Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
|||||||||||||||||||||||
Phenotype: |
MIM: 605448 MIM: 610820 | |||||||||||||||||||||||
Literature Links: |
RUNDC3A PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese)
|
|||
EUR - Not Available | |||||
AMR - Not Available |
RUNDC3A - RUN domain containing 3A | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
SLC25A39 - solute carrier family 25 member 39 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143780.2 | 851 | Missense Mutation | TCT,TTT | S,F 254 | NP_001137252.1 | |
NM_001321240.1 | 851 | Missense Mutation | TCT,TTT | S,F 231 | NP_001308169.1 | |
NM_001321241.1 | 851 | Missense Mutation | TCT,TTT | S,F 252 | NP_001308170.1 | |
NM_016016.3 | 851 | Missense Mutation | TCT,TTT | S,F 246 | NP_057100.1 | |
XM_011524880.2 | 851 | Missense Mutation | TCT,TTT | S,F 260 | XP_011523182.1 | |
XM_011524882.2 | 851 | Missense Mutation | TCT,TTT | S,F 237 | XP_011523184.1 | |
XM_011524883.2 | 851 | Missense Mutation | TCT,TTT | S,F 159 | XP_011523185.1 | |
XM_011524884.1 | 851 | Missense Mutation | TCT,TTT | S,F 159 | XP_011523186.1 | |
XM_017024737.1 | 851 | Missense Mutation | TCT,TTT | S,F 153 | XP_016880226.1 |