Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCTCAGGCAGCACCCCCGCGGGG[C/G]CGGCCTCCTCGCAGGCGCACCCAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZSCAN18 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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ZSCAN18 - zinc finger and SCAN domain containing 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145542.1 | 1085 | Missense Mutation | GCC,GGC | A,G 352 | NP_001139014.1 | |
NM_001145543.1 | 1085 | Missense Mutation | GCC,GGC | A,G 296 | NP_001139015.1 | |
NM_001145544.1 | 1085 | Missense Mutation | GCC,GGC | A,G 160 | NP_001139016.1 | |
NM_023926.4 | 1085 | Missense Mutation | GCC,GGC | A,G 296 | NP_076415.3 | |
XM_005259174.4 | 1085 | Missense Mutation | GCC,GGC | A,G 296 | XP_005259231.1 | |
XM_006723335.2 | 1085 | Missense Mutation | GCC,GGC | A,G 296 | XP_006723398.1 | |
XM_011527237.2 | 1085 | Missense Mutation | GCC,GGC | A,G 351 | XP_011525539.1 | |
XM_011527238.1 | 1085 | Missense Mutation | GCC,GGC | A,G 296 | XP_011525540.1 | |
XM_011527239.2 | 1085 | Missense Mutation | GCC,GGC | A,G 296 | XP_011525541.1 | |
XM_017027169.1 | 1085 | Missense Mutation | GCC,GGC | A,G 295 | XP_016882658.1 | |
XM_017027170.1 | 1085 | Missense Mutation | GCC,GGC | A,G 295 | XP_016882659.1 | |
XM_017027171.1 | 1085 | Missense Mutation | GCC,GGC | A,G 295 | XP_016882660.1 |