Variant #0000265130 (NC_000010.10:g.69281601T>C, NM_013266.2:c.578A>G (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.69281601T>C
DNA change (hg38) g.67521843T>C
Published as CTNNA3(NM_013266.3):c.578A>G (p.Q193R), CTNNA3(NM_013266.4):c.578A>G (p.Q193R, p.(Gln193Arg))
ISCN -
DB-ID CTNNA3_000051 See all 4 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNA3 NM_013266.2 -?/. - c.578A>G r.(?) p.(Gln193Arg)
LRRTM3 NM_178011.3 -?/. - c.*424047T>C r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.