Variant #0000923948 (NC_000003.11:g.38802155A>G, NC_000003.11(NM_006514.2):c.950+17T>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.38802155A>G
DNA change (hg38) -
Published as SCN10A(NM_006514.3):c.950+17T>C, SCN10A(NM_006514.4):c.950+17T>C
ISCN -
DB-ID SCN10A_000065 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) 0.00201 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 2023-04-16 21:50:28 +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.950+17T>C r.(=) p.(=)


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