Variant #0000509811 (NC_000002.11:g.166152415C>T, NM_021007.2:c.82C>T (SCN2A))

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.166152415C>T
DNA change (hg38) g.165295905C>T
Published as SCN2A(NM_001040142.1):c.82C>T (p.R28C, p.(Arg28Cys)), SCN2A(NM_021007.2):c.82C>T (p.R28C), SCN2A(NM_021007.3):c.82C>T (p.R28C)
ISCN -
DB-ID SCN2A_000038 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) 0.00025 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN3A NM_006922.3 ?/. - c.-92330G>A r.(?) p.(=)
SCN2A NM_021007.2 ?/. - c.82C>T r.(?) p.(Arg28Cys)


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