Variant #0001066475 (NC_000016.9:g.30970037G>A, NC_000016.9(NM_014712.1):c.-15-1G>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.30970037G>A
DNA change (hg38) -
Published as SETD1A(NM_014712.3):c.-15-1G>A
ISCN -
DB-ID ORAI3_000008
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SETD1A NM_014712.1 ?/. - c.-15-1G>A r.spl? p.?
ORAI3 NM_152288.2 ?/. - c.*4872G>A r.(=) p.(=)


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