Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTGCAGGAACCGTGACTGAATGGA[C/T]CGGGTCTGGAAGAGAAGGAGGCAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
PARP6 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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PARP6 - poly(ADP-ribose) polymerase family member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323515.1 | 2168 | Silent Mutation | CGA,CGG | R,R 530 | NP_001310444.1 | |
NM_001323516.1 | 2168 | Silent Mutation | CGA,CGG | R,R 530 | NP_001310445.1 | |
NM_001323519.1 | 2168 | Silent Mutation | CGA,CGG | R,R 529 | NP_001310448.1 | |
NM_001323521.1 | 2168 | Silent Mutation | CGA,CGG | R,R 529 | NP_001310450.1 | |
NM_001323522.1 | 2168 | Silent Mutation | CGA,CGG | R,R 549 | NP_001310451.1 | |
NM_001323523.1 | 2168 | Silent Mutation | CGA,CGG | R,R 529 | NP_001310452.1 | |
NM_001323524.1 | 2168 | Silent Mutation | CGA,CGG | R,R 529 | NP_001310453.1 | |
NM_001323525.1 | 2168 | Silent Mutation | CGA,CGG | R,R 550 | NP_001310454.1 | |
NM_001323526.1 | 2168 | Silent Mutation | CGA,CGG | R,R 529 | NP_001310455.1 | |
NM_001323528.1 | 2168 | Silent Mutation | CGA,CGG | R,R 550 | NP_001310457.1 | |
NM_001323530.1 | 2168 | Silent Mutation | CGA,CGG | R,R 530 | NP_001310459.1 | |
NM_001323531.1 | 2168 | Silent Mutation | CGA,CGG | R,R 550 | NP_001310460.1 | |
NM_001323532.1 | 2168 | Silent Mutation | CGA,CGG | R,R 549 | NP_001310461.1 | |
NM_020214.3 | 2168 | Silent Mutation | CGA,CGG | R,R 549 | NP_064599.2 | |
XM_011521805.1 | 2168 | Silent Mutation | CGA,CGG | R,R 415 | XP_011520107.1 | |
XM_017022418.1 | 2168 | Silent Mutation | CGA,CGG | R,R 394 | XP_016877907.1 |