Variant #0000329748 (NC_000003.11:g.184076765C>T, NM_004366.5:c.218G>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.184076765C>T
DNA change (hg38) g.184358977C>T
Published as CLCN2(NM_001171087.2):c.218G>A (p.(Arg73His)), CLCN2(NM_004366.5):c.218G>A (p.R73H), CLCN2(NM_004366.6):c.218G>A (p.R73H)
ISCN -
DB-ID CLCN2_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) 0.0025 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +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.218G>A r.(?) p.(Arg73His)
POLR2H NM_006232.2 ?/. - c.-4516C>T r.(?) p.(=)
FAM131A NM_144635.4 ?/. - c.*14007C>T r.(=) p.(=)


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