Variant #0000985260 (NC_000003.11:g.38802682C>T, NC_000003.11(NM_006514.2):c.883+1G>A (SCN10A))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.38802682C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SCN10A_000326
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs757136675
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-05-15 10:34:01 +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.883+1G>A r.(?) p.(?)


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