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GCAGGGGCAGGACCTCAGACATGAG[C/T]AGCCAGGTGATGGGACCCCAGCCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613104 MIM: 606813 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CACFD1 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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CACFD1 - calcium channel flower domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
SLC2A6 - solute carrier family 2 member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145099.1 | 1324 | Silent Mutation | CTA,CTG | L,L 357 | NP_001138571.1 | |
NM_017585.3 | 1324 | Silent Mutation | CTA,CTG | L,L 419 | NP_060055.2 | |
XM_011518189.2 | 1324 | Silent Mutation | CTA,CTG | L,L 213 | XP_011516491.2 | |
XM_017014236.1 | 1324 | Intron | XP_016869725.1 | |||
XM_017014237.1 | 1324 | Silent Mutation | CTA,CTG | L,L 175 | XP_016869726.1 | |
XM_017014238.1 | 1324 | Silent Mutation | CTA,CTG | L,L 175 | XP_016869727.1 |