Variant #0001041072 (NC_000016.9:g.30997073C>T, NM_014712.1:c.*1729C>T (SETD1A))

Chromosome 16
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.30997073C>T
DNA change (hg38) -
Published as HSD3B7(NM_025193.4):c.94C>T (p.(Arg32Trp))
ISCN -
DB-ID HSD3B7_000041
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) 2.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD3B7 NM_001142777.1 ?/. - c.94C>T r.(?) p.(Arg32Trp)
SETD1A NM_014712.1 ?/. - c.*1729C>T r.(=) p.(=)
HSD3B7 NM_025193.3 ?/. - c.94C>T r.(?) p.(Arg32Trp)
STX1B NM_052874.3 ?/. - c.*7069G>A r.(=) p.(=)


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