Variant #0000572064 (NC_000022.10:g.38536120G>C, PLA2G6(NM_003560.2):c.666C>G)

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38536120G>C
DNA change (hg38) g.38140113G>C
Published as PLA2G6(NM_003560.2):c.666C>G (p.T222=)
ISCN -
DB-ID PLA2G6_000157
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 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.666C>G r.(?) p.(Thr222=)