HGVS-compliant variant descriptions

(alignment method = splign)

Type Variant description Links
Transcript (:c.) NM_058216.2:c.97C>T
RefSeqGene (:g.) RefSeqGene record not available RefSeqGene record not available
Predicted effect on protein (:p.) NP_478123.1:p.(Gln33Ter)
Predicted effect on protein (:p.) NP_478123.1:p.(Q33*)
Variant description Genome Build: Chr: Pos: Ref: Alt Links
NC_000017.10:g.56770101C>T GRCh37:17:56770101:C:T
NC_000017.11:g.58692740C>T GRCh38:17:58692740:C:T

Recommended variant descriptions

View recommended variant descriptions in UCSC Genome Browser

  1. We recommend using a genomic and a transcript description in all publications
  2. We currently recommend that RefSeqGene descriptions should be used when possible

Genomic descriptions

Reference sequence type Variant description
RefSeqGene RefSeqGene record not available
Chromosomal GRCh38 NC_000017.11:g.58692740C>T

Transcript description(s)

Reference sequence type Variant description
RefSeq Transcript NM_058216.2:c.97C>T

Unable to provide variant descriptions with respect to the RefSeqGene sequence because:

  • No RefSeqGene has been created for the RAD51C gene;
  • Or, Transcript NM_058216.2 has not been annotated in the RefSeqGene record for the RAD51C gene

Transcript-level variants overlapping genome coordinates NC_000017.11:58692740

Genomic coordinates (VCF) with respect to genome build GRCh38


Aggregated data sources and clinical significance


Select Genome Build
Alignment method: