Variant #0000886623 (NC_000005.9:g.138147995_138147996del, NC_000005.9(NM_001903.2):c.588+4_588+5del (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.138147995_138147996del
DNA change (hg38) -
Published as CTNNA1(NM_001323982.2):c.588+4_588+5delCA, CTNNA1(NM_001903.5):c.588+4_588+5delCA
ISCN -
DB-ID CTNNA1_000064 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +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.588+4_588+5del r.spl? p.?
LRRTM2 NM_015564.2 -?/. - c.*60704_*60705del r.(=) p.(=)


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