Variant #0000518654 (NC_000003.11:g.184049143C>T, NM_004366.5:c.*15251G>A (CLCN2))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.184049143C>T
DNA change (hg38) g.184331355C>T
Published as EIF4G1(NM_001194946.1):c.4272C>T (p.V1424=), EIF4G1(NM_182917.4):c.4254C>T (p.V1418=)
ISCN -
DB-ID EIF4G1_000091 See all 2 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) 0.01884 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 09:23:38 +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.*15251G>A r.(=) p.(=)
FAM131A NM_144635.4 -/. - c.-6276C>T r.(?) p.(=)
EIF4G1 NM_182917.4 -/. - c.4254C>T r.(?) p.(Val1418=)


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