ClinVar

NM_000527.5(LDLR):c.1431C>T (p.Asp477=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 11113607 (on Assembly GRCh38)
• Chr19: 11224283 (on Assembly GRCh37)

Preferred name:

NM_000527.5(LDLR):c.1431C>T (p.Asp477=)

HGVS:

• NC_000019.10:g.11113607C>T
• NG_009060.1:g.29227C>T
• NM_000527.5:c.1431C>TMANE SELECT
• NM_001195798.2:c.1431C>T
• NM_001195799.2:c.1308C>T
• NM_001195800.2:c.927C>T
• NM_001195803.2:c.1050C>T
• NP_000518.1:p.Asp477=
• NP_000518.1:p.Asp477=
• NP_001182727.1:p.Asp477=
• NP_001182728.1:p.Asp436=
• NP_001182729.1:p.Asp309=
• NP_001182732.1:p.Asp350=
• LRG_274t1:c.1431C>T
• LRG_274:g.29227C>T
• LRG_274p1:p.Asp477=
• NC_000019.9:g.11224283C>T
• NM_000527.4:c.1431C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs368610522

NCBI 1000 Genomes Browser:

rs368610522

Molecular consequence:

• NM_000527.5:c.1431C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195798.2:c.1431C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195799.2:c.1308C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195800.2:c.927C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001195803.2:c.1050C>T - synonymous variant - [Sequence Ontology: SO:0001819]