Variant #0000562808 (NC_000017.10:g.63554307A>G, NM_004655.3:c.432T>C (AXIN2))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.63554307A>G
DNA change (hg38) g.65558189A>G
Published as AXIN2(NM_004655.3):c.432T>C (p.(=)), AXIN2(NM_004655.4):c.432T>C (p.I144=)
ISCN -
DB-ID AXIN2_000064 See all 2 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) 0.04396 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AXIN2 NM_004655.3 -/. - c.432T>C r.(?) p.(Ile144=)


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