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GAAATCTTTTCTTCATTCACCCTTT[A/C]CTATGACACGTTGGTCCCTGTTCTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
12 submissions
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Phenotype: |
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Literature Links: |
VWA5B1 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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VWA5B1 - von Willebrand factor A domain containing 5B1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039500.2 | Intron | NP_001034589.2 | ||||
XM_006710360.3 | Intron | XP_006710423.2 | ||||
XM_011540683.2 | Intron | XP_011538985.1 | ||||
XM_011540684.2 | Intron | XP_011538986.1 | ||||
XM_011540685.2 | Intron | XP_011538987.1 | ||||
XM_011540688.2 | Intron | XP_011538990.1 | ||||
XM_011540690.2 | Intron | XP_011538992.1 | ||||
XM_011540691.2 | Intron | XP_011538993.1 | ||||
XM_011540692.2 | Intron | XP_011538994.1 | ||||
XM_011540693.1 | Intron | XP_011538995.1 | ||||
XM_011540695.1 | Intron | XP_011538997.1 | ||||
XM_011540697.2 | Intron | XP_011538999.1 | ||||
XM_011540698.1 | Intron | XP_011539000.1 | ||||
XM_017000305.1 | Intron | XP_016855794.1 | ||||
XM_017000306.1 | Intron | XP_016855795.1 |