Variant #0000624006 (NC_000019.9:g.40882567C>T, NM_001031696.2:c.1071C>T (PLD3))

Chromosome 19
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.40882567C>T
DNA change (hg38) g.40376660C>T
Published as PLD3(NM_012268.3):c.1071C>T (p.G357=)
ISCN -
DB-ID C19orf47_000005
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) 0.00115 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-15 18:17:00 +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.1071C>T r.(?) p.(Gly357=)
C19orf47 NM_001256440.1 -?/. - c.-28146G>A r.(?) p.(=)
HIPK4 NM_144685.3 -?/. - c.*2927G>A r.(=) p.(=)


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