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GAAACGTTACCAATCTAGCAGCTAA[C/T]AACTCATCCAAGTCCACTTCATCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616073 | ||||||||||||||||||||
Literature Links: |
DEPDC1B 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 |
DEPDC1B - DEP domain containing 1B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145208.1 | 1194 | Silent Mutation | TTA,TTG | L,L 376 | NP_001138680.1 | |
NM_018369.2 | 1194 | Silent Mutation | TTA,TTG | L,L 376 | NP_060839.2 | |
XM_011543509.2 | 1194 | Silent Mutation | TTA,TTG | L,L 361 | XP_011541811.1 | |
XM_011543510.2 | 1194 | Intron | XP_011541812.1 | |||
XM_017009629.1 | 1194 | Intron | XP_016865118.1 |