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GCTCTAAGATGTGTGAATTCTTCTC[A/G]GTCAGCATATGGATGTGTCCTGTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608368 MIM: 606932 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RAD9B 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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RAD9B - RAD9 checkpoint clamp component B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286531.1 | 170 | UTR 5 | NP_001273460.1 | |||
NM_001286532.1 | 170 | UTR 5 | NP_001273461.1 | |||
NM_001286533.1 | 170 | UTR 5 | NP_001273462.1 | |||
NM_001286534.1 | 170 | UTR 5 | NP_001273463.1 | |||
NM_001286535.1 | 170 | Missense Mutation | CAG,CGG | Q,R 49 | NP_001273464.1 | |
NM_001286536.1 | 170 | Missense Mutation | CAG,CGG | Q,R 49 | NP_001273465.1 | |
NM_152442.3 | 170 | Missense Mutation | CAG,CGG | Q,R 49 | NP_689655.3 | |
XM_005253849.4 | 170 | Missense Mutation | CAG,CGG | Q,R 49 | XP_005253906.1 | |
XM_011537971.2 | 170 | Missense Mutation | CAG,CGG | Q,R 49 | XP_011536273.1 | |
XM_011537972.2 | 170 | Intron | XP_011536274.1 | |||
XM_011537974.2 | 170 | UTR 5 | XP_011536276.1 | |||
XM_017018877.1 | 170 | Intron | XP_016874366.1 | |||
XM_017018878.1 | 170 | UTR 5 | XP_016874367.1 | |||
XM_017018879.1 | 170 | UTR 5 | XP_016874368.1 | |||
XM_017018880.1 | 170 | UTR 5 | XP_016874369.1 | |||
XM_017018881.1 | 170 | UTR 5 | XP_016874370.1 | |||
XM_017018882.1 | 170 | Intron | XP_016874371.1 |
VPS29 - VPS29, retromer complex component | ||||||
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There are no transcripts associated with this gene. |