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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NAV2_chr11_19707837_20126601 | 19860082 | G | GGGCAGAG others(169): Show |
intron_variant | MODIFIER | HG00735.hp1 HG02723.hp1 |
a0003a0008 | a0003c0041a0008c0117 | a0003c0041t0028a0008c0117t0029 | a0003c0041t0028g0138 a0008c0117t0029g0160 |
2 | 166 | 0.0121 | 176 | c.439 others(193): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667373 | C | CCCTCCTT others(169): Show |
intron_variant | MODIFIER | HG02165.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0221 | 1 | 378 | 0.0027 | 176 | c.148 others(195): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667406 | T | TCCCTTAC others(169): Show |
intron_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0245 | 1 | 378 | 0.0027 | 176 | c.148 others(195): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667406 | T | TCCCTTAC others(169): Show |
intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0249 | 1 | 378 | 0.0027 | 176 | c.148 others(195): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667608 | T | TCCCTTAC others(169): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0359 | 1 | 378 | 0.0027 | 176 | c.148 others(195): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667732 | C | CTACTGGG others(169): Show |
intron_variant | MODIFIER | NA19079.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0327 | 1 | 378 | 0.0027 | 176 | c.148 others(195): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668042 | C | CCCTTACC others(169): Show |
intron_variant | MODIFIER | NA18991.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0293 | 1 | 378 | 0.0027 | 176 | c.148 others(195): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124439003 | T | TGAGACAG others(169): Show |
intron_variant | MODIFIER | HG02300.hp1 | a0010 | a0010c0007 | a0010c0007t0034 | a0010c0007t0034g0109 | 1 | 234 | 0.0043 | 176 | c.816 others(193): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 9/48 | chr12 | TogoVar | |||||||
NEU4_chr2_241804193_241822413 | 241813819 | C | CGATCCCC others(169): Show |
intron_variant | MODIFIER | HG01928.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0072 | 1 | 319 | 0.0031 | 176 | c.-3- others(189): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NEU4_chr2_241804193_241822413 | 241813827 | T | TGTCCCCA others(169): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0113 | 1 | 319 | 0.0031 | 176 | c.-3- others(189): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NEU4_chr2_241804193_241822413 | 241813882 | C | CCCCTGTC others(169): Show |
intron_variant | MODIFIER | NA19090.hp1 | a0006 | a0006c0021 | a0006c0021t0001 | a0006c0021t0001g0173 | 1 | 319 | 0.0031 | 176 | c.-3- others(189): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(169): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0035 | 1 | 322 | 0.0031 | 176 | c.127 others(193): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8656288 | A | AGCGCACC others(169): Show |
intron_variant | MODIFIER | HG01175.hp2 HG01952.hp1 HG02683.hp2 others(5): Show |
a0001a0002a0011 | a0001c0001a0002c0002a0011c0014 | a0001c0001t0015a0001c0001t0047a0001c0001t0061others(4): Show | a0001c0001t0015g0263 a0001c0001t0015g0267 a0001c0001t0047g0254 others(5): Show |
8 | 366 | 0.0219 | 176 | c.-16 others(197): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | chr19 | TogoVar | |||||||
NFILZ_chr19_8625633_8686151 | 8656447 | A | AAGCCCAC others(169): Show |
intron_variant | MODIFIER | HG01123.hp2 | a0001 | a0001c0001 | a0001c0001t0028 | a0001c0001t0028g0247 | 1 | 366 | 0.0027 | 176 | c.-16 others(197): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NGEF_chr2_232873701_233018256 | 232995572 | A | ATATATAT others(169): Show |
intron_variant | MODIFIER | NA18981.hp2 | a0002 | a0002c0008 | a0002c0008t0004 | a0002c0008t0004g0079 | 1 | 362 | 0.0028 | 176 | c.-75 others(195): Show |
NGEF | ENSG00000066248.15 | transcript | ENST00000264051.8 | protein_coding | 1/14 | chr2 | TogoVar | |||||||
NHEJ1_chr2_219064357_219165815 | 219159576 | C | CATATATA others(169): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0228 | 1 | 350 | 0.0029 | 176 | c.-1+ others(191): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | TogoVar | |||||||
NLRP12_chr19_53788741_53829314 | 53819629 | G | GTATATAT others(169): Show |
intron_variant | MODIFIER | HG03139.hp2 HG03579.hp2 NA18906.hp1 |
a0001 | a0001c0002a0001c0017 | a0001c0002t0002a0001c0017t0001 | a0001c0002t0002g0146 a0001c0017t0001g0404 a0001c0017t0001g0410 |
3 | 416 | 0.0072 | 176 | c.289 others(193): Show |
NLRP12 | ENSG00000142405.23 | transcript | ENST00000324134.11 | protein_coding | 1/9 | chr19 | TogoVar | |||||||
NLRP13_chr19_55890945_55937336 | 55930882 | A | ATATATAT others(169): Show |
intron_variant | MODIFIER | NA19087.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0195 | 1 | 440 | 0.0023 | 176 | c.319 others(193): Show |
NLRP13 | ENSG00000173572.12 | transcript | ENST00000342929.4 | protein_coding | 1/10 | chr19 | TogoVar | |||||||
NLRP13_chr19_55890945_55937336 | 55930882 | A | ATATATAT others(169): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(53): Show |
a0001a0003a0006others(2): Show | a0001c0004a0001c0010a0001c0014others(8): Show | a0001c0004t0001a0001c0010t0001a0001c0014t0001others(8): Show | a0001c0004t0001g0008 a0001c0004t0001g0105 a0001c0004t0001g0106 others(52): Show |
56 | 440 | 0.1273 | 176 | c.319 others(193): Show |
NLRP13 | ENSG00000173572.12 | transcript | ENST00000342929.4 | protein_coding | 1/10 | chr19 | TogoVar | |||||||
NLRP13_chr19_55890945_55937336 | 55930884 | A | ATATATAT others(169): Show |
intron_variant | MODIFIER | NA18977.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0200 | 1 | 440 | 0.0023 | 176 | c.319 others(193): Show |
NLRP13 | ENSG00000173572.12 | transcript | ENST00000342929.4 | protein_coding | 1/10 | chr19 | TogoVar | |||||||
NLRP8_chr19_55942832_55993629 | 55993484 | C | CCCCCTCC others(169): Show |
downstream_gene_variant | MODIFIER | HG02486.hp2 | a0000 | a0000c0008 | a0000c0008t0011 | a0000c0008t0011g0074 | 1 | 350 | 0.0029 | 176 | c.*55 others(187): Show |
NLRP8 | ENSG00000179709.8 | transcript | ENST00000291971.7 | protein_coding | 4856 | chr19 | TogoVar | |||||||
NOC4L_chr12_132139457_132157468 | 132148957 | A | ACTCACAC others(169): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0060 | 1 | 294 | 0.0034 | 176 | c.901 others(189): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132148962 | T | TACCACAC others(169): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132148962 | T | TACCACAC others(169): Show |
intron_variant | MODIFIER | NA19011.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0014 | 1 | 294 | 0.0034 | 176 | c.901 others(189): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149001 | A | ACTCACAC others(169): Show |
intron_variant | MODIFIER | NA19068.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0118 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149094 | T | TACCACAC others(169): Show |
intron_variant | MODIFIER | NA19068.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149094 | T | TACCACAC others(169): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0099 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149136 | C | CACACCAC others(169): Show |
intron_variant | MODIFIER | NA18973.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0179 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | TogoVar | |||||||
NOC4L_chr12_132139457_132157468 | 132149177 | G | GCTCCTAC others(169): Show |
intron_variant | MODIFIER | HG01358.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0223 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149226 | C | CACCACAC others(169): Show |
intron_variant | MODIFIER | NA18995.hp2 NA19079.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | 294 | 0.0068 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149265 | G | GCTCACAC others(169): Show |
intron_variant | MODIFIER | HG01071.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0262 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149270 | C | CACCACAC others(169): Show |
intron_variant | MODIFIER | NA18952.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0158 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149314 | C | CACCACAC others(169): Show |
intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0229 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149344 | C | CGCCGCCT others(169): Show |
intron_variant | MODIFIER | HG02300.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149344 | C | CGCCGCCT others(169): Show |
intron_variant | MODIFIER | HG02273.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0209 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149491 | A | ACCACACC others(169): Show |
intron_variant | MODIFIER | HG01433.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0198 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149529 | A | ACTCACAC others(169): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0109 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149652 | C | CGCCGCCT others(169): Show |
intron_variant | MODIFIER | HG00642.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0252 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149666 | T | TACCACAC others(169): Show |
intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0147 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149793 | G | GCTCACAC others(169): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0205 | 1 | 294 | 0.0034 | 176 | c.901 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150140 | G | GCTCACAC others(169): Show |
intron_variant | MODIFIER | NA19007.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032 | 1 | 294 | 0.0034 | 176 | c.902 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150188 | A | ATACCACA others(169): Show |
intron_variant | MODIFIER | HG01433.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0198 | 1 | 294 | 0.0034 | 176 | c.902 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | TogoVar | |||||||
NOC4L_chr12_132139457_132157468 | 132150189 | C | CACCACAC others(169): Show |
intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0155 | 1 | 294 | 0.0034 | 176 | c.902 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150263 | C | CGCCGCCT others(169): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0152 | 1 | 294 | 0.0034 | 176 | c.902 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150277 | C | CACCACAC others(169): Show |
intron_variant | MODIFIER | HG02273.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0209 | 1 | 294 | 0.0034 | 176 | c.902 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150277 | C | CACCACAC others(169): Show |
intron_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0214 | 1 | 294 | 0.0034 | 176 | c.902 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150277 | C | CACCACAC others(169): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0018 | a0018c0022 | a0018c0022t0001 | a0018c0022t0001g0072 | 1 | 294 | 0.0034 | 176 | c.902 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150321 | C | CACCACAC others(169): Show |
intron_variant | MODIFIER | HG01261.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0210 | 1 | 294 | 0.0034 | 176 | c.902 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150360 | G | GCTCACAC others(169): Show |
intron_variant | MODIFIER | HG00621.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0174 | 1 | 294 | 0.0034 | 176 | c.902 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150395 | C | CGCCGCCT others(169): Show |
intron_variant | MODIFIER | NA19005.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119 | 1 | 294 | 0.0034 | 176 | c.902 others(191): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |