Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTCATGAATCCACTTCTATAACAG[C/T]AAATTATTCTTTTGATTCTTGAGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
TXNDC8 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
TXNDC8 - thioredoxin domain containing 8 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003936.3 | 321 | Missense Mutation | TAC,TGC | Y,C 97 | NP_001003936.1 | |
NM_001286946.1 | 321 | Missense Mutation | TAC,TGC | Y,C 77 | NP_001273875.1 | |
NM_001286947.1 | 321 | Intron | NP_001273876.1 | |||
XM_011518463.2 | 321 | Intron | XP_011516765.1 | |||
XM_017014579.1 | 321 | Missense Mutation | TAC,TGC | Y,C 97 | XP_016870068.1 | |
XM_017014580.1 | 321 | Intron | XP_016870069.1 | |||
XM_017014581.1 | 321 | Missense Mutation | TAC,TGC | Y,C 97 | XP_016870070.1 | |
XM_017014582.1 | 321 | Missense Mutation | TAC,TGC | Y,C 77 | XP_016870071.1 | |
XM_017014583.1 | 321 | Intron | XP_016870072.1 | |||
XM_017014584.1 | 321 | Missense Mutation | TAC,TGC | Y,C 60 | XP_016870073.1 |