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CAAGTAGAGGGGCGCACACCTACCC[A/G]CAGTTGTTCACAGCCATGAGGTCGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610449 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MTCH1 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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MTCH1 - mitochondrial carrier 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271641.1 | 855 | Silent Mutation | TGC,TGT | C,C 340 | NP_001258570.1 | |
NM_014341.2 | 855 | Silent Mutation | TGC,TGT | C,C 323 | NP_055156.1 | |
XM_005248978.1 | 855 | Silent Mutation | TGC,TGT | C,C 340 | XP_005249035.1 | |
XM_005248979.1 | 855 | Silent Mutation | TGC,TGT | C,C 323 | XP_005249036.1 | |
XM_011514450.1 | 855 | Silent Mutation | TGC,TGT | C,C 167 | XP_011512752.1 | |
XM_017010642.1 | 855 | Silent Mutation | TGC,TGT | C,C 184 | XP_016866131.1 | |
XM_017010643.1 | 855 | Silent Mutation | TGC,TGT | C,C 184 | XP_016866132.1 |
PI16 - peptidase inhibitor 16 | ||||||
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There are no transcripts associated with this gene. |