Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LRRC27 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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LRRC27 - leucine rich repeat containing 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143757.1 | 442 | Intron | NP_001137229.1 | |||
NM_001143758.1 | 442 | Intron | NP_001137230.1 | |||
NM_001143759.1 | 442 | Intron | NP_001137231.1 | |||
NM_001309474.1 | 442 | Intron | NP_001296403.1 | |||
NM_030626.2 | 442 | Intron | NP_085129.1 | |||
XM_006717983.2 | 442 | Intron | XP_006718046.1 | |||
XM_006717984.2 | 442 | Intron | XP_006718047.1 | |||
XM_011540208.1 | 442 | Intron | XP_011538510.1 | |||
XM_011540209.1 | 442 | Intron | XP_011538511.1 | |||
XM_011540210.2 | 442 | Intron | XP_011538512.1 | |||
XM_017016690.1 | 442 | Intron | XP_016872179.1 | |||
XM_017016691.1 | 442 | Intron | XP_016872180.1 | |||
XM_017016692.1 | 442 | Intron | XP_016872181.1 | |||
XM_017016693.1 | 442 | Intron | XP_016872182.1 | |||
XM_017016694.1 | 442 | Intron | XP_016872183.1 |
STK32C - serine/threonine kinase 32C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318878.1 | 442 | Intron | NP_001305807.1 | |||
NM_001318879.1 | 442 | Intron | NP_001305808.1 | |||
NM_001318880.1 | 442 | UTR 3 | NP_001305809.1 | |||
NM_001318881.1 | 442 | Intron | NP_001305810.1 | |||
NM_001318882.1 | 442 | Intron | NP_001305811.1 | |||
NM_001318883.1 | 442 | Silent Mutation | NP_001305812.1 | |||
NM_173575.3 | 442 | Intron | NP_775846.2 | |||
XM_011539688.1 | 442 | Intron | XP_011537990.1 | |||
XM_011539690.2 | 442 | Intron | XP_011537992.1 | |||
XM_011539693.2 | 442 | Intron | XP_011537995.1 | |||
XM_011539694.1 | 442 | Intron | XP_011537996.1 | |||
XM_011539695.1 | 442 | Intron | XP_011537997.1 | |||
XM_011539696.1 | 442 | Intron | XP_011537998.1 | |||
XM_017016100.1 | 442 | Intron | XP_016871589.1 | |||
XM_017016101.1 | 442 | Intron | XP_016871590.1 |
Set Membership: |
HapMap |