Product Details

SNP ID

rs191441128

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:5332995 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGGGCCGCAGCAGCCCCGCAGGC[C/G]ACCGCTTGCGCACCTTGACCTCGCT

Phenotype

Polymorphism

C/G, 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	8620	Missense Mutation	TCG,TGG	S1925W	NP_001073964.2
XM_017012728.1	8620	Missense Mutation	TCG,TGG	S1925W	XP_016868217.1
XM_017012729.1	8620	Missense Mutation	TCG,TGG	S1925W	XP_016868218.1
XM_017012730.1	8620	Missense Mutation	TCG,TGG	S1924W	XP_016868219.1
XM_017012731.1	8620	Missense Mutation	TCG,TGG	S1882W	XP_016868220.1
XM_017012732.1	8620	Missense Mutation	TCG,TGG	S1881W	XP_016868221.1
XM_017012733.1	8620	Missense Mutation	TCG,TGG	S1877W	XP_016868222.1
XM_017012734.1	8620	Missense Mutation	TCG,TGG	S1875W	XP_016868223.1
XM_017012735.1	8620	Missense Mutation	TCG,TGG	S1851W	XP_016868224.1
XM_017012736.1	8620	Missense Mutation	TCG,TGG	S1851W	XP_016868225.1
XM_017012737.1	8620	Missense Mutation	TCG,TGG	S1851W	XP_016868226.1
XM_017012738.1	8620	Missense Mutation	TCG,TGG	S1851W	XP_016868227.1
XM_017012739.1	8620	Missense Mutation	TCG,TGG	S1925W	XP_016868228.1
XM_017012740.1	8620	Missense Mutation	TCG,TGG	S1925W	XP_016868229.1

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