Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGACAAGATGTACCAGGTCCCACTA[C/T]CACTGGATCGGGATGGGACCCTGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615187 | ||||||||||||||||||||
Literature Links: |
PGAP2 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 |
PGAP2 - post-GPI attachment to proteins 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145438.2 | 357 | Missense Mutation | CCA,TCA | P,S 64 | NP_001138910.1 | |
NM_001256235.1 | 357 | UTR 5 | NP_001243164.1 | |||
NM_001256236.1 | 357 | Missense Mutation | CCA,TCA | P,S 64 | NP_001243165.1 | |
NM_001256237.1 | 357 | Missense Mutation | CCA,TCA | P,S 64 | NP_001243166.1 | |
NM_001256238.1 | 357 | Missense Mutation | CCA,TCA | P,S 7 | NP_001243167.1 | |
NM_001256239.1 | 357 | Missense Mutation | CCA,TCA | P,S 7 | NP_001243168.1 | |
NM_001256240.1 | 357 | Missense Mutation | CCA,TCA | P,S 7 | NP_001243169.1 | |
NM_001283038.1 | 357 | Missense Mutation | CCA,TCA | P,S 64 | NP_001269967.1 | |
NM_001283039.1 | 357 | Intron | NP_001269968.1 | |||
NM_001283040.1 | 357 | Intron | NP_001269969.1 | |||
NM_014489.3 | 357 | Missense Mutation | CCA,TCA | P,S 7 | NP_055304.1 | |
XM_006718181.3 | 357 | Intron | XP_006718244.1 | |||
XM_006718183.3 | 357 | Silent Mutation | TAC,TAT | Y,Y 18 | XP_006718246.1 | |
XM_006718185.2 | 357 | Intron | XP_006718248.1 | |||
XM_006718186.2 | 357 | UTR 5 | XP_006718249.1 | |||
XM_006718190.3 | 357 | Missense Mutation | CCA,TCA | P,S 7 | XP_006718253.1 | |
XM_006718191.3 | 357 | Missense Mutation | CCA,TCA | P,S 7 | XP_006718254.1 | |
XM_006718192.1 | 357 | UTR 5 | XP_006718255.1 | |||
XM_006718193.2 | 357 | Intron | XP_006718256.1 | |||
XM_011519990.2 | 357 | Missense Mutation | CCA,TCA | P,S 83 | XP_011518292.2 | |
XM_011519991.2 | 357 | Missense Mutation | CCA,TCA | P,S 83 | XP_011518293.2 | |
XM_011519992.1 | 357 | Silent Mutation | TAC,TAT | Y,Y 18 | XP_011518294.1 | |
XM_011519993.2 | 357 | Missense Mutation | CCA,TCA | P,S 83 | XP_011518295.2 | |
XM_011519994.2 | 357 | Missense Mutation | CCA,TCA | P,S 83 | XP_011518296.2 | |
XM_011519995.2 | 357 | Intron | XP_011518297.1 | |||
XM_011519996.1 | 357 | Silent Mutation | TAC,TAT | Y,Y 18 | XP_011518298.1 | |
XM_011519997.1 | 357 | UTR 5 | XP_011518299.1 | |||
XM_011519998.2 | 357 | UTR 5 | XP_011518300.1 | |||
XM_011519999.1 | 357 | UTR 5 | XP_011518301.1 | |||
XM_011520000.1 | 357 | Intron | XP_011518302.1 | |||
XM_011520001.1 | 357 | Missense Mutation | CCA,TCA | P,S 7 | XP_011518303.1 | |
XM_011520002.1 | 357 | Missense Mutation | CCA,TCA | P,S 7 | XP_011518304.1 | |
XM_011520003.2 | 357 | Missense Mutation | CCA,TCA | P,S 7 | XP_011518305.1 | |
XM_011520004.2 | 357 | Missense Mutation | CCA,TCA | P,S 7 | XP_011518306.1 | |
XM_011520005.2 | 357 | Intron | XP_011518307.1 | |||
XM_011520006.2 | 357 | UTR 5 | XP_011518308.1 | |||
XM_011520007.2 | 357 | UTR 5 | XP_011518309.1 | |||
XM_017017556.1 | 357 | Missense Mutation | CCA,TCA | P,S 7 | XP_016873045.1 | |
XM_017017557.1 | 357 | Missense Mutation | CCA,TCA | P,S 58 | XP_016873046.1 | |
XM_017017558.1 | 357 | Intron | XP_016873047.1 | |||
XM_017017559.1 | 357 | Silent Mutation | TAC,TAT | Y,Y 18 | XP_016873048.1 | |
XM_017017560.1 | 357 | Silent Mutation | TAC,TAT | Y,Y 18 | XP_016873049.1 |