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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
LRRC23_chr12_6899822_6919229 | 6909259 | T | TTATATAA others(345): Show |
intron_variant | MODIFIER | HG01074.hp2 HG01496.hp1 HG04115.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0163 a0002c0002t0002g0222 a0002c0002t0002g0223 |
3 | 316 | 0.0095 | 352 | c.622 others(367): Show |
LRRC23 | ENSG00000010626.15 | transcript | ENST00000443597.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
LRRC23_chr12_6899822_6919229 | 6909259 | T | TTATATAA others(345): Show |
intron_variant | MODIFIER | HG01081.hp1 HG01358.hp2 HG01361.hp1 others(32): Show |
a0002a0006 | a0002c0002a0006c0007 | a0002c0002t0002a0006c0007t0002 | a0002c0002t0002g0006 a0002c0002t0002g0016 a0002c0002t0002g0035 others(25): Show |
35 | 316 | 0.1108 | 352 | c.622 others(367): Show |
LRRC23 | ENSG00000010626.15 | transcript | ENST00000443597.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
LRRC23_chr12_6899822_6919229 | 6909259 | T | TTATATAA others(345): Show |
intron_variant | MODIFIER | NA19074.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0136 | 1 | 316 | 0.0032 | 352 | c.622 others(367): Show |
LRRC23 | ENSG00000010626.15 | transcript | ENST00000443597.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
LRRC23_chr12_6899822_6919229 | 6909259 | T | TTATATAA others(345): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0139 | 1 | 316 | 0.0032 | 352 | c.622 others(367): Show |
LRRC23 | ENSG00000010626.15 | transcript | ENST00000443597.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
LRRC27_chr10_132327193_132386508 | 132364472 | T | TACACCCA others(345): Show |
intron_variant | MODIFIER | HG00423.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0236 | 1 | 290 | 0.0035 | 352 | c.129 others(369): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
LURAP1_chr1_46198334_46226256 | 46213358 | A | AAAGTATA others(345): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0114 | 1 | 356 | 0.0028 | 352 | c.199 others(369): Show |
LURAP1 | ENSG00000171357.6 | transcript | ENST00000371980.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
MAP3K21_chr1_233322724_233390148 | 233383384 | T | TAAAAGCT others(345): Show |
3_prime_UTR_variant | MODIFIER | HG00642.hp2 HG02055.hp1 HG04115.hp2 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0014 | a0002c0002t0014g0004 a0002c0002t0014g0064 a0002c0002t0014g0145 others(1): Show |
4 | 372 | 0.0108 | 352 | c.*68 others(361): Show |
MAP3K21 | ENSG00000143674.11 | transcript | ENST00000366624.8 | protein_coding | 10/10 | 688 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
MEGF6_chr1_3482951_3616508 | 3596429 | T | TCAGGGCA others(345): Show |
intron_variant | MODIFIER | HG02015.hp1 HG02080.hp1 HG02165.hp2 |
a0007a0008 | a0007c0008a0008c0021 | a0007c0008t0001a0008c0021t0001 | a0007c0008t0001g0132 a0007c0008t0001g0133 a0008c0021t0001g0017 |
3 | 292 | 0.0103 | 352 | c.267 others(367): Show |
MEGF6 | ENSG00000162591.17 | transcript | ENST00000356575.9 | protein_coding | 2/36 | chr1 | TogoVar | |||||||
MEGF6_chr1_3482951_3616508 | 3596595 | C | CGTCTCCA others(345): Show |
intron_variant | MODIFIER | HG01975.hp2 | a0004 | a0004c0004 | a0004c0004t0002 | a0004c0004t0002g0097 | 1 | 292 | 0.0034 | 352 | c.267 others(369): Show |
MEGF6 | ENSG00000162591.17 | transcript | ENST00000356575.9 | protein_coding | 2/36 | chr1 | TogoVar | |||||||
MELK_chr9_36567895_36682682 | 36670763 | T | TAAAAAGG others(345): Show |
intron_variant | MODIFIER | NA19240.hp1 | a0003 | a0003c0005 | a0003c0005t0004 | a0003c0005t0004g0209 | 1 | 242 | 0.0041 | 352 | c.150 others(369): Show |
MELK | ENSG00000165304.8 | transcript | ENST00000298048.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
METTL22_chr16_8616698_8654654 | 8640836 | G | GGATGGAT others(345): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0128 | 1 | 390 | 0.0026 | 352 | c.773 others(367): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
MIER2_chr19_300573_349796 | 310636 | A | AACGGCCC others(345): Show |
intron_variant | MODIFIER | HG02109.hp1 HG03195.hp2 |
a0001 | a0001c0014 | a0001c0014t0002 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | 384 | 0.0052 | 352 | c.984 others(369): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | TogoVar | |||||||
MIER2_chr19_300573_349796 | 310636 | A | AACGGCCC others(345): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02895.hp1 |
a0001 | a0001c0005 | a0001c0005t0002 | a0001c0005t0002g0226 a0001c0005t0002g0227 |
2 | 384 | 0.0052 | 352 | c.984 others(369): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | TogoVar | |||||||
MIER2_chr19_300573_349796 | 310636 | A | AACGGCCC others(345): Show |
intron_variant | MODIFIER | HG01099.hp1 HG01109.hp1 HG01192.hp1 others(21): Show |
a0001a0008 | a0001c0001a0001c0002a0008c0026 | a0001c0001t0002a0001c0002t0002a0008c0026t0002 | a0001c0001t0002g0022 a0001c0001t0002g0150 a0001c0002t0002g0089 others(20): Show |
24 | 384 | 0.0625 | 352 | c.984 others(369): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | TogoVar | |||||||
MIER2_chr19_300573_349796 | 310636 | A | AACGGCCC others(345): Show |
intron_variant | MODIFIER | HG01361.hp2 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0143 | 1 | 384 | 0.0026 | 352 | c.984 others(369): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | TogoVar | |||||||
MIER2_chr19_300573_349796 | 310636 | A | AACGGCCC others(345): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(14): Show |
a0001 | a0001c0003a0001c0011a0001c0022 | a0001c0003t0002a0001c0011t0002a0001c0022t0002 | a0001c0003t0002g0014 a0001c0003t0002g0131 a0001c0003t0002g0132 others(13): Show |
17 | 384 | 0.0443 | 352 | c.984 others(369): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | TogoVar | |||||||
MMACHC_chr1_45495300_45518382 | 45497762 | T | TGTCAGCC others(345): Show |
upstream_gene_variant | MODIFIER | HG02809.hp2 | a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0014 | 1 | 386 | 0.0026 | 352 | c.-25 others(363): Show |
MMACHC | ENSG00000132763.15 | transcript | ENST00000401061.9 | protein_coding | 2537 | chr1 | TogoVar | |||||||
MMACHC_chr1_45495300_45518382 | 45497762 | T | TGTCAGCC others(345): Show |
upstream_gene_variant | MODIFIER | HG03942.hp2 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0011 | a0001c0001t0008g0003 a0001c0001t0011g0038 |
2 | 386 | 0.0052 | 352 | c.-25 others(363): Show |
MMACHC | ENSG00000132763.15 | transcript | ENST00000401061.9 | protein_coding | 2537 | chr1 | TogoVar | |||||||
MROH9_chr1_170930534_171069765 | 170994904 | T | TAAGATTA others(345): Show |
intron_variant | MODIFIER | HG01192.hp1 HG02300.hp2 |
a0002a0003 | a0002c0015a0003c0006 | a0002c0015t0004a0003c0006t0001 | a0002c0015t0004g0180 a0003c0006t0001g0198 |
2 | 226 | 0.0089 | 352 | c.119 others(369): Show |
MROH9 | ENSG00000117501.15 | transcript | ENST00000367759.9 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
MSH4_chr1_75791882_75918242 | 75885668 | T | TTATTATA others(345): Show |
intron_variant | MODIFIER | HG01123.hp1 HG02004.hp2 HG02148.hp1 others(2): Show |
a0005 | a0005c0006 | a0005c0006t0001 | a0005c0006t0001g0078 a0005c0006t0001g0079 a0005c0006t0001g0080 others(2): Show |
5 | 332 | 0.0151 | 352 | c.210 others(371): Show |
MSH4 | ENSG00000057468.7 | transcript | ENST00000263187.4 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
MUC4_chr3_195741771_195816929 | 195770986 | C | CGGGTTGG others(345): Show |
intron_variant | MODIFIER | HG02257.hp1 HG02895.hp1 HG03834.hp2 others(3): Show |
a0014a0064a0065others(3): Show | a0014c0022a0064c0195a0065c0196others(3): Show | a0014c0022t0004a0064c0195t0003a0065c0196t0003others(3): Show | a0014c0022t0004g0246 a0064c0195t0003g0207 a0065c0196t0003g0208 others(3): Show |
6 | 249 | 0.0241 | 352 | c.132 others(371): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 5/24 | chr3 | TogoVar | |||||||
MUC4_chr3_195741771_195816929 | 195771018 | T | TGGGTTGG others(345): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0075 | 1 | 249 | 0.0040 | 352 | c.132 others(371): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 5/24 | chr3 | TogoVar | |||||||
MUC4_chr3_195741771_195816929 | 195771110 | T | TGGCCGGG others(345): Show |
intron_variant | MODIFIER | HG02486.hp1 HG02615.hp2 HG03098.hp1 |
a0048a0049a0050 | a0048c0146a0049c0145a0050c0147 | a0048c0146t0004a0049c0145t0008a0050c0147t0004 | a0048c0146t0004g0233 a0049c0145t0008g0055 a0050c0147t0004g0231 |
3 | 249 | 0.0121 | 352 | c.132 others(371): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 5/24 | chr3 | TogoVar | |||||||
MUC4_chr3_195741771_195816929 | 195771146 | C | CGGGTTGG others(345): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0052 | a0052c0140 | a0052c0140t0002 | a0052c0140t0002g0062 | 1 | 249 | 0.0040 | 352 | c.132 others(371): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 5/24 | chr3 | TogoVar | |||||||
MUC4_chr3_195741771_195816929 | 195771402 | C | CGGGTTGG others(345): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0177 | a0177c0035 | a0177c0035t0002 | a0177c0035t0002g0196 | 1 | 249 | 0.0040 | 352 | c.132 others(371): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 5/24 | chr3 | TogoVar | |||||||
MYDGF_chr19_4652545_4675342 | 4663226 | C | CCTCCAAT others(345): Show |
intron_variant | MODIFIER | NA19057.hp2 | a0003 | a0003c0004 | a0003c0004t0002 | a0003c0004t0002g0111 | 1 | 410 | 0.0024 | 352 | c.287 others(369): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | TogoVar | |||||||
MYDGF_chr19_4652545_4675342 | 4663507 | T | TCCACCCA others(345): Show |
intron_variant | MODIFIER | HG03927.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0308 | 1 | 410 | 0.0024 | 352 | c.287 others(369): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | TogoVar | |||||||
MYO3A_chr10_25929229_26217532 | 26076043 | T | TCTACTTT others(345): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0003 | a0003c0022 | a0003c0022t0005 | a0003c0022t0005g0278 | 1 | 280 | 0.0036 | 352 | c.135 others(371): Show |
MYO3A | ENSG00000095777.17 | transcript | ENST00000642920.2 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
MYT1L_chr2_1784113_2336275 | 1952717 | T | TCCTTCCT others(345): Show |
intron_variant | MODIFIER | HG02897.hp2 HG03209.hp1 HG04204.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0008a0001c0002t0002others(3): Show | a0001c0001t0001g0050 a0001c0001t0008g0009 a0001c0002t0002g0048 others(3): Show |
6 | 104 | 0.0577 | 352 | c.153 others(369): Show |
MYT1L | ENSG00000186487.21 | transcript | ENST00000647738.2 | protein_coding | 8/24 | chr2 | TogoVar | |||||||
MYT1_chr20_64159452_64247253 | 64233262 | T | TCCCCTTT others(345): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0220 | 1 | 223 | 0.0045 | 352 | c.289 others(369): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
NACC2_chr9_136001537_136100289 | 136023108 | G | GGAGGGAG others(345): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0009 | a0001c0009t0083 | a0001c0009t0083g0052 | 1 | 348 | 0.0029 | 352 | c.887 others(369): Show |
NACC2 | ENSG00000148411.8 | transcript | ENST00000277554.4 | protein_coding | 2/5 | chr9 | TogoVar | |||||||
NBPF10_chr1_146059711_146149804 | 146109343 | C | CACACACA others(345): Show |
intron_variant | MODIFIER | HG01993.hp2 | a0120 | a0120c0135 | a0120c0135t0002 | a0120c0135t0002g0129 | 1 | 283 | 0.0035 | 352 | c.450 others(369): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 35/89 | chr1 | TogoVar | |||||||
NBPF10_chr1_146059711_146149804 | 146109343 | C | CACACACA others(345): Show |
intron_variant | MODIFIER | HG01175.hp2 | a0011 | a0011c0007 | a0011c0007t0002 | a0011c0007t0002g0126 | 1 | 283 | 0.0035 | 352 | c.450 others(369): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 35/89 | chr1 | TogoVar | |||||||
NBPF10_chr1_146059711_146149804 | 146109343 | C | CACACACA others(345): Show |
intron_variant | MODIFIER | HG01928.hp1 | a0129 | a0129c0137 | a0129c0137t0002 | a0129c0137t0002g0136 | 1 | 283 | 0.0035 | 352 | c.450 others(369): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 35/89 | chr1 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667721 | C | CGCCTTAC others(345): Show |
intron_variant | MODIFIER | HG00741.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0107 | 1 | 378 | 0.0027 | 352 | c.148 others(371): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NFILZ_chr19_8625633_8686151 | 8656480 | C | CCACAGCC others(345): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0115 | a0001c0001t0115g0350 | 1 | 366 | 0.0027 | 352 | c.-16 others(373): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | chr19 | TogoVar | |||||||
NGEF_chr2_232873701_233018256 | 232995356 | C | CTGTGTAC others(345): Show |
intron_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0007 | a0001c0007t0007 | a0001c0007t0007g0042 | 1 | 362 | 0.0028 | 352 | c.-75 others(371): Show |
NGEF | ENSG00000066248.15 | transcript | ENST00000264051.8 | protein_coding | 1/14 | chr2 | TogoVar | |||||||
NME4_chr16_392199_405754 | 397703 | G | GGGGGGTG others(345): Show |
intron_variant | MODIFIER | NA18987.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0127 | 1 | 356 | 0.0028 | 352 | c.91+ others(365): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
NME4_chr16_392199_405754 | 397703 | G | GGGGGGTG others(345): Show |
intron_variant | MODIFIER | HG02040.hp2 NA18947.hp2 NA18983.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 a0001c0001t0001g0056 |
5 | 356 | 0.0140 | 352 | c.91+ others(365): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
NME4_chr16_392199_405754 | 397703 | G | GGGGGGTG others(345): Show |
intron_variant | MODIFIER | HG01070.hp2 HG01071.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 | 2 | 356 | 0.0056 | 352 | c.91+ others(365): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
NME4_chr16_392199_405754 | 397707 | T | TGTGGGGG others(345): Show |
intron_variant | MODIFIER | HG02486.hp1 HG03471.hp2 HG03486.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0017 a0001c0002t0001g0212 |
3 | 356 | 0.0084 | 352 | c.91+ others(365): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149036 | C | CGCCGCCT others(345): Show |
intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0260 | 1 | 294 | 0.0034 | 352 | c.901 others(367): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149358 | C | CACCACAC others(345): Show |
intron_variant | MODIFIER | NA19065.hp2 NA19079.hp2 NA19083.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0028 |
3 | 294 | 0.0102 | 352 | c.901 others(367): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149608 | C | CGCCGCCT others(345): Show |
intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0208 | 1 | 294 | 0.0034 | 352 | c.901 others(367): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149705 | A | ACTCACAC others(345): Show |
intron_variant | MODIFIER | NA19081.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 | 1 | 294 | 0.0034 | 352 | c.901 others(367): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150057 | C | CACCACAC others(345): Show |
intron_variant | MODIFIER | HG02074.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 | 1 | 294 | 0.0034 | 352 | c.902 others(367): 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(345): Show |
intron_variant | MODIFIER | HG00621.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0174 | 1 | 294 | 0.0034 | 352 | c.902 others(367): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150316 | G | GCTCACAC others(345): Show |
intron_variant | MODIFIER | HG02683.hp1 | a0008 | a0008c0012 | a0008c0012t0001 | a0008c0012t0001g0233 | 1 | 294 | 0.0034 | 352 | c.902 others(367): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150360 | G | GCTCCTAC others(345): Show |
intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0247 | 1 | 294 | 0.0034 | 352 | c.902 others(367): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150396 | G | GCCGCCTC others(345): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0065 | 1 | 294 | 0.0034 | 352 | c.902 others(367): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |