ClinVar

NM_000527.5(LDLR):c.1936C>T (p.Leu646=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 11120182 (on Assembly GRCh38)
• Chr19: 11230858 (on Assembly GRCh37)

Preferred name:

NM_000527.5(LDLR):c.1936C>T (p.Leu646=)

HGVS:

• NC_000019.10:g.11120182C>T
• NG_009060.1:g.35802C>T
• NM_000527.5:c.1936C>TMANE SELECT
• NM_001195798.2:c.1936C>T
• NM_001195799.2:c.1813C>T
• NM_001195800.2:c.1432C>T
• NM_001195803.2:c.1555C>T
• NP_000518.1:p.Leu646=
• NP_000518.1:p.Leu646=
• NP_001182727.1:p.Leu646=
• NP_001182728.1:p.Leu605=
• NP_001182729.1:p.Leu478=
• NP_001182732.1:p.Leu519=
• LRG_274t1:c.1936C>T
• LRG_274:g.35802C>T
• LRG_274p1:p.Leu646=
• NC_000019.9:g.11230858C>T
• NM_000527.4:c.1936C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_000527.5:c.1936C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195798.2:c.1936C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195799.2:c.1813C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195800.2:c.1432C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195803.2:c.1555C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

1