Variant #0000558069 (NC_000016.9:g.336866A>G, NM_003502.3:c.*1256T>C (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.336866A>G
DNA change (hg38) g.286866A>G
Published as PDIA2(NM_006849.2):c.1454A>G (p.(Glu485Gly))
ISCN -
DB-ID ARHGDIG_000017
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) 3.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGDIG NM_001176.3 ?/. - c.*4052A>G r.(=) p.(=)
AXIN1 NM_003502.3 ?/. - c.*1256T>C r.(=) p.(=)
PDIA2 NM_006849.2 ?/. - c.1454A>G r.(?) p.(Glu485Gly)


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