Variant #0000948484 (NC_000005.9:g.138145835G>A, NM_001903.2:c.410G>A (CTNNA1))

Chromosome 5
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.138145835G>A
DNA change (hg38) -
Published as CTNNA1(NM_001903.5):c.410G>A (p.R137Q)
ISCN -
DB-ID CTNNA1_000086
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) 2.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNA1 NM_001903.2 ?/. - c.410G>A r.(?) p.(Arg137Gln)
LRRTM2 NM_015564.2 ?/. - c.*62864C>T r.(=) p.(=)


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