All transcript variants in gene PDYN

Information The variants shown are described using the NM_024411.4 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.632T>G likely pathogenic r.(?) p.(Leu211Trp) g.1961102A>C - PDYN(NM_024411.4):c.632T>G (p.L211W) - PDYN_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL
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