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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN6_chr3_1088024_1409217 | 1098789 | C | CATATATA others(1): Show |
intron_variant | MODIFIER | HG00609.hp2 HG04204.hp2 NA18951.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0001a0001c0003t0001a0001c0004t0001 | a0001c0001t0001g0082a0001c0003t0001g0081a0001c0004t0001g0080others(1): Show | 4 | 232 | 0.0172 | 8 | c.-83 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1106521 | T | TACACACA others(1): Show |
intron_variant | MODIFIER | HG01978.hp2 HG03130.hp1 HG03239.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0003a0001c0003t0001others(1): Show | a0001c0001t0001g0024a0001c0002t0003g0069a0001c0003t0001g0144others(1): Show | 4 | 232 | 0.0172 | 8 | c.-83 others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1142966 | G | GTATATAT others(1): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02922.hp1 NA18522.hp2 |
a0001 | a0001c0008a0001c0019 | a0001c0008t0001a0001c0019t0001 | a0001c0008t0001g0197a0001c0008t0001g0214a0001c0019t0001g0202 | 3 | 232 | 0.0129 | 8 | c.-82 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1158844 | A | ATATGTGT others(1): Show |
intron_variant | MODIFIER | HG01256.hp2 HG01258.hp1 |
a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0014a0001c0007t0001g0015 | 2 | 232 | 0.0086 | 8 | c.55+ others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1158967 | C | CATATATA others(1): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02258.hp1 |
a0003 | a0003c0015 | a0003c0015t0001 | a0003c0015t0001g0007a0003c0015t0001g0008 | 2 | 232 | 0.0086 | 8 | c.55+ others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1172620 | C | CTGTGTGT others(1): Show |
intron_variant | MODIFIER | HG02615.hp1 NA21309.hp2 |
a0001a0002 | a0001c0002a0002c0014 | a0001c0002t0001a0002c0014t0001 | a0001c0002t0001g0227a0002c0014t0001g0232 | 2 | 232 | 0.0086 | 8 | c.55+ others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245197 | G | GATATATA others(1): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02258.hp1 |
a0003 | a0003c0015 | a0003c0015t0001 | a0003c0015t0001g0007a0003c0015t0001g0008 | 2 | 232 | 0.0086 | 8 | c.358 others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1265047 | T | TTTTTTTT others(1): Show |
intron_variant | MODIFIER | HG01952.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0006others(2): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0001others(2): Show | a0001c0001t0001g0129a0001c0003t0001g0077a0001c0006t0001g0183others(4): Show | 7 | 232 | 0.0302 | 8 | c.359 others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1277346 | C | CTTTTTTT others(1): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01106.hp1 HG01109.hp2 others(11): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(5): Show | a0001c0001t0001g0035a0001c0001t0001g0086a0001c0002t0001g0139others(11): Show | 14 | 232 | 0.0603 | 8 | c.359 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1280459 | A | ATTTTTTT others(1): Show |
intron_variant | MODIFIER | HG01109.hp2 HG01169.hp1 HG02559.hp1 others(8): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(3): Show | a0001c0002t0004a0001c0003t0001a0001c0004t0001others(3): Show | a0001c0002t0004g0228a0001c0003t0001g0042a0001c0003t0001g0219others(8): Show | 11 | 232 | 0.0474 | 8 | c.454 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1300449 | C | CAGGAAGG others(1): Show |
intron_variant | MODIFIER | HG00639.hp2 HG01109.hp2 HG01952.hp1 others(14): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0007others(7): Show | a0001c0001t0001g0126a0001c0002t0001g0018a0001c0002t0001g0160others(14): Show | 17 | 232 | 0.0733 | 8 | c.761 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1300557 | A | AAAAGAAA others(1): Show |
intron_variant | MODIFIER | HG01255.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
a0001 | a0001c0002a0001c0003a0001c0005others(1): Show | a0001c0002t0009a0001c0003t0001a0001c0005t0001others(1): Show | a0001c0002t0009g0205a0001c0003t0001g0030a0001c0005t0001g0181others(1): Show | 4 | 232 | 0.0172 | 8 | c.761 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1308287 | T | TTGTGTGT others(1): Show |
intron_variant | MODIFIER | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(14): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(6): Show | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0156others(14): Show | 17 | 232 | 0.0733 | 8 | c.761 others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1312319 | A | AATATATA others(1): Show |
intron_variant | MODIFIER | HG00733.hp2 HG02074.hp1 HG03669.hp1 |
a0001 | a0001c0002a0001c0009 | a0001c0002t0001a0001c0009t0001 | a0001c0002t0001g0084a0001c0002t0001g0098a0001c0009t0001g0114 | 3 | 232 | 0.0129 | 8 | c.762 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1332495 | A | AAAGGAAG others(1): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(30): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0004others(9): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0001others(10): Show | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0044others(30): Show | 33 | 232 | 0.1422 | 8 | c.136 others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1384812 | C | CACACACA others(1): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
a0001a0003a0006 | a0001c0013a0003c0015a0006c0027 | a0001c0013t0001a0003c0015t0001a0006c0027t0001 | a0001c0013t0001g0199a0001c0013t0001g0208a0003c0015t0001g0007others(2): Show | 5 | 232 | 0.0216 | 8 | c.251 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1384952 | G | GTCGCCTC others(1): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
a0001a0003a0006 | a0001c0013a0001c0025a0003c0015others(1): Show | a0001c0013t0001a0001c0025t0001a0003c0015t0001others(1): Show | a0001c0013t0001g0199a0001c0013t0001g0208a0001c0025t0001g0192others(3): Show | 6 | 232 | 0.0259 | 8 | c.251 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTNAP1_chr17_42677531_42704993 | 42686469 | G | GTTTTTTT others(1): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(29): Show |
a0001a0005 | a0001c0001a0001c0005a0005c0015 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(3): Show | a0001c0001t0001g0055a0001c0001t0002g0003a0001c0001t0002g0026others(15): Show | 32 | 364 | 0.0879 | 8 | c.900 others(23): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
CNTNAP1_chr17_42677531_42704993 | 42686475 | T | TTTTGTTT others(1): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0110 | 11 | 364 | 0.0302 | 8 | c.900 others(23): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146144139 | A | ATATTTAT others(1): Show |
intron_variant | MODIFIER | HG02486.hp2 HG02630.hp1 HG03139.hp1 |
a0001 | a0001c0003a0001c0008a0001c0012 | a0001c0003t0011a0001c0008t0001a0001c0012t0004 | a0001c0003t0011g0023a0001c0008t0001g0025a0001c0012t0004g0026 | 3 | 40 | 0.0750 | 8 | c.97+ others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146171027 | A | AAAATAAA others(1): Show |
intron_variant | MODIFIER | HG01891.hp1 HG03098.hp2 |
a0001a0004 | a0001c0002a0004c0014 | a0001c0002t0001a0004c0014t0021 | a0001c0002t0001g0021a0004c0014t0021g0022 | 2 | 40 | 0.0500 | 8 | c.97+ others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146222541 | A | AGTGTGTG others(1): Show |
intron_variant | MODIFIER | HG02630.hp2 NA19030.hp2 |
a0001a0002 | a0001c0002a0002c0016 | a0001c0002t0002a0002c0016t0004 | a0001c0002t0002g0013a0002c0016t0004g0024 | 2 | 40 | 0.0500 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146231015 | A | AAAATAAA others(1): Show |
intron_variant | MODIFIER | HG02896.hp1 HG03139.hp2 NA18522.hp2 |
a0001a0005 | a0001c0001a0001c0011a0005c0020 | a0001c0001t0007a0001c0011t0016a0005c0020t0005 | a0001c0001t0007g0018a0001c0011t0016g0019a0005c0020t0005g0016 | 3 | 40 | 0.0750 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146231042 | A | ATAAATAA others(1): Show |
intron_variant | MODIFIER | HG00735.hp1 NA21309.hp1 |
a0001 | a0001c0006a0001c0010 | a0001c0006t0014a0001c0010t0002 | a0001c0006t0014g0033a0001c0010t0002g0014 | 2 | 40 | 0.0500 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146285949 | T | TTTCCTTC others(1): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0006a0001c0003t0013a0001c0004t0003others(1): Show | a0001c0001t0006g0009a0001c0003t0013g0010a0001c0004t0003g0035others(2): Show | 5 | 40 | 0.1250 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146309829 | A | AAAGGAAG others(1): Show |
intron_variant | MODIFIER | HG03225.hp1 HG03225.hp2 NA18522.hp1 |
a0001 | a0001c0009a0001c0013a0001c0018 | a0001c0009t0019a0001c0013t0003a0001c0018t0002 | a0001c0009t0019g0027a0001c0013t0003g0039a0001c0018t0002g0012 | 3 | 40 | 0.0750 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146324777 | T | TTATATAT others(1): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0006a0001c0003t0013a0001c0004t0003others(1): Show | a0001c0001t0006g0009a0001c0003t0013g0010a0001c0004t0003g0035others(2): Show | 5 | 40 | 0.1250 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146358022 | T | TTTTATTT others(1): Show |
intron_variant | MODIFIER | HG01891.hp2 HG03098.hp2 HG03225.hp2 |
a0001 | a0001c0001a0001c0002a0001c0018 | a0001c0001t0006a0001c0002t0001a0001c0018t0002 | a0001c0001t0006g0009a0001c0002t0001g0021a0001c0018t0002g0012 | 3 | 40 | 0.0750 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146373405 | T | TACACACA others(1): Show |
intron_variant | MODIFIER | HG03098.hp2 HG03225.hp1 |
a0001 | a0001c0002a0001c0009 | a0001c0002t0001a0001c0009t0019 | a0001c0002t0001g0021a0001c0009t0019g0027 | 2 | 40 | 0.0500 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146395779 | T | TAGATGAT others(1): Show |
intron_variant | MODIFIER | HG02451.hp1 HG02922.hp1 NA18522.hp1 |
a0001 | a0001c0001a0001c0002a0001c0013 | a0001c0001t0012a0001c0002t0001a0001c0013t0003 | a0001c0001t0012g0034a0001c0002t0001g0007a0001c0013t0003g0039 | 3 | 40 | 0.0750 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146443230 | T | TAATAAAT others(1): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(10): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0001t0006g0009others(13): Show | 16 | 40 | 0.4000 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146444661 | C | CTTTTTTT others(1): Show |
intron_variant | MODIFIER | HG01891.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
a0001 | a0001c0001a0001c0009a0001c0010 | a0001c0001t0006a0001c0001t0007a0001c0009t0019others(1): Show | a0001c0001t0006g0009a0001c0001t0007g0018a0001c0009t0019g0027others(1): Show | 4 | 40 | 0.1000 | 8 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146450935 | A | ATATTTAT others(1): Show |
intron_variant | MODIFIER | HG02486.hp2 HG02630.hp2 HG02886.hp2 others(4): Show |
a0001 | a0001c0002a0001c0003a0001c0005others(3): Show | a0001c0002t0001a0001c0002t0002a0001c0003t0011others(4): Show | a0001c0002t0001g0021a0001c0002t0002g0013a0001c0003t0011g0023others(4): Show | 7 | 40 | 0.1750 | 8 | c.98- others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146474999 | A | ACGCGCGC others(1): Show |
intron_variant | MODIFIER | HG02630.hp2 HG02976.hp1 HG03139.hp1 |
a0001 | a0001c0002a0001c0008a0001c0015 | a0001c0002t0002a0001c0008t0001a0001c0015t0001 | a0001c0002t0002g0013a0001c0008t0001g0025a0001c0015t0001g0011 | 3 | 40 | 0.0750 | 8 | c.98- others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146525570 | A | ATCTATCT others(1): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02976.hp2 HG03098.hp1 |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0003t0020a0001c0005t0008 | a0001c0001t0001g0003a0001c0003t0020g0017a0001c0005t0008g0005 | 3 | 40 | 0.0750 | 8 | c.98- others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146591414 | T | TGCAGTGG others(1): Show |
intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(34): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(28): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(34): Show | 37 | 40 | 0.9250 | 8 | c.98- others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146594433 | T | TACACACA others(1): Show |
intron_variant | MODIFIER | HG02897.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
a0001 | a0001c0002a0001c0006a0001c0008 | a0001c0002t0001a0001c0006t0009a0001c0008t0001 | a0001c0002t0001g0008a0001c0002t0001g0021a0001c0006t0009g0028others(1): Show | 4 | 40 | 0.1000 | 8 | c.98- others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146596595 | C | CAGAGAGA others(1): Show |
intron_variant | MODIFIER | HG02886.hp2 HG03225.hp2 |
a0001 | a0001c0005a0001c0018 | a0001c0005t0022a0001c0018t0002 | a0001c0005t0022g0032a0001c0018t0002g0012 | 2 | 40 | 0.0500 | 8 | c.98- others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146617017 | T | TTTTGTTT others(1): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(20): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(17): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0001t0006g0009others(20): Show | 23 | 40 | 0.5750 | 8 | c.98- others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146617017 | T | TTTTTTTT others(1): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02486.hp1 others(8): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0005others(6): Show | a0001c0001t0007a0001c0003t0011a0001c0003t0013others(8): Show | a0001c0001t0007g0020a0001c0003t0011g0023a0001c0003t0013g0010others(8): Show | 11 | 40 | 0.2750 | 8 | c.98- others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146622243 | A | ATATCTAT others(1): Show |
intron_variant | MODIFIER | HG00735.hp1 HG02886.hp1 HG03225.hp1 others(1): Show |
a0001 | a0001c0003a0001c0006a0001c0009 | a0001c0003t0013a0001c0003t0023a0001c0006t0014others(1): Show | a0001c0003t0013g0010a0001c0003t0023g0030a0001c0006t0014g0033others(1): Show | 4 | 40 | 0.1000 | 8 | c.98- others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146694883 | A | AATTCTGA others(1): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02717.hp2 HG02922.hp1 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0002a0001c0001t0012a0001c0005t0008 | a0001c0001t0002g0006a0001c0001t0012g0034a0001c0005t0008g0005 | 3 | 40 | 0.0750 | 8 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146761284 | T | TGGAAGGA others(1): Show |
intron_variant | MODIFIER | HG02451.hp1 HG02896.hp1 HG03139.hp2 others(1): Show |
a0001a0005 | a0001c0002a0001c0011a0005c0020 | a0001c0002t0001a0001c0002t0010a0001c0011t0016others(1): Show | a0001c0002t0001g0007a0001c0002t0010g0002a0001c0011t0016g0019others(1): Show | 4 | 40 | 0.1000 | 8 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146770317 | T | TACACACA others(1): Show |
intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 NA21309.hp1 |
a0001 | a0001c0004a0001c0010 | a0001c0004t0003a0001c0010t0002 | a0001c0004t0003g0035a0001c0004t0003g0036a0001c0010t0002g0014 | 3 | 40 | 0.0750 | 8 | c.98- others(23): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146842994 | C | CTTTTTTT others(1): Show |
intron_variant | MODIFIER | HG02886.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
a0001a0005 | a0001c0005a0001c0010a0001c0011others(1): Show | a0001c0005t0022a0001c0010t0002a0001c0011t0016others(1): Show | a0001c0005t0022g0032a0001c0010t0002g0014a0001c0011t0016g0019others(1): Show | 4 | 40 | 0.1000 | 8 | c.402 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146856297 | G | GATACATA others(1): Show |
intron_variant | MODIFIER | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
a0001a0002 | a0001c0002a0001c0009a0002c0017 | a0001c0002t0010a0001c0009t0019a0002c0017t0015 | a0001c0002t0010g0002a0001c0009t0019g0027a0002c0017t0015g0037 | 3 | 40 | 0.0750 | 8 | c.402 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146937364 | A | AATAAAAA others(1): Show |
intron_variant | MODIFIER | HG00735.hp1 HG03239.hp2 |
a0001 | a0001c0002a0001c0006 | a0001c0002t0002a0001c0006t0014 | a0001c0002t0002g0040a0001c0006t0014g0033 | 2 | 40 | 0.0500 | 8 | c.402 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147081583 | T | TTGTGTGT others(1): Show |
intron_variant | MODIFIER | NA18522.hp2 NA20129.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0007a0001c0003t0023 | a0001c0001t0007g0018a0001c0003t0023g0030 | 2 | 40 | 0.0500 | 8 | c.551 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147090322 | C | CGTGTGTG others(1): Show |
intron_variant | MODIFIER | HG00735.hp2 HG02451.hp1 HG02896.hp1 others(5): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0018a0001c0002t0001a0001c0004t0003others(4): Show | a0001c0001t0018g0001a0001c0002t0001g0007a0001c0004t0003g0035others(5): Show | 8 | 40 | 0.2000 | 8 | c.551 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147102282 | G | GAAAAAAA others(1): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(11): Show | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0001t0007g0020others(11): Show | 14 | 40 | 0.3500 | 8 | c.551 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |