Variant #0000952179 (NC_000017.10:g.1939344T>C, NM_001383.3:c.359T>C (DPH1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1939344T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID DPH1_000005 See all 7 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs200530055
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00029 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-12-02 09:05:01 +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.359T>C r.(?) p.(Leu120Pro)


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