ClinVar

NM_001243279.3(ACSF3):c.456C>T (p.Tyr152=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

16q24.3

Genomic location:

• Chr16: 89101137 (on Assembly GRCh38)
• Chr16: 89167545 (on Assembly GRCh37)

Preferred name:

NM_001243279.3(ACSF3):c.456C>T (p.Tyr152=)

HGVS:

• NC_000016.10:g.89101137C>T
• NG_031961.1:g.12329C>T
• NM_001127214.4:c.456C>T
• NM_001243279.3:c.456C>TMANE SELECT
• NM_001284316.2:c.-129-1467C>T
• NM_174917.5:c.456C>T
• NP_001120686.1:p.Tyr152=
• NP_001230208.1:p.Tyr152=
• NP_777577.2:p.Tyr152=
• NC_000016.9:g.89167545C>T
• NR_104293.2:n.794C>T
• NR_147928.2:n.794C>T
• NR_147929.2:n.794C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs147899198

NCBI 1000 Genomes Browser:

rs147899198

Molecular consequence:

• NM_001284316.2:c.-129-1467C>T - intron variant - [Sequence Ontology: SO:0001627]
• NR_104293.2:n.794C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_147928.2:n.794C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_147929.2:n.794C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_001127214.4:c.456C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001243279.3:c.456C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_174917.5:c.456C>T - synonymous variant - [Sequence Ontology: SO:0001819]