Incidental Mutations

16 incidental mutations are currently displayed, and affect 16 genes.
2 are Possibly Damaging.
6 are Probably Damaging.
6 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 16 of 16] 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 4474 APN Abca5 0.149 IGL00487 G1 11 110309450 T A critical splice acceptor site Het probably null phenotype 04/20/2012
2 26569 APN Dusp23 0.062 IGL00487 G1 1 172631632 T C utr 3 prime Het probably benign 04/17/2013
3 6674 APN Invs 0.732 IGL00487 G1 4 48407689 Q555* C T nonsense Het probably null phenotype 04/20/2012
4 5048 APN Mak16 0.968 IGL00487 G1 8 31166750 N9D T C missense Het probably benign 0.000 04/20/2012
5 4467 APN Mrps7 0.962 IGL00487 G1 11 115604858 I74T T C missense Het possibly damaging 0.783 phenotype 04/20/2012
6 5296 APN Nlrp4a 0.081 IGL00487 G1 7 26449985 V339G T G missense Het possibly damaging 0.514 04/20/2012
7 12796 APN Nucb1 0.000 IGL00487 G1 7 45501651 L102P A G missense Het probably damaging 1.000 phenotype 12/06/2012
8 4977 APN Pdp2 0.150 IGL00487 G1 8 104594197 M226T T C missense Het probably benign 0.000 phenotype 04/20/2012
9 5029 APN Pik3r2 0.000 IGL00487 G1 8 70770429 D449G T C missense Het probably damaging 0.999 phenotype 04/20/2012
10 13838 APN Rnf157 0.000 IGL00487 G1 11 116362355 P76S G A missense Het probably benign 0.204 phenotype 12/06/2012
11 332203 APN Senp6 1.000 IGL00487 G1 9 80113838 Q267K C A missense Het probably damaging 0.998 phenotype 08/05/2015
12 7497 APN Slc9a2 0.065 IGL00487 G1 1 40742658 E349G A G missense Het probably damaging 0.990 phenotype 04/20/2012
13 4836 APN Snx14 1.000 IGL00487 G1 9 88402190 S475Y G T missense Het probably damaging 0.990 phenotype 04/20/2012
14 5310 APN Vmn1r180 0.079 IGL00487 G1 7 23952523 H37L A T missense Het probably benign 0.363 04/20/2012
15 332204 APN Wdr66 0.082 IGL00487 G1 5 123274177 I84S T G missense Het probably damaging 1.000 phenotype 08/05/2015
16 4832 APN Xrn1 0.917 IGL00487 G1 9 96038949 H1371L A T missense Het probably benign 0.045 phenotype 04/20/2012
[records 1 to 16 of 16]