ClinVar

NM_004360.5(CDH1):c.1565+175C>T

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68815934 (on Assembly GRCh38)
• Chr16: 68849837 (on Assembly GRCh37)

Preferred name:

NM_004360.5(CDH1):c.1565+175C>T

HGVS:

• NC_000016.10:g.68815934C>T
• NG_008021.1:g.83643C>T
• NM_001317184.2:c.1382+175C>T
• NM_001317185.2:c.17+175C>T
• NM_001317186.2:c.-255+175C>T
• NM_004360.5:c.1565+175C>TMANE SELECT
• LRG_301:g.83643C>T
• NC_000016.9:g.68849837C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs6499199

NCBI 1000 Genomes Browser:

rs6499199

Molecular consequence:

• NM_001317184.2:c.1382+175C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001317185.2:c.17+175C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001317186.2:c.-255+175C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_004360.5:c.1565+175C>T - intron variant - [Sequence Ontology: SO:0001627]