Product Details

SNP ID

rs665461

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:144287456 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTGTCCGCTTGGCTTCCTTTTCT[A/G]CTATCTCAATCGTTCCTAGGTTTTG

Phenotype

MIM: 128240

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

UTRN PubMed Links

Additional Information

For this assay, SNP(s) [rs76176754] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

UTRN

Gene Name

utrophin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007124.2		Intron			NP_009055.2
XM_005267127.4		Intron			XP_005267184.1
XM_005267130.2		Intron			XP_005267187.1
XM_005267133.2		Intron			XP_005267190.1
XM_006715560.3		Intron			XP_006715623.1
XM_011536101.2		Intron			XP_011534403.1
XM_011536102.2		Intron			XP_011534404.1
XM_011536106.2		Intron			XP_011534408.1
XM_011536107.2		Intron			XP_011534409.1
XM_011536109.2		Intron			XP_011534411.1
XM_017011243.1		Intron			XP_016866732.1
XM_017011244.1		Intron			XP_016866733.1
XM_017011245.1		Intron			XP_016866734.1

View Full Product Details