ClinVar

NM_170707.4(LMNA):c.-5C>A

Gene:

LMNA:lamin A/C [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q22

Genomic location:

• Chr1: 156114914 (on Assembly GRCh38)
• Chr1: 156084705 (on Assembly GRCh37)

Preferred name:

NM_170707.4(LMNA):c.-5C>A

HGVS:

• NC_000001.11:g.156114914C>A
• NG_008692.2:g.37342C>A
• NM_001282625.2:c.-5C>A
• NM_001282626.2:c.-5C>A
• NM_005572.4:c.-5C>A
• NM_170707.4:c.-5C>AMANE SELECT
• NM_170708.4:c.-5C>A
• LRG_254t1:c.-5C>A
• LRG_254:g.37342C>A
• NC_000001.10:g.156084705C>A
• NM_005572.3:c.-5C>A

This HGVS expression did not pass validation

Links:

dbSNP: rs886045362

NCBI 1000 Genomes Browser:

rs886045362

Molecular consequence:

• NM_001282625.2:c.-5C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001282626.2:c.-5C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_005572.4:c.-5C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_170707.4:c.-5C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_170708.4:c.-5C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]