Variant #0001027326 (NC_000020.10:g.46288186G>A, NM_006534.3:c.*6025G>A (NCOA3))

Chromosome 20
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.46288186G>A
DNA change (hg38) -
Published as SULF2(NM_001161841.2):c.2539C>T (p.R847C)
ISCN -
DB-ID SULF2_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) 0 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +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     
NCOA3 NM_006534.3 ?/. - c.*6025G>A r.(=) p.(=)
SULF2 NM_018837.3 ?/. - c.2539C>T r.(?) p.(Arg847Cys)


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