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SNP ID

rs147882980

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:218419435 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGCCCCATCCCACTTTGGGTGTCA[C/T]CATCCCAATTGCCCTGGAACTTCTA

Phenotype

MIM: 193040

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

VIL1 PubMed Links

Gene Details

Gene

VIL1

Gene Name

villin 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007127.2		Intron			NP_009058.2

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