Product Details

SNP ID

rs147606485

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:13818965 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGCTCACTTGCACGTGTACATCTC[C/T]GTGCGCTCGCTGCACGTGTTGCACT

Phenotype

MIM: 601570

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WNT7A PubMed Links

Gene Details

Gene

WNT7A

Gene Name

Wnt family member 7A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004625.3	1334	Silent Mutation	ACA,ACG	T343T	NP_004616.2
XM_011534091.2	1334	Silent Mutation	ACA,ACG	T276T	XP_011532393.1

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