Variant #0000933851 (NC_000016.9:g.56900547_56900598dup, NC_000016.9(NM_000339.2):c.283-438_283-387dup (SLC12A3))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.56900547_56900598dup
DNA change (hg38) g.56866635_56866686dup
Published as -
ISCN -
DB-ID SLC12A3_000197 See all 2 reported entries
Variant remarks in vitro midigene splicing assay; suggested clinical classification variant “likely pathogenic"
Reference PubMed: Viering 2023, Journal: Viering 2023
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-10-06 17:19:51 +02:00 (CEST)
Date last edited 2023-10-12 14:34:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC12A3 NM_000339.2 +/. 1i c.283-438_283-387dup r.[282_283ins283-385_283-74,282_283ins283-385_283-95] p.?


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