Variant #0000924360 (NC_000005.9:g.484688_484689dup, NM_004174.2:c.880_881dup (SLC9A3))

Chromosome 5
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.484688_484689dup
DNA change (hg38) -
Published as SLC9A3(NM_004174.4):c.880_881dupTC (p.Y295Pfs*6)
ISCN -
DB-ID SLC9A3_000011
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC9A3 NM_004174.2 +/. - c.880_881dup r.(?) p.(Tyr295Profs*6)


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