ClinVar

NM_182758.4(WDR72):c.*1734T>C

Gene:

WDR72:WD repeat domain 72 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q21.3

Genomic location:

• Chr15: 53515965 (on Assembly GRCh38)
• Chr15: 53808162 (on Assembly GRCh37)

Preferred name:

NM_182758.4(WDR72):c.*1734T>C

HGVS:

• NC_000015.10:g.53515965A>G
• NG_017034.2:g.248698T>C
• NM_001277176.2:c.*1734T>C
• NM_182758.4:c.*1734T>CMANE SELECT
• NC_000015.9:g.53808162A>G
• NM_182758.3:c.*1734T>C
• NR_102334.2:n.5283T>C
• NR_102335.2:n.2109T>C
• NR_102336.1:n.2086T>C

This HGVS expression did not pass validation

Links:

dbSNP: rs72745124

NCBI 1000 Genomes Browser:

rs72745124

Molecular consequence:

• NM_001277176.2:c.*1734T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_182758.4:c.*1734T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NR_102334.2:n.5283T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_102335.2:n.2109T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_102336.1:n.2086T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]