Variant #0000658489 (NC_000019.9:g.12790506C>G, NM_016145.3:c.-10289G>C (WDR83OS))

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.12790506C>G
DNA change (hg38) g.12679692C>G
Published as DHPS(NM_001206974.1):c.396G>C (p.(Glu132Asp))
ISCN -
DB-ID DHPS_000009
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) 0.00927 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 2020-03-23 16:13:27 +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     
DHPS NM_001930.3 -?/. - c.522G>C r.(?) p.(Glu174Asp)
WDR83OS NM_016145.3 -?/. - c.-10289G>C r.(?) p.(=)
WDR83 NM_032332.3 -?/. - c.*4020C>G r.(=) p.(=)


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