Variant #0000526008 (NC_000005.9:g.74047274G>A, NM_000521.3:c.*30274G>A (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.74047274G>A
DNA change (hg38) g.74751449G>A
Published as GFM2(NM_001281302.2):c.445C>T (p.R149*)
ISCN -
DB-ID HEXB_000036
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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.*30274G>A r.(=) p.(=)
GFM2 NM_032380.3 +/. - c.349C>T r.(?) p.(Arg117Ter)


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