Product Details
- SNP ID
-
rs145805649
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:72163745 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CATACCTTTCTCCACTTCATCTCAG[G/T]GATGAGGACTTCCTGCAGTAAGACA
- Phenotype
-
- Polymorphism
- G/T, Transversion 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 |
821 |
Missense Mutation |
ACT,CCT |
T205P |
NP_001012660.1 |
XM_011521327.2 |
821 |
Missense Mutation |
ACT,CCT |
T204P |
XP_011519629.1 |
XM_011521328.2 |
821 |
Missense Mutation |
ACT,CCT |
T203P |
XP_011519630.1 |
XM_011521329.2 |
821 |
Missense Mutation |
ACT,CCT |
T195P |
XP_011519631.1 |
XM_011521330.2 |
821 |
Missense Mutation |
ACT,CCT |
T193P |
XP_011519632.1 |
XM_011521331.2 |
821 |
Missense Mutation |
ACT,CCT |
T186P |
XP_011519633.1 |
XM_011521332.2 |
821 |
Missense Mutation |
ACT,CCT |
T169P |
XP_011519634.1 |
XM_011521333.2 |
821 |
Missense Mutation |
ACT,CCT |
T169P |
XP_011519635.1 |
XM_017021997.1 |
821 |
Missense Mutation |
ACT,CCT |
T167P |
XP_016877486.1 |
XM_017021998.1 |
821 |
Missense Mutation |
ACT,CCT |
T167P |
XP_016877487.1 |
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