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CTTCTGGCCCGAGCTCTTGCTGGTG[A/G]GAAACGCCAGGTACTCCCTGCGGCC
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 | |||
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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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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 | 2576 | Missense Mutation | CCC,CTC | P,L 585 | NP_061137.1 | |
XM_005256031.3 | 2576 | Missense Mutation | CCC,CTC | P,L 585 | XP_005256088.1 | |
XM_005256032.3 | 2576 | Missense Mutation | CCC,CTC | P,L 585 | XP_005256089.1 | |
XM_011523207.1 | 2576 | Missense Mutation | CCC,CTC | P,L 585 | XP_011521509.1 | |
XM_011523208.2 | 2576 | Missense Mutation | CCC,CTC | P,L 585 | XP_011521510.1 | |
XM_011523209.2 | 2576 | Missense Mutation | CCC,CTC | P,L 585 | XP_011521511.1 | |
XM_011523210.2 | 2576 | Intron | XP_011521512.1 | |||
XM_017023405.1 | 2576 | Missense Mutation | CCC,CTC | P,L 585 | XP_016878894.1 | |
XM_017023406.1 | 2576 | Missense Mutation | CCC,CTC | P,L 585 | XP_016878895.1 | |
XM_017023407.1 | 2576 | Missense Mutation | CCC,CTC | P,L 585 | XP_016878896.1 | |
XM_017023408.1 | 2576 | Missense Mutation | CCC,CTC | P,L 585 | XP_016878897.1 |