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ATTTACCTTCAGAATTTCTAGTCTT[G/T]GCTTATTGTCCTTGGGGATTTTGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MIR5006 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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MIR5006 - microRNA 5006 | ||||||
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There are no transcripts associated with this gene. |
VWA8 - von Willebrand factor A domain containing 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001009814.1 | 5421 | Intron | NP_001009814.1 | |||
NM_015058.1 | 5421 | Missense Mutation | NP_055873.1 | |||
XM_006719791.3 | 5421 | Missense Mutation | XP_006719854.1 | |||
XM_011535007.2 | 5421 | Intron | XP_011533309.1 | |||
XM_017020469.1 | 5421 | Missense Mutation | XP_016875958.1 | |||
XM_017020470.1 | 5421 | Intron | XP_016875959.1 | |||
XM_017020471.1 | 5421 | Intron | XP_016875960.1 | |||
XM_017020472.1 | 5421 | Missense Mutation | XP_016875961.1 | |||
XM_017020473.1 | 5421 | Missense Mutation | XP_016875962.1 | |||
XM_017020474.1 | 5421 | Intron | XP_016875963.1 |