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TGGACATAAACTCGTTGAAGCGTTT[C/G]GAGTACTGCTCAGGGTTCACAGTCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603261 MIM: 602176 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PIP4K2B 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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PIP4K2B - phosphatidylinositol-5-phosphate 4-kinase type 2 beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003559.4 | 1656 | Silent Mutation | TCC,TCG | S,S 404 | NP_003550.1 | |
XM_011525326.2 | 1656 | Silent Mutation | TCC,TCG | S,S 431 | XP_011523628.1 | |
XM_011525327.2 | 1656 | Silent Mutation | TCC,TCG | S,S 367 | XP_011523629.1 | |
XM_011525329.2 | 1656 | Intron | XP_011523631.1 | |||
XM_011525330.2 | 1656 | Silent Mutation | TCC,TCG | S,S 272 | XP_011523632.1 | |
XM_017025196.1 | 1656 | Silent Mutation | TCC,TCG | S,S 340 | XP_016880685.1 | |
XM_017025197.1 | 1656 | Silent Mutation | TCC,TCG | S,S 266 | XP_016880686.1 | |
XM_017025198.1 | 1656 | Silent Mutation | TCC,TCG | S,S 245 | XP_016880687.1 | |
XM_017025199.1 | 1656 | Silent Mutation | TCC,TCG | S,S 236 | XP_016880688.1 |
PSMB3 - proteasome subunit beta 3 | ||||||
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There are no transcripts associated with this gene. |