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GCCCTCACCTCTCACAGCCTCCATC[A/G]CTCCCAGAGCGACCTGGCGTTGGGT
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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There are no transcripts associated with this gene. |
SLC25A39 - solute carrier family 25 member 39 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143780.2 | 956 | Missense Mutation | GCG,GTG | A,V 289 | NP_001137252.1 | |
NM_001321240.1 | 956 | Missense Mutation | GCG,GTG | A,V 266 | NP_001308169.1 | |
NM_001321241.1 | 956 | Missense Mutation | GCG,GTG | A,V 287 | NP_001308170.1 | |
NM_016016.3 | 956 | Missense Mutation | GCG,GTG | A,V 281 | NP_057100.1 | |
XM_011524880.2 | 956 | Missense Mutation | GCG,GTG | A,V 295 | XP_011523182.1 | |
XM_011524882.2 | 956 | Missense Mutation | GCG,GTG | A,V 272 | XP_011523184.1 | |
XM_011524883.2 | 956 | Missense Mutation | GCG,GTG | A,V 194 | XP_011523185.1 | |
XM_011524884.1 | 956 | Missense Mutation | GCG,GTG | A,V 194 | XP_011523186.1 | |
XM_017024737.1 | 956 | Missense Mutation | GCG,GTG | A,V 188 | XP_016880226.1 |