Variant #0000537920 (NC_000009.11:g.32489407T>C, NM_014314.3:c.734A>G (DDX58))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32489407T>C
DNA change (hg38) g.32489409T>C
Published as DDX58(NM_014314.3):c.734A>G (p.N245S), DDX58(NM_014314.4):c.734A>G (p.N245S)
ISCN -
DB-ID DDX58_000017 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) 0.00175 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX58 NM_014314.3 -/. - c.734A>G r.(?) p.(Asn245Ser)


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