ClinVar

NM_004360.5(CDH1):c.2622C>T (p.Asp874=)

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68833472 (on Assembly GRCh38)
• Chr16: 68867375 (on Assembly GRCh37)

Preferred name:

NM_004360.5(CDH1):c.2622C>T (p.Asp874=)

HGVS:

• NC_000016.10:g.68833472C>T
• NG_008021.1:g.101181C>T
• NM_001317184.2:c.2439C>T
• NM_001317185.2:c.1074C>T
• NM_001317186.2:c.657C>T
• NM_004360.5:c.2622C>TMANE SELECT
• NP_001304113.1:p.Asp813=
• NP_001304114.1:p.Asp358=
• NP_001304115.1:p.Asp219=
• NP_004351.1:p.Asp874=
• LRG_301t1:c.2622C>T
• LRG_301:g.101181C>T
• NC_000016.9:g.68867375C>T
• NM_004360.3:c.2622C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs1555518285

NCBI 1000 Genomes Browser:

rs1555518285

Molecular consequence:

• NM_001317184.2:c.2439C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001317185.2:c.1074C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001317186.2:c.657C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_004360.5:c.2622C>T - synonymous variant - [Sequence Ontology: SO:0001819]