Variant #0000725858 (NC_000016.9:g.56921879G>A, NM_000339.2:c.2221G>A (SLC12A3))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.56921879G>A
DNA change (hg38) -
Published as SLC12A3(NM_000339.2):c.2221G>A (p.G741R), SLC12A3(NM_000339.3):c.2221G>A (p.G741R), SLC12A3(NM_001126108.2):c.2221G>A (p.(Gly741Arg))
ISCN -
DB-ID SLC12A3_000092 See all 9 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00038 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC12A3 NM_000339.2 +/. - c.2221G>A r.(?) p.(Gly741Arg)


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