Variant #0000690945 (NC_000011.9:g.118023371G>T, NM_174934.3:c.18C>A (SCN4B))

Chromosome 11
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.118023371G>T
DNA change (hg38) -
Published as SCN4B(NM_174934.3):c.18C>A (p.D6E), SCN4B(NM_174934.4):c.18C>A (p.D6E)
ISCN -
DB-ID SCN4B_000011 See all 3 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) 0.00012 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN4B NM_001142348.1 -?/. - c.18C>A r.(?) p.(Asp6Glu)
SCN4B NM_174934.3 -?/. - c.18C>A r.(?) p.(Asp6Glu)


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