Product Details

SNP ID

rs4258614

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:50668131 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGCACACAGGGCTGAACACTCGA[C/G]TTGGTGACCAGGAAACCAGGGAGCA

Phenotype

MIM: 613281

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

LOC101927272 PubMed Links

Additional Information

For this assay, SNP(s) [rs78629804] 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

LOC101927272

Gene Name

uncharacterized LOC101927272

There are no transcripts associated with this gene.

Gene

SNX20

Gene Name

sorting nexin 20

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001144972.1	1473	Intron			NP_001138444.1
NM_153337.2	1473	UTR 3			NP_699168.1
NM_182854.3	1473	Intron			NP_878274.1

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