Variant #0001033944 (NC_000003.11:g.38805039T>G, NM_006514.2:c.648A>C (SCN10A))

Chromosome 3
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.38805039T>G
DNA change (hg38) -
Published as SCN10A(NM_006514.3):c.648A>C (p.T216=), SCN10A(NM_006514.4):c.648A>C (p.T216=)
ISCN -
DB-ID SCN10A_000068 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) 0.00054 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN10A NM_006514.2 -?/. - c.648A>C r.(?) p.(Thr216=)


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