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TGCCCCCTTTCCTGTTGCTGGAAGC[C/T]GTCTGTGTTTTCCTGTTTTCCAGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
VWA2 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 |
VWA2 - von Willebrand factor A domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001272046.1 | 295 | Silent Mutation | GCC,GCT | A,A 9 | NP_001258975.1 | |
NM_001320804.1 | 295 | Silent Mutation | GCC,GCT | A,A 9 | NP_001307733.1 | |
XM_011539754.2 | 295 | UTR 5 | XP_011538056.1 | |||
XM_011539757.2 | 295 | Silent Mutation | GCC,GCT | A,A 9 | XP_011538059.1 | |
XM_017016177.1 | 295 | Silent Mutation | GCC,GCT | A,A 19 | XP_016871666.1 | |
XM_017016178.1 | 295 | Silent Mutation | GCC,GCT | A,A 19 | XP_016871667.1 | |
XM_017016179.1 | 295 | Silent Mutation | GCC,GCT | A,A 15 | XP_016871668.1 | |
XM_017016180.1 | 295 | Intron | XP_016871669.1 | |||
XM_017016181.1 | 295 | Silent Mutation | GCC,GCT | A,A 19 | XP_016871670.1 |