ClinVar

NM_000245.4(MET):c.2265-3C>T

Gene:

MET:MET proto-oncogene, receptor tyrosine kinase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q31.2

Genomic location:

• Chr7: 116759388 (on Assembly GRCh38)
• Chr7: 116399442 (on Assembly GRCh37)

Preferred name:

NM_000245.4(MET):c.2265-3C>T

HGVS:

• NC_000007.14:g.116759388C>T
• NG_008996.1:g.91984C>T
• NM_000245.4:c.2265-3C>TMANE SELECT
• NM_001127500.3:c.2316C>T
• NM_001324401.3:c.2265-3C>T
• NM_001324402.2:c.975-3C>T
• NP_001120972.1:p.Ala772=
• NP_001120972.1:p.Ala772=
• LRG_662t1:c.2316C>T
• LRG_662:g.91984C>T
• LRG_662p1:p.Ala772=
• NC_000007.13:g.116399442C>T
• NM_001127500.1:c.2316C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_000245.4:c.2265-3C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001324401.3:c.2265-3C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001324402.2:c.975-3C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001127500.3:c.2316C>T - synonymous variant - [Sequence Ontology: SO:0001819]