ClinVar

NM_000551.4(VHL):c.413C>T (p.Pro138Leu)

Genes:

LOC107303340:3p25 von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase Alu-mediated recombination region [Gene]
VHL:von Hippel-Lindau tumor suppressor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p25.3

Genomic location:

• Chr3: 10146586 (on Assembly GRCh38)
• Chr3: 10188270 (on Assembly GRCh37)

Preferred name:

NM_000551.4(VHL):c.413C>T (p.Pro138Leu)

HGVS:

• NC_000003.12:g.10146586C>T
• NG_008212.3:g.9952C>T
• NG_046756.1:g.4348C>T
• NM_000551.4:c.413C>TMANE SELECT
• NM_001354723.2:c.*18-3201C>T
• NM_198156.3:c.341-3201C>T
• NP_000542.1:p.Pro138Leu
• LRG_322t1:c.413C>T
• LRG_322:g.9952C>T
• NC_000003.11:g.10188270C>T
• NM_000551.3:c.413C>T

This HGVS expression did not pass validation

Protein change:

P138L; PRO138LEU

Links:

OMIM: 608537.0035; dbSNP: rs780178275

NCBI 1000 Genomes Browser:

rs780178275

Molecular consequence:

• NM_001354723.2:c.*18-3201C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_198156.3:c.341-3201C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_000551.4:c.413C>T - missense variant - [Sequence Ontology: SO:0001583]