ClinVar

NM_001378964.1(CDON):c.*2377TA[10]

Gene:

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

Variant type:

Microsatellite

Cytogenetic location:

11q24.2

Genomic location:

• Chr11: 125958547 - 125958548 (on Assembly GRCh38)
• Chr11: 125828442 - 125828443 (on Assembly GRCh37)

Preferred name:

NM_001378964.1(CDON):c.*2377TA[10]

HGVS:

• NC_000011.10:g.125958549AT[10]
• NG_029776.1:g.109728TA[10]
• NM_001243597.2:c.*2377TA[10]
• NM_001378964.1:c.*2377TA[10]MANE SELECT
• NM_016952.5:c.*2377TA[10]
• NC_000011.9:g.125828444AT[10]
• NM_016952.4:c.*2393_*2394dupTA

This HGVS expression did not pass validation

Links:

dbSNP: rs140500280

NCBI 1000 Genomes Browser:

rs140500280

Molecular consequence:

• NM_001243597.2:c.*2377TA[10] - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001378964.1:c.*2377TA[10] - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_016952.5:c.*2377TA[10] - 3 prime UTR variant - [Sequence Ontology: SO:0001624]