Variant #0000566924 (NC_000019.9:g.35524939C>A, NM_199037.3:c.744C>A (SCN1B))

Chromosome 19
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.35524939C>A
DNA change (hg38) g.35034035C>A
Published as SCN1B(NM_199037.5):c.744C>A (p.S248R)
ISCN -
DB-ID SCN1B_000009 See all 30 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) 0.14573 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN1B NM_001037.4 -/. - c.448+296C>A r.(=) p.(=)
SCN1B NM_199037.3 -/. - c.744C>A r.(?) p.(Ser248Arg)


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