Variant #0000609401 (NC_000005.9:g.11346632C>T, NM_001332.2:c.1480G>A (CTNND2))

Chromosome 5
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.11346632C>T
DNA change (hg38) g.11346520C>T
Published as CTNND2(NM_001332.3):c.1480G>A (p.G494S), CTNND2(NM_001332.4):c.1480G>A (p.G494S)
ISCN -
DB-ID CTNND2_000031 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) 0.0002 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNND2 NM_001332.2 ?/. - c.1480G>A r.(?) p.(Gly494Ser)


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