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
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