Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGTTGCTGCTCCTGTCCCTGGTCA[C/T]GGGAACTCAGCTCGGTCCACGGACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615144 | ||||||||||||||||||||
Literature Links: |
PRSS55 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 |
PRSS55 - protease, serine 55 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001197020.1 | 296 | Missense Mutation | ACG,ATG | T,M 14 | NP_001183949.1 | |
NM_198464.3 | 296 | Missense Mutation | ACG,ATG | T,M 14 | NP_940866.2 | |
XM_005272372.3 | 296 | Missense Mutation | ACG,ATG | T,M 79 | XP_005272429.2 | |
XM_011543814.2 | 296 | Missense Mutation | ACG,ATG | T,M 79 | XP_011542116.2 | |
XM_017013182.1 | 296 | Missense Mutation | ACG,ATG | T,M 79 | XP_016868671.1 |