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TGGGATATATACATTTATTGGGTAA[C/T]ACTTTCAAAGTCAGGAGATTATAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607817 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
VPS13B 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
|
VPS13B - vacuolar protein sorting 13 homolog B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015243.2 | Intron | NP_056058.2 | ||||
NM_017890.4 | Intron | NP_060360.3 | ||||
NM_152564.4 | Intron | NP_689777.3 | ||||
NM_181661.2 | Intron | NP_858047.2 | ||||
XM_005250800.3 | Intron | XP_005250857.1 | ||||
XM_005250801.4 | Intron | XP_005250858.1 | ||||
XM_006716510.3 | Intron | XP_006716573.1 | ||||
XM_011516848.2 | Intron | XP_011515150.1 | ||||
XM_011516849.2 | Intron | XP_011515151.1 | ||||
XM_011516850.2 | Intron | XP_011515152.1 | ||||
XM_011516851.2 | Intron | XP_011515153.1 | ||||
XM_011516852.2 | Intron | XP_011515154.1 | ||||
XM_011516853.2 | Intron | XP_011515155.1 | ||||
XM_011516854.2 | Intron | XP_011515156.1 | ||||
XM_011516859.2 | Intron | XP_011515161.1 | ||||
XM_011516861.1 | Intron | XP_011515163.1 | ||||
XM_011516865.1 | Intron | XP_011515167.1 | ||||
XM_011516866.2 | Intron | XP_011515168.1 | ||||
XM_017013109.1 | Intron | XP_016868598.1 | ||||
XM_017013110.1 | Intron | XP_016868599.1 | ||||
XM_017013111.1 | Intron | XP_016868600.1 | ||||
XM_017013112.1 | Intron | XP_016868601.1 |