Variant #0000925042 (NC_000009.11:g.35094287A>C, NM_032634.3:c.581T>G (PIGO))

Chromosome 9
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.35094287A>C
DNA change (hg38) -
Published as PIGO(NM_001201484.1):c.581T>G (p.(Phe194Cys)), PIGO(NM_032634.3):c.581T>G (p.F194C), PIGO(NM_032634.4):c.581T>G (p.F194C)
ISCN -
DB-ID PIGO_000036 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) 4.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIGO NM_032634.3 ?/. - c.581T>G r.(?) p.(Phe194Cys)


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