Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGAGTTTAAATCCTTGAGTTTAGA[A/G]GGCTTGTGTTGCTGATACCTTGGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MTFR2 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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MTFR2 - mitochondrial fission regulator 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099286.2 | 1365 | Missense Mutation | CCT,CTT | P,L 380 | NP_001092756.1 | |
NM_001318738.1 | 1365 | Missense Mutation | CCT,CTT | P,L 337 | NP_001305667.1 | |
NM_138419.4 | 1365 | Missense Mutation | CCT,CTT | P,L 380 | NP_612428.2 | |
XM_011535410.2 | 1365 | Missense Mutation | CCT,CTT | P,L 337 | XP_011533712.1 | |
XM_011535412.2 | 1365 | Missense Mutation | CCT,CTT | P,L 337 | XP_011533714.1 | |
XM_011535413.2 | 1365 | Missense Mutation | CCT,CTT | P,L 337 | XP_011533715.1 |