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 D225G T C missense Het probably benign 0.001 phenotype 12/06/2012
2 12429 APN Abca12 1.000 IGL00556 G1 1 71353757 I108V T C missense Het probably benign 0.001 phenotype 12/06/2012
3 5838 APN Atad2 0.436 IGL00556 G1 15 58100080 I723T A G missense Het probably damaging 1.000 phenotype 04/20/2012
4 12519 APN Cct4 0.958 IGL00556 G1 11 22997656 V233E T A missense Het possibly damaging 0.633 phenotype 12/06/2012
5 4988 APN Ces1a 0.000 IGL00556 G1 8 93045059 Y37H A G missense Het probably benign 0.027 04/20/2012
6 4852 APN Cgnl1 0.000 IGL00556 G1 9 71656056 R863Q C T missense Het probably benign 0.002 phenotype 04/20/2012
7 5726 APN Fam13b 0.273 IGL00556 G1 18 34497435 D90G T C missense Het probably damaging 0.993 04/20/2012
8 6856 APN Fhdc1 0.273 IGL00556 G1 3 84457242 D232E A T missense Het possibly damaging 0.812 04/20/2012
9 332597 APN Gm6370 0.052 IGL00556 G1 5 146493913 T303A A G missense Het probably benign 0.003 08/05/2015
10 5835 APN Gsdmc2 0.076 IGL00556 G1 15 63828271 A G splice site Het probably benign 04/20/2012
11 4170 APN Kif13b 0.000 IGL00556 G1 14 64744888 N516K T A missense Het probably damaging 0.999 phenotype 04/20/2012
12 4509 APN Med1 1.000 IGL00556 G1 11 98155684 A G intron Het probably benign phenotype 04/20/2012
13 4157 APN Med4 0.963 IGL00556 G1 14 73517267 M190T T C missense Het probably damaging 0.998 phenotype 04/20/2012
14 332598 APN Myo15b 0.077 IGL00556 G1 11 115891916 V1534A T C missense Het possibly damaging 0.686 08/05/2015
15 7215 APN Neb 0.840 IGL00556 G1 2 52191949 R1722G T C missense Het probably benign 0.157 phenotype 04/20/2012
16 12704 APN Obp2b 0.053 IGL00556 G1 2 25738581 I116F A T missense Het probably damaging 0.999 phenotype 12/06/2012
17 4102 APN Rims2 0.475 IGL00556 G1 15 39456674 A G splice site Het probably null phenotype 04/20/2012
18 5271 APN Siglecg 0.072 IGL00556 G1 7 43411795 I431F A T missense Het probably benign 0.017 phenotype 04/20/2012
19 5202 APN Thap12 0.962 IGL00556 G1 7 98716137 V504D T A missense Het possibly damaging 0.820 04/20/2012
20 3073 APN Tlr7 0.168 IGL00556 G1 X 167308475 M5R A C missense Het possibly damaging 0.945 phenotype 04/20/2012
21 14662 APN Tubgcp6 0.960 IGL00556 G1 15 89100962 V1641A A G missense Het probably damaging 0.999 phenotype 12/06/2012
22 6415 APN Ugt2b1 0.099 IGL00556 G1 5 86926196 L101F T A missense Het probably benign 0.004 phenotype 04/20/2012
23 14878 APN Xdh 0.518 IGL00556 G1 17 73884435 *1336R A T makesense Het probably null phenotype 12/06/2012
[records 1 to 23 of 23]