ClinVar

NM_130797.4(DPP6):c.243+11150C>A

Gene:

DPP6:dipeptidyl peptidase like 6 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q36.2

Genomic location:

• Chr7: 154064213 (on Assembly GRCh38)
• Chr7: 153761298 (on Assembly GRCh37)

Preferred name:

NM_130797.4(DPP6):c.243+11150C>A

HGVS:

• NC_000007.14:g.154064213C>A
• NG_033878.2:g.321228C>A
• NM_001039350.3:c.51+176479C>A
• NM_001290253.2:c.243+11150C>A
• NM_001364497.2:c.60+315205C>A
• NM_001364498.2:c.60+315205C>A
• NM_001364499.2:c.60+315205C>A
• NM_001364500.2:c.60+315205C>A
• NM_001364501.2:c.51+176479C>A
• NM_130797.4:c.243+11150C>AMANE SELECT
• NC_000007.13:g.153761298C>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001039350.3:c.51+176479C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001290253.2:c.243+11150C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001364497.2:c.60+315205C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001364498.2:c.60+315205C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001364499.2:c.60+315205C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001364500.2:c.60+315205C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001364501.2:c.51+176479C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_130797.4:c.243+11150C>A - intron variant - [Sequence Ontology: SO:0001627]

Observations:

8