Incidental Mutations

13 incidental mutations are currently displayed, and affect 13 genes.
3 are Possibly Damaging.
6 are Probably Damaging.
3 are Probably Benign.
1 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 13 of 13] 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 246006 UTSW Ces1a 0.000 R2347 G1 225 N 8 93025319 (GRCm38) V396M C T missense Het probably benign 0.066 0.090 2014-10-30
2 246009 UTSW Ddx6 1.000 R2347 G1 225 N 9 44607591 (GRCm38) K67E A G missense Het probably benign 0.002 phenotype 2014-10-30
3 246004 UTSW Fut2 0.000 R2347 G1 225 N 7 45650328 (GRCm38) D340G T C missense Het probably damaging 0.994 phenotype 2014-10-30
4 246002 UTSW Gm128 0.000 R2347 G1 225 N 3 95240930 (GRCm38) Y18H A G missense Het probably benign 0.022 phenotype 2014-10-30
5 246001 UTSW Gon4l 0.759 R2347 G1 225 N 3 88863517 (GRCm38) D502G A G missense Het probably damaging 0.999 phenotype 2014-10-30
6 246013 UTSW Lman2 0.239 R2347 G1 225 N 13 55352999 (GRCm38) N129I T A missense Het possibly damaging 0.910 phenotype 2014-10-30
7 246012 UTSW Nsf 1.000 R2347 G1 225 N 11 103930752 (GRCm38) E26K C T missense Het possibly damaging 0.586 0.089 2014-10-30
8 245999 UTSW Olfr1263 0.070 R2347 G1 225 N 2 90015614 (GRCm38) R228L G T missense Het possibly damaging 0.822 phenotype 2014-10-30
9 246005 UTSW Olfr527 0.053 R2347 G1 225 N 7 140336147 (GRCm38) M95K T A missense Het probably damaging 0.983 phenotype 2014-10-30
10 246008 UTSW Olfr935 0.057 R2347 G1 225 N 9 38994509 (GRCm38) *309K A T makesense Het probably null phenotype 2014-10-30
11 245998 UTSW Pappa2 0.000 R2347 G1 225 N 1 158765043 (GRCm38) C1588F C A missense Het probably damaging 1.000 phenotype 2014-10-30
12 246014 UTSW Piwil2 0.000 R2347 G1 127 N 14 70408917 (GRCm38) D390G T C missense Het probably damaging 0.979 phenotype 2014-10-30
13 246003 UTSW Rest 1.000 R2347 G1 225 N 5 77268593 (GRCm38) Y218C A G missense Het probably damaging 1.000 phenotype 2014-10-30
[records 1 to 13 of 13]