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Search variant frequencies in human genetic variation databases

      Search variant frequencies for a single gene, single exon, genomic region (GRCH37/hg19), or genomic locus based on human genetic variation databases including ExAC, ESP6500, UK10K, 1000G and dbSNP.

Search item:

	Examples:                 Single gene:	CD55
	Single exon:	NM_001114752:exon2
	Genomic position:	chr14:21853775-21855319
	Genomic locus:	chr14:21859996

Mutation effect:

stopgain

stoploss

splicing

frameshift

nonsynonymous

nonframeshift

synonymous

unknown

Mutation type:

C>T/G>A

C>G/G>C

C>A/G>T

insertion

A>T/T>A

A>G/T>C

A>C/T>G

deletion

Variant frequency:

ExAC

ESP6500

UK10K

1000G

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