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TTGCTTGTTAGCCTTTGTTTGAGTT[A/G]CCTTTTTTTTCTGTGCTTTGGCTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603331 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DYNC1I2 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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DYNC1I2 - dynein cytoplasmic 1 intermediate chain 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271785.1 | Intron | NP_001258714.1 | ||||
NM_001271786.1 | Intron | NP_001258715.1 | ||||
NM_001271787.1 | Intron | NP_001258716.1 | ||||
NM_001271788.1 | Intron | NP_001258717.1 | ||||
NM_001271789.1 | Intron | NP_001258718.1 | ||||
NM_001271790.1 | Intron | NP_001258719.1 | ||||
NM_001320882.1 | Intron | NP_001307811.1 | ||||
NM_001320883.1 | Intron | NP_001307812.1 | ||||
NM_001320884.1 | Intron | NP_001307813.1 | ||||
NM_001378.2 | Intron | NP_001369.1 | ||||
XM_006712347.3 | Intron | XP_006712410.1 | ||||
XM_017003525.1 | Intron | XP_016859014.1 |