ClinVar

NM_003977.4(AIP):c.609C>T (p.Tyr203=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.2

Genomic location:

• Chr11: 67490178 (on Assembly GRCh38)
• Chr11: 67257649 (on Assembly GRCh37)

Preferred name:

NM_003977.4(AIP):c.609C>T (p.Tyr203=)

HGVS:

• NC_000011.10:g.67490178C>T
• NG_008969.1:g.12145C>T
• NM_001302959.2:c.432C>T
• NM_001302960.2:c.609C>T
• NM_003977.4:c.609C>TMANE SELECT
• NP_001289888.1:p.Tyr144=
• NP_001289889.1:p.Tyr203=
• NP_003968.3:p.Tyr203=
• LRG_460t1:c.609C>T
• LRG_460:g.12145C>T
• NC_000011.9:g.67257649C>T
• NM_003977.2:c.609C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs146317385

NCBI 1000 Genomes Browser:

rs146317385

Molecular consequence:

• NM_001302959.2:c.432C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001302960.2:c.609C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_003977.4:c.609C>T - synonymous variant - [Sequence Ontology: SO:0001819]