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- SNP ID:
- rs78865223
- Gene
-
TTLL6 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.17: 48800802 - 48800802 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GGAACTGATGTTGTTTTGAAATGGA[C/T]ATAAAGAGAGCAGAGAAGGGGAAGT
Genomic Map
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Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610849
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Literature Links: |
TTLL6 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
| TTLL6 - tubulin tyrosine ligase like 6 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001130918.1 | Intron | NP_001124390.1 | ||||
| NM_173623.3 | Intron | NP_775894.2 | ||||
| XM_017024491.1 | Intron | XP_016879980.1 | ||||
| XM_017024492.1 | Intron | XP_016879981.1 | ||||
| XM_017024493.1 | Intron | XP_016879982.1 | ||||
| XM_017024494.1 | Intron | XP_016879983.1 | ||||
| XM_017024495.1 | Intron | XP_016879984.1 | ||||
| XM_017024496.1 | Intron | XP_016879985.1 | ||||
| XM_017024497.1 | Intron | XP_016879986.1 | ||||
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