Product Details

SNP ID

rs686546

Assay Type

Validated

NCBI dbSNP Submissions

68

Location

Chr.1:23383684 on Build GRCh38

Set Membership

HapMap JSNP Validated

Context Sequence [VIC/FAM]

GTGGCCCAGACATCACATGGTGCAC[A/G]TGCAAGTCAGAGAGCAGTTGGAAAC

Phenotype

MIM: 604128

Polymorphism

A/G, Transition 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	1542	Intron			NP_003187.1
XM_006710864.1	1542	UTR 3			XP_006710927.1
XM_011542053.2	1542	Intron			XP_011540355.1
XM_017002200.1	1542	Missense Mutation	ACG,ATG	T484M	XP_016857689.1
XM_017002201.1	1542	Missense Mutation	ACG,ATG	T463M	XP_016857690.1
XM_017002202.1	1542	Missense Mutation	ACG,ATG	T463M	XP_016857691.1
XM_017002203.1	1542	Missense Mutation	ACG,ATG	T447M	XP_016857692.1
XM_017002204.1	1542	Intron			XP_016857693.1

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