Variant #0001045488 (NC_000002.11:g.190430230C>T, NM_014585.5:c.610G>A (SLC40A1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.190430230C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC40A1_000003 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs387907377
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-06-25 14:47:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC40A1 NM_014585.5 +?/. - c.610G>A r.(?) p.(Gly204Ser)


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