Product Details

SNP ID

rs115368866

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:53704196 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTTTAGTGGCAGCATGAAGCGCAC[C/G]CCGACTGCCGAGGAACGAGAGCGCG

Phenotype

MIM: 610966 MIM: 610937

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FTO PubMed Links

Gene Details

Gene

FTO

Gene Name

fat mass and obesity associated

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080432.2	198	Silent Mutation	ACC,ACG	T4T	NP_001073901.1
XM_011523313.2	198	Silent Mutation	ACC,ACG	T4T	XP_011521615.1
XM_011523314.2	198	Silent Mutation	ACC,ACG	T4T	XP_011521616.1
XM_011523315.2	198	Silent Mutation	ACC,ACG	T4T	XP_011521617.1
XM_011523316.2	198	Silent Mutation	ACC,ACG	T4T	XP_011521618.1
XM_017023654.1	198	Silent Mutation	ACC,ACG	T4T	XP_016879143.1
XM_017023655.1	198	Silent Mutation	ACC,ACG	T4T	XP_016879144.1
XM_017023656.1	198	Silent Mutation	ACC,ACG	T4T	XP_016879145.1
XM_017023657.1	198	Silent Mutation	ACC,ACG	T4T	XP_016879146.1
XM_017023658.1	198	Silent Mutation	ACC,ACG	T4T	XP_016879147.1

Gene

RPGRIP1L

Gene Name

RPGRIP1 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005255867.1	198	Intron			XP_005255924.1
XM_005255868.1	198	Intron			XP_005255925.1
XM_011522970.1	198	Intron			XP_011521272.1
XM_011522971.2	198	Intron			XP_011521273.1
XM_011522973.2	198	Intron			XP_011521275.1
XM_017023094.1	198	Intron			XP_016878583.1
XM_017023095.1	198	Intron			XP_016878584.1
XM_017023096.1	198	Intron			XP_016878585.1
XM_017023097.1	198	Intron			XP_016878586.1
XM_017023098.1	198	Intron			XP_016878587.1
XM_017023099.1	198	Intron			XP_016878588.1
XM_017023100.1	198	Intron			XP_016878589.1

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