ClinVar

NM_000551.4(VHL):c.-64C>T

Gene:

VHL:von Hippel-Lindau tumor suppressor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p25.3

Genomic location:

• Chr3: 10141784 (on Assembly GRCh38)
• Chr3: 10183468 (on Assembly GRCh37)

Preferred name:

NM_000551.4(VHL):c.-64C>T

HGVS:

• NC_000003.12:g.10141784C>T
• NG_008212.3:g.5150C>T
• NM_000551.4:c.-64C>TMANE SELECT
• NM_001354723.2:c.-64C>T
• NM_198156.3:c.-64C>T
• LRG_322t1:c.-64C>T
• LRG_322:g.5150C>T
• NC_000003.11:g.10183468C>T
• NM_000551.3:c.-64C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs772944298

NCBI 1000 Genomes Browser:

rs772944298

Molecular consequence:

• NM_000551.4:c.-64C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001354723.2:c.-64C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_198156.3:c.-64C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]