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GGAGAGCCTGTCTTTTTACTCAACA[A/G]ACTGTTGAAGAAGCTGGCCAACACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611406 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DYNC1LI2 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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DYNC1LI2 - dynein cytoplasmic 1 light intermediate chain 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286157.1 | 1337 | Silent Mutation | CTG,TTG | L,L 359 | NP_001273086.1 | |
NM_001323955.1 | 1337 | Silent Mutation | CTG,TTG | L,L 397 | NP_001310884.1 | |
NM_006141.2 | 1337 | Silent Mutation | CTG,TTG | L,L 436 | NP_006132.1 | |
XM_017023008.1 | 1337 | Silent Mutation | CTG,TTG | L,L 436 | XP_016878497.1 |