Product Details

SNP ID

rs1612422

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:138348852 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGTCGCTTTGTTCCGGGGCGGGAG[G/T]TGTGGCCGCCCTCCGGGCTCGGCCG

Phenotype

MIM: 608435

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

MRAS PubMed Links

Additional Information

For this assay, SNP(s) [rs569475578] 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

MRAS

Gene Name

muscle RAS oncogene homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001085049.2	3	Intron			NP_001078518.1
NM_001252090.1	3	Intron			NP_001239019.1
NM_001252091.1	3	Intron			NP_001239020.1
NM_001252092.1	3	UTR 5			NP_001239021.1
NM_001252093.1	3	Intron			NP_001239022.1
NM_012219.4	3	Intron			NP_036351.3
XM_005247228.1	3	UTR 5			XP_005247285.1
XM_005247229.2	3	Intron			XP_005247286.1
XM_017005887.1	3	Intron			XP_016861376.1

View Full Product Details