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AAAGGAATGTGATACCAAGTGTGAC[C/G]CGAGTCCTTCAGCAGACCATGACAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615076 MIM: 605937 | ||||||||||||||||||||
Literature Links: |
MGME1 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 |
MGME1 - mitochondrial genome maintenance exonuclease 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001310338.1 | 660 | Silent Mutation | ACC,ACG | T,T 134 | NP_001297267.1 | |
NM_001310339.1 | 660 | Silent Mutation | ACC,ACG | T,T 134 | NP_001297268.1 | |
NM_052865.3 | 660 | Silent Mutation | ACC,ACG | T,T 134 | NP_443097.1 | |
XM_005260867.2 | 660 | Silent Mutation | ACC,ACG | T,T 134 | XP_005260924.1 | |
XM_005260870.3 | 660 | Silent Mutation | ACC,ACG | T,T 134 | XP_005260927.1 | |
XM_006723663.3 | 660 | Silent Mutation | ACC,ACG | T,T 134 | XP_006723726.1 | |
XM_011529394.1 | 660 | Silent Mutation | ACC,ACG | T,T 134 | XP_011527696.1 | |
XM_011529395.1 | 660 | Intron | XP_011527697.1 | |||
XM_017028127.1 | 660 | Silent Mutation | ACC,ACG | T,T 134 | XP_016883616.1 | |
XM_017028128.1 | 660 | Silent Mutation | ACC,ACG | T,T 134 | XP_016883617.1 |
SNORD17 - small nucleolar RNA, C/D box 17 | ||||||
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There are no transcripts associated with this gene. |
SNX5 - sorting nexin 5 | ||||||
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There are no transcripts associated with this gene. |