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GCTTACCAGGACTACTGCACTCCAT[C/G]GTGCCATTGGCAGCTGAGGAGCCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
9 submissions
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Phenotype: |
MIM: 609595 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RSPO1 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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RSPO1 - R-spondin 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001038633.3 | 1309 | Silent Mutation | ACC,ACG | T,T 139 | NP_001033722.1 | |
NM_001242908.1 | 1309 | Silent Mutation | ACC,ACG | T,T 139 | NP_001229837.1 | |
NM_001242909.1 | 1309 | Silent Mutation | ACC,ACG | T,T 112 | NP_001229838.1 | |
NM_001242910.1 | 1309 | Silent Mutation | ACC,ACG | T,T 139 | NP_001229839.1 | |
XM_006710583.3 | 1309 | Silent Mutation | ACC,ACG | T,T 139 | XP_006710646.1 |