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AAGCCGTGACAAGCAGGGCAGAGTC[A/G]GGGGAGAAGTCACAAGAGACAACAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600407 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RFC5 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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RFC5 - replication factor C subunit 5 | ||||||
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There are no transcripts associated with this gene. |
WSB2 - WD repeat and SOCS box containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278557.1 | 810 | Silent Mutation | CCC,CCT | P,P 266 | NP_001265486.1 | |
NM_001278558.1 | 810 | Silent Mutation | CCC,CCT | P,P 39 | NP_001265487.1 | |
NM_018639.4 | 810 | Silent Mutation | CCC,CCT | P,P 249 | NP_061109.1 | |
XM_017019642.1 | 810 | Silent Mutation | CCC,CCT | P,P 39 | XP_016875131.1 |