Product Details
- SNP ID
-
rs142712382
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:72163338 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCCAGTGCTCCTGGGCTCCTCCTCC[A/G]GCTCATCCTCCTCATAGACAGCATT
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
GRAMD2
PubMed Links
Gene Details
- Gene
- GRAMD2
- Gene Name
- GRAM domain containing 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001012642.2 |
1092 |
Missense Mutation |
CCG,CTG |
P295L |
NP_001012660.1 |
XM_011521327.2 |
1092 |
Missense Mutation |
CCG,CTG |
P294L |
XP_011519629.1 |
XM_011521328.2 |
1092 |
Missense Mutation |
CCG,CTG |
P293L |
XP_011519630.1 |
XM_011521329.2 |
1092 |
Missense Mutation |
CCG,CTG |
P285L |
XP_011519631.1 |
XM_011521330.2 |
1092 |
Missense Mutation |
CCG,CTG |
P283L |
XP_011519632.1 |
XM_011521331.2 |
1092 |
Missense Mutation |
CCG,CTG |
P276L |
XP_011519633.1 |
XM_011521332.2 |
1092 |
Missense Mutation |
CCG,CTG |
P259L |
XP_011519634.1 |
XM_011521333.2 |
1092 |
Missense Mutation |
CCG,CTG |
P259L |
XP_011519635.1 |
XM_017021997.1 |
1092 |
Missense Mutation |
CCG,CTG |
P257L |
XP_016877486.1 |
XM_017021998.1 |
1092 |
Missense Mutation |
CCG,CTG |
P257L |
XP_016877487.1 |
View Full Product Details