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Search Thermo Fisher Scientific
GGGGCGGATGGTGACCATGATGTCT[C/T]GGAAGTCGATGGCTGTGACTCTCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603859 | ||||||||||||||||||||
Literature Links: |
SLC25A13 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SLC25A13 - solute carrier family 25 member 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001160210.1 | 722 | Missense Mutation | CAA,CGA | Q,R 184 | NP_001153682.1 | |
NM_014251.2 | 722 | Missense Mutation | CAA,CGA | Q,R 184 | NP_055066.1 | |
XM_006715831.3 | 722 | Missense Mutation | CAA,CGA | Q,R 195 | XP_006715894.1 | |
XM_011515727.2 | 722 | Missense Mutation | CAA,CGA | Q,R 195 | XP_011514029.1 | |
XM_017011663.1 | 722 | Missense Mutation | CAA,CGA | Q,R 181 | XP_016867152.1 | |
XM_017011664.1 | 722 | UTR 5 | XP_016867153.1 | |||
XM_017011665.1 | 722 | UTR 5 | XP_016867154.1 |