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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CELF4_chr18_37238040_37570798 | 37283949 | T | TATAGCCC others(665): Show |
intron_variant | MODIFIER | HG01258.hp1 HG02451.hp1 HG02723.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(5): Show | a0001c0001t0001g0159 a0001c0001t0007g0096 a0001c0001t0007g0120 others(6): Show |
9 | 47 | 0.1915 | 672 | c.449 others(689): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 3/12 | chr18 | TogoVar | |||||||
CELF4_chr18_37238040_37570798 | 37283949 | T | TATAGCCC others(665): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0014 | 1 | 39 | 0.0256 | 672 | c.449 others(689): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 3/12 | chr18 | TogoVar | |||||||
CELF4_chr18_37238040_37570798 | 37283949 | T | TATAGCCC others(665): Show |
intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0128 | 1 | 39 | 0.0256 | 672 | c.449 others(689): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 3/12 | chr18 | TogoVar | |||||||
CELSR1_chr22_46356174_46542620 | 46366255 | A | AGAAAGGT others(665): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0036 | a0036c0041 | a0036c0041t0002 | a0036c0041t0002g0054 | 1 | 3 | 0.3333 | 672 | c.830 others(689): Show |
CELSR1 | ENSG00000075275.18 | transcript | ENST00000674500.2 | protein_coding | 30/34 | chr22 | TogoVar | |||||||
CENPI_chrX_101093204_101171126 | 101137985 | T | TCTGTCTT others(665): Show |
intron_variant | MODIFIER | HG02523.hp1 NA19074.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0234 a0001c0002t0002g0256 |
2 | 105 | 0.0190 | 672 | c.147 others(691): Show |
CENPI | ENSG00000102384.14 | transcript | ENST00000682095.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
CENPI_chrX_101093204_101171126 | 101137985 | T | TCTGTCTT others(665): Show |
intron_variant | MODIFIER | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(66): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0006a0001c0002t0008others(3): Show | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0048 others(63): Show |
69 | 172 | 0.4012 | 672 | c.147 others(691): Show |
CENPI | ENSG00000102384.14 | transcript | ENST00000682095.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
CENPI_chrX_101093204_101171126 | 101137985 | T | TCTTTCTT others(665): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0046 | 1 | 104 | 0.0096 | 672 | c.147 others(691): Show |
CENPI | ENSG00000102384.14 | transcript | ENST00000682095.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
CENPI_chrX_101093204_101171126 | 101137985 | T | TCTTTCTT others(665): Show |
intron_variant | MODIFIER | HG03710.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0029 | 1 | 104 | 0.0096 | 672 | c.147 others(691): Show |
CENPI | ENSG00000102384.14 | transcript | ENST00000682095.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
CENPI_chrX_101093204_101171126 | 101137985 | T | TCTTTCTT others(665): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0265 | 1 | 104 | 0.0096 | 672 | c.147 others(691): Show |
CENPI | ENSG00000102384.14 | transcript | ENST00000682095.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
CENPI_chrX_101093204_101171126 | 101137985 | T | TCTTTCTT others(665): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(96): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(6): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(95): Show |
99 | 202 | 0.4901 | 672 | c.147 others(691): Show |
CENPI | ENSG00000102384.14 | transcript | ENST00000682095.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
CENPI_chrX_101093204_101171126 | 101137986 | C | CTTTCTTT others(665): Show |
intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0142 | 1 | 190 | 0.0053 | 672 | c.147 others(691): Show |
CENPI | ENSG00000102384.14 | transcript | ENST00000682095.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
CENPI_chrX_101093204_101171126 | 101137986 | C | CTTTCTTT others(665): Show |
intron_variant | MODIFIER | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0018 | a0001c0001t0004g0004 a0001c0001t0004g0121 a0001c0001t0004g0124 others(10): Show |
14 | 203 | 0.0690 | 672 | c.147 others(691): Show |
CENPI | ENSG00000102384.14 | transcript | ENST00000682095.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
CFAP47_chrX_35914734_36390317 | 35966189 | A | ACTAATAT others(665): Show |
intron_variant | MODIFIER | HG01346.hp2 | a0024 | a0024c0025 | a0024c0025t0004 | a0024c0025t0004g0181 | 1 | 58 | 0.0172 | 672 | c.141 others(689): Show |
CFAP47 | ENSG00000165164.14 | transcript | ENST00000378653.8 | protein_coding | 8/63 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
CFAP47_chrX_35914734_36390317 | 35966203 | A | GATATTAG others(665): Show |
intron_variant | MODIFIER | HG03669.hp1 NA18966.hp1 NA18968.hp1 |
a0001a0002 | a0001c0029a0002c0002 | a0001c0029t0001a0002c0002t0001 | a0001c0029t0001g0083 a0002c0002t0001g0167 a0002c0002t0001g0170 |
3 | 123 | 0.0244 | 672 | c.141 others(689): Show |
CFAP47 | ENSG00000165164.14 | transcript | ENST00000378653.8 | protein_coding | 8/63 | chrX | TogoVar | |||||||
CFAP47_chrX_35914734_36390317 | 35966203 | A | GATATTAG others(665): Show |
intron_variant | MODIFIER | HG00408.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0164 | 1 | 121 | 0.0083 | 672 | c.141 others(689): Show |
CFAP47 | ENSG00000165164.14 | transcript | ENST00000378653.8 | protein_coding | 8/63 | chrX | TogoVar | |||||||
CFAP61_chr20_20047532_20365698 | 20320485 | A | ATTATATA others(665): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0007 | a0007c0010 | a0007c0010t0003 | a0007c0010t0003g0133 | 1 | 201 | 0.0050 | 672 | c.342 others(693): Show |
CFAP61 | ENSG00000089101.19 | transcript | ENST00000245957.10 | protein_coding | 25/26 | chr20 | TogoVar | |||||||
CHMP1A_chr16_89639435_89662708 | 89647539 | A | AGTGGAGA others(665): Show |
intron_variant | MODIFIER | HG01070.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0077 | 1 | 355 | 0.0028 | 672 | c.253 others(687): Show |
CHMP1A | ENSG00000131165.16 | transcript | ENST00000397901.8 | protein_coding | 4/6 | chr16 | TogoVar | |||||||
CHMP1A_chr16_89639435_89662708 | 89647539 | A | AGTGGAGA others(665): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0065 | 1 | 355 | 0.0028 | 672 | c.253 others(687): Show |
CHMP1A | ENSG00000131165.16 | transcript | ENST00000397901.8 | protein_coding | 4/6 | chr16 | TogoVar | |||||||
CHMP1A_chr16_89639435_89662708 | 89647648 | G | GGACCCAG others(665): Show |
intron_variant | MODIFIER | HG02896.hp1 HG03471.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0176 a0001c0001t0001g0274 |
2 | 142 | 0.0141 | 672 | c.253 others(687): Show |
CHMP1A | ENSG00000131165.16 | transcript | ENST00000397901.8 | protein_coding | 4/6 | chr16 | TogoVar | |||||||
CHMP1A_chr16_89639435_89662708 | 89648278 | A | AGACCCAG others(665): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0095 | 1 | 279 | 0.0036 | 672 | c.253 others(687): Show |
CHMP1A | ENSG00000131165.16 | transcript | ENST00000397901.8 | protein_coding | 4/6 | chr16 | TogoVar | |||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | HG00609.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0193 | 1 | 8 | 0.1250 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | HG01081.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0128 | 1 | 8 | 0.1250 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | HG00642.hp2 HG02071.hp2 NA18948.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 a0001c0001t0001g0174 |
5 | 12 | 0.4167 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | HG01256.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0130 | 1 | 8 | 0.1250 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | NA18997.hp1 NA19010.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0085 a0001c0001t0001g0197 |
2 | 9 | 0.2222 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | NA19087.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0131 | 1 | 8 | 0.1250 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | HG04184.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0135 | 1 | 8 | 0.1250 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0137 | 1 | 8 | 0.1250 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0198 | 1 | 8 | 0.1250 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00673.hp2 HG01070.hp2 others(21): Show |
a0001a0003a0035 | a0001c0001a0001c0024a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0008a0001c0024t0001others(3): Show | a0001c0001t0001g0003 a0001c0001t0001g0100 a0001c0001t0001g0146 others(5): Show |
24 | 31 | 0.7742 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0147 | 1 | 8 | 0.1250 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | HG00741.hp2 HG02074.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | 9 | 0.2222 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795593 | T | TGCTGCCC others(665): Show |
intron_variant | MODIFIER | NA18975.hp2 NA19085.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0049 | 2 | 9 | 0.2222 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CHTF18_chr16_783620_803074 | 795610 | C | CCCCCGGC others(665): Show |
intron_variant | MODIFIER | HG02055.hp2 | a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0165 | 1 | 420 | 0.0024 | 672 | c.217 others(687): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110385410 | T | TGTGGATA others(665): Show |
intron_variant | MODIFIER | NA19074.hp1 | a0001 | a0001c0015 | a0001c0015t0001 | a0001c0015t0001g0227 | 1 | 301 | 0.0033 | 672 | c.180 others(691): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110385410 | T | TGTGGATA others(665): Show |
intron_variant | MODIFIER | NA18945.hp2 | a0001 | a0001c0025 | a0001c0025t0001 | a0001c0025t0001g0201 | 1 | 301 | 0.0033 | 672 | c.180 others(691): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110385530 | C | CGTGGATA others(665): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0362 | 1 | 196 | 0.0051 | 672 | c.180 others(691): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL9A3_chr20_62812050_62846159 | 62825130 | A | AGGGAGGG others(665): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0066 | 1 | 220 | 0.0045 | 672 | c.630 others(687): Show |
COL9A3 | ENSG00000092758.18 | transcript | ENST00000649368.1 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
COL9A3_chr20_62812050_62846159 | 62825130 | A | AGGGAGGG others(665): Show |
intron_variant | MODIFIER | NA18971.hp1 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0127 | 1 | 220 | 0.0045 | 672 | c.630 others(687): Show |
COL9A3 | ENSG00000092758.18 | transcript | ENST00000649368.1 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
COMMD9_chr11_36267292_36294424 | 36287046 | A | ATATGTAT others(665): Show |
intron_variant | MODIFIER | HG03831.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0210 | 1 | 274 | 0.0036 | 672 | c.51+ others(687): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | TogoVar | |||||||
CTDP1_chr18_79674803_79759503 | 79752598 | G | GTAAGGAA others(665): Show |
intron_variant | MODIFIER | NA18963.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0057 | 1 | 350 | 0.0029 | 672 | c.274 others(691): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CXorf51B_chrX_146804771_146815411 | 146812146 | C | CATGTGTA others(665): Show |
downstream_gene_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 49 | 0.0204 | 672 | c.*18 others(683): Show |
CXorf51B | ENSG00000235699.3 | transcript | ENST00000438525.3 | protein_coding | 1736 | chrX | TogoVar | |||||||
DCDC2_chr6_24166755_24363059 | 24238180 | G | GGGAGGAA others(665): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0035 | a0001c0001t0035g0129 | 1 | 164 | 0.0061 | 672 | c.923 others(691): Show |
DCDC2 | ENSG00000146038.12 | transcript | ENST00000378454.8 | protein_coding | 7/9 | chr6 | TogoVar | |||||||
DCDC2_chr6_24166755_24363059 | 24238180 | G | GGGAGGAA others(665): Show |
intron_variant | MODIFIER | NA18983.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0110 | 1 | 164 | 0.0061 | 672 | c.923 others(691): Show |
DCDC2 | ENSG00000146038.12 | transcript | ENST00000378454.8 | protein_coding | 7/9 | chr6 | TogoVar | |||||||
DEAF1_chr11_639233_700222 | 642838 | C | CCAGGCGG others(665): Show |
downstream_gene_variant | MODIFIER | HG00558.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0179 | 1 | 144 | 0.0069 | 672 | c.*17 others(683): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1394 | chr11 | TogoVar | |||||||
DRD4_chr11_632269_645706 | 642838 | C | CCAGGCGG others(665): Show |
downstream_gene_variant | MODIFIER | HG00558.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 172 | 0.0058 | 672 | c.*22 others(683): Show |
DRD4 | ENSG00000069696.7 | transcript | ENST00000176183.6 | protein_coding | 2133 | chr11 | TogoVar | |||||||
EFNA2_chr19_1280873_1306431 | 1282324 | G | GGGGGAAG others(665): Show |
upstream_gene_variant | MODIFIER | HG01081.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0005 | 1 | 15 | 0.0667 | 672 | c.-38 others(683): Show |
EFNA2 | ENSG00000099617.4 | transcript | ENST00000215368.4 | protein_coding | 3548 | chr19 | TogoVar | |||||||
EFNA2_chr19_1280873_1306431 | 1282324 | G | GGGGGAAG others(665): Show |
upstream_gene_variant | MODIFIER | HG01516.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0088 | 1 | 15 | 0.0667 | 672 | c.-38 others(683): Show |
EFNA2 | ENSG00000099617.4 | transcript | ENST00000215368.4 | protein_coding | 3548 | chr19 | TogoVar | |||||||
EFNA2_chr19_1280873_1306431 | 1282407 | G | GGGAGGAA others(665): Show |
upstream_gene_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0001 | 1 | 285 | 0.0035 | 672 | c.-37 others(683): Show |
EFNA2 | ENSG00000099617.4 | transcript | ENST00000215368.4 | protein_coding | 3465 | chr19 | TogoVar | |||||||
EML1_chr14_99788413_99947060 | 99928107 | G | GTGATGGT others(665): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0054 | 1 | 152 | 0.0066 | 672 | c.190 others(691): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | TogoVar |