ClinVar

NM_000527.5(LDLR):c.1013G>A (p.Cys338Tyr)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 11110724 (on Assembly GRCh38)
• Chr19: 11221400 (on Assembly GRCh37)

Preferred name:

NM_000527.5(LDLR):c.1013G>A (p.Cys338Tyr)

HGVS:

• NC_000019.10:g.11110724G>A
• NG_009060.1:g.26344G>A
• NM_000527.5:c.1013G>AMANE SELECT
• NM_001195798.2:c.1013G>A
• NM_001195799.2:c.890G>A
• NM_001195800.2:c.509G>A
• NM_001195803.2:c.632G>A
• NP_000518.1:p.Cys338Tyr
• NP_000518.1:p.Cys338Tyr
• NP_001182727.1:p.Cys338Tyr
• NP_001182728.1:p.Cys297Tyr
• NP_001182729.1:p.Cys170Tyr
• NP_001182732.1:p.Cys211Tyr
• LRG_274t1:c.1013G>A
• LRG_274:g.26344G>A
• LRG_274p1:p.Cys338Tyr
• NC_000019.9:g.11221400G>A
• NM_000527.4:c.1013G>A
• c.1013G>A

This HGVS expression did not pass validation

Protein change:

C170Y

Links:

LDLR-LOVD, British Heart Foundation: LDLR_000620;

Molecular consequence:

• NM_000527.5:c.1013G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001195798.2:c.1013G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001195799.2:c.890G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001195800.2:c.509G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001195803.2:c.632G>A - missense variant - [Sequence Ontology: SO:0001583]