Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCAGGACCAAAGGCTCATCTTGGAG[C/T]GGTTGCAGGTCATGTACACTGTCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 137241 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GIPR 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 | 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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GIPR - gastric inhibitory polypeptide receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000164.3 | 562 | Missense Mutation | CGG,TGG | R,W 136 | NP_000155.1 | |
NM_001308418.1 | 562 | Missense Mutation | CGG,TGG | R,W 100 | NP_001295347.1 | |
XM_011526709.2 | 562 | Missense Mutation | CGG,TGG | R,W 136 | XP_011525011.1 | |
XM_011526710.2 | 562 | Missense Mutation | CGG,TGG | R,W 136 | XP_011525012.1 | |
XM_011526711.2 | 562 | Missense Mutation | CGG,TGG | R,W 100 | XP_011525013.1 | |
XM_011526713.2 | 562 | Intron | XP_011525015.1 | |||
XM_011526714.2 | 562 | UTR 5 | XP_011525016.1 | |||
XM_011526715.2 | 562 | UTR 5 | XP_011525017.1 | |||
XM_011526716.2 | 562 | Missense Mutation | CGG,TGG | R,W 136 | XP_011525018.1 | |
XM_017026584.1 | 562 | Intron | XP_016882073.1 | |||
XM_017026585.1 | 562 | Intron | XP_016882074.1 | |||
XM_017026586.1 | 562 | Intron | XP_016882075.1 | |||
XM_017026587.1 | 562 | Intron | XP_016882076.1 |
MIR642A - microRNA 642a | ||||||
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There are no transcripts associated with this gene. |
MIR642B - microRNA 642b | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |