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Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300242 | |||||||||||||||||||||||
Literature Links: |
SLC25A14 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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 | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
SLC25A14 - solute carrier family 25 member 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282195.1 | 400 | Missense Mutation | GAG,GCG | E,A 55 | NP_001269124.1 | |
NM_001282196.1 | 400 | Missense Mutation | GAG,GCG | E,A 52 | NP_001269125.1 | |
NM_001282197.1 | 400 | Missense Mutation | GAG,GCG | E,A 52 | NP_001269126.1 | |
NM_001282198.1 | 400 | Missense Mutation | GAG,GCG | E,A 20 | NP_001269127.1 | |
XM_005262489.4 | 400 | Intron | XP_005262546.1 | |||
XM_011531402.2 | 400 | Missense Mutation | GAG,GCG | E,A 64 | XP_011529704.1 | |
XM_011531403.1 | 400 | Intron | XP_011529705.1 | |||
XM_017029936.1 | 400 | Missense Mutation | GAG,GCG | E,A 20 | XP_016885425.1 | |
XM_017029937.1 | 400 | Missense Mutation | GAG,GCG | E,A 64 | XP_016885426.1 | |
XM_017029938.1 | 400 | Missense Mutation | GAG,GCG | E,A 55 | XP_016885427.1 | |
XM_017029939.1 | 400 | Missense Mutation | GAG,GCG | E,A 52 | XP_016885428.1 | |
XM_017029940.1 | 400 | Intron | XP_016885429.1 | |||
XM_017029941.1 | 400 | UTR 5 | XP_016885430.1 | |||
XM_017029942.1 | 400 | UTR 5 | XP_016885431.1 | |||
XM_017029943.1 | 400 | Intron | XP_016885432.1 |
Set Membership: |
HapMap |