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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN5_chr11_99015949_100363885 | 100276527 | CAAA | C | intron_variant | MODIFIER | HG01081.hp1 HG02886.hp2 HG03041.hp1 others(6): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(6): Show | a0001c0001t0001g0020a0001c0001t0004g0029a0001c0001t0010g0023others(6): Show | 9 | 66 | 0.1364 | -3 | c.231 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100333408 | GAAA | G | intron_variant | MODIFIER | HG02004.hp1 HG02257.hp1 HG02602.hp2 others(2): Show |
a0001a0003a0004 | a0001c0001a0003c0003a0003c0011others(1): Show | a0001c0001t0001a0003c0003t0017a0003c0011t0019others(1): Show | a0001c0001t0001g0053a0001c0001t0001g0054a0003c0003t0017g0065others(2): Show | 5 | 66 | 0.0758 | -3 | c.273 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100344920 | TATA | T | intron_variant | MODIFIER | HG03041.hp1 NA20300.hp2 |
a0009a0012 | a0009c0012a0012c0013 | a0009c0012t0008a0012c0013t0008 | a0009c0012t0008g0026a0012c0013t0008g0031 | 2 | 66 | 0.0303 | -3 | c.303 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1088474 | CTTA | C | upstream_gene_variant | MODIFIER | HG01952.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
a0001a0005 | a0001c0002a0001c0003a0001c0005others(4): Show | a0001c0002t0001a0001c0003t0001a0001c0005t0001others(4): Show | a0001c0002t0001g0209a0001c0003t0001g0219a0001c0005t0001g0005others(11): Show | 14 | 232 | 0.0603 | -3 | c.-47 others(14): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4549 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1098230 | TATA | T | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(45): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0009others(17): Show | a0001c0001t0001g0190a0001c0001t0001g0198a0001c0002t0001g0209others(45): Show | 48 | 232 | 0.2069 | -3 | c.-83 others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1116698 | CTTT | C | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(4): Show | a0001c0001t0001g0131a0001c0002t0001g0160a0001c0004t0001g0158others(5): Show | 8 | 232 | 0.0345 | -3 | c.-83 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1152001 | TTAA | T | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
a0001a0003 | a0001c0003a0001c0005a0001c0006others(3): Show | a0001c0003t0001a0001c0005t0001a0001c0006t0001others(3): Show | a0001c0003t0001g0219a0001c0005t0001g0005a0001c0006t0001g0037others(5): Show | 8 | 232 | 0.0345 | -3 | c.55+ others(18): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1152723 | AATT | A | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0005others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0004others(10): Show | a0001c0001t0001g0190a0001c0002t0001g0227a0001c0002t0004g0228others(16): Show | 19 | 232 | 0.0819 | -3 | c.55+ others(18): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1160662 | TAAA | T | intron_variant | MODIFIER | HG00609.hp2 HG00738.hp1 HG00738.hp2 others(58): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(16): Show | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0071others(58): Show | 61 | 232 | 0.2629 | -3 | c.55+ others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1161308 | TAGC | T | intron_variant | MODIFIER | HG00609.hp2 HG00738.hp1 HG00738.hp2 others(58): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(16): Show | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0071others(58): Show | 61 | 232 | 0.2629 | -3 | c.55+ others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1174651 | TCTC | T | intron_variant | MODIFIER | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
a0001a0002a0003 | a0001c0002a0001c0005a0001c0006others(7): Show | a0001c0002t0001a0001c0002t0004a0001c0005t0001others(8): Show | a0001c0002t0001g0227a0001c0002t0004g0228a0001c0005t0001g0005others(13): Show | 16 | 232 | 0.0690 | -3 | c.55+ others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1181945 | GACA | G | intron_variant | MODIFIER | HG00642.hp1 HG00733.hp1 HG01109.hp1 others(4): Show |
a0001a0005 | a0001c0004a0001c0005a0001c0008others(1): Show | a0001c0004t0002a0001c0005t0001a0001c0008t0001others(1): Show | a0001c0004t0002g0038a0001c0004t0002g0039a0001c0005t0001g0157others(4): Show | 7 | 232 | 0.0302 | -3 | c.55+ others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1200922 | GTTC | G | intron_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(26): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(8): Show | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0067others(26): Show | 29 | 232 | 0.1250 | -3 | c.56- others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1233427 | TGAA | T | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(114): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(25): Show | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0035others(114): Show | 117 | 232 | 0.5043 | -3 | c.358 others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245218 | ATAT | A | intron_variant | MODIFIER | HG01256.hp2 HG01258.hp1 HG02056.hp1 others(25): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(6): Show | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0035others(25): Show | 28 | 232 | 0.1207 | -3 | c.358 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245271 | ATAT | A | intron_variant | MODIFIER | HG01884.hp2 HG02451.hp1 HG03471.hp2 others(1): Show |
a0001 | a0001c0005 | a0001c0005t0001a0001c0005t0004 | a0001c0005t0001g0188a0001c0005t0001g0189a0001c0005t0001g0193others(1): Show | 4 | 232 | 0.0172 | -3 | c.358 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245273 | ATAC | A | intron_variant | MODIFIER | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(24): Show |
a0001 | a0001c0002a0001c0004a0001c0005others(4): Show | a0001c0002t0001a0001c0002t0003a0001c0004t0001others(5): Show | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0084others(24): Show | 27 | 232 | 0.1164 | -3 | c.358 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245275 | ACAC | A | intron_variant | MODIFIER | HG02922.hp2 NA20905.hp2 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0001a0001c0005t0001 | a0001c0002t0001g0018a0001c0005t0001g0196 | 2 | 232 | 0.0086 | -3 | c.358 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245292 | TAAC | T | intron_variant | MODIFIER | HG00609.hp1 HG02165.hp1 HG02257.hp1 others(8): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(2): Show | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0082others(8): Show | 11 | 232 | 0.0474 | -3 | c.358 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245305 | TATA | T | intron_variant | MODIFIER | HG01952.hp2 HG03579.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0001 | a0001c0001t0001g0190a0001c0006t0001g0183 | 2 | 232 | 0.0086 | -3 | c.358 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245624 | TCAC | T | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(3): Show |
a0001a0003 | a0001c0006a0001c0019a0003c0015 | a0001c0006t0001a0001c0019t0001a0003c0015t0001 | a0001c0006t0001g0195a0001c0006t0001g0200a0001c0006t0001g0201others(3): Show | 6 | 232 | 0.0259 | -3 | c.358 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1255416 | GGAA | G | intron_variant | MODIFIER | HG01109.hp2 HG02559.hp1 NA21309.hp2 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0001a0001c0002t0004a0001c0005t0001 | a0001c0002t0001g0227a0001c0002t0004g0228a0001c0005t0001g0113 | 3 | 232 | 0.0129 | -3 | c.359 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1267905 | TTGA | T | intron_variant | MODIFIER | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(12): Show |
a0001a0002a0004 | a0001c0005a0001c0006a0001c0008others(5): Show | a0001c0005t0001a0001c0006t0001a0001c0008t0001others(5): Show | a0001c0005t0001g0196a0001c0005t0001g0203a0001c0006t0001g0111others(12): Show | 15 | 232 | 0.0647 | -3 | c.359 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1272725 | GCCT | G | intron_variant | MODIFIER | HG02145.hp1 HG02965.hp2 HG03579.hp1 |
a0001a0004 | a0001c0007a0004c0016 | a0001c0007t0001a0004c0016t0001 | a0001c0007t0001g0012a0004c0016t0001g0002a0004c0016t0001g0003 | 3 | 232 | 0.0129 | -3 | c.359 others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1281464 | CTTT | C | intron_variant | MODIFIER | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(109): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(24): Show | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0027others(109): Show | 112 | 232 | 0.4828 | -3 | c.454 others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1289676 | GTTT | G | intron_variant | MODIFIER | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(38): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(11): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0004others(15): Show | a0001c0001t0001g0190a0001c0002t0001g0209a0001c0002t0004g0228others(38): Show | 41 | 232 | 0.1767 | -3 | c.455 others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1312192 | CTAA | C | intron_variant | MODIFIER | HG00738.hp2 HG02622.hp2 |
a0001 | a0001c0006a0001c0022 | a0001c0006t0002a0001c0022t0001 | a0001c0006t0002g0178a0001c0022t0001g0137 | 2 | 232 | 0.0086 | -3 | c.762 others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1312614 | CAAA | C | intron_variant | MODIFIER | HG00733.hp2 HG01884.hp1 HG02074.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0008others(7): Show | a0001c0001t0001g0198a0001c0002t0001g0084a0001c0002t0001g0098others(17): Show | 20 | 232 | 0.0862 | -3 | c.762 others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1334376 | ATTT | A | intron_variant | MODIFIER | HG01169.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
a0001a0003 | a0001c0006a0001c0019a0001c0025others(1): Show | a0001c0006t0001a0001c0019t0001a0001c0025t0001others(1): Show | a0001c0006t0001g0184a0001c0006t0001g0200a0001c0019t0001g0202others(3): Show | 6 | 232 | 0.0259 | -3 | c.136 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1348574 | AATT | A | intron_variant | MODIFIER | HG01884.hp1 HG02965.hp1 HG02970.hp1 others(6): Show |
a0001 | a0001c0003a0001c0006a0001c0007others(1): Show | a0001c0003t0001a0001c0006t0001a0001c0007t0001others(1): Show | a0001c0003t0001g0042a0001c0006t0001g0229a0001c0007t0001g0133others(6): Show | 9 | 232 | 0.0388 | -3 | c.136 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1353823 | ATCT | A | intron_variant | MODIFIER | HG02109.hp2 HG02257.hp2 HG02280.hp1 others(9): Show |
a0001 | a0001c0005a0001c0006a0001c0008others(5): Show | a0001c0005t0001a0001c0005t0004a0001c0006t0001others(6): Show | a0001c0005t0001g0189a0001c0005t0001g0193a0001c0005t0001g0207others(9): Show | 12 | 232 | 0.0517 | -3 | c.149 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1381325 | TTTG | T | intron_variant | MODIFIER | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
a0001 | a0001c0005a0001c0006a0001c0007others(1): Show | a0001c0005t0001a0001c0006t0001a0001c0007t0001others(3): Show | a0001c0005t0001g0159a0001c0006t0001g0184a0001c0007t0001g0001others(18): Show | 21 | 232 | 0.0905 | -3 | c.216 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1384076 | ATAG | A | intron_variant | MODIFIER | HG02647.hp1 HG02717.hp2 HG02723.hp2 |
a0001 | a0001c0005a0001c0006 | a0001c0005t0001a0001c0006t0001 | a0001c0005t0001g0163a0001c0005t0001g0203a0001c0006t0001g0223 | 3 | 232 | 0.0129 | -3 | c.251 others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1395128 | TAAG | T | intron_variant | MODIFIER | HG02559.hp2 HG02647.hp1 HG02976.hp2 others(2): Show |
a0001 | a0001c0005a0001c0008 | a0001c0005t0001a0001c0008t0001 | a0001c0005t0001g0163a0001c0008t0001g0010a0001c0008t0001g0143others(2): Show | 5 | 232 | 0.0216 | -3 | c.270 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1400485 | GACA | G | intron_variant | MODIFIER | HG01074.hp1 HG01109.hp1 HG01109.hp2 others(22): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0009others(8): Show | a0001c0001t0001g0067a0001c0001t0001g0082a0001c0001t0001g0088others(22): Show | 25 | 232 | 0.1078 | -3 | c.270 others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1405146 | CTAT | C | downstream_gene_variant | MODIFIER | HG02055.hp1 HG02258.hp1 |
a0003 | a0003c0015 | a0003c0015t0001 | a0003c0015t0001g0007a0003c0015t0001g0008 | 2 | 232 | 0.0086 | -3 | c.*17 others(14): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 930 | chr3 | TogoVar | ||||||
CNTNAP1_chr17_42677531_42704993 | 42677534 | GAGA | G | upstream_gene_variant | MODIFIER | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
a0001a0002a0004 | a0001c0002a0001c0010a0001c0011others(4): Show | a0001c0002t0001a0001c0010t0001a0001c0011t0001others(4): Show | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0010t0001g0104others(13): Show | 22 | 364 | 0.0604 | -3 | c.-52 others(14): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 4996 | chr17 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146114863 | GTAT | G | upstream_gene_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(4): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0010others(3): Show | a0001c0001t0007a0001c0003t0020a0001c0010t0002others(3): Show | a0001c0001t0007g0018a0001c0001t0007g0020a0001c0003t0020g0017others(4): Show | 7 | 40 | 0.1750 | -3 | c.-20 others(14): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1937 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146155685 | CATT | C | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0006a0001c0001t0007a0001c0002t0001others(13): Show | a0001c0001t0006g0009a0001c0001t0007g0020a0001c0002t0001g0008others(14): Show | 17 | 40 | 0.4250 | -3 | c.97+ others(20): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146172032 | ATTT | A | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0007a0001c0002t0001a0001c0003t0011others(6): Show | a0001c0001t0007g0018a0001c0001t0007g0020a0001c0002t0001g0021others(7): Show | 10 | 40 | 0.2500 | -3 | c.97+ others(20): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146176094 | ACTT | A | intron_variant | MODIFIER | HG02630.hp1 NA19030.hp2 |
a0001a0002 | a0001c0012a0002c0016 | a0001c0012t0004a0002c0016t0004 | a0001c0012t0004g0026a0002c0016t0004g0024 | 2 | 40 | 0.0500 | -3 | c.97+ others(20): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146183606 | AAAT | A | intron_variant | MODIFIER | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
a0001 | a0001c0002a0001c0003a0001c0004 | a0001c0002t0002a0001c0003t0011a0001c0004t0003 | a0001c0002t0002g0013a0001c0003t0011g0023a0001c0004t0003g0035others(1): Show | 4 | 40 | 0.1000 | -3 | c.97+ others(20): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146225578 | CCTT | C | intron_variant | MODIFIER | HG01891.hp2 HG02886.hp1 HG02897.hp1 |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0006a0001c0002t0001a0001c0003t0013 | a0001c0001t0006g0009a0001c0002t0001g0008a0001c0003t0013g0010 | 3 | 40 | 0.0750 | -3 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146247805 | GAGA | G | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0035a0001c0004t0003g0036 | 2 | 40 | 0.0500 | -3 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146252886 | AATG | A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(20): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(17): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(20): Show | 23 | 40 | 0.5750 | -3 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146266886 | ATTT | A | intron_variant | MODIFIER | HG01891.hp2 HG02886.hp1 HG02896.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(5): Show | a0001c0001t0006a0001c0003t0013a0001c0003t0023others(6): Show | a0001c0001t0006g0009a0001c0003t0013g0010a0001c0003t0023g0030others(7): Show | 10 | 40 | 0.2500 | -3 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146269351 | CAAT | C | intron_variant | MODIFIER | HG02897.hp1 NA20129.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0023 | a0001c0002t0001g0008a0001c0003t0023g0030 | 2 | 40 | 0.0500 | -3 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146279962 | TATC | T | intron_variant | MODIFIER | HG02486.hp2 HG03540.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0010a0001c0003t0011 | a0001c0002t0010g0002a0001c0003t0011g0023 | 2 | 40 | 0.0500 | -3 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146288793 | ATTT | A | intron_variant | MODIFIER | HG02486.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
a0001 | a0001c0002a0001c0003a0001c0009others(1): Show | a0001c0002t0010a0001c0003t0011a0001c0009t0019others(1): Show | a0001c0002t0010g0002a0001c0003t0011g0023a0001c0009t0019g0027others(1): Show | 4 | 40 | 0.1000 | -3 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146320922 | TATA | T | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG03139.hp2 others(1): Show |
a0001a0004 | a0001c0002a0001c0009a0001c0011others(1): Show | a0001c0002t0001a0001c0009t0019a0001c0011t0016others(1): Show | a0001c0002t0001g0007a0001c0009t0019g0027a0001c0011t0016g0019others(1): Show | 4 | 40 | 0.1000 | -3 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |