Product Details

SNP ID

rs202209402

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:62666399 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCCTCCAACCGTGCCCACAGGCT[C/T]ACTGGCTGATAGTTGCCTGGCGGAC

Phenotype

MIM: 616097

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C11orf98 PubMed Links

Additional Information

For this assay, SNP(s) [rs531793220] 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

C11orf98

Gene Name

chromosome 11 open reading frame 98

There are no transcripts associated with this gene.

Gene

LBHD1

Gene Name

LBH domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024099.3	699	Intron			NP_077004.2

Gene

METTL12

Gene Name

methyltransferase like 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001043229.1	699	Missense Mutation	TCA,TTA	S24L	NP_001036694.1
XM_005274232.4	699	Missense Mutation	TCA,TTA	S147L	XP_005274289.1

Gene

SNORA57

Gene Name

small nucleolar RNA, H/ACA box 57

There are no transcripts associated with this gene.

Gene

UQCC3

Gene Name

ubiquinol-cytochrome c reductase complex assembly factor 3

There are no transcripts associated with this gene.

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