Incidental Mutations

22 incidental mutations are currently displayed, and affect 22 genes.
5 are Possibly Damaging.
6 are Probably Damaging.
8 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 22 of 22] 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 28652 APN Abca13 0.000 IGL00977 G1 11 9399284 F3619L T A missense Het probably damaging 0.998 phenotype 04/17/2013
2 27159 APN Asic5 0.000 IGL00977 G1 3 82004646 V183E T A missense Het possibly damaging 0.482 phenotype 04/17/2013
3 28424 APN Atp2b1 1.000 IGL00977 G1 10 98986975 V164A T C missense Het possibly damaging 0.877 phenotype 04/17/2013
4 28425 APN Bend3 1.000 IGL00977 G1 10 43510949 Q446R A G missense Het possibly damaging 0.954 04/17/2013
5 29200 APN Ccdc80 0.082 IGL00977 G1 16 45096264 T461K C A missense Het probably benign 0.074 phenotype 04/17/2013
6 26760 APN Cep350 0.959 IGL00977 G1 1 155932865 E655V T A missense Het probably null 0.994 phenotype 04/17/2013
7 26759 APN Chil1 0.078 IGL00977 G1 1 134187973 F232L T C missense Het possibly damaging 0.890 phenotype 04/17/2013
8 26761 APN Degs1 0.198 IGL00977 G1 1 182279209 I162F T A missense Het probably benign 0.344 phenotype 04/17/2013
9 27343 APN Dhdds 1.000 IGL00977 G1 4 134000260 A T splice site Het probably benign phenotype 04/17/2013
10 28423 APN Herc4 0.841 IGL00977 G1 10 63311567 Y821F A T missense Het probably damaging 0.995 phenotype 04/17/2013
11 28083 APN Hpf1 0.000 IGL00977 G1 8 60905719 H303R A G missense Het probably benign 0.105 04/17/2013
12 28787 APN Kcnk10 0.076 IGL00977 G1 12 98518533 C115S A T missense Het probably damaging 0.992 phenotype 04/17/2013
13 29199 APN Map3k13 0.000 IGL00977 G1 16 21921764 S614P T C missense Het probably benign 0.001 phenotype 04/17/2013
14 29461 APN Me2 0.000 IGL00977 G1 18 73791177 N321K A T missense Het probably benign 0.240 phenotype 04/17/2013
15 28422 APN Med16 1.000 IGL00977 G1 10 79907625 M1K A T start codon destroyed Het probably null 0.624 04/17/2013
16 28998 APN Mycbp2 1.000 IGL00977 G1 14 103172642 F2651L A G missense Het probably damaging 0.976 phenotype 04/17/2013
17 27019 APN Prrc2b 1.000 IGL00977 G1 2 32213810 T1100I C T missense Het probably benign 0.053 04/17/2013
18 27018 APN Scn9a 1.000 IGL00977 G1 2 66484301 Q1680L T A missense Het probably damaging 0.991 phenotype 04/17/2013
19 29463 APN Sh3rf2 0.000 IGL00977 G1 18 42111218 T250A A G missense Het probably benign 0.001 04/17/2013
20 29462 APN Tmem173 0.000 IGL00977 G1 18 35734567 E359K C T missense Het probably damaging 0.993 phenotype 04/17/2013
21 26758 APN Tpp2 0.455 IGL00977 G1 1 43983291 F950L T C missense Het possibly damaging 0.901 phenotype 04/17/2013
22 306638 APN Vmn2r-ps159 0.593 IGL00977 G1 4 156334196 C A exon Het noncoding transcript 04/16/2015
[records 1 to 22 of 22]