Product Details

SNP ID

rs35772513

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:62710461 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATCTTGGCAGAGCCCCAGCCTGTT[G/T]TCTTAATTGAGAGCTCAGGGTCTAA

Phenotype

MIM: 613337

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

LOC105371855 PubMed Links

Additional Information

For this assay, SNP(s) [rs111749478] 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

LOC105371855

Gene Name

uncharacterized LOC105371855

There are no transcripts associated with this gene.

Gene

MARCH10

Gene Name

membrane associated ring-CH-type finger 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001100875.2		Intron			NP_001094345.1
NM_001288779.1		Intron			NP_001275708.1
NM_001288780.1		Intron			NP_001275709.1
NM_152598.3		Intron			NP_689811.2
XM_005257095.2		Intron			XP_005257152.2
XM_005257096.2		Intron			XP_005257153.2
XM_005257097.3		Intron			XP_005257154.2
XM_005257098.2		Intron			XP_005257155.2
XM_005257100.2		Intron			XP_005257157.2
XM_005257102.2		Intron			XP_005257159.2
XM_005257103.1		Intron			XP_005257160.1
XM_005257106.4		Intron			XP_005257163.2
XM_011524435.1		Intron			XP_011522737.1
XM_011524436.1		Intron			XP_011522738.1
XM_011524437.1		Intron			XP_011522739.1

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