Product Details

SNP ID

rs62246398

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:47024713 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCCTCAATGCAACAAATACTCTA[A/C]AACTACTATTTTAACATAACATAGT

Phenotype

MIM: 612778

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SETD2 PubMed Links

Gene Details

Gene

SETD2

Gene Name

SET domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014159.6		Intron			NP_054878.5
XM_011533631.2		Intron			XP_011531933.1
XM_011533632.2		Intron			XP_011531934.1
XM_011533633.2		Intron			XP_011531935.1
XM_011533634.1		Intron			XP_011531936.1
XM_017006270.1		Intron			XP_016861759.1

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