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GTCATCTTGGCCAACTCCAGGGTCC[C/T]TGTGTATGGAGCACTTGATGTCCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 607807 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ABCA13 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
|
ABCA13 - ATP binding cassette subfamily A member 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152701.4 | Intron | NP_689914.3 | ||||
XM_011515130.2 | Intron | XP_011513432.1 | ||||
XM_011515131.2 | Intron | XP_011513433.1 | ||||
XM_011515132.2 | Intron | XP_011513434.1 | ||||
XM_011515133.2 | Intron | XP_011513435.1 | ||||
XM_011515134.2 | Intron | XP_011513436.1 | ||||
XM_011515136.2 | Intron | XP_011513438.2 | ||||
XM_011515137.2 | Intron | XP_011513439.1 | ||||
XM_011515138.2 | Intron | XP_011513440.1 | ||||
XM_011515139.2 | Intron | XP_011513441.1 | ||||
XM_011515141.2 | Intron | XP_011513443.1 | ||||
XM_011515142.2 | Intron | XP_011513444.1 | ||||
XM_011515143.2 | Intron | XP_011513445.1 | ||||
XM_011515144.2 | Intron | XP_011513446.1 | ||||
XM_011515145.2 | Intron | XP_011513447.1 | ||||
XM_011515146.2 | Intron | XP_011513448.1 | ||||
XM_011515147.2 | Intron | XP_011513449.1 | ||||
XM_011515148.2 | Intron | XP_011513450.1 | ||||
XM_011515149.2 | Intron | XP_011513451.1 | ||||
XM_017011767.1 | Intron | XP_016867256.1 | ||||
XM_017011768.1 | Intron | XP_016867257.1 | ||||
XM_017011769.1 | Intron | XP_016867258.1 |