Variant #0000613068 (NC_000011.9:g.118023368T>C, NM_174934.3:c.21A>G (SCN4B))

Chromosome 11
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.118023368T>C
DNA change (hg38) g.118152653T>C
Published as SCN4B(NM_174934.4):c.21A>G (p.G7=)
ISCN -
DB-ID SCN4B_000025
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 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +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     
SCN4B NM_001142348.1 -/. - c.21A>G r.(?) p.(Gly7=)
SCN4B NM_174934.3 -/. - c.21A>G r.(?) p.(Gly7=)


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