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GCGAGGAGGTGAGAAGGAGCACAGA[A/G]CCGCTGCTGTCCACGGCGGCCAGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612341 MIM: 604885 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GGT6 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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GGT6 - gamma-glutamyltransferase 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122890.2 | 1059 | Silent Mutation | GGC,GGT | G,G 360 | NP_001116362.1 | |
NM_001288702.1 | 1059 | Silent Mutation | GGC,GGT | G,G 366 | NP_001275631.1 | |
NM_001288703.1 | 1059 | Missense Mutation | CTC,TTC | L,F 164 | NP_001275632.1 | |
NM_001288704.1 | 1059 | Missense Mutation | CTC,TTC | L,F 132 | NP_001275633.1 | |
NM_153338.3 | 1059 | Silent Mutation | GGC,GGT | G,G 328 | NP_699169.2 |
MYBBP1A - MYB binding protein 1a | ||||||
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There are no transcripts associated with this gene. |