| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| MYOM2_chr8_2040046_2150456 | 2120675 | T | TATATATA others(42): Show |
intron_variant | MODIFIER | HG00408.hp2 HG01346.hp1 HG01928.hp2 others(5): Show |
a0004a0022a0041others(3): Show | a0004c0007a0022c0043a0022c0066others(4): Show | a0004c0007t0001a0022c0043t0001a0022c0066t0005others(4): Show | a0004c0007t0001g0284a0022c0043t0001g0239a0022c0043t0001g0382others(5): Show | 8 | 403 | 0.0199 | 49 | c.345 others(68): Show |
MYOM2 | ENSG00000036448.10 | transcript | ENST00000262113.9 | protein_coding | 28/36 | chr8 | TogoVar | ||||||
| MYSM1_chr1_58649743_58705062 | 58698102 | A | ATATATAT others(42): Show |
intron_variant | MODIFIER | HG02559.hp1 | a0002 | a0002c0005 | a0002c0005t0016 | a0002c0005t0016g0259 | 1 | 410 | 0.0024 | 49 | c.68+ others(64): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | TogoVar | ||||||
| MYSM1_chr1_58649743_58705062 | 58698102 | A | ATATATAT others(42): Show |
intron_variant | MODIFIER | HG01978.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0077 | 1 | 410 | 0.0024 | 49 | c.68+ others(64): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | TogoVar | ||||||
| MYT1_chr20_64159452_64247253 | 64173537 | C | CTTTCCTA others(42): Show |
intron_variant | MODIFIER | HG01081.hp1 HG02486.hp2 HG02683.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0013 | a0001c0001t0003a0001c0002t0002a0001c0002t0006others(1): Show | a0001c0001t0003g0061a0001c0002t0002g0138a0001c0002t0006g0174others(1): Show | 4 | 223 | 0.0179 | 49 | c.-99 others(66): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | chr20 | TogoVar | ||||||
| NAALADL2_chr3_174854334_175815548 | 175132229 | A | ACCTCCCG others(42): Show |
intron_variant | MODIFIER | HG00639.hp2 HG01074.hp1 HG01074.hp2 others(26): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0013a0002c0005others(13): Show | a0001c0001t0002a0001c0001t0012a0001c0001t0035others(26): Show | a0001c0001t0002g0012a0001c0001t0012g0031a0001c0001t0035g0027others(26): Show | 29 | 64 | 0.4531 | 49 | c.545 others(68): Show |
NAALADL2 | ENSG00000177694.16 | transcript | ENST00000454872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
| NAALADL2_chr3_174854334_175815548 | 175132245 | G | GGCTGGCC others(42): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0005 | a0005c0006 | a0005c0006t0001 | a0005c0006t0001g0057 | 1 | 64 | 0.0156 | 49 | c.545 others(68): Show |
NAALADL2 | ENSG00000177694.16 | transcript | ENST00000454872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
| NALF1_chr13_107158510_107872496 | 107783176 | G | GTCCGGGA others(42): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00738.hp1 others(20): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0002g0053others(20): Show | 23 | 128 | 0.1797 | 49 | c.915 others(68): Show |
NALF1 | ENSG00000204442.4 | transcript | ENST00000375915.4 | protein_coding | 1/2 | chr13 | TogoVar | ||||||
| NAPEPLD_chr7_103094776_103154099 | 103099593 | T | TGTGTGTG others(42): Show |
downstream_gene_variant | MODIFIER | HG00738.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0207 | 1 | 381 | 0.0026 | 49 | c.*38 others(60): Show |
NAPEPLD | ENSG00000161048.12 | transcript | ENST00000465647.6 | protein_coding | 182 | chr7 | TogoVar | ||||||
| NAV1_chr1_201534127_201831969 | 201642525 | T | TTTTTCTT others(42): Show |
intron_variant | MODIFIER | HG01361.hp2 | a0001 | a0001c0026 | a0001c0026t0069 | a0001c0026t0069g0169 | 1 | 210 | 0.0048 | 49 | c.827 others(66): Show |
NAV1 | ENSG00000134369.16 | transcript | ENST00000685211.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
| NAV2_chr11_19707837_20126601 | 19860082 | G | GGGCGGGG others(42): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0003 | a0003c0027 | a0003c0027t0008 | a0003c0027t0008g0158 | 1 | 166 | 0.0060 | 49 | c.439 others(66): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| NAV3_chr12_77825894_78218010 | 78154280 | T | TATAATAT others(42): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
a0004a0013 | a0004c0017a0004c0043a0013c0030 | a0004c0017t0015a0004c0017t0021a0004c0043t0061others(1): Show | a0004c0017t0015g0155a0004c0017t0021g0176a0004c0043t0061g0003others(1): Show | 4 | 186 | 0.0215 | 49 | c.478 others(68): Show |
NAV3 | ENSG00000067798.16 | transcript | ENST00000397909.7 | protein_coding | 22/39 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| NBAS_chr2_15161916_15566334 | 15220084 | C | CCCCCCCC others(42): Show |
intron_variant | MODIFIER | HG03491.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0215 | 1 | 224 | 0.0045 | 49 | c.623 others(68): Show |
NBAS | ENSG00000151779.14 | transcript | ENST00000281513.10 | protein_coding | 47/51 | chr2 | TogoVar | ||||||
| NCAM2_chr21_20993409_21548329 | 21264961 | G | GTATGTGT others(42): Show |
intron_variant | MODIFIER | HG00558.hp1 HG00733.hp2 HG03704.hp2 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002a0002c0002t0006others(1): Show | a0002c0002t0001g0094a0002c0002t0002g0045a0002c0002t0006g0023others(1): Show | 4 | 132 | 0.0303 | 49 | c.56- others(66): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
| NCMAP_chr1_24551087_24614328 | 24604649 | T | TGTGTGTG others(42): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0390 | 1 | 402 | 0.0025 | 49 | c.168 others(64): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | TogoVar | ||||||
| NCOA3_chr20_47496887_47661872 | 47541390 | C | CCTCCCCT others(42): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0130 | 1 | 316 | 0.0032 | 49 | c.-99 others(68): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
| NCOR1_chr17_16024157_16220534 | 16077454 | A | AGAGGAGA others(42): Show |
intron_variant | MODIFIER | NA19054.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0208 | 1 | 282 | 0.0036 | 49 | c.350 others(68): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 26/45 | chr17 | TogoVar | ||||||
| NCOR1_chr17_16024157_16220534 | 16077511 | A | AGGGGAGG others(42): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0256 | 1 | 282 | 0.0036 | 49 | c.350 others(68): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 26/45 | chr17 | TogoVar | ||||||
| NCOR1_chr17_16024157_16220534 | 16095667 | G | GGGGGGGT others(42): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0017 | a0001c0017t0021 | a0001c0017t0021g0166 | 1 | 282 | 0.0036 | 49 | c.282 others(68): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 21/45 | chr17 | TogoVar | ||||||
| NCOR1_chr17_16024157_16220534 | 16106883 | A | ATATATAT others(42): Show |
intron_variant | MODIFIER | NA18982.hp2 NA19012.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0153a0001c0001t0002g0154 | 2 | 282 | 0.0071 | 49 | c.218 others(68): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 19/45 | chr17 | TogoVar | ||||||
| NDUFAF8_chr17_81234318_81246310 | 81245010 | C | CAAAAGTG others(42): Show |
downstream_gene_variant | MODIFIER | NA18967.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0007 | 1 | 288 | 0.0035 | 49 | c.*39 others(60): Show |
NDUFAF8 | ENSG00000224877.4 | transcript | ENST00000431388.3 | protein_coding | 3701 | chr17 | TogoVar | ||||||
| NEK11_chr3_131021877_131355465 | 131317821 | A | AGGGAGGG others(42): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02630.hp1 HG02970.hp2 others(4): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0010a0002c0002t0001g0076a0002c0002t0001g0078others(4): Show | 7 | 292 | 0.0240 | 49 | c.171 others(70): Show |
NEK11 | ENSG00000114670.14 | transcript | ENST00000383366.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
| NEU4_chr2_241804193_241822413 | 241805963 | T | TCTGCAGG others(42): Show |
upstream_gene_variant | MODIFIER | NA18977.hp1 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0143 | 1 | 319 | 0.0031 | 49 | c.-33 others(60): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 3229 | chr2 | TogoVar | ||||||
| NF1_chr17_31089977_31382675 | 31335275 | T | TATATATA others(42): Show |
intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(2): Show |
a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0007a0001c0003t0003g0008a0001c0003t0003g0009others(2): Show | 5 | 252 | 0.0198 | 49 | c.600 others(66): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 40/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| NFATC1_chr18_79390930_79534323 | 79395681 | C | CCCCCCTC others(42): Show |
upstream_gene_variant | MODIFIER | HG03130.hp2 | a0007 | a0007c0033 | a0007c0033t0026 | a0007c0033t0026g0101 | 1 | 322 | 0.0031 | 49 | c.-54 others(58): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 248 | chr18 | TogoVar | ||||||
| NFATC1_chr18_79390930_79534323 | 79395681 | C | CCCCCCTC others(42): Show |
upstream_gene_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0013 | a0001c0013t0025 | a0001c0013t0025g0046 | 1 | 322 | 0.0031 | 49 | c.-54 others(58): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 248 | chr18 | TogoVar | ||||||
| NFATC1_chr18_79390930_79534323 | 79494807 | C | CCGCCGGG others(42): Show |
intron_variant | MODIFIER | NA19067.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0160 | 1 | 322 | 0.0031 | 49 | c.278 others(68): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 9/9 | chr18 | TogoVar | ||||||
| NFATC1_chr18_79390930_79534323 | 79495970 | A | AGTGTCAC others(42): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00733.hp2 HG01256.hp2 others(13): Show |
a0001a0002a0003 | a0001c0027a0001c0029a0001c0053others(2): Show | a0001c0027t0008a0001c0029t0004a0001c0053t0003others(5): Show | a0001c0027t0008g0013a0001c0027t0008g0030a0001c0029t0004g0096others(13): Show | 16 | 322 | 0.0497 | 49 | c.278 others(68): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
| NGEF_chr2_232873701_233018256 | 232905895 | G | GGGGGGTC others(42): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | a0001c0001t0001g0049a0001c0001t0001g0165a0001c0001t0001g0337others(228): Show | 232 | 362 | 0.6409 | 49 | c.829 others(68): Show |
NGEF | ENSG00000066248.15 | transcript | ENST00000264051.8 | protein_coding | 5/14 | chr2 | TogoVar | ||||||
| NGEF_chr2_232873701_233018256 | 232906509 | T | TGGGAGGG others(42): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0002 | a0002c0006 | a0002c0006t0030 | a0002c0006t0030g0341 | 1 | 362 | 0.0028 | 49 | c.829 others(68): Show |
NGEF | ENSG00000066248.15 | transcript | ENST00000264051.8 | protein_coding | 5/14 | chr2 | TogoVar | ||||||
| NGEF_chr2_232873701_233018256 | 232906509 | T | TGGGAGGG others(42): Show |
intron_variant | MODIFIER | HG01109.hp1 HG02647.hp1 HG03195.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0013others(1): Show | a0001c0001t0014a0001c0004t0024a0001c0013t0001others(1): Show | a0001c0001t0014g0129a0001c0001t0014g0130a0001c0004t0024g0010others(4): Show | 7 | 362 | 0.0193 | 49 | c.829 others(68): Show |
NGEF | ENSG00000066248.15 | transcript | ENST00000264051.8 | protein_coding | 5/14 | chr2 | TogoVar | ||||||
| NGEF_chr2_232873701_233018256 | 232906558 | C | CGGGAGGG others(42): Show |
intron_variant | MODIFIER | HG02083.hp1 NA19057.hp2 |
a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0098a0001c0007t0001g0199 | 2 | 362 | 0.0055 | 49 | c.829 others(68): Show |
NGEF | ENSG00000066248.15 | transcript | ENST00000264051.8 | protein_coding | 5/14 | chr2 | TogoVar | ||||||
| NIBAN1_chr1_184786032_184979508 | 184913138 | T | TATATATA others(42): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0008 | a0008c0017 | a0008c0017t0001 | a0008c0017t0001g0250 | 1 | 256 | 0.0039 | 49 | c.56- others(66): Show |
NIBAN1 | ENSG00000135842.17 | transcript | ENST00000367511.4 | protein_coding | 1/13 | chr1 | TogoVar | ||||||
| NID2_chr14_51999809_52074059 | 52030567 | A | AGAAAGAA others(42): Show |
intron_variant | MODIFIER | HG00639.hp1 HG01109.hp2 HG02109.hp2 |
a0004 | a0004c0012 | a0004c0012t0002 | a0004c0012t0002g0302a0004c0012t0002g0303a0004c0012t0002g0307 | 3 | 372 | 0.0081 | 49 | c.225 others(66): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | TogoVar | ||||||
| NINL_chr20_25447697_25590531 | 25549210 | C | CCCCGGCA others(42): Show |
intron_variant | MODIFIER | HG00544.hp1 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0030 | 1 | 310 | 0.0032 | 49 | c.-11 others(68): Show |
NINL | ENSG00000101004.16 | transcript | ENST00000278886.11 | protein_coding | 1/23 | chr20 | TogoVar | ||||||
| NLK_chr17_28037677_28201381 | 28172264 | A | AAATTCCT others(42): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02976.hp2 HG03486.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0013 | 3 | 108 | 0.0278 | 49 | c.104 others(66): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | TogoVar | ||||||
| NLRP2_chr19_54961374_55006138 | 54999009 | T | TGGGGGGC others(42): Show |
intron_variant | MODIFIER | HG02004.hp2 HG02896.hp2 HG02970.hp2 others(1): Show |
a0021a0022a0023others(1): Show | a0021c0062a0022c0061a0023c0059others(1): Show | a0021c0062t0015a0022c0061t0015a0023c0059t0016others(1): Show | a0021c0062t0015g0376a0022c0061t0015g0291a0023c0059t0016g0276others(1): Show | 4 | 429 | 0.0093 | 49 | c.305 others(68): Show |
NLRP2 | ENSG00000022556.16 | transcript | ENST00000448584.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
| NLRP8_chr19_55942832_55993629 | 55993412 | C | CTCTCCCC others(42): Show |
downstream_gene_variant | MODIFIER | HG02896.hp1 | a0000 | a0000c0071 | a0000c0071t0037 | a0000c0071t0037g0015 | 1 | 350 | 0.0029 | 49 | c.*54 others(60): Show |
NLRP8 | ENSG00000179709.8 | transcript | ENST00000291971.7 | protein_coding | 4784 | chr19 | TogoVar | ||||||
| NME2_chr17_51161411_51176744 | 51176422 | A | AAAAAAAA others(42): Show |
downstream_gene_variant | MODIFIER | NA18967.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 413 | 0.0024 | 49 | c.*48 others(60): Show |
NME2 | ENSG00000243678.12 | transcript | ENST00000512737.6 | protein_coding | 4679 | chr17 | TogoVar | ||||||
| NOC2L_chr1_939203_964256 | 939436 | C | CCCCCTCA others(42): Show |
downstream_gene_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073 | 1 | 422 | 0.0024 | 49 | c.*52 others(60): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4766 | chr1 | TogoVar | ||||||
| NOC4L_chr12_132139457_132157468 | 132150015 | T | TCACACCA others(42): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0053 | 1 | 294 | 0.0034 | 49 | c.902 others(64): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| NOC4L_chr12_132139457_132157468 | 132150015 | T | TCACACCA others(42): Show |
intron_variant | MODIFIER | NA18966.hp2 NA18970.hp1 NA18983.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0033a0001c0001t0001g0265a0001c0003t0001g0135 | 3 | 294 | 0.0102 | 49 | c.902 others(64): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| NOC4L_chr12_132139457_132157468 | 132150015 | T | TCACACCA others(42): Show |
intron_variant | MODIFIER | HG02300.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107 | 1 | 294 | 0.0034 | 49 | c.902 others(64): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| NOC4L_chr12_132139457_132157468 | 132150015 | T | TCACACCA others(42): Show |
intron_variant | MODIFIER | HG00609.hp1 HG00673.hp2 HG02004.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0006 | a0001c0001t0001a0001c0003t0001a0001c0006t0001 | a0001c0001t0001g0150a0001c0001t0001g0162a0001c0003t0001g0147others(2): Show | 5 | 294 | 0.0170 | 49 | c.902 others(64): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| NOC4L_chr12_132139457_132157468 | 132150015 | T | TCACACCA others(42): Show |
intron_variant | MODIFIER | HG00642.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0252 | 1 | 294 | 0.0034 | 49 | c.902 others(64): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| NOC4L_chr12_132139457_132157468 | 132150015 | T | TCATACCA others(42): Show |
intron_variant | MODIFIER | HG00733.hp2 | a0008 | a0008c0012 | a0008c0012t0001 | a0008c0012t0001g0232 | 1 | 294 | 0.0034 | 49 | c.902 others(64): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| NOC4L_chr12_132139457_132157468 | 132150015 | T | TCATACCA others(42): Show |
intron_variant | MODIFIER | HG01433.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0198 | 1 | 294 | 0.0034 | 49 | c.902 others(64): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| NOC4L_chr12_132139457_132157468 | 132150015 | T | TCCTACCA others(42): Show |
intron_variant | MODIFIER | HG02273.hp2 HG02818.hp1 HG03540.hp1 others(2): Show |
a0001a0003 | a0001c0001a0001c0007a0003c0008 | a0001c0001t0001a0001c0007t0001a0003c0008t0001 | a0001c0001t0001g0190a0001c0001t0001g0209a0001c0001t0001g0250others(2): Show | 5 | 294 | 0.0170 | 49 | c.902 others(64): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| NOL4L_chr20_32438059_32590333 | 32488803 | C | CCTTTCTT others(42): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0001 | a0001c0003 | a0001c0003t0009 | a0001c0003t0009g0061 | 1 | 196 | 0.0051 | 49 | c.700 others(68): Show |
NOL4L | ENSG00000197183.15 | transcript | ENST00000621426.7 | protein_coding | 4/10 | chr20 | TogoVar | ||||||
| NOMO1_chr16_14828721_14901157 | 14867176 | A | ATATATAT others(42): Show |
intron_variant | MODIFIER | NA19084.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 | 1 | 337 | 0.0030 | 49 | c.180 others(66): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
| NOS1AP_chr1_162064691_162375475 | 162261539 | A | AGAGAGAG others(42): Show |
intron_variant | MODIFIER | HG01106.hp1 HG01261.hp1 HG02280.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0030others(2): Show | a0001c0001t0001g0055a0001c0001t0001g0144a0001c0001t0002g0077others(3): Show | 6 | 182 | 0.0330 | 49 | c.178 others(68): Show |
NOS1AP | ENSG00000198929.13 | transcript | ENST00000361897.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |