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TGGGCTCTCCCCAGTGTGGATGCGC[C/T]GGTGAGCACTGAACTGGGAACTGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZSCAN32 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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ZSCAN32 - zinc finger and SCAN domain containing 32 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284527.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 624 | NP_001271456.1 | |
NM_001284528.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 335 | NP_001271457.1 | |
NM_001284529.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 335 | NP_001271458.1 | |
NM_001324340.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 412 | NP_001311269.1 | |
NM_001324341.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 412 | NP_001311270.1 | |
NM_001324342.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 412 | NP_001311271.1 | |
NM_001324343.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 491 | NP_001311272.1 | |
NM_001324344.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 412 | NP_001311273.1 | |
NM_001324345.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 412 | NP_001311274.1 | |
NM_001324346.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 551 | NP_001311275.1 | |
NM_017810.3 | 2134 | Missense Mutation | CAG,CGG | Q,R 412 | NP_060280.2 | |
XM_005255403.2 | 2134 | Missense Mutation | CAG,CGG | Q,R 537 | XP_005255460.1 | |
XM_011522555.2 | 2134 | Missense Mutation | CAG,CGG | Q,R 624 | XP_011520857.1 | |
XM_017023371.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 624 | XP_016878860.1 | |
XM_017023372.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 537 | XP_016878861.1 | |
XM_017023373.1 | 2134 | Missense Mutation | CAG,CGG | Q,R 537 | XP_016878862.1 |