Product Details

SNP ID

rs904643

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:124301507 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCCTCCAGTGCTCGGCCTCCCTG[C/T]GGGGCACGGTACATGGACTGTGGAC

Phenotype

MIM: 615927

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM101A PubMed Links

Additional Information

For this assay, SNP(s) [rs77263762] 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

FAM101A

Gene Name

family with sequence similarity 101 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_181709.4		Intron			NP_859060.3

Gene

LOC105370045

Gene Name

filamin-interacting protein FAM101A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011539088.1		Intron			XP_011537390.1

Gene

ZNF664-FAM101A

Gene Name

filamin-interacting protein FAM101A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001204299.1		Intron			NP_001191228.1

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