Product Details

SNP ID

rs2677913

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:82763007 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TATGGTCTGTTTTGTTGAACATTCC[A/G]CGTGCACTTGAGAAAAATGTCTGTT

Phenotype

MIM: 604649

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TBCD PubMed Links

Gene Details

Gene

TBCD

Gene Name

tubulin folding cofactor D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005993.4		Intron			NP_005984.3
XM_005256396.4		Intron			XP_005256453.1
XM_005256399.4		Intron			XP_005256456.1
XM_005256404.4		Intron			XP_005256461.1
XM_006722290.2		Intron			XP_006722353.1
XM_006722291.3		Intron			XP_006722354.1
XM_006722292.2		Intron			XP_006722355.1
XM_011523589.1		Intron			XP_011521891.1
XM_011523590.1		Intron			XP_011521892.1
XM_011523591.1		Intron			XP_011521893.1
XM_011523593.1		Intron			XP_011521895.1
XM_011523594.1		Intron			XP_011521896.1
XM_011523595.2		Intron			XP_011521897.1
XM_011523597.2		Intron			XP_011521899.1
XM_011523598.1		Intron			XP_011521900.1
XM_011523599.2		Intron			XP_011521901.1
XM_011523600.2		Intron			XP_011521902.1
XM_017024987.1		Intron			XP_016880476.1
XM_017024988.1		Intron			XP_016880477.1
XM_017024989.1		Intron			XP_016880478.1
XM_017024990.1		Intron			XP_016880479.1

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