Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCCTCGATCCCTGGGAACCTATGG[C/G]CAGGGAGGCTCTCAGAGGTATCTGT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF620 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 - 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 |
ZNF620 - zinc finger protein 620 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256167.1 | 385 | Intron | NP_001243096.1 | |||
NM_001256168.1 | 385 | Intron | NP_001243097.1 | |||
NM_175888.3 | 385 | Missense Mutation | GCC,GGC | A,G 79 | NP_787084.1 | |
XM_005265011.3 | 385 | Missense Mutation | GCC,GGC | A,G 79 | XP_005265068.1 | |
XM_005265012.3 | 385 | Missense Mutation | GCC,GGC | A,G 79 | XP_005265069.1 | |
XM_017006064.1 | 385 | Missense Mutation | GCC,GGC | A,G 124 | XP_016861553.1 | |
XM_017006065.1 | 385 | Intron | XP_016861554.1 | |||
XM_017006066.1 | 385 | Missense Mutation | GCC,GGC | A,G 40 | XP_016861555.1 | |
XM_017006067.1 | 385 | Missense Mutation | GCC,GGC | A,G 40 | XP_016861556.1 | |
XM_017006068.1 | 385 | Intron | XP_016861557.1 | |||
XM_017006069.1 | 385 | Intron | XP_016861558.1 |