Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTGCTTGGGCCTCTCGCAGGGACC[A/G]GCCCAGACCAGCGGCGAACTTCTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611045 MIM: 605315 | ||||||||||||||||||||
Literature Links: |
G6PC3 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 |
G6PC3 - glucose-6-phosphatase catalytic subunit 3 | ||||||
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There are no transcripts associated with this gene. |
HDAC5 - histone deacetylase 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001015053.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1071 | NP_001015053.1 | |
NM_005474.4 | 3606 | Missense Mutation | CGG,TGG | R,W 1070 | NP_005465.2 | |
XM_005256905.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1070 | XP_005256962.1 | |
XM_005256906.4 | 3606 | Missense Mutation | CGG,TGG | R,W 1070 | XP_005256963.1 | |
XM_011524149.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1062 | XP_011522451.1 | |
XM_011524150.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1061 | XP_011522452.1 | |
XM_017023988.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1109 | XP_016879477.1 | |
XM_017023989.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1109 | XP_016879478.1 | |
XM_017023990.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1108 | XP_016879479.1 | |
XM_017023991.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1108 | XP_016879480.1 | |
XM_017023992.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1104 | XP_016879481.1 | |
XM_017023993.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1100 | XP_016879482.1 | |
XM_017023994.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1080 | XP_016879483.1 | |
XM_017023995.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1061 | XP_016879484.1 | |
XM_017023996.1 | 3606 | Missense Mutation | CGG,TGG | R,W 1029 | XP_016879485.1 |