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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
RNF150_chr4_140854807_141138469 | 140973752 | CTGTAATC others(6): Show |
C | intron_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0095 | 1 | 184 | 0.0054 | -13 | c.485 others(30): Show |
RNF150 | ENSG00000170153.11 | transcript | ENST00000515673.7 | protein_coding | 1/6 | chr4 | TogoVar | |||||||
RNF150_chr4_140854807_141138469 | 141000001 | AGAAGAAG others(6): Show |
A | intron_variant | MODIFIER | HG02129.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0114 | 1 | 184 | 0.0054 | -13 | c.485 others(32): Show |
RNF150 | ENSG00000170153.11 | transcript | ENST00000515673.7 | protein_coding | 1/6 | chr4 | TogoVar | |||||||
RNF150_chr4_140854807_141138469 | 141078801 | AAAAAAAA others(6): Show |
A | intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032 | 1 | 184 | 0.0054 | -13 | c.484 others(32): Show |
RNF150 | ENSG00000170153.11 | transcript | ENST00000515673.7 | protein_coding | 1/6 | chr4 | TogoVar | |||||||
RNF152_chr18_61803067_61898007 | 61855676 | CCCACACT others(6): Show |
C | intron_variant | MODIFIER | HG00408.hp2 | a0001 | a0001c0001 | a0001c0001t0032 | a0001c0001t0032g0193 | 1 | 310 | 0.0032 | -13 | c.-13 others(34): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | TogoVar | |||||||
RNF152_chr18_61803067_61898007 | 61895794 | CTTTTTTT others(6): Show |
C | upstream_gene_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0061 | 1 | 310 | 0.0032 | -13 | c.-31 others(24): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2788 | chr18 | TogoVar | |||||||
RNF157_chr17_76137474_76245493 | 76230855 | AAAAAGAG others(6): Show |
A | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(37): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0006 a0001c0001t0001g0127 a0001c0001t0001g0128 others(37): Show |
40 | 234 | 0.1709 | -13 | c.88+ others(28): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | TogoVar | |||||||
RNF168_chr3_196463783_196508768 | 196471196 | CAAAAAAA others(6): Show |
C | 3_prime_UTR_variant | MODIFIER | HG01070.hp2 HG01981.hp2 |
a0002 | a0002c0002 | a0002c0002t0034 | a0002c0002t0034g0010 | 2 | 350 | 0.0057 | -13 | c.*61 others(22): Show |
RNF168 | ENSG00000163961.4 | transcript | ENST00000318037.3 | protein_coding | 6/6 | 610 | chr3 | TogoVar | ||||||
RNF168_chr3_196463783_196508768 | 196484473 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0001 | a0001c0001t0091 | a0001c0001t0091g0287 | 1 | 350 | 0.0029 | -13 | c.559 others(28): Show |
RNF168 | ENSG00000163961.4 | transcript | ENST00000318037.3 | protein_coding | 3/5 | chr3 | TogoVar | |||||||
RNF169_chr11_74743849_74847413 | 74785160 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | NA18964.hp1 NA18993.hp1 |
a0001 | a0001c0001 | a0001c0001t0026 | a0001c0001t0026g0191 a0001c0001t0026g0255 |
2 | 354 | 0.0057 | -13 | c.503 others(30): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
RNF169_chr11_74743849_74847413 | 74785186 | GATATATA others(6): Show |
G | intron_variant | MODIFIER | HG00423.hp1 HG02129.hp1 HG03927.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0190 a0001c0001t0003g0201 a0001c0001t0003g0212 others(3): Show |
6 | 354 | 0.0170 | -13 | c.503 others(30): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
RNF175_chr4_153705160_153765024 | 153716063 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
a0004a0007 | a0004c0004a0007c0007 | a0004c0004t0001a0007c0007t0001 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0228 others(12): Show |
20 | 394 | 0.0508 | -13 | c.631 others(28): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | TogoVar | |||||||
RNF17_chr13_24759169_24884921 | 24815427 | GGGTGTGT others(6): Show |
G | intron_variant | MODIFIER | NA19087.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0253 | 1 | 426 | 0.0024 | -13 | c.209 others(34): Show |
RNF17 | ENSG00000132972.19 | transcript | ENST00000255324.10 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
RNF180_chr5_64160843_64377869 | 64234578 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02258.hp1 HG02896.hp2 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0028 | a0001c0001t0003g0028 a0001c0001t0003g0077 a0001c0001t0028g0193 |
3 | 250 | 0.0120 | -13 | c.122 others(34): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
RNF185_chr22_31155182_31212019 | 31164583 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0331 | 1 | 378 | 0.0027 | -13 | c.-49 others(30): Show |
RNF185 | ENSG00000138942.17 | transcript | ENST00000326132.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
RNF19B_chr1_32931449_32969809 | 32952429 | TAAAAAAA others(6): Show |
T | intron_variant | MODIFIER | NA19086.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0123 | 1 | 330 | 0.0030 | -13 | c.636 others(30): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | TogoVar | |||||||
RNF208_chr9_137215259_137227240 | 137225111 | AGCCCCGC others(6): Show |
A | upstream_gene_variant | MODIFIER | HG04199.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 390 | 0.0026 | -13 | c.-36 others(24): Show |
RNF208 | ENSG00000212864.4 | transcript | ENST00000391553.3 | protein_coding | 2872 | chr9 | TogoVar | |||||||
RNF212_chr4_1066478_1118564 | 1079030 | CATGGGAC others(6): Show |
C | intron_variant | MODIFIER | HG03492.hp1 NA19070.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0061 a0001c0001t0005g0045 |
2 | 406 | 0.0049 | -13 | c.510 others(28): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | TogoVar | |||||||
RNF213_chr17_80255852_80403794 | 80278228 | TCTCCCGG others(6): Show |
T | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp1 |
a0021 | a0021c0022 | a0021c0022t0006a0021c0022t0012 | a0021c0022t0006g0169 a0021c0022t0012g0170 |
2 | 292 | 0.0069 | -13 | c.261 others(30): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 3/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80281112 | TCACACCA others(6): Show |
T | intron_variant | MODIFIER | HG01884.hp1 | a0022 | a0022c0111 | a0022c0111t0076 | a0022c0111t0076g0171 | 1 | 292 | 0.0034 | -13 | c.262 others(30): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 3/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80303554 | TTTCTTTT others(6): Show |
T | intron_variant | MODIFIER | HG02559.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
a0005a0013a0060others(1): Show | a0005c0106a0013c0020a0060c0133others(1): Show | a0005c0106t0021a0013c0020t0003a0060c0133t0006others(1): Show | a0005c0106t0021g0270 a0013c0020t0003g0277 a0060c0133t0006g0010 others(1): Show |
4 | 292 | 0.0137 | -13 | c.221 others(32): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 11/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80304538 | GCTGAGGC others(6): Show |
G | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(23): Show |
a0001a0004a0005others(10): Show | a0001c0004a0001c0006a0004c0011others(13): Show | a0001c0004t0072a0001c0006t0009a0004c0011t0005others(20): Show | a0001c0004t0072g0164 a0001c0006t0009g0181 a0004c0011t0005g0210 others(23): Show |
26 | 292 | 0.0890 | -13 | c.221 others(32): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 11/67 | chr17 | TogoVar | |||||||
RNF213_chr17_80255852_80403794 | 80373271 | CCCCCTCA others(6): Show |
C | intron_variant | MODIFIER | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(25): Show |
a0008a0014a0017others(12): Show | a0008c0013a0008c0027a0014c0017others(15): Show | a0008c0013t0028a0008c0013t0044a0008c0027t0018others(20): Show | a0008c0013t0028g0241 a0008c0013t0028g0250 a0008c0013t0044g0236 others(25): Show |
28 | 292 | 0.0959 | -13 | c.129 others(32): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 49/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF213_chr17_80255852_80403794 | 80391760 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02015.hp1 HG02071.hp2 |
a0051a0053 | a0051c0059a0053c0040 | a0051c0059t0060a0053c0040t0061 | a0051c0059t0060g0137 a0053c0040t0061g0233 |
2 | 292 | 0.0069 | -13 | c.154 others(34): Show |
RNF213 | ENSG00000173821.20 | transcript | ENST00000582970.6 | protein_coding | 67/67 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF216_chr7_5615047_5786663 | 5660265 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00735.hp1 HG02015.hp2 others(6): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0014others(1): Show | a0001c0001t0001a0001c0002t0003a0001c0002t0039others(2): Show | a0001c0001t0001g0164 a0001c0001t0001g0229 a0001c0002t0003g0148 others(6): Show |
9 | 274 | 0.0329 | -13 | c.206 others(32): Show |
RNF216 | ENSG00000011275.19 | transcript | ENST00000389902.8 | protein_coding | 13/16 | chr7 | TogoVar | |||||||
RNF216_chr7_5615047_5786663 | 5738087 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00609.hp2 HG02040.hp1 HG02040.hp2 others(5): Show |
a0001 | a0001c0001a0001c0015 | a0001c0001t0001a0001c0001t0008a0001c0001t0040others(1): Show | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0001g0115 others(5): Show |
8 | 274 | 0.0292 | -13 | c.112 others(32): Show |
RNF216 | ENSG00000011275.19 | transcript | ENST00000389902.8 | protein_coding | 5/16 | chr7 | TogoVar | |||||||
RNF216_chr7_5615047_5786663 | 5740104 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG03453.hp1 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0040 a0001c0001t0009g0041 |
2 | 274 | 0.0073 | -13 | c.104 others(30): Show |
RNF216 | ENSG00000011275.19 | transcript | ENST00000389902.8 | protein_coding | 4/16 | chr7 | TogoVar | |||||||
RNF216_chr7_5615047_5786663 | 5742586 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG01109.hp2 HG02258.hp2 NA18906.hp2 |
a0001 | a0001c0005 | a0001c0005t0001a0001c0005t0005 | a0001c0005t0001g0009 a0001c0005t0001g0010 a0001c0005t0005g0008 |
3 | 274 | 0.0110 | -13 | c.202 others(28): Show |
RNF216 | ENSG00000011275.19 | transcript | ENST00000389902.8 | protein_coding | 3/16 | chr7 | TogoVar | |||||||
RNF216_chr7_5615047_5786663 | 5770024 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0099 | 1 | 274 | 0.0037 | -13 | c.-69 others(30): Show |
RNF216 | ENSG00000011275.19 | transcript | ENST00000389902.8 | protein_coding | 1/16 | chr7 | TogoVar | |||||||
RNF220_chr1_44400255_44656723 | 44493516 | AAAAATAA others(6): Show |
A | intron_variant | MODIFIER | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0035 a0001c0001t0001g0048 a0001c0001t0001g0079 others(29): Show |
32 | 218 | 0.1468 | -13 | c.625 others(32): Show |
RNF220 | ENSG00000187147.19 | transcript | ENST00000361799.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF220_chr1_44400255_44656723 | 44627035 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(2): Show | a0001c0001t0002g0160 a0001c0001t0003g0039 a0001c0001t0003g0041 others(14): Show |
17 | 218 | 0.0780 | -13 | c.906 others(28): Show |
RNF220 | ENSG00000187147.19 | transcript | ENST00000361799.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF224_chr9_137222502_137234640 | 137225111 | AGCCCCGC others(6): Show |
A | upstream_gene_variant | MODIFIER | HG04199.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 394 | 0.0025 | -13 | c.-29 others(24): Show |
RNF224 | ENSG00000233198.4 | transcript | ENST00000445101.4 | protein_coding | 2390 | chr9 | TogoVar | |||||||
RNF225_chr19_58390656_58402079 | 58390954 | TATATTCT others(6): Show |
T | upstream_gene_variant | MODIFIER | NA18946.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0000 | 1 | 422 | 0.0024 | -13 | c.-51 others(24): Show |
RNF225 | ENSG00000269855.3 | transcript | ENST00000601382.3 | protein_coding | 4701 | chr19 | TogoVar | |||||||
RNF24_chr20_3922311_4020558 | 3928747 | CAAAAAAA others(6): Show |
C | 3_prime_UTR_variant | MODIFIER | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(74): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010a0001c0001t0013others(7): Show | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0051 others(73): Show |
77 | 362 | 0.2127 | -13 | c.*53 others(24): Show |
RNF24 | ENSG00000101236.17 | transcript | ENST00000358395.11 | protein_coding | 6/6 | 5303 | chr20 | TogoVar | ||||||
RNF24_chr20_3922311_4020558 | 3998574 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02896.hp2 HG03540.hp2 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0033a0001c0001t0054 | a0001c0001t0033g0033 a0001c0001t0033g0034 a0001c0001t0054g0035 |
3 | 362 | 0.0083 | -13 | c.-8+ others(30): Show |
RNF24 | ENSG00000101236.17 | transcript | ENST00000358395.11 | protein_coding | 1/5 | chr20 | TogoVar | |||||||
RNF24_chr20_3922311_4020558 | 4008385 | ATATATTA others(6): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(152): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0315 others(150): Show |
155 | 362 | 0.4282 | -13 | c.-8+ others(28): Show |
RNF24 | ENSG00000101236.17 | transcript | ENST00000358395.11 | protein_coding | 1/5 | chr20 | TogoVar | |||||||
RNF2_chr1_185040558_185107603 | 185076268 | GTTTTTTT others(6): Show |
G | intron_variant | MODIFIER | HG00544.hp1 HG02717.hp1 HG02738.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0091 a0001c0001t0003g0052 a0001c0001t0003g0148 others(8): Show |
12 | 350 | 0.0343 | -13 | c.-2- others(30): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF32_chr7_156635774_156682130 | 156641858 | GAACTTAT others(6): Show |
G | intron_variant | MODIFIER | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(9): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0004t0006 | a0001c0001t0002g0018 a0001c0004t0006g0014 a0001c0004t0006g0093 others(4): Show |
12 | 448 | 0.0268 | -13 | c.-78 others(30): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | TogoVar | |||||||
RNF38_chr9_36331400_36405269 | 36347120 | CGGGGGGG others(6): Show |
C | intron_variant | MODIFIER | HG01071.hp2 HG01074.hp1 HG01123.hp2 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0247 others(24): Show |
27 | 402 | 0.0672 | -13 | c.126 others(32): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | TogoVar | |||||||
RNF43_chr17_58348676_58422534 | 58370060 | GTTTTTTT others(6): Show |
G | intron_variant | MODIFIER | NA19058.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0116 | 1 | 352 | 0.0028 | -13 | c.375 others(28): Show |
RNF43 | ENSG00000108375.13 | transcript | ENST00000407977.7 | protein_coding | 3/9 | chr17 | TogoVar | |||||||
RNF44_chr5_176521712_176542402 | 176525337 | AACAAACA others(6): Show |
A | downstream_gene_variant | MODIFIER | NA19084.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 444 | 0.0023 | -13 | c.*36 others(24): Show |
RNF44 | ENSG00000146083.12 | transcript | ENST00000274811.9 | protein_coding | 1374 | chr5 | TogoVar | |||||||
RNF4_chr4_2464106_2520857 | 2518307 | CTTTTTTT others(6): Show |
C | downstream_gene_variant | MODIFIER | HG00738.hp2 HG01081.hp2 HG03017.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0118 |
3 | 378 | 0.0079 | -13 | c.*44 others(24): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2451 | chr4 | TogoVar | |||||||
RNF4_chr4_2464106_2520857 | 2520783 | AAAAAAAT others(6): Show |
A | downstream_gene_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0184 | 1 | 378 | 0.0027 | -13 | c.*69 others(24): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4927 | chr4 | TogoVar | |||||||
RNF8_chr6_37348983_37399734 | 37378600 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0015 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(3): Show |
6 | 324 | 0.0185 | -13 | c.123 others(32): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
RNFT2_chr12_116733315_116858631 | 116743232 | AAAAAAAA others(6): Show |
A | intron_variant | MODIFIER | HG02486.hp2 NA18975.hp2 NA18980.hp2 |
a0001 | a0001c0003a0001c0006 | a0001c0003t0006a0001c0003t0042a0001c0006t0005 | a0001c0003t0006g0230 a0001c0003t0042g0229 a0001c0006t0005g0017 |
3 | 268 | 0.0112 | -13 | c.83+ others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | TogoVar | |||||||
RNFT2_chr12_116733315_116858631 | 116806376 | AAAAAAAT others(6): Show |
A | intron_variant | MODIFIER | HG00673.hp1 NA19054.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0015 | a0001c0001t0001g0207 a0001c0001t0015g0112 |
2 | 268 | 0.0075 | -13 | c.882 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RNGTT_chr6_88604897_88968618 | 88913204 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01175.hp1 HG01496.hp1 HG02145.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(2): Show | a0001c0001t0003g0197 a0001c0001t0003g0205 a0001c0001t0004g0003 others(9): Show |
12 | 220 | 0.0546 | -13 | c.368 others(30): Show |
RNGTT | ENSG00000111880.16 | transcript | ENST00000369485.9 | protein_coding | 4/15 | chr6 | TogoVar | |||||||
RNMT_chr18_13721673_13769556 | 13744159 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02155.hp1 | a0005 | a0005c0005 | a0005c0005t0001 | a0005c0005t0001g0142 | 1 | 376 | 0.0027 | -13 | c.113 others(32): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
RNPEP_chr1_201977648_202011143 | 201983196 | CGGGAGGA others(6): Show |
C | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
a0001a0002 | a0001c0003a0001c0005a0001c0013others(3): Show | a0001c0003t0001a0001c0005t0001a0001c0013t0001others(3): Show | a0001c0003t0001g0046 a0001c0003t0001g0047 a0001c0003t0001g0048 others(14): Show |
19 | 454 | 0.0419 | -13 | c.447 others(27): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNPEP_chr1_201977648_202011143 | 201984821 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG01099.hp2 HG01109.hp2 HG01346.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0001others(1): Show | a0001c0001t0001g0153 a0001c0001t0001g0180 a0001c0001t0001g0305 others(3): Show |
6 | 454 | 0.0132 | -13 | c.447 others(30): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RO60_chr1_193054612_193096219 | 193088162 | CTTTTTTT others(6): Show |
C | 3_prime_UTR_variant | MODIFIER | HG01069.hp2 HG01099.hp2 |
a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0023 a0001c0001t0022g0055 |
2 | 336 | 0.0060 | -13 | c.*34 others(24): Show |
RO60 | ENSG00000116747.13 | transcript | ENST00000400968.7 | protein_coding | 9/9 | 3450 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |