Variant #0000615242 (NC_000015.9:g.35085453A>G, NM_005159.4:c.447T>C (ACTC1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.35085453A>G
DNA change (hg38) g.34793252A>G
Published as ACTC1(NM_005159.4):c.447T>C (p.R149=), ACTC1(NM_005159.5):c.447T>C (p.(Arg149=))
ISCN -
DB-ID ACTC1_000140 See all 3 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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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 -?/. - c.447T>C r.(?) p.(Arg149=)


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