Variant #0000509961 (NC_000002.11:g.166930067A>G, NM_001165963.1:c.65T>C (SCN1A))

Chromosome 2
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.166930067A>G
DNA change (hg38) g.166073557A>G
Published as SCN1A(NM_001202435.3):c.65T>C (p.L22P), SCN1A(NM_006920.4):c.65T>C (p.L22P)
ISCN -
DB-ID SCN1A_000379 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
SCN1A NM_001165963.1 ?/. - c.65T>C r.(?) p.(Leu22Pro) -
SCN1A NM_006920.4 ?/. - c.65T>C r.(?) p.(Leu22Pro) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.