Incidental Mutations

27 incidental mutations are currently displayed, and affect 26 genes.
3 are Possibly Damaging.
11 are Probably Damaging.
10 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27] 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 29288 APN Abca17 0.000 IGL00941 G1 17 24317130 I521S A C missense Het probably damaging 0.999 04/17/2013
2 28551 APN Ace 1.000 IGL00941 G1 11 105979550 K265I A T missense Het probably benign 0.212 phenotype 04/17/2013
3 28352 APN Acss3 0.087 IGL00941 G1 10 107053326 A G critical splice donor site 2 bp Het probably null 04/17/2013
4 28550 APN Aldh3a2 0.114 IGL00941 G1 11 61262256 Y215H A G missense Het probably damaging 1.000 phenotype 04/17/2013
5 27113 APN Clk2 0.259 IGL00941 G1 3 89175422 M393V A G missense Het probably damaging 0.993 phenotype 04/17/2013
6 29069 APN Cyc1 0.954 IGL00941 G1 15 76345165 I242V A G missense Het probably benign 0.392 phenotype 04/17/2013
7 28549 APN Evpl 0.000 IGL00941 G1 11 116227901 L657F G A missense Het probably benign 0.059 phenotype 04/17/2013
8 28548 APN Fbxw10 0.065 IGL00941 G1 11 62873501 V675M G A missense Het probably damaging 1.000 phenotype 04/17/2013
9 27841 APN Fgf21 0.069 IGL00941 G1 7 45615173 V45A A G missense Het probably damaging 0.997 phenotype 04/17/2013
10 28351 APN Gm5134 0.097 IGL00941 G1 10 76000421 I412T T C missense Het possibly damaging 0.698 04/17/2013
11 27451 APN Gnat3 0.000 IGL00941 G1 5 18003751 T C splice site Het probably benign phenotype 04/17/2013
12 28861 APN Hk3 0.087 IGL00941 G1 13 55014426 C T critical splice donor site 1 bp Het probably null phenotype 04/17/2013
13 27273 APN Ifna12 0.057 IGL00941 G1 4 88603314 A T utr 5 prime Het probably benign 04/17/2013
14 27272 APN Ipp 0.000 IGL00941 G1 4 116532659 M471V A G missense Het possibly damaging 0.931 phenotype 04/17/2013
15 28191 APN Kcnj1 0.067 IGL00941 G1 9 32396498 V73I G A missense Het probably benign 0.012 phenotype 04/17/2013
16 278096 APN Kin 0.962 IGL00941 G1 2 10080704 R25H G A missense Het probably damaging 0.999 phenotype 04/16/2015
17 278097 APN Kin 0.962 IGL00941 G1 2 10080706 W26R T C missense Het probably damaging 1.000 phenotype 04/16/2015
18 27842 APN Mical2 0.217 IGL00941 G1 7 112321445 T C splice site Het probably benign phenotype 04/17/2013
19 29287 APN Mllt1 1.000 IGL00941 G1 17 56895086 S428R A T missense Het probably damaging 0.998 phenotype 04/17/2013
20 27645 APN Ppm1k 0.062 IGL00941 G1 6 57524755 H141L T A missense Het probably benign 0.048 phenotype 04/17/2013
21 28553 APN Sept4 0.544 IGL00941 G1 11 87589773 C392F G T missense Het probably damaging 1.000 phenotype 04/17/2013
22 28552 APN Slc26a11 0.080 IGL00941 G1 11 119379901 F550L T C missense Het probably benign 0.003 phenotype 04/17/2013
23 278098 APN Ssb 1.000 IGL00941 G1 2 69870835 T A critical splice donor site 2 bp Het probably null phenotype 04/16/2015
24 26669 APN Stk36 0.000 IGL00941 G1 1 74623934 M588K T A missense Het possibly damaging 0.845 phenotype 04/17/2013
25 27112 APN Ubqln4 0.750 IGL00941 G1 3 88564501 A415T G A missense Het probably benign 0.236 04/17/2013
26 28752 APN Zfp839 0.055 IGL00941 G1 12 110860948 S424R C A missense Het probably damaging 0.998 04/17/2013
27 28554 APN Zkscan6 0.148 IGL00941 G1 11 65814747 G95W G T missense Het probably damaging 1.000 04/17/2013
[records 1 to 27 of 27]