Variant #0000565217 (NC_000018.9:g.59828420G>A, NM_176787.4:c.167C>T (PIGN))

Chromosome 18
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.59828420G>A
DNA change (hg38) g.62161187G>A
Published as PIGN(NM_012327.5):c.167C>T (p.(Ala56Val)), PIGN(NM_176787.4):c.167C>T (p.A56V)
ISCN -
DB-ID PIGN_000046 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) 0.01246 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIGN NM_176787.4 -/. - c.167C>T r.(?) p.(Ala56Val)


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