Variant #0000562800 (NC_000017.10:g.63534420G>A, NM_004655.3:c.1101C>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.63534420G>A
DNA change (hg38) g.65538302G>A
Published as AXIN2(NM_004655.3):c.1101C>T (p.P367=, p.(Pro367=)), AXIN2(NM_004655.4):c.1101C>T (p.P367=)
ISCN -
DB-ID AXIN2_000086 See all 5 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) 0.00081 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +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.1101C>T r.(?) p.(Pro367=)


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