ClinVar

NM_000527.5(LDLR):c.1187-11C>T

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 11113267 (on Assembly GRCh38)
• Chr19: 11223943 (on Assembly GRCh37)

Preferred name:

NM_000527.5(LDLR):c.1187-11C>T

HGVS:

• NC_000019.10:g.11113267C>T
• NG_009060.1:g.28887C>T
• NM_000527.5:c.1187-11C>TMANE SELECT
• NM_001195798.2:c.1187-11C>T
• NM_001195799.2:c.1064-11C>T
• NM_001195800.2:c.683-11C>T
• NM_001195803.2:c.806-11C>T
• LRG_274t1:c.1187-11C>T
• LRG_274:g.28887C>T
• NC_000019.9:g.11223943C>T
• NC_000019.9:g.11223943C>T
• NM_000527.4:c.1187-11C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs897774579

NCBI 1000 Genomes Browser:

rs897774579

Molecular consequence:

• NM_000527.5:c.1187-11C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001195798.2:c.1187-11C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001195799.2:c.1064-11C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001195800.2:c.683-11C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001195803.2:c.806-11C>T - intron variant - [Sequence Ontology: SO:0001627]

Observations:

4