Product Details

SNP ID

rs141194619

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:128822367 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAATCCTACGTAAAGTACCAGGT[C/T]ATCGGCAAGAACCACGTGGCAGTGC

Phenotype

MIM: 600440

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ENDOG PubMed Links

Additional Information

For this assay, SNP(s) [rs2280844] 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

ENDOG

Gene Name

endonuclease G

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004435.2	1570	Silent Mutation	GTC,GTT	V217V	NP_004426.2
XM_011518347.2	1570	UTR 3			XP_011516649.1

Gene

SPOUT1

Gene Name

SPOUT domain containing methyltransferase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016390.3	1570	UTR 3			NP_057474.2
XM_017014804.1	1570	UTR 3			XP_016870293.1

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