified |
probably benign |
|
R5173:Chd3
|
UTSW |
11 |
69,260,069 (GRCm39) |
unclassified |
probably benign |
|
R5287:Chd3
|
UTSW |
11 |
69,239,895 (GRCm39) |
splice site |
probably null |
|
R5403:Chd3
|
UTSW |
11 |
69,239,895 (GRCm39) |
splice site |
probably null |
|
R5511:Chd3
|
UTSW |
11 |
69,252,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R5666:Chd3
|
UTSW |
11 |
69,244,177 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5702:Chd3
|
UTSW |
11 |
69,252,261 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6045:Chd3
|
UTSW |
11 |
69,242,944 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6063:Chd3
|
UTSW |
11 |
69,240,063 (GRCm39) |
missense |
probably benign |
|
R6211:Chd3
|
UTSW |
11 |
69,243,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R6215:Chd3
|
UTSW |
11 |
69,247,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R6217:Chd3
|
UTSW |
11 |
69,236,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Chd3
|
UTSW |
11 |
69,244,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R6329:Chd3
|
UTSW |
11 |
69,252,510 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6349:Chd3
|
UTSW |
11 |
69,254,857 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6414:Chd3
|
UTSW |
11 |
69,243,371 (GRCm39) |
critical splice donor site |
probably null |
|
R6453:Chd3
|
UTSW |
11 |
69,240,938 (GRCm39) |
nonsense |
probably null |
|
R6548:Chd3
|
UTSW |
11 |
69,252,886 (GRCm39) |
nonsense |
probably null |
|
R6582:Chd3
|
UTSW |
11 |
69,259,982 (GRCm39) |
unclassified |
probably benign |
|
R6721:Chd3
|
UTSW |
11 |
69,260,045 (GRCm39) |
unclassified |
probably benign |
|
R6776:Chd3
|
UTSW |
11 |
69,245,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R6900:Chd3
|
UTSW |
11 |
69,245,271 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7085:Chd3
|
UTSW |
11 |
69,260,027 (GRCm39) |
missense |
unknown |
|
R7136:Chd3
|
UTSW |
11 |
69,239,264 (GRCm39) |
missense |
probably null |
0.37 |
R7164:Chd3
|
UTSW |
11 |
69,253,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R7200:Chd3
|
UTSW |
11 |
69,254,921 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7238:Chd3
|
UTSW |
11 |
69,254,873 (GRCm39) |
missense |
probably benign |
0.31 |
R7316:Chd3
|
UTSW |
11 |
69,236,394 (GRCm39) |
missense |
probably damaging |
0.99 |
R7560:Chd3
|
UTSW |
11 |
69,247,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R7684:Chd3
|
UTSW |
11 |
69,248,692 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7748:Chd3
|
UTSW |
11 |
69,246,459 (GRCm39) |
missense |
probably benign |
0.00 |
R7820:Chd3
|
UTSW |
11 |
69,244,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R7885:Chd3
|
UTSW |
11 |
69,247,451 (GRCm39) |
missense |
probably benign |
0.13 |
R8150:Chd3
|
UTSW |
11 |
69,254,510 (GRCm39) |
missense |
probably benign |
0.02 |
R8161:Chd3
|
UTSW |
11 |
69,241,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Chd3
|
UTSW |
11 |
69,251,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Chd3
|
UTSW |
11 |
69,241,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R8423:Chd3
|
UTSW |
11 |
69,245,252 (GRCm39) |
nonsense |
probably null |
|
R8690:Chd3
|
UTSW |
11 |
69,246,648 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8828:Chd3
|
UTSW |
11 |
69,247,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R8857:Chd3
|
UTSW |
11 |
69,253,146 (GRCm39) |
missense |
probably benign |
0.22 |
R9124:Chd3
|
UTSW |
11 |
69,260,162 (GRCm39) |
missense |
unknown |
|
R9170:Chd3
|
UTSW |
11 |
69,241,648 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9213:Chd3
|
UTSW |
11 |
69,255,628 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9285:Chd3
|
UTSW |
11 |
69,249,954 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9293:Chd3
|
UTSW |
11 |
69,244,027 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9368:Chd3
|
UTSW |
11 |
69,251,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R9521:Chd3
|
UTSW |
11 |
69,249,133 (GRCm39) |
missense |
probably benign |
0.01 |
R9544:Chd3
|
UTSW |
11 |
69,241,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R9554:Chd3
|
UTSW |
11 |
69,251,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R9588:Chd3
|
UTSW |
11 |
69,241,046 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Chd3
|
UTSW |
11 |
69,247,084 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Chd3
|
UTSW |
11 |
69,245,271 (GRCm39) |
missense |
possibly damaging |
0.64 |
Z1186:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1186:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1187:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1187:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1188:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1188:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1189:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1189:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1190:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1190:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1191:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1192:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1192:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
|