Variant #0001045363 (NC_000017.10:g.63554453G>A, NM_004655.3:c.286C>T (AXIN2))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.63554453G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID AXIN2_000124
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2144588573
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-06-16 11:22:01 +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     
AXIN2 NM_004655.3 +?/. - c.286C>T r.(?) p.(Arg96Ter)


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