Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCTTTTCGAGGTCAGTTGATGAAG[A/G]CCAGATAGGAGTCAATATTTTCTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607441 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
EPSTI1 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)
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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)
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EUR
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AMR
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EPSTI1 - epithelial stromal interaction 1 (breast) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005266596.1 | 1494 | Missense Mutation | CCT,TCT | P,S 327 | XP_005266653.1 | |
XM_005266597.1 | 1494 | UTR 3 | XP_005266654.1 | |||
XM_006719896.3 | 1494 | Intron | XP_006719959.1 | |||
XM_011535312.1 | 1494 | Missense Mutation | CCT,TCT | P,S 211 | XP_011533614.1 | |
XM_011535313.1 | 1494 | Missense Mutation | CCT,TCT | P,S 211 | XP_011533615.1 | |
XM_011535314.1 | 1494 | Missense Mutation | CCT,TCT | P,S 156 | XP_011533616.1 | |
XM_017020853.1 | 1494 | Missense Mutation | CCT,TCT | P,S 211 | XP_016876342.1 | |
XM_017020854.1 | 1494 | Missense Mutation | CCT,TCT | P,S 211 | XP_016876343.1 | |
XM_017020855.1 | 1494 | Missense Mutation | CCT,TCT | P,S 211 | XP_016876344.1 |