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 at Omim

Genes at Clinical Genomics Database

Genes at HGMD

Summary

Number of Variants: 9
Number of Genes: 1

Export to: CSV
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FAM210B

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 gt_so_4086_igt_1r 20 rs17362677
dbSNP Clinvar
54935242 225.009 A T . 0/1 0 MOTIF[MA0139.1:CTCF] MODIFIER None 0.10184 0.10180 0.00 None None None None None None FAM210B|0.003888312|87.18%
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 gt_so_4086_igt_1r 16 rs7202692
dbSNP Clinvar
83434063 219.009 C T . 0/1 0 MOTIF[MA0139.1:CTCF] MODIFIER None 0.74701 0.74700 None None None None None None CDH13|0.953699546|2.14%
View gt_so_4086_igt_1r 19 rs2301669
dbSNP Clinvar
19453560 225.009 C A . 0/1 0 MOTIF[MA0139.1:CTCF] MODIFIER None 0.52436 0.52440 0.42822 None None None None None None MAU2|0.230960956|33.29%
View gt_so_4086_igt_1r 21 rs66854923
dbSNP Clinvar
9590334 225.009 C A . 0/1 0 MOTIF[MA0139.1:CTCF] MODIFIER None 0.86002 0.86000 None None None None None None None
View gt_so_4086_igt_1r 7 rs3813708
dbSNP Clinvar
65305632 186.009 C A . 0/1 0 MOTIF[MA0139.1:CTCF] MODIFIER None 0.14177 0.14180 None None None None None None None
View gt_so_4086_igt_1r 15 rs2253603
dbSNP Clinvar
40565055 221.999 G A . 1/1 0 MOTIF[MA0139.1:CTCF] MODIFIER None 0.45447 0.45450 0.42673 None None None None None None PAK6|0.183662894|38.57%
View gt_so_4086_igt_1r 17 rs2189336
dbSNP Clinvar
5326162 221.999 G A . 1/1 0 MOTIF[MA0139.1:CTCF] MODIFIER None 0.77875 0.77880 0.39428 None None None None None None RPAIN|0.023237381|72.57%
View gt_so_4086_igt_1r 17 rs820387
dbSNP Clinvar
73746146 221.999 T C . 1/1 0 MOTIF[MA0139.1:CTCF] MODIFIER None 0.74062 0.74060 0.21313 None None None None None None ITGB4|0.346553835|24.38%
View gt_so_4086_igt_1r 1 rs2531506
dbSNP Clinvar
148902392 15.1417 G A . 0/1 0 MOTIF[MA0139.1:CTCF] MODIFIER None None None None None None None None
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