Product Details

SNP ID

rs5945029

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:102127219 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAAGGGCTGCAGGAAAGCGCCCAG[C/T]TGAGGATGATATACCCAGGAAAGCC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TCEAL2 PubMed Links

Gene Details

Gene

TCEAL2

Gene Name

transcription elongation factor A like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_080390.3	608	Missense Mutation	GCT,GTT	A130V	NP_525129.1

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