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GGATAGAGTCAGAAGGGGTGGGCAC[A/G]AGGAAGTGGCCGCCCCTGACCATGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609303 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC25A18 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
SLC25A18 - solute carrier family 25 member 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303484.1 | Intron | NP_001290413.1 | ||||
NM_031481.2 | Intron | NP_113669.1 | ||||
XM_011546149.2 | Intron | XP_011544451.1 | ||||
XM_011546150.2 | Intron | XP_011544452.1 | ||||
XM_011546151.2 | Intron | XP_011544453.1 | ||||
XM_011546152.1 | Intron | XP_011544454.1 | ||||
XM_011546153.2 | Intron | XP_011544455.1 | ||||
XM_011546154.2 | Intron | XP_011544456.1 | ||||
XM_017028968.1 | Intron | XP_016884457.1 | ||||
XM_017028969.1 | Intron | XP_016884458.1 | ||||
XM_017028970.1 | Intron | XP_016884459.1 | ||||
XM_017028971.1 | Intron | XP_016884460.1 | ||||
XM_017028972.1 | Intron | XP_016884461.1 | ||||
XM_017028973.1 | Intron | XP_016884462.1 | ||||
XM_017028974.1 | Intron | XP_016884463.1 | ||||
XM_017028975.1 | Intron | XP_016884464.1 |