ClinVar

NM_000527.5(LDLR):c.891C>T (p.Asn297=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 11107465 (on Assembly GRCh38)
• Chr19: 11218141 (on Assembly GRCh37)

Preferred name:

NM_000527.5(LDLR):c.891C>T (p.Asn297=)

HGVS:

• NC_000019.10:g.11107465C>T
• NG_009060.1:g.23085C>T
• NM_000527.5:c.891C>TMANE SELECT
• NM_001195798.2:c.891C>T
• NM_001195799.2:c.768C>T
• NM_001195800.2:c.387C>T
• NM_001195803.2:c.510C>T
• NP_000518.1:p.Asn297=
• NP_001182727.1:p.Asn297=
• NP_001182728.1:p.Asn256=
• NP_001182729.1:p.Asn129=
• NP_001182732.1:p.Asn170=
• LRG_274t1:c.891C>T
• LRG_274:g.23085C>T
• NC_000019.9:g.11218141C>T
• NM_000527.4:c.891C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs1266870060

NCBI 1000 Genomes Browser:

rs1266870060

Molecular consequence:

• NM_000527.5:c.891C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195798.2:c.891C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195799.2:c.768C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195800.2:c.387C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195803.2:c.510C>T - synonymous variant - [Sequence Ontology: SO:0001819]