Variant #0001042104 (NC_000017.10:g.63533919T>C, NM_004655.3:c.1235A>G (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.63533919T>C
DNA change (hg38) -
Published as AXIN2(NM_004655.3):c.1235A>G (p.(Asn412Ser), p.N412S), AXIN2(NM_004655.4):c.1235A>G (p.N412S)
ISCN -
DB-ID AXIN2_000009 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) 0.00985 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-05-05 21:14:00 +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.1235A>G r.(?) p.(Asn412Ser)


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