Product Details
- SNP ID
-
rs77926705
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:75645438 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTGCCAACAGTGGAGCTTCAGCGAC[G/T]CTGTCCTGTGAAGCGGCCCTCCATT
- Phenotype
-
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
G3BP2
PubMed Links
Gene Details
- Gene
- G3BP2
- Gene Name
- G3BP stress granule assembly factor 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_012297.4 |
1601 |
Missense Mutation |
AGT,CGT |
S481R |
NP_036429.2 |
NM_203504.2 |
1601 |
Missense Mutation |
AGT,CGT |
S448R |
NP_987100.1 |
NM_203505.2 |
1601 |
Missense Mutation |
AGT,CGT |
S481R |
NP_987101.1 |
XM_005263382.2 |
1601 |
Missense Mutation |
AGT,CGT |
S481R |
XP_005263439.1 |
XM_005263383.3 |
1601 |
Missense Mutation |
AGT,CGT |
S481R |
XP_005263440.1 |
XM_011532441.2 |
1601 |
Missense Mutation |
AGT,CGT |
S481R |
XP_011530743.1 |
XM_017008876.1 |
1601 |
Missense Mutation |
AGT,CGT |
S481R |
XP_016864365.1 |
XM_017008877.1 |
1601 |
Missense Mutation |
AGT,CGT |
S481R |
XP_016864366.1 |
XM_017008878.1 |
1601 |
Missense Mutation |
AGT,CGT |
S448R |
XP_016864367.1 |
XM_017008879.1 |
1601 |
Missense Mutation |
AGT,CGT |
S448R |
XP_016864368.1 |
View Full Product Details