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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNRIP1_chr2_68288010_68324949 | 68305274 | ATGTGTGT others(9): Show |
A | intron_variant | MODIFIER | HG02055.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0264 | 1 | 424 | 0.0024 | -16 | c.331 others(35): Show |
CNRIP1 | ENSG00000119865.9 | transcript | ENST00000263655.4 | protein_coding | 2/2 | chr2 | TogoVar | ||||||
CNST_chr1_246561456_246673595 | 246571685 | ATTTACTT others(9): Show |
A | intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0172 | 1 | 320 | 0.0031 | -16 | c.-52 others(33): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | TogoVar | ||||||
CNST_chr1_246561456_246673595 | 246585666 | TACACACA others(9): Show |
T | intron_variant | MODIFIER | HG02647.hp1 HG02976.hp2 HG03209.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(1): Show | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0002g0188others(3): Show | 6 | 320 | 0.0188 | -16 | c.-51 others(33): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CNTD1_chr17_42793861_42816587 | 42801533 | ATATATAT others(9): Show |
A | intron_variant | MODIFIER | NA19030.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0050 | 1 | 306 | 0.0033 | -16 | c.170 others(33): Show |
CNTD1 | ENSG00000176563.10 | transcript | ENST00000588408.6 | protein_coding | 1/6 | chr17 | TogoVar | ||||||
CNTFR_chr9_34546433_34594724 | 34555935 | GCCATCTC others(9): Show |
G | intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0095 | 1 | 402 | 0.0025 | -16 | c.768 others(31): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | TogoVar | ||||||
CNTLN_chr9_17130040_17508923 | 17237354 | TACACACA others(9): Show |
T | intron_variant | MODIFIER | HG00597.hp1 HG02886.hp1 |
a0001a0003 | a0001c0004a0003c0002 | a0001c0004t0002a0003c0002t0001 | a0001c0004t0002g0002a0003c0002t0001g0125 | 2 | 218 | 0.0092 | -16 | c.849 others(31): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17248656 | AATGCTGT others(9): Show |
A | intron_variant | MODIFIER | HG01109.hp1 HG02109.hp1 HG02895.hp1 others(2): Show |
a0011a0013 | a0011c0015a0013c0019 | a0011c0015t0002a0013c0019t0002 | a0011c0015t0002g0213a0011c0015t0002g0214a0011c0015t0002g0215others(2): Show | 5 | 218 | 0.0229 | -16 | c.849 others(35): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17274453 | ATATCTAT others(9): Show |
A | intron_variant | MODIFIER | HG00621.hp1 NA18612.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0167a0001c0001t0001g0175 | 2 | 218 | 0.0092 | -16 | c.983 others(31): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17274495 | ATCTATCT others(9): Show |
A | intron_variant | MODIFIER | HG01109.hp1 HG02109.hp1 |
a0013 | a0013c0019 | a0013c0019t0002 | a0013c0019t0002g0119a0013c0019t0002g0120 | 2 | 218 | 0.0092 | -16 | c.983 others(31): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17295993 | AGAGAGTG others(9): Show |
A | intron_variant | MODIFIER | HG01109.hp1 HG02109.hp1 |
a0013 | a0013c0019 | a0013c0019t0002 | a0013c0019t0002g0119a0013c0019t0002g0120 | 2 | 218 | 0.0092 | -16 | c.984 others(33): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17302105 | CACACACA others(9): Show |
C | intron_variant | MODIFIER | HG00738.hp2 | a0002 | a0002c0008 | a0002c0008t0001 | a0002c0008t0001g0035 | 1 | 218 | 0.0046 | -16 | c.114 others(35): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17318838 | TTCCATCC others(9): Show |
T | intron_variant | MODIFIER | HG00408.hp1 HG00738.hp2 HG01070.hp1 others(17): Show |
a0001a0002a0015 | a0001c0014a0002c0006a0002c0008others(2): Show | a0001c0014t0001a0002c0006t0001a0002c0006t0002others(5): Show | a0001c0014t0001g0038a0002c0006t0001g0029a0002c0006t0001g0030others(17): Show | 20 | 218 | 0.0917 | -16 | c.134 others(35): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17325374 | ATGTATGT others(9): Show |
A | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(25): Show |
a0001a0004a0008others(3): Show | a0001c0030a0004c0003a0004c0020others(5): Show | a0001c0030t0002a0004c0003t0001a0004c0003t0002others(10): Show | a0001c0030t0002g0048a0004c0003t0001g0135a0004c0003t0001g0136others(25): Show | 28 | 218 | 0.1284 | -16 | c.134 others(35): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17353179 | CTCCTGGC others(9): Show |
C | intron_variant | MODIFIER | HG01074.hp1 HG01192.hp1 HG02257.hp1 others(1): Show |
a0010 | a0010c0012 | a0010c0012t0002a0010c0012t0003 | a0010c0012t0002g0018a0010c0012t0002g0019a0010c0012t0002g0020others(1): Show | 4 | 218 | 0.0184 | -16 | c.188 others(37): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17483668 | GATTTCTC others(9): Show |
G | intron_variant | MODIFIER | NA18943.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0005 | 1 | 218 | 0.0046 | -16 | c.385 others(33): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40707046 | GCACACAC others(9): Show |
G | intron_variant | MODIFIER | NA19010.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0089 | 1 | 230 | 0.0044 | -16 | c.-77 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40830791 | GTATATAT others(9): Show |
G | intron_variant | MODIFIER | HG02895.hp2 HG02897.hp1 |
a0001 | a0001c0004 | a0001c0004t0007 | a0001c0004t0007g0003a0001c0004t0007g0004 | 2 | 230 | 0.0087 | -16 | c.-76 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40872208 | TTGTTTGT others(9): Show |
T | intron_variant | MODIFIER | HG01106.hp1 HG01169.hp1 HG01515.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0001g0188a0001c0001t0003g0023a0001c0001t0003g0084others(13): Show | 16 | 230 | 0.0696 | -16 | c.-76 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40947774 | TATATATA others(9): Show |
T | intron_variant | MODIFIER | HG02055.hp1 NA19043.hp1 |
a0001 | a0001c0003 | a0001c0003t0003a0001c0003t0019 | a0001c0003t0003g0065a0001c0003t0019g0056 | 2 | 230 | 0.0087 | -16 | c.168 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40947776 | TATATATA others(9): Show |
T | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(12): Show |
a0001a0003 | a0001c0003a0003c0008 | a0001c0003t0002a0001c0003t0003a0001c0003t0005others(3): Show | a0001c0003t0002g0128a0001c0003t0003g0061a0001c0003t0005g0070others(12): Show | 15 | 230 | 0.0652 | -16 | c.168 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40947778 | TATATACA others(9): Show |
T | intron_variant | MODIFIER | NA18988.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0108 | 1 | 230 | 0.0044 | -16 | c.168 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40950097 | GGTGTGTG others(9): Show |
G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0012others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0049others(30): Show | 33 | 230 | 0.1435 | -16 | c.168 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40975178 | TTATATAT others(9): Show |
T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(45): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0042others(45): Show | 48 | 230 | 0.2087 | -16 | c.180 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40977770 | TGTTTTGT others(9): Show |
T | intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0003 | a0001c0003t0016 | a0001c0003t0016g0226 | 1 | 230 | 0.0044 | -16 | c.180 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 15/23 | chr12 | TogoVar | ||||||
CNTN2_chr1_205038212_205083289 | 205048910 | CGTGTGTG others(9): Show |
C | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0316 | 1 | 380 | 0.0026 | -16 | c.-86 others(33): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CNTN2_chr1_205038212_205083289 | 205069005 | TTTTGTTT others(9): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
a0001a0004a0007others(1): Show | a0001c0001a0001c0012a0004c0005others(2): Show | a0001c0001t0003a0001c0001t0011a0001c0001t0018others(9): Show | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0024others(44): Show | 57 | 380 | 0.1500 | -16 | c.212 others(33): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CNTN3_chr3_74257568_74619659 | 74285790 | GATATATA others(9): Show |
G | intron_variant | MODIFIER | HG02083.hp2 HG02129.hp1 HG02965.hp2 others(4): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0011 | a0001c0001t0002a0001c0001t0003a0001c0001t0014others(3): Show | a0001c0001t0002g0038a0001c0001t0003g0061a0001c0001t0014g0051others(4): Show | 7 | 174 | 0.0402 | -16 | c.251 others(33): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 19/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74339892 | CAGATAGA others(9): Show |
C | intron_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0136 | 1 | 174 | 0.0058 | -16 | c.136 others(35): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 11/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74344397 | GTTTTTTT others(9): Show |
G | intron_variant | MODIFIER | HG01952.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
a0001a0003 | a0001c0001a0001c0008a0001c0009others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0008t0002others(2): Show | a0001c0001t0001g0099a0001c0001t0002g0072a0001c0008t0002g0068others(2): Show | 5 | 174 | 0.0287 | -16 | c.136 others(35): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 11/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74460772 | CATATATA others(9): Show |
C | intron_variant | MODIFIER | HG02615.hp2 HG02922.hp2 NA20300.hp1 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0022a0003c0003t0002a0003c0003t0007 | a0001c0001t0022g0013a0003c0003t0002g0079a0003c0003t0007g0020 | 3 | 174 | 0.0172 | -16 | c.358 others(35): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2120393 | ATATATAT others(9): Show |
A | intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0025 | a0001c0025t0001 | a0001c0025t0001g0100 | 1 | 116 | 0.0086 | -16 | c.-14 others(37): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2383736 | TCTCTCTT others(9): Show |
T | intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0060 | 1 | 116 | 0.0086 | -16 | c.-89 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2400250 | AAGCTTGT others(9): Show |
A | intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0004 | a0001c0004t0006 | a0001c0004t0006g0068 | 1 | 116 | 0.0086 | -16 | c.-89 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2405595 | GTAGATAG others(9): Show |
G | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0024 | a0001c0024t0015 | a0001c0024t0015g0057 | 1 | 116 | 0.0086 | -16 | c.-89 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2547230 | ATATTTAT others(9): Show |
A | intron_variant | MODIFIER | HG01261.hp1 HG02602.hp2 HG02738.hp1 |
a0001 | a0001c0002a0001c0003a0001c0007 | a0001c0002t0001a0001c0003t0001a0001c0007t0004 | a0001c0002t0001g0038a0001c0003t0001g0037a0001c0007t0004g0066 | 3 | 116 | 0.0259 | -16 | c.-88 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2591352 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0115 | 1 | 116 | 0.0086 | -16 | c.55+ others(33): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2647380 | CATAAATA others(9): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(18): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0049others(66): Show | 69 | 116 | 0.5948 | -16 | c.55+ others(33): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2932800 | CTTTATTT others(9): Show |
C | intron_variant | MODIFIER | HG02074.hp1 HG02132.hp1 HG02523.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0002g0030others(5): Show | 8 | 116 | 0.0690 | -16 | c.135 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2983213 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | HG02647.hp1 HG03041.hp1 HG03453.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0033a0001c0001t0001g0059a0001c0002t0001g0027 | 3 | 116 | 0.0259 | -16 | c.135 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99063507 | CATAAATA others(9): Show |
C | intron_variant | MODIFIER | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(18): Show |
a0001a0003a0004others(5): Show | a0001c0001a0003c0003a0003c0011others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(18): Show | a0001c0001t0001g0053a0001c0001t0003g0060a0001c0001t0004g0010others(18): Show | 21 | 66 | 0.3182 | -16 | c.-21 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99178314 | CCACACAC others(9): Show |
C | intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0014 | 1 | 66 | 0.0152 | -16 | c.-20 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99236453 | CACACACT others(9): Show |
C | intron_variant | MODIFIER | HG00733.hp1 HG01081.hp2 NA19043.hp1 |
a0001a0011 | a0001c0001a0011c0009 | a0001c0001t0009a0001c0001t0010a0011c0009t0005 | a0001c0001t0009g0063a0001c0001t0010g0047a0011c0009t0005g0056 | 3 | 66 | 0.0455 | -16 | c.-20 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99284600 | GGTGTGTG others(9): Show |
G | intron_variant | MODIFIER | HG01081.hp1 HG01496.hp1 HG02109.hp1 others(2): Show |
a0002a0005a0006 | a0002c0002a0005c0005a0006c0006 | a0002c0002t0021a0005c0005t0010a0005c0005t0018others(2): Show | a0002c0002t0021g0055a0005c0005t0010g0006a0005c0005t0018g0028others(2): Show | 5 | 66 | 0.0758 | -16 | c.-20 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99422516 | TTTTATAT others(9): Show |
T | intron_variant | MODIFIER | HG02004.hp2 HG02886.hp2 |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0004c0004t0020 | a0001c0001t0001g0004a0004c0004t0020g0024 | 2 | 66 | 0.0303 | -16 | c.-71 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99422518 | TTATATAT others(9): Show |
T | intron_variant | MODIFIER | HG00733.hp2 HG01243.hp1 HG03041.hp1 others(4): Show |
a0001a0002a0006others(1): Show | a0001c0001a0002c0002a0006c0006others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0014others(4): Show | a0001c0001t0004g0029a0001c0001t0005g0048a0001c0001t0014g0016others(4): Show | 7 | 66 | 0.1061 | -16 | c.-71 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99598359 | TCTCTCTC others(9): Show |
T | intron_variant | MODIFIER | HG02723.hp1 HG02723.hp2 HG02965.hp1 others(5): Show |
a0001a0003a0006others(1): Show | a0001c0001a0003c0003a0006c0006others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(5): Show | a0001c0001t0001g0008a0001c0001t0004g0044a0001c0001t0005g0048others(5): Show | 8 | 66 | 0.1212 | -16 | c.55+ others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99684880 | TAATTGTT others(9): Show |
T | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 HG02109.hp2 others(3): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0003a0002c0002t0003a0002c0002t0008others(1): Show | a0001c0001t0003g0021a0001c0001t0003g0022a0002c0002t0003g0036others(3): Show | 6 | 66 | 0.0909 | -16 | c.55+ others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99857062 | CCCTCCCT others(9): Show |
C | intron_variant | MODIFIER | HG02004.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054 | 1 | 66 | 0.0152 | -16 | c.577 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99934933 | TATATATA others(9): Show |
T | intron_variant | MODIFIER | HG00738.hp2 HG01243.hp1 HG02895.hp1 |
a0002a0004 | a0002c0002a0004c0004 | a0002c0002t0004a0002c0002t0005a0004c0004t0002 | a0002c0002t0004g0039a0002c0002t0005g0015a0004c0004t0002g0041 | 3 | 66 | 0.0455 | -16 | c.673 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100094765 | AAAGGAAG others(9): Show |
A | intron_variant | MODIFIER | HG01081.hp1 HG01243.hp1 |
a0002a0005 | a0002c0002a0005c0005 | a0002c0002t0004a0005c0005t0018 | a0002c0002t0004g0039a0005c0005t0018g0028 | 2 | 66 | 0.0303 | -16 | c.158 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |