Product Details

SNP ID
rs200185512
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:43308367 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGTGGCAGCGCTCACATTTCAGG[A/C]AGAAGCGGTGCCAGTTCTTGCCCAG
Phenotype
MIM: 604995
Polymorphism
A/C, Transversion 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 86 Missense Mutation TGC,TTC C29F NP_996805.2
XM_005249103.3 86 Missense Mutation TGC,TTC C29F XP_005249160.1
XM_011514609.2 86 Missense Mutation TGC,TTC C29F XP_011512911.1
XM_017010856.1 86 Missense Mutation TGC,TTC C29F XP_016866345.1
XM_017010857.1 86 Missense Mutation TGC,TTC C29F XP_016866346.1
Gene
SLC22A7
Gene Name
solute carrier family 22 member 7
There are no transcripts associated with this gene.

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