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DNAH2TCGACCTGCAGATGAGCGATTACCT[A/G]CGAATCCTAGAACACGCCATTCACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
DNAH2 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 |
| DNAH2 - dynein axonemal heavy chain 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001303270.1 | 10603 | Intron | NP_001290199.1 | |||
| NM_020877.3 | 10603 | Silent Mutation | CTA,CTG | L,L 3425 | NP_065928.2 | |
| XM_011523663.1 | 10603 | Silent Mutation | CTA,CTG | L,L 3507 | XP_011521965.1 | |
| XM_011523664.2 | 10603 | Silent Mutation | CTA,CTG | L,L 3507 | XP_011521966.1 | |
| XM_011523666.1 | 10603 | Silent Mutation | CTA,CTG | L,L 3444 | XP_011521968.1 | |
| XM_011523667.2 | 10603 | Silent Mutation | CTA,CTG | L,L 3425 | XP_011521969.1 | |
| XM_011523668.1 | 10603 | Silent Mutation | CTA,CTG | L,L 2971 | XP_011521970.1 | |
| XM_011523669.2 | 10603 | Silent Mutation | CTA,CTG | L,L 2839 | XP_011521971.1 | |
| XM_011523670.2 | 10603 | Silent Mutation | CTA,CTG | L,L 3507 | XP_011521972.1 | |
| XM_017024218.1 | 10603 | Silent Mutation | CTA,CTG | L,L 2842 | XP_016879707.1 | |
| XM_017024219.1 | 10603 | Silent Mutation | CTA,CTG | L,L 3507 | XP_016879708.1 | |