ClinVar

NM_000527.5(LDLR):c.666C>T (p.Cys222=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 11105572 (on Assembly GRCh38)
• Chr19: 11216248 (on Assembly GRCh37)

Preferred name:

NM_000527.5(LDLR):c.666C>T (p.Cys222=)

Other names:

NM_000527.5(LDLR):c.666C>T; p.Cys222=

HGVS:

• NC_000019.10:g.11105572C>T
• NG_009060.1:g.21192C>T
• NM_000527.5:c.666C>TMANE SELECT
• NM_001195798.2:c.666C>T
• NM_001195799.2:c.543C>T
• NM_001195800.2:c.314-1820C>T
• NM_001195803.2:c.314-993C>T
• NP_000518.1:p.Cys222=
• NP_000518.1:p.Cys222=
• NP_001182727.1:p.Cys222=
• NP_001182728.1:p.Cys181=
• LRG_274t1:c.666C>T
• LRG_274:g.21192C>T
• LRG_274p1:p.Cys222=
• NC_000019.9:g.11216248C>T
• NC_000019.9:g.11216248C>T
• NM_000527.4:c.666C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs756613387

NCBI 1000 Genomes Browser:

rs756613387

Molecular consequence:

• NM_001195800.2:c.314-1820C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001195803.2:c.314-993C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_000527.5:c.666C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195798.2:c.666C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195799.2:c.543C>T - synonymous variant - [Sequence Ontology: SO:0001819]