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See other TMTC4 GT Assays ›
SNP ID:
rs9585476
Gene
TMTC4
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.13: 100642174 - 100642174 on Build GRCh38
Polymorphism:
C/G, Transversion substitution
Context Sequence [VIC/FAM]:

TCTTTATAGGAGGGAAAAGGACACA[C/G]AGAAAAAGCAGGCCCCAGCCATGTT

Assay ID C__11492097_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

Literature Links:

 TMTC4 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.39)
(0.61)
Caucasian
G (0.26)
(0.74)
CEPH (CEU)
G (0.27)
(0.73)
EAS
C (0.39)
(0.61)
African American
G (0.38)
(0.62)
YRI (Yoruba)
G (0.27)
(0.73)
SAS
G (0.40)
(0.60)
Chinese - Not Available JPT (Japanese)
C (0.39)
(0.61)
AFR
G (0.37)
(0.63)
Japanese - Not Available CHB (Han Chinese)
C (0.33)
(0.67)
EUR
G (0.30)
(0.70)
AMR
G (0.24)
(0.76)
TMTC4 - transmembrane and tetratricopeptide repeat containing 4
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001079669.2 Intron NP_001073137.1
NM_001286453.1 Intron NP_001273382.1
NM_032813.3 Intron NP_116202.2
XM_011521121.2 Intron XP_011519423.1
XM_011521122.2 Intron XP_011519424.1
XM_011521123.2 Intron XP_011519425.1
XM_011521124.2 Intron XP_011519426.1
XM_011521125.1 Intron XP_011519427.1
XM_017020796.1 Intron XP_016876285.1
XM_017020797.1 Intron XP_016876286.1
XM_017020798.1 Intron XP_016876287.1
XM_017020799.1 Intron XP_016876288.1
XM_017020800.1 Intron XP_016876289.1

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More Information


Set Membership:

 HapMap Validated

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