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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTCTCT others(13): Show |
intron_variant | MODIFIER | HG01123.hp2 NA18940.hp1 NA18964.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010a0001c0001t0001g0264 | 5 | 394 | 0.0127 | 20 | c.120 others(37): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTCTGT others(13): Show |
intron_variant | MODIFIER | HG02630.hp2 HG02965.hp2 HG02970.hp1 |
a0004a0022 | a0004c0004a0022c0017 | a0004c0004t0005a0022c0017t0004 | a0004c0004t0005g0179a0004c0004t0005g0182a0022c0017t0004g0289 | 3 | 394 | 0.0076 | 20 | c.120 others(37): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTGTGT others(13): Show |
intron_variant | MODIFIER | HG00544.hp1 HG00673.hp1 HG01074.hp2 others(23): Show |
a0003a0005 | a0003c0003a0005c0005 | a0003c0003t0001a0003c0003t0003a0005c0005t0004 | a0003c0003t0001g0205a0003c0003t0003g0009a0003c0003t0003g0030others(14): Show | 26 | 394 | 0.0660 | 20 | c.120 others(37): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF3_chr1_21435137_21489900 | 21479848 | G | GTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053 | 1 | 394 | 0.0025 | 20 | c.120 others(37): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF9_chr1_149047186_149108551 | 149060924 | C | CACACACA others(13): Show |
intron_variant | MODIFIER | HG02109.hp2 HG02886.hp2 |
a0007 | a0007c0007 | a0007c0007t0031a0007c0007t0062 | a0007c0007t0031g0157a0007c0007t0062g0159 | 2 | 344 | 0.0058 | 20 | c.230 others(37): Show |
NBPF9 | ENSG00000269713.9 | transcript | ENST00000698832.1 | protein_coding | 23/29 | chr1 | TogoVar | ||||||
NBR1_chr17_43166214_43216688 | 43177572 | A | AACACACA others(13): Show |
intron_variant | MODIFIER | HG02559.hp1 | a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0149 | 1 | 314 | 0.0032 | 20 | c.103 others(35): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NCALD_chr8_101681542_101795969 | 101715003 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG01074.hp1 HG02109.hp2 HG03710.hp1 |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0011 | a0001c0001t0010g0217a0001c0001t0010g0247a0001c0001t0011g0111 | 3 | 300 | 0.0100 | 20 | c.378 others(37): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113011964 | T | TTTCCTTC others(13): Show |
intron_variant | MODIFIER | HG00558.hp2 HG01884.hp1 HG02004.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(3): Show | a0001c0001t0001g0073a0001c0001t0004g0116a0001c0001t0010g0208others(4): Show | 7 | 242 | 0.0289 | 20 | c.52+ others(37): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113017635 | T | TTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG01109.hp1 HG01884.hp1 HG02148.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(5): Show | a0001c0001t0001g0210a0001c0001t0002g0015a0001c0001t0002g0176others(7): Show | 10 | 242 | 0.0413 | 20 | c.52+ others(37): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113173591 | G | GATATATA others(13): Show |
intron_variant | MODIFIER | HG04199.hp2 NA19070.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013 | a0001c0001t0001g0062a0001c0001t0013g0043 | 2 | 242 | 0.0083 | 20 | c.53- others(37): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113185062 | T | TTATATAT others(13): Show |
intron_variant | MODIFIER | NA20752.hp2 | a0001 | a0001c0001 | a0001c0001t0031 | a0001c0001t0031g0060 | 1 | 242 | 0.0041 | 20 | c.53- others(37): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113185079 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | NA18962.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0211 | 1 | 242 | 0.0041 | 20 | c.53- others(37): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113185079 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG02615.hp1 NA19087.hp1 NA20752.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0001t0020a0001c0002t0004 | a0001c0001t0009g0125a0001c0001t0020g0229a0001c0002t0004g0204 | 3 | 242 | 0.0124 | 20 | c.53- others(37): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113185079 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG00323.hp2 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0026a0001c0001t0028 | a0001c0001t0026g0228a0001c0001t0028g0207 | 2 | 242 | 0.0083 | 20 | c.53- others(37): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21009883 | C | CTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG00733.hp1 HG03225.hp1 NA19240.hp2 |
a0002a0003a0004 | a0002c0002a0003c0006a0004c0013 | a0002c0002t0001a0003c0006t0003a0004c0013t0002 | a0002c0002t0001g0018a0003c0006t0003g0030a0004c0013t0002g0014 | 3 | 132 | 0.0227 | 20 | c.55+ others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21214746 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG02965.hp1 NA19090.hp1 |
a0002 | a0002c0002a0002c0003 | a0002c0002t0001a0002c0003t0008 | a0002c0002t0001g0019a0002c0003t0008g0009 | 2 | 132 | 0.0152 | 20 | c.56- others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21214746 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG02976.hp2 HG03239.hp2 HG03704.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0002a0001c0001t0016a0001c0001t0020others(4): Show | a0001c0001t0002g0004a0001c0001t0016g0103a0001c0001t0020g0131others(4): Show | 7 | 132 | 0.0530 | 20 | c.56- others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21272934 | T | TCACACAC others(13): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00609.hp1 HG01071.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(1): Show | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0084others(4): Show | 7 | 132 | 0.0530 | 20 | c.56- others(35): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21331517 | C | CTCTCTCT others(13): Show |
intron_variant | MODIFIER | HG02965.hp2 HG02970.hp2 |
a0002 | a0002c0003 | a0002c0003t0004a0002c0003t0023 | a0002c0003t0004g0130a0002c0003t0023g0060 | 2 | 132 | 0.0152 | 20 | c.738 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21331517 | C | CTCTCTCT others(13): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0002 | a0002c0002 | a0002c0002t0009 | a0002c0002t0009g0002 | 1 | 132 | 0.0076 | 20 | c.738 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21331517 | C | CTCTCTCT others(13): Show |
intron_variant | MODIFIER | HG03041.hp1 HG03540.hp1 |
a0002 | a0002c0003 | a0002c0003t0005a0002c0003t0013 | a0002c0003t0005g0008a0002c0003t0013g0118 | 2 | 132 | 0.0152 | 20 | c.738 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21331517 | C | CTCTCTCT others(13): Show |
intron_variant | MODIFIER | NA18955.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0078 | 1 | 132 | 0.0076 | 20 | c.738 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21331534 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0003 | a0003c0006 | a0003c0006t0003 | a0003c0006t0003g0030 | 1 | 132 | 0.0076 | 20 | c.738 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21431123 | T | TTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG01346.hp2 HG02523.hp1 HG02559.hp2 others(7): Show |
a0001a0002a0005 | a0001c0001a0001c0004a0002c0002others(2): Show | a0001c0001t0001a0001c0004t0001a0001c0004t0007others(7): Show | a0001c0001t0001g0037a0001c0004t0001g0101a0001c0004t0007g0077others(7): Show | 10 | 132 | 0.0758 | 20 | c.148 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21433742 | C | CAATAAAA others(13): Show |
intron_variant | MODIFIER | HG00733.hp2 HG03540.hp2 NA18979.hp2 others(2): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0006 | a0001c0001t0001a0002c0002t0006a0002c0002t0007others(2): Show | a0001c0001t0001g0083a0002c0002t0006g0023a0002c0002t0007g0051others(2): Show | 5 | 132 | 0.0379 | 20 | c.165 others(39): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21437474 | C | CTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG03195.hp1 HG03225.hp1 HG03579.hp2 others(1): Show |
a0001a0002a0004 | a0001c0007a0002c0002a0004c0013 | a0001c0007t0004a0002c0002t0002a0002c0002t0003others(1): Show | a0001c0007t0004g0106a0002c0002t0002g0075a0002c0002t0003g0050others(1): Show | 4 | 132 | 0.0303 | 20 | c.165 others(39): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21467412 | G | GTATATAT others(13): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00673.hp1 HG00733.hp1 others(25): Show |
a0001a0002 | a0001c0001a0001c0007a0001c0012others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0084others(25): Show | 28 | 132 | 0.2121 | 20 | c.177 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21467426 | T | TTATATAT others(13): Show |
intron_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0004 | 1 | 132 | 0.0076 | 20 | c.177 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21473373 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | HG02622.hp2 HG03041.hp2 |
a0002 | a0002c0002a0002c0003 | a0002c0002t0004a0002c0003t0002 | a0002c0002t0004g0049a0002c0003t0002g0013 | 2 | 132 | 0.0152 | 20 | c.189 others(39): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21479583 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG00280.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0046 | 1 | 132 | 0.0076 | 20 | c.207 others(39): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAPD2_chr12_6489102_6536955 | 6513715 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG00642.hp1 HG01358.hp1 HG01952.hp1 others(21): Show |
a0001a0008 | a0001c0001a0001c0009a0001c0032others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(4): Show | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(21): Show | 24 | 432 | 0.0556 | 20 | c.588 others(35): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTGT others(13): Show |
intron_variant | MODIFIER | HG01109.hp2 HG02257.hp1 HG02630.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0352a0001c0001t0002g0364a0001c0001t0002g0383 | 3 | 432 | 0.0069 | 20 | c.158 others(37): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTTT others(13): Show |
intron_variant | MODIFIER | NA19002.hp1 | a0005 | a0005c0006 | a0005c0006t0003 | a0005c0006t0003g0130 | 1 | 432 | 0.0023 | 20 | c.158 others(37): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCAPD3_chr11_134145113_134228967 | 134177882 | C | CCTTTCTT others(13): Show |
intron_variant | MODIFIER | HG02895.hp1 HG02897.hp2 HG03139.hp1 others(3): Show |
a0001a0002a0004 | a0001c0001a0001c0022a0002c0003others(1): Show | a0001c0001t0009a0001c0001t0018a0001c0022t0002others(2): Show | a0001c0001t0009g0096a0001c0001t0018g0358a0001c0001t0018g0359others(3): Show | 6 | 370 | 0.0162 | 20 | c.278 others(37): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 22/34 | chr11 | TogoVar | ||||||
NCAPD3_chr11_134145113_134228967 | 134212375 | T | TTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG03486.hp2 NA19078.hp2 |
a0001a0006 | a0001c0001a0006c0009 | a0001c0001t0002a0006c0009t0032 | a0001c0001t0002g0147a0006c0009t0032g0094 | 2 | 370 | 0.0054 | 20 | c.383 others(37): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 3/34 | chr11 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648527 | C | CCAAATGG others(13): Show |
intron_variant | MODIFIER | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
a0001a0003 | a0001c0001a0001c0004a0001c0005others(1): Show | a0001c0001t0001a0001c0004t0001a0001c0005t0001others(1): Show | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0222others(57): Show | 60 | 378 | 0.1587 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648527 | C | CCAAATGG others(13): Show |
intron_variant | MODIFIER | HG01934.hp1 HG01943.hp2 HG02273.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0066a0001c0001t0001g0116a0001c0001t0002g0238 | 3 | 378 | 0.0079 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648567 | C | CCAAATGG others(13): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
a0001a0005a0007others(5): Show | a0001c0001a0001c0004a0001c0018others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0131others(142): Show | 147 | 378 | 0.3889 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648587 | C | CCAAATGG others(13): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01169.hp2 HG01952.hp1 others(4): Show |
a0001a0014 | a0001c0001a0014c0020 | a0001c0001t0001a0014c0020t0001 | a0001c0001t0001g0341a0001c0001t0001g0346a0001c0001t0001g0347others(4): Show | 7 | 378 | 0.0185 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648597 | G | GACAACCA others(13): Show |
intron_variant | MODIFIER | HG02559.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0224a0001c0005t0001g0225a0001c0005t0001g0228others(4): Show | 7 | 378 | 0.0185 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648617 | G | GACAACCA others(13): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0215 | 1 | 378 | 0.0027 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648747 | C | CCAAATGG others(13): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0346 | 1 | 378 | 0.0027 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648767 | C | CCAAATGG others(13): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01169.hp2 HG02965.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0347a0001c0001t0001g0349a0001c0001t0001g0350others(1): Show | 4 | 378 | 0.0106 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648777 | C | CACAACCA others(13): Show |
intron_variant | MODIFIER | HG03831.hp1 NA18980.hp2 NA18986.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0222a0001c0001t0001g0248a0001c0001t0001g0268 | 3 | 378 | 0.0079 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648797 | C | CACAACCA others(13): Show |
intron_variant | MODIFIER | HG00438.hp1 HG02080.hp2 HG02155.hp1 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0028a0001c0001t0001g0223a0001c0001t0001g0243others(19): Show | 22 | 378 | 0.0582 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648797 | C | CACAACCA others(13): Show |
intron_variant | MODIFIER | NA18983.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0271 | 1 | 378 | 0.0027 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648817 | C | CACAACCA others(13): Show |
intron_variant | MODIFIER | HG02630.hp1 HG04115.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010a0001c0001t0001g0227 | 2 | 378 | 0.0053 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158648847 | G | CCAAATGG others(13): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02818.hp1 HG03540.hp2 |
a0001a0004 | a0001c0001a0004c0007 | a0001c0001t0001a0004c0007t0002 | a0001c0001t0001g0355a0001c0001t0001g0356a0004c0007t0002g0216 | 3 | 378 | 0.0079 | 20 | c.307 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 24/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158660401 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG01943.hp1 HG02300.hp1 HG02451.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0001t0001g0283others(3): Show | 6 | 378 | 0.0159 | 20 | c.198 others(39): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 16/27 | chr7 | TogoVar | ||||||
NCBP2L_chrX_107772733_107800829 | 107781676 | A | ATCTATCT others(13): Show |
intron_variant | MODIFIER | HG02723.hp2 HG02976.hp1 HG03579.hp1 |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0004a0002c0003t0003 | a0001c0002t0004g0240a0002c0003t0003g0231a0002c0003t0003g0232 | 3 | 303 | 0.0099 | 20 | c.-73 others(37): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar |