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GATGGCGGTACTTCGGTTCAGGCGG[A/T]GGCATCCTTACCAAGGAATCTGCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603423 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRDM1 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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PRDM1 - PR domain 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198.3 | 260 | Missense Mutation | GAG,GTG | E,V 80 | NP_001189.2 | |
NM_182907.2 | 260 | Intron | NP_878911.1 | |||
XM_006715550.3 | 260 | Missense Mutation | GAG,GTG | E,V 94 | XP_006715613.1 | |
XM_011536062.2 | 260 | Missense Mutation | GAG,GTG | E,V 94 | XP_011534364.1 | |
XM_011536063.2 | 260 | Missense Mutation | GAG,GTG | E,V 44 | XP_011534365.1 | |
XM_011536064.2 | 260 | Intron | XP_011534366.1 | |||
XM_017011187.1 | 260 | Missense Mutation | GAG,GTG | E,V 44 | XP_016866676.1 |