Product Details

SNP ID

rs202179083

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:74772263 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACGGCCTCAGTGCCAAGGCCCTTAC[C/T]CCTGCAGCTGGGCTCTAGGAGAGAC

Phenotype

MIM: 604990

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NAT9 PubMed Links

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	443	Missense Mutation	AGT,GGT	S116G	NP_001292006.1
NM_001305078.1	443	Missense Mutation	AGT,GGT	S117G	NP_001292007.1
NM_001305079.1	443	Missense Mutation	AGT,GGT	S117G	NP_001292008.1
NM_001305080.1	443	Missense Mutation	AGT,GGT	S117G	NP_001292009.1
NM_001305081.1	443	Missense Mutation	AGT,GGT	S116G	NP_001292010.1
NM_001305082.1	443	Missense Mutation	AGT,GGT	S122G	NP_001292011.1
NM_001305083.1	443	Missense Mutation	AGT,GGT	S116G	NP_001292012.1
NM_001305084.1	443	Missense Mutation	AGT,GGT	S117G	NP_001292013.1
NM_001305085.1	443	Missense Mutation	AGT,GGT	S116G	NP_001292014.1
NM_001305086.1	443	Missense Mutation	AGT,GGT	S116G	NP_001292015.1
NM_001305087.1	443	Missense Mutation	AGT,GGT	S92G	NP_001292016.1
NM_001305088.1	443	Missense Mutation	AGT,GGT	S86G	NP_001292017.1
NM_015654.4	443	Missense Mutation	AGT,GGT	S117G	NP_056469.2
XM_005257212.4	443	Missense Mutation	AGT,GGT	S86G	XP_005257269.1
XM_006721813.3	443	Missense Mutation	AGT,GGT	S86G	XP_006721876.1
XM_011524607.2	443	Intron			XP_011522909.1
XM_017024437.1	443	Missense Mutation	AGT,GGT	S92G	XP_016879926.1
XM_017024438.1	443	Intron			XP_016879927.1
XM_017024439.1	443	Missense Mutation	AGT,GGT	S116G	XP_016879928.1
XM_017024440.1	443	Intron			XP_016879929.1
XM_017024441.1	443	Missense Mutation	AGT,GGT	S86G	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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