Variant #0000726348 (NC_000017.10:g.40261336G>A, NM_024119.2:c.630C>T (DHX58))

Chromosome 17
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.40261336G>A
DNA change (hg38) -
Published as DHX58(NM_024119.3):c.630C>T (p.H210=)
ISCN -
DB-ID DHX58_000004
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) 3.0E-5 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 2021-02-08 18:36:18 +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     
KAT2A NM_021078.2 -?/. - c.*4331C>T r.(=) p.(=)
DHX58 NM_024119.2 -?/. - c.630C>T r.(?) p.(His210=)


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