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AGCAGACTGTCAGGAAGGGTCCTCG[C/T]GGGTCTCTGGATGGGGTTTGGATCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611108 MIM: 608498 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
VWC2 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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VWC2 - von Willebrand factor C domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198570.4 | Intron | NP_940972.2 |
ZPBP - zona pellucida binding protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159878.1 | Intron | NP_001153350.1 | ||||
NM_007009.2 | Intron | NP_008940.2 | ||||
XM_011515095.2 | Intron | XP_011513397.1 | ||||
XM_011515096.2 | Intron | XP_011513398.1 | ||||
XM_011515097.1 | Intron | XP_011513399.1 | ||||
XM_011515100.2 | Intron | XP_011513402.1 | ||||
XM_011515101.2 | Intron | XP_011513403.1 | ||||
XM_011515102.2 | Intron | XP_011513404.1 | ||||
XM_011515103.1 | Intron | XP_011513405.1 | ||||
XM_017011707.1 | Intron | XP_016867196.1 |