Product Details

SNP ID
rs142733714
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:103357718 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGTCAAAAAATGGAAGGAAAACCA[C/G]AAAATGAGAGTGAACCAAAGCATGA
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
TCEAL9 PubMed Links

Gene Details

Gene
TCEAL9
Gene Name
transcription elongation factor A like 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001006612.1 256 Missense Mutation CAA,GAA Q12E NP_001006613.1
NM_001006613.1 256 Missense Mutation CAA,GAA Q12E NP_001006614.1
NM_001006614.1 256 Missense Mutation CAA,GAA Q12E NP_001006615.1
NM_016303.2 256 Missense Mutation CAA,GAA Q12E NP_057387.1

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