Product Details

SNP ID

rs202133904

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:10973625 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGGACCTGGTCCTCGAAGAAGGAC[C/T]CATCGTAATTTCTTGTGGAATTCTG

Phenotype

MIM: 604275

Polymorphism

C/T, 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	3486	Missense Mutation	GAG,GGG	E1078G	NP_001275644.1
NM_001288716.1	3486	Missense Mutation	GAG,GGG	E832G	NP_001275645.1
NM_001288717.1	3486	Missense Mutation	GAG,GGG	E736G	NP_001275646.1
NM_001332.3	3486	Missense Mutation	GAG,GGG	E1169G	NP_001323.1
XM_005248251.3	3486	Missense Mutation	GAG,GGG	E1194G	XP_005248308.1
XM_005248252.2	3486	Missense Mutation	GAG,GGG	E1180G	XP_005248309.1
XM_005248253.1	3486	Missense Mutation	GAG,GGG	E1103G	XP_005248310.1
XM_011513967.2	3486	Missense Mutation	GAG,GGG	E1103G	XP_011512269.1
XM_017009072.1	3486	Missense Mutation	GAG,GGG	E948G	XP_016864561.1
XM_017009073.1	3486	Missense Mutation	GAG,GGG	E934G	XP_016864562.1
XM_017009074.1	3486	Missense Mutation	GAG,GGG	E923G	XP_016864563.1
XM_017009075.1	3486	Missense Mutation	GAG,GGG	E857G	XP_016864564.1
XM_017009076.1	3486	Missense Mutation	GAG,GGG	E857G	XP_016864565.1

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