ClinVar

NM_002148.4(HOXD10):c.*468A>T

Gene:

HOXD10:homeobox D10 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q31.1

Genomic location:

• Chr2: 176119699 (on Assembly GRCh38)
• Chr2: 176984427 (on Assembly GRCh37)

Preferred name:

NM_002148.4(HOXD10):c.*468A>T

HGVS:

• NC_000002.12:g.176119699A>T
• NG_008133.2:g.12936A>T
• NG_009225.1:g.2015A>T
• NM_002148.4:c.*468A>TMANE SELECT
• LRG_246t1:c.*468A>T
• LRG_246:g.12936A>T
• NC_000002.11:g.176984427A>T
• NM_002148.3:c.*468A>T

This HGVS expression did not pass validation

Links:

dbSNP: rs532592274

NCBI 1000 Genomes Browser:

rs532592274

Molecular consequence:

• NM_002148.4:c.*468A>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]

Observations:

2