Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
2 are Possibly Damaging.
10 are Probably Damaging.
10 are Probably Benign.
2 are Probably Null.
2 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 25 of 25] 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 91591 APN Acaca 1.000 IGL01591 G1 11 84243320 G420W G T missense Het probably damaging 1.000 phenotype 12/09/2013
2 91603 APN Adamts17 0.151 IGL01591 G1 7 67004396 R458H G A missense Het probably damaging 0.998 phenotype 12/09/2013
3 91598 APN Adprhl2 0.253 IGL01591 G1 4 126318481 T82A T C missense Het probably damaging 0.995 phenotype 12/09/2013
4 91592 APN Ccdc158 0.212 IGL01591 G1 5 92662041 I203L T A missense Het probably benign 0.280 12/09/2013
5 91588 APN Commd10 0.370 IGL01591 G1 18 46963668 S47R C A missense Het probably benign 0.000 12/09/2013
6 91586 APN Crb1 0.250 IGL01591 G1 1 139237339 T1016A T C missense Het probably damaging 0.999 phenotype 12/09/2013
7 91599 APN Crhbp 0.119 IGL01591 G1 13 95443787 I95F T A missense Het probably damaging 0.965 phenotype 12/09/2013
8 91605 APN Cyp3a11 0.208 IGL01591 G1 5 145875481 A T splice site Het probably benign 12/09/2013
9 91595 APN Dsel 0.211 IGL01591 G1 1 111859695 Y1037H A G missense Het probably benign 0.075 phenotype 12/09/2013
10 91600 APN Epha1 0.260 IGL01591 G1 6 42360551 D898G T C missense Het probably damaging 0.997 phenotype 12/09/2013
11 91607 APN Esr2 0.783 IGL01591 G1 12 76121724 T A utr 3 prime Het probably benign phenotype 12/09/2013
12 91606 APN Exosc10 0.952 IGL01591 G1 4 148562887 T A unclassified Het probably benign phenotype 12/09/2013
13 91602 APN Fat4 1.000 IGL01591 G1 3 39010375 R4827* A T nonsense Het probably null phenotype 12/09/2013
14 91597 APN Gm11596 0.141 IGL01591 G1 11 99792798 C165* A T nonsense Het probably null 12/09/2013
15 91604 APN Heatr5b 0.453 IGL01591 G1 17 78808472 S852P A G missense Het probably benign 0.011 12/09/2013
16 91589 APN Mcm3ap 1.000 IGL01591 G1 10 76470805 P251S C T missense Het probably benign 0.000 phenotype 12/09/2013
17 91596 APN Nmur2 0.163 IGL01591 G1 11 56026999 V388A A G missense Het probably benign 0.000 phenotype 12/09/2013
18 91585 APN Parp14 0.392 IGL01591 G1 16 35858507 T364A T C missense Het possibly damaging 0.714 phenotype 12/09/2013
19 91590 APN Rarb 0.000 IGL01591 G1 14 16434207 I370F T A missense Het possibly damaging 0.928 phenotype 12/09/2013
20 91601 APN Rnf32 0.057 IGL01591 G1 5 29224274 I283N T A missense Het probably damaging 0.998 phenotype 12/09/2013
21 91587 APN Smg8 0.437 IGL01591 G1 11 87085153 V77A A G missense Het probably damaging 0.996 12/09/2013
22 91594 APN Tnn 0.237 IGL01591 G1 1 160125574 E632G T C missense Het probably damaging 1.000 12/09/2013
23 91584 APN Trip11 1.000 IGL01591 G1 12 101883345 S1487T A T missense Het probably damaging 0.982 phenotype 12/09/2013
24 91583 APN Vmn2r58 0.344 IGL01591 G1 7 41865329 K72R T C missense Het probably benign 0.028 12/09/2013
25 91593 APN Vmn2r92 0.095 IGL01591 G1 17 18185161 I856V A G missense Het unknown 12/09/2013
[records 1 to 25 of 25]