Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCCATGGATTGTCAAAGGGAAAAG[A/G]GCGGTGAGTGGTCCCATCCAATCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
TTLL9 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 |
TTLL9 - tubulin tyrosine ligase like 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008409.2 | 199 | Missense Mutation | GAG,GGG | E,G 37 | NP_001008409.1 | |
XM_005260309.2 | 199 | Missense Mutation | GAG,GGG | E,G 19 | XP_005260366.1 | |
XM_006723723.2 | 199 | Intron | XP_006723786.1 | |||
XM_006723724.2 | 199 | UTR 5 | XP_006723787.1 | |||
XM_011528617.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526919.1 | |
XM_011528618.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526920.1 | |
XM_011528619.1 | 199 | Missense Mutation | GAG,GGG | E,G 32 | XP_011526921.1 | |
XM_011528620.2 | 199 | Missense Mutation | GAG,GGG | E,G 32 | XP_011526922.1 | |
XM_011528621.1 | 199 | Missense Mutation | GAG,GGG | E,G 32 | XP_011526923.1 | |
XM_011528622.1 | 199 | Missense Mutation | GAG,GGG | E,G 32 | XP_011526924.1 | |
XM_011528623.2 | 199 | Missense Mutation | GAG,GGG | E,G 19 | XP_011526925.1 | |
XM_011528624.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526926.1 | |
XM_011528625.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526927.1 | |
XM_011528626.1 | 199 | UTR 5 | XP_011526928.1 | |||
XM_011528627.2 | 199 | UTR 5 | XP_011526929.1 | |||
XM_011528628.1 | 199 | UTR 5 | XP_011526930.1 | |||
XM_011528629.1 | 199 | UTR 5 | XP_011526931.1 | |||
XM_011528630.1 | 199 | Intron | XP_011526932.1 | |||
XM_011528631.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526933.1 | |
XM_011528632.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526934.1 | |
XM_011528633.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526935.1 | |
XM_011528634.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526936.1 | |
XM_011528635.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526937.1 | |
XM_011528637.2 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526939.1 | |
XM_011528638.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526940.1 | |
XM_011528639.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526941.1 | |
XM_011528640.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526942.1 | |
XM_011528641.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526943.1 | |
XM_011528643.2 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526945.1 | |
XM_011528644.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_011526946.1 | |
XM_011528646.1 | 199 | UTR 5 | XP_011526948.1 | |||
XM_017027694.1 | 199 | Intron | XP_016883183.1 | |||
XM_017027695.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_016883184.1 | |
XM_017027696.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_016883185.1 | |
XM_017027697.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_016883186.1 | |
XM_017027698.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_016883187.1 | |
XM_017027699.1 | 199 | Missense Mutation | GAG,GGG | E,G 19 | XP_016883188.1 | |
XM_017027700.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_016883189.1 | |
XM_017027701.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_016883190.1 | |
XM_017027702.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_016883191.1 | |
XM_017027703.1 | 199 | Missense Mutation | GAG,GGG | E,G 37 | XP_016883192.1 |