Product Details

SNP ID
rs63749888
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:102885221 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGACACATCTACATGTTTAGTTTCA[C/G]AATGGCTTCGGTTATTGCCTTTCCT
Phenotype
MIM: 611507 MIM: 611527
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
CISD2 PubMed Links
Additional Information
For this assay, SNP(s) [rs35282200] 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
CISD2
Gene Name
CDGSH iron sulfur domain 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001008388.4 1582 Missense Mutation CAA,GAA Q37E NP_001008389.1
Gene
SLC9B1
Gene Name
solute carrier family 9 member B1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001100874.2 1582 UTR 3 NP_001094344.1
NM_139173.3 1582 Intron NP_631912.2
XM_006714093.3 1582 Intron XP_006714156.1
XM_011531622.1 1582 Intron XP_011529924.1
XM_011531623.1 1582 Intron XP_011529925.1

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