Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGCAGCTGGGGTCCAGCTCCCCCC[C/G]TCCTGCCCGCGGGGTTCAGCCCCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
PWWP2B 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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PWWP2B - PWWP domain containing 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098637.1 | 286 | Missense Mutation | CCT,CGT | P,R 86 | NP_001092107.1 | |
NM_138499.3 | 286 | Missense Mutation | CCT,CGT | P,R 86 | NP_612508.3 | |
XM_006717659.3 | 286 | Missense Mutation | CCT,CGT | P,R 86 | XP_006717722.1 | |
XM_011539387.2 | 286 | Missense Mutation | CCT,CGT | P,R 86 | XP_011537689.1 |