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TTTTTGAGCAGCTGGGGGCCTACAT[A/C]CAGGAGAGCGCCACCTTCCTTGAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
17 submissions
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Phenotype: |
MIM: 608507 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MFN2 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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MFN2 - mitofusin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127660.1 | 616 | Silent Mutation | ATA,ATC | I,I 50 | NP_001121132.1 | |
NM_014874.3 | 616 | Silent Mutation | ATA,ATC | I,I 50 | NP_055689.1 | |
XM_005263543.3 | 616 | Silent Mutation | ATA,ATC | I,I 50 | XP_005263600.1 | |
XM_005263545.3 | 616 | Silent Mutation | ATA,ATC | I,I 50 | XP_005263602.1 | |
XM_005263547.3 | 616 | Silent Mutation | ATA,ATC | I,I 50 | XP_005263604.1 | |
XM_005263548.3 | 616 | Silent Mutation | ATA,ATC | I,I 50 | XP_005263605.1 |