Variant #0001045884 (NC_000003.11:g.148939510A>G, NM_032383.3:c.*49501A>G (HPS3))

Chromosome 3
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.148939510A>G
DNA change (hg38) -
Published as CP(NM_000096.4):c.70T>C (p.Y24H)
ISCN -
DB-ID CP_000113
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CP NM_000096.3 ?/. - c.70T>C r.(?) p.(Tyr24His)
HPS3 NM_032383.3 ?/. - c.*49501A>G r.(=) p.(=)


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