Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACACAACTCGAGTCACCCGTGTTAC[C/G]CAGTGTGAGTGCAAATTCCACTGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
12 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) - 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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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 | 1999 | Intron | NP_001295193.1 | |||
NM_017744.4 | 1999 | Intron | NP_060214.2 | |||
NM_138727.3 | 1999 | Intron | NP_620055.1 | |||
NM_138728.2 | 1999 | Intron | NP_620056.1 | |||
NM_138729.3 | 1999 | Intron | NP_620057.1 | |||
XM_005270963.4 | 1999 | Intron | XP_005271020.1 | |||
XM_005270964.3 | 1999 | Intron | XP_005271021.1 | |||
XM_011541627.2 | 1999 | Intron | XP_011539929.1 | |||
XM_011541628.2 | 1999 | Intron | XP_011539930.1 | |||
XM_011541629.2 | 1999 | Intron | XP_011539931.1 | |||
XM_011541630.2 | 1999 | Intron | XP_011539932.1 | |||
XM_011541631.2 | 1999 | Intron | XP_011539933.1 | |||
XM_017001534.1 | 1999 | Intron | XP_016857023.1 | |||
XM_017001535.1 | 1999 | Intron | XP_016857024.1 | |||
XM_017001536.1 | 1999 | Intron | XP_016857025.1 | |||
XM_017001537.1 | 1999 | Intron | XP_016857026.1 | |||
XM_017001538.1 | 1999 | 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 | 1999 | Silent Mutation | ACC,ACG | T,T 261 | NP_001278809.1 | |
NM_004185.4 | 1999 | Silent Mutation | ACC,ACG | T,T 334 | NP_004176.2 | |
NM_024494.2 | 1999 | Silent Mutation | ACC,ACG | T,T 353 | NP_078613.1 |