ClinVar

NM_181552.4(CUX1):c.141+8G>A

Gene:

CUX1:cut like homeobox 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q22.1

Genomic location:

• Chr7: 101916233 (on Assembly GRCh38)
• Chr7: 101559513 (on Assembly GRCh37)

Preferred name:

NM_181552.4(CUX1):c.141+8G>A

HGVS:

• NC_000007.14:g.101916233G>A
• NG_029476.2:g.105330G>A
• NM_001202543.2:c.174+8G>A
• NM_001202544.3:c.174+8G>A
• NM_001202545.3:c.174+8G>A
• NM_001202546.3:c.63+100140G>A
• NM_001913.5:c.174+8G>A
• NM_181500.4:c.174+8G>A
• NM_181552.4:c.141+8G>AMANE SELECT
• LRG_1123t1:c.141+8G>A
• LRG_1123t2:c.174+8G>A
• LRG_1123:g.105330G>A
• NC_000007.13:g.101559513G>A
• NM_001202543.1:c.174+8G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001202543.2:c.174+8G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001202544.3:c.174+8G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001202545.3:c.174+8G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001202546.3:c.63+100140G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001913.5:c.174+8G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_181500.4:c.174+8G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_181552.4:c.141+8G>A - intron variant - [Sequence Ontology: SO:0001627]