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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN5_chr11_99015949_100363885 | 99099549 | TACACAC | T | intron_variant | MODIFIER | HG01081.hp2 HG01123.hp1 HG02886.hp1 others(5): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0010others(4): Show | a0001c0001t0003g0060 a0001c0001t0005g0048 a0001c0001t0010g0023 others(5): Show |
8 | 66 | 0.1212 | -6 | c.-21 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99178314 | CCACACA | C | intron_variant | MODIFIER | HG01169.hp2 HG02132.hp1 NA20300.hp1 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0005a0001c0001t0016a0006c0006t0001 | a0001c0001t0005g0048 a0001c0001t0016g0049 a0006c0006t0001g0005 |
3 | 66 | 0.0455 | -6 | c.-20 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99178590 | TTATATC | T | intron_variant | MODIFIER | HG02109.hp1 HG06807.hp1 |
a0005a0006 | a0005c0005a0006c0006 | a0005c0005t0010a0006c0006t0013 | a0005c0005t0010g0006 a0006c0006t0013g0025 |
2 | 66 | 0.0303 | -6 | c.-20 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99206566 | TTGTGTA | T | intron_variant | MODIFIER | HG00733.hp1 HG00738.hp1 HG01081.hp2 others(14): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(9): Show | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0060 others(14): Show |
17 | 66 | 0.2576 | -6 | c.-20 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99236469 | AACACAC | A | intron_variant | MODIFIER | HG00733.hp2 HG00735.hp2 HG00738.hp2 others(32): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0003c0003others(6): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(22): Show | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0052 others(32): Show |
35 | 66 | 0.5303 | -6 | c.-20 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99236493 | CACACAG | C | intron_variant | MODIFIER | HG02886.hp2 HG02895.hp1 HG02965.hp1 others(2): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0004others(2): Show | a0001c0001t0010a0002c0002t0005a0004c0004t0020others(2): Show | a0001c0001t0010g0023 a0002c0002t0005g0015 a0004c0004t0020g0024 others(2): Show |
5 | 66 | 0.0758 | -6 | c.-20 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99246303 | ATTATTT | A | intron_variant | MODIFIER | HG01099.hp1 HG02735.hp1 NA18939.hp2 others(2): Show |
a0001a0003a0004others(1): Show | a0001c0001a0003c0003a0004c0004others(1): Show | a0001c0001t0004a0001c0001t0006a0003c0003t0002others(2): Show | a0001c0001t0004g0010 a0001c0001t0006g0032 a0003c0003t0002g0002 others(2): Show |
5 | 66 | 0.0758 | -6 | c.-20 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 99253897 | TTATATA | T | intron_variant | MODIFIER | HG02257.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0004others(2): Show | a0001c0001t0015a0002c0002t0005a0004c0004t0020others(2): Show | a0001c0001t0015g0064 a0002c0002t0005g0015 a0004c0004t0020g0024 others(2): Show |
5 | 66 | 0.0758 | -6 | c.-20 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99267920 | GCACACA | G | intron_variant | MODIFIER | HG01169.hp1 HG02004.hp2 HG02132.hp2 others(2): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(2): Show | a0001c0001t0001g0004 a0001c0001t0004g0029 a0001c0001t0009g0043 others(2): Show |
5 | 66 | 0.0758 | -6 | c.-20 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99284600 | GGTGTGT | G | intron_variant | MODIFIER | HG01169.hp1 HG02004.hp2 HG02602.hp2 others(3): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0053 others(3): Show |
6 | 66 | 0.0909 | -6 | c.-20 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99306746 | GATAATA | G | intron_variant | MODIFIER | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0003c0003others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(20): Show | a0001c0001t0001g0053 a0001c0001t0003g0060 a0001c0001t0004g0010 others(23): Show |
26 | 66 | 0.3939 | -6 | c.-20 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99329914 | GACACAC | G | intron_variant | MODIFIER | HG00735.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(10): Show | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0052 others(12): Show |
15 | 66 | 0.2273 | -6 | c.-71 others(23): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99338919 | GATATAT | G | intron_variant | MODIFIER | HG01081.hp1 HG01099.hp1 HG01169.hp2 others(13): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0003c0003others(6): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(11): Show | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0004g0010 others(13): Show |
16 | 66 | 0.2424 | -6 | c.-71 others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99373062 | AGCGGGG | A | intron_variant | MODIFIER | HG00733.hp1 HG00735.hp1 HG01081.hp2 others(4): Show |
a0001a0003a0006others(1): Show | a0001c0001a0003c0003a0006c0006others(1): Show | a0001c0001t0009a0001c0001t0010a0001c0001t0012others(4): Show | a0001c0001t0009g0063 a0001c0001t0010g0047 a0001c0001t0012g0018 others(4): Show |
7 | 66 | 0.1061 | -6 | c.-71 others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 99408442 | AAGAAAG | A | intron_variant | MODIFIER | HG02109.hp2 HG02258.hp1 HG02723.hp2 others(1): Show |
a0001a0004a0010 | a0001c0001a0004c0004a0010c0010 | a0001c0001t0003a0001c0001t0004a0004c0004t0002others(1): Show | a0001c0001t0003g0021 a0001c0001t0004g0044 a0004c0004t0002g0001 others(1): Show |
4 | 66 | 0.0606 | -6 | c.-71 others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99422516 | TTTTATA | T | intron_variant | MODIFIER | HG01081.hp2 HG02258.hp2 NA19043.hp2 |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0005 | a0001c0001t0010a0002c0002t0008a0005c0005t0003 | a0001c0001t0010g0047 a0002c0002t0008g0019 a0005c0005t0003g0045 |
3 | 66 | 0.0455 | -6 | c.-71 others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99430386 | TATATAC | T | intron_variant | MODIFIER | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(5): Show | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
13 | 66 | 0.1970 | -6 | c.-71 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99450257 | AATATAT | A | intron_variant | MODIFIER | HG01169.hp2 HG01934.hp2 HG02886.hp1 others(1): Show |
a0003a0006 | a0003c0003a0006c0006 | a0003c0003t0002a0003c0003t0017a0006c0006t0001 | a0003c0003t0002g0011 a0003c0003t0002g0027 a0003c0003t0017g0065 others(1): Show |
4 | 66 | 0.0606 | -6 | c.-70 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99560268 | GTATTAT | G | intron_variant | MODIFIER | HG00735.hp2 NA18957.hp2 NA19000.hp2 |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0004 | a0001c0001t0011a0003c0003t0002a0004c0004t0002 | a0001c0001t0011g0062 a0003c0003t0002g0002 a0004c0004t0002g0001 |
3 | 66 | 0.0455 | -6 | c.55+ others(21): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99617121 | TAACAAA | T | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 HG02109.hp2 others(6): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(4): Show | a0001c0001t0001g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(6): Show |
9 | 66 | 0.1364 | -6 | c.55+ others(23): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99625919 | TATATAC | T | intron_variant | MODIFIER | HG02258.hp1 HG02895.hp1 NA18522.hp2 others(1): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0014a0002c0002t0005a0003c0003t0007others(1): Show | a0001c0001t0014g0016 a0002c0002t0005g0015 a0003c0003t0007g0057 others(1): Show |
4 | 66 | 0.0606 | -6 | c.55+ others(23): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99630247 | CATATAT | C | intron_variant | MODIFIER | HG02258.hp1 HG02895.hp1 |
a0002a0010 | a0002c0002a0010c0010 | a0002c0002t0005a0010c0010t0011 | a0002c0002t0005g0015 a0010c0010t0011g0009 |
2 | 66 | 0.0303 | -6 | c.55+ others(23): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99637010 | CAAAAAA | C | intron_variant | MODIFIER | HG00738.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0004others(2): Show | a0001c0001t0003a0002c0002t0003a0002c0002t0004others(6): Show | a0001c0001t0003g0021 a0001c0001t0003g0022 a0002c0002t0003g0036 others(8): Show |
11 | 66 | 0.1667 | -6 | c.55+ others(23): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99669470 | GTGTATA | G | intron_variant | MODIFIER | HG02895.hp2 NA18522.hp1 |
a0002a0004 | a0002c0002a0004c0004 | a0002c0002t0004a0004c0004t0013 | a0002c0002t0004g0007 a0004c0004t0013g0050 |
2 | 66 | 0.0303 | -6 | c.55+ others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99710567 | ATGTGTG | A | intron_variant | MODIFIER | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(20): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0003c0003others(5): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(15): Show | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0053 others(20): Show |
23 | 66 | 0.3485 | -6 | c.56- others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99732262 | ATAGAGT | A | intron_variant | MODIFIER | HG02886.hp2 HG03130.hp1 NA19000.hp1 others(1): Show |
a0001a0004a0005others(1): Show | a0001c0001a0004c0004a0005c0005others(1): Show | a0001c0001t0014a0004c0004t0020a0005c0005t0001others(1): Show | a0001c0001t0014g0016 a0004c0004t0020g0024 a0005c0005t0001g0035 others(1): Show |
4 | 66 | 0.0606 | -6 | c.56- others(23): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99735007 | CAAAACA | C | intron_variant | MODIFIER | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(21): Show |
a0001a0002a0004others(5): Show | a0001c0001a0002c0002a0004c0004others(5): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(17): Show | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0004g0010 others(21): Show |
24 | 66 | 0.3636 | -6 | c.56- others(23): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99841875 | CATACAT | C | intron_variant | MODIFIER | HG01081.hp2 HG01099.hp1 HG01169.hp2 others(4): Show |
a0001a0005a0006others(1): Show | a0001c0001a0005c0005a0006c0006others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(4): Show | a0001c0001t0001g0054 a0001c0001t0004g0010 a0001c0001t0010g0047 others(4): Show |
7 | 66 | 0.1061 | -6 | c.278 others(23): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99889291 | GGTGTGT | G | intron_variant | MODIFIER | HG00735.hp2 HG01243.hp1 HG01934.hp2 others(5): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0011a0002c0002t0004others(5): Show | a0001c0001t0001g0004 a0001c0001t0011g0062 a0002c0002t0004g0039 others(5): Show |
8 | 66 | 0.1212 | -6 | c.578 others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99934943 | TATATAC | T | intron_variant | MODIFIER | HG02109.hp1 HG02132.hp2 HG02976.hp2 |
a0004a0005 | a0004c0004a0005c0005 | a0004c0004t0002a0005c0005t0001a0005c0005t0010 | a0004c0004t0002g0051 a0005c0005t0001g0017 a0005c0005t0010g0006 |
3 | 66 | 0.0455 | -6 | c.673 others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99961980 | ATATAGT | A | intron_variant | MODIFIER | HG00735.hp1 HG00738.hp1 HG01099.hp2 others(14): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(9): Show | a0001c0001t0001g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(14): Show |
17 | 66 | 0.2576 | -6 | c.877 others(23): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100043848 | AATTAGG | A | intron_variant | MODIFIER | HG02602.hp1 HG02735.hp1 NA18939.hp2 others(1): Show |
a0001a0003a0007 | a0001c0001a0003c0003a0007c0007 | a0001c0001t0006a0003c0003t0002a0007c0007t0023 | a0001c0001t0006g0032 a0001c0001t0006g0066 a0003c0003t0002g0002 others(1): Show |
4 | 66 | 0.0606 | -6 | c.981 others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 9/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 100091424 | CTTTTTT | C | intron_variant | MODIFIER | HG01123.hp1 HG01243.hp1 HG01243.hp2 others(11): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(8): Show | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0060 others(11): Show |
14 | 66 | 0.2121 | -6 | c.158 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100161830 | TACACAC | T | intron_variant | MODIFIER | HG00735.hp2 HG01081.hp2 HG02004.hp2 others(1): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(1): Show | a0001c0001t0001g0004 a0001c0001t0010g0047 a0001c0001t0011g0062 others(1): Show |
4 | 66 | 0.0606 | -6 | c.158 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100176851 | GGTGTGT | G | intron_variant | MODIFIER | HG00738.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
a0002a0005 | a0002c0002a0005c0005 | a0002c0002t0003a0002c0002t0008a0005c0005t0018 | a0002c0002t0003g0036 a0002c0002t0003g0037 a0002c0002t0008g0019 others(1): Show |
4 | 66 | 0.0606 | -6 | c.158 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100204297 | AATATAT | A | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 NA19043.hp2 |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0008 | a0002c0002t0003g0036 a0002c0002t0003g0037 a0002c0002t0008g0019 |
3 | 66 | 0.0455 | -6 | c.188 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100342152 | GACACAC | G | intron_variant | MODIFIER | HG02004.hp1 HG02257.hp1 HG02602.hp2 others(4): Show |
a0001a0003 | a0001c0001a0003c0003a0003c0011 | a0001c0001t0001a0003c0003t0002a0003c0003t0007others(2): Show | a0001c0001t0001g0053 a0001c0001t0001g0054 a0003c0003t0002g0027 others(4): Show |
7 | 66 | 0.1061 | -6 | c.303 others(23): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1131422 | TCCTTGA | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(228): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(24): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(41): Show | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(228): Show |
231 | 232 | 0.9957 | -6 | 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 | 1142968 | GTATATA | G | intron_variant | MODIFIER | HG01070.hp2 HG01496.hp2 HG02145.hp2 others(10): Show |
a0001a0002 | a0001c0004a0001c0005a0001c0006others(3): Show | a0001c0004t0001a0001c0005t0001a0001c0006t0001others(4): Show | a0001c0004t0001g0060 a0001c0005t0001g0182 a0001c0006t0001g0028 others(10): Show |
13 | 232 | 0.0560 | -6 | c.-82 others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1145483 | CAGAATT | C | intron_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(110): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(25): Show | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0044 others(110): Show |
113 | 232 | 0.4871 | -6 | c.-82 others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1158776 | ATGTGTG | A | intron_variant | MODIFIER | HG00609.hp2 HG00738.hp1 HG00738.hp2 others(54): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(13): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(15): Show | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0071 others(54): Show |
57 | 232 | 0.2457 | -6 | c.55+ others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1158953 | TACACAC | T | intron_variant | MODIFIER | HG01884.hp1 HG02148.hp1 HG02602.hp2 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(5): Show | a0001c0001t0001g0029 a0001c0002t0001g0068 a0001c0002t0001g0138 others(11): Show |
14 | 232 | 0.0603 | -6 | c.55+ others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1160344 | GTATATA | G | intron_variant | MODIFIER | HG00609.hp2 HG00738.hp1 HG00738.hp2 others(58): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(16): Show | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0054 others(58): Show |
61 | 232 | 0.2629 | -6 | c.55+ others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1161769 | TACACAC | T | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
a0001a0003 | a0001c0003a0001c0005a0001c0010others(2): Show | a0001c0003t0001a0001c0005t0001a0001c0010t0001others(2): Show | a0001c0003t0001g0219 a0001c0005t0001g0005 a0001c0010t0001g0009 others(4): Show |
7 | 232 | 0.0302 | -6 | c.55+ others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1172620 | CTGTGTG | C | intron_variant | MODIFIER | HG00741.hp2 HG03654.hp1 HG03669.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0086 a0001c0002t0002g0021 a0001c0003t0001g0031 others(1): Show |
4 | 232 | 0.0172 | -6 | c.55+ others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1201097 | TTTTGTG | T | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG01074.hp1 others(17): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0006others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(6): Show | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0067 others(17): Show |
20 | 232 | 0.0862 | -6 | c.56- others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1201099 | TTGTGTG | T | intron_variant | MODIFIER | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(16): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0008others(8): Show | a0001c0001t0001g0071 a0001c0001t0001g0198 a0001c0002t0001g0227 others(16): Show |
19 | 232 | 0.0819 | -6 | c.56- others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245197 | GATATAT | G | intron_variant | MODIFIER | HG01070.hp2 HG01123.hp1 HG01255.hp1 others(11): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(2): Show | a0001c0002t0001a0001c0003t0001a0001c0004t0001others(2): Show | a0001c0002t0001g0068 a0001c0002t0001g0094 a0001c0002t0001g0117 others(11): Show |
14 | 232 | 0.0603 | -6 | c.358 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245233 | TATACAC | T | intron_variant | MODIFIER | HG02559.hp2 HG02976.hp1 |
a0001a0002 | a0001c0008a0002c0017 | a0001c0008t0001a0002c0017t0001 | a0001c0008t0001g0212 a0002c0017t0001g0179 |
2 | 232 | 0.0086 | -6 | c.358 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245295 | CATATAT | C | intron_variant | MODIFIER | HG00738.hp2 HG02723.hp1 NA18747.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0022others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0022t0001others(1): Show | a0001c0001t0001g0044 a0001c0002t0001g0062 a0001c0002t0001g0063 others(3): Show |
6 | 232 | 0.0259 | -6 | c.358 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |