Product Details

SNP ID

rs4849842

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:120255090 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAGTTAGAAACATCATTAGAGACC[A/T]TTCTTGAAAGCTAAATTTGGAGACA

Phenotype

MIM: 179551

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

RALB PubMed Links

Additional Information

For this assay, SNP(s) [rs138292165] 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

RALB

Gene Name

RALB Ras like proto-oncogene B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002881.2		Intron			NP_002872.1
XM_005263724.1		Intron			XP_005263781.1
XM_005263727.1		Intron			XP_005263784.1
XM_005263728.1		Intron			XP_005263785.1
XM_005263729.2		Intron			XP_005263786.1
XM_011511573.1		Intron			XP_011509875.1
XM_011511574.1		Intron			XP_011509876.1
XM_017004621.1		Intron			XP_016860110.1
XM_017004622.1		Intron			XP_016860111.1

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