Product Details

SNP ID
rs140362028
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:43307869 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTCCAAAGAGAGCCCCATAGCATG[A/G]CTTGTGGCAGTATGGCCTCCCATTG
Phenotype
MIM: 604995
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CRIP3 PubMed Links

Gene Details

Gene
CRIP3
Gene Name
cysteine rich protein 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_206922.2 166 Missense Mutation CCA,TCA P56S NP_996805.2
XM_005249103.3 166 Missense Mutation CCA,TCA P56S XP_005249160.1
XM_011514609.2 166 Missense Mutation CCA,TCA P56S XP_011512911.1
XM_017010856.1 166 Missense Mutation CCA,TCA P56S XP_016866345.1
XM_017010857.1 166 Missense Mutation CCA,TCA P56S XP_016866346.1
Gene
SLC22A7
Gene Name
solute carrier family 22 member 7
There are no transcripts associated with this gene.

View Full Product Details