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TCTTCCAGTAGTTTTCTTTTTTGCA[A/G]TAAGTTTTTTTCCATGGTAAGTGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 614191 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DEPDC5 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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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
|
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AMR
|
DEPDC5 - DEP domain containing 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007188.2 | Intron | NP_001007189.1 | ||||
NM_001136029.2 | Intron | NP_001129501.1 | ||||
NM_001242896.1 | Intron | NP_001229825.1 | ||||
NM_001242897.1 | Intron | NP_001229826.1 | ||||
NM_014662.4 | Intron | NP_055477.1 | ||||
XM_005261862.1 | Intron | XP_005261919.1 | ||||
XM_011530557.2 | Intron | XP_011528859.1 | ||||
XM_011530558.2 | Intron | XP_011528860.1 | ||||
XM_011530559.2 | Intron | XP_011528861.1 | ||||
XM_011530560.2 | Intron | XP_011528862.1 | ||||
XM_011530561.2 | Intron | XP_011528863.1 | ||||
XM_011530562.2 | Intron | XP_011528864.1 | ||||
XM_011530563.2 | Intron | XP_011528865.1 | ||||
XM_011530565.2 | Intron | XP_011528867.1 | ||||
XM_011530568.2 | Intron | XP_011528870.1 | ||||
XM_011530569.2 | Intron | XP_011528871.1 | ||||
XM_017029109.1 | Intron | XP_016884598.1 | ||||
XM_017029110.1 | Intron | XP_016884599.1 | ||||
XM_017029111.1 | Intron | XP_016884600.1 | ||||
XM_017029112.1 | Intron | XP_016884601.1 | ||||
XM_017029113.1 | Intron | XP_016884602.1 | ||||
XM_017029114.1 | Intron | XP_016884603.1 | ||||
XM_017029115.1 | Intron | XP_016884604.1 |