Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTATGCGCTGTGATCGCGGGCCTCT[A/G]CCTGCTGCTGGTGCCCACTGCCGGG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
PROM2 - prominin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001165977.2 | 469 | Missense Mutation | TAC,TGC | Y,C 116 | NP_001159449.1 | |
NM_001165978.2 | 469 | Missense Mutation | TAC,TGC | Y,C 116 | NP_001159450.1 | |
NM_001321070.1 | 469 | UTR 5 | NP_001307999.1 | |||
NM_144707.3 | 469 | Missense Mutation | TAC,TGC | Y,C 116 | NP_653308.2 | |
XM_006712301.2 | 469 | Intron | XP_006712364.1 | |||
XM_011510672.2 | 469 | Missense Mutation | TAC,TGC | Y,C 116 | XP_011508974.1 |