ClinVar

NM_004360.5(CDH1):c.1680G>T (p.Thr560=)

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68819394 (on Assembly GRCh38)
• Chr16: 68853297 (on Assembly GRCh37)

Preferred name:

NM_004360.5(CDH1):c.1680G>T (p.Thr560=)

HGVS:

• NC_000016.10:g.68819394G>T
• NG_008021.1:g.87103G>T
• NM_001317184.2:c.1497G>T
• NM_001317185.2:c.132G>T
• NM_001317186.2:c.-254-2607G>T
• NM_004360.3:c.1680G>T
• NM_004360.5:c.1680G>TMANE SELECT
• NP_001304113.1:p.Thr499=
• NP_001304114.1:p.Thr44=
• NP_004351.1:p.Thr560=
• LRG_301t1:c.1680G>T
• LRG_301:g.87103G>T
• NC_000016.9:g.68853297G>T
• NM_004360.4:c.1680G>T

This HGVS expression did not pass validation

Links:

dbSNP: rs35741240

NCBI 1000 Genomes Browser:

rs35741240

Molecular consequence:

• NM_001317186.2:c.-254-2607G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001317184.2:c.1497G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001317185.2:c.132G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_004360.5:c.1680G>T - synonymous variant - [Sequence Ontology: SO:0001819]