Variant #0000001446 (NC_000009.11:g.35068298T>C, VCP(NM_007126.3):c.79A>G)

Individual ID 00001446
Chromosome 9
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.35068298T>C
Reference Rohrer JD1, Warren JD, Reiman D, Uphill J, Beck J, Collinge J, Rossor MN, Isaacs AM, Mead S.(2011)
DB-ID VCP_000015
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00056 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
VCP NM_007126.3 ./. 2 c.79A>G r.(?) p.(Ile27Val) 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     
0000001446 ? ? VCP 1 Y Yang