Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2 |
A |
T |
3: 59,914,474 (GRCm39) |
N26Y |
probably damaging |
Het |
Aass |
C |
T |
6: 23,092,329 (GRCm39) |
D194N |
probably damaging |
Het |
Acp7 |
T |
C |
7: 28,313,822 (GRCm39) |
Y404C |
probably damaging |
Het |
Acsl1 |
A |
T |
8: 46,979,410 (GRCm39) |
I421L |
probably benign |
Het |
Adgrb3 |
A |
T |
1: 25,865,569 (GRCm39) |
D91E |
probably damaging |
Het |
Adgrg3 |
T |
C |
8: 95,767,153 (GRCm39) |
S503P |
probably damaging |
Het |
Adgrg6 |
A |
T |
10: 14,317,243 (GRCm39) |
C526S |
probably damaging |
Het |
Arhgap32 |
A |
T |
9: 32,150,644 (GRCm39) |
I15F |
possibly damaging |
Het |
Arid1b |
G |
T |
17: 5,045,325 (GRCm39) |
|
probably benign |
Het |
Asnsd1 |
A |
G |
1: 53,387,378 (GRCm39) |
V83A |
probably benign |
Het |
Atg101 |
A |
G |
15: 101,191,213 (GRCm39) |
|
probably benign |
Het |
Atp8a1 |
T |
C |
5: 67,840,056 (GRCm39) |
|
probably benign |
Het |
Aurkb |
T |
A |
11: 68,939,188 (GRCm39) |
L137Q |
probably damaging |
Het |
AY702103 |
A |
T |
17: 50,547,029 (GRCm39) |
|
noncoding transcript |
Het |
B3gnt9 |
A |
G |
8: 105,980,477 (GRCm39) |
S304P |
probably benign |
Het |
Babam2 |
T |
C |
5: 32,164,656 (GRCm39) |
V310A |
probably damaging |
Het |
Batf |
A |
G |
12: 85,755,327 (GRCm39) |
D60G |
possibly damaging |
Het |
Baz1a |
A |
T |
12: 54,988,300 (GRCm39) |
I283K |
probably benign |
Het |
Bmerb1 |
A |
C |
16: 13,911,786 (GRCm39) |
E44A |
possibly damaging |
Het |
Bst1 |
T |
G |
5: 43,976,261 (GRCm39) |
|
probably benign |
Het |
C2 |
C |
A |
17: 35,082,650 (GRCm39) |
V490L |
probably damaging |
Het |
Cacna1e |
T |
C |
1: 154,347,311 (GRCm39) |
E952G |
possibly damaging |
Het |
Ccnyl1 |
A |
G |
1: 64,757,417 (GRCm39) |
D262G |
probably damaging |
Het |
Cdc42bpa |
A |
T |
1: 179,902,223 (GRCm39) |
K493N |
probably damaging |
Het |
Cenpe |
A |
G |
3: 134,949,469 (GRCm39) |
T85A |
probably benign |
Het |
Ces2e |
T |
A |
8: 105,655,341 (GRCm39) |
|
probably null |
Het |
Cpm |
A |
G |
10: 117,506,202 (GRCm39) |
N188D |
possibly damaging |
Het |
Cspg4b |
A |
G |
13: 113,456,615 (GRCm39) |
D887G |
probably benign |
Het |
Ctnnd2 |
A |
T |
15: 30,887,315 (GRCm39) |
M781L |
probably benign |
Het |
Ctnnd2 |
A |
G |
15: 31,009,259 (GRCm39) |
T1094A |
probably benign |
Het |
Cux1 |
T |
C |
5: 136,337,154 (GRCm39) |
K657R |
probably damaging |
Het |
Ddx54 |
G |
A |
5: 120,764,488 (GRCm39) |
V732M |
probably damaging |
Het |
Ecrg4 |
G |
T |
1: 43,781,481 (GRCm39) |
R121L |
possibly damaging |
Het |
Efna5 |
T |
C |
17: 62,958,040 (GRCm39) |
D72G |
probably benign |
Het |
Eva1c |
T |
A |
16: 90,694,343 (GRCm39) |
|
probably null |
Het |
Evi5l |
T |
C |
8: 4,252,909 (GRCm39) |
|
probably benign |
Het |
Fasl |
A |
G |
1: 161,614,703 (GRCm39) |
L120P |
probably benign |
Het |
H2-M9 |
A |
T |
17: 36,952,716 (GRCm39) |
|
probably null |
Het |
Hdgf |
C |
A |
3: 87,821,884 (GRCm39) |
N198K |
possibly damaging |
Het |
Hspa9 |
A |
T |
18: 35,082,090 (GRCm39) |
M172K |
possibly damaging |
Het |
Il1r1 |
A |
C |
1: 40,351,580 (GRCm39) |
L406F |
probably damaging |
Het |
Il31 |
T |
C |
5: 123,618,498 (GRCm39) |
D96G |
probably damaging |
Het |
Inhbc |
A |
G |
10: 127,193,146 (GRCm39) |
I290T |
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,290,693 (GRCm39) |
V3589D |
possibly damaging |
Het |
Lrrc14 |
A |
T |
15: 76,600,540 (GRCm39) |
|
probably benign |
Het |
Lyst |
G |
A |
13: 13,848,983 (GRCm39) |
A2057T |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,266,141 (GRCm39) |
|
probably null |
Het |
Mapk10 |
C |
A |
5: 103,137,590 (GRCm39) |
G209V |
probably damaging |
Het |
Mcoln1 |
A |
G |
8: 3,555,923 (GRCm39) |
I73V |
probably damaging |
Het |
Met |
G |
T |
6: 17,513,383 (GRCm39) |
R411L |
probably benign |
Het |
Mplkipl1 |
C |
T |
19: 61,164,364 (GRCm39) |
G24R |
unknown |
Het |
Mrpl4 |
G |
A |
9: 20,918,793 (GRCm39) |
R176Q |
probably damaging |
Het |
Mrtfb |
G |
A |
16: 13,150,570 (GRCm39) |
G102D |
probably damaging |
Het |
Mtmr3 |
T |
C |
11: 4,441,067 (GRCm39) |
T528A |
possibly damaging |
Het |
Mtmr7 |
A |
T |
8: 41,034,583 (GRCm39) |
N246K |
probably damaging |
Het |
Mycbp2 |
G |
T |
14: 103,457,415 (GRCm39) |
T1627K |
probably benign |
Het |
Necab3 |
A |
G |
2: 154,397,502 (GRCm39) |
|
probably null |
Het |
Nr1d1 |
C |
T |
11: 98,660,710 (GRCm39) |
C419Y |
probably damaging |
Het |
Nwd1 |
C |
A |
8: 73,393,928 (GRCm39) |
A397E |
probably damaging |
Het |
Oas1f |
A |
T |
5: 120,986,390 (GRCm39) |
K114N |
probably damaging |
Het |
Or13a18 |
T |
A |
7: 140,190,611 (GRCm39) |
C169* |
probably null |
Het |
Or1e35 |
C |
A |
11: 73,797,737 (GRCm39) |
V194F |
possibly damaging |
Het |
Or51ab3 |
G |
T |
7: 103,201,361 (GRCm39) |
R123L |
probably benign |
Het |
Or5k8 |
A |
T |
16: 58,644,469 (GRCm39) |
I201N |
possibly damaging |
Het |
Or5w13 |
T |
A |
2: 87,523,987 (GRCm39) |
K80* |
probably null |
Het |
Osbpl8 |
T |
C |
10: 111,127,357 (GRCm39) |
S814P |
probably benign |
Het |
Pcdhgb7 |
A |
T |
18: 37,886,183 (GRCm39) |
Q451L |
probably benign |
Het |
Pde7b |
C |
T |
10: 20,294,538 (GRCm39) |
R300Q |
probably damaging |
Het |
Pgghg |
A |
G |
7: 140,521,409 (GRCm39) |
|
probably null |
Het |
Plcg1 |
A |
G |
2: 160,589,688 (GRCm39) |
|
probably benign |
Het |
Plxna2 |
A |
T |
1: 194,494,458 (GRCm39) |
I1892L |
probably benign |
Het |
Ppt2 |
A |
G |
17: 34,844,875 (GRCm39) |
V123A |
probably benign |
Het |
Prdx5 |
G |
T |
19: 6,884,341 (GRCm39) |
|
probably benign |
Het |
Prpf40b |
A |
G |
15: 99,214,197 (GRCm39) |
D819G |
probably benign |
Het |
Prss3l |
A |
T |
6: 41,422,246 (GRCm39) |
I53N |
probably damaging |
Het |
Psap |
T |
G |
10: 60,136,630 (GRCm39) |
C536W |
probably damaging |
Het |
Rab3gap1 |
T |
C |
1: 127,870,156 (GRCm39) |
C919R |
probably benign |
Het |
Racgap1 |
C |
A |
15: 99,524,087 (GRCm39) |
S440I |
probably benign |
Het |
Rec8 |
C |
T |
14: 55,862,215 (GRCm39) |
R480C |
probably damaging |
Het |
Reg3d |
A |
G |
6: 78,354,442 (GRCm39) |
L53S |
probably benign |
Het |
Rnft2 |
T |
A |
5: 118,370,471 (GRCm39) |
S244C |
probably damaging |
Het |
Scn2a |
T |
C |
2: 65,582,371 (GRCm39) |
V1573A |
probably benign |
Het |
Selenoo |
G |
T |
15: 88,979,910 (GRCm39) |
G353* |
probably null |
Het |
Siva1 |
A |
G |
12: 112,611,501 (GRCm39) |
Y34C |
probably damaging |
Het |
Slc2a4 |
C |
T |
11: 69,835,600 (GRCm39) |
|
probably benign |
Het |
Slc39a12 |
A |
T |
2: 14,405,136 (GRCm39) |
T243S |
probably benign |
Het |
Slc9b2 |
T |
C |
3: 135,038,279 (GRCm39) |
I453T |
probably damaging |
Het |
Spag17 |
A |
G |
3: 100,010,559 (GRCm39) |
T2018A |
probably benign |
Het |
Tbc1d24 |
A |
T |
17: 24,427,865 (GRCm39) |
D32E |
probably benign |
Het |
Tet1 |
T |
A |
10: 62,655,253 (GRCm39) |
H1556L |
possibly damaging |
Het |
Tmem59 |
A |
T |
4: 107,047,915 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,731,296 (GRCm39) |
|
probably benign |
Het |
Uimc1 |
A |
T |
13: 55,225,307 (GRCm39) |
L89H |
probably damaging |
Het |
Vipas39 |
A |
G |
12: 87,291,317 (GRCm39) |
I343T |
probably damaging |
Het |
Vmn2r71 |
G |
T |
7: 85,269,817 (GRCm39) |
V443L |
probably benign |
Het |
Zbtb14 |
G |
A |
17: 69,695,342 (GRCm39) |
D347N |
possibly damaging |
Het |
Zfp980 |
G |
T |
4: 145,428,627 (GRCm39) |
C452F |
probably damaging |
Het |
Zmym5 |
T |
A |
14: 57,049,693 (GRCm39) |
|
probably benign |
Het |
Znfx1 |
T |
C |
2: 166,883,673 (GRCm39) |
T145A |
possibly 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 |
|
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 |
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 |
|