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TGGGGTCCTGTGGGACCCCCGCCCT[C/T]GGCAGCCTCCTGTTCCTGCTCTTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601051 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR662 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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MIR662 - microRNA 662 | ||||||
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There are no transcripts associated with this gene. |
MSLN - mesothelin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001177355.2 | 235 | Silent Mutation | CTC,CTT | L,L 18 | NP_001170826.1 | |
NM_005823.5 | 235 | Silent Mutation | CTC,CTT | L,L 18 | NP_005814.2 | |
NM_013404.4 | 235 | Silent Mutation | CTC,CTT | L,L 18 | NP_037536.2 | |
XM_005255034.4 | 235 | Silent Mutation | CTC,CTT | L,L 18 | XP_005255091.1 | |
XM_011522348.2 | 235 | Silent Mutation | CTC,CTT | L,L 18 | XP_011520650.1 | |
XM_017022853.1 | 235 | Silent Mutation | CTC,CTT | L,L 28 | XP_016878342.1 | |
XM_017022854.1 | 235 | Silent Mutation | CTC,CTT | L,L 28 | XP_016878343.1 | |
XM_017022855.1 | 235 | Silent Mutation | CTC,CTT | L,L 28 | XP_016878344.1 | |
XM_017022856.1 | 235 | Silent Mutation | CTC,CTT | L,L 28 | XP_016878345.1 | |
XM_017022857.1 | 235 | Silent Mutation | CTC,CTT | L,L 18 | XP_016878346.1 | |
XM_017022858.1 | 235 | Silent Mutation | CTC,CTT | L,L 18 | XP_016878347.1 |