Variant #0000324351 (NC_000016.9:g.334380C>T, NM_003502.3:c.*3742G>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.334380C>T
DNA change (hg38) g.284380C>T
Published as PDIA2(NM_006849.2):c.200-7C>T (p.(=))
ISCN -
DB-ID ARHGDIG_000007
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.*1566C>T r.(=) p.(=)
AXIN1 NM_003502.3 -?/. - c.*3742G>A r.(=) p.(=)
PDIA2 NM_006849.2 -?/. - c.200-7C>T r.(=) p.(=)


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