Variant #0000617618 (NC_000019.9:g.40877595G>A, NM_001031696.2:c.694G>A (PLD3))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.40877595G>A
DNA change (hg38) g.40371688G>A
Published as PLD3(NM_012268.3):c.694G>A (p.V232M), PLD3(NM_012268.4):c.694G>A (p.V232M)
ISCN -
DB-ID PLD3_000010 See all 5 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) 0.00311 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 2019-12-04 15:24:38 +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     
PLD3 NM_001031696.2 ?/. - c.694G>A r.(?) p.(Val232Met)
C19orf47 NM_001256440.1 ?/. - c.-23174C>T r.(?) p.(=)


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