Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGATTCAGCAGATGTATCAACTATA[A/G]GTTGCTTTGGTGGTGTTGCCAACAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601743 MIM: 609022 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
OSMR 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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OSMR - oncostatin M receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168355.2 | 5014 | Intron | NP_001161827.1 | |||
NM_001323504.1 | 5014 | Intron | NP_001310433.1 | |||
NM_001323505.1 | 5014 | Intron | NP_001310434.1 | |||
NM_001323506.1 | 5014 | Intron | NP_001310435.1 | |||
NM_001323507.1 | 5014 | Intron | NP_001310436.1 | |||
NM_003999.2 | 5014 | Intron | NP_003990.1 | |||
XM_005248384.1 | 5014 | Intron | XP_005248441.1 | |||
XM_005248386.2 | 5014 | Intron | XP_005248443.1 | |||
XM_005248387.2 | 5014 | Intron | XP_005248444.1 | |||
XM_011514161.2 | 5014 | Intron | XP_011512463.1 | |||
XM_017010019.1 | 5014 | Intron | XP_016865508.1 | |||
XM_017010020.1 | 5014 | Intron | XP_016865509.1 |
RICTOR - RPTOR independent companion of MTOR complex 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001285439.1 | 5014 | Missense Mutation | CCT,CTT | P,L 1724 | NP_001272368.1 | |
NM_001285440.1 | 5014 | Missense Mutation | CCT,CTT | P,L 1377 | NP_001272369.1 | |
NM_152756.4 | 5014 | Missense Mutation | CCT,CTT | P,L 1700 | NP_689969.2 | |
XM_006714463.3 | 5014 | Missense Mutation | CCT,CTT | P,L 1662 | XP_006714526.1 | |
XM_011514005.2 | 5014 | Missense Mutation | CCT,CTT | P,L 1686 | XP_011512307.1 | |
XM_011514006.2 | 5014 | Missense Mutation | CCT,CTT | P,L 1661 | XP_011512308.1 | |
XM_017009311.1 | 5014 | Missense Mutation | CCT,CTT | P,L 1708 | XP_016864800.1 | |
XM_017009312.1 | 5014 | Missense Mutation | CCT,CTT | P,L 1684 | XP_016864801.1 | |
XM_017009313.1 | 5014 | Missense Mutation | CCT,CTT | P,L 1671 | XP_016864802.1 | |
XM_017009314.1 | 5014 | Missense Mutation | CCT,CTT | P,L 1439 | XP_016864803.1 | |
XM_017009315.1 | 5014 | Missense Mutation | CCT,CTT | P,L 1415 | XP_016864804.1 |