Product Details

SNP ID
rs4863656
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:139496517 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTACACGTTCCCAGGTGATTCTTCT[C/G]GCCACTGAAATTGGAGAAGCAACTG
Phenotype
MIM: 606594
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SETD7 PubMed Links

Gene Details

Gene
SETD7
Gene Name
SET domain containing lysine methyltransferase 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001306199.1 1557 Missense Mutation CAG,GAG Q309E NP_001293128.1
NM_001306200.1 1557 Intron NP_001293129.1
NM_030648.3 1557 Intron NP_085151.1
XM_017008661.1 1557 Intron XP_016864150.1

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