Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
C |
T |
12: 72,953,008 (GRCm39) |
E242K |
possibly damaging |
Het |
A930011G23Rik |
A |
G |
5: 99,370,263 (GRCm39) |
M499T |
possibly damaging |
Het |
Abcb8 |
G |
A |
5: 24,605,779 (GRCm39) |
V196M |
possibly damaging |
Het |
Ahnak |
T |
C |
19: 8,988,331 (GRCm39) |
M3205T |
possibly damaging |
Het |
Ankrd1 |
A |
G |
19: 36,092,433 (GRCm39) |
Y265H |
probably damaging |
Het |
Apeh |
A |
G |
9: 107,965,024 (GRCm39) |
S446P |
probably benign |
Het |
Apip |
C |
A |
2: 102,922,226 (GRCm39) |
Y197* |
probably null |
Het |
Arhgef11 |
T |
G |
3: 87,635,901 (GRCm39) |
V925G |
probably damaging |
Het |
Arid4b |
T |
C |
13: 14,362,062 (GRCm39) |
V929A |
probably damaging |
Het |
Asah2 |
T |
A |
19: 32,030,306 (GRCm39) |
D122V |
probably benign |
Het |
B2m |
A |
T |
2: 121,982,128 (GRCm39) |
D116V |
possibly damaging |
Het |
Bhmt-ps1 |
A |
G |
4: 26,369,184 (GRCm39) |
|
noncoding transcript |
Het |
Cacna1g |
T |
A |
11: 94,334,899 (GRCm39) |
I803F |
probably damaging |
Het |
Ccdc43 |
A |
T |
11: 102,581,111 (GRCm39) |
V113E |
probably damaging |
Het |
Cenpj |
A |
T |
14: 56,772,238 (GRCm39) |
Y388* |
probably null |
Het |
Chil3 |
C |
T |
3: 106,071,524 (GRCm39) |
D47N |
possibly damaging |
Het |
Colgalt2 |
A |
G |
1: 152,375,710 (GRCm39) |
T361A |
possibly damaging |
Het |
Cops3 |
C |
A |
11: 59,726,193 (GRCm39) |
|
probably benign |
Het |
Crb2 |
G |
T |
2: 37,673,326 (GRCm39) |
G74V |
probably damaging |
Het |
Cspg4b |
G |
T |
13: 113,464,196 (GRCm39) |
G1453C |
probably damaging |
Het |
Cyp20a1 |
A |
T |
1: 60,405,878 (GRCm39) |
Y224F |
probably damaging |
Het |
Diaph3 |
A |
G |
14: 87,378,602 (GRCm39) |
|
probably benign |
Het |
Dnah3 |
A |
T |
7: 119,550,904 (GRCm39) |
Y3127* |
probably null |
Het |
Eef1akmt3 |
A |
C |
10: 126,877,224 (GRCm39) |
S14A |
possibly damaging |
Het |
Ehf |
C |
A |
2: 103,097,202 (GRCm39) |
R250L |
probably damaging |
Het |
Eps8l1 |
G |
A |
7: 4,463,915 (GRCm39) |
R13Q |
possibly damaging |
Het |
Frem2 |
A |
C |
3: 53,563,736 (GRCm39) |
V257G |
possibly damaging |
Het |
Gc |
T |
C |
5: 89,587,448 (GRCm39) |
T259A |
probably benign |
Het |
Gm4952 |
A |
T |
19: 12,604,376 (GRCm39) |
N263Y |
probably benign |
Het |
Gpcpd1 |
T |
A |
2: 132,388,794 (GRCm39) |
H326L |
probably damaging |
Het |
Helz |
T |
C |
11: 107,510,994 (GRCm39) |
F617L |
probably damaging |
Het |
Hoxb4 |
T |
C |
11: 96,209,662 (GRCm39) |
Y23H |
probably damaging |
Het |
Hsf4 |
T |
A |
8: 105,999,330 (GRCm39) |
|
probably null |
Het |
Ift56 |
A |
T |
6: 38,368,475 (GRCm39) |
Y174F |
probably damaging |
Het |
Ighv1-81 |
T |
C |
12: 115,883,924 (GRCm39) |
D109G |
probably damaging |
Het |
Irx4 |
T |
C |
13: 73,417,032 (GRCm39) |
V476A |
probably benign |
Het |
Katnb1 |
T |
A |
8: 95,823,922 (GRCm39) |
|
probably null |
Het |
L3mbtl1 |
A |
G |
2: 162,807,692 (GRCm39) |
Y490C |
probably damaging |
Het |
Lemd2 |
A |
G |
17: 27,412,806 (GRCm39) |
|
probably null |
Het |
Lrrc38 |
A |
T |
4: 143,096,438 (GRCm39) |
T250S |
probably damaging |
Het |
Map3k8 |
A |
T |
18: 4,349,215 (GRCm39) |
Y34* |
probably null |
Het |
Mgst1 |
T |
A |
6: 138,130,507 (GRCm39) |
F79I |
probably benign |
Het |
Midn |
T |
C |
10: 79,991,189 (GRCm39) |
S357P |
probably benign |
Het |
Mmp3 |
T |
A |
9: 7,447,640 (GRCm39) |
D208E |
probably benign |
Het |
Mrps26 |
A |
G |
2: 130,406,862 (GRCm39) |
E163G |
probably damaging |
Het |
Mycbpap |
A |
T |
11: 94,393,983 (GRCm39) |
M371K |
probably benign |
Het |
Mynn |
A |
C |
3: 30,661,191 (GRCm39) |
N91T |
probably damaging |
Het |
Nek11 |
A |
G |
9: 105,177,265 (GRCm39) |
L292P |
probably damaging |
Het |
Nid1 |
A |
T |
13: 13,684,596 (GRCm39) |
R1228W |
probably damaging |
Het |
Nphs2 |
T |
C |
1: 156,148,499 (GRCm39) |
Y121H |
probably damaging |
Het |
Or1f19 |
T |
G |
16: 3,410,299 (GRCm39) |
L13R |
probably damaging |
Het |
Or4p7 |
G |
A |
2: 88,222,284 (GRCm39) |
R231H |
probably benign |
Het |
Or5ac22 |
C |
A |
16: 59,135,236 (GRCm39) |
C178F |
probably damaging |
Het |
Or5ap2 |
T |
A |
2: 85,680,237 (GRCm39) |
I147N |
probably benign |
Het |
Or5d38 |
A |
C |
2: 87,954,684 (GRCm39) |
I215S |
probably benign |
Het |
Or7e176 |
T |
C |
9: 20,171,313 (GRCm39) |
I59T |
probably damaging |
Het |
Or9q2 |
T |
C |
19: 13,772,915 (GRCm39) |
H20R |
probably benign |
Het |
P2rx7 |
C |
T |
5: 122,808,542 (GRCm39) |
T308M |
probably damaging |
Het |
Prdx6 |
C |
T |
1: 161,069,263 (GRCm39) |
|
probably benign |
Het |
Rad54b |
T |
A |
4: 11,615,579 (GRCm39) |
D862E |
probably damaging |
Het |
Ripor1 |
A |
G |
8: 106,343,814 (GRCm39) |
Y344C |
probably damaging |
Het |
Rnf112 |
T |
C |
11: 61,344,291 (GRCm39) |
M43V |
probably benign |
Het |
Rp1l1 |
A |
G |
14: 64,269,655 (GRCm39) |
N1747S |
probably benign |
Het |
Rps27 |
A |
G |
3: 90,120,306 (GRCm39) |
V22A |
probably damaging |
Het |
Spaca1 |
A |
G |
4: 34,044,236 (GRCm39) |
V86A |
possibly damaging |
Het |
Spdef |
A |
G |
17: 27,937,136 (GRCm39) |
Y156H |
probably damaging |
Het |
Specc1 |
A |
C |
11: 62,009,784 (GRCm39) |
E433D |
possibly damaging |
Het |
Srpra |
T |
A |
9: 35,126,326 (GRCm39) |
F506L |
probably benign |
Het |
Stxbp5 |
A |
G |
10: 9,636,610 (GRCm39) |
|
probably benign |
Het |
Syne1 |
C |
T |
10: 5,002,777 (GRCm39) |
R8046Q |
probably damaging |
Het |
Tbx5 |
T |
A |
5: 120,021,090 (GRCm39) |
S365R |
probably benign |
Het |
Terb1 |
G |
T |
8: 105,174,580 (GRCm39) |
P698Q |
probably benign |
Het |
Tmbim7 |
T |
A |
5: 3,711,948 (GRCm39) |
Y27* |
probably null |
Het |
Tmem106c |
C |
A |
15: 97,862,909 (GRCm39) |
A60E |
possibly damaging |
Het |
Ttc6 |
T |
A |
12: 57,720,609 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,562,714 (GRCm39) |
I28747V |
possibly damaging |
Het |
Unc13a |
C |
T |
8: 72,083,148 (GRCm39) |
|
probably null |
Het |
Wdr81 |
T |
C |
11: 75,342,750 (GRCm39) |
D839G |
probably benign |
Het |
Wfdc15a |
G |
C |
2: 164,041,725 (GRCm39) |
Q33E |
probably benign |
Het |
Zfp456 |
T |
C |
13: 67,515,065 (GRCm39) |
R214G |
probably benign |
Het |
Zfp457 |
T |
A |
13: 67,442,164 (GRCm39) |
Y137F |
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 |
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 |
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 |
|