Variant #0000889632 (NC_000011.9:g.118015894C>G, NM_174934.3:c.112G>C (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.118015894C>G
DNA change (hg38) -
Published as SCN4B(NM_174934.3):c.112G>C (p.A38P)
ISCN -
DB-ID SCN4B_000029
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) 0.00036 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN4B NM_001142348.1 -?/. - c.62-3843G>C r.(=) p.(=)
SCN4B NM_174934.3 -?/. - c.112G>C r.(?) p.(Ala38Pro)


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