Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
6 are Possibly Damaging.
9 are Probably Damaging.
9 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 28 of 28] 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 414617 APN 1600012P17Rik 0.088 IGL03255 1 158969351 A G unclassified Het noncoding transcript 08/02/2016
2 414623 APN Alpk3 0.402 IGL03255 7 81092562 D709G A G missense Het probably benign 0.008 phenotype 08/02/2016
3 414610 APN AY761184 0.073 IGL03255 8 21703518 T29A T C missense Het possibly damaging 0.707 08/02/2016
4 414620 APN Capn3 0.315 IGL03255 2 120489708 R309L G T missense Het probably damaging 1.000 phenotype 08/02/2016
5 414624 APN Card11 0.000 IGL03255 5 140898331 I398V T C missense Het possibly damaging 0.727 phenotype 08/02/2016
6 414611 APN Cps1 1.000 IGL03255 1 67145801 Y162* T A nonsense Het probably null phenotype 08/02/2016
7 414609 APN Defa26 0.111 IGL03255 8 21618241 D20V A T missense Het probably damaging 1.000 08/02/2016
8 414621 APN Dnah8 0.385 IGL03255 17 30741381 L2244R T G missense Het probably damaging 1.000 phenotype 08/02/2016
9 414628 APN Fhad1 0.083 IGL03255 4 141972880 N353I T A missense Het possibly damaging 0.794 08/02/2016
10 414631 APN Flt1 1.000 IGL03255 5 147588521 T A splice site Het probably benign phenotype 08/02/2016
11 414613 APN Glyr1 0.411 IGL03255 16 5048757 G A unclassified Het probably null 08/02/2016
12 414618 APN Gm10220 0.437 IGL03255 5 26116901 S258P A G missense Het possibly damaging 0.930 08/02/2016
13 414625 APN Lama3 1.000 IGL03255 18 12539703 D845V A T missense Het probably damaging 0.997 phenotype 08/02/2016
14 414626 APN Myh2 0.250 IGL03255 11 67193225 L1558Q T A missense Het probably damaging 0.997 phenotype 08/02/2016
15 414622 APN Nelfb 1.000 IGL03255 2 25203195 H482N G T missense Het probably benign 0.206 phenotype 08/02/2016
16 414614 APN Olfr290 0.201 IGL03255 7 84916517 L246P T C missense Het possibly damaging 0.953 phenotype 08/02/2016
17 414619 APN Olfr482 0.088 IGL03255 7 108094817 V251A A G missense Het probably damaging 1.000 phenotype 08/02/2016
18 414627 APN Ppfia2 0.000 IGL03255 10 106896507 T972A A G missense Het possibly damaging 0.764 0.146 phenotype 08/02/2016
19 414629 APN Slc5a4a 0.106 IGL03255 10 76150512 V85M G A missense Het probably damaging 0.999 08/02/2016
20 414616 APN Slc6a12 0.000 IGL03255 6 121354287 C166G T G missense Het probably damaging 0.991 phenotype 08/02/2016
21 414632 APN Tm7sf3 0.209 IGL03255 6 146606120 T C unclassified Het probably benign 08/02/2016
22 414634 APN Tmem94 0.257 IGL03255 11 115792068 G T unclassified Het probably benign 08/02/2016
23 414630 APN Tmod2 0.000 IGL03255 9 75577258 T C splice site Het probably benign phenotype 08/02/2016
24 414612 APN Tmprss11c 0.000 IGL03255 5 86271482 I73F T A missense Het probably damaging 0.988 08/02/2016
25 414607 APN Vmn1r10 0.276 IGL03255 6 57113926 M168V A G missense Het probably benign 0.054 08/02/2016
26 414608 APN Vmn2r77 0.077 IGL03255 7 86811923 M819K T A missense Het probably benign 0.041 08/02/2016
27 414633 APN Vmo1 0.172 IGL03255 11 70514410 C T critical splice donor site 1 bp Het probably null 08/02/2016
28 414615 APN Ywhab 0.000 IGL03255 2 164014016 D104G A G missense Het probably benign 0.011 phenotype 08/02/2016
[records 1 to 28 of 28]