Variant #0000680548 (NC_000016.9:g.30997015C>A, NM_014712.1:c.*1671C>A (SETD1A))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.30997015C>A
DNA change (hg38) -
Published as HSD3B7(NM_001142777.2):c.36C>A (p.Y12*)
ISCN -
DB-ID HSD3B7_000019
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD3B7 NM_001142777.1 +/. - c.36C>A r.(?) p.(Tyr12Ter)
SETD1A NM_014712.1 +/. - c.*1671C>A r.(=) p.(=)
HSD3B7 NM_025193.3 +/. - c.36C>A r.(?) p.(Tyr12Ter)
STX1B NM_052874.3 +/. - c.*7127G>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.