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TTACCCTGAGCTTGCCAATACCTTC[A/G]CCATCTGCTCGTGCATCAAAAACTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610937 | ||||||||||||||||||||
Literature Links: |
RPGRIP1L 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 |
RPGRIP1L - RPGRIP1 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005255867.1 | 3902 | Silent Mutation | GGC,GGT | G,G 1252 | XP_005255924.1 | |
XM_005255868.1 | 3902 | Silent Mutation | GGC,GGT | G,G 1244 | XP_005255925.1 | |
XM_011522970.1 | 3902 | Intron | XP_011521272.1 | |||
XM_011522971.2 | 3902 | Intron | XP_011521273.1 | |||
XM_011522973.2 | 3902 | Intron | XP_011521275.1 | |||
XM_017023094.1 | 3902 | Silent Mutation | GGC,GGT | G,G 1290 | XP_016878583.1 | |
XM_017023095.1 | 3902 | Silent Mutation | GGC,GGT | G,G 1210 | XP_016878584.1 | |
XM_017023096.1 | 3902 | Intron | XP_016878585.1 | |||
XM_017023097.1 | 3902 | Intron | XP_016878586.1 | |||
XM_017023098.1 | 3902 | Silent Mutation | GGC,GGT | G,G 701 | XP_016878587.1 | |
XM_017023099.1 | 3902 | Silent Mutation | GGC,GGT | G,G 701 | XP_016878588.1 | |
XM_017023100.1 | 3902 | Intron | XP_016878589.1 |