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CTGCTAGAATACTCGGGCTCCGCTG[C/G]AGTTTGTTGTAAGGGCTGTATTTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612344 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF385B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
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
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ZNF385B - zinc finger protein 385B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001113397.1 | 1093 | Silent Mutation | CTC,CTG | L,L 315 | NP_001106868.1 | |
NM_001113398.1 | 1093 | Silent Mutation | CTC,CTG | L,L 289 | NP_001106869.1 | |
NM_001282725.1 | 1093 | Silent Mutation | CTC,CTG | L,L 289 | NP_001269654.1 | |
NM_152520.4 | 1093 | Silent Mutation | CTC,CTG | L,L 391 | NP_689733.3 | |
XM_011510713.2 | 1093 | Silent Mutation | CTC,CTG | L,L 446 | XP_011509015.1 | |
XM_011510714.2 | 1093 | Silent Mutation | CTC,CTG | L,L 433 | XP_011509016.1 | |
XM_011510715.2 | 1093 | Silent Mutation | CTC,CTG | L,L 419 | XP_011509017.1 | |
XM_011510716.2 | 1093 | Silent Mutation | CTC,CTG | L,L 349 | XP_011509018.1 | |
XM_011510717.2 | 1093 | Silent Mutation | CTC,CTG | L,L 349 | XP_011509019.1 | |
XM_011510719.2 | 1093 | Silent Mutation | CTC,CTG | L,L 329 | XP_011509021.1 | |
XM_011510720.2 | 1093 | Silent Mutation | CTC,CTG | L,L 329 | XP_011509022.1 | |
XM_011510721.2 | 1093 | Silent Mutation | CTC,CTG | L,L 316 | XP_011509023.1 | |
XM_011510723.2 | 1093 | Intron | XP_011509025.1 | |||
XM_017003435.1 | 1093 | Silent Mutation | CTC,CTG | L,L 406 | XP_016858924.1 | |
XM_017003436.1 | 1093 | Silent Mutation | CTC,CTG | L,L 329 | XP_016858925.1 | |
XM_017003437.1 | 1093 | Silent Mutation | CTC,CTG | L,L 323 | XP_016858926.1 | |
XM_017003438.1 | 1093 | Silent Mutation | CTC,CTG | L,L 289 | XP_016858927.1 | |
XM_017003439.1 | 1093 | Silent Mutation | CTC,CTG | L,L 289 | XP_016858928.1 | |
XM_017003440.1 | 1093 | Silent Mutation | CTC,CTG | L,L 277 | XP_016858929.1 | |
XM_017003441.1 | 1093 | Intron | XP_016858930.1 |