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CCGAGGGAAGTTACTTCGGCTTCGC[C/G]GTGGATTTCTTCGTGCCCAGCGCGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 193210 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ITGAV 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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ITGAV - integrin subunit alpha V | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144999.2 | 432 | Intron | NP_001138471.1 | |||
NM_001145000.2 | 432 | Silent Mutation | GCC,GCG | A,A 52 | NP_001138472.1 | |
NM_002210.4 | 432 | Silent Mutation | GCC,GCG | A,A 52 | NP_002201.1 |