Variant #0000722507 (NC_000009.11:g.35066777T>C, NM_007126.3:c.340A>G (VCP))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.35066777T>C
DNA change (hg38) -
Published as VCP(NM_001354928.1):c.205A>G (p.I69V), VCP(NM_007126.3):c.340A>G (p.I114V, p.(Ile114Val)), VCP(NM_007126.5):c.340A>G (p.I114V)
ISCN -
DB-ID VCP_000050 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VCP NM_007126.3 ?/. - c.340A>G r.(?) p.(Ile114Val)


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