Product Details

SNP ID
rs1052147
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:103630159 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTCCAGGAAGGACCTGTTTGAGGG[G/T]CGCCCTCCCATGGAGCAGCCTCCTT
Phenotype
MIM: 300237
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
TCEAL1 PubMed Links

Gene Details

Gene
TCEAL1
Gene Name
transcription elongation factor A like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001006639.1 405 Silent Mutation GGG,GGT G81G NP_001006640.1
NM_001006640.1 405 Silent Mutation GGG,GGT G81G NP_001006641.1
NM_004780.2 405 Silent Mutation GGG,GGT G81G NP_004771.2

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