Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCTTAATGGGTAATGCTATTACCC[A/G]TTGCCTAACTAGGTTTGCAGTAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
30 submissions
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Phenotype: |
MIM: 601968 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ST7L 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)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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ST7L - suppression of tumorigenicity 7 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308264.1 | Intron | NP_001295193.1 | ||||
NM_017744.4 | Intron | NP_060214.2 | ||||
NM_138727.3 | Intron | NP_620055.1 | ||||
NM_138728.2 | Intron | NP_620056.1 | ||||
NM_138729.3 | Intron | NP_620057.1 | ||||
XM_005270963.4 | Intron | XP_005271020.1 | ||||
XM_005270964.3 | Intron | XP_005271021.1 | ||||
XM_011541627.2 | Intron | XP_011539929.1 | ||||
XM_011541628.2 | Intron | XP_011539930.1 | ||||
XM_011541629.2 | Intron | XP_011539931.1 | ||||
XM_011541630.2 | Intron | XP_011539932.1 | ||||
XM_011541631.2 | Intron | XP_011539933.1 | ||||
XM_017001534.1 | Intron | XP_016857023.1 | ||||
XM_017001535.1 | Intron | XP_016857024.1 | ||||
XM_017001536.1 | Intron | XP_016857025.1 | ||||
XM_017001537.1 | Intron | XP_016857026.1 | ||||
XM_017001538.1 | Intron | XP_016857027.1 |
WNT2B - Wnt family member 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291880.1 | Intron | NP_001278809.1 | ||||
NM_004185.4 | Intron | NP_004176.2 | ||||
NM_024494.2 | Intron | NP_078613.1 |
Set Membership: |
HapMap |