ClinVar

NM_000016.6(ACADM):c.31-37C>T

Gene:

ACADM:acyl-CoA dehydrogenase medium chain [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p31.1

Genomic location:

• Chr1: 75728364 (on Assembly GRCh38)
• Chr1: 76194049 (on Assembly GRCh37)

Preferred name:

NM_000016.6(ACADM):c.31-37C>T

HGVS:

• NC_000001.11:g.75728364C>T
• NG_007045.2:g.9007C>T
• NM_000016.6:c.31-37C>TMANE SELECT
• NM_001127328.3:c.31-25C>T
• NM_001286042.2:c.10+3547C>T
• NM_001286043.2:c.31-37C>T
• NM_001286044.2:c.-268+3547C>T
• LRG_838:g.9007C>T
• NC_000001.10:g.76194049C>T
• NM_000016.4:c.31-37C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs201590881

NCBI 1000 Genomes Browser:

rs201590881

Molecular consequence:

• NM_000016.6:c.31-37C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001127328.3:c.31-25C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001286042.2:c.10+3547C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001286043.2:c.31-37C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001286044.2:c.-268+3547C>T - intron variant - [Sequence Ontology: SO:0001627]