ClinVar

NM_004360.5(CDH1):c.1566-218A>T

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68819062 (on Assembly GRCh38)
• Chr16: 68852965 (on Assembly GRCh37)

Preferred name:

NM_004360.5(CDH1):c.1566-218A>T

HGVS:

• NC_000016.10:g.68819062A>T
• NG_008021.1:g.86771A>T
• NM_001317184.2:c.1383-218A>T
• NM_001317185.2:c.18-218A>T
• NM_001317186.2:c.-254-2939A>T
• NM_004360.5:c.1566-218A>TMANE SELECT
• LRG_301:g.86771A>T
• NC_000016.9:g.68852965A>T

This HGVS expression did not pass validation

Links:

dbSNP: rs34245865

NCBI 1000 Genomes Browser:

rs34245865

Molecular consequence:

• NM_001317184.2:c.1383-218A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001317185.2:c.18-218A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001317186.2:c.-254-2939A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_004360.5:c.1566-218A>T - intron variant - [Sequence Ontology: SO:0001627]