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GGTGCTGGTGACGTACCTGGTTCAG[A/G]TTGTCGCTGCAGGAGACCTTGCTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607875 MIM: 606538 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
INPP5K 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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INPP5K - inositol polyphosphate-5-phosphatase K | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135642.1 | 1345 | Silent Mutation | AAC,AAT | N,N 316 | NP_001129114.1 | |
NM_016532.3 | 1345 | Silent Mutation | AAC,AAT | N,N 392 | NP_057616.2 | |
NM_130766.2 | 1345 | Silent Mutation | AAC,AAT | N,N 316 | NP_570122.1 | |
XM_005256683.2 | 1345 | Silent Mutation | AAC,AAT | N,N 316 | XP_005256740.1 | |
XM_005256685.1 | 1345 | Silent Mutation | AAC,AAT | N,N 300 | XP_005256742.1 | |
XM_005256686.1 | 1345 | Silent Mutation | AAC,AAT | N,N 300 | XP_005256743.1 | |
XM_011523934.1 | 1345 | Silent Mutation | AAC,AAT | N,N 316 | XP_011522236.1 | |
XM_011523936.2 | 1345 | Silent Mutation | AAC,AAT | N,N 257 | XP_011522238.1 | |
XM_017024755.1 | 1345 | Silent Mutation | AAC,AAT | N,N 316 | XP_016880244.1 | |
XM_017024756.1 | 1345 | Silent Mutation | AAC,AAT | N,N 316 | XP_016880245.1 | |
XM_017024757.1 | 1345 | Silent Mutation | AAC,AAT | N,N 300 | XP_016880246.1 | |
XM_017024758.1 | 1345 | Silent Mutation | AAC,AAT | N,N 257 | XP_016880247.1 | |
XM_017024759.1 | 1345 | Silent Mutation | AAC,AAT | N,N 257 | XP_016880248.1 |
MYO1C - myosin IC | ||||||
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There are no transcripts associated with this gene. |