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CCCGCTTAGATCGGAAGTAGTTGCT[A/G]GCAATGTTTTCACTGTTGCTCCGAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 602202 MIM: 605037 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DDOST 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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DDOST - dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit | ||||||
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There are no transcripts associated with this gene. |
KIF17 - kinesin family member 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122819.2 | 2907 | Silent Mutation | GCC,GCT | A,A 948 | NP_001116291.1 | |
NM_001287212.1 | 2907 | Silent Mutation | GCC,GCT | A,A 849 | NP_001274141.1 | |
NM_020816.3 | 2907 | Silent Mutation | GCC,GCT | A,A 949 | NP_065867.2 | |
XM_005245950.3 | 2907 | Silent Mutation | GCC,GCT | A,A 949 | XP_005246007.1 | |
XM_005245951.3 | 2907 | Silent Mutation | GCC,GCT | A,A 948 | XP_005246008.1 | |
XM_011541837.1 | 2907 | Missense Mutation | CCA,CTA | P,L 948 | XP_011540139.1 | |
XM_011541838.1 | 2907 | Missense Mutation | CCA,CTA | P,L 947 | XP_011540140.1 | |
XM_011541839.2 | 2907 | Silent Mutation | GCC,GCT | A,A 949 | XP_011540141.1 | |
XM_011541840.2 | 2907 | Silent Mutation | GCC,GCT | A,A 948 | XP_011540142.1 | |
XM_011541841.2 | 2907 | Missense Mutation | CCA,CTA | P,L 948 | XP_011540143.1 | |
XM_011541842.1 | 2907 | Silent Mutation | GCC,GCT | A,A 949 | XP_011540144.1 | |
XM_011541843.1 | 2907 | Missense Mutation | CCA,CTA | P,L 948 | XP_011540145.1 | |
XM_011541844.2 | 2907 | Silent Mutation | GCC,GCT | A,A 949 | XP_011540146.1 | |
XM_011541845.2 | 2907 | Missense Mutation | CCA,CTA | P,L 948 | XP_011540147.1 | |
XM_011541846.2 | 2907 | Missense Mutation | CCA,CTA | P,L 848 | XP_011540148.1 | |
XM_011541847.2 | 2907 | Missense Mutation | CCA,CTA | P,L 474 | XP_011540149.1 |