Variant #0000615955 (NC_000016.9:g.30997051C>A, NM_014712.1:c.*1707C>A (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.30997051C>A
DNA change (hg38) g.30985730C>A
Published as HSD3B7(NM_001142777.1):c.72C>A (p.(His24Gln))
ISCN -
DB-ID HSD3B7_000015
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
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.72C>A r.(?) p.(His24Gln)
SETD1A NM_014712.1 ?/. - c.*1707C>A r.(=) p.(=)
HSD3B7 NM_025193.3 ?/. - c.72C>A r.(?) p.(His24Gln)
STX1B NM_052874.3 ?/. - c.*7091G>T r.(=) p.(=)


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