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CTGATCCTACCAACTCTATGAGCCA[A/C]CTCTTACCTGTGTTTTATAGATGAC
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615569 | ||||||||||||||||||||||||||||||||
Literature Links: |
SFXN1 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
SFXN1 - sideroflexin 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322977.1 | Intron | NP_001309906.1 | ||||
NM_001322978.1 | Intron | NP_001309907.1 | ||||
NM_001322980.1 | Intron | NP_001309909.1 | ||||
NM_001322981.1 | Intron | NP_001309910.1 | ||||
NM_001322982.1 | Intron | NP_001309911.1 | ||||
NM_001322983.1 | Intron | NP_001309912.1 | ||||
NM_022754.6 | Intron | NP_073591.2 |
Set Membership: |
HapMap |