ClinVar

NM_018486.3(HDAC8):c.164+19A>T

Gene:

HDAC8:histone deacetylase 8 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xq13.1

Genomic location:

• ChrX: 72572038 (on Assembly GRCh38)
• ChrX: 71791888 (on Assembly GRCh37)

Preferred name:

NM_018486.3(HDAC8):c.164+19A>T

HGVS:

• NC_000023.11:g.72572038T>A
• NG_015851.1:g.6066A>T
• NM_001166418.2:c.164+19A>T
• NM_001166419.2:c.164+19A>T
• NM_001166420.2:c.164+19A>T
• NM_001166422.2:c.164+19A>T
• NM_001166448.2:c.164+19A>T
• NM_018486.3:c.164+19A>TMANE SELECT
• NC_000023.10:g.71791888T>A

This HGVS expression did not pass validation

Links:

dbSNP: rs188536186

NCBI 1000 Genomes Browser:

rs188536186

Molecular consequence:

• NM_001166418.2:c.164+19A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001166419.2:c.164+19A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001166420.2:c.164+19A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001166422.2:c.164+19A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001166448.2:c.164+19A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_018486.3:c.164+19A>T - intron variant - [Sequence Ontology: SO:0001627]