Variant #0001056668 (NC_000019.9:g.40880407G>A, NM_001031696.2:c.899G>A (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.40880407G>A
DNA change (hg38) -
Published as PLD3(NM_012268.3):c.899G>A (p.C300Y)
ISCN -
DB-ID PLD3_000007 See all 4 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) 0.00086 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLD3 NM_001031696.2 -?/. - c.899G>A r.(?) p.(Cys300Tyr)
C19orf47 NM_001256440.1 -?/. - c.-25986C>T r.(?) p.(=)
HIPK4 NM_144685.3 -?/. - c.*5087C>T r.(=) p.(=)


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