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TGCCTGCTAATACTGAAAAAAATCT[G/T]TGGCAAAATCCAACACACATTTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C10orf128 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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C10orf128 - chromosome 10 open reading frame 128 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010863.2 | Intron | NP_001010863.1 | ||||
NM_001288740.1 | Intron | NP_001275669.1 | ||||
NM_001288741.1 | Intron | NP_001275670.1 | ||||
NM_001288742.1 | Intron | NP_001275671.1 | ||||
NM_001288743.1 | Intron | NP_001275672.1 | ||||
XM_011539378.2 | Intron | XP_011537680.1 | ||||
XM_011539379.1 | Intron | XP_011537681.1 | ||||
XM_011539380.1 | Intron | XP_011537682.1 | ||||
XM_011539382.1 | Intron | XP_011537684.1 | ||||
XM_011539383.2 | Intron | XP_011537685.1 | ||||
XM_011539384.1 | Intron | XP_011537686.1 | ||||
XM_011539385.1 | Intron | XP_011537687.1 | ||||
XM_017015792.1 | Intron | XP_016871281.1 | ||||
XM_017015793.1 | Intron | XP_016871282.1 | ||||
XM_017015794.1 | Intron | XP_016871283.1 | ||||
XM_017015795.1 | Intron | XP_016871284.1 | ||||
XM_017015796.1 | Intron | XP_016871285.1 | ||||
XM_017015797.1 | Intron | XP_016871286.1 |
FAM170B-AS1 - FAM170B antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |