regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CECR2_chr22_17364460_17563151 | 17533700 | T | TTTTGTTT others(5): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0002 | a0002c0010 | a0002c0010t0041 | a0002c0010t0041g0269 | 1 | 324 | 0.0031 | 12 | c.110 others(31): Show |
CECR2 | ENSG00000099954.19 | transcript | ENST00000262608.13 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
CECR2_chr22_17364460_17563151 | 17545374 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG02717.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0009 | a0001c0001t0002g0080a0001c0001t0002g0215a0001c0001t0009g0187 | 3 | 324 | 0.0093 | 12 | c.286 others(31): Show |
CECR2 | ENSG00000099954.19 | transcript | ENST00000262608.13 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
CECR2_chr22_17364460_17563151 | 17550132 | C | CTTTATTT others(5): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0009 | a0001c0009t0075 | a0001c0009t0075g0195 | 1 | 324 | 0.0031 | 12 | c.427 others(29): Show |
CECR2 | ENSG00000099954.19 | transcript | ENST00000262608.13 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
CECR2_chr22_17364460_17563151 | 17552774 | G | GTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG01243.hp2 HG01884.hp2 HG02647.hp2 others(1): Show |
a0001a0014 | a0001c0001a0014c0021 | a0001c0001t0006a0001c0001t0017a0001c0001t0020others(1): Show | a0001c0001t0006g0003a0001c0001t0017g0312a0001c0001t0020g0051others(1): Show | 4 | 324 | 0.0124 | 12 | c.439 others(27): Show |
CECR2 | ENSG00000099954.19 | transcript | ENST00000262608.13 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
CELA1_chr12_51323442_51351679 | 51324943 | C | CAAATAAA others(5): Show |
downstream_gene_variant | MODIFIER | HG02572.hp1 HG03098.hp1 |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0002a0002c0006t0001 | a0001c0001t0002g0144a0002c0006t0001g0016 | 2 | 406 | 0.0049 | 12 | c.*36 others(23): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3498 | chr12 | TogoVar | ||||||
CELA1_chr12_51323442_51351679 | 51347994 | C | CAAAAAAA others(5): Show |
upstream_gene_variant | MODIFIER | HG02615.hp2 HG03041.hp1 |
a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0086a0002c0004t0002g0087 | 2 | 406 | 0.0049 | 12 | c.-13 others(23): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1316 | chr12 | TogoVar | ||||||
CELA1_chr12_51323442_51351679 | 51347995 | A | AAAATAAA others(5): Show |
upstream_gene_variant | MODIFIER | HG00280.hp1 HG02055.hp2 HG02074.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0024others(3): Show | 6 | 406 | 0.0148 | 12 | c.-13 others(23): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1317 | chr12 | TogoVar | ||||||
CELA1_chr12_51323442_51351679 | 51348043 | T | TAAATAAA others(5): Show |
upstream_gene_variant | MODIFIER | HG02258.hp1 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | 406 | 0.0049 | 12 | c.-14 others(23): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1365 | chr12 | TogoVar | ||||||
CELA2B_chr1_15471104_15496395 | 15478201 | C | CATATATA others(5): Show |
intron_variant | MODIFIER | NA18993.hp1 NA19072.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | 414 | 0.0048 | 12 | c.129 others(29): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CELA2B_chr1_15471104_15496395 | 15490220 | A | ATATCTAT others(5): Show |
intron_variant | MODIFIER | NA18973.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0131 | 1 | 414 | 0.0024 | 12 | c.793 others(29): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CELA3A_chr1_21996657_22017542 | 22008152 | C | CTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG02738.hp1 HG03927.hp1 HG04115.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0079a0001c0003t0001g0080a0001c0003t0001g0088 | 3 | 419 | 0.0072 | 12 | c.642 others(27): Show |
CELA3A | ENSG00000142789.20 | transcript | ENST00000290122.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CELA3B_chr1_21972022_21994354 | 21972454 | C | CAAAAAAA others(5): Show |
upstream_gene_variant | MODIFIER | HG00544.hp1 HG00733.hp2 HG01952.hp2 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(10): Show | 21 | 444 | 0.0473 | 12 | c.-45 others(23): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4567 | chr1 | TogoVar | ||||||
CELA3B_chr1_21972022_21994354 | 21983548 | A | AATGATGA others(5): Show |
intron_variant | MODIFIER | HG01515.hp2 HG01517.hp1 |
a0000 | a0000c0018a0000c0019 | a0000c0018t0002a0000c0019t0002 | a0000c0018t0002g0173a0000c0019t0002g0174 | 2 | 444 | 0.0045 | 12 | c.363 others(27): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CELA3B_chr1_21972022_21994354 | 21992488 | A | AGAACCAG others(5): Show |
downstream_gene_variant | MODIFIER | NA19009.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107 | 1 | 444 | 0.0023 | 12 | c.*32 others(23): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3135 | chr1 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47489935 | G | GTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG02486.hp1 HG03540.hp2 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0019 | a0001c0001t0004g0006a0001c0001t0004g0008a0001c0001t0019g0185 | 3 | 340 | 0.0088 | 12 | c.72- others(25): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47533631 | A | AATACATA others(5): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0059 | 1 | 340 | 0.0029 | 12 | c.-15 others(33): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47533635 | A | AATAAATA others(5): Show |
intron_variant | MODIFIER | NA18939.hp2 NA18953.hp2 NA19002.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0100others(1): Show | 4 | 340 | 0.0118 | 12 | c.-15 others(33): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47533635 | A | AATACATA others(5): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(60): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0002g0283others(60): Show | 63 | 340 | 0.1853 | 12 | c.-15 others(33): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47541686 | C | CAAAGAAA others(5): Show |
intron_variant | MODIFIER | HG02922.hp2 HG03453.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | 340 | 0.0059 | 12 | c.-15 others(33): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47547065 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG00741.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0118 | 1 | 340 | 0.0029 | 12 | c.-15 others(31): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47553014 | C | CGCTGCCT others(5): Show |
5_prime_UTR_variant | MODIFIER | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 10 | 340 | 0.0294 | 12 | c.-18 others(21): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/15 | 53492 | chr11 | TogoVar | |||||
CELF1_chr11_47460937_47558132 | 47557524 | C | CTTTTTTT others(5): Show |
upstream_gene_variant | MODIFIER | HG02451.hp1 HG02976.hp2 HG03098.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0024a0001c0003t0011 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0309 | 3 | 340 | 0.0088 | 12 | c.-46 others(23): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4393 | chr11 | TogoVar | ||||||
CELF2_chr10_11012872_11341675 | 11025237 | G | GTATATAT others(5): Show |
intron_variant | MODIFIER | HG00741.hp2 HG01255.hp2 HG02080.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0008a0001c0001t0013a0001c0002t0018others(2): Show | a0001c0001t0008g0081a0001c0001t0013g0083a0001c0002t0018g0084others(2): Show | 5 | 194 | 0.0258 | 12 | c.74+ others(27): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11025239 | G | GTATATAT others(5): Show |
intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0111 | 1 | 194 | 0.0052 | 12 | c.74+ others(27): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11025239 | G | GTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG01952.hp2 HG03490.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0004 | a0001c0001t0001g0030a0001c0003t0004g0029 | 2 | 194 | 0.0103 | 12 | c.74+ others(27): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11032146 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02258.hp1 HG02451.hp1 |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0003a0001c0003t0004a0001c0004t0001 | a0001c0001t0003g0149a0001c0003t0004g0024a0001c0004t0001g0152 | 3 | 194 | 0.0155 | 12 | c.74+ others(29): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11054507 | G | GTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG01433.hp2 HG01891.hp2 HG02615.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(7): Show | a0001c0001t0003g0038a0001c0001t0005g0044a0001c0001t0007g0042others(9): Show | 12 | 194 | 0.0619 | 12 | c.74+ others(29): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11086578 | T | TAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG01433.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0026a0001c0002t0003a0001c0003t0001others(2): Show | a0001c0001t0026g0065a0001c0002t0003g0048a0001c0003t0001g0046others(2): Show | 5 | 194 | 0.0258 | 12 | c.74+ others(29): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11106207 | T | TTTTATTT others(5): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(7): Show | a0001c0001t0001g0026a0001c0001t0001g0189a0001c0001t0006g0127others(10): Show | 13 | 194 | 0.0670 | 12 | c.75- others(29): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11119864 | T | TCTCCCCC others(5): Show |
intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0071 | 1 | 194 | 0.0052 | 12 | c.75- others(29): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11148843 | A | AACACACA others(5): Show |
intron_variant | MODIFIER | HG01952.hp1 HG01978.hp2 NA19086.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0008a0001c0002t0015 | a0001c0001t0004g0138a0001c0002t0008g0028a0001c0002t0015g0143 | 3 | 194 | 0.0155 | 12 | c.75- others(29): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11197025 | A | AAAAGAAA others(5): Show |
intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0096 | 1 | 194 | 0.0052 | 12 | c.272 others(31): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11197083 | G | GAAAGAAG others(5): Show |
intron_variant | MODIFIER | HG02896.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0005a0001c0001t0019a0001c0001t0036others(2): Show | a0001c0001t0005g0044a0001c0001t0019g0051a0001c0001t0036g0016others(2): Show | 5 | 194 | 0.0258 | 12 | c.272 others(31): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11202901 | A | ATCTCTCT others(5): Show |
intron_variant | MODIFIER | NA18522.hp1 NA19090.hp2 |
a0001 | a0001c0005a0001c0006 | a0001c0005t0053a0001c0006t0042 | a0001c0005t0053g0185a0001c0006t0042g0190 | 2 | 194 | 0.0103 | 12 | c.272 others(31): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11262940 | C | CTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG00735.hp2 HG00741.hp2 HG01517.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0013a0001c0001t0043others(1): Show | a0001c0001t0001g0177a0001c0001t0013g0083a0001c0001t0043g0008others(1): Show | 4 | 194 | 0.0206 | 12 | c.539 others(29): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11280989 | C | CGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0050others(6): Show | a0001c0001t0001g0123a0001c0001t0003g0071a0001c0001t0050g0173others(7): Show | 10 | 194 | 0.0516 | 12 | c.841 others(29): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11285826 | G | GGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG02698.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0072 | 1 | 194 | 0.0052 | 12 | c.842 others(29): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11323424 | A | AAATAATA others(5): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(20): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(11): Show | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0114others(20): Show | 23 | 194 | 0.1186 | 12 | c.129 others(31): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF3_chr1_151695058_151721803 | 151696461 | T | TTTTCTTT others(5): Show |
downstream_gene_variant | MODIFIER | HG02148.hp2 HG02717.hp2 HG03942.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(2): Show | a0001c0001t0003g0003a0001c0001t0003g0050a0001c0001t0003g0124others(4): Show | 12 | 432 | 0.0278 | 12 | c.*69 others(23): Show |
CELF3 | ENSG00000159409.15 | transcript | ENST00000290583.9 | protein_coding | 3596 | chr1 | TogoVar | ||||||
CELF3_chr1_151695058_151721803 | 151696498 | T | TTTCGTTC others(5): Show |
downstream_gene_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG02148.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0015others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0026others(4): Show | 14 | 432 | 0.0324 | 12 | c.*69 others(23): Show |
CELF3 | ENSG00000159409.15 | transcript | ENST00000290583.9 | protein_coding | 3559 | chr1 | TogoVar | ||||||
CELF3_chr1_151695058_151721803 | 151696498 | T | TTTCTTTC others(5): Show |
downstream_gene_variant | MODIFIER | HG00438.hp2 HG01175.hp1 HG02486.hp2 others(9): Show |
a0001a0003 | a0001c0001a0001c0004a0003c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(4): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0003g0003others(7): Show | 12 | 432 | 0.0278 | 12 | c.*69 others(23): Show |
CELF3 | ENSG00000159409.15 | transcript | ENST00000290583.9 | protein_coding | 3559 | chr1 | TogoVar | ||||||
CELF3_chr1_151695058_151721803 | 151696522 | G | GTTCTTTC others(5): Show |
downstream_gene_variant | MODIFIER | HG00438.hp1 HG00639.hp1 HG01099.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0007a0001c0001t0051 | a0001c0001t0006g0013a0001c0001t0006g0038a0001c0001t0007g0006others(4): Show | 10 | 432 | 0.0232 | 12 | c.*69 others(23): Show |
CELF3 | ENSG00000159409.15 | transcript | ENST00000290583.9 | protein_coding | 3535 | chr1 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37338759 | C | CGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG02818.hp2 NA19066.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0016 | a0001c0001t0006g0017a0001c0001t0016g0070 | 2 | 184 | 0.0109 | 12 | c.370 others(31): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 2/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37380792 | A | AATCCATC others(5): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(59): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0081others(59): Show | 62 | 184 | 0.3370 | 12 | c.370 others(31): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 2/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37444617 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0005a0001c0001t0017a0001c0001t0040others(2): Show | a0001c0001t0005g0140a0001c0001t0017g0021a0001c0001t0040g0097others(2): Show | 5 | 184 | 0.0272 | 12 | c.369 others(31): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 2/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37444652 | A | ACACACAC others(5): Show |
intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0040 | 1 | 184 | 0.0054 | 12 | c.369 others(31): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 2/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37470836 | C | CTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0001 | 1 | 184 | 0.0054 | 12 | c.369 others(31): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 2/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37470890 | C | CAGAGAGA others(5): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0002 | a0001c0002t0024 | a0001c0002t0024g0181 | 1 | 184 | 0.0054 | 12 | c.369 others(31): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 2/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37522128 | C | CCCAGCAT others(5): Show |
intron_variant | MODIFIER | HG02486.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0012a0001c0001t0023a0001c0001t0039others(1): Show | a0001c0001t0012g0032a0001c0001t0023g0121a0001c0001t0039g0122others(1): Show | 4 | 184 | 0.0217 | 12 | c.287 others(31): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 1/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37547160 | G | GGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG02074.hp1 HG02486.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0023 | a0001c0001t0002g0133a0001c0001t0023g0121 | 2 | 184 | 0.0109 | 12 | c.286 others(31): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 1/12 | chr18 | TogoVar |