ClinVar

NM_006744.4(RBP4):c.355+212G>A

Gene:

RBP4:retinol binding protein 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10q23.33

Genomic location:

• Chr10: 93600181 (on Assembly GRCh38)
• Chr10: 95359938 (on Assembly GRCh37)

Preferred name:

NM_006744.4(RBP4):c.355+212G>A

HGVS:

• NC_000010.11:g.93600181C>T
• NG_009104.1:g.6056G>A
• NM_001323517.1:c.355+212G>A
• NM_001323518.2:c.349+212G>A
• NM_006744.4:c.355+212G>AMANE SELECT
• NC_000010.10:g.95359938C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs11187548

NCBI 1000 Genomes Browser:

rs11187548

Molecular consequence:

• NM_001323517.1:c.355+212G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001323518.2:c.349+212G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_006744.4:c.355+212G>A - intron variant - [Sequence Ontology: SO:0001627]