Variant #0000265089 (NC_000005.9:g.138119081T>G, NC_000005.9(NM_001903.2):c.301+20T>G (CTNNA1))

Chromosome 5
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.138119081T>G
DNA change (hg38) g.138783392T>G
Published as CTNNA1(NM_001290307.3):c.301+20T>G, CTNNA1(NM_001903.5):c.301+20T>G
ISCN -
DB-ID CTNNA1_000004 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) 0.00066 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNA1 NM_001903.2 -?/. - c.301+20T>G r.(=) p.(=)
LRRTM2 NM_015564.2 -?/. - c.*89618A>C r.(=) p.(=)


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