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AGTGTGCTTGTTTTCGAACGTCCAT[C/G]TGGGATGAGACGCTCTACAAAGCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613433 MIM: 612194 MIM: 616292 | ||||||||||||||||||||
Literature Links: |
HAUS6 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 |
HAUS6 - HAUS augmin like complex subunit 6 | ||||||
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There are no transcripts associated with this gene. |
RRAGA - Ras related GTP binding A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006570.4 | 778 | Missense Mutation | ATC,ATG | I,M 164 | NP_006561.1 |
SAXO1 - stabilizer of axonemal microtubules 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287049.1 | 778 | Intron | NP_001273978.1 | |||
NM_001287050.1 | 778 | Intron | NP_001273979.1 | |||
NM_153707.3 | 778 | Intron | NP_714918.2 | |||
XM_011517744.1 | 778 | Intron | XP_011516046.1 | |||
XM_011517745.1 | 778 | Intron | XP_011516047.1 | |||
XM_011517746.2 | 778 | Intron | XP_011516048.1 | |||
XM_011517747.2 | 778 | Intron | XP_011516049.1 | |||
XM_017014314.1 | 778 | Intron | XP_016869803.1 | |||
XM_017014315.1 | 778 | Intron | XP_016869804.1 |