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TAAAAAGAACAGGAGAATATTTTAG[A/C]ATTCATTGTTCATTTGACCTTTATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609360 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RNLS 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
|
RNLS - renalase, FAD dependent amine oxidase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031709.2 | Intron | NP_001026879.2 | ||||
NM_018363.3 | Intron | NP_060833.1 | ||||
XM_005269946.1 | Intron | XP_005270003.1 | ||||
XM_005269947.1 | Intron | XP_005270004.1 | ||||
XM_005269948.2 | Intron | XP_005270005.1 | ||||
XM_005269949.4 | Intron | XP_005270006.1 | ||||
XM_005269950.3 | Intron | XP_005270007.1 | ||||
XM_011539924.2 | Intron | XP_011538226.1 | ||||
XM_011539927.2 | Intron | XP_011538229.1 | ||||
XM_017016380.1 | Intron | XP_016871869.1 | ||||
XM_017016381.1 | Intron | XP_016871870.1 | ||||
XM_017016382.1 | Intron | XP_016871871.1 | ||||
XM_017016383.1 | Intron | XP_016871872.1 | ||||
XM_017016384.1 | Intron | XP_016871873.1 | ||||
XM_017016385.1 | Intron | XP_016871874.1 |