Variant #0000001442 (NC_000009.11:g.35065360C>T, VCP(NM_007126.3):c.464G>A)

Individual ID 00001442
Chromosome 9
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.35065360C>T
Reference Gitcho MA1, Strider J, Carter D, Taylor-Reinwald L, Forman MS, Goate AM, Cairns NJ.(2009)
DB-ID VCP_000011 See all 2 reported entries
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     
VCP NM_007126.3 ./. 5 c.464G>A r.(?) p.(Arg155His) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001442 ? ? VCP 1 Y Yang