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SNP ID

hCV26953307

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:5315204 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCTGGGGTCCCCAGCTTGGAGCT[C/T]CCAAGACCCTGGTCTGTCCCGGGGA

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		Intron			NP_001073964.2

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