ClinVar

NM_001144757.3(SCG5):c.459G>A (p.Pro153=)

Genes:

ARHGAP11A-SCG5:ARHGAP11A-SCG5 readthrough [Gene - HGNC]
SCG5:secretogranin V [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q13.3

Genomic location:

• Chr15: 32684639 (on Assembly GRCh38)
• Chr15: 32976840 (on Assembly GRCh37)

Preferred name:

NM_001144757.3(SCG5):c.459G>A (p.Pro153=)

HGVS:

• NC_000015.10:g.32684639G>A
• NG_051230.1:g.48027G>A
• NM_001144757.3:c.459G>AMANE SELECT
• NM_001368319.1:c.1698G>A
• NM_001394278.1:c.459G>A
• NM_001394279.1:c.456G>A
• NM_003020.5:c.456G>A
• NP_001138229.1:p.Pro153=
• NP_001355248.1:p.Pro566=
• NP_001381207.1:p.Pro153=
• NP_001381208.1:p.Pro152=
• NP_003011.1:p.Pro152=
• NC_000015.9:g.32976840G>A
• NM_001144757.1:c.459G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs35500536

NCBI 1000 Genomes Browser:

rs35500536

Molecular consequence:

• NM_001144757.3:c.459G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001368319.1:c.1698G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001394278.1:c.459G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001394279.1:c.456G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_003020.5:c.456G>A - synonymous variant - [Sequence Ontology: SO:0001819]