Variants
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rs1555444334

  • Pathogenic
  • Likely pathogenic

Your Genotype

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Description

The PKD1 c.12445-2A>C variant was not identified in the literature nor was it identified in the Clinvitae, ClinVar, GeneInsight COGR, MutDB, ADPKD Mutation, PKD1-LOVD, and PKD1-LOVD 3.0 databases. Furthermore, the variant was not listed in the 1000 Genomes Project, the Exome Aggregation Consortium (August 8, 2016) and NHLBI GO Exome Sequencing projects nor was it identified in dbSNP. The c.12445-2A>C variant is predicted to cause abnormal splicing because the nucleotide substitution occurs in the invariant region of the splice consensus sequence. In addition, 5 of 5 in silico or computational prediction software programs (SpliceSiteFinder, MaxEntScan, NNSPLICE, GeneSplicer, HumanSpliceFinder) predict a greater than 10% difference in splicing, predicting the loss of the 3’ splice site in intron 45. In summary, based on the above information, this variant meets our laboratory’s criteria to be classified as pathogenic.

Reference Allele

T


Alternative Allele

A

G

Chromosome

16


Location

2090196


Variant Type

SNP

Genes

ClinVar

Name

NM_001009944.3(PKD1):c.12445-2A>C


Allele

G


Clinical Significance

Pathogenic

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