ClinVar

NM_001164277.2(SLC37A4):c.886T>C (p.Tyr296His)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.3

Genomic location:

• Chr11: 119026065 (on Assembly GRCh38)
• Chr11: 118896775 (on Assembly GRCh37)

Preferred name:

NM_001164277.2(SLC37A4):c.886T>C (p.Tyr296His)

HGVS:

• NC_000011.10:g.119026065A>G
• NG_013331.1:g.9841T>C
• NM_001164277.2:c.886T>CMANE SELECT
• NM_001164278.2:c.886T>C
• NM_001164279.2:c.667T>C
• NM_001164280.2:c.886T>C
• NM_001467.6:c.886T>C
• NP_001157749.1:p.Tyr296His
• NP_001157749.1:p.Tyr296His
• NP_001157750.1:p.Tyr296His
• NP_001157751.1:p.Tyr223His
• NP_001157752.1:p.Tyr296His
• NP_001458.1:p.Tyr296His
• LRG_187t1:c.886T>C
• LRG_187:g.9841T>C
• LRG_187p1:p.Tyr296His
• NC_000011.9:g.118896775A>G
• NM_001164277.1:c.886T>C

This HGVS expression did not pass validation

Protein change:

Y223H

Links:

dbSNP: rs763008231

NCBI 1000 Genomes Browser:

rs763008231

Molecular consequence:

• NM_001164277.2:c.886T>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_001164278.2:c.886T>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_001164279.2:c.667T>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_001164280.2:c.886T>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_001467.6:c.886T>C - missense variant - [Sequence Ontology: SO:0001583]