Variant #0000572052 (NC_000022.10:g.38528888C>T, PLA2G6(NM_003560.2):c.1027G>A)

Chromosome 22
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.38528888C>T
DNA change (hg38) g.38132881C>T
Published as PLA2G6(NM_003560.2):c.1027G>A (p.A343T)
ISCN -
DB-ID PLA2G6_000122 See all 4 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) 0.01086 View details
Owner VKGL-NL_AMC
Database submission license No license selected
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLA2G6 NM_003560.2 -/. - c.1027G>A r.(?) p.(Ala343Thr)