Incidental Mutations

18 incidental mutations are currently displayed, and affect 18 genes.
2 are Possibly Damaging.
5 are Probably Damaging.
10 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 18 of 18] 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 8558 APN Acsm2 0.000 IGL00782 G1 7 119573168 E78V A T missense Het probably damaging 0.999 12/06/2012
2 9162 APN Atxn7 0.000 IGL00782 G1 14 14096218 I508V A G missense Het possibly damaging 0.781 phenotype 12/06/2012
3 9590 APN Cecr2 1.000 IGL00782 G1 6 120761621 N1075S A G missense Het probably benign 0.002 phenotype 12/06/2012
4 9728 APN Clcn3 0.748 IGL00782 G1 8 60922792 I689T A G missense Het probably damaging 0.988 phenotype 12/06/2012
5 9782 APN Cntnap3 0.073 IGL00782 G1 13 64745805 T C splice site Het probably benign phenotype 12/06/2012
6 10108 APN Defb11 0.101 IGL00782 G1 8 21905494 I56V T C missense Het probably benign 0.012 12/06/2012
7 10529 APN Ercc5 1.000 IGL00782 G1 1 44163935 N244S A G missense Het probably damaging 1.000 phenotype 12/06/2012
8 10884 APN Gabrg3 0.000 IGL00782 G1 7 57381667 S42P A G missense Het probably damaging 0.989 phenotype 12/06/2012
9 11214 APN Hcrtr2 0.065 IGL00782 G1 9 76230497 A T utr 3 prime Het probably benign phenotype 12/06/2012
10 8498 APN Jcad 0.000 IGL00782 G1 18 4675073 L945S T C missense Het probably benign 0.004 12/06/2012
11 11816 APN Lrp2 1.000 IGL00782 G1 2 69501645 M1589V T C missense Het probably benign 0.138 phenotype 12/06/2012
12 13170 APN Prkg1 0.524 IGL00782 G1 19 30578753 C T splice site Het probably benign phenotype 12/06/2012
13 13905 APN Samd1 0.902 IGL00782 G1 8 83999617 F464S T C missense Het probably damaging 1.000 12/06/2012
14 14087 APN Slc35b3 0.607 IGL00782 G1 13 38943140 S213P A G missense Het possibly damaging 0.819 phenotype 12/06/2012
15 14341 APN Taar1 0.101 IGL00782 G1 10 23920446 N14S A G missense Het probably benign 0.003 phenotype 12/06/2012
16 10372 APN Tinf2 1.000 IGL00782 G1 14 55680464 A G splice site 3430 bp Het probably null phenotype 12/06/2012
17 14757 APN Utrn 0.000 IGL00782 G1 10 12652811 N2140S T C missense Het probably benign 0.134 phenotype 12/06/2012
18 15000 APN Zfp780b 0.064 IGL00782 G1 7 27964761 D123G T C missense Het probably benign 0.000 12/06/2012
[records 1 to 18 of 18]