Product Details

SNP ID

rs191755162

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:92969744 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCTGCGATGTCAGAGAACGGCTCC[C/T]TCGCCAACTGCTGCGAGGCGGGCGG

Phenotype

MIM: 600804

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MTNR1B PubMed Links

Gene Details

Gene

MTNR1B

Gene Name

melatonin receptor 1B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005959.3	122	Missense Mutation	CTC,TTC	L7F	NP_005950.1
XM_011542839.2	122	Missense Mutation	CTC,TTC	L7F	XP_011541141.1
XM_017017777.1	122	Intron			XP_016873266.1

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