Variant #0000948085 (NC_000003.11:g.184064514G>C, NM_004366.5:c.2577C>G (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.184064514G>C
DNA change (hg38) -
Published as CLCN2(NM_001171087.2):c.2526C>G (p.(Asp842Glu))
ISCN -
DB-ID FAM131A_000052
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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN2 NM_004366.5 ?/. - c.2577C>G r.(?) p.(Asp859Glu)
FAM131A NM_144635.4 ?/. - c.*1756G>C r.(=) p.(=)


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