Variant #0000277773 (NC_000010.10:g.103825568C>T, NM_024747.5:c.337C>T (HPS6))

Chromosome 10
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.103825568C>T
DNA change (hg38) g.102065811C>T
Published as HPS6(NM_024747.5):c.337C>T (p.R113W), HPS6(NM_024747.6):c.337C>T (p.R113W)
ISCN -
DB-ID HPS6_000012 See all 3 reported entries
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) 0.00234 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HPS6 NM_024747.5 ?/. - c.337C>T r.(?) p.(Arg113Trp)


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