Product Details

SNP ID

rs148177060

Assay Type

Functionally tested

NCBI dbSNP Submissions

19

Location

Chr.1:54807979 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGTAGCACCCGGGGGCTGCTCAGC[G/T]CTGGGGAGGTTCGCTTCCGAGGACT

Phenotype

MIM: 616446

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

LEXM PubMed Links

Gene Details

Gene

LEXM

Gene Name

lymphocyte expansion molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001110533.1	502	Missense Mutation	GCT,TCT	A150S	NP_001104003.1
NM_152607.2	502	Missense Mutation	GCT,TCT	A150S	NP_689820.2
XM_017000480.1	502	Missense Mutation	GCT,TCT	A150S	XP_016855969.1
XM_017000481.1	502	Missense Mutation	GCT,TCT	A150S	XP_016855970.1

Gene

TTC22

Gene Name

tetratricopeptide repeat domain 22

There are no transcripts associated with this gene.

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