ClinVar

NM_003039.3(SLC2A5):c.-25G>A

Gene:

SLC2A5:solute carrier family 2 member 5 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p36.23

Genomic location:

• Chr1: 9069561 (on Assembly GRCh38)
• Chr1: 9129620 (on Assembly GRCh37)

Preferred name:

NM_003039.3(SLC2A5):c.-25G>A

HGVS:

• NC_000001.11:g.9069561C>T
• NG_050918.1:g.28847G>A
• NM_001135585.2:c.-25G>A
• NM_001328619.2:c.-25G>A
• NM_001328620.2:c.-119G>A
• NM_001328621.2:c.-81G>A
• NM_003039.3:c.-25G>AMANE SELECT
• NC_000001.10:g.9129620C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs5438

NCBI 1000 Genomes Browser:

rs5438

Molecular consequence:

• NM_001135585.2:c.-25G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001328619.2:c.-25G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001328620.2:c.-119G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001328621.2:c.-81G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_003039.3:c.-25G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]