Variant #0000518667 (NC_000003.11:g.184070901C>T, NM_004366.5:c.2063G>A (CLCN2))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.184070901C>T
DNA change (hg38) g.184353113C>T
Published as CLCN2(NM_001171087.2):c.2012G>A (p.(Arg671Gln)), CLCN2(NM_004366.6):c.2063G>A (p.R688Q)
ISCN -
DB-ID CLCN2_000006 See all 4 reported entries
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) 0.01521 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN2 NM_004366.5 -?/. - c.2063G>A r.(?) p.(Arg688Gln)
FAM131A NM_144635.4 -?/. - c.*8143C>T r.(=) p.(=)


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