Variant #0000548481 (NC_000012.11:g.52115549_52115557del, NM_014191.3:c.1855_1863del (SCN8A))

Chromosome 12
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.52115549_52115557del
DNA change (hg38) g.51721765_51721773del
Published as SCN8A(NM_001177984.2):c.1838_1846del (p.(Ser615_Tyr617del)), SCN8A(NM_014191.3):c.1855_1863delGGCTACAGC (p.G619_S621del)
ISCN -
DB-ID SCN8A_000028 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN8A NM_014191.3 ?/. - c.1855_1863del r.(?) p.(Gly619_Ser621del)


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