Product Details

SNP ID

rs201111117

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:7786793 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGATGTGAGCATGTACAGTCTTG[A/G]GGAGCTGGCCACTATCGCTTCAGAA

Phenotype

MIM: 603427 MIM: 603657

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PER3 PubMed Links

Gene Details

Gene

PER3

Gene Name

period circadian clock 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001289861.1	486	Missense Mutation	GAG,GGG	E116G	NP_001276790.1
NM_001289862.1	486	Missense Mutation	GAG,GGG	E116G	NP_001276791.1
NM_001289863.1	486	Missense Mutation	GAG,GGG	E116G	NP_001276792.1
NM_001289864.1	486	UTR 5			NP_001276793.1
NM_016831.2	486	Missense Mutation	GAG,GGG	E116G	NP_058515.1
XM_005263524.3	486	Missense Mutation	GAG,GGG	E116G	XP_005263581.1
XM_011542385.2	486	Missense Mutation	GAG,GGG	E116G	XP_011540687.1
XM_011542390.2	486	Missense Mutation	GAG,GGG	E116G	XP_011540692.1
XM_017002723.1	486	Missense Mutation	GAG,GGG	E116G	XP_016858212.1
XM_017002724.1	486	Missense Mutation	GAG,GGG	E116G	XP_016858213.1
XM_017002725.1	486	Missense Mutation	GAG,GGG	E116G	XP_016858214.1
XM_017002726.1	486	Missense Mutation	GAG,GGG	E116G	XP_016858215.1
XM_017002727.1	486	Missense Mutation	GAG,GGG	E60G	XP_016858216.1
XM_017002728.1	486	Intron			XP_016858217.1
XM_017002729.1	486	Intron			XP_016858218.1
XM_017002730.1	486	Intron			XP_016858219.1
XM_017002731.1	486	Intron			XP_016858220.1
XM_017002732.1	486	Intron			XP_016858221.1
XM_017002733.1	486	UTR 5			XP_016858222.1
XM_017002734.1	486	UTR 5			XP_016858223.1
XM_017002735.1	486	UTR 5			XP_016858224.1
XM_017002736.1	486	UTR 5			XP_016858225.1
XM_017002737.1	486	Intron			XP_016858226.1
XM_017002738.1	486	Intron			XP_016858227.1

Gene

VAMP3

Gene Name

vesicle associated membrane protein 3

There are no transcripts associated with this gene.

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