Variant #0000885657 (NC_000003.11:g.184071958G>T, NM_004366.5:c.1652C>A (CLCN2))

Chromosome 3
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.184071958G>T
DNA change (hg38) -
Published as CLCN2(NM_004366.5):c.1652C>A (p.(Ser551Tyr))
ISCN -
DB-ID FAM131A_000042
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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN2 NM_004366.5 ?/. - c.1652C>A r.(?) p.(Ser551Tyr)
FAM131A NM_144635.4 ?/. - c.*9200G>T r.(=) p.(=)


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