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GGTCTTGTCCCGCCAGCCCACATTT[C/T]GTGGGTCTGTCCACAGCAGTCGTAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
7 submissions
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Phenotype: |
MIM: 158340 MIM: 188062 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR92B 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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MIR92B - microRNA 92b | ||||||
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There are no transcripts associated with this gene. |
MUC1 - mucin 1, cell surface associated | ||||||
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There are no transcripts associated with this gene. |
THBS3 - thrombospondin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252607.1 | 2656 | Missense Mutation | CAA,CGA | Q,R 858 | NP_001239536.1 | |
NM_001252608.1 | 2656 | Missense Mutation | CAA,CGA | Q,R 747 | NP_001239537.1 | |
NM_007112.4 | 2656 | Missense Mutation | CAA,CGA | Q,R 867 | NP_009043.1 | |
XM_006711498.3 | 2656 | Missense Mutation | CAA,CGA | Q,R 924 | XP_006711561.1 | |
XM_011509926.2 | 2656 | Missense Mutation | CAA,CGA | Q,R 927 | XP_011508228.1 | |
XM_011509927.2 | 2656 | Missense Mutation | CAA,CGA | Q,R 918 | XP_011508229.1 | |
XM_011509928.2 | 2656 | Missense Mutation | CAA,CGA | Q,R 896 | XP_011508230.1 | |
XM_011509929.1 | 2656 | Missense Mutation | CAA,CGA | Q,R 870 | XP_011508231.1 | |
XM_011509930.2 | 2656 | Missense Mutation | CAA,CGA | Q,R 927 | XP_011508232.1 | |
XM_011509931.1 | 2656 | Missense Mutation | CAA,CGA | Q,R 832 | XP_011508233.1 | |
XM_011509932.2 | 2656 | Missense Mutation | CAA,CGA | Q,R 832 | XP_011508234.1 | |
XM_011509933.1 | 2656 | Missense Mutation | CAA,CGA | Q,R 832 | XP_011508235.1 | |
XM_011509934.1 | 2656 | Missense Mutation | CAA,CGA | Q,R 691 | XP_011508236.1 | |
XM_011509935.1 | 2656 | Missense Mutation | CAA,CGA | Q,R 691 | XP_011508237.1 | |
XM_011509936.1 | 2656 | Missense Mutation | CAA,CGA | Q,R 615 | XP_011508238.1 | |
XM_017002206.1 | 2656 | Missense Mutation | CAA,CGA | Q,R 399 | XP_016857695.1 |