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ATGGCACCGTGCGCCGCTTCCTCTC[A/G]GTGGTGCAGCTCAATCCTTTCCCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
PROM2 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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PROM2 - prominin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001165977.2 | 338 | Silent Mutation | TCA,TCG | S,S 72 | NP_001159449.1 | |
NM_001165978.2 | 338 | Silent Mutation | TCA,TCG | S,S 72 | NP_001159450.1 | |
NM_001321070.1 | 338 | UTR 5 | NP_001307999.1 | |||
NM_144707.3 | 338 | Silent Mutation | TCA,TCG | S,S 72 | NP_653308.2 | |
XM_006712301.2 | 338 | Intron | XP_006712364.1 | |||
XM_011510672.2 | 338 | Silent Mutation | TCA,TCG | S,S 72 | XP_011508974.1 |