Product Details

SNP ID

rs145086613

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:56417952 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTCCTGTTCCTCGTCGCTGTCCA[C/G]CAATTGTCGTTTCTTGGGTGCTGCC

Phenotype

MIM: 603887

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

TIMELESS PubMed Links

Gene Details

Gene

TIMELESS

Gene Name

timeless circadian clock

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011538939.2	3654	Missense Mutation	CTG,GTG	L1170V	XP_011537241.1

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