ClinVar

NM_001382430.1(AKT1):c.633+12C>T

Gene:

AKT1:AKT serine/threonine kinase 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q32.33

Genomic location:

• Chr14: 104774926 (on Assembly GRCh38)
• Chr14: 105241263 (on Assembly GRCh37)

Preferred name:

NM_001382430.1(AKT1):c.633+12C>T

HGVS:

• NC_000014.9:g.104774926G>A
• NG_012188.1:g.25819C>T
• NM_001014431.2:c.633+12C>T
• NM_001014432.2:c.633+12C>T
• NM_001382430.1:c.633+12C>TMANE SELECT
• NM_001382431.1:c.633+12C>T
• NM_001382432.1:c.633+12C>T
• NM_001382433.1:c.633+12C>T
• NM_005163.2:c.633+12C>T
• LRG_721t2:c.633+12C>T
• LRG_721:g.25819C>T
• NC_000014.8:g.105241263G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001014431.2:c.633+12C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001014432.2:c.633+12C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382430.1:c.633+12C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382431.1:c.633+12C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382432.1:c.633+12C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382433.1:c.633+12C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_005163.2:c.633+12C>T - intron variant - [Sequence Ontology: SO:0001627]