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SELECT VARIANTS FROM EXCLUDE VARIANTS FROM
INDIVIDUALS:

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 GROUPS:

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GENE LIST:
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 EXCLUDE GROUPS:

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SELECT YOUR DISEASES:
OMIM:
CLINICAL GENOMICS DATABASE:
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MUTATION TYPE:
 CHR:

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VARIANT EFFECT FUNCTIONAL CLASS IMPACT
DBSNP BUILD:


EXCLUDE VARIANTS AT VARISNP 		READ DEPTH:

QUAL:
VARIANTS PER GENE:
SHOW ONLY VARIANTS PRESENT IN COMMON GENES BETWEEN ALL THE INDIVIDUALS SELECTED
SHOW ONLY VARIANTS AT EXACTLY SAME POSITION BETWEEN ALL THE INDIVIDUALS SELECTED
EXCLUDE ALL VARIANTS PRESENT IN LATEST DBSNP BUILD
SHOW ONLY VARIANTS PRESENT AT HGMD

FREQUENCIES

1000 GENOMES FREQUENCY

EXCLUDE ALL VARIANTS PRESENT IN 1000GENOMES 		DBSNP FREQUENCY

EXCLUDE ALL VARIANTS PRESENT IN DBSNP 		ESP6500 FREQUENCY

EXCLUDE ALL VARIANTS PRESENT IN EXOME SEQUENCING PROJECT

SCORES

SIFT SCORE

EXCLUDE VARIANTS WITHOUT SIFT SCORE 		POLYPHEN2 SCORE

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CADD

EXCLUDE VARIANTS WITHOUT CADD SCORE 		MCAP

EXCLUDE VARIANTS WITHOUT M-CAP SCORE
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+ Genes 1

Genes:
MYO9B,

+ Genes associated with diseases 1

Genes at Omim

MYO9B,
MYO9B {Celiac disease, susceptibility to, 4}, 609753 (3)

Genes at Clinical Genomics Database

Genes at HGMD

Summary

Number of Variants: 7
Number of Genes: 1

Export to: CSV
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MYO9B
Omim - GeneCards - NCBI
Options Individual Chr
 RsId
 Pos
 Qual
 Ref
 Alt
 Filter Gen
 Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View grc14378018_exome 19 rs7256689
dbSNP Clinvar 		17273893 18.592 G T . 0/1 17 SYNONYMOUS_CODING LOW None 0.74820 0.74820 0.25821 None None None None None None MYO9B|0.037345575|66.66%
View grc14378018_exome 19 rs1545620
dbSNP Clinvar 		17303774 93.5867 T G . 0/1 19 NON_SYNONYMOUS_CODING MODERATE None 0.64437 0.64440 0.47533 1.00 0.00 None None None None None None MYO9B|0.037345575|66.66%
View grc14378018_exome 19 rs1064305
dbSNP Clinvar 		17305440 1484.13 T C,A . 0/1 109 SYNONYMOUS_CODING LOW None 0.64417 0.64420 0.48861 None None None None None None MYO9B|0.037345575|66.66%
View grc14378018_exome 19 rs2279003
dbSNP Clinvar 		17306031 178.533 T C . 0/1 33 SYNONYMOUS_CODING LOW None 0.75919 0.75920 0.31003 None None None None None None MYO9B|0.037345575|66.66%
View grc14378018_exome 19 rs2305765
dbSNP Clinvar 		17312992 1484.13 C T . 0/1 123 SYNONYMOUS_CODING LOW None 0.60044 0.60040 0.44220 None None None None None None MYO9B|0.037345575|66.66%
View grc14378018_exome 19 rs7248508
dbSNP Clinvar 		17316782 1484.13 T C . 0/1 76 NON_SYNONYMOUS_CODING MODERATE None 0.63159 0.63160 0.48094 0.71 0.00 None None None None None None MYO9B|0.037345575|66.66%
View grc14378018_exome 19 rs8110964
dbSNP Clinvar 		17317955 1484.13 A G . 0/1 102 SYNONYMOUS_CODING LOW None 0.63139 0.63140 0.47937 None None None None None None MYO9B|0.037345575|66.66%
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