Incidental Mutations

23 incidental mutations are currently displayed, and affect 23 genes.
5 are Possibly Damaging.
6 are Probably Damaging.
10 are Probably Benign.
2 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 23 of 23] 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 12420 APN 4930402H24Rik 0.000 IGL00556 G1 2 130784457 (GRCm38) D225G T C missense Het probably benign 0.001 phenotype 2012-12-06
2 12429 APN Abca12 1.000 IGL00556 G1 1 71353757 (GRCm38) I108V T C missense Het probably benign 0.001 phenotype 2012-12-06
3 5838 APN Atad2 0.434 IGL00556 G1 15 58100080 (GRCm38) I723T A G missense Het probably damaging 1.000 phenotype 2012-04-20
4 12519 APN Cct4 0.959 IGL00556 G1 11 22997656 (GRCm38) V233E T A missense Het possibly damaging 0.633 phenotype 2012-12-06
5 4988 APN Ces1a 0.000 IGL00556 G1 8 93045059 (GRCm38) Y37H A G missense Het probably benign 0.027 2012-04-20
6 4852 APN Cgnl1 0.000 IGL00556 G1 9 71656056 (GRCm38) R863Q C T missense Het probably benign 0.002 phenotype 2012-04-20
7 5726 APN Fam13b 0.179 IGL00556 G1 18 34497435 (GRCm38) D90G T C missense Het probably damaging 0.993 2012-04-20
8 6856 APN Fhdc1 0.332 IGL00556 G1 3 84457242 (GRCm38) D232E A T missense Het possibly damaging 0.812 2012-04-20
9 332597 APN Gm6370 0.051 IGL00556 G1 5 146493913 (GRCm38) T303A A G missense Het probably benign 0.003 2015-08-05
10 5835 APN Gsdmc2 0.077 IGL00556 G1 15 63828271 (GRCm38) A G splice site Het probably benign 2012-04-20
11 4170 APN Kif13b 0.000 IGL00556 G1 14 64744888 (GRCm38) N516K T A missense Het probably damaging 0.999 phenotype 2012-04-20
12 4509 APN Med1 1.000 IGL00556 G1 11 98155684 (GRCm38) A G intron Het probably benign phenotype 2012-04-20
13 4157 APN Med4 0.964 IGL00556 G1 14 73517267 (GRCm38) M190T T C missense Het probably damaging 0.998 phenotype 2012-04-20
14 332598 APN Myo15b 0.065 IGL00556 G1 11 115891916 (GRCm38) V1534A T C missense Het possibly damaging 0.686 2015-08-05
15 7215 APN Neb 0.831 IGL00556 G1 2 52191949 (GRCm38) R1722G T C missense Het probably benign 0.157 phenotype 2012-04-20
16 12704 APN Obp2b 0.059 IGL00556 G1 2 25738581 (GRCm38) I116F A T missense Het probably damaging 0.999 phenotype 2012-12-06
17 4102 APN Rims2 0.444 IGL00556 G1 15 39456674 (GRCm38) A G splice site Het probably null phenotype 2012-04-20
18 5271 APN Siglecg 0.081 IGL00556 G1 7 43411795 (GRCm38) I431F A T missense Het probably benign 0.017 phenotype 2012-04-20
19 5202 APN Thap12 0.951 IGL00556 G1 7 98716137 (GRCm38) V504D T A missense Het possibly damaging 0.820 2012-04-20
20 3073 APN Tlr7 0.168 IGL00556 G1 X 167308475 (GRCm38) M5R A C missense Het possibly damaging 0.945 phenotype 2012-04-20
21 14662 APN Tubgcp6 0.965 IGL00556 G1 15 89100962 (GRCm38) V1641A A G missense Het probably damaging 0.999 phenotype 2012-12-06
22 6415 APN Ugt2b1 0.081 IGL00556 G1 5 86926196 (GRCm38) L101F T A missense Het probably benign 0.004 phenotype 2012-04-20
23 14878 APN Xdh 0.320 IGL00556 G1 17 73884435 (GRCm38) *1336R A T makesense Het probably null phenotype 2012-12-06
[records 1 to 23 of 23]