Product Details
- SNP ID
-
rs145193373
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:28113122 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGTCGGCGATGGTCCTGGGCAGCCT[C/T]GTCCGGCCCCAGACGAAGCGAAGGA
- 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 |
7619 |
Silent Mutation |
ACA,ACG |
T4727T |
NP_004658.3 |
| XM_005268276.4 |
7619 |
Silent Mutation |
ACA,ACG |
T4689T |
XP_005268333.1 |
| XM_006720726.3 |
7619 |
Silent Mutation |
ACA,ACG |
T4722T |
XP_006720789.1 |
| XM_006720727.3 |
7619 |
Silent Mutation |
ACA,ACG |
T4641T |
XP_006720790.1 |
| XM_011522131.2 |
7619 |
Silent Mutation |
ACA,ACG |
T4566T |
XP_011520433.1 |
| XM_011522133.2 |
7619 |
Silent Mutation |
ACA,ACG |
T3642T |
XP_011520435.1 |
| XM_017022695.1 |
7619 |
Silent Mutation |
ACA,ACG |
T4689T |
XP_016878184.1 |
| XM_017022696.1 |
7619 |
Silent Mutation |
ACA,ACG |
T4689T |
XP_016878185.1 |
| XM_017022697.1 |
7619 |
Silent Mutation |
ACA,ACG |
T2449T |
XP_016878186.1 |
| XM_017022698.1 |
7619 |
Silent Mutation |
ACA,ACG |
T2449T |
XP_016878187.1 |
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