Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
61 submissions
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Phenotype: |
MIM: 609321 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SASS6 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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SASS6 - SAS-6 centriolar assembly protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304829.1 | 232 | Intron | NP_001291758.1 | |||
NM_194292.2 | 232 | Intron | NP_919268.1 | |||
XM_017000486.1 | 232 | Intron | XP_016855975.1 |
TRMT13 - tRNA methyltransferase 13 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_019083.2 | 232 | Missense Mutation | GCG,GTG | A,V 48 | NP_061956.2 | |
XM_005270945.3 | 232 | Missense Mutation | GCG,GTG | A,V 48 | XP_005271002.1 | |
XM_005270946.2 | 232 | UTR 5 | XP_005271003.1 | |||
XM_017001504.1 | 232 | Missense Mutation | GCG,GTG | A,V 48 | XP_016856993.1 | |
XM_017001505.1 | 232 | Missense Mutation | GCG,GTG | A,V 48 | XP_016856994.1 |
Set Membership: |
HapMap |