Product Details

SNP ID

rs885095

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:126712981 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGCTGGCGGTCATCCACGTTCCTC[G/T]CTTTCTCTATATTCATGACAAGTCT

Phenotype

MIM: 615634

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CHCHD6 PubMed Links

Additional Information

For this assay, SNP(s) [rs142790602] 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

CHCHD6

Gene Name

coiled-coil-helix-coiled-coil-helix domain containing 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320610.1		Intron			NP_001307539.1
NM_032343.2		Intron			NP_115719.1
XM_011513234.1		Intron			XP_011511536.1
XM_011513235.2		Intron			XP_011511537.1
XM_017007320.1		Intron			XP_016862809.1
XM_017007321.1		Intron			XP_016862810.1
XM_017007322.1		Intron			XP_016862811.1

View Full Product Details