Variant #0001068211 (NC_000003.11:g.9483932A>G, NC_000003.11(NM_001080517.1):c.1077+3A>G (SETD5))

Chromosome 3
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.9483932A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID SETD5_000157
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1260031095
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-11 15:36:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SETD5 NM_001080517.1 ?/. - c.1077+3A>G r.(?) p.(?)


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