Variant #0000255152 (NC_000002.11:g.166911255A>G, NM_001165963.1:c.495T>C (SCN1A))

Chromosome 2
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.166911255A>G
DNA change (hg38) g.166054745A>G
Published as SCN1A(NM_001165963.4):c.495T>C (p.Y165=), SCN1A(NM_001202435.2):c.495T>C (p.Y165=)
ISCN -
DB-ID SCN1A_000267 See all 2 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
SCN1A NM_001165963.1 -?/. - c.495T>C r.(?) p.(Tyr165=) -
SCN1A NM_006920.4 -?/. - c.495T>C r.(?) p.(Tyr165=) -


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