Human Reference Genome:    GRCh37/hg19     GRCh38/hg38

Visulization Components: 

X-Axis MAF  (General, in gnomAD) MAF  (Maximum, in gnomAD) Amino Acid Position

Y-Axis CADD  (Phred-like Score) EIGEN  (Phred-like Score) LINSIGHT  (Probability) MAF  (General, in gnomAD) MAF  (Maximum, in gnomAD)

MAF Range:

-

Disease Information:

	Mode of Inheritance:	AD     AR
	Disease Prevalence:		(in decimal)

Population: (based on gnomAD)
General   (123,136 exomes)
AFR: African / African American  (7,652 exomes)
AMR: Admixed American / Latino  (16,791 exomes)
ASJ: Ashkenazi Jewish  (4,925 exomes)
EAS: East Asian  (8,624 exomes)
FIN: Finnish  (11,150 exomes)
NFE: Non-Finnish European  (55,860 exomes)
SAS: South Asian  (15,391 exomes)

Mutation Consequence:
All

3-UTR 5-UTR Frameshift Inframe Deletion Inframe Insertion Intronic Missense

Splice Acceptor Splice Donor Splice Region Start Lost Stop Gained Stop Lost Synonymous

Gene-Level Cutoff on CADD Score:
None
MSC (Mutation Significance Cutoff) at 99%  95%  90%  Confidence Internval

Mutation Impact:    All     High     Moderate     Modifier     Low

Loss of Function:     All     High-Confidence     Low-Confidence

Only the Variants in More Than 1 Individual (AC > 1)

Only the Variants Having Homozygous Alleles (HOM > 1)

Only the Variants Having Hemizygous Alleles, for Sex-Linked Genes (HEMI > 1)


User's Mutations? :    No    Yes

Please provide the first 5 columns of the mutations (<= 100) in VCF format. If ID is empty, fill it by a dot.