ClinVar

NM_002449.5(MSX2):c.-17C>G

Gene:

MSX2:msh homeobox 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

5q35.2

Genomic location:

• Chr5: 174724643 (on Assembly GRCh38)
• Chr5: 174151646 (on Assembly GRCh37)

Preferred name:

NM_002449.5(MSX2):c.-17C>G

HGVS:

• NC_000005.10:g.174724643C>G
• NG_008124.1:g.5072C>G
• NM_001363626.2:c.-17C>G
• NM_002449.5:c.-17C>GMANE SELECT
• NC_000005.9:g.174151646C>G
• NM_002449.4:c.-17C>G

This HGVS expression did not pass validation

Links:

dbSNP: rs4647952

NCBI 1000 Genomes Browser:

rs4647952

Molecular consequence:

• NM_001363626.2:c.-17C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_002449.5:c.-17C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]