Variant #0000859996 (NC_000005.9:g.74035829C>T, NM_000521.3:c.*18829C>T (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.74035829C>T
DNA change (hg38) -
Published as GFM2(NM_001281302.1):c.1160G>A (p.R387H)
ISCN -
DB-ID HEXB_000055
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 2022-05-09 15:51:19 +02:00 (CEST)
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.*18829C>T r.(=) p.(=)
GFM2 NM_032380.3 ?/. - c.1064G>A r.(?) p.(Arg355His)


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