Product Details

SNP ID

rs35103191

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:80262063 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGTTTTCTGGTCTGTGGTTCCCCA[G/T]TGTAGCATTGGAGAAGGAAACACTT

Phenotype

MIM: 613768 MIM: 610117

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

RNF213 PubMed Links

Additional Information

For this assay, SNP(s) [rs143410054] 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

RNF213

Gene Name

ring finger protein 213

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256071.2		Intron			NP_001243000.2
NM_020954.3		Intron			NP_066005.2
XM_005257545.4		Intron			XP_005257602.2
XM_005257546.4		Intron			XP_005257603.2
XM_006721995.3		Intron			XP_006722058.1
XM_011525084.2		Intron			XP_011523386.1
XM_011525086.2		Intron			XP_011523388.1
XM_011525087.2		Intron			XP_011523389.1
XM_017024905.1		Intron			XP_016880394.1

Gene

SLC26A11

Gene Name

solute carrier family 26 member 11

There are no transcripts associated with this gene.

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