Incidental Mutations

39 incidental mutations are currently displayed, and affect 39 genes.
7 are Possibly Damaging.
15 are Probably Damaging.
13 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 39 of 39] 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 103181 APN Acsm5 0.198 IGL01662 G1 7 119538288 I402F A T missense Het probably damaging 1.000 01/21/2014
2 103212 APN Acvr2b 1.000 IGL01662 G1 9 119432504 Y388H T C missense Het probably damaging 1.000 phenotype 01/21/2014
3 103193 APN Adh1 0.000 IGL01662 G1 3 138282751 D162N G A missense Het possibly damaging 0.956 phenotype 01/21/2014
4 103191 APN C6 0.091 IGL01662 G1 15 4792754 R585I G T missense Het probably damaging 1.000 phenotype 01/21/2014
5 103214 APN Ccdc169 0.110 IGL01662 G1 3 55163311 T A splice site Het probably null 01/21/2014
6 103199 APN Cdh13 0.000 IGL01662 G1 8 118675177 M106K T A missense Het probably damaging 0.988 phenotype 01/21/2014
7 103201 APN Cep78 0.577 IGL01662 G1 19 15960995 E530K C T missense Het probably damaging 1.000 01/21/2014
8 103202 APN Cyfip1 1.000 IGL01662 G1 7 55896739 L533Q T A missense Het probably damaging 0.999 phenotype 01/21/2014
9 103205 APN Etl4 0.621 IGL01662 G1 2 20806649 V1181A T C missense Het probably benign 0.041 phenotype 01/21/2014
10 103211 APN Fam105a 0.072 IGL01662 G1 15 27658065 D290N C T missense Het probably damaging 1.000 01/21/2014
11 103209 APN Fam122a 0.500 IGL01662 G1 19 24476584 V258A A G missense Het probably benign 0.004 01/21/2014
12 103215 APN Galnt7 0.427 IGL01662 G1 8 57531735 T G splice site Het probably benign phenotype 01/21/2014
13 103187 APN Gm11595 0.085 IGL01662 G1 11 99772672 R61C G A missense Het unknown 01/21/2014
14 103210 APN Gucy1a1 0.113 IGL01662 G1 3 82109253 I143F T A missense Het possibly damaging 0.626 phenotype 01/21/2014
15 103195 APN Hmcn1 0.000 IGL01662 G1 1 150737299 N1410D T C missense Het possibly damaging 0.460 phenotype 01/21/2014
16 103184 APN Ltbp2 0.831 IGL01662 G1 12 84809246 T741I G A missense Het probably benign 0.002 phenotype 01/21/2014
17 103197 APN Mdc1 0.945 IGL01662 G1 17 35852505 S982P T C missense Het probably benign 0.005 phenotype 01/21/2014
18 103217 APN Mfsd4b2 0.091 IGL01662 G1 10 39922197 A G splice site Het probably benign 01/21/2014
19 103200 APN Mrgprb5 0.053 IGL01662 G1 7 48168424 I188L T G missense Het probably benign 0.022 01/21/2014
20 103204 APN Naip6 0.121 IGL01662 G1 13 100300354 S554C T A missense Het probably damaging 0.997 phenotype 01/21/2014
21 103208 APN Nav2 0.612 IGL01662 G1 7 49571209 N1715D A G missense Het probably damaging 0.999 phenotype 01/21/2014
22 103194 APN Nav3 0.000 IGL01662 G1 10 109769258 S985T A T missense Het possibly damaging 0.565 phenotype 01/21/2014
23 103189 APN Nme7 0.254 IGL01662 G1 1 164328297 Q22R A G missense Het probably benign 0.019 phenotype 01/21/2014
24 103185 APN Olfr556 0.153 IGL01662 G1 7 102670720 W267R T C missense Het probably damaging 0.999 phenotype 01/21/2014
25 103190 APN Ppp1r9a 0.638 IGL01662 G1 6 5115322 E815G A G missense Het probably damaging 1.000 phenotype 01/21/2014
26 103198 APN Ppp2r2c 0.316 IGL01662 G1 5 36926400 I95N T A missense Het probably damaging 1.000 phenotype 01/21/2014
27 103206 APN Ppp4r4 0.211 IGL01662 G1 12 103602966 E717K G A missense Het possibly damaging 0.552 phenotype 01/21/2014
28 103213 APN Prdm2 0.000 IGL01662 G1 4 143133568 S1051P A G missense Het possibly damaging 0.734 phenotype 01/21/2014
29 103186 APN Rnf214 0.813 IGL01662 G1 9 45899786 D193G T C missense Het probably damaging 0.996 01/21/2014
30 103192 APN Sirpb1b 0.065 IGL01662 G1 3 15543184 T167K G T missense Het probably damaging 1.000 01/21/2014
31 103183 APN Slc16a3 0.000 IGL01662 G1 11 120956706 S240* C A nonsense Het probably null phenotype 01/21/2014
32 103218 APN Snx14 1.000 IGL01662 G1 9 88385838 T A splice site Het probably benign phenotype 01/21/2014
33 103216 APN Sorbs2 0.000 IGL01662 G1 8 45803829 A G splice site Het probably benign phenotype 01/21/2014
34 103196 APN Stk-ps2 0.093 IGL01662 G1 1 46029362 A T unclassified Het noncoding transcript 01/21/2014
35 103180 APN Taar7b 0.119 IGL01662 G1 10 23999976 D13V A T missense Het probably benign 0.016 01/21/2014
36 103188 APN Trp53bp1 0.000 IGL01662 G1 2 121236025 E740G T C missense Het probably damaging 1.000 phenotype 01/21/2014
37 103203 APN Unc79 1.000 IGL01662 G1 12 103149020 A2054V C T missense Het possibly damaging 0.921 phenotype 01/21/2014
38 103182 APN Zfp106 0.000 IGL01662 G1 2 120523553 V211A A G missense Het probably benign 0.174 phenotype 01/21/2014
39 103207 APN Zfp112 0.138 IGL01662 G1 7 24125954 H449R A G missense Het probably benign 0.438 01/21/2014
[records 1 to 39 of 39]