Variant #0001020216 (NC_000003.11:g.47162183C>G, NM_014159.6:c.3943G>C (SETD2))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47162183C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID SETD2_000125
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2107744841
Origin CLASSIFICATION record
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 2025-01-05 16:05:02 +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     
SETD2 NM_014159.6 -?/. - c.3943G>C r.(?) p.(Gly1315Arg)


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