Variant #0001066596 (NC_000017.10:g.1939344T>C, NM_001383.3:c.374T>C (DPH1))

Chromosome 17
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.1939344T>C
DNA change (hg38) -
Published as DPH1(NM_001383.6):c.359T>C (p.(Leu120Pro))
ISCN -
DB-ID DPH1_000005 See all 7 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) 0.00029 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +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     
DPH1 NM_001383.3 ?/. - c.374T>C r.(?) p.(Leu125Pro)
OVCA2 NM_080822.2 ?/. - c.-5998T>C r.(?) p.(=)


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