Variant #0000612541 (NC_000010.10:g.69299333C>T, NM_013266.2:c.387G>A (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.69299333C>T
DNA change (hg38) g.67539575C>T
Published as CTNNA3(NM_013266.3):c.387G>A (p.L129=), CTNNA3(NM_013266.4):c.387G>A (p.L129=)
ISCN -
DB-ID CTNNA3_000092 See all 3 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) 9.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.387G>A r.(?) p.(Leu129=)
LRRTM3 NM_178011.3 -?/. - c.*441779C>T r.(=) p.(=)


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