Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAAGTTGACTTCTGGTGCAGTTTCT[C/T]GTCCCGTTGAAGGGTAAAGTACTTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606639 MIM: 609305 | ||||||||||||||||||||
Literature Links: |
GFM1 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 |
GFM1 - G elongation factor mitochondrial 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308164.1 | 486 | Intron | NP_001295093.1 | |||
NM_001308166.1 | 486 | Intron | NP_001295095.1 | |||
NM_024996.5 | 486 | Intron | NP_079272.4 | |||
XM_006713795.1 | 486 | Intron | XP_006713858.1 |
LXN - latexin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020169.3 | 486 | Missense Mutation | CAA,CGA | Q,R 81 | NP_064554.3 | |
XM_017006876.1 | 486 | Missense Mutation | CAA,CGA | Q,R 81 | XP_016862365.1 |