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GTCATGGTTTGGTGATATGCACTTC[A/G]CTGCTTCCGTTCCCGTTGGTGGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 164013 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NFRKB 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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NFRKB - nuclear factor related to kappaB binding protein | ||||||
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There are no transcripts associated with this gene. |
PRDM10 - PR domain 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020228.2 | 5451 | Silent Mutation | AGC,AGT | S,S 1153 | NP_064613.2 | |
NM_199437.1 | 5451 | Silent Mutation | AGC,AGT | S,S 1149 | NP_955469.1 | |
NM_199438.1 | 5451 | Silent Mutation | AGC,AGT | S,S 1054 | NP_955470.1 | |
NM_199439.1 | 5451 | Silent Mutation | AGC,AGT | S,S 1016 | NP_955471.1 | |
XM_011542912.2 | 5451 | Silent Mutation | AGC,AGT | S,S 1136 | XP_011541214.1 | |
XM_017018023.1 | 5451 | Silent Mutation | AGC,AGT | S,S 1050 | XP_016873512.1 |