Product Details

SNP ID

rs150659339

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:184164362 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCTATGGAGCGCACGGGAGGCAT[C/T]GGGGACTCCCGACCCCCATCCTTCC

Phenotype

MIM: 601368

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

DVL3 PubMed Links

Gene Details

Gene

DVL3

Gene Name

dishevelled segment polarity protein 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004423.3	652	Silent Mutation	ATC,ATT	I109I	NP_004414.3
XM_005247172.2	652	Silent Mutation	ATC,ATT	I109I	XP_005247229.1
XM_011512513.2	652	UTR 5			XP_011510815.1

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