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GAATTCAACCCTTATTCGACATCAG[A/G]TGATCCATAGTGGAGAAAAACGCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF394 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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ZNF394 - zinc finger protein 394 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032164.2 | 1288 | Intron | NP_115540.2 | |||
XM_017012710.1 | 1288 | Intron | XP_016868199.1 | |||
XM_017012711.1 | 1288 | Intron | XP_016868200.1 |
ZNF789 - zinc finger protein 789 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001013258.1 | 1288 | Intron | NP_001013276.1 | |||
NM_213603.2 | 1288 | Missense Mutation | ATG,GTG | M,V 305 | NP_998768.2 | |
XM_011516067.2 | 1288 | Missense Mutation | ATG,GTG | M,V 298 | XP_011514369.1 | |
XM_011516070.2 | 1288 | Missense Mutation | ATG,GTG | M,V 288 | XP_011514372.1 | |
XM_011516073.2 | 1288 | Missense Mutation | ATG,GTG | M,V 210 | XP_011514375.1 | |
XM_017012018.1 | 1288 | Missense Mutation | ATG,GTG | M,V 305 | XP_016867507.1 | |
XM_017012019.1 | 1288 | Missense Mutation | ATG,GTG | M,V 288 | XP_016867508.1 | |
XM_017012020.1 | 1288 | Missense Mutation | ATG,GTG | M,V 288 | XP_016867509.1 | |
XM_017012021.1 | 1288 | Missense Mutation | ATG,GTG | M,V 288 | XP_016867510.1 | |
XM_017012022.1 | 1288 | Missense Mutation | ATG,GTG | M,V 288 | XP_016867511.1 | |
XM_017012023.1 | 1288 | Missense Mutation | ATG,GTG | M,V 267 | XP_016867512.1 | |
XM_017012024.1 | 1288 | Missense Mutation | ATG,GTG | M,V 247 | XP_016867513.1 | |
XM_017012025.1 | 1288 | Missense Mutation | ATG,GTG | M,V 210 | XP_016867514.1 | |
XM_017012026.1 | 1288 | Missense Mutation | ATG,GTG | M,V 210 | XP_016867515.1 | |
XM_017012027.1 | 1288 | Missense Mutation | ATG,GTG | M,V 210 | XP_016867516.1 |