Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579F01Rik |
T |
C |
3: 137,879,457 (GRCm39) |
H72R |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,227,937 (GRCm39) |
N660I |
probably damaging |
Het |
Actr8 |
C |
T |
14: 29,715,041 (GRCm39) |
R619* |
probably null |
Het |
Adam18 |
C |
A |
8: 25,104,843 (GRCm39) |
G657V |
probably damaging |
Het |
Adcyap1 |
A |
G |
17: 93,510,227 (GRCm39) |
E85G |
probably benign |
Het |
Akr1c14 |
A |
G |
13: 4,137,302 (GRCm39) |
Y305C |
probably damaging |
Het |
Ankdd1b |
T |
A |
13: 96,591,388 (GRCm39) |
H37L |
possibly damaging |
Het |
Ap4e1 |
T |
C |
2: 126,903,636 (GRCm39) |
L846P |
probably benign |
Het |
Aqp9 |
A |
T |
9: 71,039,966 (GRCm39) |
Y105* |
probably null |
Het |
Arid1b |
C |
T |
17: 5,387,538 (GRCm39) |
Q1664* |
probably null |
Het |
Aup1 |
A |
G |
6: 83,031,588 (GRCm39) |
|
probably benign |
Het |
Bnip1 |
C |
A |
17: 27,005,684 (GRCm39) |
S64* |
probably null |
Het |
Calcr |
T |
A |
6: 3,687,621 (GRCm39) |
Q422L |
probably damaging |
Het |
Ccdc162 |
T |
A |
10: 41,539,147 (GRCm39) |
D407V |
possibly damaging |
Het |
Ccdc66 |
G |
T |
14: 27,208,441 (GRCm39) |
S760R |
probably benign |
Het |
Cd22 |
T |
A |
7: 30,577,193 (GRCm39) |
E38V |
probably damaging |
Het |
Cggbp1 |
T |
C |
16: 64,676,383 (GRCm39) |
Y150H |
probably damaging |
Het |
Col4a2 |
T |
A |
8: 11,496,238 (GRCm39) |
F1620I |
probably damaging |
Het |
Col6a2 |
T |
C |
10: 76,435,662 (GRCm39) |
T858A |
probably benign |
Het |
Dnah7a |
T |
A |
1: 53,580,273 (GRCm39) |
D1554V |
probably damaging |
Het |
Dnajc25 |
A |
T |
4: 59,013,678 (GRCm39) |
Q132L |
probably benign |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Ehbp1l1 |
A |
C |
19: 5,768,795 (GRCm39) |
I836S |
possibly damaging |
Het |
Elf1 |
A |
G |
14: 79,810,779 (GRCm39) |
Q288R |
possibly damaging |
Het |
Fbn1 |
C |
A |
2: 125,150,393 (GRCm39) |
V2608L |
possibly damaging |
Het |
Frmpd1 |
T |
C |
4: 45,268,551 (GRCm39) |
I232T |
possibly damaging |
Het |
Fuca1 |
T |
A |
4: 135,662,137 (GRCm39) |
I355N |
probably damaging |
Het |
Gcnt4 |
A |
G |
13: 97,083,781 (GRCm39) |
D359G |
probably damaging |
Het |
Gm5134 |
T |
C |
10: 75,790,494 (GRCm39) |
M30T |
possibly damaging |
Het |
Grk1 |
T |
G |
8: 13,455,704 (GRCm39) |
L196R |
probably damaging |
Het |
Igkv14-126 |
A |
C |
6: 67,873,548 (GRCm39) |
D92A |
probably damaging |
Het |
Kmt2c |
A |
G |
5: 25,520,600 (GRCm39) |
S1837P |
probably benign |
Het |
Lhx4 |
T |
A |
1: 155,578,300 (GRCm39) |
T281S |
probably benign |
Het |
Lrrc55 |
G |
T |
2: 85,026,653 (GRCm39) |
H124N |
probably benign |
Het |
Marchf8 |
T |
A |
6: 116,383,277 (GRCm39) |
I566N |
possibly damaging |
Het |
Mycbp2 |
G |
A |
14: 103,393,288 (GRCm39) |
A3091V |
probably benign |
Het |
Nlrp4b |
A |
G |
7: 10,458,847 (GRCm39) |
N355S |
probably benign |
Het |
Nmur2 |
A |
G |
11: 55,920,411 (GRCm39) |
V278A |
probably benign |
Het |
Nod1 |
T |
C |
6: 54,921,689 (GRCm39) |
M210V |
probably benign |
Het |
Nt5c1b |
T |
A |
12: 10,422,138 (GRCm39) |
C63* |
probably null |
Het |
Or1e1f |
A |
G |
11: 73,855,568 (GRCm39) |
I45V |
possibly damaging |
Het |
Or1j17 |
A |
T |
2: 36,578,694 (GRCm39) |
K227* |
probably null |
Het |
Or4g7 |
C |
T |
2: 111,309,573 (GRCm39) |
A148V |
possibly damaging |
Het |
Or5d37 |
G |
A |
2: 87,924,008 (GRCm39) |
P91S |
probably damaging |
Het |
Or7g21 |
A |
C |
9: 19,032,253 (GRCm39) |
M1L |
probably benign |
Het |
Or8b37 |
T |
C |
9: 37,959,121 (GRCm39) |
V201A |
probably benign |
Het |
Or8g24 |
C |
T |
9: 38,989,199 (GRCm39) |
V281I |
probably benign |
Het |
Osbp2 |
T |
A |
11: 3,665,153 (GRCm39) |
S517C |
probably damaging |
Het |
Pcdha1 |
C |
T |
18: 37,065,301 (GRCm39) |
P655L |
probably damaging |
Het |
Pdcd6 |
A |
G |
13: 74,452,098 (GRCm39) |
Y181H |
probably damaging |
Het |
Perp |
G |
A |
10: 18,731,502 (GRCm39) |
G154S |
probably damaging |
Het |
Perp |
G |
T |
10: 18,731,503 (GRCm39) |
G154V |
probably damaging |
Het |
Pira13 |
T |
C |
7: 3,825,850 (GRCm39) |
T340A |
probably damaging |
Het |
Prokr1 |
T |
G |
6: 87,558,774 (GRCm39) |
T204P |
possibly damaging |
Het |
Prpf3 |
A |
T |
3: 95,739,890 (GRCm39) |
C630S |
probably damaging |
Het |
Pter |
C |
A |
2: 12,985,359 (GRCm39) |
H230N |
probably damaging |
Het |
Ptprs |
A |
T |
17: 56,724,427 (GRCm39) |
Y1167* |
probably null |
Het |
Rad54l2 |
T |
C |
9: 106,595,121 (GRCm39) |
I279V |
possibly damaging |
Het |
Rora |
T |
A |
9: 69,280,468 (GRCm39) |
L347Q |
probably damaging |
Het |
Runx1t1 |
T |
G |
4: 13,785,136 (GRCm39) |
M1R |
probably null |
Het |
Sdcbp |
A |
G |
4: 6,381,064 (GRCm39) |
S70G |
probably benign |
Het |
Serpinb12 |
A |
G |
1: 106,881,493 (GRCm39) |
Y210C |
probably damaging |
Het |
Sipa1 |
T |
C |
19: 5,701,517 (GRCm39) |
E1015G |
probably damaging |
Het |
Slc15a2 |
A |
C |
16: 36,572,144 (GRCm39) |
L740R |
possibly damaging |
Het |
Specc1 |
A |
G |
11: 62,047,379 (GRCm39) |
E916G |
probably damaging |
Het |
Spta1 |
T |
C |
1: 174,041,743 (GRCm39) |
I1371T |
possibly damaging |
Het |
Tagln3 |
T |
C |
16: 45,533,365 (GRCm39) |
M130V |
probably benign |
Het |
Tchh |
A |
T |
3: 93,353,752 (GRCm39) |
E1064V |
unknown |
Het |
Tdp1 |
A |
T |
12: 99,880,330 (GRCm39) |
S464C |
probably damaging |
Het |
Tdp1 |
G |
C |
12: 99,880,331 (GRCm39) |
S464T |
probably benign |
Het |
Tenm3 |
T |
C |
8: 48,729,884 (GRCm39) |
Y1374C |
probably damaging |
Het |
Tmprss3 |
A |
T |
17: 31,402,833 (GRCm39) |
Y455* |
probably null |
Het |
Ttc5 |
A |
G |
14: 51,003,385 (GRCm39) |
V433A |
possibly damaging |
Het |
Wnt5a |
A |
T |
14: 28,240,449 (GRCm39) |
R180* |
probably null |
Het |
Zfp53 |
A |
G |
17: 21,728,372 (GRCm39) |
D135G |
probably benign |
Het |
Zfp619 |
T |
A |
7: 39,186,969 (GRCm39) |
C1000S |
probably damaging |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
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 |
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 |
R7226:Chd3
|
UTSW |
11 |
69,260,037 (GRCm39) |
missense |
unknown |
|
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 |
|