ClinVar

NR_185838.1(ATXN8OS):n.983T>C

Gene:

ATXN8OS:ATXN8 opposite strand lncRNA [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

13q21.33

Genomic location:

• Chr13: 70147713 (on Assembly GRCh38)
• Chr13: 70721845 (on Assembly GRCh37)

Preferred name:

NR_185838.1(ATXN8OS):n.983T>C

HGVS:

• NC_000013.11:g.70147713T>C
• NC_000013.10:g.70721845T>C
• NR_185838.1:n.983T>C
• NR_185839.1:n.812T>C
• NR_185840.1:n.1451T>C

This HGVS expression did not pass validation

Molecular consequence:

• NR_185838.1:n.983T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_185839.1:n.812T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_185840.1:n.1451T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Observations:

1