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CCGCCCCGGGCACCGCGGTGCTGCT[G/T]GTCACGGCCAACGTGGGCTCGCTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600106 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
INPP5A 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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INPP5A - inositol polyphosphate-5-phosphatase A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321042.1 | 355 | Intron | NP_001307971.1 | |||
NM_005539.4 | 355 | Silent Mutation | CTG,CTT | L,L 14 | NP_005530.3 | |
XM_017016204.1 | 355 | Intron | XP_016871693.1 | |||
XM_017016205.1 | 355 | Silent Mutation | CTG,CTT | L,L 14 | XP_016871694.1 |
LOC107984282 - uncharacterized LOC107984282 | ||||||
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There are no transcripts associated with this gene. |