Variant #0000259611 (NC_000015.9:g.35084477G>A, NM_005159.4:c.622C>T (ACTC1))

Chromosome 15
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.35084477G>A
DNA change (hg38) g.34792276G>A
Published as ACTC1(NM_005159.4):c.622C>T (p.R208C), ACTC1(NM_005159.5):c.622C>T (p.R208C)
ISCN -
DB-ID ACTC1_000085 See all 2 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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     
ACTC1 NM_005159.4 ?/. - c.622C>T r.(?) p.(Arg208Cys)


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