Product Details

SNP ID

rs143932195

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:63555836 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGTTCCTGACCTCGGACCTGAGTC[C/T]GCACCTGCTCAAGCGCCACCACGCC

Phenotype

MIM: 611265

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FNDC11 PubMed Links

Additional Information

For this assay, SNP(s) [rs3746348] 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

FNDC11

Gene Name

fibronectin type III domain containing 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001319152.1	249	Missense Mutation	CCG,CTG	P58L	NP_001306081.1
NM_001319153.1	249	Missense Mutation	CCG,CTG	P58L	NP_001306082.1
NM_024059.3	249	Missense Mutation	CCG,CTG	P58L	NP_076964.1
XM_011529041.2	249	Missense Mutation	CCG,CTG	P58L	XP_011527343.1
XM_017028060.1	249	Missense Mutation	CCG,CTG	P63L	XP_016883549.1

Gene

HELZ2

Gene Name

helicase with zinc finger 2

There are no transcripts associated with this gene.

Gene

SRMS

Gene Name

src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites

There are no transcripts associated with this gene.

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