Incidental Mutations

15 incidental mutations are currently displayed, and affect 15 genes.
1 are Possibly Damaging.
7 are Probably Damaging.
6 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 15 of 15] 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 92144 APN Atp7b 0.711 IGL01600 G1 8 22027525 C A splice site 5 bp Het probably null phenotype 12/09/2013
2 92140 APN Ccr7 0.308 IGL01600 G1 11 99145145 V317A A G missense Het probably benign 0.452 phenotype 12/09/2013
3 92135 APN Dna2 1.000 IGL01600 G1 10 62950806 I111K T A missense Het probably damaging 0.965 phenotype 12/09/2013
4 92134 APN Egflam 0.000 IGL01600 G1 15 7219764 S858P A G missense Het probably damaging 1.000 phenotype 12/09/2013
5 92137 APN Glt28d2 0.226 IGL01600 G1 3 85871983 Y61C T C missense Het probably damaging 1.000 12/09/2013
6 92138 APN Kbtbd12 0.122 IGL01600 G1 6 88618558 A97T C T missense Het probably benign 0.084 12/09/2013
7 92141 APN Myh4 0.197 IGL01600 G1 11 67260189 E1890G A G missense Het possibly damaging 0.847 phenotype 12/09/2013
8 92143 APN Notch3 0.000 IGL01600 G1 17 32144498 G1197V C A missense Het probably damaging 1.000 phenotype 12/09/2013
9 92132 APN Olfr1257 0.060 IGL01600 G1 2 89881662 M279L A T missense Het probably benign 0.017 phenotype 12/09/2013
10 92142 APN Pcdh10 0.244 IGL01600 G1 3 45379487 I79L A T missense Het probably damaging 0.980 phenotype 12/09/2013
11 92131 APN Runx1t1 0.821 IGL01600 G1 4 13841871 V181D T A missense Het probably damaging 1.000 phenotype 12/09/2013
12 92139 APN Snx25 1.000 IGL01600 G1 8 46116310 D183E A T missense Het probably benign 0.002 12/09/2013
13 92145 APN Srsf11 1.000 IGL01600 G1 3 158019442 G A splice site Het probably benign phenotype 12/09/2013
14 92136 APN Tox 0.000 IGL01600 G1 4 6697585 V406A A G missense Het probably damaging 0.976 phenotype 12/09/2013
15 92133 APN Vmn2r68 0.080 IGL01600 G1 7 85222260 H605L T A missense Het probably benign 0.386 12/09/2013
[records 1 to 15 of 15]