Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGTCGCCATCCAGGCCGCCCATCA[C/T]CTGGAAAGGGAAGAGAGCGTTGTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
|
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Phenotype: |
MIM: 602758 MIM: 610568 | ||||||||||||||||||||
Literature Links: |
PI4KB 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 |
PI4KB - phosphatidylinositol 4-kinase beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198774.1 | 2577 | Missense Mutation | ATG,GTG | M,V 702 | NP_001185703.1 | |
XM_005245264.3 | 2577 | Missense Mutation | ATG,GTG | M,V 714 | XP_005245321.1 | |
XM_011509634.1 | 2577 | Missense Mutation | ATG,GTG | M,V 729 | XP_011507936.1 | |
XM_011509635.1 | 2577 | Missense Mutation | ATG,GTG | M,V 717 | XP_011507937.1 | |
XM_011509636.2 | 2577 | Missense Mutation | ATG,GTG | M,V 717 | XP_011507938.1 | |
XM_011509637.2 | 2577 | Missense Mutation | ATG,GTG | M,V 717 | XP_011507939.1 | |
XM_011509638.1 | 2577 | Missense Mutation | ATG,GTG | M,V 714 | XP_011507940.1 | |
XM_017001486.1 | 2577 | Missense Mutation | ATG,GTG | M,V 702 | XP_016856975.1 | |
XM_017001487.1 | 2577 | Missense Mutation | ATG,GTG | M,V 702 | XP_016856976.1 | |
XM_017001488.1 | 2577 | Missense Mutation | ATG,GTG | M,V 702 | XP_016856977.1 | |
XM_017001489.1 | 2577 | Missense Mutation | ATG,GTG | M,V 717 | XP_016856978.1 | |
XM_017001490.1 | 2577 | Missense Mutation | ATG,GTG | M,V 717 | XP_016856979.1 | |
XM_017001491.1 | 2577 | Missense Mutation | ATG,GTG | M,V 717 | XP_016856980.1 | |
XM_017001492.1 | 2577 | Missense Mutation | ATG,GTG | M,V 702 | XP_016856981.1 |
ZNF687 - zinc finger protein 687 | ||||||
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There are no transcripts associated with this gene. |