Variant #0000301899 (NC_000003.11:g.38645420T>C, NM_198056.2:c.1673A>G (SCN5A))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38645420T>C
DNA change (hg38) g.38603929T>C
Published as SCN5A(NM_000335.5):c.1673A>G (p.(His558Arg)), SCN5A(NM_001099404.2):c.1673A>G (p.H558R), SCN5A(NM_198056.2):c.1673A>G (p.H558R)
ISCN -
DB-ID SCN5A_000217 See all 16 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) 0.2208 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN5A NM_198056.2 -/. - c.1673A>G r.(?) p.(His558Arg)


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