Product Details

SNP ID
rs1726757
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:74017552 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGAAAGAAAATGTGGGGCTTCCTG[A/G]GGCTCTTCAAATTGAGTGGCTAACC
Phenotype
MIM: 615944 MIM: 602044
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C2CD3 PubMed Links

Gene Details

Gene
C2CD3
Gene Name
C2 calcium dependent domain containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286577.1 Intron NP_001273506.1
NM_015531.5 Intron NP_056346.3
XM_011544904.1 Intron XP_011543206.1
XM_011544905.1 Intron XP_011543207.1
XM_017017510.1 Intron XP_016872999.1
XM_017017511.1 Intron XP_016873000.1
XM_017017512.1 Intron XP_016873001.1
XM_017017513.1 Intron XP_016873002.1
XM_017017514.1 Intron XP_016873003.1
XM_017017515.1 Intron XP_016873004.1
XM_017017516.1 Intron XP_016873005.1
Gene
UCP3
Gene Name
uncoupling protein 3
There are no transcripts associated with this gene.

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