ClinVar

NM_004360.5(CDH1):c.805G>A (p.Gly269Arg)

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68810314 (on Assembly GRCh38)
• Chr16: 68844217 (on Assembly GRCh37)

Preferred name:

NM_004360.5(CDH1):c.805G>A (p.Gly269Arg)

HGVS:

• NC_000016.10:g.68810314G>A
• NG_008021.1:g.78023G>A
• NM_001317184.2:c.805G>A
• NM_001317185.2:c.-811G>A
• NM_001317186.2:c.-1015G>A
• NM_004360.5:c.805G>AMANE SELECT
• NP_001304113.1:p.Gly269Arg
• NP_004351.1:p.Gly269Arg
• LRG_301t1:c.805G>A
• LRG_301:g.78023G>A
• NC_000016.9:g.68844217G>A
• NM_004360.3:c.805G>A
• NM_004360.4:c.805G>A

This HGVS expression did not pass validation

Protein change:

G269R

Links:

dbSNP: rs750979600

NCBI 1000 Genomes Browser:

rs750979600

Molecular consequence:

• NM_001317185.2:c.-811G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001317186.2:c.-1015G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001317184.2:c.805G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_004360.5:c.805G>A - missense variant - [Sequence Ontology: SO:0001583]