Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCACTCTTCCTCAGGTCCGAGACGG[C/T]GTACACACAGGCCCCCTCCTGGGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 137168 | ||||||||||||||||||||
Literature Links: |
GGT5 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 |
GGT5 - gamma-glutamyltransferase 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099781.2 | 2130 | Missense Mutation | ACC,GCC | T,A 574 | NP_001093251.1 | |
NM_001099782.2 | 2130 | Missense Mutation | ACC,GCC | T,A 541 | NP_001093252.1 | |
NM_001302464.1 | 2130 | UTR 3 | NP_001289393.1 | |||
NM_001302465.1 | 2130 | Missense Mutation | ACC,GCC | T,A 497 | NP_001289394.1 | |
NM_004121.3 | 2130 | Missense Mutation | ACC,GCC | T,A 573 | NP_004112.2 | |
XM_005261557.2 | 2130 | Missense Mutation | ACC,GCC | T,A 605 | XP_005261614.1 | |
XM_005261558.2 | 2130 | Missense Mutation | ACC,GCC | T,A 604 | XP_005261615.1 | |
XM_011530133.1 | 2130 | Missense Mutation | ACC,GCC | T,A 610 | XP_011528435.1 | |
XM_011530134.1 | 2130 | Missense Mutation | ACC,GCC | T,A 579 | XP_011528436.1 | |
XM_011530135.1 | 2130 | Missense Mutation | ACC,GCC | T,A 578 | XP_011528437.1 | |
XM_011530136.1 | 2130 | UTR 3 | XP_011528438.1 | |||
XM_011530137.2 | 2130 | UTR 3 | XP_011528439.1 | |||
XM_017028768.1 | 2130 | Missense Mutation | ACC,GCC | T,A 572 | XP_016884257.1 | |
XM_017028769.1 | 2130 | Missense Mutation | ACC,GCC | T,A 547 | XP_016884258.1 |