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AGGAGTTTTATAACTTGGACAGTCT[A/G]TCCTTACTAGAAGTTGTTGACTTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603297 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DYNC2H1 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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DYNC2H1 - dynein cytoplasmic 2 heavy chain 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080463.1 | 789 | Silent Mutation | CTA,CTG | L,L 215 | NP_001073932.1 | |
NM_001377.2 | 789 | Silent Mutation | CTA,CTG | L,L 215 | NP_001368.2 | |
XM_006718903.2 | 789 | Silent Mutation | CTA,CTG | L,L 215 | XP_006718966.1 | |
XM_017018291.1 | 789 | Silent Mutation | CTA,CTG | L,L 215 | XP_016873780.1 | |
XM_017018292.1 | 789 | Silent Mutation | CTA,CTG | L,L 9 | XP_016873781.1 | |
XM_017018293.1 | 789 | Silent Mutation | CTA,CTG | L,L 215 | XP_016873782.1 |