Product Details

SNP ID

rs149170494

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:68316074 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATGATTACCACCAGGAGATTGCAA[C/G]GTACTGGGTTGGTTTACAGCAGGCT

Phenotype

MIM: 610087

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

PRMT7 PubMed Links

Gene Details

Gene

PRMT7

Gene Name

protein arginine methyltransferase 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184824.1	236	Missense Mutation	ACG,AGG	T32R	NP_001171753.1
NM_001290018.1	236	Missense Mutation	ACG,AGG	T32R	NP_001276947.1
NM_019023.2	236	Missense Mutation	ACG,AGG	T32R	NP_061896.1
XM_011523112.2	236	Missense Mutation	ACG,AGG	T32R	XP_011521414.1
XM_011523113.2	236	Missense Mutation	ACG,AGG	T32R	XP_011521415.1
XM_011523115.2	236	Missense Mutation	ACG,AGG	T32R	XP_011521417.1
XM_011523116.2	236	Missense Mutation	ACG,AGG	T32R	XP_011521418.1
XM_011523121.2	236	Missense Mutation	CAA,GAA	Q12E	XP_011521423.1
XM_011523124.2	236	UTR 5			XP_011521426.1
XM_011523125.2	236	UTR 5			XP_011521427.1
XM_011523126.2	236	UTR 5			XP_011521428.1
XM_011523128.2	236	UTR 5			XP_011521430.1
XM_011523131.2	236	UTR 5			XP_011521433.1
XM_017023290.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878779.1
XM_017023291.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878780.1
XM_017023292.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878781.1
XM_017023293.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878782.1
XM_017023294.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878783.1
XM_017023295.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878784.1
XM_017023296.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878785.1
XM_017023297.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878786.1
XM_017023298.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878787.1
XM_017023299.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878788.1
XM_017023300.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878789.1
XM_017023301.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878790.1
XM_017023302.1	236	UTR 5			XP_016878791.1
XM_017023303.1	236	UTR 5			XP_016878792.1
XM_017023304.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878793.1
XM_017023305.1	236	Missense Mutation	CAA,GAA	Q12E	XP_016878794.1
XM_017023306.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878795.1
XM_017023307.1	236	UTR 5			XP_016878796.1
XM_017023308.1	236	UTR 5			XP_016878797.1
XM_017023309.1	236	UTR 5			XP_016878798.1
XM_017023310.1	236	UTR 5			XP_016878799.1
XM_017023311.1	236	UTR 5			XP_016878800.1
XM_017023312.1	236	Missense Mutation	ACG,AGG	T32R	XP_016878801.1
XM_017023313.1	236	UTR 5			XP_016878802.1
XM_017023314.1	236	UTR 5			XP_016878803.1
XM_017023315.1	236	UTR 5			XP_016878804.1
XM_017023316.1	236	UTR 5			XP_016878805.1

Gene

SLC7A6OS

Gene Name

solute carrier family 7 member 6 opposite strand

There are no transcripts associated with this gene.

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