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ACCAGCAAGTACACCGGCACCCACA[A/G]GGAGCGCTTTGATGAGAGTGGCAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605272 MIM: 616956 | ||||||||||||||||||||
Literature Links: |
MIR6717 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
MIR6717 - microRNA 6717 | ||||||
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There are no transcripts associated with this gene. |
RNASE13 - ribonuclease A family member 13 (inactive) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012264.3 | 580 | Intron | NP_001012264.1 |
TPPP2 - tubulin polymerization promoting protein family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173846.4 | 580 | Missense Mutation | AAG,AGG | K,R 131 | NP_776245.2 | |
XM_005267324.4 | 580 | Missense Mutation | AAG,AGG | K,R 131 | XP_005267381.1 | |
XM_011536416.1 | 580 | Intron | XP_011534718.1 | |||
XM_011536417.2 | 580 | Intron | XP_011534719.1 | |||
XM_011536418.1 | 580 | Intron | XP_011534720.1 | |||
XM_011536420.2 | 580 | Intron | XP_011534722.1 | |||
XM_017020966.1 | 580 | Missense Mutation | AAG,AGG | K,R 131 | XP_016876455.1 |