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TGTTTTCTTCATTGGCAGTAAAAAT[G/T]GGGTAATGCTTTCTTTTTTTCAATT
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 |
---|---|---|
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 |
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 | 224 | Missense Mutation | GGG,TGG | G,W 42 | NP_001180393.1 | |
NM_015522.3 | 224 | Missense Mutation | GGG,TGG | G,W 42 | NP_056337.1 | |
NM_016008.3 | 224 | Missense Mutation | GGG,TGG | G,W 42 | NP_057092.2 | |
XM_005264364.4 | 224 | Missense Mutation | GGG,TGG | G,W 42 | XP_005264421.1 | |
XM_005264365.4 | 224 | Missense Mutation | GGG,TGG | G,W 42 | XP_005264422.1 |
PLEKHH2 - pleckstrin homology, MyTH4 and FERM domain containing H2 | ||||||
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There are no transcripts associated with this gene. |