Variant #0001002301 (NC_000016.9:g.335097G>C, NM_003502.3:c.*3025C>G (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.335097G>C
DNA change (hg38) -
Published as PDIA2(NM_006849.2):c.692G>C (p.(Arg231Pro))
ISCN -
DB-ID ARHGDIG_000025
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.*2283G>C r.(=) p.(=)
AXIN1 NM_003502.3 -?/. - c.*3025C>G r.(=) p.(=)
PDIA2 NM_006849.2 -?/. - c.692G>C r.(?) p.(Arg231Pro)


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