Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
2 are Possibly Damaging.
11 are Probably Damaging.
7 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 25 of 25] 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 29286 APN Anks1 0.000 IGL00940 G1 17 28057354 N1024D A G missense Het probably damaging 0.999 phenotype 04/17/2013
2 28860 APN Cts7 0.236 IGL00940 G1 13 61356909 A G critical splice donor site 2 bp Het probably null 04/17/2013
3 28189 APN Dock3 0.777 IGL00940 G1 9 106911377 T A splice site Het probably benign phenotype 04/17/2013
4 27270 APN Fbxo6 0.113 IGL00940 G1 4 148146110 F232L A G missense Het probably benign 0.054 0.090 phenotype 04/17/2013
5 27111 APN Hsd3b6 0.076 IGL00940 G1 3 98806624 F120I A T missense Het probably damaging 0.999 04/17/2013
6 27840 APN Il4ra 0.068 IGL00940 G1 7 125569175 G A critical splice donor site 1 bp Het probably null phenotype 04/17/2013
7 29585 APN Irs4 0.082 IGL00940 G1 X 141722144 F1019I A T missense Het unknown phenotype 04/17/2013
8 28749 APN Klc1 0.262 IGL00940 G1 12 111787498 T464A A G missense Het probably damaging 0.998 phenotype 04/17/2013
9 27642 APN Mical3 0.186 IGL00940 G1 6 121022410 T660A T C missense Het possibly damaging 0.548 04/17/2013
10 28350 APN Ndufs7 1.000 IGL00940 G1 10 80255121 V158E T A missense Het probably damaging 0.982 phenotype 04/17/2013
11 29584 APN Nhs 0.000 IGL00940 G1 X 161837230 N1510I T A missense Het probably damaging 0.999 phenotype 04/17/2013
12 26924 APN Olfr1085 1.000 IGL00940 G1 2 86657726 H244P T G missense Het probably damaging 0.980 phenotype 04/17/2013
13 27839 APN Olfr78 0.063 IGL00940 G1 7 102742262 V247A A G missense Het probably damaging 0.999 phenotype 04/17/2013
14 28751 APN Pole2 1.000 IGL00940 G1 12 69215360 T148I G A missense Het probably damaging 0.996 phenotype 04/17/2013
15 27269 APN Pramel1 0.000 IGL00940 G1 4 143397556 L267H T A missense Het probably damaging 1.000 04/17/2013
16 26925 APN Rag1 0.416 IGL00940 G1 2 101642388 E803G T C missense Het probably damaging 0.997 phenotype 04/17/2013
17 28190 APN Rassf1 0.128 IGL00940 G1 9 107558311 G T splice site Het probably benign phenotype 04/17/2013
18 27271 APN Rnf220 0.765 IGL00940 G1 4 117307675 K210R T C missense Het probably benign 0.017 04/17/2013
19 278094 APN Setd7 1.000 IGL00940 G1 3 51533038 D194V T A missense Het probably damaging 1.000 phenotype 04/16/2015
20 27644 APN Snd1 0.928 IGL00940 G1 6 28745175 T C intron Het probably benign phenotype 04/17/2013
21 278095 APN Ssb 1.000 IGL00940 G1 2 69870835 T A critical splice donor site 2 bp Het probably null phenotype 04/16/2015
22 27643 APN Tex37 0.000 IGL00940 G1 6 70913388 R140L C A missense Het probably benign 0.115 04/17/2013
23 26667 APN Tlr5 0.240 IGL00940 G1 1 182974196 V355A T C missense Het possibly damaging 0.842 phenotype 04/17/2013
24 26668 APN Ush2a 0.485 IGL00940 G1 1 188357961 R414* A T nonsense Het probably null phenotype 04/17/2013
25 28750 APN Zfyve26 0.000 IGL00940 G1 12 79280900 S559P A G missense Het probably benign 0.000 phenotype 04/17/2013
[records 1 to 25 of 25]