ClinVar

NM_004360.5(CDH1):c.2646C>T (p.Asp882=)

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68833496 (on Assembly GRCh38)
• Chr16: 68867399 (on Assembly GRCh37)

Preferred name:

NM_004360.5(CDH1):c.2646C>T (p.Asp882=)

HGVS:

• NC_000016.10:g.68833496C>T
• NG_008021.1:g.101205C>T
• NM_001317184.2:c.2463C>T
• NM_001317185.2:c.1098C>T
• NM_001317186.2:c.681C>T
• NM_004360.5:c.2646C>TMANE SELECT
• NP_001304113.1:p.Asp821=
• NP_001304114.1:p.Asp366=
• NP_001304115.1:p.Asp227=
• NP_004351.1:p.Asp882=
• LRG_301t1:c.2646C>T
• LRG_301:g.101205C>T
• NC_000016.9:g.68867399C>T
• NM_004360.3:c.2646C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs1555518315

NCBI 1000 Genomes Browser:

rs1555518315

Molecular consequence:

• NM_001317184.2:c.2463C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001317185.2:c.1098C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001317186.2:c.681C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_004360.5:c.2646C>T - synonymous variant - [Sequence Ontology: SO:0001819]