Incidental Mutations

18 incidental mutations are currently displayed, and affect 18 genes.
7 are Possibly Damaging.
3 are Probably Damaging.
5 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
2 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 8527 APN Abca5 0.159 IGL00675 G1 11 110304985 D549E A T missense Het probably damaging 0.995 phenotype 12/06/2012
2 8540 APN Abcc9 0.198 IGL00675 G1 6 142664621 F606L A G missense Het probably damaging 1.000 phenotype 12/06/2012
3 9372 APN Canx 0.344 IGL00675 G1 11 50300996 S363P A G missense Het possibly damaging 0.609 phenotype 12/06/2012
4 9552 APN Cdh6 0.362 IGL00675 G1 15 13041439 D513G T C missense Het possibly damaging 0.798 phenotype 12/06/2012
5 9972 APN Cyp11a1 1.000 IGL00675 G1 9 58019313 G111W G T missense Het probably damaging 1.000 phenotype 12/06/2012
6 10254 APN Dnm1l 1.000 IGL00675 G1 16 16333827 A G critical splice donor site 2 bp Het probably null phenotype 12/06/2012
7 10316 APN Dsg1b 0.254 IGL00675 G1 18 20391918 L137* T A nonsense Het probably null phenotype 12/06/2012
8 11554 APN Kcnh5 0.000 IGL00675 G1 12 75114189 A T critical splice donor site 2 bp Het probably null phenotype 12/06/2012
9 11578 APN Kcnu1 0.000 IGL00675 G1 8 25851849 E74G A G missense Het probably benign 0.000 phenotype 12/06/2012
10 12392 APN Nlrp9b 0.094 IGL00675 G1 7 20023186 I116K T A missense Het possibly damaging 0.633 phenotype 12/06/2012
11 12768 APN Notch2 1.000 IGL00675 G1 3 98111675 Y718H T C missense Het possibly damaging 0.766 phenotype 12/06/2012
12 13168 APN Prkdc 0.974 IGL00675 G1 16 15787158 L2980P T C missense Het probably benign 0.046 phenotype 12/06/2012
13 13910 APN Samm50 0.948 IGL00675 G1 15 84200375 S171F C T missense Het possibly damaging 0.819 phenotype 12/06/2012
14 14503 APN Saraf 0.165 IGL00675 G1 8 34167808 S288T T A missense Het probably benign 0.006 12/06/2012
15 14692 APN Ubr5 1.000 IGL00675 G1 15 38018284 V865I C T missense Het possibly damaging 0.838 phenotype 12/06/2012
16 14711 APN Uhrf1bp1 0.000 IGL00675 G1 17 27876917 C T splice site Het probably benign 12/06/2012
17 14802 APN Vnn3 0.061 IGL00675 G1 10 23867168 K425N G T missense Het possibly damaging 0.769 12/06/2012
18 8436 APN Zswim8 0.978 IGL00675 G1 14 20716901 T C unclassified Het probably benign 12/06/2012
[records 1 to 18 of 18]