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Search Thermo Fisher Scientific
CCAGCTGGAGCAAGGAGAAGCAGCA[C/T]GGGGCCCAGATCCCTGGACACTTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF619 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 |
ZNF619 - zinc finger protein 619 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145082.2 | 369 | Missense Mutation | CGG,TGG | R,W 120 | NP_001138554.1 | |
NM_001145083.1 | 369 | Missense Mutation | CGG,TGG | R,W 36 | NP_001138555.1 | |
NM_001145093.2 | 369 | Missense Mutation | CGG,TGG | R,W 80 | NP_001138565.1 | |
XM_006713112.2 | 369 | Missense Mutation | CGG,TGG | R,W 79 | XP_006713175.1 | |
XM_006713113.3 | 369 | Missense Mutation | CGG,TGG | R,W 35 | XP_006713176.1 | |
XM_011533607.1 | 369 | Missense Mutation | CGG,TGG | R,W 119 | XP_011531909.1 | |
XM_011533608.1 | 369 | Missense Mutation | ACG,ATG | T,M 47 | XP_011531910.1 | |
XM_017006225.1 | 369 | Missense Mutation | ACG,ATG | T,M 47 | XP_016861714.1 |