Variant #0000725765 (NC_000016.9:g.334697C>T, NM_003502.3:c.*3425G>A (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.334697C>T
DNA change (hg38) -
Published as PDIA2(NM_006849.4):c.445C>T (p.R149W)
ISCN -
DB-ID ARHGDIG_000020
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGDIG NM_001176.3 ?/. - c.*1883C>T r.(=) p.(=)
AXIN1 NM_003502.3 ?/. - c.*3425G>A r.(=) p.(=)
PDIA2 NM_006849.2 ?/. - c.445C>T r.(?) p.(Arg149Trp)


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