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CAGACAGTGAAGTGAGTATTCTAAA[C/T]GATCATGGCCTGCCATGAAGGCCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611409 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
OCA2 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
|
OCA2 - OCA2 melanosomal transmembrane protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000275.2 | Intron | NP_000266.2 | ||||
NM_001300984.1 | Intron | NP_001287913.1 | ||||
XM_011521640.2 | Intron | XP_011519942.1 | ||||
XM_017022255.1 | Intron | XP_016877744.1 | ||||
XM_017022256.1 | Intron | XP_016877745.1 | ||||
XM_017022257.1 | Intron | XP_016877746.1 | ||||
XM_017022258.1 | Intron | XP_016877747.1 | ||||
XM_017022259.1 | Intron | XP_016877748.1 | ||||
XM_017022260.1 | Intron | XP_016877749.1 | ||||
XM_017022261.1 | Intron | XP_016877750.1 | ||||
XM_017022262.1 | Intron | XP_016877751.1 | ||||
XM_017022263.1 | Intron | XP_016877752.1 | ||||
XM_017022264.1 | Intron | XP_016877753.1 | ||||
XM_017022265.1 | Intron | XP_016877754.1 |