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TCTGTAGCAAGTCCAATCTTTCCAA[A/G]CATCAGCGAGTCCACACTGGAGAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 194510 MIM: 601261 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF3 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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ZNF3 - zinc finger protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278284.1 | 1527 | Intron | NP_001265213.1 | |||
NM_001278287.1 | 1527 | Intron | NP_001265216.1 | |||
NM_001278290.1 | 1527 | Intron | NP_001265219.1 | |||
NM_001278291.1 | 1527 | Intron | NP_001265220.1 | |||
NM_001278292.1 | 1527 | Intron | NP_001265221.1 | |||
NM_001318135.1 | 1527 | Intron | NP_001305064.1 | |||
NM_001318136.1 | 1527 | Intron | NP_001305065.1 | |||
NM_001318137.1 | 1527 | UTR 3 | NP_001305066.1 | |||
NM_017715.3 | 1527 | UTR 3 | NP_060185.2 | |||
NM_032924.4 | 1527 | Intron | NP_116313.3 | |||
XM_006716111.1 | 1527 | Intron | XP_006716174.1 | |||
XM_017012582.1 | 1527 | Intron | XP_016868071.1 | |||
XM_017012583.1 | 1527 | Intron | XP_016868072.1 |
ZSCAN21 - zinc finger and SCAN domain containing 21 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_145914.2 | 1527 | Silent Mutation | AAA,AAG | K,K 461 | NP_666019.1 | |
XM_005250568.4 | 1527 | Silent Mutation | AAA,AAG | K,K 461 | XP_005250625.1 | |
XM_006716113.3 | 1527 | Silent Mutation | AAA,AAG | K,K 461 | XP_006716176.1 | |
XM_017012584.1 | 1527 | Silent Mutation | AAA,AAG | K,K 461 | XP_016868073.1 | |
XM_017012585.1 | 1527 | Missense Mutation | AAC,AGC | N,S 427 | XP_016868074.1 |