Product Details

SNP ID

rs16827019

Assay Type

Functionally tested

NCBI dbSNP Submissions

22

Location

Chr.1:40172082 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTATTTAAGAAATAAATGCATGGTA[C/T]TCCATCAGAAATTGCATTGATTTTA

Phenotype

MIM: 180610

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RLF PubMed Links

Gene Details

Gene

RLF

Gene Name

rearranged L-myc fusion

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012421.3		Intron			NP_036553.2
XM_017002016.1		Intron			XP_016857505.1
XM_017002017.1		Intron			XP_016857506.1
XM_017002018.1		Intron			XP_016857507.1

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