ClinVar

NM_001015878.2(AURKC):c.-99dup

Gene:

AURKC:aurora kinase C [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

19q13.43

Genomic location:

• Chr19: 57231146 - 57231147 (on Assembly GRCh38)
• Chr19: 57742514 - 57742515 (on Assembly GRCh37)

Preferred name:

NM_001015878.2(AURKC):c.-99dup

HGVS:

• NC_000019.10:g.57231150dup
• NG_012134.1:g.5142dup
• NM_001015878.2:c.-99dupMANE SELECT
• NM_001015879.2:c.1+36dup
• NM_003160.3:c.-45+31dup
• NC_000019.9:g.57742518dup
• NM_001015878.1:c.-99dupC

This HGVS expression did not pass validation

Links:

dbSNP: rs74179426

NCBI 1000 Genomes Browser:

rs74179426

Molecular consequence:

• NM_001015878.2:c.-99dup - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001015879.2:c.1+36dup - intron variant - [Sequence Ontology: SO:0001627]
• NM_003160.3:c.-45+31dup - intron variant - [Sequence Ontology: SO:0001627]