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AGGTGCGGGGGAACCCAGAGGGACA[A/T]GGGGTAGTTGCCTTTGGCCAAACCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
|
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Phenotype: |
MIM: 610824 | ||||||||||||||||||||
Literature Links: |
SLC25A44 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 |
SLC25A44 - solute carrier family 25 member 44 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286184.1 | 1361 | Missense Mutation | CAA,CAT | Q,H 158 | NP_001273113.1 | |
NM_014655.3 | 1361 | Missense Mutation | CAA,CAT | Q,H 158 | NP_055470.1 | |
XM_006711657.3 | 1361 | Missense Mutation | CAA,CAT | Q,H 158 | XP_006711720.1 | |
XM_011510180.1 | 1361 | Missense Mutation | CAA,CAT | Q,H 158 | XP_011508482.1 | |
XM_011510181.1 | 1361 | Missense Mutation | CAA,CAT | Q,H 158 | XP_011508483.1 | |
XM_017002904.1 | 1361 | Missense Mutation | CAA,CAT | Q,H 158 | XP_016858393.1 | |
XM_017002905.1 | 1361 | Missense Mutation | CAA,CAT | Q,H 158 | XP_016858394.1 | |
XM_017002906.1 | 1361 | Missense Mutation | CAA,CAT | Q,H 158 | XP_016858395.1 | |
XM_017002907.1 | 1361 | Missense Mutation | CAA,CAT | Q,H 158 | XP_016858396.1 | |
XM_017002908.1 | 1361 | Missense Mutation | CAA,CAT | Q,H 158 | XP_016858397.1 |