Product Details

SNP ID

rs141014675

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:3192427 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGTGCCCTTACTTCTCTTCAGAAC[A/G]GTGGTCCTCCTGGTCACTGATGTCA

Phenotype

MIM: 608998

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TSSC1 PubMed Links

Gene Details

Gene

TSSC1

Gene Name

tumor suppressing subtransferable candidate 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_006711893.2	1074	Missense Mutation	CGT,TGT	R226C	XP_006711956.1
XM_011510383.2	1074	Missense Mutation	CGT,TGT	R365C	XP_011508685.1
XM_011510384.2	1074	Missense Mutation	CGT,TGT	R353C	XP_011508686.1
XM_011510385.2	1074	Missense Mutation	CGT,TGT	R338C	XP_011508687.1
XM_011510387.2	1074	Missense Mutation	CGT,TGT	R182C	XP_011508689.1
XM_017004818.1	1074	Missense Mutation	CGT,TGT	R226C	XP_016860307.1

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