Variant #0000915194 (NC_000019.9:g.35521779G>T, NC_000019.9(NM_199037.3):c.40+15G>T (SCN1B))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.35521779G>T
DNA change (hg38) -
Published as SCN1B(NM_001037.5):c.40+15G>T, SCN1B(NM_199037.5):c.40+15G>T
ISCN -
DB-ID SCN4B_000005 See all 20 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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     
SCN1B NM_001037.4 -/. - c.40+15G>T r.(=) p.(=)
GRAMD1A NM_020895.3 -/. - c.*4734G>T r.(=) p.(=)
SCN1B NM_199037.3 -/. - c.40+15G>T r.(=) p.(=)


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