ClinVar

NM_000018.4(ACADVL):c.1605+7G>C

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

17p13.1

Genomic location:

• Chr17: 7224400 (on Assembly GRCh38)
• Chr17: 7127719 (on Assembly GRCh37)

Preferred name:

NM_000018.4(ACADVL):c.1605+7G>C

HGVS:

• NC_000017.11:g.7224400G>C
• NG_007975.1:g.9567G>C
• NG_008391.2:g.651C>G
• NG_033038.1:g.15145C>G
• NM_000018.4:c.1605+7G>CMANE SELECT
• NM_001033859.3:c.1539+7G>C
• NM_001270447.2:c.1674+7G>C
• NM_001270448.2:c.1377+7G>C
• NC_000017.10:g.7127719G>C
• NM_000018.3:c.1605+7G>C

This HGVS expression did not pass validation

Links:

dbSNP: rs572010910

NCBI 1000 Genomes Browser:

rs572010910

Molecular consequence:

• NM_000018.4:c.1605+7G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001033859.3:c.1539+7G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001270447.2:c.1674+7G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001270448.2:c.1377+7G>C - intron variant - [Sequence Ontology: SO:0001627]