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TGCTTCTCTATATGTTGAAGTTGCA[C/T]GGACTCTGCCCCAGTTACTTGACCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605184 | ||||||||||||||||||||
Literature Links: |
PAIP1 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 |
PAIP1 - poly(A) binding protein interacting protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006451.4 | 1389 | Missense Mutation | CAT,CGT | H,R 381 | NP_006442.2 | |
NM_182789.3 | 1389 | Missense Mutation | CAT,CGT | H,R 302 | NP_877590.1 | |
NM_183323.2 | 1389 | Intron | NP_899152.1 | |||
XM_005248230.3 | 1389 | Intron | XP_005248287.1 | |||
XM_017008956.1 | 1389 | Intron | XP_016864445.1 |