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TACATACCTATCACAAATACTGAAA[C/T]AGCCTGTTGGGAAGCGGTGCTGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
TXNDC11 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 |
TXNDC11 - thioredoxin domain containing 11 | ||||||
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There are no transcripts associated with this gene. |
ZC3H7A - zinc finger CCCH-type containing 7A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014153.3 | 2670 | Missense Mutation | TAT,TGT | Y,C 903 | NP_054872.2 | |
XM_006720877.2 | 2670 | Missense Mutation | TAT,TGT | Y,C 903 | XP_006720940.1 | |
XM_011522463.1 | 2670 | Missense Mutation | TAT,TGT | Y,C 903 | XP_011520765.1 | |
XM_011522464.2 | 2670 | Missense Mutation | TAT,TGT | Y,C 664 | XP_011520766.1 | |
XM_017023174.1 | 2670 | Missense Mutation | TAT,TGT | Y,C 802 | XP_016878663.1 | |
XM_017023175.1 | 2670 | Missense Mutation | TAT,TGT | Y,C 512 | XP_016878664.1 |