ClinVar

NM_000018.4(ACADVL):c.1332+27C>T

Gene:

ACADVL:acyl-CoA dehydrogenase very long chain [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17p13.1

Genomic location:

• Chr17: 7223902 (on Assembly GRCh38)
• Chr17: 7127221 (on Assembly GRCh37)

Preferred name:

NM_000018.4(ACADVL):c.1332+27C>T

HGVS:

• NC_000017.11:g.7223902C>T
• NG_007975.1:g.9069C>T
• NG_008391.2:g.1149G>A
• NG_033038.1:g.15643G>A
• NM_000018.4:c.1332+27C>TMANE SELECT
• NM_001033859.3:c.1266+27C>T
• NM_001270447.2:c.1401+27C>T
• NM_001270448.2:c.1104+27C>T
• NC_000017.10:g.7127221C>T
• NM_000018.3:c.1332+27C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs200161683

NCBI 1000 Genomes Browser:

rs200161683

Molecular consequence:

• NM_000018.4:c.1332+27C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001033859.3:c.1266+27C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001270447.2:c.1401+27C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001270448.2:c.1104+27C>T - intron variant - [Sequence Ontology: SO:0001627]