Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCCGGCCTGGCACGACGAGTTCGT[C/T]ACCGATGTGTGCAACGGACGCAAGA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176975 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC102724965 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)
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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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LOC102724965 - collagen alpha-2(I) chain-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_011533229.2 | 996 | Intron | XP_011531531.2 |
PRKCE - protein kinase C epsilon | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005400.2 | 996 | Silent Mutation | GTC,GTT | V,V 70 | NP_005391.1 | |
XM_005264428.1 | 996 | Silent Mutation | GTC,GTT | V,V 70 | XP_005264485.1 | |
XM_005264431.3 | 996 | Silent Mutation | GTC,GTT | V,V 70 | XP_005264488.1 | |
XM_006712050.3 | 996 | Intron | XP_006712113.1 | |||
XM_011532971.2 | 996 | Intron | XP_011531273.1 | |||
XM_011532975.2 | 996 | Intron | XP_011531277.1 | |||
XM_011532978.1 | 996 | Intron | XP_011531280.1 | |||
XM_011532980.2 | 996 | Intron | XP_011531282.1 | |||
XM_011532981.2 | 996 | Intron | XP_011531283.1 | |||
XM_011532982.1 | 996 | Intron | XP_011531284.1 | |||
XM_011532983.2 | 996 | Intron | XP_011531285.1 | |||
XM_017004486.1 | 996 | Intron | XP_016859975.1 | |||
XM_017004487.1 | 996 | Intron | XP_016859976.1 | |||
XM_017004488.1 | 996 | Intron | XP_016859977.1 | |||
XM_017004489.1 | 996 | Intron | XP_016859978.1 | |||
XM_017004490.1 | 996 | Intron | XP_016859979.1 | |||
XM_017004491.1 | 996 | Intron | XP_016859980.1 | |||
XM_017004492.1 | 996 | Silent Mutation | GTC,GTT | V,V 70 | XP_016859981.1 |
Set Membership: |
HapMap |