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CTGAAGGACCTGGAGGCGGAGAACC[A/G]GCGGCTTCAGCTGCAGCTGGAGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605448 MIM: 610820 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RUNDC3A 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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RUNDC3A - RUN domain containing 3A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144825.1 | 1055 | Missense Mutation | CAG,CGG | Q,R 287 | NP_001138297.1 | |
NM_001144826.1 | 1055 | Missense Mutation | CAG,CGG | Q,R 282 | NP_001138298.1 | |
NM_006695.4 | 1055 | Missense Mutation | CAG,CGG | Q,R 287 | NP_006686.1 | |
XM_005256964.3 | 1055 | Missense Mutation | CAG,CGG | Q,R 282 | XP_005257021.1 | |
XM_017024035.1 | 1055 | Missense Mutation | CAG,CGG | Q,R 287 | XP_016879524.1 | |
XM_017024036.1 | 1055 | Missense Mutation | CAG,CGG | Q,R 283 | XP_016879525.1 | |
XM_017024037.1 | 1055 | Missense Mutation | CAG,CGG | Q,R 282 | XP_016879526.1 | |
XM_017024038.1 | 1055 | Missense Mutation | CAG,CGG | Q,R 287 | XP_016879527.1 | |
XM_017024039.1 | 1055 | Missense Mutation | CAG,CGG | Q,R 287 | XP_016879528.1 | |
XM_017024040.1 | 1055 | Missense Mutation | CAG,CGG | Q,R 283 | XP_016879529.1 |
RUNDC3A-AS1 - RUNDC3A antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |
SLC25A39 - solute carrier family 25 member 39 | ||||||
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There are no transcripts associated with this gene. |