Variant #0000852266 (NC_000009.11:g.35095169T>C, NM_032634.3:c.394A>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.35095169T>C
DNA change (hg38) -
Published as PIGO(NM_001201484.1):c.394A>G (p.(Met132Val)), PIGO(NM_032634.3):c.394A>G (p.M132V), PIGO(NM_032634.4):c.394A>G (p.M132V)
ISCN -
DB-ID PIGO_000038 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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STOML2 NM_013442.1 ?/. - c.*4863A>G r.(=) p.(=)
PIGO NM_032634.3 ?/. - c.394A>G r.(?) p.(Met132Val)


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