ClinVar

NM_001079675.5(ETV4):c.-52+205AC[25]

Gene:

ETV4:ETS variant transcription factor 4 [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

17q21.31

Genomic location:

• Chr17: 43545934 - 43545935 (on Assembly GRCh38)
• Chr17: 41623302 - 41623303 (on Assembly GRCh37)

Preferred name:

NM_001079675.5(ETV4):c.-52+205AC[25]

HGVS:

• NC_000017.11:g.43545935GT[25]
• NM_001079675.5:c.-52+205AC[25]MANE SELECT
• NM_001261437.3:c.-58+205AC[25]
• NC_000017.10:g.41623303GT[25]

This HGVS expression did not pass validation

Links:

dbSNP: rs531139204

NCBI 1000 Genomes Browser:

rs531139204

Molecular consequence:

• NM_001079675.5:c.-52+205AC[25] - intron variant - [Sequence Ontology: SO:0001627]
• NM_001261437.3:c.-58+205AC[25] - intron variant - [Sequence Ontology: SO:0001627]