Variant #0000526002 (NC_000005.9:g.74014629C>T, NM_000521.3:c.1250C>T (HEXB))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74014629C>T
DNA change (hg38) g.74718804C>T
Published as HEXB(NM_001292004.1):c.575C>T (p.P192L), HEXB(NM_001292004.2):c.575C>T (p.P192L)
ISCN -
DB-ID HEXB_000030 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) 0.00061 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +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     
HEXB NM_000521.3 +/. - c.1250C>T r.(?) p.(Pro417Leu)
ENC1 NM_003633.3 +/. - c.-78511G>A r.(?) p.(=)
GFM2 NM_032380.3 +/. - c.*2851G>A r.(=) p.(=)


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