ClinVar

NM_001039591.3(USP9X):c.436-237T>A

Gene:

USP9X:ubiquitin specific peptidase 9 X-linked [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xp11.4

Genomic location:

• ChrX: 41136567 (on Assembly GRCh38)
• ChrX: 40995820 (on Assembly GRCh37)

Preferred name:

NM_001039591.3(USP9X):c.436-237T>A

HGVS:

• NC_000023.11:g.41136567T>A
• NG_012547.1:g.55933T>A
• NM_001039590.3:c.436-237T>A
• NM_001039591.3:c.436-237T>AMANE SELECT
• NC_000023.10:g.40995820T>A

This HGVS expression did not pass validation

Links:

dbSNP: rs5918120

NCBI 1000 Genomes Browser:

rs5918120

Molecular consequence:

• NM_001039590.3:c.436-237T>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001039591.3:c.436-237T>A - intron variant - [Sequence Ontology: SO:0001627]