Variant #0000540225 (NC_000010.10:g.67829127C>T, NM_013266.2:c.2098G>A (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.67829127C>T
DNA change (hg38) g.66069369C>T
Published as CTNNA3(NM_013266.3):c.2098G>A (p.D700N), CTNNA3(NM_013266.4):c.2098G>A (p.D700N)
ISCN -
DB-ID CTNNA3_000114 See all 2 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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +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.2098G>A r.(?) p.(Asp700Asn)
LRRTM3 NM_178011.3 ?/. - c.-857215C>T r.(?) p.(=)


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