view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTNAP2_chr7_146111801_148425998 | 147086397 | CTTTCTT | C | intron_variant | MODIFIER | HG02486.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0007a0001c0002t0002a0001c0003t0020others(2): Show | a0001c0001t0007g0020 a0001c0002t0002g0013 a0001c0003t0020g0017 others(2): Show |
5 | 40 | 0.1250 | -6 | c.551 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147104873 | CATATAT | C | intron_variant | MODIFIER | HG02896.hp1 HG03139.hp1 NA20129.hp2 |
a0001a0005 | a0001c0003a0001c0008a0005c0020 | a0001c0003t0023a0001c0008t0001a0005c0020t0005 | a0001c0003t0023g0030 a0001c0008t0001g0025 a0005c0020t0005g0016 |
3 | 40 | 0.0750 | -6 | c.551 others(23): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147301590 | CTCTGTG | C | intron_variant | MODIFIER | HG02451.hp2 HG02922.hp1 HG03225.hp2 |
a0001 | a0001c0001a0001c0018 | a0001c0001t0002a0001c0001t0012a0001c0018t0002 | a0001c0001t0002g0006 a0001c0001t0012g0034 a0001c0018t0002g0012 |
3 | 40 | 0.0750 | -6 | c.149 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147347435 | TATATGC | T | intron_variant | MODIFIER | HG02717.hp1 HG03239.hp2 |
a0001a0002 | a0001c0002a0002c0017 | a0001c0002t0002a0002c0017t0015 | a0001c0002t0002g0040 a0002c0017t0015g0037 |
2 | 40 | 0.0500 | -6 | c.149 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147469527 | TTTTTTC | T | intron_variant | MODIFIER | HG02717.hp1 HG02886.hp1 HG03098.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0013others(2): Show | a0001c0001t0001g0003 a0001c0002t0002g0040 a0001c0003t0013g0010 others(2): Show |
5 | 40 | 0.1250 | -6 | c.167 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147472204 | CTTTTTT | C | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(20): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(17): Show | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0006g0009 others(20): Show |
23 | 40 | 0.5750 | -6 | c.167 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147502737 | GTGTGTA | G | intron_variant | MODIFIER | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
a0001a0005 | a0001c0005a0001c0010a0001c0011others(2): Show | a0001c0005t0008a0001c0005t0022a0001c0010t0002others(3): Show | a0001c0005t0008g0005 a0001c0005t0022g0032 a0001c0010t0002g0014 others(3): Show |
6 | 40 | 0.1500 | -6 | c.177 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147510850 | CATATAT | C | intron_variant | MODIFIER | HG02451.hp2 HG03540.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0010 | a0001c0001t0002g0006 a0001c0002t0010g0002 |
2 | 40 | 0.0500 | -6 | c.177 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147569359 | ACCTCCC | A | intron_variant | MODIFIER | HG00735.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
a0001a0002 | a0001c0003a0001c0006a0001c0013others(1): Show | a0001c0003t0020a0001c0006t0014a0001c0013t0003others(1): Show | a0001c0003t0020g0017 a0001c0006t0014g0033 a0001c0013t0003g0039 others(1): Show |
4 | 40 | 0.1000 | -6 | c.189 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147575107 | ATGTGTG | A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(6): Show | a0001c0001t0001g0003 a0001c0001t0002g0006 a0001c0001t0006g0009 others(6): Show |
9 | 40 | 0.2250 | -6 | c.189 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147575371 | GGTGTGT | G | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02451.hp2 others(12): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0005others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(11): Show | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0002g0006 others(12): Show |
15 | 40 | 0.3750 | -6 | c.189 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147576091 | CTATTAT | C | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp2 others(8): Show |
a0001 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(8): Show | a0001c0001t0001g0003 a0001c0001t0002g0006 a0001c0001t0006g0009 others(8): Show |
11 | 40 | 0.2750 | -6 | c.189 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147599481 | CAAAAAA | C | intron_variant | MODIFIER | HG02451.hp2 HG02886.hp1 HG02922.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0013others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(4): Show | a0001c0001t0001g0003 a0001c0001t0002g0006 a0001c0001t0012g0034 others(4): Show |
7 | 40 | 0.1750 | -6 | c.189 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147601644 | AATATAT | A | intron_variant | MODIFIER | HG02630.hp1 HG02886.hp2 HG03098.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0022others(3): Show | a0001c0001t0001g0038 a0001c0002t0001g0021 a0001c0005t0022g0032 others(3): Show |
6 | 40 | 0.1500 | -6 | c.189 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147607390 | TTCTCTC | T | intron_variant | MODIFIER | HG00735.hp1 HG02976.hp2 |
a0001 | a0001c0003a0001c0006 | a0001c0003t0020a0001c0006t0014 | a0001c0003t0020g0017 a0001c0006t0014g0033 |
2 | 40 | 0.0500 | -6 | c.189 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147615277 | CAAAAAA | C | intron_variant | MODIFIER | HG02486.hp1 HG02630.hp1 HG02630.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0007a0001c0001t0012a0001c0002t0002others(5): Show | a0001c0001t0007g0020 a0001c0001t0012g0034 a0001c0002t0002g0013 others(6): Show |
9 | 40 | 0.2250 | -6 | c.189 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147629406 | AAATAAT | A | intron_variant | MODIFIER | HG00735.hp2 HG02451.hp1 HG02630.hp2 others(12): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(9): Show | a0001c0001t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0008 others(12): Show |
15 | 40 | 0.3750 | -6 | c.189 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147802794 | GGGGAGA | G | intron_variant | MODIFIER | HG02630.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
a0001 | a0001c0002a0001c0004a0001c0005others(1): Show | a0001c0002t0010a0001c0004t0005a0001c0005t0008others(1): Show | a0001c0002t0010g0002 a0001c0004t0005g0004 a0001c0005t0008g0005 others(1): Show |
4 | 40 | 0.1000 | -6 | c.209 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147861999 | CAAAAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp2 HG02897.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0006a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0006g0009 a0001c0002t0001g0008 a0001c0002t0001g0021 others(2): Show |
5 | 40 | 0.1250 | -6 | c.209 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147880854 | GGTGTGT | G | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG02451.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(2): Show | a0001c0001t0018a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0018g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(5): Show |
8 | 40 | 0.2000 | -6 | c.209 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147894959 | TTCTTTC | T | intron_variant | MODIFIER | HG00735.hp2 HG02896.hp1 HG03139.hp2 |
a0001a0005 | a0001c0011a0001c0019a0005c0020 | a0001c0011t0016a0001c0019t0006a0005c0020t0005 | a0001c0011t0016g0019 a0001c0019t0006g0015 a0005c0020t0005g0016 |
3 | 40 | 0.0750 | -6 | c.209 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147894961 | CTTTCTT | C | intron_variant | MODIFIER | HG02630.hp1 HG02717.hp2 HG03540.hp1 |
a0001 | a0001c0002a0001c0005a0001c0012 | a0001c0002t0010a0001c0005t0008a0001c0012t0004 | a0001c0002t0010g0002 a0001c0005t0008g0005 a0001c0012t0004g0026 |
3 | 40 | 0.0750 | -6 | c.209 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147925152 | AGAGAAG | A | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp2 HG02717.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0018a0001c0002t0001a0001c0003t0004others(3): Show | a0001c0001t0018g0001 a0001c0002t0001g0007 a0001c0003t0004g0029 others(3): Show |
6 | 40 | 0.1500 | -6 | c.225 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147943766 | CAAAAAA | C | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0006a0001c0001t0007a0001c0002t0002others(1): Show | a0001c0001t0006g0009 a0001c0001t0007g0020 a0001c0002t0002g0040 others(2): Show |
5 | 40 | 0.1250 | -6 | c.225 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147947454 | CAAAAAA | C | intron_variant | MODIFIER | HG01891.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0006a0001c0001t0007a0001c0002t0002others(4): Show | a0001c0001t0006g0009 a0001c0001t0007g0018 a0001c0002t0002g0013 others(5): Show |
8 | 40 | 0.2000 | -6 | c.225 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148057950 | CTTATTA | C | intron_variant | MODIFIER | HG02630.hp2 NA18522.hp2 NA19030.hp2 |
a0001a0002 | a0001c0001a0001c0002a0002c0016 | a0001c0001t0007a0001c0002t0002a0002c0016t0004 | a0001c0001t0007g0018 a0001c0002t0002g0013 a0002c0016t0004g0024 |
3 | 40 | 0.0750 | -6 | c.238 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148062028 | AGTGTGT | A | intron_variant | MODIFIER | HG03225.hp2 NA21309.hp1 |
a0001 | a0001c0010a0001c0018 | a0001c0010t0002a0001c0018t0002 | a0001c0010t0002g0014 a0001c0018t0002g0012 |
2 | 40 | 0.0500 | -6 | c.238 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148096279 | ATGTGTG | A | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp2 HG02896.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(4): Show | a0001c0001t0001g0003 a0001c0001t0002g0006 a0001c0001t0006g0009 others(5): Show |
8 | 40 | 0.2000 | -6 | c.238 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148097367 | AAAAAAT | A | intron_variant | MODIFIER | HG03098.hp2 HG03239.hp1 NA19030.hp1 |
a0001a0003 | a0001c0001a0001c0002a0003c0007 | a0001c0001t0001a0001c0002t0001a0003c0007t0017 | a0001c0001t0001g0038 a0001c0002t0001g0021 a0003c0007t0017g0031 |
3 | 40 | 0.0750 | -6 | c.238 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148101350 | AGTGTGT | A | intron_variant | MODIFIER | HG02451.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
a0001a0002 | a0001c0002a0001c0004a0001c0005others(1): Show | a0001c0002t0001a0001c0004t0005a0001c0005t0022others(1): Show | a0001c0002t0001g0007 a0001c0004t0005g0004 a0001c0005t0022g0032 others(1): Show |
4 | 40 | 0.1000 | -6 | c.238 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148106493 | GATATAT | G | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0001a0001c0008a0001c0010others(1): Show | a0001c0001t0002a0001c0001t0006a0001c0008t0001others(2): Show | a0001c0001t0002g0006 a0001c0001t0006g0009 a0001c0008t0001g0025 others(2): Show |
5 | 40 | 0.1250 | -6 | c.238 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148112415 | GTATTAT | G | intron_variant | MODIFIER | HG01891.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
a0001a0004a0005 | a0001c0002a0001c0003a0004c0014others(1): Show | a0001c0002t0001a0001c0002t0002a0001c0003t0023others(2): Show | a0001c0002t0001g0008 a0001c0002t0002g0013 a0001c0003t0023g0030 others(2): Show |
5 | 40 | 0.1250 | -6 | c.238 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148125685 | GTGTGTA | G | intron_variant | MODIFIER | HG03098.hp1 HG03540.hp2 NA19030.hp2 |
a0001a0002 | a0001c0001a0001c0003a0002c0016 | a0001c0001t0001a0001c0003t0004a0002c0016t0004 | a0001c0001t0001g0003 a0001c0003t0004g0029 a0002c0016t0004g0024 |
3 | 40 | 0.0750 | -6 | c.255 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148181741 | CTTTTTT | C | intron_variant | MODIFIER | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(2): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0006others(1): Show | a0001c0002t0001a0001c0002t0002a0001c0003t0011others(2): Show | a0001c0002t0001g0007 a0001c0002t0002g0040 a0001c0003t0011g0023 others(2): Show |
5 | 40 | 0.1250 | -6 | c.301 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148187109 | TACACAC | T | intron_variant | MODIFIER | HG02630.hp1 HG02896.hp1 |
a0001a0005 | a0001c0012a0005c0020 | a0001c0012t0004a0005c0020t0005 | a0001c0012t0004g0026 a0005c0020t0005g0016 |
2 | 40 | 0.0500 | -6 | c.301 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148190854 | CAGAGAG | C | intron_variant | MODIFIER | HG00735.hp1 HG02451.hp2 HG02486.hp2 others(12): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(11): Show | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0002g0006 others(12): Show |
15 | 40 | 0.3750 | -6 | c.301 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148227884 | CGTGTGT | C | intron_variant | MODIFIER | HG02717.hp2 HG02976.hp1 |
a0001 | a0001c0005a0001c0015 | a0001c0005t0008a0001c0015t0001 | a0001c0005t0008g0005 a0001c0015t0001g0011 |
2 | 40 | 0.0500 | -6 | c.324 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148257922 | AACACAC | A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp2 others(24): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(19): Show | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0002g0006 others(24): Show |
27 | 40 | 0.6750 | -6 | c.338 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148294039 | CAAAAAA | C | intron_variant | MODIFIER | HG00735.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0007a0001c0002t0002a0001c0003t0004others(2): Show | a0001c0001t0007g0018 a0001c0002t0002g0013 a0001c0003t0004g0029 others(2): Show |
5 | 40 | 0.1250 | -6 | c.347 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148328976 | GAAAAAA | G | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp2 HG02897.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(1): Show | a0001c0001t0002g0006 a0001c0001t0006g0009 a0001c0002t0001g0008 others(1): Show |
4 | 40 | 0.1000 | -6 | c.347 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148339974 | AGTGTGT | A | intron_variant | MODIFIER | HG01891.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0015others(3): Show | a0001c0001t0006a0001c0003t0013a0001c0015t0001others(3): Show | a0001c0001t0006g0009 a0001c0003t0013g0010 a0001c0015t0001g0011 others(3): Show |
6 | 40 | 0.1500 | -6 | c.347 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148365684 | ATATATG | A | intron_variant | MODIFIER | HG03139.hp2 HG03239.hp1 HG03239.hp2 |
a0001a0003 | a0001c0002a0001c0011a0003c0007 | a0001c0002t0002a0001c0011t0016a0003c0007t0017 | a0001c0002t0002g0040 a0001c0011t0016g0019 a0003c0007t0017g0031 |
3 | 40 | 0.0750 | -6 | c.347 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148365817 | CATGCAT | C | intron_variant | MODIFIER | HG02976.hp1 HG02976.hp2 |
a0001 | a0001c0003a0001c0015 | a0001c0003t0020a0001c0015t0001 | a0001c0003t0020g0017 a0001c0015t0001g0011 |
2 | 40 | 0.0500 | -6 | c.347 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 148365919 | TGTATAC | T | intron_variant | MODIFIER | HG02717.hp2 NA20129.hp1 |
a0001 | a0001c0005a0001c0006 | a0001c0005t0008a0001c0006t0009 | a0001c0005t0008g0005 a0001c0006t0009g0028 |
2 | 40 | 0.0500 | -6 | c.347 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 148366256 | GTGTGTA | G | intron_variant | MODIFIER | HG02922.hp1 HG03540.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0012a0001c0002t0010 | a0001c0001t0012g0034 a0001c0002t0010g0002 |
2 | 40 | 0.0500 | -6 | c.347 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148369181 | CTTTTTT | C | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(6): Show | a0001c0001t0002g0006 a0001c0001t0006g0009 a0001c0001t0012g0034 others(6): Show |
9 | 40 | 0.2250 | -6 | c.347 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148385736 | GTTTTTT | G | intron_variant | MODIFIER | HG02976.hp1 HG03139.hp2 HG03239.hp1 others(1): Show |
a0001a0003 | a0001c0002a0001c0011a0001c0015others(1): Show | a0001c0002t0002a0001c0011t0016a0001c0015t0001others(1): Show | a0001c0002t0002g0040 a0001c0011t0016g0019 a0001c0015t0001g0011 others(1): Show |
4 | 40 | 0.1000 | -6 | c.371 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148413401 | AATATAT | A | intron_variant | MODIFIER | HG02896.hp1 HG02922.hp2 HG03098.hp2 others(2): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0007a0001c0002t0001a0001c0004t0005others(2): Show | a0001c0001t0007g0018 a0001c0002t0001g0021 a0001c0004t0005g0004 others(2): Show |
5 | 40 | 0.1250 | -6 | c.379 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41902215 | AAAAAAG | A | intron_variant | MODIFIER | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(4): Show |
a0004a0011a0033 | a0004c0004a0011c0037a0011c0040others(1): Show | a0004c0004t0005a0011c0037t0007a0011c0040t0007others(1): Show | a0004c0004t0005g0030 a0004c0004t0005g0031 a0004c0004t0005g0032 others(4): Show |
7 | 108 | 0.0648 | -6 | c.344 others(25): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | TogoVar | |||||||
CNTNAP3B_chr9_41885536_42134426 | 41904311 | GTTTTTT | G | intron_variant | MODIFIER | HG02109.hp2 HG02559.hp2 HG02622.hp2 others(2): Show |
a0008a0026a0027 | a0008c0006a0026c0025a0027c0026 | a0008c0006t0010a0026c0025t0019a0027c0026t0020 | a0008c0006t0010g0069 a0008c0006t0010g0070 a0008c0006t0010g0071 others(2): Show |
5 | 108 | 0.0463 | -6 | c.344 others(25): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | TogoVar |