Product Details
- SNP ID
-
rs139334295
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:81875811 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGACGCCCAACCGGATTAGCACTCG[C/T]CTGACCACCATCACGCGGGCGCCCA
- Phenotype
-
MIM: 605533
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
NRG3
PubMed Links
Gene Details
- Gene
- NRG3
- Gene Name
- neuregulin 3
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001010848.3 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
NP_001010848.2 |
| NM_001165972.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
NP_001159444.1 |
| NM_001165973.1 |
501 |
Intron |
|
|
NP_001159445.1 |
| XM_005269444.4 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_005269501.1 |
| XM_011539172.2 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_011537474.1 |
| XM_011539173.2 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_011537475.1 |
| XM_011539175.2 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_011537477.1 |
| XM_011539178.2 |
501 |
Intron |
|
|
XP_011537480.1 |
| XM_017015573.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016871062.1 |
| XM_017015574.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016871063.1 |
| XM_017015575.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016871064.1 |
| XM_017015576.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016871065.1 |
| XM_017015577.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016871066.1 |
| XM_017015578.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016871067.1 |
| XM_017015579.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016871068.1 |
| XM_017015580.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016871069.1 |
| XM_017015581.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016871070.1 |
| XM_017015582.1 |
501 |
Intron |
|
|
XP_016871071.1 |
| XM_017015583.1 |
501 |
Intron |
|
|
XP_016871072.1 |
| XM_017015584.1 |
501 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016871073.1 |
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