Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
6 are Possibly Damaging.
9 are Probably Damaging.
8 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 26 of 26] 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 295395 APN 4930430A15Rik 0.066 IGL02485 2 111228325 V94E A T missense Het probably damaging 0.971 04/16/2015
2 295385 APN Agl 0.315 IGL02485 3 116779080 S841P A G missense Het probably benign 0.000 phenotype 04/16/2015
3 295408 APN BC003331 0.798 IGL02485 1 150363489 A G critical splice donor site 2 bp Het probably null 04/16/2015
4 295405 APN Cd59b 0.054 IGL02485 2 104081104 A C splice site Het probably benign phenotype 04/16/2015
5 295397 APN Dopey2 0.000 IGL02485 16 93770822 L1379P T C missense Het probably damaging 1.000 04/16/2015
6 295394 APN Ercc2 1.000 IGL02485 7 19394045 A433T G A missense Het possibly damaging 0.830 phenotype 04/16/2015
7 295409 APN Gm17175 0.062 IGL02485 14 51569611 T C utr 3 prime Het probably benign 04/16/2015
8 295387 APN Gm5150 0.063 IGL02485 3 15990752 I103N A T missense Het probably damaging 1.000 04/16/2015
9 295384 APN Igf1 1.000 IGL02485 10 87864746 M11V A G missense Het probably benign 0.000 phenotype 04/16/2015
10 295391 APN Incenp 1.000 IGL02485 19 9893368 N299S T C missense Het unknown phenotype 04/16/2015
11 295400 APN Maneal 0.000 IGL02485 4 124856770 S398T A T missense Het probably damaging 1.000 04/16/2015
12 295389 APN Map1a 0.431 IGL02485 2 121299288 N195S A G missense Het probably damaging 0.999 phenotype 04/16/2015
13 295398 APN Mars2 1.000 IGL02485 1 55237591 F118L T C missense Het possibly damaging 0.867 phenotype 04/16/2015
14 295399 APN Mast4 0.277 IGL02485 13 102735496 S2263P A G missense Het probably benign 0.021 0.068 phenotype 04/16/2015
15 295404 APN Mrgprb1 0.051 IGL02485 7 48447717 R149L C A missense Het possibly damaging 0.881 04/16/2015
16 295388 APN Myo1d 0.000 IGL02485 11 80666581 D511G T C missense Het probably damaging 0.998 04/16/2015
17 295406 APN Ntan1 0.000 IGL02485 16 13834676 T C intron Het probably benign phenotype 04/16/2015
18 295390 APN Nxf2 IGL02485 X 134956467 F158L A G missense Het probably damaging 0.992 phenotype 04/16/2015
19 295396 APN Olfr1513 0.171 IGL02485 14 52350044 M1L T A start codon destroyed Het possibly damaging 0.886 phenotype 04/16/2015
20 295401 APN Trpm1 0.000 IGL02485 7 64269114 A734V C T missense Het possibly damaging 0.522 phenotype 04/16/2015
21 295402 APN Upf2 1.000 IGL02485 2 6027291 E883K G A missense Het unknown phenotype 04/16/2015
22 295403 APN Ush1c 0.000 IGL02485 7 46229250 I83V T C missense Het probably damaging 0.994 phenotype 04/16/2015
23 295393 APN Vmn2r60 0.125 IGL02485 7 42195466 T751N C A missense Het possibly damaging 0.543 04/16/2015
24 295392 APN Zfp146 0.168 IGL02485 7 30162590 I9T A G missense Het probably benign 0.000 04/16/2015
25 295407 APN Zfp592 0.911 IGL02485 7 81037970 G A splice site Het probably benign phenotype 04/16/2015
26 295386 APN Zswim8 0.963 IGL02485 14 20711887 L243F C T missense Het probably damaging 0.979 04/16/2015
[records 1 to 26 of 26]