Variant #0000801913 (NC_000005.9:g.138118862T>C, NC_000005.9(NM_001903.2):c.106-4T>C (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.138118862T>C
DNA change (hg38) -
Published as CTNNA1(NM_001323982.1):c.106-4T>C
ISCN -
DB-ID CTNNA1_000044
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.106-4T>C r.spl? p.?
LRRTM2 NM_015564.2 -?/. - c.*89837A>G r.(=) p.(=)


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