Variant #0000347204 (NC_000005.9:g.74016497T>C, NM_000521.3:c.1538T>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.74016497T>C
DNA change (hg38) g.74720672T>C
Published as -
ISCN -
DB-ID HEXB_000025
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +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.1538T>C r.(?) p.(Leu513Pro)
ENC1 NM_003633.3 ?/. - c.-80379A>G r.(?) p.(=)
GFM2 NM_032380.3 ?/. - c.*983A>G r.(=) p.(=)


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