Product Details

SNP ID

rs10272647

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:5332734 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCGGGCGCGGTGCTGACGGGCGCA[G/T]GTGCAGCAGCCGAGGCGTCGTGCAG

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

TNRC18 PubMed Links

Gene Details

Gene

TNRC18

Gene Name

trinucleotide repeat containing 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080495.2	8881	Missense Mutation	CAT,CCT	H2012P	NP_001073964.2
XM_017012728.1	8881	Missense Mutation	CAT,CCT	H2012P	XP_016868217.1
XM_017012729.1	8881	Missense Mutation	CAT,CCT	H2012P	XP_016868218.1
XM_017012730.1	8881	Missense Mutation	CAT,CCT	H2011P	XP_016868219.1
XM_017012731.1	8881	Missense Mutation	CAT,CCT	H1969P	XP_016868220.1
XM_017012732.1	8881	Missense Mutation	CAT,CCT	H1968P	XP_016868221.1
XM_017012733.1	8881	Missense Mutation	CAT,CCT	H1964P	XP_016868222.1
XM_017012734.1	8881	Missense Mutation	CAT,CCT	H1962P	XP_016868223.1
XM_017012735.1	8881	Missense Mutation	CAT,CCT	H1938P	XP_016868224.1
XM_017012736.1	8881	Missense Mutation	CAT,CCT	H1938P	XP_016868225.1
XM_017012737.1	8881	Missense Mutation	CAT,CCT	H1938P	XP_016868226.1
XM_017012738.1	8881	Missense Mutation	CAT,CCT	H1938P	XP_016868227.1
XM_017012739.1	8881	Missense Mutation	CAT,CCT	H2012P	XP_016868228.1
XM_017012740.1	8881	Missense Mutation	CAT,CCT	H2012P	XP_016868229.1

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