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AAGATTGGCTCTCTCATGTAACACA[A/G]TGTATGAATGGGAGACCCAAAACAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
|
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Phenotype: |
MIM: 147264 | ||||||||||||||||||||
Literature Links: |
INPP5B 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 |
INPP5B - inositol polyphosphate-5-phosphatase B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297434.1 | 2262 | Silent Mutation | NP_001284363.1 | |||
NM_005540.2 | 2262 | Silent Mutation | NP_005531.2 | |||
XM_006710621.3 | 2262 | Intron | XP_006710684.2 | |||
XM_011541392.2 | 2262 | Silent Mutation | XP_011539694.1 | |||
XM_011541393.2 | 2262 | Silent Mutation | XP_011539695.1 | |||
XM_017001206.1 | 2262 | Silent Mutation | XP_016856695.1 | |||
XM_017001207.1 | 2262 | Silent Mutation | XP_016856696.1 | |||
XM_017001208.1 | 2262 | Intron | XP_016856697.1 | |||
XM_017001209.1 | 2262 | Silent Mutation | XP_016856698.1 |