Product Details

SNP ID

rs202096813

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:150410364 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTGGCGCAGCCGGCTATGTCCCT[C/G]CCTCCGCAGCCGGGCCCTGCAGTGG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

TSC22D2 PubMed Links

Gene Details

Gene

TSC22D2

Gene Name

TSC22 domain family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303264.1	2030	Silent Mutation	CTC,CTG	L338L	NP_001290193.1
NM_014779.3	2030	Silent Mutation	CTC,CTG	L338L	NP_055594.1
XM_011513337.2	2030	Silent Mutation	CTC,CTG	L338L	XP_011511639.1

View Full Product Details