Variant #0000283429 (NC_000001.10:g.87380778_87380779del, NM_012262.3:c.59_60del (HS2ST1))

Chromosome 1
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.87380778_87380779del
DNA change (hg38) g.86915095_86915096del
Published as HS2ST1(NM_012262.4):c.59_60delTC (p.F20Cfs*34)
ISCN -
DB-ID HS2ST1_000001
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HS2ST1 NM_012262.3 ?/. - c.59_60del r.(?) p.(Phe20CysfsTer34)


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