Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCGCCCCCAATAAGGAGCCAGTGAA[A/T]TACGGGGAGCTGGTGGTGCTCGGGT
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 - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 385 | Missense Mutation | AAA,AAT | K,N 18 | NP_067078.1 | |
XM_005267890.4 | 385 | Missense Mutation | AAA,AAT | K,N 18 | XP_005267947.1 | |
XM_006720211.3 | 385 | Intron | XP_006720274.1 | |||
XM_011536990.2 | 385 | Intron | XP_011535292.1 | |||
XM_011536992.2 | 385 | Intron | XP_011535294.1 | |||
XM_017021478.1 | 385 | Intron | XP_016876967.1 | |||
XM_017021479.1 | 385 | Intron | XP_016876968.1 |