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AAGAATGAACTGCCTCTCAGGAAAA[A/G]AGCAATATTGTTGTCTCTATGAAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607494 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
INPP4B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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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
|
INPP4B - inositol polyphosphate-4-phosphatase type II B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001101669.1 | 5868 | Intron | NP_001095139.1 | |||
NM_003866.2 | 5868 | Intron | NP_003857.2 | |||
XM_005263323.3 | 5868 | Intron | XP_005263380.1 | |||
XM_005263325.3 | 5868 | Intron | XP_005263382.1 | |||
XM_011532391.2 | 5868 | Intron | XP_011530693.1 | |||
XM_011532392.2 | 5868 | Intron | XP_011530694.1 | |||
XM_017008794.1 | 5868 | UTR 3 | XP_016864283.1 | |||
XM_017008795.1 | 5868 | Intron | XP_016864284.1 | |||
XM_017008796.1 | 5868 | Intron | XP_016864285.1 | |||
XM_017008797.1 | 5868 | Intron | XP_016864286.1 | |||
XM_017008798.1 | 5868 | Intron | XP_016864287.1 |