ClinVar

NM_001164277.2(SLC37A4):c.891G>T (p.Gly297=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.3

Genomic location:

• Chr11: 119026060 (on Assembly GRCh38)
• Chr11: 118896770 (on Assembly GRCh37)

Preferred name:

NM_001164277.2(SLC37A4):c.891G>T (p.Gly297=)

HGVS:

• NC_000011.10:g.119026060C>A
• NG_013331.1:g.9846G>T
• NM_001164277.2:c.891G>TMANE SELECT
• NM_001164278.2:c.891G>T
• NM_001164279.2:c.672G>T
• NM_001164280.2:c.891G>T
• NM_001467.6:c.891G>T
• NP_001157749.1:p.Gly297=
• NP_001157749.1:p.Gly297=
• NP_001157750.1:p.Gly297=
• NP_001157751.1:p.Gly224=
• NP_001157752.1:p.Gly297=
• NP_001458.1:p.Gly297=
• LRG_187t1:c.891G>T
• LRG_187:g.9846G>T
• LRG_187p1:p.Gly297=
• NC_000011.9:g.118896770C>A
• NC_000011.9:g.118896770C>A
• NM_001164277.1:c.891G>T

This HGVS expression did not pass validation

Links:

dbSNP: rs1388277495

NCBI 1000 Genomes Browser:

rs1388277495

Molecular consequence:

• NM_001164277.2:c.891G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001164278.2:c.891G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001164279.2:c.672G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001164280.2:c.891G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001467.6:c.891G>T - synonymous variant - [Sequence Ontology: SO:0001819]