Product Details

SNP ID

rs17552409

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:100398175 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTAGGAACGCTCCTGTAAATGGA[A/G]TAATGGAATTTTTAAATGTGAGAGA

Phenotype

MIM: 608350

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

EMCN PubMed Links

Additional Information

For this assay, SNP(s) [rs74410782] 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

EMCN

Gene Name

endomucin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001159694.1	1203	UTR 3			NP_001153166.1
NM_016242.3	1203	UTR 3			NP_057326.2
XM_011532024.2	1203	Intron			XP_011530326.1
XM_017008290.1	1203	Intron			XP_016863779.1

Gene

SNORA101A

Gene Name

small nucleolar RNA, H/ACA box 101A

There are no transcripts associated with this gene.

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