Genomic Map

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Assay Details

Species:	Human
dbSNP Submissions:	NA
Phenotype:	MIM: 608435
Literature Links:	MRAS PubMed Links
Allele Nomenclature:
Minor Allele Frequency:

1000Genome

Applied Biosystems^®

HapMap

Global

C (0.38)

(0.62)

Caucasian

G (0.31)

(0.69)

CEPH (CEU) - Not Available

EAS

C (0.27)

(0.73)

African American

G (0.49)

(0.51)

YRI (Yoruba)

T (0.34)

(0.66)

SAS

C (0.29)

(0.71)

Chinese - Not Available

JPT (Japanese)

C (0.39)

(0.61)

AFR

T (0.38)

(0.62)

Japanese - Not Available

CHB (Han Chinese)

C (0.16)

(0.84)

EUR

C (0.33)

(0.67)

AMR

C (0.25)

(0.75)

MRAS - muscle RAS oncogene homolog
Transcript Accession	SNP Location	SNP Type	Observed Codons	Observed Amino Acid	Protein ID
NM_001085049.2		Intron			NP_001078518.1
NM_001252090.1		Intron			NP_001239019.1
NM_001252091.1		Intron			NP_001239020.1
NM_001252092.1		Intron			NP_001239021.1
NM_001252093.1		Intron			NP_001239022.1
NM_012219.4		Intron			NP_036351.3
XM_005247228.1		Intron			XP_005247285.1
XM_005247229.2		Intron			XP_005247286.1
XM_017005887.1		Intron			XP_016861376.1

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More Information

Additional Information:

For this assay, SNP(s) [rs9289557] 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.