regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACYP2_chr2_53966113_54310300 | 53967649 | C | CAAAAAA | upstream_gene_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(35): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(7): Show | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(35): Show | 38 | 272 | 0.1397 | 6 | c.-37 others(17): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 3463 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 53973855 | A | ATGTGTG | intron_variant | MODIFIER | HG01109.hp1 HG02683.hp1 HG02735.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0253 | 3 | 272 | 0.0110 | 6 | c.62+ others(17): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 53982828 | C | CTGTGTG | intron_variant | MODIFIER | HG00597.hp1 HG01243.hp1 HG01346.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0211others(7): Show | 10 | 272 | 0.0368 | 6 | c.62+ others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 53982872 | G | GTGTGTA | intron_variant | MODIFIER | HG01074.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | 272 | 0.0221 | 6 | c.62+ others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54013255 | A | ATATGTG | intron_variant | MODIFIER | HG01255.hp2 NA18951.hp2 NA18967.hp1 |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0004a0001c0002t0015a0002c0003t0002 | a0001c0001t0004g0272a0001c0002t0015g0097a0002c0003t0002g0090 | 3 | 272 | 0.0110 | 6 | c.63- others(23): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54015645 | T | TCACACA | intron_variant | MODIFIER | HG02145.hp2 HG02615.hp2 HG03195.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0173others(3): Show | 6 | 272 | 0.0221 | 6 | c.63- others(23): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54017272 | C | CTTTTCT | intron_variant | MODIFIER | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(32): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(5): Show | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(32): Show | 35 | 272 | 0.1287 | 6 | c.63- others(23): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54019609 | T | TTTATTA | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(29): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(3): Show | a0001c0001t0001g0196a0001c0001t0001g0221a0001c0001t0004g0170others(29): Show | 32 | 272 | 0.1177 | 6 | c.63- others(23): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54027837 | C | CTTTCTT | intron_variant | MODIFIER | HG02630.hp1 HG02896.hp2 HG03195.hp1 others(3): Show |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0015 | a0001c0002t0003g0070a0001c0002t0003g0073a0001c0002t0003g0074others(3): Show | 6 | 272 | 0.0221 | 6 | c.63- others(23): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54038673 | C | CTATATA | intron_variant | MODIFIER | HG01515.hp2 HG02132.hp1 HG04184.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0177a0001c0001t0001g0214a0001c0001t0001g0235others(2): Show | 5 | 272 | 0.0184 | 6 | c.63- others(23): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54039819 | T | TTGTGTG | intron_variant | MODIFIER | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(37): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0124others(37): Show | 40 | 272 | 0.1471 | 6 | c.63- others(23): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54074578 | T | TTGTGTG | intron_variant | MODIFIER | HG00738.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0132a0001c0002t0003g0080a0001c0002t0003g0081others(2): Show | 5 | 272 | 0.0184 | 6 | c.277 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54078411 | C | CATATAT | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(16): Show | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0115others(166): Show | 169 | 272 | 0.6213 | 6 | c.277 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54125751 | A | AAAAAAC | intron_variant | MODIFIER | HG00099.hp1 HG00738.hp2 HG01070.hp1 others(55): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(11): Show | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0001g0116others(55): Show | 58 | 272 | 0.2132 | 6 | c.278 others(23): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201594 | C | CTTTCTT | intron_variant | MODIFIER | HG01175.hp1 HG02735.hp2 HG06807.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(1): Show | a0001c0001t0001g0119a0001c0001t0004g0225a0001c0001t0004g0251others(4): Show | 7 | 272 | 0.0257 | 6 | c.404 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201622 | T | TTCTTTC | intron_variant | MODIFIER | NA18981.hp2 NA19056.hp2 NA19085.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0187 | 3 | 272 | 0.0110 | 6 | c.404 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54202706 | C | CTTTTTT | intron_variant | MODIFIER | HG02027.hp1 HG02056.hp1 HG03516.hp1 others(6): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0002t0002a0004c0006t0001 | a0001c0001t0001g0180a0001c0001t0001g0221a0001c0001t0001g0229others(6): Show | 9 | 272 | 0.0331 | 6 | c.404 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54219857 | A | ATGTGTG | intron_variant | MODIFIER | HG01099.hp1 HG01256.hp1 HG01934.hp2 others(20): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(3): Show | a0001c0001t0001g0147a0001c0001t0001g0174a0001c0001t0001g0175others(20): Show | 23 | 272 | 0.0846 | 6 | c.404 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54219881 | G | GTGTGTA | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG01071.hp2 others(31): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0003others(5): Show | a0001c0001t0001g0142a0001c0001t0001g0155a0001c0001t0001g0162others(31): Show | 34 | 272 | 0.1250 | 6 | c.404 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54219905 | A | ATTTTTT | intron_variant | MODIFIER | HG00423.hp2 HG01071.hp2 HG03239.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0002a0001c0002t0005others(1): Show | a0001c0001t0001g0132a0001c0002t0002g0026a0001c0002t0002g0044others(3): Show | 6 | 272 | 0.0221 | 6 | c.404 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54221520 | C | CTTTTTT | intron_variant | MODIFIER | HG01109.hp2 HG01255.hp1 HG01346.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003a0001c0002t0006 | a0001c0001t0001g0105a0001c0001t0001g0193a0001c0001t0001g0233others(5): Show | 8 | 272 | 0.0294 | 6 | c.404 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54255566 | G | GGGGCCC | intron_variant | MODIFIER | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0003 | a0001c0001t0001g0267a0001c0002t0002g0107a0001c0002t0003g0070others(4): Show | 7 | 272 | 0.0257 | 6 | c.405 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54266590 | C | CTTTTTT | intron_variant | MODIFIER | HG00408.hp2 HG00558.hp1 HG01070.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0118others(17): Show | 20 | 272 | 0.0735 | 6 | c.405 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54276619 | T | TCACACA | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG01243.hp2 others(13): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(4): Show | a0001c0001t0001g0188a0001c0001t0001g0239a0001c0001t0001g0241others(13): Show | 16 | 272 | 0.0588 | 6 | c.405 others(25): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54298344 | T | TTAAATA | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(152): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0010a0001c0002t0001others(8): Show | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0113others(152): Show | 155 | 272 | 0.5699 | 6 | c.405 others(23): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADA2_chr22_17173790_17224435 | 17174366 | T | TACACAC | downstream_gene_variant | MODIFIER | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0013others(2): Show | a0001c0001t0004a0001c0001t0010a0001c0003t0010others(3): Show | a0001c0001t0004g0338a0001c0001t0010g0052a0001c0003t0010g0088others(10): Show | 13 | 408 | 0.0319 | 6 | c.*71 others(17): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 4423 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17216789 | C | CACACAT | intron_variant | MODIFIER | HG00642.hp2 HG01074.hp1 HG02015.hp2 others(1): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0007 | a0001c0001t0001a0001c0005t0002a0002c0007t0007 | a0001c0001t0001g0200a0001c0005t0002g0198a0001c0005t0002g0199others(1): Show | 4 | 408 | 0.0098 | 6 | c.-47 others(23): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
ADAD1_chr4_122374011_122434784 | 122398317 | G | GGTGTGT | intron_variant | MODIFIER | HG02257.hp1 HG03195.hp2 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0036a0001c0001t0001g0071a0001c0001t0002g0213 | 3 | 376 | 0.0080 | 6 | c.724 others(23): Show |
ADAD1 | ENSG00000164113.11 | transcript | ENST00000296513.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ADAD1_chr4_122374011_122434784 | 122413851 | C | CATATAT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(55): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0030others(46): Show | 58 | 376 | 0.1543 | 6 | c.124 others(25): Show |
ADAD1 | ENSG00000164113.11 | transcript | ENST00000296513.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ADAD2_chr16_84186157_84202166 | 84197184 | C | CTGTGTG | downstream_gene_variant | MODIFIER | HG01891.hp1 HG03098.hp1 HG03486.hp2 |
a0006a0010 | a0006c0016a0006c0027a0010c0040 | a0006c0016t0007a0006c0027t0007a0010c0040t0007 | a0006c0016t0007g0065a0006c0027t0007g0047a0010c0040t0007g0061 | 3 | 470 | 0.0064 | 6 | c.*21 others(15): Show |
ADAD2 | ENSG00000140955.11 | transcript | ENST00000315906.10 | protein_coding | 19 | chr16 | TogoVar | ||||||
ADAL_chr15_43325672_43359569 | 43326034 | A | ATTTTTT | upstream_gene_variant | MODIFIER | HG00280.hp1 HG00733.hp2 HG01516.hp2 others(9): Show |
a0001a0002 | a0001c0001a0001c0006a0002c0004 | a0001c0001t0004a0001c0001t0015a0001c0006t0004others(1): Show | a0001c0001t0004g0025a0001c0001t0004g0050a0001c0001t0004g0059others(7): Show | 12 | 386 | 0.0311 | 6 | c.-52 others(17): Show |
ADAL | ENSG00000168803.16 | transcript | ENST00000562188.7 | protein_coding | 4637 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58586912 | A | AGTGTGT | downstream_gene_variant | MODIFIER | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(2): Show | a0001c0001t0001g0058a0001c0001t0001g0064a0001c0001t0001g0108others(10): Show | 13 | 342 | 0.0380 | 6 | c.*10 others(19): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 1896 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58586916 | A | AGTGTGT | downstream_gene_variant | MODIFIER | HG01257.hp1 HG01993.hp1 HG02004.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(9): Show | a0001c0001t0004g0222a0001c0001t0005g0272a0001c0001t0006g0017others(11): Show | 14 | 342 | 0.0409 | 6 | c.*10 others(19): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 1892 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58647248 | A | ATTTTTT | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(25): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(10): Show | a0001c0001t0001g0106a0001c0001t0001g0123a0001c0001t0001g0146others(25): Show | 28 | 342 | 0.0819 | 6 | c.586 others(23): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 5/15 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58655696 | G | GTGTGTA | intron_variant | MODIFIER | HG00423.hp1 HG00609.hp2 HG01515.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0048others(2): Show | a0001c0001t0001g0149a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | 342 | 0.0234 | 6 | c.585 others(23): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 5/15 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58655711 | G | GTATATA | intron_variant | MODIFIER | HG01070.hp1 HG02074.hp1 HG02109.hp1 others(4): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0012a0001c0001t0034a0001c0001t0036others(4): Show | a0001c0001t0012g0045a0001c0001t0034g0081a0001c0001t0036g0015others(4): Show | 7 | 342 | 0.0205 | 6 | c.585 others(23): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 5/15 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58685545 | A | AATATAT | intron_variant | MODIFIER | HG01943.hp2 HG02074.hp1 HG02630.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0012a0001c0001t0022others(4): Show | a0001c0001t0006g0017a0001c0001t0012g0027a0001c0001t0022g0055others(4): Show | 7 | 342 | 0.0205 | 6 | c.207 others(23): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 2/15 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58714292 | T | TACACAC | intron_variant | MODIFIER | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | a0001c0001t0001g0184a0001c0001t0001g0282a0001c0001t0001g0288others(62): Show | 65 | 342 | 0.1901 | 6 | c.206 others(23): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 2/15 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58726567 | C | CAAAAAA | intron_variant | MODIFIER | HG02004.hp2 HG02965.hp2 HG03516.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0014a0001c0001t0025others(3): Show | a0001c0001t0001g0175a0001c0001t0014g0278a0001c0001t0025g0284others(3): Show | 6 | 342 | 0.0175 | 6 | c.56- others(21): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 1/15 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58729962 | A | AAAAAAC | intron_variant | MODIFIER | NA18964.hp2 NA18967.hp2 NA18977.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0110a0001c0002t0001a0001c0002t0010 | a0001c0001t0110g0116a0001c0002t0001g0115a0001c0002t0001g0117others(4): Show | 7 | 342 | 0.0205 | 6 | c.56- others(23): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 1/15 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58750657 | C | CGTGTGT | upstream_gene_variant | MODIFIER | HG00609.hp1 HG01175.hp1 HG02055.hp1 others(8): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(3): Show | a0001c0001t0003g0249a0001c0001t0003g0254a0001c0001t0003g0255others(8): Show | 11 | 342 | 0.0322 | 6 | c.-11 others(17): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 951 | chr15 | TogoVar | ||||||
ADAM10_chr15_58583809_58754707 | 58750792 | A | AGTGTGT | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(173): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(53): Show | a0001c0001t0001g0100a0001c0001t0001g0106a0001c0001t0001g0108others(173): Show | 176 | 342 | 0.5146 | 6 | c.-12 others(17): Show |
ADAM10 | ENSG00000137845.15 | transcript | ENST00000260408.8 | protein_coding | 1086 | chr15 | TogoVar | ||||||
ADAM11_chr17_44753988_44786846 | 44765610 | C | CTTTTTT | intron_variant | MODIFIER | HG01884.hp1 HG03195.hp1 HG03540.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0005a0001c0002t0003a0001c0002t0006 | a0001c0001t0005g0149a0001c0002t0003g0183a0001c0002t0003g0184others(3): Show | 6 | 336 | 0.0179 | 6 | c.238 others(23): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ADAM11_chr17_44753988_44786846 | 44774097 | A | AAAAAAG | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0004a0001c0005others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(17): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 200 | 336 | 0.5952 | 6 | c.993 others(21): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ADAM12_chr10_126007391_126393477 | 126082363 | G | GTTTTTT | intron_variant | MODIFIER | HG00140.hp2 HG01109.hp2 HG01167.hp1 others(15): Show |
a0001a0002 | a0001c0002a0001c0008a0001c0012others(8): Show | a0001c0002t0002a0001c0002t0011a0001c0002t0019others(12): Show | a0001c0002t0002g0038a0001c0002t0011g0178a0001c0002t0019g0188others(15): Show | 18 | 252 | 0.0714 | 6 | c.114 others(27): Show |
ADAM12 | ENSG00000148848.15 | transcript | ENST00000448723.2 | protein_coding | 11/22 | chr10 | TogoVar | ||||||
ADAM12_chr10_126007391_126393477 | 126086704 | T | TATATAA | intron_variant | MODIFIER | HG00099.hp1 HG00639.hp1 HG00673.hp1 others(11): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0004others(5): Show | a0001c0002t0001a0001c0003t0003a0001c0003t0007others(8): Show | a0001c0002t0001g0209a0001c0002t0001g0220a0001c0003t0003g0195others(11): Show | 14 | 252 | 0.0556 | 6 | c.114 others(25): Show |
ADAM12 | ENSG00000148848.15 | transcript | ENST00000448723.2 | protein_coding | 11/22 | chr10 | TogoVar | ||||||
ADAM12_chr10_126007391_126393477 | 126138817 | C | CTTTTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(55): Show |
a0001a0002a0003others(6): Show | a0001c0002a0001c0003a0001c0004others(24): Show | a0001c0002t0001a0001c0002t0005a0001c0002t0008others(42): Show | a0001c0002t0001g0185a0001c0002t0005g0210a0001c0002t0008g0017others(55): Show | 58 | 252 | 0.2302 | 6 | c.340 others(23): Show |
ADAM12 | ENSG00000148848.15 | transcript | ENST00000448723.2 | protein_coding | 4/22 | chr10 | TogoVar | ||||||
ADAM12_chr10_126007391_126393477 | 126159307 | C | CAAAAAA | intron_variant | MODIFIER | HG02145.hp1 HG02723.hp2 HG02895.hp2 others(5): Show |
a0001a0002a0006 | a0001c0002a0001c0004a0001c0021others(4): Show | a0001c0002t0017a0001c0004t0023a0001c0021t0021others(4): Show | a0001c0002t0017g0013a0001c0004t0023g0173a0001c0021t0021g0076others(5): Show | 8 | 252 | 0.0318 | 6 | c.261 others(23): Show |
ADAM12 | ENSG00000148848.15 | transcript | ENST00000448723.2 | protein_coding | 3/22 | chr10 | TogoVar | ||||||
ADAM12_chr10_126007391_126393477 | 126243489 | A | ATGTGTG | intron_variant | MODIFIER | HG01109.hp2 HG01175.hp1 HG02071.hp1 others(10): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0008others(7): Show | a0001c0002t0001a0001c0002t0019a0001c0003t0007others(8): Show | a0001c0002t0001g0044a0001c0002t0001g0097a0001c0002t0001g0205others(10): Show | 13 | 252 | 0.0516 | 6 | c.260 others(25): Show |
ADAM12 | ENSG00000148848.15 | transcript | ENST00000448723.2 | protein_coding | 3/22 | chr10 | TogoVar | ||||||
ADAM12_chr10_126007391_126393477 | 126311094 | T | TACACAC | intron_variant | MODIFIER | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(34): Show |
a0001a0002a0004 | a0001c0002a0001c0003a0001c0004others(16): Show | a0001c0002t0001a0001c0002t0006a0001c0003t0003others(27): Show | a0001c0002t0001g0066a0001c0002t0001g0209a0001c0002t0006g0208others(34): Show | 37 | 252 | 0.1468 | 6 | c.186 others(25): Show |
ADAM12 | ENSG00000148848.15 | transcript | ENST00000448723.2 | protein_coding | 2/22 | chr10 | TogoVar |