Variant #0000608435 (NC_000003.11:g.184071129C>T, NM_004366.5:c.1937G>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.184071129C>T
DNA change (hg38) g.184353341C>T
Published as CLCN2(NM_001171087.2):c.1886G>A (p.(Arg629Gln)), CLCN2(NM_004366.5):c.1937G>A (p.R646Q), CLCN2(NM_004366.6):c.1937G>A (p.R646Q)
ISCN -
DB-ID FAM131A_000019 See all 3 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) 0.0004 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN2 NM_004366.5 -?/. - c.1937G>A r.(?) p.(Arg646Gln)
FAM131A NM_144635.4 -?/. - c.*8371C>T r.(=) p.(=)


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