Variant #0000258544 (NC_000017.10:g.63554469G>A, NM_004655.3:c.270C>T (AXIN2))

Chromosome 17
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.63554469G>A
DNA change (hg38) g.65558351G>A
Published as AXIN2(NM_004655.3):c.270C>T (p.D90=, p.(Asp90=)), AXIN2(NM_004655.4):c.270C>T (p.D90=)
ISCN -
DB-ID AXIN2_000065 See all 6 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) 0.00089 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
AXIN2 NM_004655.3 -?/. - c.270C>T r.(?) p.(Asp90=)


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