Variant #0000655409 (NC_000005.9:g.74014717T>A, NM_000521.3:c.1338T>A (HEXB))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74014717T>A
DNA change (hg38) g.74718892T>A
Published as HEXB(NM_001292004.1):c.663T>A (p.S221=)
ISCN -
DB-ID HEXB_000043
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +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.1338T>A r.(?) p.(Ser446=)
ENC1 NM_003633.3 -?/. - c.-78599A>T r.(?) p.(=)
GFM2 NM_032380.3 -?/. - c.*2763A>T r.(=) p.(=)


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