Variant #0000854513 (NC_000016.9:g.396193G>A, NM_003502.3:c.833C>T (AXIN1))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.396193G>A
DNA change (hg38) -
Published as AXIN1(NM_003502.3):c.833C>T (p.(Pro278Leu)), AXIN1(NM_003502.4):c.833C>T (p.P278L)
ISCN -
DB-ID AXIN1_000014 See all 3 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) 0.00051 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AXIN1 NM_003502.3 ?/. - c.833C>T r.(?) p.(Pro278Leu)


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