Product Details

SNP ID

rs61737506

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:174398334 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCGTGGCATTACCTCCAGCAACAGT[C/T]GATAACAGGATTATTTTTGGAAAAA

Phenotype

MIM: 605228 MIM: 614967

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CIR1 PubMed Links

Additional Information

For this assay, SNP(s) [rs10497410] are located under a probe 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

CIR1

Gene Name

corepressor interacting with RBPJ, 1

There are no transcripts associated with this gene.

Gene

SCRN3

Gene Name

secernin 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001193528.1	1146	Intron			NP_001180457.1
NM_024583.4	1146	Silent Mutation	GTC,GTT	V17V	NP_078859.2
XM_005246853.2	1146	Silent Mutation	GTC,GTT	V37V	XP_005246910.1
XM_005246854.4	1146	Silent Mutation	GTC,GTT	V17V	XP_005246911.1
XM_005246855.2	1146	Silent Mutation	GTC,GTT	V17V	XP_005246912.1
XM_005246856.2	1146	Silent Mutation	GTC,GTT	V17V	XP_005246913.1
XM_005246857.2	1146	Silent Mutation	GTC,GTT	V17V	XP_005246914.1
XM_011511839.2	1146	Intron			XP_011510141.1
XM_017004909.1	1146	Silent Mutation	GTC,GTT	V17V	XP_016860398.1
XM_017004910.1	1146	Silent Mutation	GTC,GTT	V17V	XP_016860399.1

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