ClinVar

NM_018486.3(HDAC8):c.164+186G>C

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

Xq13.1

Genomic location:

• ChrX: 72571871 (on Assembly GRCh38)
• ChrX: 71791721 (on Assembly GRCh37)

Preferred name:

NM_018486.3(HDAC8):c.164+186G>C

HGVS:

• NC_000023.11:g.72571871C>G
• NG_015851.1:g.6233G>C
• NM_001166418.2:c.164+186G>C
• NM_001166419.2:c.164+186G>C
• NM_001166420.2:c.164+186G>C
• NM_001166422.2:c.164+186G>C
• NM_001166448.2:c.164+186G>C
• NM_018486.3:c.164+186G>CMANE SELECT
• NC_000023.10:g.71791721C>G

This HGVS expression did not pass validation

Links:

dbSNP: rs192758726

NCBI 1000 Genomes Browser:

rs192758726

Molecular consequence:

• NM_001166418.2:c.164+186G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001166419.2:c.164+186G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001166420.2:c.164+186G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001166422.2:c.164+186G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001166448.2:c.164+186G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_018486.3:c.164+186G>C - intron variant - [Sequence Ontology: SO:0001627]