Product Details

SNP ID
rs104893644
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:27092366 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGAGATGGCAGCGCGGAGGCAAC[A/G]CGTCCAACTCCTGCACCGTTCTCTC
Phenotype
MIM: 606137 MIM: 130660 MIM: 614058
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CGREF1 PubMed Links

Gene Details

Gene
CGREF1
Gene Name
cell growth regulator with EF-hand domain 1
There are no transcripts associated with this gene.

Gene
EMILIN1
Gene Name
elastin microfibril interfacer 1
There are no transcripts associated with this gene.

Gene
KHK
Gene Name
ketohexokinase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000221.2 649 Missense Mutation ACG,GCG T43A NP_000212.1
NM_006488.2 649 Missense Mutation ACG,GCG T43A NP_006479.1
XM_005264294.3 649 Missense Mutation ACG,GCG T43A XP_005264351.1
XM_005264296.3 649 Missense Mutation ACG,GCG T43A XP_005264353.1
XM_005264298.3 649 Intron XP_005264355.1
XM_006712008.3 649 Missense Mutation ACG,GCG T43A XP_006712071.1
XM_006712009.3 649 Missense Mutation ACG,GCG T43A XP_006712072.1
XM_006712010.3 649 Missense Mutation ACG,GCG T43A XP_006712073.1
XM_006712011.3 649 Missense Mutation ACG,GCG T43A XP_006712074.1
XM_006712012.3 649 Missense Mutation ACG,GCG T43A XP_006712075.1
XM_006712013.3 649 Missense Mutation ACG,GCG T43A XP_006712076.1
XM_006712014.3 649 Intron XP_006712077.1
XM_017004060.1 649 Missense Mutation ACG,GCG T43A XP_016859549.1
XM_017004061.1 649 Missense Mutation ACG,GCG T43A XP_016859550.1

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