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See other PRMT7 GT Assays ›
SNP ID:
rs8063446
Gene
PRMT7 SLC7A6 SLC7A6OS
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.16: 68310460 - 68310460 on Build GRCh38
Polymorphism:
A/C, Transversion substitution
Context Sequence [VIC/FAM]:

GTGTACTCGGACTCCTGGCCGCTCG[A/C]GGTGGTCCCCAAGGATCGGCGGCTG

Assay ID C__25939050_20
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 610087 MIM: 605641

Literature Links:

 PRMT7 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.11)
(0.89)
Caucasian - Not Available CEPH (CEU)
C (0.09)
(0.91)
EAS
C (0.06)
(0.94)
African American - Not Available YRI (Yoruba)
C (0.13)
(0.87)
SAS
C (0.12)
(0.88)
Chinese - Not Available JPT (Japanese)
C (0.06)
(0.94)
AFR
C (0.16)
(0.84)
Japanese - Not Available CHB (Han Chinese)
C (0.01)
(0.99)
EUR
C (0.13)
(0.87)
AMR
C (0.08)
(0.92)
PRMT7 - protein arginine methyltransferase 7
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001184824.1 385 Intron NP_001171753.1
NM_001290018.1 385 Intron NP_001276947.1
NM_019023.2 385 Intron NP_061896.1
XM_011523112.2 385 Intron XP_011521414.1
XM_011523113.2 385 Intron XP_011521415.1
XM_011523115.2 385 Intron XP_011521417.1
XM_011523116.2 385 Intron XP_011521418.1
XM_011523121.2 385 Intron XP_011521423.1
XM_011523124.2 385 Intron XP_011521426.1
XM_011523125.2 385 Intron XP_011521427.1
XM_011523126.2 385 Intron XP_011521428.1
XM_011523128.2 385 Intron XP_011521430.1
XM_011523131.2 385 Intron XP_011521433.1
XM_017023290.1 385 Intron XP_016878779.1
XM_017023291.1 385 Intron XP_016878780.1
XM_017023292.1 385 Intron XP_016878781.1
XM_017023293.1 385 Intron XP_016878782.1
XM_017023294.1 385 Intron XP_016878783.1
XM_017023295.1 385 Intron XP_016878784.1
XM_017023296.1 385 Intron XP_016878785.1
XM_017023297.1 385 Intron XP_016878786.1
XM_017023298.1 385 Intron XP_016878787.1
XM_017023299.1 385 Intron XP_016878788.1
XM_017023300.1 385 Intron XP_016878789.1
XM_017023301.1 385 Intron XP_016878790.1
XM_017023302.1 385 Intron XP_016878791.1
XM_017023303.1 385 Intron XP_016878792.1
XM_017023304.1 385 Intron XP_016878793.1
XM_017023305.1 385 Intron XP_016878794.1
XM_017023306.1 385 Intron XP_016878795.1
XM_017023307.1 385 Intron XP_016878796.1
XM_017023308.1 385 Intron XP_016878797.1
XM_017023309.1 385 Intron XP_016878798.1
XM_017023310.1 385 Intron XP_016878799.1
XM_017023311.1 385 Intron XP_016878800.1
XM_017023312.1 385 Intron XP_016878801.1
XM_017023313.1 385 Intron XP_016878802.1
XM_017023314.1 385 Intron XP_016878803.1
XM_017023315.1 385 Intron XP_016878804.1
XM_017023316.1 385 Intron XP_016878805.1
SLC7A6 - solute carrier family 7 member 6
There are no transcripts associated with this gene.
SLC7A6OS - solute carrier family 7 member 6 opposite strand
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_032178.2 385 Missense Mutation GCG,TCG A,S 116 NP_115554.2
XM_011523372.2 385 Missense Mutation GCG,TCG A,S 116 XP_011521674.1

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