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CACTGGCATCTACCACAATTAGAGT[A/G]AGCAGCGTCTGCAGTGCCAGGGCAA
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 |
---|---|---|
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 |
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 | 915 | Silent Mutation | CTC,CTT | L,L 237 | NP_001306596.1 | |
NM_006996.2 | 915 | Silent Mutation | CTC,CTT | L,L 438 | NP_008927.1 |