ClinVar

NM_004360.5(CDH1):c.2412C>T (p.Pro804=)

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68829770 (on Assembly GRCh38)
• Chr16: 68863673 (on Assembly GRCh37)

Preferred name:

NM_004360.5(CDH1):c.2412C>T (p.Pro804=)

HGVS:

• NC_000016.10:g.68829770C>T
• NG_008021.1:g.97479C>T
• NM_001317184.2:c.2229C>T
• NM_001317185.2:c.864C>T
• NM_001317186.2:c.447C>T
• NM_004360.5:c.2412C>TMANE SELECT
• NP_001304113.1:p.Pro743=
• NP_001304114.1:p.Pro288=
• NP_001304115.1:p.Pro149=
• NP_004351.1:p.Pro804=
• LRG_301t1:c.2412C>T
• LRG_301:g.97479C>T
• NC_000016.9:g.68863673C>T
• NM_004360.3:c.2412C>T
• NM_004360.4:c.2412C>T
• p.P804P
• p.Pro804Pro

This HGVS expression did not pass validation

Links:

dbSNP: rs202075199

NCBI 1000 Genomes Browser:

rs202075199

Molecular consequence:

• NM_001317184.2:c.2229C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001317185.2:c.864C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001317186.2:c.447C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_004360.5:c.2412C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

1