Product Details

SNP ID

rs2298633

Assay Type

Functionally tested

NCBI dbSNP Submissions

25

Location

Chr.1:23383748 on Build GRCh38

Set Membership

HapMap JSNP

Context Sequence [VIC/FAM]

GTGACCACACTCTGTTCCTTCAGGA[C/G]ACTTGGCAGGAAGGAGCACTCTGGG

Phenotype

MIM: 604128

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

TCEA3 PubMed Links

Gene Details

Gene

TCEA3

Gene Name

transcription elongation factor A3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003196.2	1478	Intron			NP_003187.1
XM_006710864.1	1478	UTR 3			XP_006710927.1
XM_011542053.2	1478	Intron			XP_011540355.1
XM_017002200.1	1478	Missense Mutation	CTC,GTC	L463V	XP_016857689.1
XM_017002201.1	1478	Missense Mutation	CTC,GTC	L442V	XP_016857690.1
XM_017002202.1	1478	Missense Mutation	CTC,GTC	L442V	XP_016857691.1
XM_017002203.1	1478	Missense Mutation	CTC,GTC	L426V	XP_016857692.1
XM_017002204.1	1478	Intron			XP_016857693.1

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