Product Details

SNP ID

rs147153174

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:184164320 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCCAGCCCCCTTCTGTGCTGATAA[C/T]CCATCGGAGCTGCCACCACCTATGG

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	610	Silent Mutation	AAC,AAT	N95N	NP_004414.3
XM_005247172.2	610	Silent Mutation	AAC,AAT	N95N	XP_005247229.1
XM_011512513.2	610	UTR 5			XP_011510815.1

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