Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612723 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DYNC2LI1 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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DYNC2LI1 - dynein cytoplasmic 2 light intermediate chain 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193464.1 | 198 | Missense Mutation | TCT,TTT | S,F 33 | NP_001180393.1 | |
NM_015522.3 | 198 | Missense Mutation | TCT,TTT | S,F 33 | NP_056337.1 | |
NM_016008.3 | 198 | Missense Mutation | TCT,TTT | S,F 33 | NP_057092.2 | |
XM_005264364.4 | 198 | Missense Mutation | TCT,TTT | S,F 33 | XP_005264421.1 | |
XM_005264365.4 | 198 | Missense Mutation | TCT,TTT | S,F 33 | XP_005264422.1 |
PLEKHH2 - pleckstrin homology, MyTH4 and FERM domain containing H2 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |