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GGCCTGCAGGTGGGGCCGGGTCACC[C/G]CCAGCCGCAGCAGGCACAGCACCAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610823 | ||||||||||||||||||||
Literature Links: |
SLC25A42 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 |
SLC25A42 - solute carrier family 25 member 42 | ||||||
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There are no transcripts associated with this gene. |
TMEM161A - transmembrane protein 161A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256766.1 | 952 | Missense Mutation | GCG,GGG | A,G 225 | NP_001243695.1 | |
NM_017814.2 | 952 | Missense Mutation | GCG,GGG | A,G 328 | NP_060284.1 | |
XM_011528117.2 | 952 | Missense Mutation | GCG,GGG | A,G 126 | XP_011526419.1 | |
XM_017026916.1 | 952 | Missense Mutation | GCG,GGG | A,G 303 | XP_016882405.1 |