Variant #0000559047 (NC_000016.9:g.72132856G>A, NM_014003.3:c.795G>A (DHX38))

Chromosome 16
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.72132856G>A
DNA change (hg38) g.72098957G>A
Published as DHX38(NM_014003.3):c.795G>A (p.T265=), DHX38(NM_014003.4):c.795G>A (p.T265=)
ISCN -
DB-ID DHX38_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) 0.00091 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHX38 NM_014003.3 -/. - c.795G>A r.(?) p.(Thr265=)
TXNL4B NM_017853.2 -/. - c.-5628C>T r.(?) p.(=)


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