ClinVar

NM_000527.5(LDLR):c.1911C>A (p.Ser637=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 11120157 (on Assembly GRCh38)
• Chr19: 11230833 (on Assembly GRCh37)

Preferred name:

NM_000527.5(LDLR):c.1911C>A (p.Ser637=)

HGVS:

• NC_000019.10:g.11120157C>A
• NG_009060.1:g.35777C>A
• NM_000527.5:c.1911C>AMANE SELECT
• NM_001195798.2:c.1911C>A
• NM_001195799.2:c.1788C>A
• NM_001195800.2:c.1407C>A
• NM_001195803.2:c.1530C>A
• NP_000518.1:p.Ser637=
• NP_000518.1:p.Ser637=
• NP_001182727.1:p.Ser637=
• NP_001182728.1:p.Ser596=
• NP_001182729.1:p.Ser469=
• NP_001182732.1:p.Ser510=
• LRG_274t1:c.1911C>A
• LRG_274:g.35777C>A
• LRG_274p1:p.Ser637=
• NC_000019.9:g.11230833C>A
• NM_000527.4:c.1911C>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_000527.5:c.1911C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195798.2:c.1911C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195799.2:c.1788C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195800.2:c.1407C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195803.2:c.1530C>A - synonymous variant - [Sequence Ontology: SO:0001819]