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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
RNF17_chr13_24759169_24884921 | 24882257 | T | TAGATATA others(17): Show |
downstream_gene_variant | MODIFIER | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
a0002a0008 | a0002c0003a0008c0013 | a0002c0003t0001a0008c0013t0001 | a0002c0003t0001g0329 a0002c0003t0001g0330 a0002c0003t0001g0331 others(27): Show |
30 | 426 | 0.0704 | 24 | c.*25 others(35): Show |
RNF17 | ENSG00000132972.19 | transcript | ENST00000255324.10 | protein_coding | 2337 | chr13 | TogoVar | |||||||
RNF180_chr5_64160843_64377869 | 64192903 | G | GTATATAT others(17): Show |
intron_variant | MODIFIER | HG02818.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0178 a0001c0001t0002g0206 a0001c0001t0003g0194 others(2): Show |
5 | 250 | 0.0200 | 24 | c.1-7 others(37): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
RNF180_chr5_64160843_64377869 | 64192903 | G | GTGTATAT others(17): Show |
intron_variant | MODIFIER | HG03098.hp2 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | 250 | 0.0080 | 24 | c.1-7 others(37): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
RNF183_chr9_113292093_113308376 | 113308170 | A | AAAAAAAA others(17): Show |
upstream_gene_variant | MODIFIER | HG00099.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 | 1 | 440 | 0.0023 | 24 | c.-55 others(35): Show |
RNF183 | ENSG00000165188.14 | transcript | ENST00000489339.2 | protein_coding | 4795 | chr9 | TogoVar | |||||||
RNF183_chr9_113292093_113308376 | 113308170 | A | AAAAGAAA others(17): Show |
upstream_gene_variant | MODIFIER | NA18939.hp2 NA18971.hp2 NA19000.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 3 | 440 | 0.0068 | 24 | c.-55 others(35): Show |
RNF183 | ENSG00000165188.14 | transcript | ENST00000489339.2 | protein_coding | 4795 | chr9 | TogoVar | |||||||
RNF185_chr22_31155182_31212019 | 31171156 | C | CTTACTTA others(17): Show |
intron_variant | MODIFIER | HG00741.hp2 NA18954.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0002 | a0001c0001t0002g0229 a0001c0002t0002g0228 |
2 | 378 | 0.0053 | 24 | c.-49 others(43): Show |
RNF185 | ENSG00000138942.17 | transcript | ENST00000326132.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
RNF187_chr1_228482382_228501188 | 228487374 | T | TCCCCGAC others(17): Show |
upstream_gene_variant | MODIFIER | NA18991.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0034 | 1 | 422 | 0.0024 | 24 | c.-11 others(33): Show |
RNF187 | ENSG00000168159.15 | transcript | ENST00000305943.9 | protein_coding | 7 | chr1 | TogoVar | |||||||
RNF207_chr1_6201119_6226299 | 6224610 | T | TTAAAGAA others(17): Show |
downstream_gene_variant | MODIFIER | NA18906.hp2 | a0003 | a0003c0008 | a0003c0008t0010 | a0003c0008t0010g0015 | 1 | 366 | 0.0027 | 24 | c.*52 others(35): Show |
RNF207 | ENSG00000158286.13 | transcript | ENST00000377939.5 | protein_coding | 3312 | chr1 | TogoVar | |||||||
RNF20_chr9_101528853_101568344 | 101543295 | G | GCCAGGGC others(17): Show |
intron_variant | MODIFIER | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(27): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0002a0001c0004t0003 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0004t0002g0006 others(6): Show |
30 | 406 | 0.0739 | 24 | c.629 others(41): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
RNF20_chr9_101528853_101568344 | 101543375 | G | GGCACTGT others(17): Show |
intron_variant | MODIFIER | NA18947.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053 | 1 | 406 | 0.0025 | 24 | c.629 others(41): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
RNF20_chr9_101528853_101568344 | 101543468 | A | AGCACTGT others(17): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0011 | a0001c0011t0007 | a0001c0011t0007g0064 | 1 | 406 | 0.0025 | 24 | c.629 others(41): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80314179 | T | TGGTGGTG others(17): Show |
intron_variant | MODIFIER | NA18944.hp2 NA18954.hp2 NA19086.hp1 |
a0001 | a0001c0003a0001c0004 | a0001c0003t0001a0001c0003t0002a0001c0004t0023 | a0001c0003t0001g0108 a0001c0003t0002g0109 a0001c0004t0023g0106 |
3 | 292 | 0.0103 | 24 | c.281 others(43): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80314257 | T | TGGTGGTG others(17): Show |
intron_variant | MODIFIER | NA18944.hp2 NA18954.hp2 NA19086.hp1 |
a0001 | a0001c0003a0001c0004 | a0001c0003t0001a0001c0003t0002a0001c0004t0023 | a0001c0003t0001g0108 a0001c0003t0002g0109 a0001c0004t0023g0106 |
3 | 292 | 0.0103 | 24 | c.281 others(43): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80315102 | A | ATGGTGGT others(17): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0107 | a0107c0086 | a0107c0086t0006 | a0107c0086t0006g0291 | 1 | 292 | 0.0034 | 24 | c.281 others(43): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80315244 | T | TGGTGGTG others(17): Show |
intron_variant | MODIFIER | HG02055.hp2 NA18979.hp2 NA18990.hp1 |
a0001a0005a0052 | a0001c0004a0005c0007a0052c0046 | a0001c0004t0072a0005c0007t0009a0052c0046t0013 | a0001c0004t0072g0164 a0005c0007t0009g0218 a0052c0046t0013g0198 |
3 | 292 | 0.0103 | 24 | c.281 others(43): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80315322 | T | TGGAGGTG others(17): Show |
intron_variant | MODIFIER | NA18973.hp2 NA19062.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0226 a0001c0001t0002g0227 |
2 | 292 | 0.0069 | 24 | c.281 others(43): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80315353 | G | GGTGGTGG others(17): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0107 | a0107c0086 | a0107c0086t0006 | a0107c0086t0006g0291 | 1 | 292 | 0.0034 | 24 | c.281 others(43): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80315353 | G | GGTGGTGG others(17): Show |
intron_variant | MODIFIER | HG04228.hp2 | a0091 | a0091c0141 | a0091c0141t0001 | a0091c0141t0001g0284 | 1 | 292 | 0.0034 | 24 | c.281 others(43): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80315366 | A | ACAGTGGT others(17): Show |
intron_variant | MODIFIER | HG00642.hp2 HG01106.hp2 |
a0001a0004 | a0001c0006a0004c0011 | a0001c0006t0009a0004c0011t0005 | a0001c0006t0009g0181 a0004c0011t0005g0224 |
2 | 292 | 0.0069 | 24 | c.281 others(43): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | chr17 | TogoVar | |||||||
RNF213_chr17_80255852_80403794 | 80315399 | G | GTGATGGT others(17): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0022 | a0022c0111 | a0022c0111t0076 | a0022c0111t0076g0171 | 1 | 292 | 0.0034 | 24 | c.281 others(43): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 15/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF214_chr11_117227671_117291454 | 117251438 | C | CAGTAGGG others(17): Show |
intron_variant | MODIFIER | HG01081.hp2 HG02109.hp1 HG02257.hp1 others(33): Show |
a0001a0004 | a0001c0001a0004c0006 | a0001c0001t0001a0001c0001t0003a0004c0006t0003 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(30): Show |
36 | 360 | 0.1000 | 24 | c.959 others(41): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | TogoVar | |||||||
RNF214_chr11_117227671_117291454 | 117251438 | C | CAGTAGGG others(17): Show |
intron_variant | MODIFIER | HG02055.hp1 HG03139.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0080 a0001c0001t0005g0081 |
2 | 360 | 0.0056 | 24 | c.959 others(41): Show |
RNF214 | ENSG00000167257.11 | transcript | ENST00000300650.9 | protein_coding | 6/14 | chr11 | TogoVar | |||||||
RNF215_chr22_30373821_30392411 | 30376487 | C | CCAGCCCT others(17): Show |
downstream_gene_variant | MODIFIER | HG01175.hp2 HG02055.hp1 HG02451.hp2 others(2): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0001a0001c0003t0003others(1): Show | a0001c0002t0001g0001 a0001c0003t0001g0003 a0001c0003t0003g0017 others(1): Show |
5 | 432 | 0.0116 | 24 | c.*30 others(35): Show |
RNF215 | ENSG00000099999.15 | transcript | ENST00000382363.8 | protein_coding | 2333 | chr22 | TogoVar | |||||||
RNF216_chr7_5615047_5786663 | 5671805 | C | CAAAAAAA others(17): Show |
intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0016 | a0001c0016t0006 | a0001c0016t0006g0049 | 1 | 274 | 0.0037 | 24 | c.206 others(45): Show |
RNF216 | ENSG00000011275.19 | transcript | ENST00000389902.8 | protein_coding | 13/16 | chr7 | TogoVar | |||||||
RNF216_chr7_5615047_5786663 | 5768346 | T | TACACACA others(17): Show |
intron_variant | MODIFIER | HG00738.hp2 HG02818.hp1 HG03225.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0249 a0001c0001t0002g0271 a0001c0001t0004g0223 others(2): Show |
5 | 274 | 0.0183 | 24 | c.-69 others(41): Show |
RNF216 | ENSG00000011275.19 | transcript | ENST00000389902.8 | protein_coding | 1/16 | chr7 | TogoVar | |||||||
RNF220_chr1_44400255_44656723 | 44583215 | G | GATATATA others(17): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0020 | 1 | 218 | 0.0046 | 24 | c.626 others(43): Show |
RNF220 | ENSG00000187147.19 | transcript | ENST00000361799.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF222_chr17_8385702_8402827 | 8388995 | A | ACTTACTT others(17): Show |
downstream_gene_variant | MODIFIER | NA18995.hp2 | a0002 | a0002c0002 | a0002c0002t0012 | a0002c0002t0012g0018 | 1 | 436 | 0.0023 | 24 | c.*38 others(35): Show |
RNF222 | ENSG00000189051.6 | transcript | ENST00000399398.3 | protein_coding | 1706 | chr17 | TogoVar | |||||||
RNF223_chr1_1065967_1079306 | 1077303 | G | GAGCTGAG others(17): Show |
upstream_gene_variant | MODIFIER | HG01175.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 324 | 0.0031 | 24 | c.-32 others(35): Show |
RNF223 | ENSG00000237330.3 | transcript | ENST00000453464.3 | protein_coding | 2998 | chr1 | TogoVar | |||||||
RNF24_chr20_3922311_4020558 | 3966469 | A | AGTGTGTG others(17): Show |
intron_variant | MODIFIER | HG01261.hp1 HG01993.hp2 HG02300.hp2 |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0012 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0012g0180 |
3 | 362 | 0.0083 | 24 | c.-7- others(39): Show |
RNF24 | ENSG00000101236.17 | transcript | ENST00000358395.11 | protein_coding | 1/5 | chr20 | TogoVar | |||||||
RNF2_chr1_185040558_185107603 | 185076268 | G | GTTTTTTT others(17): Show |
intron_variant | MODIFIER | HG02148.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0169 | 1 | 350 | 0.0029 | 24 | c.-2- others(41): 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(17): Show |
intron_variant | MODIFIER | HG01433.hp2 HG02056.hp1 HG02572.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0015 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0004g0201 others(2): Show |
5 | 350 | 0.0143 | 24 | c.-2- others(39): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF2_chr1_185040558_185107603 | 185082366 | T | TTTTTTTT others(17): Show |
intron_variant | MODIFIER | NA18971.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0277 | 1 | 350 | 0.0029 | 24 | c.-2- others(39): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF32_chr7_156635774_156682130 | 156678874 | A | ATGGGGGG others(17): Show |
downstream_gene_variant | MODIFIER | NA18974.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0139 | 1 | 448 | 0.0022 | 24 | c.*22 others(35): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1745 | chr7 | TogoVar | |||||||
RNF32_chr7_156635774_156682130 | 156680399 | A | AGTGTGTG others(17): Show |
downstream_gene_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0004 | a0001c0004t0006 | a0001c0004t0006g0093 | 1 | 448 | 0.0022 | 24 | c.*37 others(35): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3270 | chr7 | TogoVar | |||||||
RNF32_chr7_156635774_156682130 | 156680403 | A | AGAGAGAG others(17): Show |
downstream_gene_variant | MODIFIER | HG02922.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0191 | 1 | 448 | 0.0022 | 24 | c.*37 others(35): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3274 | chr7 | TogoVar | |||||||
RNF34_chr12_121395118_121429348 | 121406283 | A | AGTTGTTG others(17): Show |
intron_variant | MODIFIER | HG00558.hp2 HG00673.hp2 HG01071.hp2 others(39): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0001c0001t0002a0003c0003t0002 | a0001c0001t0001g0009 a0001c0001t0001g0103 a0001c0001t0001g0104 others(29): Show |
42 | 350 | 0.1200 | 24 | c.6+6 others(37): Show |
RNF34 | ENSG00000170633.17 | transcript | ENST00000361234.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNF40_chr16_30757322_30781307 | 30770119 | A | ATGGATTT others(17): Show |
intron_variant | MODIFIER | HG01928.hp1 HG01928.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0054 a0001c0001t0002g0049 |
2 | 230 | 0.0087 | 24 | c.258 others(41): Show |
RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
RNF44_chr5_176521712_176542402 | 176529405 | G | GCGTCACC others(17): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0177 | 1 | 444 | 0.0023 | 24 | c.113 others(39): Show |
RNF44 | ENSG00000146083.12 | transcript | ENST00000274811.9 | protein_coding | 9/10 | chr5 | TogoVar | |||||||
RNF4_chr4_2464106_2520857 | 2466647 | T | TTGTGTGT others(17): Show |
upstream_gene_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0299 a0001c0001t0002g0207 a0001c0001t0003g0218 others(32): Show |
35 | 378 | 0.0926 | 24 | c.-27 others(35): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2458 | chr4 | TogoVar | |||||||
RNF4_chr4_2464106_2520857 | 2484067 | T | TCCCCCCC others(17): Show |
intron_variant | MODIFIER | HG00673.hp1 HG01169.hp1 HG01496.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0007 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0002g0175 others(5): Show |
8 | 378 | 0.0212 | 24 | c.-15 others(43): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116743213 | T | TAAAAAAA others(17): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0187 | 1 | 268 | 0.0037 | 24 | c.83+ others(39): 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(17): Show |
intron_variant | MODIFIER | HG00140.hp1 HG02055.hp2 NA19062.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0019a0001c0001t0056 | a0001c0001t0001g0205 a0001c0001t0019g0124 a0001c0001t0056g0220 |
3 | 268 | 0.0112 | 24 | c.882 others(41): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116785249 | C | CTGTGTGT others(17): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0017 | a0001c0017t0032 | a0001c0017t0032g0044 | 1 | 268 | 0.0037 | 24 | c.882 others(41): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116788810 | T | TGGTGGAT others(17): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0017 | a0001c0017t0032 | a0001c0017t0032g0044 | 1 | 268 | 0.0037 | 24 | c.882 others(41): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116794646 | A | AGGAGGGA others(17): Show |
intron_variant | MODIFIER | HG00741.hp1 NA18971.hp2 |
a0001 | a0001c0004a0001c0006 | a0001c0004t0001a0001c0006t0050 | a0001c0004t0001g0083 a0001c0006t0050g0013 |
2 | 268 | 0.0075 | 24 | c.882 others(43): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116794646 | A | AGGAGGGA others(17): Show |
intron_variant | MODIFIER | HG02040.hp1 | a0002 | a0002c0010 | a0002c0010t0002 | a0002c0010t0002g0254 | 1 | 268 | 0.0037 | 24 | c.882 others(43): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116794656 | A | AAGGGAGG others(17): Show |
intron_variant | MODIFIER | HG03453.hp2 HG03579.hp1 NA18906.hp2 |
a0001 | a0001c0005a0001c0013a0001c0019 | a0001c0005t0013a0001c0013t0013a0001c0019t0055 | a0001c0005t0013g0154 a0001c0013t0013g0158 a0001c0019t0055g0059 |
3 | 268 | 0.0112 | 24 | c.882 others(43): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116794668 | A | AAGGGAGG others(17): Show |
intron_variant | MODIFIER | HG02293.hp2 HG02300.hp2 NA19005.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0146 a0001c0001t0001g0217 a0001c0001t0003g0131 |
3 | 268 | 0.0112 | 24 | c.882 others(43): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116794672 | A | AAGGGAGG others(17): Show |
intron_variant | MODIFIER | HG01243.hp1 HG01243.hp2 HG02280.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0005a0001c0002t0004a0001c0002t0005others(8): Show | a0001c0001t0005g0105 a0001c0002t0004g0005 a0001c0002t0005g0064 others(9): Show |
12 | 268 | 0.0448 | 24 | c.882 others(43): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116832146 | A | AATATATA others(17): Show |
intron_variant | MODIFIER | HG02132.hp2 | a0002 | a0002c0010 | a0002c0010t0002 | a0002c0010t0002g0002 | 1 | 268 | 0.0037 | 24 | c.883 others(41): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |