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CTGGTCTGATGCCAGACTTGGGCGT[C/G]AAAGTTGTGCGTGGATGCGGCCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608159 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRSS21 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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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PRSS21 - protease, serine 21 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270452.1 | Intron | NP_001257381.1 | ||||
NM_006799.3 | Intron | NP_006790.1 | ||||
NM_144956.2 | Intron | NP_659205.1 | ||||
NM_144957.2 | Intron | NP_659206.1 | ||||
XM_017022875.1 | Intron | XP_016878364.1 | ||||
XM_017022876.1 | Intron | XP_016878365.1 | ||||
XM_017022877.1 | Intron | XP_016878366.1 | ||||
XM_017022878.1 | Intron | XP_016878367.1 |