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SNP ID: rs113477098
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:68301112 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTGGAAAAGACTCACTCCCCTAAC[A/G]TAAGTTTTCACTGTGGTGGGATGGT
Phenotype: MIM: 610087 MIM: 605641
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: PRMT7 PubMed Links

Gene Details

Gene: PRMT7
Gene Name: protein arginine methyltransferase 7

There are no transcripts associated with this gene.

Gene: SLC7A6
Gene Name: solute carrier family 7 member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001076785.2	1132	UTR 3			NP_001070253.1
NM_003983.5	1132	UTR 3			NP_003974.3
XM_011523433.1	1132	UTR 3			XP_011521735.1
XM_011523434.1	1132	UTR 3			XP_011521736.1
XM_011523438.1	1132	UTR 3			XP_011521740.1
XM_011523439.1	1132	UTR 3			XP_011521741.1
XM_017023851.1	1132	UTR 3			XP_016879340.1

Gene: SLC7A6OS
Gene Name: solute carrier family 7 member 6 opposite strand

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032178.2	1132	UTR 3			NP_115554.2
XM_011523372.2	1132	Intron			XP_011521674.1

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