Variant #0000557922 (NC_000016.9:g.30964762T>A, NM_014712.1:c.-4539T>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.30964762T>A
DNA change (hg38) g.30953441T>A
Published as ORAI3(NM_152288.2):c.485T>A (p.(Phe162Tyr))
ISCN -
DB-ID FBXL19_000002
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXL19 NM_001099784.2 ?/. - c.*6211T>A r.(=) p.(=)
SETD1A NM_014712.1 ?/. - c.-4539T>A r.(?) p.(=)
ORAI3 NM_152288.2 ?/. - c.485T>A r.(?) p.(Phe162Tyr)


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