Variant #0000261350 (NC_000017.10:g.63533919T>C, NM_004655.3:c.1235A>G (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.63533919T>C
DNA change (hg38) g.65537801T>C
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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.1235A>G r.(?) p.(Asn412Ser)


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