Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
3 are Possibly Damaging.
9 are Probably Damaging.
13 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] per page Full List
 
ID question?
Source question?
Gene question?
E-score question?
 
Stock # question?
Gen question?
Quality
-
Vld question?
Strain question?
Chr question?
Position question?
 
Mutation question?
Ref
Var
Type question?
Exon Dist question?
 
Zygosity question?
Predicted Effect question?
PPH Score question?
-
Meta Score question?
 
MGI Phenotype question?
Posted question?
 
1 88536 APN Akr1c12 0.000 IGL01479 G1 13 4272935 (GRCm38) K225R T C missense Het probably benign 0.010 2013-11-18
2 88543 APN Amn 1.000 IGL01479 G1 12 111271793 (GRCm38) A47E C A missense Het probably damaging 0.969 phenotype 2013-11-18
3 88542 APN Arhgef1 0.435 IGL01479 G1 7 24912603 (GRCm38) I137T T C missense Het probably benign 0.010 phenotype 2013-11-18
4 88541 APN Cep57l1 1.000 IGL01479 G1 10 41728639 (GRCm38) K165E T C missense Het possibly damaging 0.952 2013-11-18
5 88562 APN Chfr 0.197 IGL01479 G1 5 110144993 (GRCm38) A G unclassified Het probably benign phenotype 2013-11-18
6 88556 APN Dnah9 0.250 IGL01479 G1 11 65955717 (GRCm38) V2923A A G missense Het probably benign 0.140 phenotype 2013-11-18
7 88537 APN Dnaja2 0.711 IGL01479 G1 8 85553951 (GRCm38) Y35C T C missense Het probably damaging 1.000 phenotype 2013-11-18
8 88540 APN Dnajc2 0.956 IGL01479 G1 5 21757893 (GRCm38) T481A T C missense Het probably damaging 0.996 phenotype 2013-11-18
9 88561 APN Foxred2 0.000 IGL01479 G1 15 77952289 (GRCm38) A G splice site 6 bp Het probably null 2013-11-18
10 88550 APN Gin1 0.000 IGL01479 G1 1 97792372 (GRCm38) T364I C T missense Het possibly damaging 0.953 2013-11-18
11 88552 APN Glt8d2 0.113 IGL01479 G1 10 82660736 (GRCm38) V163I C T missense Het probably damaging 1.000 phenotype 2013-11-18
12 88545 APN Gm10118 0.101 IGL01479 G1 10 63926820 (GRCm38) T C intron Het probably benign 2013-11-18
13 88563 APN Hps5 0.095 IGL01479 G1 7 46762942 (GRCm38) C T critical splice donor site 1 bp Het probably null phenotype 2013-11-18
14 88548 APN Kdm4c 0.000 IGL01479 G1 4 74343501 (GRCm38) K638E A G missense Het probably benign 0.177 phenotype 2013-11-18
15 88551 APN L3mbtl2 1.000 IGL01479 G1 15 81676392 (GRCm38) T285A A G missense Het probably benign 0.052 phenotype 2013-11-18
16 88549 APN Mab21l1 0.000 IGL01479 G1 3 55783832 (GRCm38) Y280C A G missense Het probably damaging 0.999 phenotype 2013-11-18
17 88559 APN Mcoln2 0.091 IGL01479 G1 3 146175652 (GRCm38) T A splice site Het probably benign phenotype 2013-11-18
18 88554 APN Myo9b 0.718 IGL01479 G1 8 71359342 (GRCm38) R1926L G T missense Het probably damaging 1.000 phenotype 2013-11-18
19 88544 APN Rrp12 0.943 IGL01479 G1 19 41865202 (GRCm38) V1251A A G missense Het probably benign 0.051 2013-11-18
20 88547 APN Rtn4rl1 0.194 IGL01479 G1 11 75265342 (GRCm38) D200G A G missense Het probably damaging 1.000 phenotype 2013-11-18
21 88535 APN Sbsn 0.072 IGL01479 G1 7 30752357 (GRCm38) A266T G A missense Het possibly damaging 0.904 2013-11-18
22 88555 APN Sgca 0.251 IGL01479 G1 11 94963378 (GRCm38) C335* A T nonsense Het probably null phenotype 2013-11-18
23 88560 APN Spag1 0.781 IGL01479 G1 15 36233199 (GRCm38) T C splice site Het probably benign phenotype 2013-11-18
24 88546 APN Sult6b1 0.081 IGL01479 G1 17 78905576 (GRCm38) V82D A T missense Het probably benign 0.004 2013-11-18
25 88553 APN Tigit 0.063 IGL01479 G1 16 43659522 (GRCm38) T137A T C missense Het probably benign 0.001 phenotype 2013-11-18
26 88557 APN Tmem125 0.096 IGL01479 G1 4 118541623 (GRCm38) Q204* G A nonsense Het probably null 2013-11-18
27 88539 APN Tmem59l 0.057 IGL01479 G1 8 70486098 (GRCm38) R111Q C T missense Het probably benign 0.003 phenotype 2013-11-18
28 88538 APN Vmn2r95 0.085 IGL01479 G1 17 18443862 (GRCm38) G448R G A missense Het probably damaging 1.000 2013-11-18
29 88558 APN Zfp64 0.866 IGL01479 G1 2 168951679 (GRCm38) H49R T C missense Het probably damaging 0.998 2013-11-18
[records 1 to 29 of 29]