ClinVar

NM_004360.5(CDH1):c.6C>T (p.Gly2=)

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68737421 (on Assembly GRCh38)
• Chr16: 68771324 (on Assembly GRCh37)

Preferred name:

NM_004360.5(CDH1):c.6C>T (p.Gly2=)

HGVS:

• NC_000016.10:g.68737421C>T
• NG_008021.1:g.5130C>T
• NM_001317184.2:c.6C>T
• NM_001317185.2:c.-1610C>T
• NM_001317186.2:c.-1814C>T
• NM_004360.5:c.6C>TMANE SELECT
• NP_001304113.1:p.Gly2=
• NP_004351.1:p.Gly2=
• LRG_301t1:c.6C>T
• LRG_301:g.5130C>T
• NC_000016.9:g.68771324C>T
• NM_004360.3:c.6C>T
• p.G2G

This HGVS expression did not pass validation

Links:

dbSNP: rs786201283

NCBI 1000 Genomes Browser:

rs786201283

Molecular consequence:

• NM_001317185.2:c.-1610C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001317186.2:c.-1814C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001317184.2:c.6C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_004360.5:c.6C>T - synonymous variant - [Sequence Ontology: SO:0001819]