Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTAAGCGCCCTGGGAGCTTTATTT[A/G]AATGTTCCTGTTCCTCTTCCCTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
13 submissions
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Phenotype: |
MIM: 602135 MIM: 609365 | ||||||||||||||||||||
Literature Links: |
DNALI1 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 |
DNALI1 - dynein axonemal light intermediate chain 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003462.3 | 2172 | Intron | NP_003453.2 | |||
XM_005271172.2 | 2172 | Intron | XP_005271229.1 |
GNL2 - G protein nucleolar 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323623.1 | 2172 | Missense Mutation | TCA,TTA | S,L 738 | NP_001310552.1 | |
NM_001323624.1 | 2172 | Missense Mutation | TCA,TTA | S,L 487 | NP_001310553.1 | |
NM_013285.2 | 2172 | Missense Mutation | TCA,TTA | S,L 670 | NP_037417.1 |