ClinVar

NM_000350.3(ABCA4):c.4297G>A (p.Val1433Ile)

Gene:

ABCA4:ATP binding cassette subfamily A member 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p22.1

Genomic location:

• Chr1: 94030483 (on Assembly GRCh38)
• Chr1: 94496039 (on Assembly GRCh37)

Preferred name:

NM_000350.3(ABCA4):c.4297G>A (p.Val1433Ile)

HGVS:

• NC_000001.11:g.94030483C>T
• NG_009073.1:g.95667G>A
• NG_009073.2:g.95665G>A
• NM_000350.3:c.4297G>AMANE SELECT
• NM_001425324.1:c.4075G>A
• NP_000341.2:p.Val1433Ile
• NP_001412253.1:p.Val1359Ile
• NC_000001.10:g.94496039C>T
• NM_000350.2:c.4297G>A
• P78363:p.Val1433Ile

This HGVS expression did not pass validation

Protein change:

V1359I

Links:

UniProtKB: P78363#VAR_008449; dbSNP: rs56357060

NCBI 1000 Genomes Browser:

rs56357060

Molecular consequence:

• NM_000350.3:c.4297G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001425324.1:c.4075G>A - missense variant - [Sequence Ontology: SO:0001583]