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TTTAGTTGAGGTGAAAAAACTGCTT[C/T]ATAAGTTCGTATGTTGTAAAAGCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 139080 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC25A16 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SLC25A16 - solute carrier family 25 member 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324312.1 | 1123 | UTR 3 | NP_001311241.1 | |||
NM_001324313.1 | 1123 | Intron | NP_001311242.1 | |||
NM_001324314.1 | 1123 | Missense Mutation | ATA,ATG | I,M 227 | NP_001311243.1 | |
NM_001324315.1 | 1123 | Missense Mutation | ATA,ATG | I,M 227 | NP_001311244.1 | |
NM_001324317.1 | 1123 | Missense Mutation | ATA,ATG | I,M 191 | NP_001311246.1 | |
NM_152707.3 | 1123 | Missense Mutation | ATA,ATG | I,M 325 | NP_689920.1 | |
XM_011540211.2 | 1123 | Missense Mutation | ATA,ATG | I,M 325 | XP_011538513.1 | |
XM_017016695.1 | 1123 | Intron | XP_016872184.1 |