Variant #0000948573 (NC_000005.9:g.74017533T>C, NM_000521.3:c.*533T>C (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.74017533T>C
DNA change (hg38) -
Published as GFM2(NM_001281302.1):c.2383A>G (p.M795V), GFM2(NM_032380.5):c.2287A>G (p.M763V)
ISCN -
DB-ID HEXB_000054 See all 2 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) 5.0E-5 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 2023-11-27 17:35:39 +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     
HEXB NM_000521.3 ?/. - c.*533T>C r.(=) p.(=)
ENC1 NM_003633.3 ?/. - c.-81415A>G r.(?) p.(=)
GFM2 NM_032380.3 ?/. - c.2287A>G r.(?) p.(Met763Val)


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