Variant #0000933812 (NC_000020.10:g.39317457G>A, NM_005461.4:c.34C>T (MAFB))

Chromosome 20
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.39317457G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID MAFB_000015
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1185769365
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 2023-10-02 09:35:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAFB NM_005461.4 ?/. - c.34C>T r.(?) p.(Pro12Ser)


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