Variant #0000558056 (NC_000016.9:g.333208_333210dup, NM_003502.3:c.*4926_*4928dup (AXIN1))

Chromosome 16
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.333208_333210dup
DNA change (hg38) g.283208_283210dup
Published as PDIA2(NM_006849.4):c.39_41dupGCT (p.L14dup)
ISCN -
DB-ID ARHGDIG_000003
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGDIG NM_001176.3 -?/. - c.*394_*396dup r.(=) p.(=)
AXIN1 NM_003502.3 -?/. - c.*4926_*4928dup r.(=) p.(=)
PDIA2 NM_006849.2 -?/. - c.39_41dup r.(?) p.(Leu14dup)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.