ClinVar

NM_000527.5(LDLR):c.1428C>T (p.Pro476=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 11113604 (on Assembly GRCh38)
• Chr19: 11224280 (on Assembly GRCh37)

Preferred name:

NM_000527.5(LDLR):c.1428C>T (p.Pro476=)

HGVS:

• NC_000019.10:g.11113604C>T
• NG_009060.1:g.29224C>T
• NM_000527.5:c.1428C>TMANE SELECT
• NM_001195798.2:c.1428C>T
• NM_001195799.2:c.1305C>T
• NM_001195800.2:c.924C>T
• NM_001195803.2:c.1047C>T
• NP_000518.1:p.Pro476=
• NP_000518.1:p.Pro476=
• NP_001182727.1:p.Pro476=
• NP_001182728.1:p.Pro435=
• NP_001182729.1:p.Pro308=
• NP_001182732.1:p.Pro349=
• LRG_274t1:c.1428C>T
• LRG_274:g.29224C>T
• LRG_274p1:p.Pro476=
• NC_000019.9:g.11224280C>T
• NM_000527.4:c.1428C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs543392107

NCBI 1000 Genomes Browser:

rs543392107

Molecular consequence:

• NM_000527.5:c.1428C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195798.2:c.1428C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195799.2:c.1305C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195800.2:c.924C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195803.2:c.1047C>T - synonymous variant - [Sequence Ontology: SO:0001819]