ClinVar

NM_001164277.2(SLC37A4):c.898C>T (p.Arg300Cys)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.3

Genomic location:

• Chr11: 119026053 (on Assembly GRCh38)
• Chr11: 118896763 (on Assembly GRCh37)

Preferred name:

NM_001164277.2(SLC37A4):c.898C>T (p.Arg300Cys)

HGVS:

• NC_000011.10:g.119026053G>A
• NG_013331.1:g.9853C>T
• NM_001164277.2:c.898C>TMANE SELECT
• NM_001164278.2:c.898C>T
• NM_001164279.2:c.679C>T
• NM_001164280.2:c.898C>T
• NM_001467.6:c.898C>T
• NP_001157749.1:p.Arg300Cys
• NP_001157749.1:p.Arg300Cys
• NP_001157750.1:p.Arg300Cys
• NP_001157751.1:p.Arg227Cys
• NP_001157752.1:p.Arg300Cys
• NP_001458.1:p.Arg300Cys
• LRG_187t1:c.898C>T
• LRG_187:g.9853C>T
• LRG_187p1:p.Arg300Cys
• NC_000011.9:g.118896763G>A
• NM_001164277.1:c.898C>T

This HGVS expression did not pass validation

Protein change:

R227C

Links:

UniProtKB/Swiss-Prot: VAR_066397; dbSNP: rs193302880

NCBI 1000 Genomes Browser:

rs193302880

Molecular consequence:

• NM_001164277.2:c.898C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001164278.2:c.898C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001164279.2:c.679C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001164280.2:c.898C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001467.6:c.898C>T - missense variant - [Sequence Ontology: SO:0001583]

Observations:

3