SELECT VARIANTS FROM EXCLUDE VARIANTS FROM
INDIVIDUALS:

SNP LIST:
GROUPS:

SAVED GENE LIST:

GENE LIST:
INDIVIDUALS:

EXCLUDE SNP LIST:
EXCLUDE GROUPS:

EXCLUDE SAVED GENE LIST:

EXCLUDE GENE LIST:
SELECT YOUR DISEASES:
OMIM:
CLINICAL GENOMICS DATABASE:
HGMD:
MUTATION TYPE:
CHR:

POS:
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

EXCLUDE VARIANTS WITHOUT POLYPHEN SCORE
CADD

EXCLUDE VARIANTS WITHOUT CADD SCORE
MCAP

EXCLUDE VARIANTS WITHOUT M-CAP SCORE
OPEN RESULT IN A NEW WINDOW
RESET FILTER | Save Config | Save Analysis

Genes:

Genes at Omim

Genes at Clinical Genomics Database

Genes at HGMD

Summary

Number of Variants: 18
Number of Genes: 0

Export to: CSV
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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 1_s1 1 . 151380066 158.39 A G LowVariantFreq 0/1 264 None None None None None None None None None None
View 1_s1 1 . 151401069 416.68 T C PASS 0/1 60 None None None None None None None None None None
View 1_s1 1 rs12408139
dbSNP Clinvar
151380508 9351.48 G A PASS 0/1 342 None None None None None None None None None None
View 1_s1 1 rs2025899
dbSNP Clinvar
151380727 19273.37 A G PASS 0/1 851 None None None 0.07408 0.07408 0.09657 None None None None None None None
View 1_s1 1 . 151381549 3.48 T C LowGQX;LowVariantFreq 0/1 54 None None None None None None None None None None
View 1_s1 1 . 151381554 136.92 T C PASS 0/1 9 None None None None None None None None None None
View 1_s1 1 . 151383828 316.91 A AG PASS 0/1 37 None None None None None None None None None None
View 1_s1 1 rs759853119
dbSNP Clinvar
151384052 2542.72 TA T R8 0/1 531 None None None 0.31019 None None None None None None None
View 1_s1 1 rs748256178
dbSNP Clinvar
151384338 2705.03 T TA R8 0/1 386 None None None None None None None None None None
View 1_s1 1 . 151396981 53.96 T C LowVariantFreq 0/1 72 None None None None None None None None None None
View 1_s1 1 . 151397351 5.18 C G LowGQX;LowVariantFreq 0/1 37 None None None None None None None None None None
View 1_s1 1 rs148827204
dbSNP Clinvar
151401600 2887.29 TA T R8 0/1 575 None None None 0.50939 0.50940 None None None None None None None
View 1_s1 1 rs778483881
dbSNP Clinvar
151401631 1357.33 TA T LowVariantFreq;R8 0/1 630 None None None None None None None None None None
View 1_s1 1 rs113396244
dbSNP Clinvar
151403334 6782.45 GA G R8 0/1 1406 None None None 0.11590 None None None None None None None
View 1_s1 1 rs751552668,rs777322689
dbSNP Clinvar
151403380 110677.89 CT... C R8 1/1 1053 None None None None None None None None None None
View 1_s1 1 . 151413712 50.51 T C LowGQX;LowGQ 1/1 3 None None None None None None None None None None
View 1_s1 1 . 151414384 75.86 A G LowGQ 0/1 5 None None None None None None None None None None
View 1_s1 1 . 151414391 267.75 T TG PASS 0/1 39 None None None None None None None None None None
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