ClinVar

NM_001243279.3(ACSF3):c.-187C>T

Gene:

ACSF3:acyl-CoA synthetase family member 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q24.3

Genomic location:

• Chr16: 89098597 (on Assembly GRCh38)
• Chr16: 89165005 (on Assembly GRCh37)

Preferred name:

NM_001243279.3(ACSF3):c.-187C>T

HGVS:

• NC_000016.10:g.89098597C>T
• NG_031961.1:g.9789C>T
• NM_001127214.4:c.-20-2065C>T
• NM_001243279.3:c.-187C>TMANE SELECT
• NM_001284316.2:c.-129-4007C>T
• NM_174917.5:c.-187C>T
• NC_000016.9:g.89165005C>T
• NM_174917.3:c.-187C>T
• NR_104293.2:n.152C>T
• NR_147928.2:n.152C>T
• NR_147929.2:n.152C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs577925407

NCBI 1000 Genomes Browser:

rs577925407

Molecular consequence:

• NM_001243279.3:c.-187C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_174917.5:c.-187C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001127214.4:c.-20-2065C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001284316.2:c.-129-4007C>T - intron variant - [Sequence Ontology: SO:0001627]
• NR_104293.2:n.152C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_147928.2:n.152C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_147929.2:n.152C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]