ClinVar

NM_022124.6(CDH23):c.429+11C>T

Genes:

CDH23-AS1:CDH23 antisense RNA 1 [Gene - HGNC]
CDH23:cadherin related 23 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10q22.1

Genomic location:

• Chr10: 71511223 (on Assembly GRCh38)
• Chr10: 73270980 (on Assembly GRCh37)

Preferred name:

NM_022124.6(CDH23):c.429+11C>T

HGVS:

• NC_000010.11:g.71511223C>T
• NG_008835.1:g.119277C>T
• NM_001171930.2:c.429+11C>T
• NM_001171931.2:c.429+11C>T
• NM_001171932.2:c.429+11C>T
• NM_022124.6:c.429+11C>TMANE SELECT
• NM_052836.4:c.429+11C>T
• NC_000010.10:g.73270980C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001171930.2:c.429+11C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001171931.2:c.429+11C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001171932.2:c.429+11C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_022124.6:c.429+11C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_052836.4:c.429+11C>T - intron variant - [Sequence Ontology: SO:0001627]