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CCTTTTGATTGGAAAGTAAATCTCC[C/T]GATAAACATTAGCACAGAAAACTAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603571 MIM: 606592 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
VNN2 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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VNN2 - vanin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242350.2 | 2018 | Intron | NP_001229279.1 | |||
NM_004665.4 | 2018 | Intron | NP_004656.2 | |||
NM_078488.2 | 2018 | Intron | NP_511043.1 | |||
XM_006715593.3 | 2018 | Intron | XP_006715656.1 | |||
XM_011536231.1 | 2018 | Intron | XP_011534533.1 | |||
XM_017011407.1 | 2018 | Intron | XP_016866896.1 | |||
XM_017011408.1 | 2018 | UTR 3 | XP_016866897.1 | |||
XM_017011409.1 | 2018 | UTR 3 | XP_016866898.1 |
VNN3 - vanin 3 | ||||||
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There are no transcripts associated with this gene. |