Variant #0000912231 (NC_000005.9:g.138147943A>C, NM_001903.2:c.540A>C (CTNNA1))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.138147943A>C
DNA change (hg38) -
Published as CTNNA1(NM_001290307.2):c.540A>C (p.(Leu180=)), CTNNA1(NM_001323982.2):c.540A>C (p.L180=), CTNNA1(NM_001903.5):c.540A>C (p.L180=)
ISCN -
DB-ID CTNNA1_000007 See all 5 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) 0.03258 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNA1 NM_001903.2 -/. - c.540A>C r.(?) p.(Leu180=)
LRRTM2 NM_015564.2 -/. - c.*60756T>G r.(=) p.(=)


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