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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CACNG7_chr19_53904278_53948950 | 53921606 | T | TCCCCAGG others(20): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0016 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | 364 | 0.0302 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53921634 | T | TCCCCAGG others(20): Show |
intron_variant | MODIFIER | NA18961.hp2 NA19043.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073a0001c0001t0001g0084 | 2 | 364 | 0.0055 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53921754 | T | TATTGGTG others(20): Show |
intron_variant | MODIFIER | HG00423.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0166 | 1 | 364 | 0.0028 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53921795 | T | TCCCCAGG others(20): Show |
intron_variant | MODIFIER | HG02083.hp1 HG02135.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | 364 | 0.0055 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53921937 | T | TCTGGTCA others(20): Show |
intron_variant | MODIFIER | NA18950.hp2 NA18982.hp1 NA18998.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | 364 | 0.0082 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53922052 | T | TCATTGGT others(20): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0025 | 1 | 364 | 0.0028 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | TogoVar | ||||||
CACNG7_chr19_53904278_53948950 | 53922100 | C | CCTGGTCA others(20): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0209 | 1 | 364 | 0.0028 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53922331 | G | GAGTTGCC others(20): Show |
intron_variant | MODIFIER | HG01496.hp2 HG03834.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0212a0001c0001t0001g0335 | 2 | 364 | 0.0055 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53922581 | T | TCCCAGAT others(20): Show |
intron_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0089 | 1 | 364 | 0.0028 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53922602 | C | CAGTTGCC others(20): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(34): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(9): Show | a0001c0001t0001g0006a0001c0001t0001g0087a0001c0001t0001g0088others(33): Show | 37 | 364 | 0.1017 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53923099 | G | GCTGGTCA others(20): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0316 | 1 | 364 | 0.0028 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53923373 | C | CATTGGTG others(20): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0016 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | 364 | 0.0302 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53923413 | G | GTCCCCAG others(20): Show |
intron_variant | MODIFIER | HG02818.hp1 HG03669.hp2 HG03834.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0010 | a0001c0001t0001g0212a0001c0001t0002g0316a0001c0001t0010g0233 | 3 | 364 | 0.0082 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53923449 | C | CCTGGTAT others(20): Show |
intron_variant | MODIFIER | HG04115.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0099 | 1 | 364 | 0.0028 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53923502 | G | GCTGGTCA others(20): Show |
intron_variant | MODIFIER | HG03669.hp2 HG03834.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0212a0001c0001t0010g0233 | 2 | 364 | 0.0055 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53923825 | T | TCTGGTCA others(20): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02257.hp1 HG02897.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 9 | 364 | 0.0247 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53924305 | G | GTTGCCCC others(20): Show |
intron_variant | MODIFIER | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011a0001c0001t0020others(1): Show | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | 364 | 0.0165 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53925484 | G | GCTGGTCA others(20): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 125 | 364 | 0.3434 | 27 | c.424 others(46): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53925484 | G | GCTGGTCA others(20): Show |
intron_variant | MODIFIER | HG02886.hp1 HG03195.hp2 HG03225.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0014 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0006g0351others(1): Show | 4 | 364 | 0.0110 | 27 | c.424 others(44): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CACNG7_chr19_53904278_53948950 | 53925502 | T | TGCCCCAG others(20): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0031 | 1 | 364 | 0.0028 | 27 | c.424 others(46): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CADM1_chr11_115164236_115509415 | 115401293 | C | CAAAACTA others(20): Show |
intron_variant | MODIFIER | NA19062.hp2 | a0001 | a0001c0001 | a0001c0001t0044 | a0001c0001t0044g0108 | 1 | 164 | 0.0061 | 27 | c.124 others(48): Show |
CADM1 | ENSG00000182985.19 | transcript | ENST00000331581.11 | protein_coding | 1/11 | chr11 | TogoVar | ||||||
CADM2_chr3_84953989_86079429 | 85359666 | A | ATATATAT others(20): Show |
intron_variant | MODIFIER | HG01361.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0111 | 1 | 146 | 0.0069 | 27 | c.62- others(46): Show |
CADM2 | ENSG00000175161.14 | transcript | ENST00000383699.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CADM2_chr3_84953989_86079429 | 85359666 | A | ATATATAT others(20): Show |
intron_variant | MODIFIER | HG01516.hp2 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0087 | 1 | 146 | 0.0069 | 27 | c.62- others(46): Show |
CADM2 | ENSG00000175161.14 | transcript | ENST00000383699.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CADM2_chr3_84953989_86079429 | 85359666 | A | ATATATAT others(20): Show |
intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0019 | 1 | 146 | 0.0069 | 27 | c.62- others(46): Show |
CADM2 | ENSG00000175161.14 | transcript | ENST00000383699.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CADM2_chr3_84953989_86079429 | 85768734 | C | CATATATA others(20): Show |
intron_variant | MODIFIER | HG02257.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0003t0006a0001c0003t0024others(1): Show | a0001c0001t0003g0092a0001c0003t0006g0027a0001c0003t0006g0028others(4): Show | 7 | 146 | 0.0480 | 27 | c.89- others(44): Show |
CADM2 | ENSG00000175161.14 | transcript | ENST00000383699.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CADM2_chr3_84953989_86079429 | 85855617 | A | ATATATAT others(20): Show |
intron_variant | MODIFIER | HG02258.hp1 HG04228.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0115a0001c0001t0002g0102 | 2 | 146 | 0.0137 | 27 | c.239 others(46): Show |
CADM2 | ENSG00000175161.14 | transcript | ENST00000383699.8 | protein_coding | 3/9 | chr3 | TogoVar | ||||||
CADM2_chr3_84953989_86079429 | 86066332 | C | CAAAAAAA others(20): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0077 | 1 | 146 | 0.0069 | 27 | c.109 others(44): Show |
CADM2 | ENSG00000175161.14 | transcript | ENST00000383699.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CADPS2_chr7_122313411_122891460 | 122315296 | T | TCTCTCTC others(20): Show |
downstream_gene_variant | MODIFIER | NA19240.hp2 NA20905.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0048a0001c0001t0002g0095 | 2 | 126 | 0.0159 | 27 | c.*48 others(38): Show |
CADPS2 | ENSG00000081803.17 | transcript | ENST00000449022.7 | protein_coding | 3114 | chr7 | TogoVar | ||||||
CADPS2_chr7_122313411_122891460 | 122315298 | T | TCTCTCTC others(20): Show |
downstream_gene_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0020 | 1 | 126 | 0.0079 | 27 | c.*48 others(38): Show |
CADPS2 | ENSG00000081803.17 | transcript | ENST00000449022.7 | protein_coding | 3112 | chr7 | TogoVar | ||||||
CADPS2_chr7_122313411_122891460 | 122351372 | C | CAAAAAAA others(20): Show |
intron_variant | MODIFIER | HG02080.hp2 NA18944.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0121a0001c0003t0001g0046 | 2 | 126 | 0.0159 | 27 | c.350 others(46): Show |
CADPS2 | ENSG00000081803.17 | transcript | ENST00000449022.7 | protein_coding | 27/29 | chr7 | TogoVar | ||||||
CADPS2_chr7_122313411_122891460 | 122508449 | G | GTTTTTTT others(20): Show |
intron_variant | MODIFIER | HG00280.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0038 | 1 | 126 | 0.0079 | 27 | c.154 others(46): Show |
CADPS2 | ENSG00000081803.17 | transcript | ENST00000449022.7 | protein_coding | 9/29 | chr7 | TogoVar | ||||||
CADPS_chr3_62393348_62880416 | 62731805 | C | CAAAAAAA others(20): Show |
intron_variant | MODIFIER | HG00738.hp1 NA18986.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0118 | 2 | 160 | 0.0125 | 27 | c.888 others(46): Show |
CADPS | ENSG00000163618.18 | transcript | ENST00000383710.9 | protein_coding | 3/29 | chr3 | TogoVar | ||||||
CALB2_chr16_71353723_71395433 | 71366022 | C | CTTTTTTT others(20): Show |
intron_variant | MODIFIER | NA19000.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 | 1 | 426 | 0.0024 | 27 | c.95- others(42): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CALB2_chr16_71353723_71395433 | 71366024 | C | CTTTTTTT others(20): Show |
intron_variant | MODIFIER | HG01943.hp1 HG01981.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0358a0001c0001t0001g0359 | 2 | 426 | 0.0047 | 27 | c.95- others(42): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CALCOCO2_chr17_48826035_48870245 | 48854396 | A | ATATATAT others(20): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0326 | 1 | 328 | 0.0031 | 27 | c.912 others(44): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
CALCOCO2_chr17_48826035_48870245 | 48857497 | C | CTTTTTTT others(20): Show |
intron_variant | MODIFIER | HG01099.hp1 HG03139.hp2 NA18954.hp2 others(3): Show |
a0002a0003 | a0002c0002a0003c0006 | a0002c0002t0001a0003c0006t0015 | a0002c0002t0001g0066a0002c0002t0001g0155a0002c0002t0001g0173others(3): Show | 6 | 328 | 0.0183 | 27 | c.100 others(46): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
CALCR_chr7_93419486_93579724 | 93460572 | A | ATATATAT others(20): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0075 | 1 | 292 | 0.0034 | 27 | c.648 others(42): Show |
CALCR | ENSG00000004948.16 | transcript | ENST00000426151.7 | protein_coding | 8/13 | chr7 | TogoVar | ||||||
CALCR_chr7_93419486_93579724 | 93460572 | A | ATATATAT others(20): Show |
intron_variant | MODIFIER | HG03017.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0253 | 1 | 292 | 0.0034 | 27 | c.648 others(42): Show |
CALCR | ENSG00000004948.16 | transcript | ENST00000426151.7 | protein_coding | 8/13 | chr7 | TogoVar | ||||||
CALHM1_chr10_103448240_103463900 | 103451642 | C | CAGGAGGA others(20): Show |
downstream_gene_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0095 | 1 | 462 | 0.0022 | 27 | c.*35 others(38): Show |
CALHM1 | ENSG00000185933.7 | transcript | ENST00000329905.6 | protein_coding | 1597 | chr10 | TogoVar | ||||||
CALHM1_chr10_103448240_103463900 | 103451675 | G | GAGGAGGA others(20): Show |
downstream_gene_variant | MODIFIER | HG03130.hp1 NA18986.hp2 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0008 | a0001c0001t0005g0016a0001c0001t0008g0019 | 2 | 462 | 0.0043 | 27 | c.*35 others(38): Show |
CALHM1 | ENSG00000185933.7 | transcript | ENST00000329905.6 | protein_coding | 1564 | chr10 | TogoVar | ||||||
CALHM2_chr10_103441786_103457370 | 103451642 | C | CAGGAGGA others(20): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 | 1 | 458 | 0.0022 | 27 | c.-36 others(44): Show |
CALHM2 | ENSG00000138172.11 | transcript | ENST00000260743.10 | protein_coding | 1/3 | chr10 | TogoVar | ||||||
CALHM2_chr10_103441786_103457370 | 103451675 | G | GAGGAGGA others(20): Show |
intron_variant | MODIFIER | HG03130.hp1 NA18953.hp1 NA18986.hp2 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0004a0006c0006t0001 | a0001c0001t0004g0023a0006c0006t0001g0040 | 3 | 458 | 0.0066 | 27 | c.-36 others(44): Show |
CALHM2 | ENSG00000138172.11 | transcript | ENST00000260743.10 | protein_coding | 1/3 | chr10 | TogoVar | ||||||
CALM2_chr2_47155084_47181511 | 47167693 | C | CAAAAAAA others(20): Show |
intron_variant | MODIFIER | HG04199.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0218 | 1 | 432 | 0.0023 | 27 | c.34+ others(42): Show |
CALM2 | ENSG00000143933.20 | transcript | ENST00000272298.12 | protein_coding | 2/5 | chr2 | TogoVar | ||||||
CALM2_chr2_47155084_47181511 | 47167814 | C | CCTTTTTT others(20): Show |
intron_variant | MODIFIER | HG02451.hp1 HG02818.hp2 HG03098.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0001t0002g0299others(2): Show | 5 | 432 | 0.0116 | 27 | c.34+ others(42): Show |
CALM2 | ENSG00000143933.20 | transcript | ENST00000272298.12 | protein_coding | 2/5 | chr2 | TogoVar | ||||||
CALM2_chr2_47155084_47181511 | 47167814 | C | CTTCTTTT others(20): Show |
intron_variant | MODIFIER | HG03490.hp2 HG03492.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0334a0001c0001t0001g0360 | 2 | 432 | 0.0046 | 27 | c.34+ others(42): Show |
CALM2 | ENSG00000143933.20 | transcript | ENST00000272298.12 | protein_coding | 2/5 | chr2 | TogoVar | ||||||
CALM2_chr2_47155084_47181511 | 47167814 | C | CTTTTCTT others(20): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0383 | 1 | 432 | 0.0023 | 27 | c.34+ others(42): Show |
CALM2 | ENSG00000143933.20 | transcript | ENST00000272298.12 | protein_coding | 2/5 | chr2 | TogoVar | ||||||
CALN1_chr7_71774491_72417338 | 71971945 | A | AGAAAGAA others(20): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02451.hp1 HG02723.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0018a0001c0001t0043 | a0001c0001t0001g0061a0001c0001t0018g0063a0001c0001t0018g0126others(1): Show | 4 | 142 | 0.0282 | 27 | c.501 others(46): Show |
CALN1 | ENSG00000183166.12 | transcript | ENST00000395275.7 | protein_coding | 5/6 | chr7 | TogoVar | ||||||
CALN1_chr7_71774491_72417338 | 72205551 | A | AAATATAT others(20): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0113 | 1 | 142 | 0.0070 | 27 | c.244 others(46): Show |
CALN1 | ENSG00000183166.12 | transcript | ENST00000395275.7 | protein_coding | 3/6 | chr7 | TogoVar | ||||||
CALN1_chr7_71774491_72417338 | 72205551 | A | AAATATAT others(20): Show |
intron_variant | MODIFIER | HG00438.hp1 HG01109.hp1 HG02622.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(2): Show | a0001c0001t0001g0047a0001c0001t0001g0103a0001c0001t0001g0110others(5): Show | 8 | 142 | 0.0563 | 27 | c.244 others(46): Show |
CALN1 | ENSG00000183166.12 | transcript | ENST00000395275.7 | protein_coding | 3/6 | chr7 | TogoVar | ||||||
CALN1_chr7_71774491_72417338 | 72209279 | T | TTTCCTTC others(20): Show |
intron_variant | MODIFIER | HG00639.hp2 HG03453.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0037 | a0001c0001t0004g0071a0001c0001t0037g0072 | 2 | 142 | 0.0141 | 27 | c.244 others(46): Show |
CALN1 | ENSG00000183166.12 | transcript | ENST00000395275.7 | protein_coding | 3/6 | chr7 | TogoVar |