Product Details

SNP ID

rs148170396

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:101362577 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGTCGTTGAGGCACAGCACAGAG[A/G]AGAATAGGGAGGTTCTATCAGGTGG

Phenotype

MIM: 602938

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

BAAT PubMed Links

Gene Details

Gene

BAAT

Gene Name

bile acid-CoA:amino acid N-acyltransferase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127610.1	1318	Missense Mutation	CCT,TCT	P370S	NP_001121082.1
NM_001701.3	1318	Missense Mutation	CCT,TCT	P370S	NP_001692.1

View Full Product Details