Variant #0000267189 (NC_000010.10:g.69407239G>A, NM_013266.2:c.33C>T (CTNNA3))

Chromosome 10
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.69407239G>A
DNA change (hg38) g.67647481G>A
Published as CTNNA3(NM_013266.3):c.33C>T (p.I11=), CTNNA3(NM_013266.4):c.33C>T (p.I11=, p.(Ile11=))
ISCN -
DB-ID CTNNA3_000058 See all 5 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) 0.00168 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNA3 NM_013266.2 -?/. - c.33C>T r.(?) p.(Ile11=)
LRRTM3 NM_178011.3 -?/. - c.*549685G>A r.(=) p.(=)


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