Variant #0000540199 (NC_000010.10:g.67680203A>G, NM_013266.2:c.2573T>C (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.67680203A>G
DNA change (hg38) g.65920445A>G
Published as CTNNA3(NM_013266.3):c.2573T>C (p.L858S), CTNNA3(NM_013266.4):c.2573T>C (p.L858S, p.(Leu858Ser))
ISCN -
DB-ID CTNNA3_000099 See all 7 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) 0.00034 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNA3 NM_013266.2 -?/. - c.2573T>C r.(?) p.(Leu858Ser)
LRRTM3 NM_178011.3 -?/. - c.-1006139A>G r.(?) p.(=)


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