Incidental Mutations

21 incidental mutations are currently displayed, and affect 21 genes.
1 are Possibly Damaging.
6 are Probably Damaging.
10 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 21 of 21] 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 88776 APN Abtb1 0.216 IGL01487 G1 6 88839449 V121A A G missense Het probably damaging 0.980 phenotype 11/18/2013
2 88768 APN Carf 0.000 IGL01487 G1 1 60109379 H17R A G missense Het probably damaging 1.000 phenotype 11/18/2013
3 278535 APN Col5a2 1.000 IGL01487 G1 1 45376739 N1416S T C missense Het probably benign 0.013 phenotype 04/16/2015
4 88765 APN Ctsm 0.000 IGL01487 G1 13 61539069 R3L C A missense Het probably benign 0.080 11/18/2013
5 88772 APN Dnah3 0.105 IGL01487 G1 7 119965530 Q2626* G A nonsense Het probably null phenotype 11/18/2013
6 88773 APN Dpp3 0.461 IGL01487 G1 19 4913892 V587I C T missense Het probably benign 0.005 phenotype 11/18/2013
7 88775 APN Fank1 0.191 IGL01487 G1 7 133879909 T245A A G missense Het probably damaging 0.999 11/18/2013
8 88782 APN Golga5 0.000 IGL01487 G1 12 102495696 A G intron Het probably benign phenotype 11/18/2013
9 88774 APN Hoxb9 0.735 IGL01487 G1 11 96274788 Q228* C T nonsense Het probably null phenotype 11/18/2013
10 88778 APN Invs 0.633 IGL01487 G1 4 48398136 I441V A G missense Het probably benign 0.264 phenotype 11/18/2013
11 278534 APN Olfr344 0.096 IGL01487 G1 2 36568742 L48H T A missense Het probably damaging 1.000 phenotype 04/16/2015
12 88771 APN Psd3 0.095 IGL01487 G1 8 67697114 E1243G T C missense Het probably benign 0.008 11/18/2013
13 88779 APN Rapgefl1 0.179 IGL01487 G1 11 98847135 H392Y C T missense Het probably damaging 1.000 11/18/2013
14 88777 APN Ropn1 0.103 IGL01487 G1 16 34678469 V209A T C missense Het probably damaging 0.999 phenotype 11/18/2013
15 88783 APN Scap 0.000 IGL01487 G1 9 110377734 G A critical splice donor site 1 bp Het probably null phenotype 11/18/2013
16 88780 APN Scn5a 1.000 IGL01487 G1 9 119562623 M1T A G start codon destroyed Het probably null 0.896 phenotype 11/18/2013
17 88769 APN Serpinb11 0.000 IGL01487 G1 1 107379838 Y333F A T missense Het probably benign 0.013 11/18/2013
18 88770 APN Sf3b3 0.963 IGL01487 G1 8 110817660 Y783H A G missense Het probably benign 0.008 phenotype 11/18/2013
19 88766 APN Slc4a4 1.000 IGL01487 G1 5 89228856 M990V A G missense Het probably benign 0.190 phenotype 11/18/2013
20 88781 APN Syt3 0.230 IGL01487 G1 7 44390999 V219F G T missense Het possibly damaging 0.948 11/18/2013
21 88767 APN Tmtc4 0.000 IGL01487 G1 14 122926031 L647S A G missense Het probably benign 0.251 11/18/2013
[records 1 to 21 of 21]