Variant #0000300938 (NC_000022.10:g.38511665G>A, NM_003560.2:c.1903C>T (PLA2G6))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.38511665G>A
DNA change (hg38) g.38115658G>A
Published as PLA2G6(NM_003560.4):c.1903C>T (p.R635*)
ISCN -
DB-ID PLA2G6_000042 See all 2 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) 5.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLA2G6 NM_003560.2 +/. - c.1903C>T r.(?) p.(Arg635Ter)
BAIAP2L2 NM_025045.4 +/. - c.-5133C>T r.(?) p.(=)


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