Search Thermo Fisher Scientific
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ACGATCCTTCGGAGGTAAAGCGGTC[G/A]CTTATGTTCTGGCACTCTGATGATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601066 MIM: 603593 | ||||||||||||||||||||
Literature Links: |
OXA1L 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 |
OXA1L - OXA1L, mitochondrial inner membrane protein | ||||||
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There are no transcripts associated with this gene. |
SLC7A7 - solute carrier family 7 member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001126105.2 | 1644 | Missense Mutation | NP_001119577.1 | |||
NM_001126106.2 | 1644 | Missense Mutation | NP_001119578.1 | |||
XM_006720302.1 | 1644 | Nonsense Mutation | XP_006720365.1 | |||
XM_011537298.2 | 1644 | Nonsense Mutation | XP_011535600.1 | |||
XM_011537299.1 | 1644 | Nonsense Mutation | XP_011535601.1 |