All transcript variants in gene HPD

Information The variants shown are described using the NM_002150.2 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

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     
+?/. - c.505dup likely pathogenic r.(?) p.(Leu169Profs*4) g.122287610dup - HPD(NM_001171993.1):c.388dupC (p.L130Pfs*4) - HPD_000009 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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