Product Details

SNP ID
rs150720649
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:74772552 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTGGGGGAAACTGAGGACCATGAA[A/G]GAGCAGAAACAGGAGGGCCTCCTCC
Phenotype
MIM: 604990
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
NAT9 PubMed Links
Additional Information
For this assay, SNP(s) [rs71361635] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
NAT9
Gene Name
N-acetyltransferase 9 (putative)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001305077.1 469 Intron NP_001292006.1
NM_001305078.1 469 Intron NP_001292007.1
NM_001305079.1 469 Intron NP_001292008.1
NM_001305080.1 469 Intron NP_001292009.1
NM_001305081.1 469 Intron NP_001292010.1
NM_001305082.1 469 Intron NP_001292011.1
NM_001305083.1 469 Intron NP_001292012.1
NM_001305084.1 469 Intron NP_001292013.1
NM_001305085.1 469 Intron NP_001292014.1
NM_001305086.1 469 Intron NP_001292015.1
NM_001305087.1 469 Intron NP_001292016.1
NM_001305088.1 469 Intron NP_001292017.1
NM_015654.4 469 Intron NP_056469.2
XM_005257212.4 469 Intron XP_005257269.1
XM_006721813.3 469 Intron XP_006721876.1
XM_011524607.2 469 Missense Mutation CCT,CTT P119L XP_011522909.1
XM_017024437.1 469 Intron XP_016879926.1
XM_017024438.1 469 Missense Mutation CCT,CTT P119L XP_016879927.1
XM_017024439.1 469 Intron XP_016879928.1
XM_017024440.1 469 Missense Mutation CCT,CTT P89L XP_016879929.1
XM_017024441.1 469 Intron XP_016879930.1
Gene
SLC9A3R1
Gene Name
SLC9A3 regulator 1
There are no transcripts associated with this gene.

Gene
TMEM104
Gene Name
transmembrane protein 104
There are no transcripts associated with this gene.

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