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Search Thermo Fisher Scientific
ACTCCCTGCGGCCCTCCTCACTCTC[C/T]AGGACCCTGTCCACACATGCAGGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610087 MIM: 605777 | ||||||||||||||||||||
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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There are no transcripts associated with this gene. |
SMPD3 - sphingomyelin phosphodiesterase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018667.3 | 2538 | Silent Mutation | CTA,CTG | L,L 572 | NP_061137.1 | |
XM_005256031.3 | 2538 | Silent Mutation | CTA,CTG | L,L 572 | XP_005256088.1 | |
XM_005256032.3 | 2538 | Silent Mutation | CTA,CTG | L,L 572 | XP_005256089.1 | |
XM_011523207.1 | 2538 | Silent Mutation | CTA,CTG | L,L 572 | XP_011521509.1 | |
XM_011523208.2 | 2538 | Silent Mutation | CTA,CTG | L,L 572 | XP_011521510.1 | |
XM_011523209.2 | 2538 | Silent Mutation | CTA,CTG | L,L 572 | XP_011521511.1 | |
XM_011523210.2 | 2538 | Intron | XP_011521512.1 | |||
XM_017023405.1 | 2538 | Silent Mutation | CTA,CTG | L,L 572 | XP_016878894.1 | |
XM_017023406.1 | 2538 | Silent Mutation | CTA,CTG | L,L 572 | XP_016878895.1 | |
XM_017023407.1 | 2538 | Silent Mutation | CTA,CTG | L,L 572 | XP_016878896.1 | |
XM_017023408.1 | 2538 | Silent Mutation | CTA,CTG | L,L 572 | XP_016878897.1 |