Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATCAGGGCCAGGGACTGCACTCACC[A/G]AGGCAATGAGATAGACAATGGCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 158340 MIM: 188062 MIM: 600986 | ||||||||||||||||||||||||||||||||||||||
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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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001018016.2 | 485 | Missense Mutation | TCG,TTG | S,L 190 | NP_001018016.1 | |
NM_001018017.2 | 485 | Missense Mutation | TCG,TTG | S,L 181 | NP_001018017.1 | |
NM_001044390.2 | 485 | Missense Mutation | TCG,TTG | S,L 129 | NP_001037855.1 | |
NM_001044391.2 | 485 | Intron | NP_001037856.1 | |||
NM_001044392.2 | 485 | Intron | NP_001037857.1 | |||
NM_001044393.2 | 485 | Silent Mutation | CTC,CTT | L,L 118 | NP_001037858.1 | |
NM_001204285.1 | 485 | Missense Mutation | TCG,TTG | S,L 401 | NP_001191214.1 | |
NM_001204286.1 | 485 | Missense Mutation | TCG,TTG | S,L 410 | NP_001191215.1 | |
NM_001204287.1 | 485 | Missense Mutation | TCG,TTG | S,L 208 | NP_001191216.1 | |
NM_001204288.1 | 485 | Silent Mutation | CTC,CTT | L,L 179 | NP_001191217.1 | |
NM_001204289.1 | 485 | Missense Mutation | TCG,TTG | S,L 164 | NP_001191218.1 | |
NM_001204290.1 | 485 | Missense Mutation | TCG,TTG | S,L 143 | NP_001191219.1 | |
NM_001204291.1 | 485 | Missense Mutation | TCG,TTG | S,L 167 | NP_001191220.1 | |
NM_001204292.1 | 485 | Missense Mutation | TCG,TTG | S,L 165 | NP_001191221.1 | |
NM_001204293.1 | 485 | Intron | NP_001191222.1 | |||
NM_001204294.1 | 485 | Missense Mutation | TCG,TTG | S,L 156 | NP_001191223.1 | |
NM_001204295.1 | 485 | Missense Mutation | TCG,TTG | S,L 115 | NP_001191224.1 | |
NM_001204296.1 | 485 | Missense Mutation | TCG,TTG | S,L 138 | NP_001191225.1 | |
NM_001204297.1 | 485 | Intron | NP_001191226.1 | |||
NM_002456.5 | 485 | Missense Mutation | TCG,TTG | S,L 199 | NP_002447.4 |
THBS3 - thrombospondin 3 | ||||||
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There are no transcripts associated with this gene. |
TRIM46 - tripartite motif containing 46 | ||||||
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There are no transcripts associated with this gene. |