Product Details
- SNP ID
-
rs1566622
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:10973615 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GAGGGCGATGGTGGACCTGGTCCTC[A/G]AAGAAGGACTCATCGTAATTTCTTG
- Phenotype
-
MIM: 604275
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CTNND2
PubMed Links
Gene Details
- Gene
- CTNND2
- Gene Name
- catenin delta 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001288715.1 |
3496 |
Silent Mutation |
TTC,TTT |
F1081F |
NP_001275644.1 |
NM_001288716.1 |
3496 |
Silent Mutation |
TTC,TTT |
F835F |
NP_001275645.1 |
NM_001288717.1 |
3496 |
Silent Mutation |
TTC,TTT |
F739F |
NP_001275646.1 |
NM_001332.3 |
3496 |
Silent Mutation |
TTC,TTT |
F1172F |
NP_001323.1 |
XM_005248251.3 |
3496 |
Silent Mutation |
TTC,TTT |
F1197F |
XP_005248308.1 |
XM_005248252.2 |
3496 |
Silent Mutation |
TTC,TTT |
F1183F |
XP_005248309.1 |
XM_005248253.1 |
3496 |
Silent Mutation |
TTC,TTT |
F1106F |
XP_005248310.1 |
XM_011513967.2 |
3496 |
Silent Mutation |
TTC,TTT |
F1106F |
XP_011512269.1 |
XM_017009072.1 |
3496 |
Silent Mutation |
TTC,TTT |
F951F |
XP_016864561.1 |
XM_017009073.1 |
3496 |
Silent Mutation |
TTC,TTT |
F937F |
XP_016864562.1 |
XM_017009074.1 |
3496 |
Silent Mutation |
TTC,TTT |
F926F |
XP_016864563.1 |
XM_017009075.1 |
3496 |
Silent Mutation |
TTC,TTT |
F860F |
XP_016864564.1 |
XM_017009076.1 |
3496 |
Silent Mutation |
TTC,TTT |
F860F |
XP_016864565.1 |
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