ClinVar

NM_003977.4(AIP):c.564G>A (p.Arg188=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.2

Genomic location:

• Chr11: 67490133 (on Assembly GRCh38)
• Chr11: 67257604 (on Assembly GRCh37)

Preferred name:

NM_003977.4(AIP):c.564G>A (p.Arg188=)

HGVS:

• NC_000011.10:g.67490133G>A
• NG_008969.1:g.12100G>A
• NM_001302959.2:c.387G>A
• NM_001302960.2:c.564G>A
• NM_003977.4:c.564G>AMANE SELECT
• NP_001289888.1:p.Arg129=
• NP_001289889.1:p.Arg188=
• NP_003968.2:p.Arg188=
• NP_003968.3:p.Arg188=
• LRG_460t1:c.564G>A
• LRG_460:g.12100G>A
• LRG_460p1:p.Arg188=
• NC_000011.9:g.67257604G>A
• NM_003977.2:c.564G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001302959.2:c.387G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001302960.2:c.564G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_003977.4:c.564G>A - synonymous variant - [Sequence Ontology: SO:0001819]