Product Details

SNP ID

rs12996213

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:121220881 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTCATAAGCTATAAGCTTTAACT[A/C]CAACCACGAGAAGGTAAGAAGAGCA

Phenotype

MIM: 609785

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

TFCP2L1 PubMed Links

Additional Information

For this assay, SNP(s) [rs116740749] 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

TFCP2L1

Gene Name

transcription factor CP2-like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014553.2	4300	UTR 3			NP_055368.1
XM_017003902.1	4300	UTR 3			XP_016859391.1
XM_017003903.1	4300	UTR 3			XP_016859392.1
XM_017003904.1	4300	Intron			XP_016859393.1
XM_017003905.1	4300	Intron			XP_016859394.1

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