Product Details

SNP ID

rs113405524

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:5332868 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCGCAGCTTCCGGGCCTTGCGCCC[C/T]TTCTCCACCGCCAGCTTGGCCTTGT

Phenotype

Polymorphism

C/T, Transition 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	8747	Silent Mutation	AAA,AAG	K1967K	NP_001073964.2
XM_017012728.1	8747	Silent Mutation	AAA,AAG	K1967K	XP_016868217.1
XM_017012729.1	8747	Silent Mutation	AAA,AAG	K1967K	XP_016868218.1
XM_017012730.1	8747	Silent Mutation	AAA,AAG	K1966K	XP_016868219.1
XM_017012731.1	8747	Silent Mutation	AAA,AAG	K1924K	XP_016868220.1
XM_017012732.1	8747	Silent Mutation	AAA,AAG	K1923K	XP_016868221.1
XM_017012733.1	8747	Silent Mutation	AAA,AAG	K1919K	XP_016868222.1
XM_017012734.1	8747	Silent Mutation	AAA,AAG	K1917K	XP_016868223.1
XM_017012735.1	8747	Silent Mutation	AAA,AAG	K1893K	XP_016868224.1
XM_017012736.1	8747	Silent Mutation	AAA,AAG	K1893K	XP_016868225.1
XM_017012737.1	8747	Silent Mutation	AAA,AAG	K1893K	XP_016868226.1
XM_017012738.1	8747	Silent Mutation	AAA,AAG	K1893K	XP_016868227.1
XM_017012739.1	8747	Silent Mutation	AAA,AAG	K1967K	XP_016868228.1
XM_017012740.1	8747	Silent Mutation	AAA,AAG	K1967K	XP_016868229.1

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