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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(4793): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0020 | a0001c0020t0005 | a0001c0020t0005g0173 | 1 | 29 | 0.0345 | 4800 | c.109 others(4815): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(4793): Show |
intron_variant | MODIFIER | NA18967.hp1 NA18979.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0046 | 2 | 30 | 0.0667 | 4800 | c.109 others(4815): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(4793): Show |
intron_variant | MODIFIER | NA19011.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0249 | 1 | 29 | 0.0345 | 4800 | c.109 others(4815): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(4793): Show |
intron_variant | MODIFIER | HG01993.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0239 | 1 | 29 | 0.0345 | 4800 | c.109 others(4815): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045949 | C | TCAACACC others(4793): Show |
intron_variant | MODIFIER | NA18975.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0206 | 1 | 368 | 0.0027 | 4800 | c.109 others(4815): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | TogoVar | |||||||
BTNL9_chr5_181035266_181066521 | 181045949 | C | TCAACACC others(4793): Show |
intron_variant | MODIFIER | NA18964.hp2 NA18969.hp1 |
a0001a0002 | a0001c0001a0002c0012 | a0001c0001t0001a0002c0012t0002 | a0001c0001t0001g0222 a0002c0012t0002g0221 |
2 | 369 | 0.0054 | 4800 | c.109 others(4815): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | TogoVar | |||||||
BTNL9_chr5_181035266_181066521 | 181045949 | C | TCAACACC others(4793): Show |
intron_variant | MODIFIER | NA18947.hp1 NA19074.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012 | 2 | 369 | 0.0054 | 4800 | c.109 others(4815): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | TogoVar | |||||||
BTNL9_chr5_181035266_181066521 | 181045949 | C | TCAACACC others(4793): Show |
intron_variant | MODIFIER | NA18947.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0231 | 1 | 368 | 0.0027 | 4800 | c.109 others(4815): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | TogoVar | |||||||
CACNA1C_chr12_2047987_2702950 | 2256047 | C | CTTTACAA others(4793): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0032 | 1 | 2 | 0.5000 | 4800 | c.477 others(4821): Show |
CACNA1C | ENSG00000151067.23 | transcript | ENST00000399603.6 | protein_coding | 3/46 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585487 | C | CCTTTCCA others(4793): Show |
intron_variant | MODIFIER | NA19063.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 | 1 | 192 | 0.0052 | 4800 | c.215 others(4817): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(4794): Show |
intron_variant | MODIFIER | NA18992.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0189 | 1 | 29 | 0.0345 | 4801 | c.109 others(4816): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(4794): Show |
intron_variant | MODIFIER | HG01169.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0187 | 1 | 29 | 0.0345 | 4801 | c.109 others(4816): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(4794): Show |
intron_variant | MODIFIER | HG03831.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0247 | 1 | 29 | 0.0345 | 4801 | c.109 others(4816): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
MEGF6_chr1_3482951_3616508 | 3502017 | G | GCCTCACA others(4797): Show |
intron_variant | MODIFIER | HG03516.hp2 | a0086 | a0086c0098 | a0086c0098t0003 | a0086c0098t0003g0251 | 1 | 32 | 0.0313 | 4804 | c.218 others(4819): Show |
MEGF6 | ENSG00000162591.17 | transcript | ENST00000356575.9 | protein_coding | 17/36 | chr1 | TogoVar | |||||||
DYNC2I1_chr7_158851558_158951189 | 158915400 | C | CATTAAGG others(4799): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0174 | 1 | 267 | 0.0037 | 4806 | c.179 others(4825): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585658 | T | TTGAGGTA others(4800): Show |
intron_variant | MODIFIER | HG00408.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0211 | 1 | 13 | 0.0769 | 4807 | c.215 others(4824): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(4801): Show |
intron_variant | MODIFIER | NA18988.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0191 | 1 | 29 | 0.0345 | 4808 | c.109 others(4823): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DEAF1_chr11_639233_700222 | 642838 | C | CCAGGCGG others(4801): Show |
downstream_gene_variant | MODIFIER | HG02735.hp2 HG03017.hp2 |
a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0025 a0001c0004t0001g0029 |
2 | 145 | 0.0138 | 4808 | c.*17 others(4819): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1394 | chr11 | TogoVar | |||||||
DLEC1_chr3_38034208_38129025 | 38084560 | A | AGTAGTGG others(4801): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0275 | 1 | 158 | 0.0063 | 4808 | c.126 others(4825): Show |
DLEC1 | ENSG00000008226.20 | transcript | ENST00000308059.11 | protein_coding | 7/36 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
DRD4_chr11_632269_645706 | 642838 | C | CCAGGCGG others(4801): Show |
downstream_gene_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0018 | a0001c0018t0001 | a0001c0018t0001g0008 | 1 | 172 | 0.0058 | 4808 | c.*22 others(4819): Show |
DRD4 | ENSG00000069696.7 | transcript | ENST00000176183.6 | protein_coding | 2133 | chr11 | TogoVar | |||||||
HHAT_chr1_210323902_210681290 | 210653965 | G | GGAATAGT others(4801): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0128 | 1 | 42 | 0.0238 | 4808 | c.139 others(4829): Show |
HHAT | ENSG00000054392.13 | transcript | ENST00000261458.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
HHAT_chr1_210323902_210681290 | 210653965 | G | GGAATAGT others(4803): Show |
intron_variant | MODIFIER | HG01257.hp1 HG01258.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0089 a0001c0001t0001g0096 |
2 | 43 | 0.0465 | 4810 | c.139 others(4831): Show |
HHAT | ENSG00000054392.13 | transcript | ENST00000261458.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
HHAT_chr1_210323902_210681290 | 210653965 | G | GGAATAGT others(4803): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0212 | 1 | 42 | 0.0238 | 4810 | c.139 others(4831): Show |
HHAT | ENSG00000054392.13 | transcript | ENST00000261458.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PTPRD_chr9_8309246_10618002 | 9008027 | C | CTCATCAT others(4804): Show |
intron_variant | MODIFIER | HG00642.hp1 HG01243.hp2 HG02257.hp1 others(3): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0024a0001c0003t0023a0001c0004t0018others(3): Show | a0001c0001t0024g0032 a0001c0003t0023g0031 a0001c0004t0018g0015 others(3): Show |
6 | 23 | 0.2609 | 4811 | c.-10 others(4832): Show |
PTPRD | ENSG00000153707.19 | transcript | ENST00000381196.9 | protein_coding | 11/45 | chr9 | TogoVar | |||||||
C2orf80_chr2_208160347_208195030 | 208176941 | C | CCGTATAC others(4805): Show |
intron_variant | MODIFIER | NA19000.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0106 | 1 | 233 | 0.0043 | 4812 | c.366 others(4829): Show |
C2orf80 | ENSG00000188674.11 | transcript | ENST00000341287.9 | protein_coding | 6/8 | chr2 | TogoVar | |||||||
EPPK1_chr8_143852324_143883467 | 143865718 | G | GTCTGGGC others(4805): Show |
disruptive_inframe_insertion | MODERATE | HG04228.hp1 | a0132 | a0132c0081 | a0132c0081t0002 | a0132c0081t0002g0200 | 1 | 287 | 0.0035 | 4812 | c.753 others(4821): Show |
p.Pro others(4827): Show |
EPPK1 | ENSG00000261150.3 | transcript | ENST00000615648.2 | protein_coding | 2/2 | 7610/16005 | 7535/15267 | 2512/5088 | chr8 | TogoVar | |||
EPPK1_chr8_143852324_143883467 | 143865718 | G | GTCTGGGC others(4805): Show |
disruptive_inframe_insertion | MODERATE | HG01243.hp2 | a0072 | a0072c0190 | a0072c0190t0002 | a0072c0190t0002g0330 | 1 | 287 | 0.0035 | 4812 | c.753 others(4821): Show |
p.Pro others(4827): Show |
EPPK1 | ENSG00000261150.3 | transcript | ENST00000615648.2 | protein_coding | 2/2 | 7610/16005 | 7535/15267 | 2512/5088 | chr8 | TogoVar | |||
HHAT_chr1_210323902_210681290 | 210653965 | G | GGAATAGT others(4805): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 42 | 0.0238 | 4812 | c.139 others(4833): Show |
HHAT | ENSG00000054392.13 | transcript | ENST00000261458.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4807): Show |
upstream_gene_variant | MODIFIER | HG01346.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0023 | 1 | 8 | 0.1250 | 4814 | c.-45 others(4823): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
PTPRD_chr9_8309246_10618002 | 9008027 | C | CTCATCAT others(4807): Show |
intron_variant | MODIFIER | HG01981.hp1 | a0003 | a0003c0008 | a0003c0008t0008 | a0003c0008t0008g0003 | 1 | 18 | 0.0556 | 4814 | c.-10 others(4835): Show |
PTPRD | ENSG00000153707.19 | transcript | ENST00000381196.9 | protein_coding | 11/45 | chr9 | TogoVar | |||||||
EPPK1_chr8_143852324_143883467 | 143866194 | T | TGTGCACG others(4808): Show |
conservative_inframe_insertion | MODERATE | HG01099.hp2 | a0063 | a0063c0195 | a0063c0195t0006 | a0063c0195t0006g0235 | 1 | 422 | 0.0024 | 4815 | c.705 others(4824): Show |
p.His others(4830): Show |
EPPK1 | ENSG00000261150.3 | transcript | ENST00000615648.2 | protein_coding | 2/2 | 7134/16005 | 7059/15267 | 2353/5088 | chr8 | TogoVar | |||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(4809): Show |
intron_variant | MODIFIER | HG02273.hp2 | a0005 | a0005c0015 | a0005c0015t0001 | a0005c0015t0001g0064 | 1 | 34 | 0.0294 | 4816 | c.299 others(4831): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(4809): Show |
intron_variant | MODIFIER | HG01346.hp1 | a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0194 | 1 | 34 | 0.0294 | 4816 | c.299 others(4831): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
DHRSX_chrX_2214506_2505976 | 2320508 | T | TTGGTCTC others(4811): Show |
intron_variant | MODIFIER | HG02055.hp1 | a0005 | a0005c0008 | a0005c0008t0006 | a0005c0008t0006g0032 | 1 | 2 | 0.5000 | 4818 | c.287 others(4837): Show |
DHRSX | ENSG00000169084.15 | transcript | ENST00000334651.11 | protein_coding | 3/6 | chrX | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4811): Show |
upstream_gene_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0001 | a0001c0001t0028 | a0001c0001t0028g0037 | 1 | 8 | 0.1250 | 4818 | c.-45 others(4827): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
DHRSX_chrX_2214506_2505976 | 2320508 | T | TTGGTCTC others(4812): Show |
intron_variant | MODIFIER | HG01261.hp1 | a0003 | a0003c0003 | a0003c0003t0013 | a0003c0003t0013g0002 | 1 | 2 | 0.5000 | 4819 | c.287 others(4838): Show |
DHRSX | ENSG00000169084.15 | transcript | ENST00000334651.11 | protein_coding | 3/6 | chrX | TogoVar | |||||||
FAM120B_chr6_170301758_170412067 | 170377914 | C | CGCCCGGG others(4812): Show |
intron_variant | MODIFIER | HG01123.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0141 | 1 | 152 | 0.0066 | 4819 | c.228 others(4840): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
DHRSX_chrX_2214506_2505976 | 2320508 | T | TTGGTCTC others(4813): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0002 | a0002c0005 | a0002c0005t0004 | a0002c0005t0004g0030 | 1 | 2 | 0.5000 | 4820 | c.287 others(4839): Show |
DHRSX | ENSG00000169084.15 | transcript | ENST00000334651.11 | protein_coding | 3/6 | chrX | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1222715 | T | TGCGTCTC others(4813): Show |
intron_variant | MODIFIER | HG01975.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0006 | 1 | 28 | 0.0357 | 4820 | c.719 others(4839): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TMEM242_chr6_157284025_157328519 | 157311844 | C | CATAGTGC others(4813): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0315 | 1 | 332 | 0.0030 | 4820 | c.327 others(4837): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311844 | C | CATAGTGC others(4813): Show |
intron_variant | MODIFIER | HG01934.hp2 HG02451.hp2 |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0316 a0001c0001t0008g0317 |
2 | 333 | 0.0060 | 4820 | c.327 others(4837): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311844 | C | CATAGTGC others(4813): Show |
intron_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0318 | 1 | 332 | 0.0030 | 4820 | c.327 others(4837): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
HNRNPCL1_chr1_12842377_12853720 | 12847054 | A | ACACCGCA others(4814): Show |
downstream_gene_variant | MODIFIER | HG03195.hp2 | a0005 | a0005c0005 | a0005c0005t0008 | a0005c0005t0008g0012 | 1 | 332 | 0.0030 | 4821 | c.*35 others(4830): Show |
HNRNPCL1 | ENSG00000179172.10 | transcript | ENST00000317869.7 | protein_coding | 322 | chr1 | TogoVar | |||||||
HHAT_chr1_210323902_210681290 | 210653947 | C | CGGGAATA others(4816): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0199 | 1 | 266 | 0.0038 | 4823 | c.139 others(4844): Show |
HHAT | ENSG00000054392.13 | transcript | ENST00000261458.8 | protein_coding | 11/11 | chr1 | TogoVar | |||||||
HNRNPCL1_chr1_12842377_12853720 | 12847054 | A | ACACCGCA others(4816): Show |
downstream_gene_variant | MODIFIER | HG00642.hp2 | a0005 | a0005c0005 | a0005c0005t0008 | a0005c0005t0008g0012 | 1 | 332 | 0.0030 | 4823 | c.*35 others(4832): Show |
HNRNPCL1 | ENSG00000179172.10 | transcript | ENST00000317869.7 | protein_coding | 322 | chr1 | TogoVar | |||||||
HHAT_chr1_210323902_210681290 | 210653965 | G | GGAATAGT others(4817): Show |
intron_variant | MODIFIER | NA18977.hp1 NA18992.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0005a0001c0002t0005 | a0001c0001t0005g0217 a0001c0002t0005g0063 |
2 | 43 | 0.0465 | 4824 | c.139 others(4845): Show |
HHAT | ENSG00000054392.13 | transcript | ENST00000261458.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
HNRNPCL1_chr1_12842377_12853720 | 12847054 | A | ACACCACA others(4817): Show |
downstream_gene_variant | MODIFIER | NA18946.hp2 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0004 | 1 | 332 | 0.0030 | 4824 | c.*35 others(4833): Show |
HNRNPCL1 | ENSG00000179172.10 | transcript | ENST00000317869.7 | protein_coding | 322 | chr1 | TogoVar | |||||||
HNRNPCL1_chr1_12842377_12853720 | 12847054 | A | ACACCACA others(4817): Show |
downstream_gene_variant | MODIFIER | NA19005.hp1 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0004 | 1 | 332 | 0.0030 | 4824 | c.*35 others(4833): Show |
HNRNPCL1 | ENSG00000179172.10 | transcript | ENST00000317869.7 | protein_coding | 322 | chr1 | TogoVar | |||||||
HNRNPCL1_chr1_12842377_12853720 | 12847054 | A | ACACCACA others(4817): Show |
downstream_gene_variant | MODIFIER | NA19076.hp2 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0004 | 1 | 332 | 0.0030 | 4824 | c.*35 others(4833): Show |
HNRNPCL1 | ENSG00000179172.10 | transcript | ENST00000317869.7 | protein_coding | 322 | chr1 | TogoVar | |||||||
HNRNPCL1_chr1_12842377_12853720 | 12847054 | A | ACACCACA others(4818): Show |
downstream_gene_variant | MODIFIER | HG02135.hp2 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0004 | 1 | 332 | 0.0030 | 4825 | c.*35 others(4834): Show |
HNRNPCL1 | ENSG00000179172.10 | transcript | ENST00000317869.7 | protein_coding | 322 | chr1 | TogoVar |