ClinVar

NM_003977.4(AIP):c.468+13C>T

Gene:

AIP:aryl hydrocarbon receptor interacting protein [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.2

Genomic location:

• Chr11: 67489468 (on Assembly GRCh38)
• Chr11: 67256939 (on Assembly GRCh37)

Preferred name:

NM_003977.4(AIP):c.468+13C>T

HGVS:

• NC_000011.10:g.67489468C>T
• NG_008969.1:g.11435C>T
• NM_001302959.2:c.291+13C>T
• NM_001302960.2:c.468+13C>T
• NM_003977.4:c.468+13C>TMANE SELECT
• LRG_460t1:c.468+13C>T
• LRG_460:g.11435C>T
• NC_000011.9:g.67256939C>T
• NM_003977.2:c.468+13C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs375823655

NCBI 1000 Genomes Browser:

rs375823655

Molecular consequence:

• NM_001302959.2:c.291+13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001302960.2:c.468+13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_003977.4:c.468+13C>T - intron variant - [Sequence Ontology: SO:0001627]