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CTGAGTGATTTCCTCCTCTATAAAA[C/T]ATAGTGGTTTGTCCGATGTCTGGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612420 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
AFAP1L2 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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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 | Intron | NP_001258975.1 | ||||
NM_001320804.1 | Intron | NP_001307733.1 | ||||
XM_011539754.2 | Intron | XP_011538056.1 | ||||
XM_011539757.2 | Intron | XP_011538059.1 | ||||
XM_017016177.1 | Intron | XP_016871666.1 | ||||
XM_017016178.1 | Intron | XP_016871667.1 | ||||
XM_017016179.1 | Intron | XP_016871668.1 | ||||
XM_017016180.1 | Intron | XP_016871669.1 | ||||
XM_017016181.1 | Intron | XP_016871670.1 |