ClinVar

NM_000527.5(LDLR):c.1976C>A (p.Thr659Asn)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 11120222 (on Assembly GRCh38)
• Chr19: 11230898 (on Assembly GRCh37)

Preferred name:

NM_000527.5(LDLR):c.1976C>A (p.Thr659Asn)

Other names:

NM_000527.5(LDLR):c.1976C>A; p.Thr659Asn

HGVS:

• NC_000019.10:g.11120222C>A
• NG_009060.1:g.35842C>A
• NM_000527.5:c.1976C>AMANE SELECT
• NM_001195798.2:c.1976C>A
• NM_001195799.2:c.1853C>A
• NM_001195800.2:c.1472C>A
• NM_001195803.2:c.1595C>A
• NP_000518.1:p.Thr659Asn
• NP_000518.1:p.Thr659Asn
• NP_001182727.1:p.Thr659Asn
• NP_001182728.1:p.Thr618Asn
• NP_001182729.1:p.Thr491Asn
• NP_001182732.1:p.Thr532Asn
• LRG_274t1:c.1976C>A
• LRG_274:g.35842C>A
• LRG_274p1:p.Thr659Asn
• NC_000019.9:g.11230898C>A
• NM_000527.4:c.1976C>A
• c.1976C>A

This HGVS expression did not pass validation

Protein change:

T491N

Links:

LDLR-LOVD, British Heart Foundation: LDLR_001572; dbSNP: rs879255094

NCBI 1000 Genomes Browser:

rs879255094

Molecular consequence:

• NM_000527.5:c.1976C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001195798.2:c.1976C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001195799.2:c.1853C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001195800.2:c.1472C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001195803.2:c.1595C>A - missense variant - [Sequence Ontology: SO:0001583]