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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TENM2_chr5_166974029_168269157 | 167652599 | C | CTA | intron_variant | MODIFIER | HG01081.hp2 HG01192.hp1 HG01891.hp1 others(46): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0002a0001c0003others(32): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0029others(43): Show | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0006g0001others(46): Show | 49 | 54 | 0.9074 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167656943 | C | CTT | intron_variant | MODIFIER | HG01192.hp1 HG01192.hp2 HG01891.hp2 others(16): Show |
a0001a0003a0005others(3): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(15): Show | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0002t0001g0044others(16): Show | 19 | 54 | 0.3519 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167663141 | G | GGA | intron_variant | MODIFIER | HG02055.hp1 HG03195.hp2 NA21309.hp2 |
a0001 | a0001c0004a0001c0017a0001c0025 | a0001c0004t0009a0001c0017t0002a0001c0025t0002 | a0001c0004t0009g0025a0001c0017t0002g0053a0001c0025t0002g0052 | 3 | 54 | 0.0556 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167669862 | G | GTT | intron_variant | MODIFIER | HG01192.hp2 HG01891.hp2 HG01943.hp2 others(8): Show |
a0001a0002a0003others(3): Show | a0001c0005a0001c0010a0001c0012others(8): Show | a0001c0005t0016a0001c0010t0001a0001c0012t0023others(8): Show | a0001c0005t0016g0012a0001c0010t0001g0043a0001c0012t0023g0016others(8): Show | 11 | 54 | 0.2037 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167681625 | T | TTA | intron_variant | MODIFIER | HG01081.hp1 HG01891.hp2 HG01943.hp1 others(24): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0003others(20): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0031others(23): Show | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0002t0001g0044others(24): Show | 27 | 54 | 0.5000 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167690920 | A | AGT | intron_variant | MODIFIER | HG01943.hp2 HG02818.hp2 |
a0001a0006 | a0001c0002a0006c0013 | a0001c0002t0001a0006c0013t0027 | a0001c0002t0001g0044a0006c0013t0027g0015 | 2 | 54 | 0.0370 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167700949 | T | TAA | intron_variant | MODIFIER | HG01081.hp2 HG01192.hp1 HG01192.hp2 others(4): Show |
a0001a0002a0003others(1): Show | a0001c0003a0001c0004a0001c0010others(4): Show | a0001c0003t0001a0001c0004t0007a0001c0010t0001others(4): Show | a0001c0003t0001g0040a0001c0004t0007g0054a0001c0010t0001g0043others(4): Show | 7 | 54 | 0.1296 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167702540 | A | ATG | intron_variant | MODIFIER | HG01081.hp1 HG01891.hp2 HG02602.hp1 others(2): Show |
a0001 | a0001c0002a0001c0004a0001c0007others(2): Show | a0001c0002t0001a0001c0004t0007a0001c0007t0010others(2): Show | a0001c0002t0001g0044a0001c0004t0007g0010a0001c0007t0010g0037others(2): Show | 5 | 54 | 0.0926 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167702552 | G | GTA | intron_variant | MODIFIER | HG02451.hp2 HG02615.hp1 HG02818.hp1 others(5): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0029a0001c0003t0002others(5): Show | a0001c0001t0001g0045a0001c0001t0029g0006a0001c0003t0002g0007others(5): Show | 8 | 54 | 0.1482 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167707013 | T | TAA | intron_variant | MODIFIER | HG02145.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
a0001a0003 | a0001c0001a0001c0019a0001c0022others(3): Show | a0001c0001t0001a0001c0019t0003a0001c0022t0021others(3): Show | a0001c0001t0001g0045a0001c0019t0003g0022a0001c0022t0021g0024others(3): Show | 6 | 54 | 0.1111 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167708233 | G | GGA | intron_variant | MODIFIER | HG01192.hp1 HG01192.hp2 HG01891.hp1 others(12): Show |
a0001a0002a0003others(1): Show | a0001c0002a0001c0003a0001c0005others(10): Show | a0001c0002t0013a0001c0003t0001a0001c0003t0002others(12): Show | a0001c0002t0013g0041a0001c0003t0001g0040a0001c0003t0002g0007others(12): Show | 15 | 54 | 0.2778 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167726136 | C | CAT | intron_variant | MODIFIER | HG01891.hp1 HG01943.hp1 HG02615.hp2 others(6): Show |
a0001a0007 | a0001c0002a0001c0005a0001c0006others(4): Show | a0001c0002t0002a0001c0002t0031a0001c0005t0024others(5): Show | a0001c0002t0002g0032a0001c0002t0031g0036a0001c0005t0024g0009others(6): Show | 9 | 54 | 0.1667 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167727104 | C | CTT | intron_variant | MODIFIER | HG01192.hp1 HG01192.hp2 HG01891.hp1 others(14): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0029a0001c0002t0002others(13): Show | a0001c0001t0001g0045a0001c0001t0029g0006a0001c0002t0002g0032others(14): Show | 17 | 54 | 0.3148 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167731697 | G | GTT | intron_variant | MODIFIER | HG01081.hp1 HG01943.hp2 HG02602.hp1 others(6): Show |
a0001a0003a0006 | a0001c0003a0001c0004a0001c0007others(6): Show | a0001c0003t0022a0001c0004t0007a0001c0007t0010others(6): Show | a0001c0003t0022g0020a0001c0004t0007g0010a0001c0007t0010g0037others(6): Show | 9 | 54 | 0.1667 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167736686 | G | GAA | intron_variant | MODIFIER | HG01943.hp1 HG02145.hp2 HG02451.hp1 others(14): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0002a0001c0005others(12): Show | a0001c0001t0029a0001c0002t0001a0001c0002t0002others(14): Show | a0001c0001t0029g0006a0001c0002t0001g0044a0001c0002t0002g0032others(14): Show | 17 | 54 | 0.3148 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167746675 | C | CAG | intron_variant | MODIFIER | HG02622.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
a0001a0003 | a0001c0003a0001c0010a0001c0023others(1): Show | a0001c0003t0022a0001c0010t0001a0001c0023t0008others(1): Show | a0001c0003t0022g0020a0001c0010t0001g0043a0001c0023t0008g0004others(1): Show | 4 | 54 | 0.0741 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167751953 | T | TAC | intron_variant | MODIFIER | HG01081.hp1 HG01891.hp1 HG02602.hp1 others(10): Show |
a0001 | a0001c0003a0001c0004a0001c0006others(7): Show | a0001c0003t0022a0001c0004t0007a0001c0004t0009others(9): Show | a0001c0003t0022g0020a0001c0004t0007g0010a0001c0004t0009g0025others(10): Show | 13 | 54 | 0.2407 | 2 | c.503 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167782313 | C | CAA | intron_variant | MODIFIER | HG01192.hp2 HG02451.hp1 HG02622.hp1 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0003a0001c0005a0001c0027others(6): Show | a0001c0003t0002a0001c0005t0005a0001c0005t0016others(7): Show | a0001c0003t0002g0007a0001c0005t0005g0034a0001c0005t0016g0012others(7): Show | 10 | 54 | 0.1852 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167796613 | C | CGT | intron_variant | MODIFIER | HG02145.hp1 HG03130.hp2 HG03516.hp2 others(1): Show |
a0001a0005a0009 | a0001c0037a0005c0034a0005c0035others(1): Show | a0001c0037t0030a0005c0034t0025a0005c0035t0001others(1): Show | a0001c0037t0030g0011a0005c0034t0025g0002a0005c0035t0001g0039others(1): Show | 4 | 54 | 0.0741 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167801905 | G | GAC | intron_variant | MODIFIER | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0003a0001c0019others(9): Show | a0001c0001t0001a0001c0003t0001a0001c0019t0003others(9): Show | a0001c0001t0001g0045a0001c0003t0001g0040a0001c0019t0003g0022others(9): Show | 12 | 54 | 0.2222 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167807124 | T | TAA | intron_variant | MODIFIER | HG01943.hp2 HG02622.hp2 HG03209.hp1 others(1): Show |
a0001a0003a0006 | a0001c0003a0001c0021a0003c0020others(1): Show | a0001c0003t0022a0001c0021t0020a0003c0020t0028others(1): Show | a0001c0003t0022g0020a0001c0021t0020g0021a0003c0020t0028g0013others(1): Show | 4 | 54 | 0.0741 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167813387 | G | GCA | intron_variant | MODIFIER | HG01943.hp1 HG02145.hp1 HG03130.hp2 others(3): Show |
a0001a0005a0009 | a0001c0002a0001c0004a0001c0021others(3): Show | a0001c0002t0031a0001c0004t0009a0001c0021t0020others(3): Show | a0001c0002t0031g0036a0001c0004t0009g0025a0001c0021t0020g0021others(3): Show | 6 | 54 | 0.1111 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167815972 | T | TTG | intron_variant | MODIFIER | HG02451.hp1 HG03195.hp2 |
a0001a0002 | a0001c0017a0002c0024 | a0001c0017t0002a0002c0024t0014 | a0001c0017t0002g0053a0002c0024t0014g0048 | 2 | 54 | 0.0370 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167819058 | C | CTG | intron_variant | MODIFIER | HG01943.hp2 HG02145.hp2 HG02615.hp2 others(7): Show |
a0001a0003a0006others(2): Show | a0001c0005a0001c0006a0001c0008others(6): Show | a0001c0005t0024a0001c0006t0004a0001c0008t0003others(6): Show | a0001c0005t0024g0009a0001c0006t0004g0026a0001c0006t0004g0028others(7): Show | 10 | 54 | 0.1852 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167825865 | T | TAA | intron_variant | MODIFIER | HG02145.hp1 HG03130.hp2 HG03516.hp2 others(1): Show |
a0001a0005a0009 | a0001c0037a0005c0034a0005c0035others(1): Show | a0001c0037t0030a0005c0034t0025a0005c0035t0001others(1): Show | a0001c0037t0030g0011a0005c0034t0025g0002a0005c0035t0001g0039others(1): Show | 4 | 54 | 0.0741 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167827628 | C | CGG | intron_variant | MODIFIER | HG01192.hp1 HG01891.hp1 HG01943.hp2 others(11): Show |
a0001a0005a0006others(1): Show | a0001c0002a0001c0003a0001c0004others(10): Show | a0001c0002t0002a0001c0003t0001a0001c0004t0007others(11): Show | a0001c0002t0002g0032a0001c0003t0001g0040a0001c0004t0007g0010others(11): Show | 14 | 54 | 0.2593 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167831485 | C | CTT | intron_variant | MODIFIER | HG01081.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0013others(6): Show | a0001c0001t0001g0049a0001c0002t0001g0044a0001c0002t0013g0041others(6): Show | 9 | 54 | 0.1667 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167837067 | T | TAC | intron_variant | MODIFIER | HG03209.hp2 NA19043.hp2 |
a0001 | a0001c0002a0001c0030 | a0001c0002t0013a0001c0030t0026 | a0001c0002t0013g0041a0001c0030t0026g0014 | 2 | 54 | 0.0370 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167839553 | C | CTG | intron_variant | MODIFIER | HG02145.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
a0001a0005a0009 | a0001c0015a0005c0034a0005c0035others(1): Show | a0001c0015t0002a0005c0034t0025a0005c0035t0001others(1): Show | a0001c0015t0002g0051a0005c0034t0025g0002a0005c0035t0001g0039others(1): Show | 4 | 54 | 0.0741 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167842580 | C | CAA | intron_variant | MODIFIER | HG01192.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
a0001a0003a0004others(3): Show | a0001c0003a0001c0026a0003c0014others(4): Show | a0001c0003t0002a0001c0026t0008a0003c0014t0019others(4): Show | a0001c0003t0002g0007a0001c0026t0008g0005a0003c0014t0019g0008others(4): Show | 7 | 54 | 0.1296 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167862241 | A | ATG | intron_variant | MODIFIER | HG01081.hp1 HG01192.hp2 HG02145.hp1 others(8): Show |
a0001a0003a0004others(3): Show | a0001c0003a0001c0007a0001c0022others(7): Show | a0001c0003t0002a0001c0003t0022a0001c0007t0010others(8): Show | a0001c0003t0002g0007a0001c0003t0022g0020a0001c0007t0010g0037others(8): Show | 11 | 54 | 0.2037 | 2 | c.503 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167870554 | C | CAT | intron_variant | MODIFIER | HG01192.hp2 HG01943.hp2 HG02145.hp1 others(10): Show |
a0001a0003a0004others(4): Show | a0001c0002a0001c0003a0001c0015others(10): Show | a0001c0002t0013a0001c0003t0002a0001c0015t0002others(10): Show | a0001c0002t0013g0041a0001c0003t0002g0007a0001c0015t0002g0051others(10): Show | 13 | 54 | 0.2407 | 2 | c.503 others(19): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167878573 | C | CTG | intron_variant | MODIFIER | HG01943.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
a0001a0003a0006others(1): Show | a0001c0002a0001c0015a0001c0028others(3): Show | a0001c0002t0013a0001c0015t0002a0001c0028t0011others(3): Show | a0001c0002t0013g0041a0001c0015t0002g0051a0001c0028t0011g0042others(3): Show | 6 | 54 | 0.1111 | 2 | c.712 others(19): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167894466 | G | GAC | intron_variant | MODIFIER | HG01081.hp1 HG01081.hp2 HG01192.hp1 others(40): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0003others(28): Show | a0001c0001t0001a0001c0001t0006a0001c0002t0001others(37): Show | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0006g0001others(40): Show | 43 | 54 | 0.7963 | 2 | c.712 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167911878 | A | AAT | intron_variant | MODIFIER | HG01943.hp2 HG02622.hp2 HG03209.hp2 |
a0001a0003a0006 | a0001c0002a0003c0020a0006c0013 | a0001c0002t0013a0003c0020t0028a0006c0013t0027 | a0001c0002t0013g0041a0003c0020t0028g0013a0006c0013t0027g0015 | 3 | 54 | 0.0556 | 2 | c.712 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167918774 | C | CTT | intron_variant | MODIFIER | HG01081.hp2 HG02055.hp2 HG02622.hp1 others(3): Show |
a0001 | a0001c0002a0001c0004a0001c0019others(2): Show | a0001c0002t0001a0001c0002t0002a0001c0004t0007others(3): Show | a0001c0002t0001g0044a0001c0002t0002g0032a0001c0004t0007g0054others(3): Show | 6 | 54 | 0.1111 | 2 | c.713 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167920330 | T | TAA | intron_variant | MODIFIER | HG01192.hp2 HG02145.hp1 HG02615.hp2 others(4): Show |
a0001a0003a0005others(1): Show | a0001c0003a0001c0008a0001c0026others(4): Show | a0001c0003t0002a0001c0008t0003a0001c0026t0008others(4): Show | a0001c0003t0002g0007a0001c0008t0003g0029a0001c0026t0008g0005others(4): Show | 7 | 54 | 0.1296 | 2 | c.713 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167920515 | T | TCA | intron_variant | MODIFIER | HG01081.hp1 HG01192.hp1 HG01192.hp2 others(10): Show |
a0001a0003a0008 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0006a0001c0002t0031others(10): Show | a0001c0001t0001g0049a0001c0001t0006g0001a0001c0002t0031g0036others(10): Show | 13 | 54 | 0.2407 | 2 | c.713 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167926718 | C | CCA | intron_variant | MODIFIER | HG01192.hp2 HG01943.hp1 HG02602.hp1 others(5): Show |
a0001a0003a0004others(2): Show | a0001c0002a0001c0003a0001c0004others(5): Show | a0001c0002t0031a0001c0003t0002a0001c0004t0007others(5): Show | a0001c0002t0031g0036a0001c0003t0002g0007a0001c0004t0007g0010others(5): Show | 8 | 54 | 0.1482 | 2 | c.713 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167974037 | A | AGG | intron_variant | MODIFIER | HG02055.hp1 HG02895.hp2 |
a0001 | a0001c0025a0001c0026 | a0001c0025t0002a0001c0026t0008 | a0001c0025t0002g0052a0001c0026t0008g0005 | 2 | 54 | 0.0370 | 2 | c.948 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167989298 | G | GAA | intron_variant | MODIFIER | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(1): Show |
a0001 | a0001c0001a0001c0006a0001c0018 | a0001c0001t0029a0001c0006t0004a0001c0018t0003 | a0001c0001t0029g0006a0001c0006t0004g0026a0001c0006t0004g0028others(1): Show | 4 | 54 | 0.0741 | 2 | c.948 others(19): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 167998683 | C | CAT | intron_variant | MODIFIER | HG01081.hp2 HG01192.hp1 NA21309.hp2 |
a0001 | a0001c0003a0001c0004 | a0001c0003t0001a0001c0004t0007a0001c0004t0009 | a0001c0003t0001g0040a0001c0004t0007g0054a0001c0004t0009g0025 | 3 | 54 | 0.0556 | 2 | c.118 others(21): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 168004506 | T | TGC | intron_variant | MODIFIER | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
a0001 | a0001c0006a0001c0017a0001c0023 | a0001c0006t0004a0001c0017t0002a0001c0023t0008 | a0001c0006t0004g0026a0001c0006t0004g0028a0001c0017t0002g0053others(1): Show | 4 | 54 | 0.0741 | 2 | c.118 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 168004517 | G | GCA | intron_variant | MODIFIER | HG01081.hp2 HG01192.hp1 HG01891.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0007others(6): Show | a0001c0001t0001g0049a0001c0003t0001g0040a0001c0004t0007g0054others(6): Show | 9 | 54 | 0.1667 | 2 | c.118 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 168012774 | G | GAA | intron_variant | MODIFIER | HG01081.hp2 HG01891.hp2 HG02922.hp1 others(2): Show |
a0001a0007 | a0001c0004a0001c0012a0001c0030others(1): Show | a0001c0004t0007a0001c0004t0009a0001c0012t0023others(2): Show | a0001c0004t0007g0054a0001c0004t0009g0025a0001c0012t0023g0016others(2): Show | 5 | 54 | 0.0926 | 2 | c.118 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 168018378 | C | CTT | intron_variant | MODIFIER | HG01192.hp2 HG01943.hp2 HG02055.hp2 others(7): Show |
a0001a0003a0006others(1): Show | a0001c0010a0001c0019a0001c0026others(7): Show | a0001c0010t0001a0001c0019t0003a0001c0026t0008others(7): Show | a0001c0010t0001g0043a0001c0019t0003g0022a0001c0026t0008g0005others(7): Show | 10 | 54 | 0.1852 | 2 | c.118 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 168027104 | G | GAC | intron_variant | MODIFIER | HG01081.hp2 HG01192.hp1 HG01891.hp2 others(5): Show |
a0001a0002 | a0001c0003a0001c0004a0001c0008others(3): Show | a0001c0003t0001a0001c0003t0002a0001c0004t0007others(5): Show | a0001c0003t0001g0040a0001c0003t0002g0007a0001c0004t0007g0054others(5): Show | 8 | 54 | 0.1482 | 2 | c.118 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 168030158 | C | CTT | intron_variant | MODIFIER | HG01943.hp1 HG02622.hp1 HG03130.hp2 others(3): Show |
a0001a0005a0009 | a0001c0002a0001c0005a0001c0027others(2): Show | a0001c0002t0031a0001c0005t0005a0001c0005t0024others(3): Show | a0001c0002t0031g0036a0001c0005t0005g0034a0001c0005t0024g0009others(3): Show | 6 | 54 | 0.1111 | 2 | c.118 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 168034047 | G | GTA | intron_variant | MODIFIER | HG02970.hp2 HG04204.hp1 NA19043.hp2 others(1): Show |
a0001 | a0001c0004a0001c0016a0001c0030others(1): Show | a0001c0004t0009a0001c0016t0015a0001c0030t0026others(1): Show | a0001c0004t0009g0025a0001c0016t0015g0047a0001c0030t0026g0014others(1): Show | 4 | 54 | 0.0741 | 2 | c.118 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TENM2_chr5_166974029_168269157 | 168036677 | G | GTA | intron_variant | MODIFIER | HG01081.hp1 HG01192.hp1 HG01891.hp1 others(4): Show |
a0001a0002 | a0001c0003a0001c0005a0001c0007others(3): Show | a0001c0003t0001a0001c0005t0005a0001c0007t0010others(4): Show | a0001c0003t0001g0040a0001c0005t0005g0034a0001c0007t0010g0037others(4): Show | 7 | 54 | 0.1296 | 2 | c.118 others(23): Show |
TENM2 | ENSG00000145934.17 | transcript | ENST00000518659.6 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |