Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCCTTGTATTCAGCCCCAGGCATA[A/G]CCTTCTTGGCCACAGGGCGATGAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
RRP12 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 |
RRP12 - ribosomal RNA processing 12 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145114.1 | 3819 | Missense Mutation | GCT,GTT | A,V 1166 | NP_001138586.1 | |
NM_001284337.1 | 3819 | Missense Mutation | GCT,GTT | A,V 1127 | NP_001271266.1 | |
NM_015179.3 | 3819 | Missense Mutation | GCT,GTT | A,V 1227 | NP_055994.2 | |
XM_011539555.1 | 3819 | Missense Mutation | GCT,GTT | A,V 1199 | XP_011537857.1 | |
XM_011539556.2 | 3819 | Intron | XP_011537858.1 |