Variant #0000983204 (NC_000019.9:g.12791874_12791876del, NC_000019.9(NM_001930.3):c.207+501_207+503del (DHPS))

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.12791874_12791876del
DNA change (hg38) -
Published as DHPS(NM_001206974.1):c.55_57delGAG (p.E19del), DHPS(NM_001206974.2):c.55_57del (p.(Glu19del))
ISCN -
DB-ID DHPS_000010 See all 2 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHPS NM_001930.3 ?/. - c.207+501_207+503del r.(=) p.(=)
WDR83 NM_032332.3 ?/. - c.*5388_*5390del r.(=) p.(=)


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