Variant #0000518659 (NC_000003.11:g.184049756C>T, NM_004366.5:c.*14638G>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.184049756C>T
DNA change (hg38) g.184331968C>T
Published as EIF4G1(NM_182917.4):c.4503C>T (p.D1501=)
ISCN -
DB-ID EIF4G1_000095 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) 4.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 09:25:08 +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.*14638G>A r.(=) p.(=)
FAM131A NM_144635.4 -?/. - c.-5663C>T r.(?) p.(=)
EIF4G1 NM_182917.4 -?/. - c.4503C>T r.(?) p.(Asp1501=)


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