Variant #0000948163 (NC_000003.11:g.38835234G>A, NM_006514.2:c.268C>T (SCN10A))

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.38835234G>A
DNA change (hg38) -
Published as SCN10A(NM_006514.3):c.268C>T (p.R90W), SCN10A(NM_006514.4):c.268C>T (p.R90W)
ISCN -
DB-ID SCN10A_000185 See all 4 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) 0.00141 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 2023-11-27 17:35:39 +01:00 (CET)
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.268C>T r.(?) p.(Arg90Trp)


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