ClinVar

NM_004360.5(CDH1):c.183C>T (p.Thr61=)

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68801689 (on Assembly GRCh38)
• Chr16: 68835592 (on Assembly GRCh37)

Preferred name:

NM_004360.5(CDH1):c.183C>T (p.Thr61=)

HGVS:

• NC_000016.10:g.68801689C>T
• NG_008021.1:g.69398C>T
• NM_001317184.2:c.183C>T
• NM_001317185.2:c.-1433C>T
• NM_001317186.2:c.-1637C>T
• NM_004360.5:c.183C>TMANE SELECT
• NP_001304113.1:p.Thr61=
• NP_004351.1:p.Thr61=
• LRG_301t1:c.183C>T
• LRG_301:g.69398C>T
• NC_000016.9:g.68835592C>T
• NM_004360.3:c.183C>T
• p.T61T

This HGVS expression did not pass validation

Links:

dbSNP: rs575896144

NCBI 1000 Genomes Browser:

rs575896144

Molecular consequence:

• NM_001317185.2:c.-1433C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001317186.2:c.-1637C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001317184.2:c.183C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_004360.5:c.183C>T - synonymous variant - [Sequence Ontology: SO:0001819]