ClinVar

NM_003722.5(TP63):c.62+25276G>C

Gene:

TP63:tumor protein p63 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3q28

Genomic location:

• Chr3: 189656853 (on Assembly GRCh38)
• Chr3: 189374642 (on Assembly GRCh37)

Preferred name:

NM_003722.5(TP63):c.62+25276G>C

HGVS:

• NC_000003.12:g.189656853G>C
• NG_007550.3:g.65108G>C
• NM_001114978.2:c.62+25276G>C
• NM_001114979.2:c.62+25276G>C
• NM_001329144.2:c.62+25276G>C
• NM_001329148.2:c.62+25276G>C
• NM_001329964.2:c.56+59615G>C
• NM_003722.5:c.62+25276G>CMANE SELECT
• LRG_428t1:c.62+25276G>C
• LRG_428:g.65108G>C
• NC_000003.11:g.189374642G>C

This HGVS expression did not pass validation

Links:

dbSNP: rs9853796

NCBI 1000 Genomes Browser:

rs9853796

Molecular consequence:

• NM_001114978.2:c.62+25276G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001114979.2:c.62+25276G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001329144.2:c.62+25276G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001329148.2:c.62+25276G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001329964.2:c.56+59615G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_003722.5:c.62+25276G>C - intron variant - [Sequence Ontology: SO:0001627]