Variant #0001030012 (NC_000020.10:g.741709G>C, NM_033409.3:c.1371C>G (SLC52A3))

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.741709G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC52A3_000005 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs145431028
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00037 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-03-20 18:00:01 +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     
SLC52A3 NM_033409.3 ?/. - c.1371C>G r.(?) p.(Phe457Leu)


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