Product Details

SNP ID: rs16979058
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:13653300 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CAGCTTTCCGGTGCGCCCTGGGCGG[C/T]GTAGATCCGAAGGTGCTCGCACCCC
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: LOC107985657 PubMed Links

Gene Details

Gene: LOC107985657
Gene Name: uncharacterized LOC107985657

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_017030004.1	1591	Missense Mutation	ACC,GCC	T39A	XP_016885493.1

Gene: TCEANC
Gene Name: transcription elongation factor A N-terminal and central domain containing

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001297563.1	1591	Intron			NP_001284492.1
NM_001297564.1	1591	Intron			NP_001284493.1
NM_152634.3	1591	UTR 5			NP_689847.2
XM_017029316.1	1591	Intron			XP_016884805.1
XM_017029317.1	1591	Intron			XP_016884806.1
XM_017029318.1	1591	Intron			XP_016884807.1
XM_017029319.1	1591	UTR 5			XP_016884808.1

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