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CTGTCAGGTGTTTGTCTCCCAGGTT[C/T]CTGTGAATCCAGTTTTTGATGTAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CXorf38 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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CXorf38 - chromosome X open reading frame 38 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144970.2 | 972 | Missense Mutation | AAA,GAA | K,E 309 | NP_659407.1 | |
XM_005272589.2 | 972 | Missense Mutation | AAA,GAA | K,E 309 | XP_005272646.2 | |
XM_006724527.3 | 972 | Missense Mutation | AAA,GAA | K,E 249 | XP_006724590.2 | |
XM_006724528.2 | 972 | Missense Mutation | AAA,GAA | K,E 264 | XP_006724591.1 | |
XM_017029302.1 | 972 | Missense Mutation | AAA,GAA | K,E 320 | XP_016884791.1 | |
XM_017029303.1 | 972 | Missense Mutation | AAA,GAA | K,E 264 | XP_016884792.1 | |
XM_017029304.1 | 972 | Missense Mutation | AAA,GAA | K,E 190 | XP_016884793.1 | |
XM_017029305.1 | 972 | Missense Mutation | AAA,GAA | K,E 190 | XP_016884794.1 |
MPC1L - mitochondrial pyruvate carrier 1-like | ||||||
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There are no transcripts associated with this gene. |