Variant #0001041091 (NC_000016.9:g.334531C>T, NM_003502.3:c.*3591G>A (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.334531C>T
DNA change (hg38) -
Published as PDIA2(NM_006849.4):c.344C>T (p.(Thr115Met))
ISCN -
DB-ID ARHGDIG_000026
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) 0.00441 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGDIG NM_001176.3 -?/. - c.*1717C>T r.(=) p.(=)
AXIN1 NM_003502.3 -?/. - c.*3591G>A r.(=) p.(=)
PDIA2 NM_006849.2 -?/. - c.344C>T r.(?) p.(Thr115Met)


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