Product Details

SNP ID
rs137918449
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:28113185 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGTGTTGGAGAAGGACTCCATCAC[C/T]TCCCAGAACCACTGGATCAGCGATG
Phenotype
MIM: 605837
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HERC2 PubMed Links

Gene Details

Gene
HERC2
Gene Name
HECT and RLD domain containing E3 ubiquitin protein ligase 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004667.5 7556 Silent Mutation GAA,GAG E4706E NP_004658.3
XM_005268276.4 7556 Silent Mutation GAA,GAG E4668E XP_005268333.1
XM_006720726.3 7556 Silent Mutation GAA,GAG E4701E XP_006720789.1
XM_006720727.3 7556 Silent Mutation GAA,GAG E4620E XP_006720790.1
XM_011522131.2 7556 Silent Mutation GAA,GAG E4545E XP_011520433.1
XM_011522133.2 7556 Silent Mutation GAA,GAG E3621E XP_011520435.1
XM_017022695.1 7556 Silent Mutation GAA,GAG E4668E XP_016878184.1
XM_017022696.1 7556 Silent Mutation GAA,GAG E4668E XP_016878185.1
XM_017022697.1 7556 Silent Mutation GAA,GAG E2428E XP_016878186.1
XM_017022698.1 7556 Silent Mutation GAA,GAG E2428E XP_016878187.1

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