ClinVar

NM_000527.5(LDLR):c.378C>A (p.Phe126Leu)

Gene:

LDLR:low density lipoprotein receptor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 11105284 (on Assembly GRCh38)
• Chr19: 11215960 (on Assembly GRCh37)

Preferred name:

NM_000527.5(LDLR):c.378C>A (p.Phe126Leu)

HGVS:

• NC_000019.10:g.11105284C>A
• NG_009060.1:g.20904C>A
• NM_000527.5:c.378C>AMANE SELECT
• NM_001195798.2:c.378C>A
• NM_001195799.2:c.255C>A
• NM_001195800.2:c.314-2108C>A
• NM_001195803.2:c.314-1281C>A
• NP_000518.1:p.Phe126Leu
• NP_001182727.1:p.Phe126Leu
• NP_001182728.1:p.Phe85Leu
• LRG_274t1:c.378C>A
• LRG_274:g.20904C>A
• NC_000019.9:g.11215960C>A
• NM_000527.4:c.378C>A

This HGVS expression did not pass validation

Protein change:

F126L

Links:

dbSNP: rs762139262

NCBI 1000 Genomes Browser:

rs762139262

Molecular consequence:

• NM_001195800.2:c.314-2108C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001195803.2:c.314-1281C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_000527.5:c.378C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001195798.2:c.378C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001195799.2:c.255C>A - missense variant - [Sequence Ontology: SO:0001583]