ClinVar

NM_001164277.2(SLC37A4):c.-16C>A

Gene:

SLC37A4:solute carrier family 37 member 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.3

Genomic location:

• Chr11: 119029385 (on Assembly GRCh38)
• Chr11: 118900095 (on Assembly GRCh37)

Preferred name:

NM_001164277.2(SLC37A4):c.-16C>A

HGVS:

• NC_000011.10:g.119029385G>T
• NG_013331.1:g.6522C>A
• NM_001164277.2:c.-16C>AMANE SELECT
• NM_001164278.2:c.-16C>A
• NM_001164279.2:c.-172+7C>A
• NM_001164280.2:c.-16C>A
• NM_001467.6:c.-16C>A
• LRG_187t1:c.-16C>A
• LRG_187:g.6522C>A
• NC_000011.9:g.118900095G>T
• NM_001164277.1:c.-16C>A

This HGVS expression did not pass validation

Links:

dbSNP: rs1555191915

NCBI 1000 Genomes Browser:

rs1555191915

Molecular consequence:

• NM_001164277.2:c.-16C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001164278.2:c.-16C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001164280.2:c.-16C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001467.6:c.-16C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001164279.2:c.-172+7C>A - intron variant - [Sequence Ontology: SO:0001627]