Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCGGCGCGCGGAGCTGCGGCGGCGG[C/T]GCTGCTGAGGCTGTGAGTGCAGGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609686 | ||||||||||||||||||||
Literature Links: |
CLYBL 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 |
CLYBL - citrate lyase beta like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_206808.3 | 82 | Missense Mutation | GCG,GTG | A,V 17 | NP_996531.1 | |
XM_005254030.2 | 82 | Missense Mutation | GCG,GTG | A,V 17 | XP_005254087.1 | |
XM_005254031.2 | 82 | Missense Mutation | GCG,GTG | A,V 17 | XP_005254088.1 | |
XM_006719915.3 | 82 | Missense Mutation | GCG,GTG | A,V 17 | XP_006719978.1 | |
XM_011521051.2 | 82 | Missense Mutation | GCG,GTG | A,V 17 | XP_011519353.1 | |
XM_011521052.2 | 82 | Missense Mutation | GCG,GTG | A,V 17 | XP_011519354.1 | |
XM_017020402.1 | 82 | Missense Mutation | GCG,GTG | A,V 17 | XP_016875891.1 | |
XM_017020403.1 | 82 | UTR 5 | XP_016875892.1 | |||
XM_017020404.1 | 82 | Intron | XP_016875893.1 |