Product Details
- SNP ID
-
rs145648453
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:78019772 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCCCCGAGGCGCTGCTTCTTCTGG[C/T]CGCAGGCTGAAAGCTCCTTTGGTTT
- Phenotype
-
MIM: 606382
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
MAGI2
PubMed Links
Gene Details
- Gene
- MAGI2
- Gene Name
- membrane associated guanylate kinase, WW and PDZ domain containing 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001301128.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1290G |
NP_001288057.1 |
NM_012301.3 |
4651 |
Missense Mutation |
GAC,GGC |
D1304G |
NP_036433.2 |
XM_011516718.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1346G |
XP_011515020.1 |
XM_011516719.2 |
4651 |
Missense Mutation |
GAC,GGC |
D1226G |
XP_011515021.1 |
XM_011516720.2 |
4651 |
Missense Mutation |
GAC,GGC |
D1226G |
XP_011515022.1 |
XM_011516726.2 |
4651 |
Missense Mutation |
GAC,GGC |
D998G |
XP_011515028.1 |
XM_011516728.1 |
4651 |
Missense Mutation |
GAC,GGC |
D955G |
XP_011515030.1 |
XM_017012840.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1389G |
XP_016868329.1 |
XM_017012841.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1388G |
XP_016868330.1 |
XM_017012842.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1387G |
XP_016868331.1 |
XM_017012843.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1375G |
XP_016868332.1 |
XM_017012844.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1347G |
XP_016868333.1 |
XM_017012845.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1344G |
XP_016868334.1 |
XM_017012846.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1332G |
XP_016868335.1 |
XM_017012847.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1226G |
XP_016868336.1 |
XM_017012848.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1183G |
XP_016868337.1 |
XM_017012849.1 |
4651 |
Missense Mutation |
GAC,GGC |
D1181G |
XP_016868338.1 |
XM_017012850.1 |
4651 |
UTR 3 |
|
|
XP_016868339.1 |
XM_017012851.1 |
4651 |
Intron |
|
|
XP_016868340.1 |
XM_017012852.1 |
4651 |
Intron |
|
|
XP_016868341.1 |
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