ClinVar

NM_012448.4(STAT5B):c.2077+33TG[18]

Gene:

STAT5B:signal transducer and activator of transcription 5B [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

17q21.2

Genomic location:

• Chr17: 42207488 - 42207489 (on Assembly GRCh38)
• Chr17: 40359506 - 40359507 (on Assembly GRCh37)

Preferred name:

NM_012448.4(STAT5B):c.2077+33TG[18]

HGVS:

• NC_000017.11:g.42207488CA[18]
• NG_007271.1:g.73882TG[18]
• NM_012448.4:c.2077+33TG[18]MANE SELECT
• LRG_192:g.73882TG[18]
• NC_000017.10:g.40359506CA[18]

This HGVS expression did not pass validation

Links:

dbSNP: rs57356051

NCBI 1000 Genomes Browser:

rs57356051

Molecular consequence:

• NM_012448.4:c.2077+33TG[18] - intron variant - [Sequence Ontology: SO:0001627]