Product Details
- SNP ID
-
rs140375826
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:277427 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCCCACGGGAGTTGATGGGGATGAC[A/G]CCGATGTCCACCACGACCACCACTC
- Phenotype
-
MIM: 611380
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
DIP2C
PubMed Links
Gene Details
- Gene
- DIP2C
- Gene Name
- disco interacting protein 2 homolog C
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_014974.2 |
2950 |
Silent Mutation |
GGC,GGT |
G1523G |
NP_055789.1 |
XM_005252426.3 |
2950 |
Silent Mutation |
GGC,GGT |
G1579G |
XP_005252483.1 |
XM_005252427.3 |
2950 |
Silent Mutation |
GGC,GGT |
G1533G |
XP_005252484.1 |
XM_005252428.4 |
2950 |
Silent Mutation |
GGC,GGT |
G1589G |
XP_005252485.1 |
XM_005252430.2 |
2950 |
Silent Mutation |
GGC,GGT |
G960G |
XP_005252487.2 |
XM_011519428.2 |
2950 |
Silent Mutation |
GGC,GGT |
G1593G |
XP_011517730.1 |
XM_011519429.2 |
2950 |
Silent Mutation |
GGC,GGT |
G1583G |
XP_011517731.1 |
XM_011519430.2 |
2950 |
Silent Mutation |
GGC,GGT |
G1537G |
XP_011517732.1 |
XM_011519431.2 |
2950 |
Silent Mutation |
GGC,GGT |
G1527G |
XP_011517733.1 |
XM_011519432.1 |
2950 |
Silent Mutation |
GGC,GGT |
G1426G |
XP_011517734.1 |
XM_011519433.2 |
2950 |
Silent Mutation |
GGC,GGT |
G854G |
XP_011517735.1 |
XM_017015977.1 |
2950 |
Silent Mutation |
GGC,GGT |
G970G |
XP_016871466.1 |
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