Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCAGCTTCGGAAACGCCGAGGTCG[A/G]AAGCGTCGTTCTGACTTCACTCACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
GPATCH2L 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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GPATCH2L - G-patch domain containing 2 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322026.1 | 452 | Silent Mutation | CGA,CGG | R,R 45 | NP_001308955.1 | |
NM_001322027.1 | 452 | Silent Mutation | CGA,CGG | R,R 45 | NP_001308956.1 | |
NM_001322028.1 | 452 | Silent Mutation | CGA,CGG | R,R 45 | NP_001308957.1 | |
NM_001322029.1 | 452 | Silent Mutation | CGA,CGG | R,R 45 | NP_001308958.1 | |
NM_001322030.1 | 452 | Silent Mutation | CGA,CGG | R,R 45 | NP_001308959.1 | |
NM_001322031.1 | 452 | Silent Mutation | CGA,CGG | R,R 45 | NP_001308960.1 | |
NM_001322032.1 | 452 | Silent Mutation | CGA,CGG | R,R 45 | NP_001308961.1 | |
NM_017926.3 | 452 | Silent Mutation | CGA,CGG | R,R 45 | NP_060396.2 | |
NM_017972.3 | 452 | Silent Mutation | CGA,CGG | R,R 45 | NP_060442.2 | |
XM_006720191.2 | 452 | Silent Mutation | CGA,CGG | R,R 45 | XP_006720254.1 | |
XM_017021427.1 | 452 | Silent Mutation | CGA,CGG | R,R 58 | XP_016876916.1 | |
XM_017021428.1 | 452 | Silent Mutation | CGA,CGG | R,R 58 | XP_016876917.1 | |
XM_017021429.1 | 452 | Silent Mutation | CGA,CGG | R,R 58 | XP_016876918.1 | |
XM_017021430.1 | 452 | Silent Mutation | CGA,CGG | R,R 58 | XP_016876919.1 | |
XM_017021431.1 | 452 | Silent Mutation | CGA,CGG | R,R 58 | XP_016876920.1 | |
XM_017021432.1 | 452 | Silent Mutation | CGA,CGG | R,R 58 | XP_016876921.1 | |
XM_017021433.1 | 452 | Silent Mutation | CGA,CGG | R,R 45 | XP_016876922.1 |