Product Details

SNP ID
rs1052148
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:103630204 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCCTTGTGGAGTAGGAAAACATAA[C/G]CTTGAAGAAGGAAGCTTTAAAGAAA
Phenotype
MIM: 300237
Polymorphism
C/G, 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_001006639.1 450 Missense Mutation AAC,AAG N96K NP_001006640.1
NM_001006640.1 450 Missense Mutation AAC,AAG N96K NP_001006641.1
NM_004780.2 450 Missense Mutation AAC,AAG N96K NP_004771.2

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