ClinVar

NM_001164277.2(SLC37A4):c.626+25C>T

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.3

Genomic location:

• Chr11: 119027603 (on Assembly GRCh38)
• Chr11: 118898313 (on Assembly GRCh37)

Preferred name:

NM_001164277.2(SLC37A4):c.626+25C>T

HGVS:

• NC_000011.10:g.119027603G>A
• NG_013331.1:g.8303C>T
• NM_001164277.2:c.626+25C>TMANE SELECT
• NM_001164278.2:c.626+25C>T
• NM_001164279.2:c.407+25C>T
• NM_001164280.2:c.626+25C>T
• NM_001467.6:c.626+25C>T
• LRG_187t1:c.625+25C>T
• LRG_187:g.8303C>T
• NC_000011.9:g.118898313G>A
• NM_001164277.1:c.625+25C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs533221443

NCBI 1000 Genomes Browser:

rs533221443

Molecular consequence:

• NM_001164277.2:c.626+25C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001164278.2:c.626+25C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001164279.2:c.407+25C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001164280.2:c.626+25C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001467.6:c.626+25C>T - intron variant - [Sequence Ontology: SO:0001627]