ClinVar

NM_000062.3(SERPING1):c.210A>T (p.Ser70=)

Gene:

SERPING1:serpin family G member 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q12.1

Genomic location:

• Chr11: 57600037 (on Assembly GRCh38)
• Chr11: 57367510 (on Assembly GRCh37)

Preferred name:

NM_000062.3(SERPING1):c.210A>T (p.Ser70=)

HGVS:

• NC_000011.10:g.57600037A>T
• NG_009625.1:g.7484A>T
• NM_000062.3:c.210A>TMANE SELECT
• NM_001032295.2:c.210A>T
• NP_000053.2:p.Ser70=
• NP_000053.2:p.Ser70=
• NP_001027466.1:p.Ser70=
• LRG_105t1:c.210A>T
• LRG_105:g.7484A>T
• LRG_105p1:p.Ser70=
• NC_000011.9:g.57367510A>T
• NM_000062.2:c.210A>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_000062.3:c.210A>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001032295.2:c.210A>T - synonymous variant - [Sequence Ontology: SO:0001819]