Product Details

SNP ID
rs79796752
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:85354463 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCCCAAGTAAACTTTGCAGAGGAC[A/G]GCCAGCAGCAGCACAGCCAGGAGCA
Phenotype
MIM: 615427
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ELMOD3 PubMed Links

Gene Details

Gene
ELMOD3
Gene Name
ELMO domain containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135021.1 236 Intron NP_001128493.1
NM_001135022.1 236 Intron NP_001128494.1
NM_001135023.1 236 Intron NP_001128495.1
NM_032213.4 236 Intron NP_115589.2
XM_005264596.3 236 Intron XP_005264653.1
XM_005264597.3 236 UTR 5 XP_005264654.1
XM_005264598.3 236 Intron XP_005264655.1
XM_017005078.1 236 Intron XP_016860567.1
XM_017005079.1 236 Intron XP_016860568.1
Gene
RETSAT
Gene Name
retinol saturase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017750.3 236 Silent Mutation NP_060220.3

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