ClinVar

NM_058216.3(RAD51C):c.146-3C>T

Gene:

RAD51C:RAD51 paralog C [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17q22

Genomic location:

• Chr17: 58694928 (on Assembly GRCh38)
• Chr17: 56772289 (on Assembly GRCh37)

Preferred name:

NM_058216.3(RAD51C):c.146-3C>T

HGVS:

• NC_000017.11:g.58694928C>T
• NG_023199.1:g.7327C>T
• NG_047169.1:g.2152G>A
• NM_002876.4:c.146-3C>T
• NM_058216.3:c.146-3C>TMANE SELECT
• LRG_314t1:c.146-3C>T
• LRG_314:g.7327C>T
• NC_000017.10:g.56772289C>T
• NM_058216.1:c.146-3C>T
• NM_058216.2:c.146-3C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs765143155

NCBI 1000 Genomes Browser:

rs765143155

Molecular consequence:

• NM_002876.4:c.146-3C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_058216.3:c.146-3C>T - intron variant - [Sequence Ontology: SO:0001627]

Observations:

1