ClinVar

NM_004360.5(CDH1):c.832+168T>C

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68810509 (on Assembly GRCh38)
• Chr16: 68844412 (on Assembly GRCh37)

Preferred name:

NM_004360.5(CDH1):c.832+168T>C

HGVS:

• NC_000016.10:g.68810509T>C
• NG_008021.1:g.78218T>C
• NM_001317184.2:c.832+168T>C
• NM_001317185.2:c.-784+168T>C
• NM_001317186.2:c.-988+168T>C
• NM_004360.5:c.832+168T>CMANE SELECT
• LRG_301:g.78218T>C
• NC_000016.9:g.68844412T>C

This HGVS expression did not pass validation

Links:

dbSNP: rs16958375

NCBI 1000 Genomes Browser:

rs16958375

Molecular consequence:

• NM_001317184.2:c.832+168T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001317185.2:c.-784+168T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001317186.2:c.-988+168T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_004360.5:c.832+168T>C - intron variant - [Sequence Ontology: SO:0001627]