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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
RNF10_chr12_120529356_120582588 | 120530583 | AAAATAAA others(5): Show |
A | upstream_gene_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
a0001a0005 | a0001c0001a0001c0004a0001c0010others(2): Show | a0001c0001t0001a0001c0001t0008a0001c0004t0001others(3): Show | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0064 others(97): Show |
102 | 372 | 0.2742 | -12 | c.-42 others(23): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3772 | chr12 | TogoVar | |||||||
RNF111_chr15_58982663_59102419 | 58986202 | TGTGTTTT others(5): Show |
T | upstream_gene_variant | MODIFIER | HG01934.hp1 HG01952.hp1 HG02523.hp2 others(11): Show |
a0001a0002a0003 | a0001c0001a0001c0009a0002c0016others(1): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0023others(3): Show | a0001c0001t0003g0143 a0001c0001t0006g0114 a0001c0001t0006g0115 others(11): Show |
14 | 330 | 0.0424 | -12 | c.-18 others(23): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1460 | chr15 | TogoVar | |||||||
RNF111_chr15_58982663_59102419 | 59005313 | CCAGCCTC others(5): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(35): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(1): Show | a0001c0001t0002g0026 a0001c0001t0002g0068 a0001c0001t0002g0069 others(35): Show |
38 | 330 | 0.1152 | -12 | c.-20 others(31): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
RNF111_chr15_58982663_59102419 | 59012003 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0009 | a0001c0001t0002g0142 a0001c0001t0003g0067 a0001c0001t0003g0086 others(6): Show |
9 | 330 | 0.0273 | -12 | c.-19 others(31): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
RNF111_chr15_58982663_59102419 | 59080114 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0164 | 1 | 330 | 0.0030 | -12 | c.194 others(29): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
RNF112_chr17_19406232_19422276 | 19407053 | TTGTGTGT others(5): Show |
T | upstream_gene_variant | MODIFIER | HG00735.hp2 HG01123.hp2 HG01261.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0008 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0025 others(1): Show |
7 | 356 | 0.0197 | -12 | c.-43 others(23): Show |
RNF112 | ENSG00000128482.16 | transcript | ENST00000461366.2 | protein_coding | 4178 | chr17 | TogoVar | |||||||
RNF113B_chr13_98170785_98182269 | 98181597 | ATTATTTA others(5): Show |
A | upstream_gene_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 460 | 0.0022 | -12 | c.-43 others(23): Show |
RNF113B | ENSG00000139797.8 | transcript | ENST00000267291.7 | protein_coding | 4329 | chr13 | TogoVar | |||||||
RNF114_chr20_49931397_49958885 | 49943827 | TATATATA others(5): Show |
T | intron_variant | MODIFIER | NA18984.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0203 | 1 | 426 | 0.0024 | -12 | c.292 others(29): Show |
RNF114 | ENSG00000124226.11 | transcript | ENST00000244061.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
RNF114_chr20_49931397_49958885 | 49943873 | GATATATA others(5): Show |
G | intron_variant | MODIFIER | HG02486.hp2 HG03139.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0115 a0001c0001t0003g0116 |
2 | 426 | 0.0047 | -12 | c.292 others(29): Show |
RNF114 | ENSG00000124226.11 | transcript | ENST00000244061.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
RNF114_chr20_49931397_49958885 | 49947769 | GTTTTTTT others(5): Show |
G | intron_variant | MODIFIER | HG01106.hp1 HG01175.hp2 HG01243.hp2 others(39): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0218 a0001c0001t0001g0221 a0001c0001t0001g0250 others(36): Show |
42 | 426 | 0.0986 | -12 | c.514 others(29): Show |
RNF114 | ENSG00000124226.11 | transcript | ENST00000244061.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
RNF115_chr1_145733868_145829095 | 145789700 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG01993.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 | 1 | 272 | 0.0037 | -12 | c.103 others(27): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | TogoVar | |||||||
RNF115_chr1_145733868_145829095 | 145819271 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG02922.hp1 HG03098.hp2 |
a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0129 a0001c0001t0012g0130 |
2 | 272 | 0.0074 | -12 | c.102 others(29): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | TogoVar | |||||||
RNF11_chr1_51231273_51278447 | 51248096 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0047 | 1 | 274 | 0.0037 | -12 | c.123 others(31): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF11_chr1_51231273_51278447 | 51264281 | AAAAAAAA others(5): Show |
A | intron_variant | MODIFIER | HG02071.hp2 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0072 | 1 | 274 | 0.0037 | -12 | c.124 others(29): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF11_chr1_51231273_51278447 | 51264285 | AAAATATA others(5): Show |
A | intron_variant | MODIFIER | HG02055.hp1 HG02622.hp1 HG03516.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0005 | a0001c0001t0004g0011 a0001c0001t0004g0094 a0001c0001t0005g0056 |
4 | 274 | 0.0146 | -12 | c.124 others(29): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RNF125_chr18_32013825_32078219 | 32020002 | CTGTGTGT others(5): Show |
C | intron_variant | MODIFIER | NA19058.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0336 | 1 | 360 | 0.0028 | -12 | c.164 others(28): Show |
RNF125 | ENSG00000101695.9 | transcript | ENST00000217740.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
RNF125_chr18_32013825_32078219 | 32024197 | TTTTTTTT others(5): Show |
T | intron_variant | MODIFIER | HG01243.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0013a0001c0001t0015a0001c0001t0041others(3): Show | a0001c0001t0013g0110 a0001c0001t0015g0349 a0001c0001t0041g0348 others(4): Show |
7 | 360 | 0.0194 | -12 | c.164 others(29): Show |
RNF125 | ENSG00000101695.9 | transcript | ENST00000217740.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
RNF125_chr18_32013825_32078219 | 32031486 | GAAAAAAA others(5): Show |
G | intron_variant | MODIFIER | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0005a0001c0006t0011 | a0001c0001t0005g0147 a0001c0001t0005g0148 a0001c0006t0011g0149 |
3 | 360 | 0.0083 | -12 | c.165 others(29): Show |
RNF125 | ENSG00000101695.9 | transcript | ENST00000217740.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
RNF125_chr18_32013825_32078219 | 32041832 | GTGTTAGC others(5): Show |
G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0006others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(78): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(208): Show |
212 | 360 | 0.5889 | -12 | c.319 others(27): Show |
RNF125 | ENSG00000101695.9 | transcript | ENST00000217740.4 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
RNF130_chr5_179950067_180076759 | 180015437 | CAAGCTGG others(5): Show |
C | intron_variant | MODIFIER | HG02155.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0265 | 1 | 340 | 0.0029 | -12 | c.443 others(29): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | TogoVar | |||||||
RNF130_chr5_179950067_180076759 | 180015445 | AAAAGGAG others(5): Show |
A | intron_variant | MODIFIER | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(1): Show | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0003t0001g0155 others(3): Show |
6 | 340 | 0.0177 | -12 | c.443 others(29): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | TogoVar | |||||||
RNF130_chr5_179950067_180076759 | 180015490 | AGGAAAGG others(5): Show |
A | intron_variant | MODIFIER | HG02683.hp2 HG03017.hp1 HG03704.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0091 |
3 | 340 | 0.0088 | -12 | c.443 others(29): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | TogoVar | |||||||
RNF130_chr5_179950067_180076759 | 180015562 | GAAGGAGT others(5): Show |
G | intron_variant | MODIFIER | HG00408.hp2 HG00735.hp1 HG01123.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0309 a0001c0002t0001g0046 a0001c0002t0001g0123 others(5): Show |
8 | 340 | 0.0235 | -12 | c.443 others(29): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | TogoVar | |||||||
RNF130_chr5_179950067_180076759 | 180055269 | AAAAAAAA others(5): Show |
A | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00735.hp1 others(37): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(3): Show | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(37): Show |
40 | 340 | 0.1177 | -12 | c.248 others(31): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | TogoVar | |||||||
RNF133_chr7_122692735_122704117 | 122692814 | ACAGCTCT others(5): Show |
A | downstream_gene_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 1 | 448 | 0.0022 | -12 | c.*49 others(23): Show |
RNF133 | ENSG00000188050.3 | transcript | ENST00000340112.3 | protein_coding | 4920 | chr7 | TogoVar | |||||||
RNF133_chr7_122692735_122704117 | 122696501 | GACCCCAT others(5): Show |
G | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(444): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0007a0002c0003others(6): Show | a0001c0001t0001a0001c0007t0001a0002c0003t0001others(6): Show | a0001c0001t0001g0000 a0001c0007t0001g0000 a0002c0003t0001g0000 others(6): Show |
447 | 448 | 0.9978 | -12 | c.*12 others(23): Show |
RNF133 | ENSG00000188050.3 | transcript | ENST00000340112.3 | protein_coding | 1233 | chr7 | TogoVar | |||||||
RNF135_chr17_30966039_31004911 | 30983320 | CATATATA others(5): Show |
C | intron_variant | MODIFIER | HG01346.hp1 HG01433.hp2 HG02145.hp2 others(10): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0003others(2): Show | a0001c0001t0001g0161 a0002c0002t0001g0007 a0002c0002t0001g0009 others(10): Show |
13 | 266 | 0.0489 | -12 | c.373 others(29): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF135_chr17_30966039_31004911 | 30983343 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | HG03139.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0076 | 1 | 266 | 0.0038 | -12 | c.373 others(29): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RNF138_chr18_32086874_32136561 | 32097878 | ATATATGT others(5): Show |
A | intron_variant | MODIFIER | NA18984.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0124 | 1 | 362 | 0.0028 | -12 | c.110 others(29): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
RNF138_chr18_32086874_32136561 | 32135035 | CAAAAAAA others(5): Show |
C | downstream_gene_variant | MODIFIER | HG00423.hp1 HG02071.hp2 HG03225.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0016a0001c0001t0021 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0132 others(9): Show |
12 | 362 | 0.0332 | -12 | c.*58 others(23): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3475 | chr18 | TogoVar | |||||||
RNF139_chr8_124469880_124493618 | 124482939 | AAAAAATA others(5): Show |
A | intron_variant | MODIFIER | HG00741.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0216 | 1 | 408 | 0.0025 | -12 | c.182 others(29): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
RNF13_chr3_149808215_149967139 | 149853455 | GGAGAGAG others(5): Show |
G | intron_variant | MODIFIER | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
a0001a0004a0007 | a0001c0001a0001c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0002t0002a0004c0005t0001others(1): Show | a0001c0001t0001g0082 a0001c0001t0001g0245 a0001c0002t0002g0240 others(8): Show |
11 | 280 | 0.0393 | -12 | c.195 others(27): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
RNF13_chr3_149808215_149967139 | 149903937 | ATCTGTCT others(5): Show |
A | intron_variant | MODIFIER | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 |
3 | 280 | 0.0107 | -12 | c.500 others(29): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
RNF141_chr11_10506673_10546187 | 10532496 | TACACACA others(5): Show |
T | intron_variant | MODIFIER | HG02738.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0091 | 1 | 374 | 0.0027 | -12 | c.143 others(29): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | TogoVar | |||||||
RNF144A_chr2_6912412_7049179 | 6990385 | TACACACA others(5): Show |
T | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00621.hp1 others(66): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0044 others(65): Show |
69 | 310 | 0.2226 | -12 | c.-11 others(29): Show |
RNF144A | ENSG00000151692.15 | transcript | ENST00000320892.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
RNF144A_chr2_6912412_7049179 | 6990425 | CACACACA others(5): Show |
C | intron_variant | MODIFIER | HG00438.hp1 HG00735.hp1 HG01256.hp1 others(31): Show |
a0001a0002 | a0001c0001a0002c0003a0002c0004 | a0001c0001t0002a0001c0001t0012a0001c0001t0024others(6): Show | a0001c0001t0002g0022 a0001c0001t0002g0113 a0001c0001t0002g0166 others(30): Show |
34 | 310 | 0.1097 | -12 | c.-11 others(29): Show |
RNF144A | ENSG00000151692.15 | transcript | ENST00000320892.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
RNF144A_chr2_6912412_7049179 | 6990562 | TACACACA others(5): Show |
T | intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0046 | 1 | 310 | 0.0032 | -12 | c.-11 others(29): Show |
RNF144A | ENSG00000151692.15 | transcript | ENST00000320892.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
RNF144A_chr2_6912412_7049179 | 7030257 | CTGTGTGT others(5): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(64): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0002a0001c0001t0005a0001c0001t0017others(5): Show | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0040 others(64): Show |
67 | 310 | 0.2161 | -12 | c.747 others(25): Show |
RNF144A | ENSG00000151692.15 | transcript | ENST00000320892.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
RNF144B_chr6_18382350_18473870 | 18406457 | AGTGTGTG others(5): Show |
A | intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0001 | a0001c0001t0070 | a0001c0001t0070g0226 | 1 | 386 | 0.0026 | -12 | c.165 others(29): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
RNF144B_chr6_18382350_18473870 | 18411462 | CATATATA others(5): Show |
C | intron_variant | MODIFIER | HG01123.hp1 HG01175.hp1 HG01257.hp1 others(44): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0002g0302 a0001c0001t0002g0311 a0001c0001t0002g0319 others(42): Show |
47 | 386 | 0.1218 | -12 | c.165 others(31): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
RNF144B_chr6_18382350_18473870 | 18411487 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | HG00408.hp2 HG00621.hp2 HG01123.hp2 others(23): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(9): Show | a0001c0001t0002g0133 a0001c0001t0002g0303 a0001c0001t0002g0313 others(22): Show |
26 | 386 | 0.0674 | -12 | c.165 others(31): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
RNF144B_chr6_18382350_18473870 | 18411489 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | HG00609.hp2 | a0001 | a0001c0001 | a0001c0001t0034 | a0001c0001t0034g0231 | 1 | 386 | 0.0026 | -12 | c.165 others(31): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
RNF144B_chr6_18382350_18473870 | 18445016 | CTTTTAGT others(5): Show |
C | intron_variant | MODIFIER | HG00423.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0327 | 1 | 386 | 0.0026 | -12 | c.331 others(29): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
RNF144B_chr6_18382350_18473870 | 18446840 | GGTGTGTG others(5): Show |
G | intron_variant | MODIFIER | HG02055.hp1 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0058a0001c0001t0065 | a0001c0001t0058g0227 a0001c0001t0065g0289 |
2 | 386 | 0.0052 | -12 | c.331 others(29): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
RNF145_chr5_159152409_159214553 | 159198239 | CTAAATAA others(5): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(42): Show |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0089 a0001c0001t0002g0033 a0001c0001t0002g0034 others(34): Show |
45 | 394 | 0.1142 | -12 | c.185 others(29): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | TogoVar | |||||||
RNF14_chr5_141964105_141995292 | 141971563 | TTTTCTTT others(5): Show |
T | intron_variant | MODIFIER | HG01175.hp2 HG03669.hp2 NA19063.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0021a0001c0001t0022 | a0001c0001t0001g0087 a0001c0001t0021g0077 a0001c0001t0022g0078 |
3 | 284 | 0.0106 | -12 | c.-7+ others(25): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
RNF14_chr5_141964105_141995292 | 141976776 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0073 a0001c0001t0002g0068 a0001c0001t0002g0069 others(15): Show |
27 | 284 | 0.0951 | -12 | c.307 others(29): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
RNF150_chr4_140854807_141138469 | 140899974 | CTGTGTGT others(5): Show |
C | intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0040 | a0001c0001t0040g0013 | 1 | 184 | 0.0054 | -12 | c.119 others(33): Show |
RNF150 | ENSG00000170153.11 | transcript | ENST00000515673.7 | protein_coding | 6/6 | chr4 | TogoVar | |||||||
RNF150_chr4_140854807_141138469 | 140939606 | TTGTGTGT others(5): Show |
T | intron_variant | MODIFIER | HG00140.hp2 HG01070.hp2 HG01192.hp2 others(21): Show |
a0001a0005 | a0001c0001a0005c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0090 a0001c0001t0001g0121 a0001c0001t0002g0053 others(21): Show |
24 | 184 | 0.1304 | -12 | c.890 others(29): Show |
RNF150 | ENSG00000170153.11 | transcript | ENST00000515673.7 | protein_coding | 4/6 | chr4 | TogoVar | |||||||
RNF150_chr4_140854807_141138469 | 140996187 | TATCTCAT others(5): Show |
T | intron_variant | MODIFIER | HG01978.hp1 | a0001 | a0001c0001 | a0001c0001t0063 | a0001c0001t0063g0007 | 1 | 184 | 0.0054 | -12 | c.485 others(31): Show |
RNF150 | ENSG00000170153.11 | transcript | ENST00000515673.7 | protein_coding | 1/6 | chr4 | TogoVar |