Variant #0000001921 (NC_000012.11:g.32777993_32777994delAG, FGD4(NM_139241.2):c.1626_1627delAG)

Individual ID 00001921
Chromosome 12
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.32777993_32777994delAG
Reference Stendel C1, Roos A, Deconinck T, Pereira J, Castagner F, Niemann A, Kirschner J(2007)
DB-ID FGD4_000006
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
FGD4 NM_139241.2 ./. 13 c.1626_1627delAG r.(?) p.(Glu543Glyfs*5) VariO:0141 DNA deletion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001921 ? ? FGD4 1 Y Yang