Variant #0000949418 (NC_000010.10:g.68979569C>G, NM_013266.2:c.639G>C (CTNNA3))

Chromosome 10
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.68979569C>G
DNA change (hg38) -
Published as CTNNA3(NM_013266.4):c.639G>C (p.E213D)
ISCN -
DB-ID CTNNA3_000234
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNA3 NM_013266.2 ?/. - c.639G>C r.(?) p.(Glu213Asp)
LRRTM3 NM_178011.3 ?/. - c.*122015C>G r.(=) p.(=)


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