Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTGAGCTAAAGGAGAAAAAAAATA[C/T]GGTGGATCGTTCAAAACTCCTTCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
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Literature Links: |
AXDND1 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 |
AXDND1 - axonemal dynein light chain domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144696.5 | 494 | Missense Mutation | ACG,ATG | T,M 43 | NP_653297.3 | |
XM_011509165.1 | 494 | Missense Mutation | ACG,ATG | T,M 43 | XP_011507467.1 | |
XM_011509166.2 | 494 | Missense Mutation | ACG,ATG | T,M 43 | XP_011507468.1 | |
XM_011509167.2 | 494 | Missense Mutation | ACG,ATG | T,M 43 | XP_011507469.1 | |
XM_011509168.1 | 494 | Missense Mutation | ACG,ATG | T,M 43 | XP_011507470.1 | |
XM_011509169.1 | 494 | Missense Mutation | ACG,ATG | T,M 22 | XP_011507471.1 | |
XM_011509170.1 | 494 | Missense Mutation | ACG,ATG | T,M 43 | XP_011507472.1 | |
XM_011509171.1 | 494 | Missense Mutation | ACG,ATG | T,M 1 | XP_011507473.1 | |
XM_011509174.1 | 494 | Missense Mutation | ACG,ATG | T,M 43 | XP_011507476.1 | |
XM_011509175.1 | 494 | Missense Mutation | ACG,ATG | T,M 43 | XP_011507477.1 | |
XM_011509176.1 | 494 | Missense Mutation | ACG,ATG | T,M 43 | XP_011507478.1 | |
XM_011509178.2 | 494 | Missense Mutation | ACG,ATG | T,M 43 | XP_011507480.1 | |
XM_011509179.2 | 494 | Intron | XP_011507481.1 | |||
XM_011509180.1 | 494 | Missense Mutation | ACG,ATG | T,M 43 | XP_011507482.1 | |
XM_011509181.2 | 494 | Intron | XP_011507483.1 | |||
XM_017000257.1 | 494 | Intron | XP_016855746.1 | |||
XM_017000258.1 | 494 | Intron | XP_016855747.1 | |||
XM_017000259.1 | 494 | Intron | XP_016855748.1 |