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TCATACCTACTGAGTTCTTCCAAAC[A/G]TTCTGAGTTTTGAGATACAGCTTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
TTC29 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 |
TTC29 - tetratricopeptide repeat domain 29 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300761.2 | 1710 | Missense Mutation | CGT,TGT | R,C 486 | NP_001287690.1 | |
NM_001317806.1 | 1710 | Missense Mutation | CGT,TGT | R,C 459 | NP_001304735.1 | |
NM_031956.3 | 1710 | Missense Mutation | CGT,TGT | R,C 460 | NP_114162.2 | |
XM_005263270.1 | 1710 | Missense Mutation | CGT,TGT | R,C 477 | XP_005263327.1 | |
XM_006714335.1 | 1710 | Missense Mutation | CGT,TGT | R,C 485 | XP_006714398.1 | |
XM_006714336.1 | 1710 | Missense Mutation | CGT,TGT | R,C 476 | XP_006714399.1 | |
XM_006714339.2 | 1710 | Missense Mutation | CGT,TGT | R,C 424 | XP_006714402.1 | |
XM_011532310.2 | 1710 | Intron | XP_011530612.1 |