Variant #0000526003 (NC_000005.9:g.74014795C>T, NM_000521.3:c.1416C>T (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.74014795C>T
DNA change (hg38) g.74718970C>T
Published as HEXB(NM_001292004.1):c.741C>T (p.G247=)
ISCN -
DB-ID HEXB_000031
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) 4.0E-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 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.1416C>T r.(?) p.(Gly472=)
ENC1 NM_003633.3 -?/. - c.-78677G>A r.(?) p.(=)
GFM2 NM_032380.3 -?/. - c.*2685G>A r.(=) p.(=)


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