ClinVar

NM_001203.3(BMPR1B):c.144-74AC[9]

Gene:

BMPR1B:bone morphogenetic protein receptor type 1B [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

4q22.3

Genomic location:

• Chr4: 95114646 - 95114651 (on Assembly GRCh38)
• Chr4: 96035797 - 96035802 (on Assembly GRCh37)

Preferred name:

NM_001203.3(BMPR1B):c.144-74AC[9]

HGVS:

• NC_000004.12:g.95114646AC[9]
• NG_009245.1:g.361670AC[9]
• NM_001203.3:c.144-74AC[9]MANE SELECT
• NM_001256792.2:c.144-74AC[9]
• NM_001256793.2:c.234-74AC[9]
• NM_001256794.1:c.144-74AC[9]
• NC_000004.11:g.96035797AC[9]

This HGVS expression did not pass validation

Links:

dbSNP: rs10622489

NCBI 1000 Genomes Browser:

rs10622489

Molecular consequence:

• NM_001203.3:c.144-74AC[9] - intron variant - [Sequence Ontology: SO:0001627]
• NM_001256792.2:c.144-74AC[9] - intron variant - [Sequence Ontology: SO:0001627]
• NM_001256793.2:c.234-74AC[9] - intron variant - [Sequence Ontology: SO:0001627]
• NM_001256794.1:c.144-74AC[9] - intron variant - [Sequence Ontology: SO:0001627]