Incidental Mutations

9 incidental mutations are currently displayed, and affect 9 genes.
1 are Possibly Damaging.
1 are Probably Damaging.
6 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 9 of 9] 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 29153 APN 4930562C15Rik 0.112 IGL00936 G1 16 4864646 T1053A A G missense Het probably benign 0.309 04/17/2013
2 26919 APN 8030411F24Rik 0.059 IGL00936 G1 2 148785804 T124P A C missense Het probably benign 0.050 04/17/2013
3 28347 APN Col13a1 0.000 IGL00936 G1 10 61876290 M332T A G missense Het probably damaging 0.993 phenotype 04/17/2013
4 29066 APN Cyth4 0.123 IGL00936 G1 15 78619913 E361G A G missense Het probably benign 0.002 phenotype 04/17/2013
5 28184 APN Mrps22 1.000 IGL00936 G1 9 98596981 T114A T C missense Het possibly damaging 0.829 phenotype 04/17/2013
6 29067 APN Nup155 1.000 IGL00936 G1 15 8128405 T C splice site Het probably benign phenotype 04/17/2013
7 29515 APN Olfr1467 0.086 IGL00936 G1 19 13364624 T A utr 5 prime Het probably benign phenotype 04/17/2013
8 28543 APN Slc35g3 0.072 IGL00936 G1 11 69760491 T C splice site Het probably null 04/17/2013
9 28348 APN Taar7f 0.104 IGL00936 G1 10 24050168 V220A T C missense Het probably benign 0.000 04/17/2013
[records 1 to 9 of 9]