Variant #0001034433 (NC_000004.11:g.170608858A>G, NM_001829.3:c.368A>G (CLCN3))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.170608858A>G
DNA change (hg38) g.169687707A>G
Published as CLCN3(NM_001829.4):c.368A>G (p.(Tyr123Cys))
ISCN -
DB-ID CLCN3_000012
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited 2025-10-31 18:58:02 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN3 NM_001829.3 ?/. - c.368A>G r.(?) p.(Tyr123Cys)


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