Variant #0000609789 (NC_000005.9:g.74001089G>A, NM_000521.3:c.715G>A (HEXB))

Chromosome 5
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.74001089G>A
DNA change (hg38) g.74705264G>A
Published as HEXB(NM_000521.3):c.715G>A (p.V239I, p.(Val239Ile)), HEXB(NM_001292004.2):c.40G>A (p.V14I)
ISCN -
DB-ID HEXB_000018 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) 0.00036 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HEXB NM_000521.3 ?/. - c.715G>A r.(?) p.(Val239Ile)
ENC1 NM_003633.3 ?/. - c.-64971C>T r.(?) p.(=)


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