Variant #0000297060 (NC_000006.11:g.46684222C>T, NM_001168357.1:c.275G>A (PLA2G7))

Chromosome 6
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.46684222C>T
DNA change (hg38) g.46716485C>T
Published as PLA2G7(NM_005084.4):c.275G>A (p.R92H)
ISCN -
DB-ID PLA2G7_000003
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) 0.30775 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
TDRD6 NM_001010870.2 -/. - c.*14598C>T r.(=) p.(=)
PLA2G7 NM_001168357.1 -/. - c.275G>A r.(?) p.(Arg92His)


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