Product Details
- SNP ID
-
rs941952
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:104093286 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- CTGCTGGGAGTGGCCCATCCTGACC[C/T]ACGTCCTTGCCTCTGTGGGGAGCTC
- Phenotype
-
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
ASPG
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs45487897] 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
- ASPG
- Gene Name
- asparaginase
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001080464.2 |
539 |
Intron |
|
|
NP_001073933.2 |
XM_005267590.4 |
539 |
Intron |
|
|
XP_005267647.1 |
XM_017021265.1 |
539 |
Missense Mutation |
CCA,CTA |
P24L |
XP_016876754.1 |
XM_017021266.1 |
539 |
Missense Mutation |
CCA,CTA |
P24L |
XP_016876755.1 |
XM_017021267.1 |
539 |
Missense Mutation |
CCA,CTA |
P24L |
XP_016876756.1 |
XM_017021268.1 |
539 |
Intron |
|
|
XP_016876757.1 |
XM_017021269.1 |
539 |
Missense Mutation |
CCA,CTA |
P24L |
XP_016876758.1 |
XM_017021270.1 |
539 |
Missense Mutation |
CCA,CTA |
P24L |
XP_016876759.1 |
XM_017021271.1 |
539 |
Missense Mutation |
CCA,CTA |
P24L |
XP_016876760.1 |
XM_017021272.1 |
539 |
Missense Mutation |
CCA,CTA |
P24L |
XP_016876761.1 |
XM_017021273.1 |
539 |
Missense Mutation |
CCA,CTA |
P24L |
XP_016876762.1 |
XM_017021274.1 |
539 |
Intron |
|
|
XP_016876763.1 |
XM_017021275.1 |
539 |
Missense Mutation |
CCA,CTA |
P24L |
XP_016876764.1 |
XM_017021276.1 |
539 |
Missense Mutation |
CCA,CTA |
P24L |
XP_016876765.1 |
- Gene
- LOC105370691
- Gene Name
- uncharacterized LOC105370691
There are no transcripts associated with this gene.
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