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AATGTAAAATACTACCAAGGTATCC[A/G]GGCTGCCGTGAGCAGGGTGAAGGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610087 | ||||||||||||||||||||
Literature Links: |
PRMT7 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 |
PRMT7 - protein arginine methyltransferase 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184824.1 | 262 | Intron | NP_001171753.1 | |||
NM_001290018.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | NP_001276947.1 | |
NM_019023.2 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | NP_061896.1 | |
XM_011523112.2 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_011521414.1 | |
XM_011523113.2 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_011521415.1 | |
XM_011523115.2 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_011521417.1 | |
XM_011523116.2 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_011521418.1 | |
XM_011523121.2 | 262 | Silent Mutation | CCA,CCG | P,P 20 | XP_011521423.1 | |
XM_011523124.2 | 262 | UTR 5 | XP_011521426.1 | |||
XM_011523125.2 | 262 | UTR 5 | XP_011521427.1 | |||
XM_011523126.2 | 262 | UTR 5 | XP_011521428.1 | |||
XM_011523128.2 | 262 | UTR 5 | XP_011521430.1 | |||
XM_011523131.2 | 262 | UTR 5 | XP_011521433.1 | |||
XM_017023290.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878779.1 | |
XM_017023291.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878780.1 | |
XM_017023292.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878781.1 | |
XM_017023293.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878782.1 | |
XM_017023294.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878783.1 | |
XM_017023295.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878784.1 | |
XM_017023296.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878785.1 | |
XM_017023297.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878786.1 | |
XM_017023298.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878787.1 | |
XM_017023299.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878788.1 | |
XM_017023300.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878789.1 | |
XM_017023301.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878790.1 | |
XM_017023302.1 | 262 | UTR 5 | XP_016878791.1 | |||
XM_017023303.1 | 262 | UTR 5 | XP_016878792.1 | |||
XM_017023304.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878793.1 | |
XM_017023305.1 | 262 | Silent Mutation | CCA,CCG | P,P 20 | XP_016878794.1 | |
XM_017023306.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878795.1 | |
XM_017023307.1 | 262 | UTR 5 | XP_016878796.1 | |||
XM_017023308.1 | 262 | UTR 5 | XP_016878797.1 | |||
XM_017023309.1 | 262 | UTR 5 | XP_016878798.1 | |||
XM_017023310.1 | 262 | UTR 5 | XP_016878799.1 | |||
XM_017023311.1 | 262 | UTR 5 | XP_016878800.1 | |||
XM_017023312.1 | 262 | Missense Mutation | CAG,CGG | Q,R 53 | XP_016878801.1 | |
XM_017023313.1 | 262 | UTR 5 | XP_016878802.1 | |||
XM_017023314.1 | 262 | UTR 5 | XP_016878803.1 | |||
XM_017023315.1 | 262 | UTR 5 | XP_016878804.1 | |||
XM_017023316.1 | 262 | UTR 5 | XP_016878805.1 |