Variant #0000509960 (NC_000002.11:g.166915084G>C, NM_001165963.1:c.379C>G (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.166915084G>C
DNA change (hg38) g.166058574G>C
Published as SCN1A(NM_001165963.4):c.379C>G (p.H127D)
ISCN -
DB-ID SCN1A_000025 See all 5 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) 7.0E-5 View details
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)
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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.379C>G r.(?) p.(His127Asp) -
SCN1A NM_006920.4 ?/. - c.379C>G r.(?) p.(His127Asp) -


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