Variant #0000517809 (NC_000003.11:g.128780764A>G, NM_000174.3:c.182A>G (GP9))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.128780764A>G
DNA change (hg38) g.129061921A>G
Published as GP9(NM_000174.4):c.182A>G (p.N61S), GP9(NM_000174.5):c.182A>G (p.(Asn61Ser))
ISCN -
DB-ID GP9_000001 See all 40 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) 0.0005 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GP9 NM_000174.3 +/. - c.182A>G r.(?) p.(Asn61Ser)


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