ClinVar

NM_000352.6(ABCC8):c.3329+11C>A

Gene:

ABCC8:ATP binding cassette subfamily C member 8 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.1

Genomic location:

• Chr11: 17406611 (on Assembly GRCh38)
• Chr11: 17428158 (on Assembly GRCh37)

Preferred name:

NM_000352.6(ABCC8):c.3329+11C>A

HGVS:

• NC_000011.10:g.17406611G>T
• NG_008867.1:g.75292C>A
• NM_000352.6:c.3329+11C>AMANE SELECT
• NM_001287174.3:c.3332+11C>A
• NM_001351295.2:c.3395+11C>A
• NM_001351296.2:c.3329+11C>A
• NM_001351297.2:c.3326+11C>A
• LRG_790t1:c.3329+11C>A
• LRG_790t2:c.3332+11C>A
• LRG_790:g.75292C>A
• NC_000011.9:g.17428158G>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_000352.6:c.3329+11C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001287174.3:c.3332+11C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001351295.2:c.3395+11C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001351296.2:c.3329+11C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001351297.2:c.3326+11C>A - intron variant - [Sequence Ontology: SO:0001627]