ClinVar

NM_001365715.1(LRCH3):c.827C>T (p.Ala276Val)

Gene:

LRCH3:leucine rich repeats and calponin homology domain containing 3 [Gene - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3q29

Genomic location:

• Chr3: 197829613 (on Assembly GRCh38)
• Chr3: 197556484 (on Assembly GRCh37)

Preferred name:

NM_001365715.1(LRCH3):c.827C>T (p.Ala276Val)

HGVS:

• NC_000003.12:g.197829613C>T
• NM_001363887.1:c.827C>T
• NM_001365715.1:c.827C>TMANE SELECT
• NM_001365716.1:c.827C>T
• NM_001365717.1:c.827C>T
• NM_001365718.1:c.827C>T
• NM_001365719.2:c.827C>T
• NM_032773.4:c.827C>T
• NP_001350816.1:p.Ala276Val
• NP_001352644.1:p.Ala276Val
• NP_001352645.1:p.Ala276Val
• NP_001352646.1:p.Ala276Val
• NP_001352647.1:p.Ala276Val
• NP_001352648.1:p.Ala276Val
• NP_116162.1:p.Ala276Val
• NC_000003.11:g.197556484C>T
• NM_032773.2:c.827C>T
• NR_158582.1:n.852C>T

This HGVS expression did not pass validation

Protein change:

A276V

Molecular consequence:

• NM_001363887.1:c.827C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001365715.1:c.827C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001365716.1:c.827C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001365717.1:c.827C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001365718.1:c.827C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001365719.2:c.827C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_032773.4:c.827C>T - missense variant - [Sequence Ontology: SO:0001583]
• NR_158582.1:n.852C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]