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SNP ID

rs138953994

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:10026654 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCAGCCAGCTAAGGCATTCTCACT[C/T]GTGTGTTTTCTGTTCCTTGCCGCCC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WWC3 PubMed Links

Gene Details

Gene

WWC3

Gene Name

WWC family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015691.3		Intron			NP_056506.2

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