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TCGTACGGTTCCCTAATTCACAAGT[C/T]ATCTGTTCAAGAGCAGTTTTTTTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609759 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRDM7 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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PRDM7 - PR domain 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098173.1 | Intron | NP_001091643.1 | ||||
XM_005256274.3 | Intron | XP_005256331.1 | ||||
XM_011522829.1 | Intron | XP_011521131.1 | ||||
XM_011522831.2 | Intron | XP_011521133.1 | ||||
XM_017022882.1 | Intron | XP_016878371.1 | ||||
XM_017022883.1 | Intron | XP_016878372.1 | ||||
XM_017022884.1 | Intron | XP_016878373.1 |