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Search Thermo Fisher Scientific
CTCAAGTATCCCATCCGTGAGTTTC[A/G]GCTGCTTCCCAATCACGGCGTAGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
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Literature Links: |
TTC39A PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
TTC39A - tetratricopeptide repeat domain 39A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080494.3 | 1520 | Missense Mutation | CCG,CTG | P,L 439 | NP_001073963.1 | |
NM_001144832.2 | 1520 | Missense Mutation | CCG,CTG | P,L 442 | NP_001138304.1 | |
NM_001297662.1 | 1520 | Intron | NP_001284591.1 | |||
NM_001297663.1 | 1520 | Missense Mutation | CCG,CTG | P,L 438 | NP_001284592.1 | |
NM_001297664.1 | 1520 | Missense Mutation | CCG,CTG | P,L 411 | NP_001284593.1 | |
NM_001297665.1 | 1520 | Missense Mutation | CCG,CTG | P,L 474 | NP_001284594.1 | |
NM_001297666.1 | 1520 | Missense Mutation | CCG,CTG | P,L 82 | NP_001284595.1 | |
NM_001297667.1 | 1520 | Missense Mutation | CCG,CTG | P,L 15 | NP_001284596.1 | |
XM_005270644.2 | 1520 | Missense Mutation | CCG,CTG | P,L 435 | XP_005270701.1 | |
XM_006710471.2 | 1520 | Missense Mutation | CCG,CTG | P,L 470 | XP_006710534.1 | |
XM_011541048.2 | 1520 | Missense Mutation | CCG,CTG | P,L 477 | XP_011539350.1 | |
XM_011541049.2 | 1520 | Missense Mutation | CCG,CTG | P,L 475 | XP_011539351.1 | |
XM_011541050.2 | 1520 | Missense Mutation | CCG,CTG | P,L 473 | XP_011539352.1 | |
XM_011541051.2 | 1520 | Missense Mutation | CCG,CTG | P,L 446 | XP_011539353.1 | |
XM_011541052.2 | 1520 | Missense Mutation | CCG,CTG | P,L 446 | XP_011539354.1 | |
XM_011541053.2 | 1520 | Missense Mutation | CCG,CTG | P,L 446 | XP_011539355.1 | |
XM_011541054.2 | 1520 | Missense Mutation | CCG,CTG | P,L 411 | XP_011539356.1 | |
XM_017000715.1 | 1520 | Missense Mutation | CCG,CTG | P,L 411 | XP_016856204.1 |