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CGTGAGCCACTATGCCCAGCCCATA[C/T]AGCAATTTAAAAAAATTTTTTTATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610465 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACSF2 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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ACSF2 - acyl-CoA synthetase family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288968.1 | Intron | NP_001275897.1 | ||||
NM_001288969.1 | Intron | NP_001275898.1 | ||||
NM_001288970.1 | Intron | NP_001275899.1 | ||||
NM_001288971.1 | Intron | NP_001275900.1 | ||||
NM_001288972.1 | Intron | NP_001275901.1 | ||||
NM_025149.5 | Intron | NP_079425.3 | ||||
XM_006722110.3 | Intron | XP_006722173.1 | ||||
XM_011525294.1 | Intron | XP_011523596.1 |