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TGTGACCTCCTTTGTGCAACTTATG[A/C]TCATCCACACTTTTACAGCCTTTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF708 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
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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
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ZNF708 - zinc finger protein 708 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297560.1 | 366 | Intron | NP_001284489.1 | |||
NM_001297561.1 | 366 | Intron | NP_001284490.1 | |||
NM_021269.2 | 366 | Intron | NP_067092.2 | |||
XM_017027201.1 | 366 | Intron | XP_016882690.1 | |||
XM_017027202.1 | 366 | Missense Mutation | XP_016882691.1 | |||
XM_017027203.1 | 366 | Missense Mutation | XP_016882692.1 | |||
XM_017027204.1 | 366 | Missense Mutation | XP_016882693.1 |