Variant #0000327132 (NC_000002.11:g.80529610C>T, NC_000002.11(NM_004389.3):c.1057-90726C>T (CTNNA2))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.80529610C>T
DNA change (hg38) g.80302485C>T
Published as CTNNA2(NM_001164883.1):c.1057-90726C>T (p.(=))
ISCN -
DB-ID CTNNA2_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNA2 NM_004389.3 ?/. - c.1057-90726C>T r.(=) p.(=)
LRRTM1 NM_178839.4 ?/. - c.1335G>A r.(?) p.(Val445=)


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