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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
DIAPH2_chrX_96679842_97609997 | 96962478 | TACACAC | T | intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0046 | 1 | 147 | 0.0068 | -6 | c.193 others(25): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 96962492 | CACACAT | C | intron_variant | MODIFIER | NA18970.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0049 | 1 | 147 | 0.0068 | -6 | c.193 others(25): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 96962496 | CATATAT | C | intron_variant | MODIFIER | HG02129.hp1 HG02257.hp2 HG02717.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0118a0001c0001t0001g0126a0001c0001t0001g0127others(10): Show | 13 | 147 | 0.0884 | -6 | c.193 others(25): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97047542 | CTTTTTT | C | intron_variant | MODIFIER | HG03139.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(1): Show | a0001c0001t0001g0142a0001c0001t0002g0004a0001c0001t0012g0003others(1): Show | 4 | 147 | 0.0272 | -6 | c.205 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97095098 | CTTTTTT | C | intron_variant | MODIFIER | HG01167.hp1 HG01261.hp1 HG01891.hp1 others(10): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0068a0001c0001t0001g0082a0001c0001t0001g0121others(10): Show | 13 | 147 | 0.0884 | -6 | c.224 others(25): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97112761 | CTTTCTT | C | intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0139 | 1 | 147 | 0.0068 | -6 | c.235 others(25): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97137270 | CATATAT | C | intron_variant | MODIFIER | NA19043.hp1 | a0004 | a0004c0010 | a0004c0010t0001 | a0004c0010t0001g0016 | 1 | 147 | 0.0068 | -6 | c.259 others(25): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97160093 | ACGGGGG | A | intron_variant | MODIFIER | HG00609.hp1 HG02040.hp1 HG02083.hp1 others(7): Show |
a0001a0003 | a0001c0001a0001c0005a0003c0008 | a0001c0001t0001a0001c0001t0002a0001c0005t0001others(1): Show | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0121others(7): Show | 10 | 147 | 0.0680 | -6 | c.271 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97185351 | ATGTGTG | A | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp1 HG01109.hp1 others(7): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(2): Show | a0001c0001t0001g0014a0001c0001t0001g0068a0001c0001t0001g0073others(7): Show | 10 | 147 | 0.0680 | -6 | c.271 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97185393 | GTGTATA | G | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(1): Show | a0001c0001t0001g0014a0001c0001t0001g0068a0001c0001t0001g0073others(5): Show | 8 | 147 | 0.0544 | -6 | c.271 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97185395 | GTATATA | G | intron_variant | MODIFIER | HG02717.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(1): Show | a0001c0001t0001g0082a0001c0001t0004g0137a0001c0002t0001g0015others(1): Show | 4 | 147 | 0.0272 | -6 | c.271 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97185405 | ATATATG | A | intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0002 | a0001c0002t0021 | a0001c0002t0021g0076 | 1 | 147 | 0.0068 | -6 | c.271 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97185451 | GTGTGTA | G | intron_variant | MODIFIER | HG01081.hp2 HG02257.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0018a0001c0002t0021 | a0001c0001t0018g0083a0001c0002t0021g0076 | 2 | 147 | 0.0136 | -6 | c.271 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97185474 | CATATAT | C | intron_variant | MODIFIER | HG01358.hp1 HG01981.hp1 HG02027.hp1 others(9): Show |
a0001a0004 | a0001c0001a0001c0007a0004c0010 | a0001c0001t0001a0001c0001t0002a0001c0007t0005others(1): Show | a0001c0001t0001g0091a0001c0001t0001g0104a0001c0001t0001g0111others(9): Show | 12 | 147 | 0.0816 | -6 | c.271 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97187281 | CTTTTTT | C | intron_variant | MODIFIER | HG01891.hp2 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0022 | a0001c0001t0004g0108a0001c0001t0022g0112 | 2 | 147 | 0.0136 | -6 | c.271 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97190833 | CAAAAAA | C | intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0137 | 1 | 147 | 0.0068 | -6 | c.271 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97192309 | AAAAAAG | A | intron_variant | MODIFIER | NA18962.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073 | 1 | 147 | 0.0068 | -6 | c.271 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97196219 | TACACAC | T | intron_variant | MODIFIER | HG00621.hp1 HG00673.hp1 HG01069.hp1 others(65): Show |
a0001a0002a0003 | a0001c0001a0002c0006a0003c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0023others(65): Show | 68 | 147 | 0.4626 | -6 | c.272 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97198265 | TACACAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(36): Show |
a0001 | a0001c0001a0001c0005a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0042others(36): Show | 39 | 147 | 0.2653 | -6 | c.272 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97274006 | GGTGTGT | G | intron_variant | MODIFIER | HG00609.hp1 HG01192.hp1 HG02071.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0087a0001c0001t0001g0104a0001c0001t0002g0045others(8): Show | 11 | 147 | 0.0748 | -6 | c.284 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97297076 | CTTTTTT | C | intron_variant | MODIFIER | HG01081.hp2 NA19091.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0018 | a0001c0001t0002g0088a0001c0001t0018g0083 | 2 | 147 | 0.0136 | -6 | c.284 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97300931 | TAAAAAA | T | intron_variant | MODIFIER | HG01081.hp2 HG02055.hp1 HG02809.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006a0001c0001t0018 | a0001c0001t0002g0139a0001c0001t0006g0005a0001c0001t0018g0083 | 3 | 147 | 0.0204 | -6 | c.284 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97329891 | GACACAC | G | intron_variant | MODIFIER | HG01081.hp2 HG01243.hp1 HG01934.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0066others(8): Show | 11 | 147 | 0.0748 | -6 | c.284 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97352870 | CAAAAAA | C | intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0147 | 1 | 147 | 0.0068 | -6 | c.300 others(25): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97427657 | GTTTTGT | G | intron_variant | MODIFIER | HG00621.hp1 HG00673.hp1 HG00738.hp1 others(73): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0006others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0018others(73): Show | 76 | 147 | 0.5170 | -6 | c.314 others(25): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97428479 | AGATCAC | A | intron_variant | MODIFIER | HG01081.hp2 HG01243.hp1 HG02055.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(2): Show | a0001c0001t0001g0068a0001c0001t0002g0139a0001c0001t0013g0141others(2): Show | 5 | 147 | 0.0340 | -6 | c.314 others(25): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97438359 | GTTTTTT | G | intron_variant | MODIFIER | NA19043.hp1 | a0004 | a0004c0010 | a0004c0010t0001 | a0004c0010t0001g0016 | 1 | 147 | 0.0068 | -6 | c.324 others(25): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97476039 | CATTAAT | C | intron_variant | MODIFIER | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0012others(3): Show | a0001c0001t0002g0139a0001c0001t0003g0006a0001c0001t0012g0003others(4): Show | 7 | 147 | 0.0476 | -6 | c.324 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97500763 | GATATAT | G | intron_variant | MODIFIER | HG00280.hp1 HG01071.hp2 HG01934.hp1 others(11): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(3): Show | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0037others(11): Show | 14 | 147 | 0.0952 | -6 | c.324 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97509471 | CTTTTTT | C | intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 | 1 | 147 | 0.0068 | -6 | c.324 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97553683 | AAAGAAG | A | intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0086 | 1 | 147 | 0.0068 | -6 | c.324 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97570075 | AATATAT | A | intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0040 | 1 | 147 | 0.0068 | -6 | c.324 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH2_chrX_96679842_97609997 | 97583587 | CTGGGAT | C | intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0144 | 1 | 147 | 0.0068 | -6 | c.324 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 26/26 | chrX | TogoVar | ||||||
DIAPH2_chrX_96679842_97609997 | 97588996 | AATATAT | A | intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0112 | 1 | 147 | 0.0068 | -6 | c.324 others(27): Show |
DIAPH2 | ENSG00000147202.19 | transcript | ENST00000324765.13 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
DIAPH3_chr13_59660583_60168928 | 59670583 | CTTTTTT | C | intron_variant | MODIFIER | HG01884.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0132a0001c0001t0001g0167a0001c0001t0001g0196others(3): Show | 6 | 208 | 0.0289 | -6 | c.332 others(25): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 27/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 59692137 | CTTTTTT | C | intron_variant | MODIFIER | HG00323.hp1 HG02132.hp2 HG02896.hp1 others(2): Show |
a0001a0002a0004 | a0001c0001a0002c0003a0004c0007 | a0001c0001t0001a0001c0001t0007a0002c0003t0002others(1): Show | a0001c0001t0001g0060a0001c0001t0007g0131a0002c0003t0002g0044others(2): Show | 5 | 208 | 0.0240 | -6 | c.332 others(27): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 27/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 59741164 | AATGAGT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(90): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0006others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(16): Show | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(90): Show | 93 | 208 | 0.4471 | -6 | c.331 others(27): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 27/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 59795239 | ATTATAT | A | intron_variant | MODIFIER | HG00544.hp2 HG00609.hp2 HG01070.hp1 others(35): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0001c0010others(5): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(8): Show | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(35): Show | 38 | 208 | 0.1827 | -6 | c.316 others(27): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 25/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 59799375 | GCACACA | G | intron_variant | MODIFIER | HG02717.hp1 HG03041.hp2 HG04184.hp2 others(2): Show |
a0001a0004 | a0001c0001a0004c0007 | a0001c0001t0002a0001c0001t0006a0001c0001t0011others(1): Show | a0001c0001t0002g0029a0001c0001t0002g0100a0001c0001t0006g0207others(2): Show | 5 | 208 | 0.0240 | -6 | c.316 others(27): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 25/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 59802644 | ATATTAT | A | intron_variant | MODIFIER | HG03491.hp2 HG04184.hp2 |
a0004 | a0004c0007 | a0004c0007t0002a0004c0007t0006 | a0004c0007t0002g0050a0004c0007t0006g0174 | 2 | 208 | 0.0096 | -6 | c.316 others(25): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 25/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 59836859 | TTAAGTA | T | intron_variant | MODIFIER | HG03139.hp2 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0133a0001c0001t0007g0134 | 2 | 208 | 0.0096 | -6 | c.286 others(25): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 23/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 59917889 | CAAAAAA | C | intron_variant | MODIFIER | HG02572.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0125others(4): Show | 7 | 208 | 0.0337 | -6 | c.217 others(25): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 18/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 59939835 | CGTGTGT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(17): Show |
a0001a0006 | a0001c0001a0001c0002a0006c0011 | a0001c0001t0002a0001c0001t0005a0001c0002t0001others(1): Show | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0098others(17): Show | 20 | 208 | 0.0962 | -6 | c.207 others(27): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 17/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 59948901 | GAAGGAA | G | intron_variant | MODIFIER | HG00609.hp2 NA18985.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148a0001c0001t0001g0160 | 2 | 208 | 0.0096 | -6 | c.207 others(27): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 17/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 60082260 | TAAATAG | T | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp2 HG02615.hp1 others(10): Show |
a0001a0004 | a0001c0001a0004c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(2): Show | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0196others(10): Show | 13 | 208 | 0.0625 | -6 | c.495 others(25): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 4/27 | chr13 | TogoVar | ||||||
DIAPH3_chr13_59660583_60168928 | 60138754 | GGAAGGA | G | intron_variant | MODIFIER | HG02602.hp1 HG02896.hp1 HG03139.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0155a0001c0001t0001g0188a0001c0001t0007g0131others(1): Show | 4 | 208 | 0.0192 | -6 | c.181 others(23): Show |
DIAPH3 | ENSG00000139734.19 | transcript | ENST00000400324.9 | protein_coding | 1/27 | chr13 | TogoVar | ||||||
DICER1_chr14_95081228_95162529 | 95099731 | TACACAC | T | intron_variant | MODIFIER | HG03579.hp1 NA18945.hp1 NA19004.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0007 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0004g0085others(1): Show | 4 | 306 | 0.0131 | -6 | c.420 others(21): Show |
DICER1 | ENSG00000100697.17 | transcript | ENST00000343455.8 | protein_coding | 22/26 | chr14 | TogoVar | ||||||
DICER1_chr14_95081228_95162529 | 95136086 | TACACAC | T | intron_variant | MODIFIER | HG01074.hp2 HG01123.hp2 HG01168.hp1 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0025others(1): Show | a0001c0001t0001g0041a0001c0001t0001g0108a0001c0001t0003g0005others(15): Show | 22 | 306 | 0.0719 | -6 | c.-45 others(23): Show |
DICER1 | ENSG00000100697.17 | transcript | ENST00000343455.8 | protein_coding | 1/26 | chr14 | TogoVar | ||||||
DICER1_chr14_95081228_95162529 | 95161116 | TTACAAG | T | upstream_gene_variant | MODIFIER | HG01255.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0015 | a0001c0001t0010a0001c0003t0010a0001c0003t0015others(1): Show | a0001c0001t0010g0253a0001c0003t0010g0249a0001c0003t0010g0250others(4): Show | 9 | 306 | 0.0294 | -6 | c.-39 others(17): Show |
DICER1 | ENSG00000100697.17 | transcript | ENST00000343455.8 | protein_coding | 3588 | chr14 | TogoVar | ||||||
DIDO1_chr20_62872743_62931505 | 62929693 | GTGTATA | G | upstream_gene_variant | MODIFIER | HG01433.hp1 HG02451.hp1 HG02615.hp1 others(3): Show |
a0002a0006a0013 | a0002c0015a0006c0010a0013c0030 | a0002c0015t0004a0006c0010t0004a0013c0030t0016 | a0002c0015t0004g0039a0006c0010t0004g0036a0006c0010t0004g0037others(3): Show | 6 | 320 | 0.0188 | -6 | c.-34 others(17): Show |
DIDO1 | ENSG00000101191.17 | transcript | ENST00000395343.6 | protein_coding | 3189 | chr20 | TogoVar |