Product Details

SNP ID

rs34889455

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:26297006 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAAGATTAGATCCCTGACTCATAC[A/C]ATTCACAAAAGTAAATTCCATTTAA

Phenotype

MIM: 614780

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SNX10 PubMed Links

Additional Information

For this assay, SNP(s) [rs5883023] 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

SNX10

Gene Name

sorting nexin 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199835.1		Intron			NP_001186764.1
NM_001199837.1		Intron			NP_001186766.1
NM_001199838.1		Intron			NP_001186767.1
NM_001318198.1		Intron			NP_001305127.1
NM_001318199.1		Intron			NP_001305128.1
NM_013322.2		Intron			NP_037454.2
XM_006715712.2		Intron			XP_006715775.1
XM_017012085.1		Intron			XP_016867574.1
XM_017012086.1		Intron			XP_016867575.1
XM_017012087.1		Intron			XP_016867576.1
XM_017012088.1		Intron			XP_016867577.1

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