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CCTGCTTAAACCAAATGAGTATGTC[G/A]ACTTTGCAATCTTGACACACTATTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 603941 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC181 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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CCDC181 - coiled-coil domain containing 181 | ||||||
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There are no transcripts associated with this gene. |
SLC19A2 - solute carrier family 19 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319667.1 | 2466 | UTR 3 | NP_001306596.1 | |||
NM_006996.2 | 2466 | UTR 3 | NP_008927.1 |