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TGGAGTCCGGGTTGTCCAGTGTGGC[A/G]GACTTGATGAAGATGGGGTAACTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602932 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SMAD7 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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SMAD7 - SMAD family member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190821.1 | 617 | Silent Mutation | TCC,TCT | S,S 343 | NP_001177750.1 | |
NM_001190822.1 | 617 | Silent Mutation | TCC,TCT | S,S 129 | NP_001177751.1 | |
NM_001190823.1 | 617 | Silent Mutation | TCC,TCT | S,S 156 | NP_001177752.1 | |
NM_005904.3 | 617 | Silent Mutation | TCC,TCT | S,S 344 | NP_005895.1 |