Product Details

SNP ID

rs17661062

Assay Type

Functionally tested

NCBI dbSNP Submissions

19

Location

Chr.1:150929727 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCAAGGTAAATAATGAGGTAAGGG[A/T]GAAAGTACTGTACTTTGGGCTTACT

Phenotype

MIM: 604396

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

SETDB1 PubMed Links

Gene Details

Gene

SETDB1

Gene Name

SET domain bifurcated 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145415.1		Intron			NP_001138887.1
NM_001243491.1		Intron			NP_001230420.1
NM_012432.3		Intron			NP_036564.3
XM_005245641.3		Intron			XP_005245698.1
XM_017002953.1		Intron			XP_016858442.1
XM_017002954.1		Intron			XP_016858443.1
XM_017002955.1		Intron			XP_016858444.1

View Full Product Details