Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTGCGGCAGCCAGGCCGTCGACGA[C/T]GCCCAGGTATTCCCTGAACCCGGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 612723 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DYNC2LI1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
DYNC2LI1 - dynein cytoplasmic 2 light intermediate chain 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193464.1 | 102 | Missense Mutation | ACG,ATG | T,M 1 | NP_001180393.1 | |
NM_015522.3 | 102 | Missense Mutation | ACG,ATG | T,M 1 | NP_056337.1 | |
NM_016008.3 | 102 | Missense Mutation | ACG,ATG | T,M 1 | NP_057092.2 | |
XM_005264364.4 | 102 | Missense Mutation | ACG,ATG | T,M 1 | XP_005264421.1 | |
XM_005264365.4 | 102 | Missense Mutation | ACG,ATG | T,M 1 | XP_005264422.1 |
PLEKHH2 - pleckstrin homology, MyTH4 and FERM domain containing H2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |