Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
4 are Possibly Damaging.
8 are Probably Damaging.
11 are Probably Benign.
5 are Probably Null.
3 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 28 of 28] 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 301180 APN Actr10 0.961 IGL02628 12 70954656 T A critical splice donor site 2 bp Het probably null 04/16/2015
2 301155 APN Ankhd1 0.000 IGL02628 18 36647703 V1936A T C missense Het probably benign 0.001 04/16/2015
3 301175 APN Ap3m1 0.129 IGL02628 14 21045520 E81* C A nonsense Het probably null phenotype 04/16/2015
4 301178 APN Camkk1 0.000 IGL02628 11 73029169 T C splice site Het probably benign phenotype 04/16/2015
5 301164 APN Cbwd1 0.239 IGL02628 19 24957905 E78D T A missense Het probably damaging 0.999 04/16/2015
6 301158 APN Cdc45 1.000 IGL02628 16 18798729 M200I C T missense Het probably benign 0.059 0.196 phenotype 04/16/2015
7 301171 APN Cmc1 0.193 IGL02628 9 118065308 Y33H A G missense Het probably damaging 1.000 04/16/2015
8 301159 APN Cntnap5b 0.123 IGL02628 1 100072069 D184V A T missense Het probably damaging 0.972 04/16/2015
9 301154 APN F5 1.000 IGL02628 1 164194075 D1373V A T missense Het probably damaging 0.988 phenotype 04/16/2015
10 301181 APN Fam169a 0.090 IGL02628 13 97111288 T C splice site Het probably benign 04/16/2015
11 301169 APN Fem1c 0.000 IGL02628 18 46505952 R328W G A missense Het probably damaging 1.000 phenotype 04/16/2015
12 301156 APN Gba2 0.000 IGL02628 4 43568919 R579G T C missense Het probably benign 0.010 phenotype 04/16/2015
13 301177 APN Gm42641 IGL02628 9 109058630 Q98* G A nonsense Het probably null 04/16/2015
14 301163 APN Hsd17b7 1.000 IGL02628 1 169964489 F117L A G missense Het possibly damaging 0.582 phenotype 04/16/2015
15 301168 APN Itsn1 0.000 IGL02628 16 91899623 D38G A G missense Het possibly damaging 0.790 0.358 phenotype 04/16/2015
16 301167 APN Map1a 0.445 IGL02628 2 121300104 I467T T C missense Het probably damaging 0.999 phenotype 04/16/2015
17 301162 APN Map2k4 1.000 IGL02628 11 65690741 I382F T A missense Het possibly damaging 0.835 phenotype 04/16/2015
18 301179 APN Myh1 0.000 IGL02628 11 67206262 T G unclassified Het probably benign phenotype 04/16/2015
19 301176 APN Nr1h4 0.746 IGL02628 10 89473839 A339T C T missense Het probably damaging 1.000 phenotype 04/16/2015
20 301166 APN Olfr190 0.056 IGL02628 16 59074792 M96R A C missense Het probably benign 0.013 phenotype 04/16/2015
21 301165 APN Olfr429 0.085 IGL02628 1 174089190 Y50C A G missense Het probably benign 0.000 phenotype 04/16/2015
22 301172 APN Opn4 0.000 IGL02628 14 34593057 T420S T A missense Het probably benign 0.149 phenotype 04/16/2015
23 301160 APN Rnf123 0.256 IGL02628 9 108068302 R390* G A nonsense Het probably null phenotype 04/16/2015
24 301173 APN Slc17a3 0.000 IGL02628 13 23842451 M1K T A start codon destroyed Het probably null 1.000 phenotype 04/16/2015
25 301174 APN T 0.954 IGL02628 17 8435358 I125N T A missense Het probably damaging 0.999 phenotype 04/16/2015
26 301170 APN Tns2 0.000 IGL02628 15 102111828 S710T T A missense Het probably benign 0.036 phenotype 04/16/2015
27 301157 APN Trav3-1 0.067 IGL02628 14 52581094 V75E T A missense Het probably benign 0.014 04/16/2015
28 301161 APN U2surp 0.958 IGL02628 9 95472090 Y832H A G missense Het possibly damaging 0.887 04/16/2015
[records 1 to 28 of 28]