Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCCTGACATTGGTGGTGGCGAGGG[G/T]AAGGGGCTGGACTTTGGGATTGAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
PRSS37 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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PRSS37 - protease, serine 37 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008270.2 | 1849 | Missense Mutation | ACC,CCC | T,P 119 | NP_001008271.2 | |
NM_001171951.1 | 1849 | Missense Mutation | ACC,CCC | T,P 119 | NP_001165422.1 | |
XM_005249946.4 | 1849 | Missense Mutation | ACC,CCC | T,P 119 | XP_005250003.1 | |
XM_005249947.3 | 1849 | Missense Mutation | ACC,CCC | T,P 119 | XP_005250004.1 | |
XM_011515792.2 | 1849 | Missense Mutation | ACC,CCC | T,P 56 | XP_011514094.1 | |
XM_011515793.2 | 1849 | Missense Mutation | ACC,CCC | T,P 56 | XP_011514095.1 |
Set Membership: |
HapMap |