Product Details

SNP ID

rs1043159

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.20:3251385 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ATTCAGAAAACATTTACAGTTCAGG[C/T]AGCTGAGGCACTGAAGTCCTAAGAG

Phenotype

MIM: 614146 MIM: 610206

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C20orf194 PubMed Links

Additional Information

For this assay, SNP(s) [rs144617259] 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

C20orf194

Gene Name

chromosome 20 open reading frame 194

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001009984.2	4826	UTR 3			NP_001009984.1
XM_005260684.3	4826	UTR 3			XP_005260741.1
XM_005260687.4	4826	UTR 3			XP_005260744.1
XM_011529208.2	4826	UTR 3			XP_011527510.1
XM_017027783.1	4826	UTR 3			XP_016883272.1

Gene

SLC4A11

Gene Name

solute carrier family 4 member 11

There are no transcripts associated with this gene.

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