Variant #0001024733 (NC_000003.11:g.148895654A>G, NM_032383.3:c.*5645A>G (HPS3))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.148895654A>G
DNA change (hg38) -
Published as CP(NM_000096.3):c.2991T>C (p.H997=), CP(NM_000096.4):c.2991T>C (p.H997=)
ISCN -
DB-ID CP_000009 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) 0.03384 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 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CP NM_000096.3 -/. - c.2991T>C r.(?) p.(His997=)
HPS3 NM_032383.3 -/. - c.*5645A>G r.(=) p.(=)


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