Product Details

SNP ID

rs6962301

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:155648503 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCATTCGAAATTGTGAAAGTGAAA[C/T]AAGTTTTAGTACTTCAACAGGTAAA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

LOC100506302 PubMed Links

Additional Information

For this assay, SNP(s) [rs115196199] 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.

Gene Details

Gene

LOC100506302

Gene Name

uncharacterized LOC100506302

There are no transcripts associated with this gene.

Gene

RBM33

Gene Name

RNA binding motif protein 33

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_053043.2		Intron			NP_444271.2
XM_005249531.1		Intron			XP_005249588.1
XM_005249532.1		Intron			XP_005249589.1
XM_005249533.1		Intron			XP_005249590.1
XM_005249534.1		Intron			XP_005249591.1
XM_005249535.1		Intron			XP_005249592.1
XM_011515840.1		Intron			XP_011514142.1

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