ClinVar

NM_014336.5(AIPL1):c.97-15C>T

Gene:

AIPL1:AIP like 1 HSP90 co-chaperone [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17p13.2

Genomic location:

• Chr17: 6434113 (on Assembly GRCh38)
• Chr17: 6337433 (on Assembly GRCh37)

Preferred name:

NM_014336.5(AIPL1):c.97-15C>T

HGVS:

• NC_000017.11:g.6434113G>A
• NG_008474.1:g.6087C>T
• NM_001033054.3:c.97-15C>T
• NM_001033055.3:c.96+896C>T
• NM_001285399.3:c.97-51C>T
• NM_001285400.3:c.97-81C>T
• NM_001285401.3:c.97-15C>T
• NM_001285402.2:c.-21-15C>T
• NM_001285403.4:c.97-15C>T
• NM_014336.5:c.97-15C>TMANE SELECT
• NC_000017.10:g.6337433G>A
• NM_014336.3:c.97-15C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs190887679

NCBI 1000 Genomes Browser:

rs190887679

Molecular consequence:

• NM_001033054.3:c.97-15C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001033055.3:c.96+896C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001285399.3:c.97-51C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001285400.3:c.97-81C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001285401.3:c.97-15C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001285402.2:c.-21-15C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001285403.4:c.97-15C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_014336.5:c.97-15C>T - intron variant - [Sequence Ontology: SO:0001627]