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GGTTCTAAAGAAAGAGTTCCAGGGT[G/T]CATAGCTATGCGATCAGGCAGTCCT
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 | |||
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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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C10orf142 - chromosome 10 open reading frame 142 | ||||||
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There are no transcripts associated with this gene. |
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 | Intron | NP_000600.1 | ||||
NM_001033886.2 | Intron | NP_001029058.1 | ||||
NM_001178134.1 | Intron | NP_001171605.1 | ||||
NM_001277990.1 | Intron | NP_001264919.1 | ||||
NM_199168.3 | Intron | NP_954637.1 |