ClinVar

NM_022369.4(STRA6):c.927+284C>A

Gene:

STRA6:signaling receptor and transporter of retinol STRA6 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q24.1

Genomic location:

• Chr15: 74190556 (on Assembly GRCh38)
• Chr15: 74482897 (on Assembly GRCh37)

Preferred name:

NM_022369.4(STRA6):c.927+284C>A

HGVS:

• NC_000015.10:g.74190556G>T
• NG_009207.1:g.23475C>A
• NM_001142617.2:c.927+284C>A
• NM_001142618.2:c.927+284C>A
• NM_001142619.2:c.900+284C>A
• NM_001199040.2:c.1038+284C>A
• NM_001199041.2:c.972+284C>A
• NM_001199042.2:c.1044+284C>A
• NM_022369.4:c.927+284C>AMANE SELECT
• NC_000015.9:g.74482897G>T

This HGVS expression did not pass validation

Links:

dbSNP: rs77909337

NCBI 1000 Genomes Browser:

rs77909337

Molecular consequence:

• NM_001142617.2:c.927+284C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001142618.2:c.927+284C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001142619.2:c.900+284C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001199040.2:c.1038+284C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001199041.2:c.972+284C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001199042.2:c.1044+284C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_022369.4:c.927+284C>A - intron variant - [Sequence Ontology: SO:0001627]