Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAGTGGGTCATAGAGGATTTTGGG[A/G]AGAGATTCCCCAATCTGCATCGTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603334 MIM: 614709 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DNAH3 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 | 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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DNAH3 - dynein axonemal heavy chain 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017539.2 | 12692 | Silent Mutation | CTC,CTT | L,L 4038 | NP_060009.1 | |
XM_006721062.1 | 12692 | Silent Mutation | CTC,CTT | L,L 3992 | XP_006721125.1 | |
XM_011545882.2 | 12692 | Silent Mutation | CTC,CTT | L,L 3999 | XP_011544184.1 | |
XM_011545883.1 | 12692 | Silent Mutation | CTC,CTT | L,L 3999 | XP_011544185.1 | |
XM_011545885.2 | 12692 | Intron | XP_011544187.1 | |||
XM_011545886.2 | 12692 | Silent Mutation | CTC,CTT | L,L 3662 | XP_011544188.1 | |
XM_011545888.2 | 12692 | Silent Mutation | CTC,CTT | L,L 3133 | XP_011544190.1 | |
XM_011545889.2 | 12692 | Silent Mutation | CTC,CTT | L,L 3133 | XP_011544191.1 | |
XM_017023426.1 | 12692 | Silent Mutation | CTC,CTT | L,L 3954 | XP_016878915.1 | |
XM_017023427.1 | 12692 | Silent Mutation | CTC,CTT | L,L 3918 | XP_016878916.1 | |
XM_017023428.1 | 12692 | Silent Mutation | CTC,CTT | L,L 3806 | XP_016878917.1 | |
XM_017023429.1 | 12692 | Intron | XP_016878918.1 | |||
XM_017023430.1 | 12692 | Silent Mutation | CTC,CTT | L,L 2017 | XP_016878919.1 | |
XM_017023431.1 | 12692 | Intron | XP_016878920.1 | |||
XM_017023432.1 | 12692 | Silent Mutation | CTC,CTT | L,L 4052 | XP_016878921.1 |
LYRM1 - LYR motif containing 1 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |