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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
RNF181_chr2_85590745_85602708 | 85592800 | C | CAAAAAAA others(8): Show |
upstream_gene_variant | MODIFIER | HG01243.hp2 HG01981.hp1 HG02145.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0001a0002c0002t0001others(1): Show | a0001c0001t0001g0003 a0001c0003t0001g0005 a0002c0002t0001g0004 others(1): Show |
13 | 217 | 0.0599 | 15 | c.-29 others(26): Show |
RNF181 | ENSG00000168894.10 | transcript | ENST00000306368.9 | protein_coding | 2944 | chr2 | TogoVar | |||||||
RNF182_chr6_13919952_13985310 | 13980201 | T | TTTTTATT others(8): Show |
3_prime_UTR_variant | MODIFIER | HG00733.hp2 HG02027.hp1 NA18941.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0021 a0001c0001t0010g0025 a0001c0001t0010g0228 |
4 | 104 | 0.0385 | 15 | c.*23 others(26): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2382 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
RNF183_chr9_113292093_113308376 | 113308170 | A | AAAAAAAA others(8): Show |
upstream_gene_variant | MODIFIER | HG00408.hp2 HG00673.hp1 HG01516.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0004 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0002c0002t0004g0004 |
7 | 144 | 0.0486 | 15 | c.-55 others(26): Show |
RNF183 | ENSG00000165188.14 | transcript | ENST00000489339.2 | protein_coding | 4795 | chr9 | TogoVar | |||||||
RNF183_chr9_113292093_113308376 | 113308170 | A | AAAAAAAG others(8): Show |
upstream_gene_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 138 | 0.0072 | 15 | c.-55 others(26): Show |
RNF183 | ENSG00000165188.14 | transcript | ENST00000489339.2 | protein_coding | 4795 | chr9 | TogoVar | |||||||
RNF183_chr9_113292093_113308376 | 113308170 | A | AAAGAAAG others(8): Show |
upstream_gene_variant | MODIFIER | HG02896.hp1 HG03834.hp2 NA19001.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 3 | 140 | 0.0214 | 15 | c.-55 others(26): Show |
RNF183 | ENSG00000165188.14 | transcript | ENST00000489339.2 | protein_coding | 4795 | chr9 | TogoVar | |||||||
RNF185_chr22_31155182_31212019 | 31182908 | T | TTTATTAT others(8): Show |
intron_variant | MODIFIER | HG00609.hp1 HG00741.hp2 HG01168.hp2 others(54): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0112 a0001c0001t0002g0005 a0001c0001t0002g0012 others(53): Show |
57 | 128 | 0.4453 | 15 | c.-48 others(32): Show |
RNF185 | ENSG00000138942.17 | transcript | ENST00000326132.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
RNF185_chr22_31155182_31212019 | 31182908 | T | TTTTTTAT others(8): Show |
intron_variant | MODIFIER | HG02132.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0251 | 1 | 72 | 0.0139 | 15 | c.-48 others(32): Show |
RNF185 | ENSG00000138942.17 | transcript | ENST00000326132.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
RNF19A_chr8_100252067_100314953 | 100256511 | C | CAAAAAAA others(8): Show |
downstream_gene_variant | MODIFIER | HG02145.hp2 HG02647.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0157 a0001c0001t0002g0146 |
2 | 121 | 0.0165 | 15 | c.*20 others(26): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 555 | chr8 | TogoVar | |||||||
RNF19A_chr8_100252067_100314953 | 100313902 | C | CTTTTTTT others(8): Show |
upstream_gene_variant | MODIFIER | HG01167.hp1 HG01168.hp1 HG01346.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | 166 | 0.0723 | 15 | c.-41 others(26): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3950 | chr8 | TogoVar | |||||||
RNF207_chr1_6201119_6226299 | 6214630 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02258.hp2 HG02717.hp1 others(6): Show |
a0001a0003a0008 | a0001c0001a0003c0006a0003c0012others(1): Show | a0001c0001t0001a0003c0006t0002a0003c0006t0003others(2): Show | a0001c0001t0001g0011 a0001c0001t0001g0059 a0003c0006t0002g0070 others(4): Show |
9 | 212 | 0.0425 | 15 | c.165 others(34): Show |
RNF207 | ENSG00000158286.13 | transcript | ENST00000377939.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF212B_chr14_23232936_23278477 | 23238777 | A | AATCATCA others(8): Show |
intron_variant | MODIFIER | HG01943.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0177 | 1 | 310 | 0.0032 | 15 | c.-2+ others(28): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
RNF212B_chr14_23232936_23278477 | 23238780 | A | AATAATCA others(8): Show |
intron_variant | MODIFIER | NA18995.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0173 | 1 | 301 | 0.0033 | 15 | c.-2+ others(28): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
RNF212B_chr14_23232936_23278477 | 23238780 | A | AATCATCA others(8): Show |
intron_variant | MODIFIER | HG02080.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0174 | 1 | 301 | 0.0033 | 15 | c.-2+ others(28): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
RNF212B_chr14_23232936_23278477 | 23266302 | G | GGTTGTTT others(8): Show |
intron_variant | MODIFIER | HG01071.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0118 | 1 | 366 | 0.0027 | 15 | c.634 others(32): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
RNF212B_chr14_23232936_23278477 | 23274207 | A | AAATGAAA others(8): Show |
downstream_gene_variant | MODIFIER | HG00544.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0038 | 1 | 366 | 0.0027 | 15 | c.*13 others(26): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 731 | chr14 | TogoVar | |||||||
RNF212B_chr14_23232936_23278477 | 23277802 | T | TTTTTTAG others(8): Show |
downstream_gene_variant | MODIFIER | HG01928.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0006 | 1 | 366 | 0.0027 | 15 | c.*49 others(26): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4326 | chr14 | TogoVar | |||||||
RNF213_chr17_80255852_80403794 | 80305184 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0011 | a0011c0036 | a0011c0036t0033 | a0011c0036t0033g0282 | 1 | 130 | 0.0077 | 15 | c.221 others(34): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 11/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80314367 | G | GTGATGGT others(8): Show |
intron_variant | MODIFIER | NA18944.hp2 NA18954.hp2 NA19086.hp1 |
a0001 | a0001c0003a0001c0004 | a0001c0003t0001a0001c0004t0022 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0004t0022g0106 |
3 | 290 | 0.0103 | 15 | c.281 others(34): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | chr17 | TogoVar | |||||||
RNF213_chr17_80255852_80403794 | 80314432 | G | GGTGATGG others(8): Show |
intron_variant | MODIFIER | HG03540.hp2 NA18942.hp2 |
a0004a0091 | a0004c0044a0091c0043 | a0004c0044t0012a0091c0043t0002 | a0004c0044t0012g0190 a0091c0043t0002g0055 |
2 | 290 | 0.0069 | 15 | c.281 others(34): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80314706 | G | GAGGTGAT others(8): Show |
intron_variant | MODIFIER | HG04228.hp2 | a0089 | a0089c0139 | a0089c0139t0001 | a0089c0139t0001g0284 | 1 | 267 | 0.0037 | 15 | c.281 others(34): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80314707 | A | AGGTGATG others(8): Show |
intron_variant | MODIFIER | HG02015.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0157 | 1 | 289 | 0.0035 | 15 | c.281 others(34): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80314708 | G | GGTGATGG others(8): Show |
intron_variant | MODIFIER | NA19005.hp1 NA19062.hp1 NA21309.hp2 |
a0002a0104 | a0002c0002a0104c0085 | a0002c0002t0002a0104c0085t0003 | a0002c0002t0002g0087 a0002c0002t0002g0141 a0104c0085t0003g0291 |
3 | 286 | 0.0105 | 15 | c.281 others(34): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80314886 | G | GTGGTGGT others(8): Show |
intron_variant | MODIFIER | HG02451.hp2 HG03041.hp1 HG03209.hp1 |
a0058a0075a0078 | a0058c0049a0075c0048a0078c0107 | a0058c0049t0014a0075c0048t0051a0078c0107t0023 | a0058c0049t0014g0243 a0075c0048t0051g0245 a0078c0107t0023g0081 |
3 | 256 | 0.0117 | 15 | c.281 others(34): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80315180 | G | GTGGTGGT others(8): Show |
intron_variant | MODIFIER | NA19081.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069 | 1 | 286 | 0.0035 | 15 | c.281 others(34): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF215_chr22_30373821_30392411 | 30387217 | A | ACAGCGGC others(8): Show |
conservative_inframe_insertion | MODERATE | NA18979.hp2 | a0007 | a0007c0008 | a0007c0008t0004 | a0007c0008t0004g0047 | 1 | 430 | 0.0023 | 15 | c.82_ others(20): Show |
p.Leu others(26): Show |
RNF215 | ENSG00000099999.15 | transcript | ENST00000382363.8 | protein_coding | 1/9 | 194/2011 | 96/1134 | 32/377 | chr22 | TogoVar | |||
RNF216_chr7_5615047_5786663 | 5660943 | G | GTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG03540.hp2 NA19077.hp2 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0006a0001c0008t0007 | a0001c0001t0006g0050 a0001c0008t0007g0241 |
2 | 125 | 0.0160 | 15 | c.206 others(34): Show |
RNF216 | ENSG00000011275.19 | transcript | ENST00000389902.8 | protein_coding | 13/16 | chr7 | TogoVar | |||||||
RNF216_chr7_5615047_5786663 | 5671805 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG00140.hp2 | a0001 | a0001c0006 | a0001c0006t0014 | a0001c0006t0014g0163 | 1 | 89 | 0.0112 | 15 | c.206 others(36): Show |
RNF216 | ENSG00000011275.19 | transcript | ENST00000389902.8 | protein_coding | 13/16 | chr7 | TogoVar | |||||||
RNF26_chr11_119329527_119342309 | 119333882 | T | TAGGGTAG others(8): Show |
upstream_gene_variant | MODIFIER | HG01099.hp2 HG02965.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0000 | 2 | 420 | 0.0048 | 15 | c.-12 others(26): Show |
RNF26 | ENSG00000173456.5 | transcript | ENST00000311413.5 | protein_coding | 644 | chr11 | TogoVar | |||||||
RNF2_chr1_185040558_185107603 | 185076268 | G | GTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG01975.hp1 HG01975.hp2 NA18965.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0007 | a0001c0001t0005g0311 a0001c0001t0005g0324 a0001c0001t0007g0225 |
3 | 31 | 0.0968 | 15 | c.-2- others(32): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF2_chr1_185040558_185107603 | 185077625 | G | GTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG02109.hp2 HG03471.hp2 |
a0001 | a0001c0001 | a0001c0001t0034a0001c0001t0035 | a0001c0001t0034g0187 a0001c0001t0035g0255 |
2 | 230 | 0.0087 | 15 | c.-2- others(30): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF2_chr1_185040558_185107603 | 185082345 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG01952.hp1 HG01975.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0118 a0001c0001t0007g0225 |
2 | 7 | 0.2857 | 15 | c.-2- others(30): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF34_chr12_121395118_121429348 | 121406283 | A | AGTTGTTG others(8): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0004c0004t0001 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(86): Show |
112 | 229 | 0.4891 | 15 | c.6+6 others(28): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNF34_chr12_121395118_121429348 | 121407445 | T | TAGTATAC others(8): Show |
intron_variant | MODIFIER | NA19057.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0192 | 1 | 348 | 0.0029 | 15 | c.6+7 others(28): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNF38_chr9_36331400_36405269 | 36336177 | A | AAAAATAT others(8): Show |
downstream_gene_variant | MODIFIER | HG02148.hp1 HG04115.hp2 NA19007.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0113 a0001c0001t0002g0046 a0001c0001t0002g0103 |
3 | 170 | 0.0176 | 15 | c.*35 others(26): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 222 | chr9 | TogoVar | |||||||
RNF41_chr12_56197179_56226922 | 56202127 | T | TAAAAAAA others(8): Show |
downstream_gene_variant | MODIFIER | NA19057.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0127 | 1 | 16 | 0.0625 | 15 | c.*43 others(26): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 51 | chr12 | TogoVar | |||||||
RNF4_chr4_2464106_2520857 | 2484067 | T | TCCCCCCC others(8): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG01069.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(13): Show |
16 | 42 | 0.3810 | 15 | c.-15 others(34): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
RNF4_chr4_2464106_2520857 | 2484067 | T | TCCCCCGC others(8): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0150 | 1 | 27 | 0.0370 | 15 | c.-15 others(34): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
RNF4_chr4_2464106_2520857 | 2501415 | G | GGGAGGCT others(8): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0008 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | 376 | 0.0186 | 15 | c.204 others(30): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
RNF4_chr4_2464106_2520857 | 2518307 | C | CTTTTTTT others(8): Show |
downstream_gene_variant | MODIFIER | HG00597.hp1 HG01516.hp1 HG03239.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(2): Show | a0001c0001t0003g0241 a0001c0001t0003g0251 a0001c0001t0003g0279 others(8): Show |
11 | 25 | 0.4400 | 15 | c.*44 others(26): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2451 | chr4 | TogoVar | |||||||
RNFT2_chr12_116733315_116858631 | 116743213 | T | TAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG00544.hp1 HG02055.hp2 HG02273.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(3): Show | a0001c0001t0001g0094 a0001c0001t0001g0256 a0001c0001t0004g0095 others(5): Show |
8 | 138 | 0.0580 | 15 | c.83+ others(30): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116782079 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG01099.hp2 HG02132.hp2 NA18971.hp2 |
a0001a0002 | a0001c0002a0001c0004a0002c0010 | a0001c0002t0001a0001c0004t0001a0002c0010t0002 | a0001c0002t0001g0079 a0001c0004t0001g0083 a0002c0010t0002g0002 |
3 | 16 | 0.1875 | 15 | c.882 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116785275 | G | GTGTGTGT others(8): Show |
intron_variant | MODIFIER | HG00741.hp1 HG02155.hp1 HG02965.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0006 | a0001c0001t0004a0001c0003t0005a0001c0003t0016others(2): Show | a0001c0001t0004g0143 a0001c0003t0005g0037 a0001c0003t0005g0038 others(3): Show |
6 | 195 | 0.0308 | 15 | c.882 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | TogoVar | |||||||
RNFT2_chr12_116733315_116858631 | 116800812 | T | TTAAAATA others(8): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(33): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0094 others(33): Show |
36 | 126 | 0.2857 | 15 | c.882 others(34): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116832146 | A | ATATATAT others(8): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0002 | a0001c0002t0065 | a0001c0002t0065g0093 | 1 | 114 | 0.0088 | 15 | c.883 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | TogoVar | |||||||
RNFT2_chr12_116733315_116858631 | 116832148 | A | AAAAATAT others(8): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02818.hp1 HG02970.hp1 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0064a0001c0007t0005a0001c0007t0016 | a0001c0002t0064g0263 a0001c0007t0005g0060 a0001c0007t0016g0059 |
3 | 26 | 0.1154 | 15 | c.883 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116832148 | A | AAATATAT others(8): Show |
intron_variant | MODIFIER | HG02486.hp2 HG03139.hp2 |
a0001 | a0001c0006a0001c0007 | a0001c0006t0005a0001c0007t0034 | a0001c0006t0005g0017 a0001c0007t0034g0061 |
2 | 25 | 0.0800 | 15 | c.883 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116846437 | A | ATTTTTTT others(8): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0004 | a0001c0004t0053 | a0001c0004t0053g0015 | 1 | 50 | 0.0200 | 15 | c.120 others(34): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116849845 | C | CTTCCTTC others(8): Show |
3_prime_UTR_variant | MODIFIER | HG02451.hp1 HG02735.hp2 NA18960.hp2 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0027a0001c0008t0060 | a0001c0001t0027g0121 a0001c0001t0027g0125 a0001c0008t0060g0084 |
3 | 51 | 0.0588 | 15 | c.*39 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
RNFT2_chr12_116733315_116858631 | 116850620 | C | CTTTTTTC others(8): Show |
3_prime_UTR_variant | MODIFIER | HG01261.hp2 HG02055.hp2 HG02735.hp1 |
a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 |
3 | 254 | 0.0118 | 15 | c.*11 others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
RNGTT_chr6_88604897_88968618 | 88739725 | T | TATATATA others(8): Show |
intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0176 | 1 | 33 | 0.0303 | 15 | c.143 others(36): Show |
RNGTT | ENSG00000111880.16 | transcript | ENST00000369485.9 | protein_coding | 13/15 | chr6 | TogoVar |