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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CELF1_chr11_47460937_47558132 | 47508569 | TAAA | T | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0019others(179): Show | 182 | 340 | 0.5353 | -3 | c.-15 others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47525390 | CCAA | C | intron_variant | MODIFIER | NA18961.hp1 NA18972.hp1 NA18986.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0022a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | 340 | 0.0177 | -3 | c.-15 others(24): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47531474 | TAGG | T | intron_variant | MODIFIER | HG00558.hp2 NA18964.hp2 NA19062.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009 | a0001c0001t0001g0177a0001c0001t0001g0182a0001c0001t0001g0199others(1): Show | 4 | 340 | 0.0118 | -3 | c.-15 others(24): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47540885 | AAAC | A | intron_variant | MODIFIER | HG02293.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0024a0001c0003t0011 | a0001c0001t0001g0132a0001c0001t0001g0319a0001c0001t0024g0320others(2): Show | 5 | 340 | 0.0147 | -3 | c.-15 others(24): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47545915 | ATTT | A | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(1): Show | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0130others(21): Show | 24 | 340 | 0.0706 | -3 | c.-15 others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47547065 | CAAA | C | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(4): Show | a0001c0001t0002g0077a0001c0001t0003g0014a0001c0001t0003g0015others(60): Show | 63 | 340 | 0.1853 | -3 | c.-15 others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF1_chr11_47460937_47558132 | 47547681 | AAAG | A | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(88): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(5): Show | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(88): Show | 91 | 340 | 0.2677 | -3 | c.-15 others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
CELF2_chr10_11012872_11341675 | 11040737 | GTTC | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(34): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(23): Show | a0001c0001t0001g0010a0001c0001t0001g0104a0001c0001t0001g0108others(34): Show | 37 | 194 | 0.1907 | -3 | c.74+ others(20): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11061919 | TCTC | T | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0018a0001c0003t0016 | a0001c0002t0018g0135a0001c0003t0016g0003 | 2 | 194 | 0.0103 | -3 | c.74+ others(20): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11081067 | ATTC | A | intron_variant | MODIFIER | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(25): Show | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0108others(39): Show | 42 | 194 | 0.2165 | -3 | c.74+ others(20): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11103331 | ATTT | A | intron_variant | MODIFIER | HG01517.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0017others(6): Show | a0001c0001t0001g0161a0001c0001t0003g0071a0001c0001t0003g0149others(8): Show | 11 | 194 | 0.0567 | -3 | c.75- others(20): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11107518 | TTGA | T | intron_variant | MODIFIER | HG02109.hp1 HG03540.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0010a0001c0002t0002g0061 | 2 | 194 | 0.0103 | -3 | c.75- others(20): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | chr10 | TogoVar | ||||||
CELF2_chr10_11012872_11341675 | 11144900 | GAAA | G | intron_variant | MODIFIER | HG01074.hp2 HG01081.hp2 HG02109.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0010a0001c0002t0003others(4): Show | a0001c0001t0001g0123a0001c0001t0010g0015a0001c0002t0003g0165others(4): Show | 7 | 194 | 0.0361 | -3 | c.75- others(20): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11187604 | CTCT | C | intron_variant | MODIFIER | HG01074.hp1 HG02615.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0027 | a0001c0002t0001g0088a0001c0004t0027g0066 | 2 | 194 | 0.0103 | -3 | c.271 others(22): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11190775 | TAAA | T | intron_variant | MODIFIER | HG01081.hp2 HG01517.hp2 HG02145.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0017a0001c0001t0022a0001c0002t0001others(3): Show | a0001c0001t0017g0153a0001c0001t0022g0022a0001c0002t0001g0054others(3): Show | 6 | 194 | 0.0309 | -3 | c.271 others(22): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11212737 | GTTT | G | intron_variant | MODIFIER | HG02809.hp1 HG02965.hp1 HG03130.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0019a0001c0001t0021a0001c0001t0025others(5): Show | a0001c0001t0019g0047a0001c0001t0021g0076a0001c0001t0025g0012others(5): Show | 8 | 194 | 0.0412 | -3 | c.272 others(20): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11228718 | CAAA | C | intron_variant | MODIFIER | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0002others(3): Show | a0001c0001t0001g0010a0001c0001t0003g0171a0001c0002t0002g0011others(4): Show | 7 | 194 | 0.0361 | -3 | c.354 others(22): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11234679 | CAAA | C | intron_variant | MODIFIER | HG02486.hp1 HG02559.hp1 HG03041.hp2 others(2): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0002t0002a0001c0002t0023others(2): Show | a0001c0002t0001g0054a0001c0002t0002g0052a0001c0002t0023g0053others(2): Show | 5 | 194 | 0.0258 | -3 | c.355 others(22): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11256569 | GCTT | G | intron_variant | MODIFIER | HG00099.hp2 HG00621.hp1 HG01074.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0026a0001c0001t0028others(2): Show | a0001c0001t0001g0092a0001c0001t0026g0065a0001c0001t0028g0192others(5): Show | 8 | 194 | 0.0412 | -3 | c.404 others(20): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11257336 | CAAA | C | intron_variant | MODIFIER | HG00639.hp1 HG00673.hp2 HG00735.hp1 others(33): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0001g0180others(33): Show | 36 | 194 | 0.1856 | -3 | c.404 others(18): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11269685 | TCTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(49): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(20): Show | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0085others(49): Show | 52 | 194 | 0.2680 | -3 | c.619 others(18): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11320586 | ACAT | A | intron_variant | MODIFIER | HG00741.hp2 HG01099.hp2 HG04228.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0013a0001c0004t0013 | a0001c0001t0013g0083a0001c0001t0013g0178a0001c0004t0013g0074 | 3 | 194 | 0.0155 | -3 | c.109 others(20): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF2_chr10_11012872_11341675 | 11323424 | AAAT | A | intron_variant | MODIFIER | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0050a0001c0002t0002a0001c0002t0005others(7): Show | a0001c0001t0050g0173a0001c0002t0002g0052a0001c0002t0005g0005others(9): Show | 12 | 194 | 0.0619 | -3 | c.129 others(22): Show |
CELF2 | ENSG00000048740.19 | transcript | ENST00000633077.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CELF3_chr1_151695058_151721803 | 151699318 | TCTC | T | downstream_gene_variant | MODIFIER | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0009a0001c0001t0049a0002c0002t0009 | a0001c0001t0009g0021a0001c0001t0009g0092a0001c0001t0049g0133others(1): Show | 9 | 432 | 0.0208 | -3 | c.*41 others(14): Show |
CELF3 | ENSG00000159409.15 | transcript | ENST00000290583.9 | protein_coding | 739 | chr1 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37275734 | GTCC | G | intron_variant | MODIFIER | HG01109.hp1 HG02055.hp2 HG03130.hp1 |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0031 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0031g0034 | 3 | 184 | 0.0163 | -3 | c.449 others(18): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 3/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37292035 | TAAA | T | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0050a0001c0001t0001g0065a0001c0001t0001g0071others(109): Show | 112 | 184 | 0.6087 | -3 | c.449 others(22): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 3/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37362281 | GCTC | G | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(37): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0081others(37): Show | 40 | 184 | 0.2174 | -3 | c.370 others(22): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 2/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37408501 | GCGC | G | intron_variant | MODIFIER | HG03130.hp1 NA21309.hp1 |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0031 | a0001c0001t0007g0061a0001c0001t0031g0034 | 2 | 184 | 0.0109 | -3 | c.369 others(22): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 2/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37498331 | CTCT | C | intron_variant | MODIFIER | HG01978.hp1 HG02055.hp1 HG02257.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0001t0009a0001c0001t0018others(5): Show | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0041others(9): Show | 12 | 184 | 0.0652 | -3 | c.287 others(22): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 1/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37500528 | TTTC | T | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(58): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0075others(58): Show | 61 | 184 | 0.3315 | -3 | c.287 others(22): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 1/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37505056 | CAGG | C | intron_variant | MODIFIER | HG01258.hp2 HG01261.hp2 NA18964.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0005a0001c0002t0010 | a0001c0001t0002g0095a0001c0001t0005g0105a0001c0002t0010g0094 | 3 | 184 | 0.0163 | -3 | c.287 others(22): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 1/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37544152 | CTTT | C | intron_variant | MODIFIER | HG02257.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(4): Show | a0001c0001t0001g0158a0001c0001t0004g0014a0001c0001t0005g0110others(6): Show | 9 | 184 | 0.0489 | -3 | c.286 others(22): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 1/12 | chr18 | TogoVar | ||||||
CELF4_chr18_37238040_37570798 | 37569868 | TCTC | T | upstream_gene_variant | MODIFIER | HG02572.hp1 HG02818.hp2 HG02897.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0009 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0009g0015others(1): Show | 4 | 184 | 0.0217 | -3 | c.-42 others(14): Show |
CELF4 | ENSG00000101489.20 | transcript | ENST00000420428.7 | protein_coding | 4071 | chr18 | TogoVar | ||||||
CELF5_chr19_3219661_3302076 | 3242964 | AAAT | A | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(128): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(127): Show | 131 | 262 | 0.5000 | -3 | c.260 others(20): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CELF5_chr19_3219661_3302076 | 3256534 | TTTA | T | intron_variant | MODIFIER | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0052others(89): Show | 92 | 262 | 0.3512 | -3 | c.342 others(20): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CELF5_chr19_3219661_3302076 | 3263805 | TGAA | T | intron_variant | MODIFIER | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
a0001 | a0001c0001a0001c0003a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0052a0001c0001t0001g0204a0001c0001t0002g0011others(11): Show | 14 | 262 | 0.0534 | -3 | c.343 others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CELF5_chr19_3219661_3302076 | 3287034 | CAAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(39): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(5): Show | a0001c0001t0001g0146a0001c0001t0004g0010a0001c0001t0004g0071others(39): Show | 42 | 262 | 0.1603 | -3 | c.118 others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CELF5_chr19_3219661_3302076 | 3290563 | CTTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(61): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0146a0001c0001t0001g0166a0001c0001t0001g0206others(61): Show | 64 | 262 | 0.2443 | -3 | c.133 others(20): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CELF5_chr19_3219661_3302076 | 3297533 | CAAA | C | downstream_gene_variant | MODIFIER | HG00099.hp2 HG02615.hp2 HG02723.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0122others(4): Show | 7 | 262 | 0.0267 | -3 | c.*81 others(12): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 458 | chr19 | TogoVar | ||||||
CELF5_chr19_3219661_3302076 | 3299506 | TTCC | T | downstream_gene_variant | MODIFIER | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0138a0001c0001t0002g0177a0001c0001t0003g0055others(7): Show | 10 | 262 | 0.0382 | -3 | c.*27 others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2431 | chr19 | TogoVar | ||||||
CELF5_chr19_3219661_3302076 | 3299515 | CTCT | C | downstream_gene_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0001g0100others(9): Show | 12 | 262 | 0.0458 | -3 | c.*27 others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2440 | chr19 | TogoVar | ||||||
CELF5_chr19_3219661_3302076 | 3299578 | TTTC | T | downstream_gene_variant | MODIFIER | HG02486.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0176others(1): Show | 4 | 262 | 0.0153 | -3 | c.*28 others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2503 | chr19 | TogoVar | ||||||
CELF5_chr19_3219661_3302076 | 3301009 | GTTT | G | downstream_gene_variant | MODIFIER | HG02055.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(1): Show | a0001c0001t0002g0211a0001c0001t0004g0234a0001c0001t0005g0152others(3): Show | 6 | 262 | 0.0229 | -3 | c.*42 others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3934 | chr19 | TogoVar | ||||||
CELF6_chr15_72279727_72325157 | 72320469 | TCCC | T | upstream_gene_variant | MODIFIER | HG01106.hp1 HG01496.hp1 HG01891.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(5): Show | 10 | 300 | 0.0333 | -3 | c.-59 others(12): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 313 | chr15 | TogoVar | ||||||
CELF6_chr15_72279727_72325157 | 72325154 | TTTC | T | upstream_gene_variant | MODIFIER | HG00140.hp2 HG01346.hp2 HG02257.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(5): Show | 10 | 300 | 0.0333 | -3 | c.-52 others(14): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 4998 | chr15 | TogoVar | ||||||
CELSR1_chr22_46356174_46542620 | 46356687 | TCAG | T | downstream_gene_variant | MODIFIER | HG02615.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
a0002a0026a0047others(2): Show | a0002c0012a0002c0016a0002c0051others(4): Show | a0002c0012t0003a0002c0016t0003a0002c0051t0003others(4): Show | a0002c0012t0003g0012a0002c0016t0003g0025a0002c0051t0003g0053others(4): Show | 7 | 104 | 0.0673 | -3 | c.*65 others(14): Show |
CELSR1 | ENSG00000075275.18 | transcript | ENST00000674500.2 | protein_coding | 4486 | chr22 | TogoVar | ||||||
CELSR1_chr22_46356174_46542620 | 46365947 | GGGT | G | intron_variant | MODIFIER | HG00642.hp2 HG00735.hp2 HG01106.hp1 others(16): Show |
a0003a0005a0007others(12): Show | a0003c0005a0003c0015a0005c0019others(15): Show | a0003c0005t0002a0003c0015t0001a0005c0019t0001others(15): Show | a0003c0005t0002g0036a0003c0005t0002g0065a0003c0015t0001g0022others(16): Show | 19 | 104 | 0.1827 | -3 | c.830 others(20): Show |
CELSR1 | ENSG00000075275.18 | transcript | ENST00000674500.2 | protein_coding | 30/34 | chr22 | TogoVar | ||||||
CELSR1_chr22_46356174_46542620 | 46385674 | ATTT | A | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01261.hp2 others(13): Show |
a0003a0010a0015others(12): Show | a0003c0005a0010c0069a0015c0045others(12): Show | a0003c0005t0002a0010c0069t0005a0015c0045t0001others(12): Show | a0003c0005t0002g0036a0003c0005t0002g0065a0010c0069t0005g0001others(13): Show | 16 | 104 | 0.1539 | -3 | c.673 others(20): Show |
CELSR1 | ENSG00000075275.18 | transcript | ENST00000674500.2 | protein_coding | 19/34 | chr22 | TogoVar | ||||||
CELSR1_chr22_46356174_46542620 | 46397277 | CTTT | C | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(15): Show |
a0003a0007a0008others(13): Show | a0003c0005a0007c0013a0007c0023others(14): Show | a0003c0005t0002a0007c0013t0001a0007c0023t0001others(14): Show | a0003c0005t0002g0036a0003c0005t0002g0065a0007c0013t0001g0023others(15): Show | 18 | 104 | 0.1731 | -3 | c.570 others(20): Show |
CELSR1 | ENSG00000075275.18 | transcript | ENST00000674500.2 | protein_coding | 12/34 | chr22 | TogoVar | ||||||
CELSR1_chr22_46356174_46542620 | 46456661 | TAAA | T | intron_variant | MODIFIER | HG00621.hp1 HG02647.hp1 HG02683.hp1 others(9): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0040a0002c0051others(8): Show | a0001c0001t0001a0001c0040t0001a0002c0051t0003others(8): Show | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0040t0001g0088others(9): Show | 12 | 104 | 0.1154 | -3 | c.418 others(22): Show |
CELSR1 | ENSG00000075275.18 | transcript | ENST00000674500.2 | protein_coding | 2/34 | chr22 | TogoVar |