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GCTCATAGAGGGCCTGCAGCTGCTC[A/G]CTGTGTGCGTGGAGCAGGCTGTGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603032 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SNN PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SNN - stannin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003498.5 | 2553 | Intron | NP_003489.1 | |||
XM_017023741.1 | 2553 | Intron | XP_016879230.1 | |||
XM_017023742.1 | 2553 | Intron | XP_016879231.1 |
TXNDC11 - thioredoxin domain containing 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303447.1 | 2553 | Silent Mutation | AGC,AGT | S,S 883 | NP_001290376.1 | |
NM_001324022.1 | 2553 | Silent Mutation | AGC,AGT | S,S 642 | NP_001310951.1 | |
NM_001324024.1 | 2553 | Silent Mutation | AGC,AGT | S,S 404 | NP_001310953.1 | |
NM_001324025.1 | 2553 | Silent Mutation | AGC,AGT | S,S 404 | NP_001310954.1 | |
NM_015914.6 | 2553 | Silent Mutation | AGC,AGT | S,S 856 | NP_056998.4 | |
XM_011522515.2 | 2553 | Silent Mutation | AGC,AGT | S,S 896 | XP_011520817.1 | |
XM_011522516.2 | 2553 | Silent Mutation | AGC,AGT | S,S 682 | XP_011520818.1 | |
XM_017023268.1 | 2553 | Silent Mutation | AGC,AGT | S,S 895 | XP_016878757.1 |