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CTGCGGGTACCGCTGTTCCAGCCCT[A/G]AGAGGACGAGGGGACGCTGCGCTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600835 | ||||||||||||||||||||
Literature Links: |
C10orf142 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 |
C10orf142 - chromosome 10 open reading frame 142 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258000.1 | 270 | Missense Mutation | AAG,GAG | K,E 87 | NP_001244929.1 |
CXCL12 - C-X-C motif chemokine ligand 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000609.6 | 270 | Intron | NP_000600.1 | |||
NM_001033886.2 | 270 | Intron | NP_001029058.1 | |||
NM_001178134.1 | 270 | Intron | NP_001171605.1 | |||
NM_001277990.1 | 270 | Intron | NP_001264919.1 | |||
NM_199168.3 | 270 | Intron | NP_954637.1 |