Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
1 are Possibly Damaging.
9 are Probably Damaging.
12 are Probably Benign.
4 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 277888 APN Adamtsl1 0.229 IGL00770 4 86388539 A1397T G A missense Het possibly damaging 0.654 phenotype 04/16/2015
2 277885 APN Aldob 0.480 IGL00770 4 49536843 S349P A G missense Het probably benign 0.008 phenotype 04/16/2015
3 277899 APN Cd2 0.000 IGL00770 3 101283029 A T critical splice donor site 2 bp Het probably null phenotype 04/16/2015
4 277886 APN Cmtm2a 0.061 IGL00770 8 104292930 S43P A G missense Het probably damaging 0.991 04/16/2015
5 277894 APN Cts6 0.000 IGL00770 13 61198339 T C splice site Het probably benign 04/16/2015
6 277884 APN E2f3 1.000 IGL00770 13 29918704 D68E A T missense Het probably damaging 1.000 phenotype 04/16/2015
7 277876 APN Ect2 1.000 IGL00770 3 27098443 R869W G A missense Het probably damaging 0.989 phenotype 04/16/2015
8 277896 APN Eml1 0.202 IGL00770 12 108514515 A G splice site 3 bp Het probably null phenotype 04/16/2015
9 277897 APN Fundc1 IGL00770 X 17558013 T A critical splice acceptor site Het probably null phenotype 04/16/2015
10 277895 APN Gabrb1 0.000 IGL00770 5 72108446 G T critical splice donor site 1 bp Het probably null phenotype 04/16/2015
11 277893 APN Lrrk2 0.517 IGL00770 15 91801833 T G splice site Het probably benign phenotype 04/16/2015
12 277892 APN Map3k2 0.000 IGL00770 18 32228239 P584L C T missense Het probably benign 0.002 phenotype 04/16/2015
13 277889 APN Mindy2 0.112 IGL00770 9 70631033 D340G T C missense Het probably benign 0.053 04/16/2015
14 277890 APN Nav3 0.000 IGL00770 10 109816263 D877G T C missense Het probably damaging 0.998 phenotype 04/16/2015
15 277880 APN Nol9 0.960 IGL00770 4 152052015 S515P T C missense Het probably benign 0.382 04/16/2015
16 277882 APN Osgepl1 0.180 IGL00770 1 53320246 I305V A G missense Het probably benign 0.066 04/16/2015
17 277881 APN Pign 0.848 IGL00770 1 105597756 V449A A G missense Het probably benign 0.001 phenotype 04/16/2015
18 277873 APN Rad54b 0.000 IGL00770 4 11593765 R131K G A missense Het probably benign 0.000 phenotype 04/16/2015
19 277898 APN Rgl3 0.000 IGL00770 9 21987722 A T splice site Het probably benign 04/16/2015
20 277875 APN Scn2a 1.000 IGL00770 2 65735853 D1407G A G missense Het probably damaging 1.000 phenotype 04/16/2015
21 277874 APN Sf3b3 0.969 IGL00770 8 110817638 I790N A T missense Het probably damaging 0.961 phenotype 04/16/2015
22 277887 APN Srebf1 1.000 IGL00770 11 60205139 R358Q C T missense Het probably damaging 0.960 phenotype 04/16/2015
23 277877 APN Tmem18 0.112 IGL00770 12 30588721 R133G A G missense Het unknown phenotype 04/16/2015
24 277891 APN Tnfrsf11b 0.468 IGL00770 15 54254072 R262S T G missense Het probably benign 0.160 phenotype 04/16/2015
25 277879 APN Tsc1 1.000 IGL00770 2 28665011 H171L A T missense Het probably damaging 0.996 phenotype 04/16/2015
26 277878 APN Ubr5 1.000 IGL00770 15 38006541 T1157A T C missense Het probably benign 0.274 phenotype 04/16/2015
27 277883 APN Wdcp 0.122 IGL00770 12 4855303 E608G A G missense Het probably damaging 0.998 04/16/2015
[records 1 to 27 of 27]