Variant #0000405586 (NC_000015.9:g.35083364C>T, NM_005159.4:c.941G>A (ACTC1))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.35083364C>T
DNA change (hg38) g.34791163C>T
Published as -
ISCN -
DB-ID ACTC1_000008 See all 4 reported entries
Variant remarks expression cloning yeast; reduced cell viability
Reference PubMed: Wong 2001
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-05-30 11:42:22 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACTC1 NM_005159.4 +/. 6 c.941G>A r.(?) p.Arg314His


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