Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAACCCTGTATTGGGATGTGATGT[C/T]GGAGAACTATAGAAACCTCATCTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
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Literature Links: |
ZNF684 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 |
ZNF684 - zinc finger protein 684 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152373.3 | 697 | Missense Mutation | TCG,TTG | S,L 38 | NP_689586.3 | |
XM_011540671.2 | 697 | Missense Mutation | TCG,TTG | S,L 38 | XP_011538973.1 | |
XM_011540672.2 | 697 | Missense Mutation | TCG,TTG | S,L 38 | XP_011538974.1 | |
XM_011540673.2 | 697 | Missense Mutation | TCG,TTG | S,L 38 | XP_011538975.1 | |
XM_017000290.1 | 697 | Missense Mutation | TCG,TTG | S,L 38 | XP_016855779.1 | |
XM_017000291.1 | 697 | Missense Mutation | TCG,TTG | S,L 2 | XP_016855780.1 | |
XM_017000292.1 | 697 | Intron | XP_016855781.1 |