Variant #0001049639 (NC_000002.11:g.44502922G>C, NM_000341.3:c.248G>C (SLC3A1))

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.44502922G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC3A1_000103
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs375663080
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-27 14:28:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC3A1 NM_000341.3 +?/. - c.248G>C r.(?) p.(Arg83Pro)


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