Product Details

SNP ID
rs5944856
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:102127033 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GATAAAGAAAAGCCAGAGAGTGCGG[C/G]AAAGGCAAAAGGAGAAGGAAAGTCA
Phenotype
Polymorphism
C/G, Transversion 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_080390.3 422 Missense Mutation GCA,GGA A68G NP_525129.1

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