Product Details

SNP ID

rs28395444

Assay Type

Functionally Tested

NCBI dbSNP Submissions

5

Location

Chr.1:239388185 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATGCAAACCTTCATTTGTCTGCAA[A/G]TGTTACTGGAACCTGTCCAAAGGCT

Phenotype

MIM: 118494

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CHRM3 PubMed Links

Additional Information

For this assay, SNP(s) [rs76484712] are located under a primer 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

CHRM3

Gene Name

cholinergic receptor muscarinic 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000740.2		Intron			NP_000731.1
XM_005273032.3		Intron			XP_005273089.1
XM_011544041.2		Intron			XP_011542343.1
XM_011544043.2		Intron			XP_011542345.1
XM_011544044.2		Intron			XP_011542346.1
XM_011544045.2		Intron			XP_011542347.1
XM_011544046.2		Intron			XP_011542348.1
XM_011544047.2		Intron			XP_011542349.1
XM_017000152.1		Intron			XP_016855641.1
XM_017000153.1		Intron			XP_016855642.1
XM_017000154.1		Intron			XP_016855643.1
XM_017000155.1		Intron			XP_016855644.1
XM_017000156.1		Intron			XP_016855645.1
XM_017000157.1		Intron			XP_016855646.1
XM_017000158.1		Intron			XP_016855647.1
XM_017000159.1		Intron			XP_016855648.1
XM_017000160.1		Intron			XP_016855649.1
XM_017000161.1		Intron			XP_016855650.1
XM_017000162.1		Intron			XP_016855651.1
XM_017000163.1		Intron			XP_016855652.1

Gene

LOC107983951

Gene Name

uncharacterized LOC107983951

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011544355.2		Intron			XP_011542657.1

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