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CGTGGTCAGGGTCATTATCCAGACT[C/T]CCACACACGCCAGCACGGCTTTGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602042 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GPR18 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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GPR18 - G protein-coupled receptor 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098200.1 | 932 | Missense Mutation | NP_001091670.1 | |||
NM_005292.3 | 932 | Missense Mutation | NP_005283.1 | |||
XM_006719946.3 | 932 | Missense Mutation | XP_006720009.1 |
UBAC2 - UBA domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144072.1 | 932 | Intron | NP_001137544.1 | |||
NM_177967.3 | 932 | Intron | NP_808882.1 | |||
XM_006719948.3 | 932 | Intron | XP_006720011.1 | |||
XM_011521082.2 | 932 | Intron | XP_011519384.1 | |||
XM_011521083.2 | 932 | Intron | XP_011519385.1 | |||
XM_011521084.2 | 932 | Intron | XP_011519386.1 | |||
XM_017020553.1 | 932 | Intron | XP_016876042.1 |