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CAGGGCAGGGCCTGGGAGAGGAAGC[A/G]CGGGACTCCTGCCTGGCGTCCACGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603659 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GLP2R 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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GLP2R - glucagon like peptide 2 receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004246.2 | 599 | Missense Mutation | ACG,GCG | T,A 15 | NP_004237.1 | |
XM_005256861.3 | 599 | Intron | XP_005256918.1 | |||
XM_011524077.2 | 599 | Missense Mutation | ACG,GCG | T,A 15 | XP_011522379.1 | |
XM_017025339.1 | 599 | Missense Mutation | ACG,GCG | T,A 15 | XP_016880828.1 | |
XM_017025340.1 | 599 | Missense Mutation | ACG,GCG | T,A 15 | XP_016880829.1 | |
XM_017025341.1 | 599 | Missense Mutation | ACG,GCG | T,A 15 | XP_016880830.1 |
GSG1L2 - GSG1 like 2 | ||||||
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There are no transcripts associated with this gene. |