Variant #0000801912 (NC_000005.9:g.138117693_138117694del, NM_001903.2:c.80_81del (CTNNA1))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.138117693_138117694del
DNA change (hg38) -
Published as CTNNA1(NM_001903.5):c.80_81delGA (p.R27Tfs*17)
ISCN -
DB-ID CTNNA1_000043
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 2021-09-17 14:40:49 +02:00 (CEST)
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.80_81del r.(?) p.(Arg27Thrfs*17)
LRRTM2 NM_015564.2 +/. - c.*91009_*91010del r.(=) p.(=)


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