ClinVar

NM_182758.4(WDR72):c.*2356C>T

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

15q21.3

Genomic location:

• Chr15: 53515343 (on Assembly GRCh38)
• Chr15: 53807540 (on Assembly GRCh37)

Preferred name:

NM_182758.4(WDR72):c.*2356C>T

HGVS:

• NC_000015.10:g.53515343G>A
• NG_017034.2:g.249320C>T
• NM_001277176.2:c.*2356C>T
• NM_182758.4:c.*2356C>TMANE SELECT
• NC_000015.9:g.53807540G>A
• NM_182758.3:c.*2356C>T
• NR_102334.2:n.5905C>T
• NR_102335.2:n.2731C>T
• NR_102336.1:n.2708C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs3088091

NCBI 1000 Genomes Browser:

rs3088091

Molecular consequence:

• NM_001277176.2:c.*2356C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_182758.4:c.*2356C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NR_102334.2:n.5905C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_102335.2:n.2731C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_102336.1:n.2708C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]