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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
HRNR_chr1_152207076_152229193 | 152215700 | G | GGCTGGAA others(7049): Show |
conservative_inframe_insertion | MODERATE | HG03834.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0006 | 1 | 293 | 0.0034 | 7056 | c.592 others(7065): Show |
p.Ser others(7071): Show |
HRNR | ENSG00000197915.7 | transcript | ENST00000368801.4 | protein_coding | 3/3 | 6004/9629 | 5928/8553 | 1976/2850 | chr1 | TogoVar | |||
HRNR_chr1_152207076_152229193 | 152215736 | C | CGTAGCTG others(7049): Show |
conservative_inframe_insertion | MODERATE | HG03831.hp2 | a0010 | a0010c0047 | a0010c0047t0001 | a0010c0047t0001g0054 | 1 | 158 | 0.0063 | 7056 | c.589 others(7065): Show |
p.Tyr others(7071): Show |
HRNR | ENSG00000197915.7 | transcript | ENST00000368801.4 | protein_coding | 3/3 | 5968/9629 | 5892/8553 | 1964/2850 | chr1 | TogoVar | |||
HRNR_chr1_152207076_152229193 | 152215736 | C | CGTAGCTG others(7049): Show |
conservative_inframe_insertion | MODERATE | HG01123.hp2 | a0001 | a0001c0031 | a0001c0031t0001 | a0001c0031t0001g0036 | 1 | 158 | 0.0063 | 7056 | c.589 others(7065): Show |
p.Tyr others(7071): Show |
HRNR | ENSG00000197915.7 | transcript | ENST00000368801.4 | protein_coding | 3/3 | 5968/9629 | 5892/8553 | 1964/2850 | chr1 | TogoVar | |||
HRNR_chr1_152207076_152229193 | 152215736 | C | CGTAGCTG others(7049): Show |
conservative_inframe_insertion | MODERATE | HG01517.hp1 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0030 | 1 | 158 | 0.0063 | 7056 | c.589 others(7065): Show |
p.Tyr others(7071): Show |
HRNR | ENSG00000197915.7 | transcript | ENST00000368801.4 | protein_coding | 3/3 | 5968/9629 | 5892/8553 | 1964/2850 | chr1 | TogoVar | |||
HRNR_chr1_152207076_152229193 | 152215736 | C | CGTAGCTG others(7049): Show |
conservative_inframe_insertion | MODERATE | HG01257.hp2 HG01515.hp1 HG01934.hp1 others(5): Show |
a0001 | a0001c0006a0001c0031 | a0001c0006t0001a0001c0031t0001 | a0001c0006t0001g0006 a0001c0006t0001g0030 a0001c0031t0001g0036 |
8 | 165 | 0.0485 | 7056 | c.589 others(7065): Show |
p.Tyr others(7071): Show |
HRNR | ENSG00000197915.7 | transcript | ENST00000368801.4 | protein_coding | 3/3 | 5968/9629 | 5892/8553 | 1964/2850 | chr1 | TogoVar | |||
HRNR_chr1_152207076_152229193 | 152215736 | C | CGTAGCTG others(7049): Show |
conservative_inframe_insertion | MODERATE | HG02572.hp1 HG02630.hp1 HG03486.hp2 |
a0001 | a0001c0005a0001c0109 | a0001c0005t0001a0001c0109t0001 | a0001c0005t0001g0010 a0001c0109t0001g0112 |
3 | 160 | 0.0188 | 7056 | c.589 others(7065): Show |
p.Tyr others(7071): Show |
HRNR | ENSG00000197915.7 | transcript | ENST00000368801.4 | protein_coding | 3/3 | 5968/9629 | 5892/8553 | 1964/2850 | chr1 | TogoVar | |||
HRNR_chr1_152207076_152229193 | 152215736 | C | CGTAGCTG others(7049): Show |
conservative_inframe_insertion | MODERATE | HG02055.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0010 | 1 | 158 | 0.0063 | 7056 | c.589 others(7065): Show |
p.Tyr others(7071): Show |
HRNR | ENSG00000197915.7 | transcript | ENST00000368801.4 | protein_coding | 3/3 | 5968/9629 | 5892/8553 | 1964/2850 | chr1 | TogoVar | |||
HRNR_chr1_152207076_152229193 | 152215736 | C | CGTAGCTG others(7049): Show |
conservative_inframe_insertion | MODERATE | HG03453.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0010 | 1 | 158 | 0.0063 | 7056 | c.589 others(7065): Show |
p.Tyr others(7071): Show |
HRNR | ENSG00000197915.7 | transcript | ENST00000368801.4 | protein_coding | 3/3 | 5968/9629 | 5892/8553 | 1964/2850 | chr1 | TogoVar | |||
TMEM192_chr4_165065608_165117860 | 165095953 | T | TTTTTTTT others(7051): Show |
intron_variant | MODIFIER | HG01952.hp2 | a0001 | a0001c0001 | a0001c0001t0030 | a0001c0001t0030g0123 | 1 | 328 | 0.0030 | 7058 | c.439 others(7075): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | TogoVar | |||||||
YBEY_chr21_46281342_46302751 | 46294693 | G | GTCAGCCA others(7052): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 | 1 | 198 | 0.0051 | 7059 | c.340 others(7076): Show |
YBEY | ENSG00000182362.14 | transcript | ENST00000397701.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
EXD3_chr9_137301896_137428162 | 137328303 | A | TCCCATAT others(7054): Show |
intron_variant | MODIFIER | HG01993.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0056 | 1 | 43 | 0.0233 | 7061 | c.199 others(7080): Show |
EXD3 | ENSG00000187609.16 | transcript | ENST00000340951.9 | protein_coding | 17/21 | chr9 | TogoVar | |||||||
EXD3_chr9_137301896_137428162 | 137328303 | A | TCCCATAT others(7054): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0062 | 1 | 43 | 0.0233 | 7061 | c.199 others(7080): Show |
EXD3 | ENSG00000187609.16 | transcript | ENST00000340951.9 | protein_coding | 17/21 | chr9 | TogoVar | |||||||
EXD3_chr9_137301896_137428162 | 137328303 | A | TCCCATAT others(7054): Show |
intron_variant | MODIFIER | HG02965.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0048 | 1 | 43 | 0.0233 | 7061 | c.199 others(7080): Show |
EXD3 | ENSG00000187609.16 | transcript | ENST00000340951.9 | protein_coding | 17/21 | chr9 | TogoVar | |||||||
EXD3_chr9_137301896_137428162 | 137328303 | A | TCCCATAT others(7055): Show |
intron_variant | MODIFIER | HG02965.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0011 | 1 | 43 | 0.0233 | 7062 | c.199 others(7081): Show |
EXD3 | ENSG00000187609.16 | transcript | ENST00000340951.9 | protein_coding | 17/21 | chr9 | TogoVar | |||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(7057): Show |
intron_variant | MODIFIER | NA19002.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0182 | 1 | 29 | 0.0345 | 7064 | c.109 others(7079): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DISC1_chr1_231621790_232046272 | 231799889 | T | TTCCCTCC others(7057): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0012 | a0001c0012t0017 | a0001c0012t0017g0039 | 1 | 3 | 0.3333 | 7064 | c.169 others(7081): Show |
DISC1 | ENSG00000162946.24 | transcript | ENST00000439617.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(7059): Show |
intron_variant | MODIFIER | NA18612.hp2 NA18953.hp2 NA19012.hp2 |
a0001 | a0001c0001a0001c0019 | a0001c0001t0001a0001c0019t0001 | a0001c0001t0001g0018 a0001c0001t0001g0183 a0001c0019t0001g0018 |
3 | 31 | 0.0968 | 7066 | c.109 others(7081): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181046192 | C | CACCTCCT others(7059): Show |
intron_variant | MODIFIER | NA18999.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018 | 1 | 387 | 0.0026 | 7066 | c.109 others(7081): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045918 | C | CCCAACAC others(7060): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0009 | a0001c0009t0008 | a0001c0009t0008g0123 | 1 | 380 | 0.0026 | 7067 | c.109 others(7082): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045918 | C | CCCAACAC others(7060): Show |
intron_variant | MODIFIER | HG03486.hp1 HG03579.hp2 |
a0001 | a0001c0009 | a0001c0009t0008 | a0001c0009t0008g0118 a0001c0009t0008g0119 |
2 | 381 | 0.0052 | 7067 | c.109 others(7082): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045918 | C | CCCAACAC others(7060): Show |
intron_variant | MODIFIER | HG03130.hp2 | a0001 | a0001c0009 | a0001c0009t0008 | a0001c0009t0008g0116 | 1 | 380 | 0.0026 | 7067 | c.109 others(7082): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045986 | C | CTCCTCCA others(7062): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0006 | a0001c0006t0006 | a0001c0006t0006g0065 | 1 | 353 | 0.0028 | 7069 | c.109 others(7084): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(7063): Show |
upstream_gene_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0091 | 1 | 8 | 0.1250 | 7070 | c.-45 others(7079): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
FAM120B_chr6_170301758_170412067 | 170377914 | C | CGCCCGGG others(7069): Show |
intron_variant | MODIFIER | NA19066.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0133 | 1 | 152 | 0.0066 | 7076 | c.228 others(7097): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
FAM120B_chr6_170301758_170412067 | 170377914 | C | CGCCCGGG others(7069): Show |
intron_variant | MODIFIER | HG02896.hp2 | a0002 | a0002c0003 | a0002c0003t0007 | a0002c0003t0007g0111 | 1 | 152 | 0.0066 | 7076 | c.228 others(7097): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
YBEY_chr21_46281342_46302751 | 46294687 | A | AGTGGGGA others(7069): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0141 | 1 | 274 | 0.0036 | 7076 | c.340 others(7093): Show |
YBEY | ENSG00000182362.14 | transcript | ENST00000397701.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
FAM120B_chr6_170301758_170412067 | 170377914 | C | CGCCCGGG others(7070): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0002 | a0002c0003 | a0002c0003t0007 | a0002c0003t0007g0144 | 1 | 152 | 0.0066 | 7077 | c.228 others(7098): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
AP2A2_chr11_920870_1017240 | 965201 | T | TCCCAGAT others(7073): Show |
intron_variant | MODIFIER | NA19085.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0214 | 1 | 239 | 0.0042 | 7080 | c.137 others(7097): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
DOCK1_chr10_126900428_127457516 | 126948257 | G | AGTTGGTA others(7074): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0108 | 1 | 133 | 0.0075 | 7081 | c.47- others(7098): Show |
DOCK1 | ENSG00000150760.13 | transcript | ENST00000623213.2 | protein_coding | 1/51 | chr10 | TogoVar | |||||||
FOXK2_chr17_82514732_82609602 | 82586454 | G | GGGGAAAG others(7080): Show |
intron_variant | MODIFIER | HG01361.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0111 | 1 | 280 | 0.0036 | 7087 | c.157 others(7104): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
YBEY_chr21_46281342_46302751 | 46294693 | G | GTCAGCCA others(7091): Show |
intron_variant | MODIFIER | HG02735.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0205 | 1 | 198 | 0.0051 | 7098 | c.340 others(7115): Show |
YBEY | ENSG00000182362.14 | transcript | ENST00000397701.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
FOXK2_chr17_82514732_82609602 | 82586551 | A | AGGGGAAA others(7094): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0014 | a0014c0015 | a0014c0015t0005 | a0014c0015t0005g0185 | 1 | 172 | 0.0058 | 7101 | c.157 others(7118): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
MED16_chr19_862963_898187 | 879404 | T | TCCCTGGT others(7097): Show |
intron_variant | MODIFIER | HG01099.hp2 | a0004 | a0004c0019 | a0004c0019t0001 | a0004c0019t0001g0016 | 1 | 9 | 0.1111 | 7104 | c.135 others(7121): Show |
MED16 | ENSG00000175221.16 | transcript | ENST00000325464.6 | protein_coding | 8/15 | chr19 | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11219072 | A | ATTCCCCT others(7098): Show |
intron_variant | MODIFIER | HG01433.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0056 | 1 | 144 | 0.0069 | 7105 | c.748 others(7124): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | |||||||
EHMT1_chr9_137614005_137841127 | 137716460 | T | TGGGGGAG others(7099): Show |
intron_variant | MODIFIER | HG01169.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0097 | 1 | 129 | 0.0078 | 7106 | c.86- others(7117): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
KCNIP4_chr4_20723606_21953772 | 21594807 | G | GGCACATA others(7100): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054 | 1 | 70 | 0.0143 | 7107 | c.61+ others(7126): Show |
KCNIP4 | ENSG00000185774.17 | transcript | ENST00000382152.7 | protein_coding | 1/8 | chr4 | TogoVar | |||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(7100): Show |
intron_variant | MODIFIER | NA18522.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0128 | 1 | 62 | 0.0161 | 7107 | c.286 others(7124): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
KCNIP4_chr4_20723606_21953772 | 21594807 | G | GGCACATA others(7104): Show |
intron_variant | MODIFIER | HG02809.hp2 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0011 | a0001c0001t0003g0002 a0001c0001t0011g0003 |
2 | 71 | 0.0282 | 7111 | c.61+ others(7130): Show |
KCNIP4 | ENSG00000185774.17 | transcript | ENST00000382152.7 | protein_coding | 1/8 | chr4 | TogoVar | |||||||
KCNIP4_chr4_20723606_21953772 | 21594807 | G | GGCACATA others(7104): Show |
intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 | 1 | 70 | 0.0143 | 7111 | c.61+ others(7130): Show |
KCNIP4 | ENSG00000185774.17 | transcript | ENST00000382152.7 | protein_coding | 1/8 | chr4 | TogoVar | |||||||
KCNIP4_chr4_20723606_21953772 | 21594807 | G | GGCACATA others(7108): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0027 | 1 | 70 | 0.0143 | 7115 | c.61+ others(7134): Show |
KCNIP4 | ENSG00000185774.17 | transcript | ENST00000382152.7 | protein_coding | 1/8 | chr4 | TogoVar | |||||||
KCNIP4_chr4_20723606_21953772 | 21594807 | G | GGCACATA others(7110): Show |
intron_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0077 | 1 | 70 | 0.0143 | 7117 | c.61+ others(7136): Show |
KCNIP4 | ENSG00000185774.17 | transcript | ENST00000382152.7 | protein_coding | 1/8 | chr4 | TogoVar | |||||||
ACTN2_chr1_236681499_236769631 | 236714689 | T | TACCACTG others(7112): Show |
intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0013 | a0001c0013t0002 | a0001c0013t0002g0052 | 1 | 299 | 0.0033 | 7119 | c.127 others(7136): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
KCNIP4_chr4_20723606_21953772 | 21594807 | G | GGCACATA others(7112): Show |
intron_variant | MODIFIER | HG02280.hp1 HG02280.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0013a0001c0003t0003 | a0001c0001t0013g0059 a0001c0003t0003g0029 |
2 | 71 | 0.0282 | 7119 | c.61+ others(7138): Show |
KCNIP4 | ENSG00000185774.17 | transcript | ENST00000382152.7 | protein_coding | 1/8 | chr4 | TogoVar | |||||||
KCNIP4_chr4_20723606_21953772 | 21594807 | G | GGCACATA others(7112): Show |
intron_variant | MODIFIER | HG02615.hp1 HG03098.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0034 a0001c0001t0005g0072 |
2 | 71 | 0.0282 | 7119 | c.61+ others(7138): Show |
KCNIP4 | ENSG00000185774.17 | transcript | ENST00000382152.7 | protein_coding | 1/8 | chr4 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(7114): Show |
upstream_gene_variant | MODIFIER | HG01993.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0003 | 1 | 8 | 0.1250 | 7121 | c.-45 others(7130): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
KCNIP4_chr4_20723606_21953772 | 21594807 | G | GGCACATA others(7115): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0009 | 1 | 70 | 0.0143 | 7122 | c.61+ others(7141): Show |
KCNIP4 | ENSG00000185774.17 | transcript | ENST00000382152.7 | protein_coding | 1/8 | chr4 | TogoVar | |||||||
EXD3_chr9_137301896_137428162 | 137328267 | A | ATACACCT others(7116): Show |
intron_variant | MODIFIER | HG01975.hp1 | a0017 | a0017c0015 | a0017c0015t0001 | a0017c0015t0001g0073 | 1 | 73 | 0.0137 | 7123 | c.199 others(7142): Show |
EXD3 | ENSG00000187609.16 | transcript | ENST00000340951.9 | protein_coding | 17/21 | chr9 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(7117): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0126 | 1 | 55 | 0.0182 | 7124 | c.891 others(7139): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
EXD3_chr9_137301896_137428162 | 137328267 | A | ATACACCT others(7118): Show |
intron_variant | MODIFIER | NA18951.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0077 | 1 | 73 | 0.0137 | 7125 | c.199 others(7144): Show |
EXD3 | ENSG00000187609.16 | transcript | ENST00000340951.9 | protein_coding | 17/21 | chr9 | TogoVar | |||||||
EXD3_chr9_137301896_137428162 | 137328267 | A | ATACACCT others(7118): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0031 | 1 | 73 | 0.0137 | 7125 | c.199 others(7144): Show |
EXD3 | ENSG00000187609.16 | transcript | ENST00000340951.9 | protein_coding | 17/21 | chr9 | TogoVar |