All transcript variants in gene APTX

Information The variants shown are described using the NM_175073.2 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
+/+ 7 c.601del r.(?) p.(His201Ilefs*13) - pathogenic (recessive) g.32984799del g.32984801del 643delC - APTX_000029 - PubMed: Nouri et al 2012 - - Germline - - - 0 - Rick van Minkelen
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