Product Details

SNP ID
rs61733220
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:74013467 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCAGGCAGGTTGAGGGGGAGCGAG[C/T]TAGGTCTGGGGCGACAAGGCCTTTG
Phenotype
MIM: 615944 MIM: 602044
Polymorphism
C/T, 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 7106 Missense Mutation AAC,AGC N2327S NP_001273506.1
NM_015531.5 7106 Intron NP_056346.3
XM_011544904.1 7106 Missense Mutation AAC,AGC N2337S XP_011543206.1
XM_011544905.1 7106 Intron XP_011543207.1
XM_017017510.1 7106 Intron XP_016872999.1
XM_017017511.1 7106 Missense Mutation AAC,AGC N2144S XP_016873000.1
XM_017017512.1 7106 Missense Mutation AAC,AGC N1814S XP_016873001.1
XM_017017513.1 7106 Missense Mutation AAC,AGC N1696S XP_016873002.1
XM_017017514.1 7106 Intron XP_016873003.1
XM_017017515.1 7106 Missense Mutation AAC,AGC N1435S XP_016873004.1
XM_017017516.1 7106 Missense Mutation AAC,AGC N1395S XP_016873005.1
Gene
UCP3
Gene Name
uncoupling protein 3
There are no transcripts associated with this gene.

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