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TTTTCCTGCTTCTCTTGAAAATTCA[A/G]AAGACCTGACAGTTTTGGGACTGCA
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 - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
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 | Intron | NP_001273460.1 | ||||
NM_001286532.1 | Intron | NP_001273461.1 | ||||
NM_001286533.1 | Intron | NP_001273462.1 | ||||
NM_001286534.1 | Intron | NP_001273463.1 | ||||
NM_001286535.1 | Intron | NP_001273464.1 | ||||
NM_001286536.1 | Intron | NP_001273465.1 | ||||
NM_152442.3 | Intron | NP_689655.3 | ||||
XM_005253849.4 | Intron | XP_005253906.1 | ||||
XM_011537971.2 | Intron | XP_011536273.1 | ||||
XM_011537972.2 | Intron | XP_011536274.1 | ||||
XM_011537974.2 | Intron | XP_011536276.1 | ||||
XM_017018877.1 | Intron | XP_016874366.1 | ||||
XM_017018878.1 | Intron | XP_016874367.1 | ||||
XM_017018879.1 | Intron | XP_016874368.1 | ||||
XM_017018880.1 | Intron | XP_016874369.1 | ||||
XM_017018881.1 | Intron | XP_016874370.1 | ||||
XM_017018882.1 | Intron | XP_016874371.1 |
VPS29 - VPS29, retromer complex component | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |