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GGTGGTATTGGAAATCTCATTACCT[A/G]TTTTGAAGCTGTTTGCAGATAAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614798 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PELI2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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PELI2 - pellino E3 ubiquitin protein ligase family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021255.2 | Intron | NP_067078.1 | ||||
XM_005267890.4 | Intron | XP_005267947.1 | ||||
XM_006720211.3 | Intron | XP_006720274.1 | ||||
XM_011536990.2 | Intron | XP_011535292.1 | ||||
XM_011536992.2 | Intron | XP_011535294.1 | ||||
XM_017021478.1 | Intron | XP_016876967.1 | ||||
XM_017021479.1 | Intron | XP_016876968.1 |