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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MTERF3_chr8_96234402_96266610 | 96250681 | A | AAGAAGAC others(167): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0176 | 1 | 294 | 0.0034 | 174 | c.677 others(189): Show |
MTERF3 | ENSG00000156469.9 | transcript | ENST00000287025.4 | protein_coding | 4/7 | chr8 | TogoVar | |||||||
MTHFD2L_chr4_74153118_74308099 | 74188742 | A | ATATATAT others(167): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0173 | 1 | 200 | 0.0050 | 174 | c.452 others(193): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
MTTP_chr4_99569824_99628997 | 99588843 | A | ACATATAT others(167): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0009 | a0009c0012 | a0009c0012t0007 | a0009c0012t0007g0318 | 1 | 364 | 0.0028 | 174 | c.394 others(189): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
MUC4_chr3_195741771_195816929 | 195767530 | G | GCCACCAC others(167): Show |
intron_variant | MODIFIER | HG00140.hp2 HG01106.hp1 HG03831.hp2 others(2): Show |
a0009a0174a0183 | a0009c0006a0174c0116a0183c0118 | a0009c0006t0001a0174c0116t0001a0183c0118t0001 | a0009c0006t0001g0101 a0009c0006t0001g0102 a0009c0006t0001g0133 others(2): Show |
5 | 249 | 0.0201 | 174 | c.135 others(193): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 7/24 | chr3 | TogoVar | |||||||
MUC4_chr3_195741771_195816929 | 195767530 | G | GCCACCAC others(167): Show |
intron_variant | MODIFIER | HG03688.hp2 HG03942.hp2 |
a0025 | a0025c0010 | a0025c0010t0001 | a0025c0010t0001g0078 a0025c0010t0001g0141 |
2 | 249 | 0.0080 | 174 | c.135 others(193): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 7/24 | chr3 | TogoVar | |||||||
MUC4_chr3_195741771_195816929 | 195767728 | C | CACCACCA others(167): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0080 | a0080c0170 | a0080c0170t0005 | a0080c0170t0005g0240 | 1 | 249 | 0.0040 | 174 | c.135 others(193): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 7/24 | chr3 | TogoVar | |||||||
MYCBP2_chr13_77039657_77332094 | 77174902 | T | TATATATA others(167): Show |
intron_variant | MODIFIER | HG02717.hp2 HG03041.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0020 a0001c0003t0001g0021 |
2 | 334 | 0.0060 | 174 | c.547 others(191): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | TogoVar | |||||||
MYDGF_chr19_4652545_4675342 | 4663119 | T | TCATCCTC others(167): Show |
intron_variant | MODIFIER | HG01109.hp1 HG01167.hp2 HG01515.hp1 others(4): Show |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0018 a0002c0002t0002g0095 a0002c0002t0002g0098 others(3): Show |
7 | 410 | 0.0171 | 174 | c.287 others(191): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | TogoVar | |||||||
MYDGF_chr19_4652545_4675342 | 4663181 | C | CCTCCAAT others(167): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0046 | 1 | 410 | 0.0024 | 174 | c.287 others(191): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | TogoVar | |||||||
MYDGF_chr19_4652545_4675342 | 4663507 | T | TCCACCCA others(167): Show |
intron_variant | MODIFIER | HG00733.hp1 HG01928.hp1 HG01975.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 a0001c0001t0001g0149 a0001c0001t0001g0151 others(4): Show |
8 | 410 | 0.0195 | 174 | c.287 others(191): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | TogoVar | |||||||
MYDGF_chr19_4652545_4675342 | 4663533 | C | CAGCCTCC others(167): Show |
intron_variant | MODIFIER | NA18962.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0303 | 1 | 410 | 0.0024 | 174 | c.287 others(191): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | TogoVar | |||||||
MYDGF_chr19_4652545_4675342 | 4663565 | C | CCCTCATT others(167): Show |
intron_variant | MODIFIER | HG02698.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 | 1 | 410 | 0.0024 | 174 | c.287 others(191): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | TogoVar | |||||||
MYDGF_chr19_4652545_4675342 | 4663576 | C | CAGCCTCC others(167): Show |
intron_variant | MODIFIER | NA19087.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0055 | 1 | 410 | 0.0024 | 174 | c.287 others(191): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | TogoVar | |||||||
MYNN_chr3_169768396_169794716 | 169769250 | G | GCCCCACC others(167): Show |
upstream_gene_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0091 | 1 | 350 | 0.0029 | 174 | c.-42 others(185): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4145 | chr3 | TogoVar | |||||||
MYO16_chr13_108624611_109213005 | 109023408 | T | TTATACAG others(167): Show |
intron_variant | MODIFIER | NA19011.hp2 | a0014 | a0014c0057 | a0014c0057t0001 | a0014c0057t0001g0023 | 1 | 152 | 0.0066 | 174 | c.279 others(193): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 109023447 | A | ATAAATAT others(167): Show |
intron_variant | MODIFIER | NA19010.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0027 | 1 | 152 | 0.0066 | 174 | c.279 others(193): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
MYO1F_chr19_8515778_8582442 | 8544006 | C | CGGTGGCG others(167): Show |
intron_variant | MODIFIER | HG03704.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0251 | 1 | 342 | 0.0029 | 174 | c.152 others(191): Show |
MYO1F | ENSG00000142347.20 | transcript | ENST00000644032.2 | protein_coding | 14/27 | chr19 | TogoVar | |||||||
MYT1L_chr2_1784113_2336275 | 2295565 | C | CAGAGAGA others(167): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(16): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(10): Show | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0002t0001g0046 others(16): Show |
19 | 104 | 0.1827 | 174 | c.-52 others(195): Show |
MYT1L | ENSG00000186487.21 | transcript | ENST00000647738.2 | protein_coding | 1/24 | chr2 | TogoVar | |||||||
NCAM2_chr21_20993409_21548329 | 21125508 | T | TTTACATA others(167): Show |
intron_variant | MODIFIER | HG02723.hp2 HG03209.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0032a0001c0004t0002 | a0001c0001t0032g0125 a0001c0004t0002g0096 |
2 | 132 | 0.0152 | 174 | c.55+ others(193): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667549 | C | CTCTTACC others(167): Show |
intron_variant | MODIFIER | HG03834.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0046 | 1 | 378 | 0.0027 | 174 | c.148 others(193): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667751 | C | CCTTACCT others(167): Show |
intron_variant | MODIFIER | HG01099.hp1 HG01346.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0249 a0001c0001t0001g0323 |
2 | 378 | 0.0053 | 174 | c.148 others(193): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667828 | T | TCCCTCCG others(167): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0037 | 1 | 378 | 0.0027 | 174 | c.148 others(193): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668042 | C | CCTTACCC others(167): Show |
intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0026 | 1 | 378 | 0.0027 | 174 | c.148 others(193): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668071 | T | TCCTTACC others(167): Show |
intron_variant | MODIFIER | HG02165.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0221 | 1 | 378 | 0.0027 | 174 | c.148 others(193): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124373449 | G | GCAGTGAG others(167): Show |
intron_variant | MODIFIER | HG00597.hp2 HG02027.hp1 NA19091.hp2 |
a0001a0009 | a0001c0029a0001c0093a0009c0156 | a0001c0029t0018a0001c0093t0010a0009c0156t0007 | a0001c0029t0018g0154 a0001c0093t0010g0214 a0009c0156t0007g0189 |
3 | 234 | 0.0128 | 174 | c.221 others(191): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 21/48 | chr12 | TogoVar | |||||||
NDUFV3_chr21_42888309_42918299 | 42894362 | A | ATATATAT others(167): Show |
intron_variant | MODIFIER | HG01261.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0022a0001c0001t0050 | a0001c0001t0022g0045 a0001c0001t0022g0047 a0001c0001t0022g0048 others(1): Show |
4 | 348 | 0.0115 | 174 | c.48+ others(187): Show |
NDUFV3 | ENSG00000160194.18 | transcript | ENST00000354250.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NEGR1_chr1_71390943_72287539 | 71928131 | C | CATGTATA others(167): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0017 | 1 | 64 | 0.0156 | 174 | c.409 others(191): Show |
NEGR1 | ENSG00000172260.15 | transcript | ENST00000357731.10 | protein_coding | 2/6 | chr1 | TogoVar | |||||||
NFATC1_chr18_79390930_79534323 | 79400830 | C | CCGACCCC others(167): Show |
intron_variant | MODIFIER | NA19063.hp2 | a0001 | a0001c0006 | a0001c0006t0003 | a0001c0006t0003g0183 | 1 | 322 | 0.0031 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | chr18 | TogoVar | |||||||
NFATC1_chr18_79390930_79534323 | 79400830 | C | CCGACCCC others(167): Show |
intron_variant | MODIFIER | HG00140.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0297 | 1 | 322 | 0.0031 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | chr18 | TogoVar | |||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(167): Show |
intron_variant | MODIFIER | HG01934.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0298 | 1 | 322 | 0.0031 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(167): Show |
intron_variant | MODIFIER | HG01255.hp1 | a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0307 | 1 | 322 | 0.0031 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(167): Show |
intron_variant | MODIFIER | HG00544.hp1 HG00597.hp1 HG01192.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0046a0002c0002others(1): Show | a0001c0001t0003a0001c0046t0016a0002c0002t0003others(1): Show | a0001c0001t0003g0143 a0001c0046t0016g0144 a0002c0002t0003g0141 others(2): Show |
5 | 322 | 0.0155 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(167): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0264 | 1 | 322 | 0.0031 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(167): Show |
intron_variant | MODIFIER | HG01168.hp2 | a0002 | a0002c0003 | a0002c0003t0023 | a0002c0003t0023g0123 | 1 | 322 | 0.0031 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(167): Show |
intron_variant | MODIFIER | HG01074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0233 | 1 | 322 | 0.0031 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(167): Show |
intron_variant | MODIFIER | HG03491.hp1 | a0001 | a0001c0029 | a0001c0029t0004 | a0001c0029t0004g0098 | 1 | 322 | 0.0031 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(167): Show |
intron_variant | MODIFIER | HG01975.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0253 | 1 | 322 | 0.0031 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(167): Show |
intron_variant | MODIFIER | NA18960.hp2 | a0001 | a0001c0001 | a0001c0001t0059 | a0001c0001t0059g0192 | 1 | 322 | 0.0031 | 174 | c.127 others(191): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8663394 | A | ATGGAACT others(167): Show |
intron_variant | MODIFIER | HG02027.hp1 NA18954.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0145 a0001c0001t0001g0147 |
2 | 366 | 0.0055 | 174 | c.-16 others(195): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8663415 | G | GTGGGGAA others(167): Show |
intron_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(42): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0168 a0001c0001t0001g0179 a0001c0001t0001g0185 others(42): Show |
45 | 366 | 0.1230 | 174 | c.-16 others(195): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8663415 | G | GTGGGGAA others(167): Show |
intron_variant | MODIFIER | NA19055.hp1 NA19055.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0136 | a0001c0001t0003g0033 a0001c0001t0136g0271 |
2 | 366 | 0.0055 | 174 | c.-16 others(195): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8663434 | A | AGCTGGTG others(167): Show |
intron_variant | MODIFIER | NA20805.hp2 | a0011 | a0011c0014 | a0011c0014t0165 | a0011c0014t0165g0109 | 1 | 366 | 0.0027 | 174 | c.-16 others(195): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8663434 | A | AGCTGGTG others(167): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0127 | a0001c0001t0127g0056 | 1 | 366 | 0.0027 | 174 | c.-16 others(195): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8663434 | A | AGCTGGTG others(167): Show |
intron_variant | MODIFIER | HG00099.hp2 HG01243.hp2 NA18612.hp2 |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0002a0002c0002t0023a0003c0003t0071 | a0002c0002t0002g0006 a0002c0002t0023g0004 a0003c0003t0071g0331 |
3 | 366 | 0.0082 | 174 | c.-16 others(195): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8663434 | A | AGCTGGTG others(167): Show |
intron_variant | MODIFIER | HG02056.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 | 1 | 366 | 0.0027 | 174 | c.-16 others(195): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8663491 | A | ACGCTGGT others(167): Show |
intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0001 | a0001c0001t0142 | a0001c0001t0142g0011 | 1 | 366 | 0.0027 | 174 | c.-16 others(195): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8678097 | C | CCATCCAT others(167): Show |
3_prime_UTR_variant | MODIFIER | HG02615.hp1 homoSapiens_chm13v2.hp1 |
a0002 | a0002c0002 | a0002c0002t0103a0002c0002t0166 | a0002c0002t0103g0243 a0002c0002t0166g0100 |
2 | 366 | 0.0055 | 174 | c.*47 others(183): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 6/6 | 474 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
NHSL1_chr6_138417043_138504494 | 138455536 | A | ACATGCTC others(167): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0007 | a0001c0007t0020 | a0001c0007t0020g0148 | 1 | 332 | 0.0030 | 174 | c.340 others(191): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | TogoVar | |||||||
NLRP13_chr19_55890945_55937336 | 55930882 | A | ATATATAT others(167): Show |
intron_variant | MODIFIER | NA19090.hp2 | a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0152 | 1 | 440 | 0.0023 | 174 | c.319 others(191): Show |
NLRP13 | ENSG00000173572.12 | transcript | ENST00000342929.4 | protein_coding | 1/10 | chr19 | TogoVar | |||||||
NLRP13_chr19_55890945_55937336 | 55930884 | A | ATATATAT others(167): Show |
intron_variant | MODIFIER | NA19004.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0232 | 1 | 440 | 0.0023 | 174 | c.319 others(191): Show |
NLRP13 | ENSG00000173572.12 | transcript | ENST00000342929.4 | protein_coding | 1/10 | chr19 | TogoVar |