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TCACTGTTCTCGTCATCTTCATCGT[C/T]GTAAATGTCCTCTGGTTCTTGATCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610087 MIM: 605641 | ||||||||||||||||||||
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. |
SLC7A6 - solute carrier family 7 member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001076785.2 | 751 | Intron | NP_001070253.1 | |||
NM_003983.5 | 751 | Intron | NP_003974.3 | |||
XM_011523433.1 | 751 | Intron | XP_011521735.1 | |||
XM_011523434.1 | 751 | Intron | XP_011521736.1 | |||
XM_011523438.1 | 751 | Intron | XP_011521740.1 | |||
XM_011523439.1 | 751 | Intron | XP_011521741.1 | |||
XM_017023851.1 | 751 | Intron | XP_016879340.1 |
SLC7A6OS - solute carrier family 7 member 6 opposite strand | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032178.2 | 751 | Missense Mutation | AAC,GAC | N,D 238 | NP_115554.2 | |
XM_011523372.2 | 751 | UTR 3 | XP_011521674.1 |