ClinVar

NM_001378964.1(CDON):c.3395C>T (p.Pro1132Leu)

Gene:

CDON:cell adhesion associated, oncogene regulated [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q24.2

Genomic location:

• Chr11: 125961960 (on Assembly GRCh38)
• Chr11: 125831855 (on Assembly GRCh37)

Preferred name:

NM_001378964.1(CDON):c.3395C>T (p.Pro1132Leu)

HGVS:

• NC_000011.10:g.125961960G>A
• NG_029776.1:g.106333C>T
• NM_001243597.2:c.3395C>T
• NM_001378964.1:c.3395C>TMANE SELECT
• NM_016952.5:c.3395C>T
• NP_001230526.1:p.Pro1132Leu
• NP_001365893.1:p.Pro1132Leu
• NP_058648.4:p.Pro1132Leu
• NP_058648.4:p.Pro1132Leu
• NC_000011.9:g.125831855G>A
• NM_016952.4:c.3395C>T

This HGVS expression did not pass validation

Protein change:

P1132L

Links:

dbSNP: rs754025360

NCBI 1000 Genomes Browser:

rs754025360

Molecular consequence:

• NM_001243597.2:c.3395C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001378964.1:c.3395C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_016952.5:c.3395C>T - missense variant - [Sequence Ontology: SO:0001583]