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GGGCCCCAGAGGCTGAGAACGAGCG[C/G]TCTGGAGTCACAGGAGGTGGCTGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 169730 MIM: 611115 | ||||||||||||||||||||
Literature Links: |
PGA5 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 |
PGA5 - pepsinogen 5, group I (pepsinogen A) | ||||||
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There are no transcripts associated with this gene. |
VWCE - von Willebrand factor C and EGF domains | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152718.2 | 2491 | Silent Mutation | GAC,GAG | D,E 873 | NP_689931.2 | |
XM_006718460.1 | 2491 | Missense Mutation | GAC,GAG | D,E 865 | XP_006718523.1 | |
XM_006718462.1 | 2491 | Missense Mutation | GAC,GAG | D,E 813 | XP_006718525.1 | |
XM_011544817.1 | 2491 | Missense Mutation | GAC,GAG | D,E 775 | XP_011543119.1 | |
XM_017017340.1 | 2491 | Missense Mutation | GAC,GAG | D,E 852 | XP_016872829.1 | |
XM_017017341.1 | 2491 | Missense Mutation | GAC,GAG | D,E 830 | XP_016872830.1 | |
XM_017017342.1 | 2491 | Missense Mutation | GAC,GAG | D,E 743 | XP_016872831.1 | |
XM_017017343.1 | 2491 | Missense Mutation | GAC,GAG | D,E 590 | XP_016872832.1 | |
XM_017017344.1 | 2491 | Intron | XP_016872833.1 |