ClinVar

NM_001164277.2(SLC37A4):c.871+51G>A

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.3

Genomic location:

• Chr11: 119026552 (on Assembly GRCh38)
• Chr11: 118897262 (on Assembly GRCh37)

Preferred name:

NM_001164277.2(SLC37A4):c.871+51G>A

HGVS:

• NC_000011.10:g.119026552C>T
• NG_013331.1:g.9354G>A
• NM_001164277.2:c.871+51G>AMANE SELECT
• NM_001164278.2:c.871+51G>A
• NM_001164279.2:c.652+51G>A
• NM_001164280.2:c.871+51G>A
• NM_001467.6:c.871+51G>A
• LRG_187:g.9354G>A
• NC_000011.9:g.118897262C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs77180649

NCBI 1000 Genomes Browser:

rs77180649

Molecular consequence:

• NM_001164277.2:c.871+51G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001164278.2:c.871+51G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001164279.2:c.652+51G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001164280.2:c.871+51G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001467.6:c.871+51G>A - intron variant - [Sequence Ontology: SO:0001627]