Variant #0000268798 (NC_000003.11:g.184049382C>T, NM_004366.5:c.*15012G>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.184049382C>T
DNA change (hg38) g.184331594C>T
Published as EIF4G1(NM_182917.4):c.4386C>T (p.F1462=)
ISCN -
DB-ID EIF4G1_000048 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) 0.00935 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-16 09:24:17 +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.*15012G>A r.(=) p.(=)
FAM131A NM_144635.4 -/. - c.-6037C>T r.(?) p.(=)
EIF4G1 NM_182917.4 -/. - c.4386C>T r.(?) p.(Phe1462=)


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