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CATTTTATTCTTCTTTATATCTTCT[A/G]TTTCTTTACTGAGACTTCCTATGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 614884 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
VWA3B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
VWA3B - von Willebrand factor A domain containing 3B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144992.4 | Intron | NP_659429.4 | ||||
XM_005263897.2 | Intron | XP_005263954.1 | ||||
XM_006712357.2 | Intron | XP_006712420.1 | ||||
XM_006712359.3 | Intron | XP_006712422.1 | ||||
XM_006712360.3 | Intron | XP_006712423.1 | ||||
XM_011510770.1 | Intron | XP_011509072.1 | ||||
XM_011510771.2 | Intron | XP_011509073.1 | ||||
XM_011510772.1 | Intron | XP_011509074.1 | ||||
XM_011510774.1 | Intron | XP_011509076.1 | ||||
XM_011510775.2 | Intron | XP_011509077.1 | ||||
XM_017003560.1 | Intron | XP_016859049.1 | ||||
XM_017003561.1 | Intron | XP_016859050.1 | ||||
XM_017003562.1 | Intron | XP_016859051.1 | ||||
XM_017003563.1 | Intron | XP_016859052.1 | ||||
XM_017003564.1 | Intron | XP_016859053.1 |