view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
COL3A1_chr2_188969373_189017746 | 188972936 | C | CAAAAAAA others(23): Show |
upstream_gene_variant | MODIFIER | HG00438.hp2 HG02886.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009 | a0001c0001t0001g0315a0001c0001t0009g0116 | 2 | 376 | 0.0053 | 30 | c.-15 others(41): Show |
COL3A1 | ENSG00000168542.17 | transcript | ENST00000304636.9 | protein_coding | 1436 | chr2 | TogoVar | |||||||
COL3A1_chr2_188969373_189017746 | 188997014 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG00423.hp1 HG02165.hp1 HG02886.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(1): Show | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0222others(4): Show | 7 | 376 | 0.0186 | 30 | c.176 others(45): Show |
COL3A1 | ENSG00000168542.17 | transcript | ENST00000304636.9 | protein_coding | 24/50 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110355484 | T | TGGGAGAG others(23): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0004 | a0004c0012 | a0004c0012t0004 | a0004c0012t0004g0307 | 1 | 372 | 0.0027 | 30 | c.100 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110355533 | T | TAGCTCAC others(23): Show |
intron_variant | MODIFIER | HG02056.hp2 | a0001 | a0001c0016 | a0001c0016t0007 | a0001c0016t0007g0235 | 1 | 372 | 0.0027 | 30 | c.100 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110355843 | G | GTGGAGGG others(23): Show |
intron_variant | MODIFIER | HG01515.hp2 HG03834.hp2 HG04184.hp1 |
a0002 | a0002c0006a0002c0019 | a0002c0006t0006a0002c0019t0002a0002c0019t0037 | a0002c0006t0006g0066a0002c0019t0002g0303a0002c0019t0037g0026 | 3 | 372 | 0.0081 | 30 | c.100 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 3/47 | chr13 | TogoVar | |||||||
COL4A2_chr13_110302284_110518209 | 110480906 | C | CTGGAGAC others(23): Show |
intron_variant | MODIFIER | HG01070.hp1 | a0002 | a0002c0006 | a0002c0006t0002 | a0002c0006t0002g0024 | 1 | 372 | 0.0027 | 30 | c.275 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481018 | T | TTCCGTTG others(23): Show |
intron_variant | MODIFIER | HG01433.hp2 HG01516.hp1 HG01517.hp1 |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0006a0002c0006t0001 | a0001c0001t0006g0074a0001c0001t0006g0075a0002c0006t0001g0258 | 3 | 372 | 0.0081 | 30 | c.275 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481082 | G | GTTGCTGG others(23): Show |
intron_variant | MODIFIER | HG01257.hp1 HG01258.hp1 HG01934.hp1 others(22): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0004others(10): Show | a0001c0001t0005a0001c0001t0006a0001c0003t0001others(18): Show | a0001c0001t0005g0107a0001c0001t0006g0047a0001c0003t0001g0232others(21): Show | 25 | 372 | 0.0672 | 30 | c.275 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481168 | C | CTCCGTTG others(23): Show |
intron_variant | MODIFIER | NA18955.hp1 NA19086.hp1 |
a0001a0006 | a0001c0002a0006c0027 | a0001c0002t0004a0006c0027t0012 | a0001c0002t0004g0292a0006c0027t0012g0281 | 2 | 372 | 0.0054 | 30 | c.275 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481310 | T | TTCTGTCC others(23): Show |
intron_variant | MODIFIER | HG00323.hp2 | a0002 | a0002c0017 | a0002c0017t0002 | a0002c0017t0002g0316 | 1 | 372 | 0.0027 | 30 | c.275 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481322 | A | ATTGCTGG others(23): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0002 | a0002c0055 | a0002c0055t0016 | a0002c0055t0016g0250 | 1 | 372 | 0.0027 | 30 | c.275 others(48): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481340 | T | TTCTGTCC others(23): Show |
intron_variant | MODIFIER | HG00544.hp2 HG00597.hp2 HG01069.hp1 others(9): Show |
a0001a0002a0004 | a0001c0001a0001c0004a0001c0005others(5): Show | a0001c0001t0003a0001c0001t0006a0001c0004t0001others(8): Show | a0001c0001t0003g0091a0001c0001t0006g0074a0001c0001t0006g0075others(9): Show | 12 | 372 | 0.0323 | 30 | c.275 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481352 | G | GTTGCTGG others(23): Show |
intron_variant | MODIFIER | HG03239.hp2 HG03654.hp1 |
a0001a0002 | a0001c0037a0002c0006 | a0001c0037t0020a0002c0006t0006 | a0001c0037t0020g0069a0002c0006t0006g0070 | 2 | 372 | 0.0054 | 30 | c.275 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481378 | C | CTCCGTTG others(23): Show |
intron_variant | MODIFIER | HG00738.hp1 NA19030.hp2 |
a0001a0003 | a0001c0014a0003c0067 | a0001c0014t0026a0003c0067t0050 | a0001c0014t0026g0156a0003c0067t0050g0151 | 2 | 372 | 0.0054 | 30 | c.275 others(49): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481408 | C | CTCCGTTG others(23): Show |
intron_variant | MODIFIER | HG01074.hp1 HG02015.hp2 HG02738.hp1 others(4): Show |
a0001a0003a0004others(1): Show | a0001c0003a0001c0008a0001c0011others(3): Show | a0001c0003t0002a0001c0008t0001a0001c0011t0004others(3): Show | a0001c0003t0002g0293a0001c0008t0001g0202a0001c0011t0004g0311others(4): Show | 7 | 372 | 0.0188 | 30 | c.275 others(49): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481430 | T | TTCTGTCC others(23): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0002 | a0002c0065 | a0002c0065t0014 | a0002c0065t0014g0028 | 1 | 372 | 0.0027 | 30 | c.275 others(49): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481472 | G | GTTGCTGG others(23): Show |
intron_variant | MODIFIER | HG01074.hp1 NA21309.hp2 |
a0003a0018 | a0003c0105a0018c0049 | a0003c0105t0011a0018c0049t0031 | a0003c0105t0011g0168a0018c0049t0031g0045 | 2 | 372 | 0.0054 | 30 | c.275 others(49): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481522 | C | CTGTCCTT others(23): Show |
intron_variant | MODIFIER | HG02015.hp2 HG02738.hp1 HG03516.hp1 others(2): Show |
a0001a0004 | a0001c0003a0001c0008a0001c0011others(1): Show | a0001c0003t0002a0001c0008t0001a0001c0011t0004others(1): Show | a0001c0003t0002g0293a0001c0008t0001g0202a0001c0011t0004g0311others(2): Show | 5 | 372 | 0.0134 | 30 | c.275 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110481937 | C | CTCTGTCC others(23): Show |
intron_variant | MODIFIER | HG01168.hp2 HG01169.hp1 HG02300.hp2 others(1): Show |
a0001a0010 | a0001c0002a0001c0014a0010c0036 | a0001c0002t0005a0001c0014t0001a0010c0036t0021 | a0001c0002t0005g0158a0001c0014t0001g0194a0010c0036t0021g0319others(1): Show | 4 | 372 | 0.0108 | 30 | c.275 others(47): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110493051 | A | AGGTGAAA others(23): Show |
intron_variant | MODIFIER | HG00621.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0067 | 1 | 372 | 0.0027 | 30 | c.356 others(46): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 38/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110509245 | T | TTATATAT others(23): Show |
intron_variant | MODIFIER | HG00408.hp2 HG00738.hp2 |
a0001 | a0001c0003a0001c0014 | a0001c0003t0002a0001c0014t0006 | a0001c0003t0002g0267a0001c0014t0006g0095 | 2 | 372 | 0.0054 | 30 | c.488 others(49): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 47/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A3_chr2_227159624_227319792 | 227202982 | C | CATATATG others(23): Show |
intron_variant | MODIFIER | HG03017.hp1 HG04115.hp2 |
a0009a0023 | a0009c0008a0023c0046 | a0009c0008t0001a0023c0046t0001 | a0009c0008t0001g0265a0023c0046t0001g0313 | 2 | 344 | 0.0058 | 30 | c.88- others(47): Show |
COL4A3 | ENSG00000169031.21 | transcript | ENST00000396578.8 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COL4A3_chr2_227159624_227319792 | 227203112 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG01516.hp1 | a0005 | a0005c0005 | a0005c0005t0007 | a0005c0005t0007g0280 | 1 | 344 | 0.0029 | 30 | c.88- others(47): Show |
COL4A3 | ENSG00000169031.21 | transcript | ENST00000396578.8 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COL4A3_chr2_227159624_227319792 | 227203288 | C | CCCATATG others(23): Show |
intron_variant | MODIFIER | HG00735.hp1 HG03704.hp2 NA18954.hp2 others(1): Show |
a0001a0002a0009 | a0001c0001a0002c0004a0009c0008 | a0001c0001t0001a0002c0004t0003a0009c0008t0001 | a0001c0001t0001g0131a0001c0001t0001g0184a0002c0004t0003g0125others(1): Show | 4 | 344 | 0.0116 | 30 | c.88- others(47): Show |
COL4A3 | ENSG00000169031.21 | transcript | ENST00000396578.8 | protein_coding | 1/51 | chr2 | TogoVar | |||||||
COL4A3_chr2_227159624_227319792 | 227203316 | C | CCCATATG others(23): Show |
intron_variant | MODIFIER | NA19077.hp1 NA19091.hp1 |
a0007a0009 | a0007c0006a0009c0008 | a0007c0006t0005a0009c0008t0001 | a0007c0006t0005g0149a0009c0008t0001g0270 | 2 | 344 | 0.0058 | 30 | c.88- others(47): Show |
COL4A3 | ENSG00000169031.21 | transcript | ENST00000396578.8 | protein_coding | 1/51 | chr2 | TogoVar | |||||||
COL4A3_chr2_227159624_227319792 | 227203489 | G | GTATATGT others(23): Show |
intron_variant | MODIFIER | HG03669.hp1 | a0007 | a0007c0006 | a0007c0006t0005 | a0007c0006t0005g0133 | 1 | 344 | 0.0029 | 30 | c.88- others(47): Show |
COL4A3 | ENSG00000169031.21 | transcript | ENST00000396578.8 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COL4A3_chr2_227159624_227319792 | 227203489 | G | GTATATGT others(23): Show |
intron_variant | MODIFIER | HG00639.hp2 | a0007 | a0007c0006 | a0007c0006t0005 | a0007c0006t0005g0235 | 1 | 344 | 0.0029 | 30 | c.88- others(47): Show |
COL4A3 | ENSG00000169031.21 | transcript | ENST00000396578.8 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COL4A3_chr2_227159624_227319792 | 227249230 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG01943.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0161 | 1 | 344 | 0.0029 | 30 | c.546 others(45): Show |
COL4A3 | ENSG00000169031.21 | transcript | ENST00000396578.8 | protein_coding | 9/51 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COL4A3_chr2_227159624_227319792 | 227249230 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0056 | 1 | 344 | 0.0029 | 30 | c.546 others(45): Show |
COL4A3 | ENSG00000169031.21 | transcript | ENST00000396578.8 | protein_coding | 9/51 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COL4A3_chr2_227159624_227319792 | 227249230 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02615.hp1 HG02723.hp2 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005 | a0001c0001t0002g0050a0001c0001t0002g0057a0001c0001t0005g0051 | 3 | 344 | 0.0087 | 30 | c.546 others(45): Show |
COL4A3 | ENSG00000169031.21 | transcript | ENST00000396578.8 | protein_coding | 9/51 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COL4A3_chr2_227159624_227319792 | 227249230 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG03098.hp2 NA20805.hp1 |
a0001a0011 | a0001c0001a0011c0021 | a0001c0001t0002a0011c0021t0003 | a0001c0001t0002g0266a0011c0021t0003g0323 | 2 | 344 | 0.0058 | 30 | c.546 others(45): Show |
COL4A3 | ENSG00000169031.21 | transcript | ENST00000396578.8 | protein_coding | 9/51 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COL4A4_chr2_226997714_227169205 | 227089588 | C | CATATATA others(23): Show |
intron_variant | MODIFIER | NA19006.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0077 | 1 | 284 | 0.0035 | 30 | c.145 others(47): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | TogoVar | |||||||
COL4A4_chr2_226997714_227169205 | 227089611 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG03041.hp1 NA19030.hp2 |
a0007 | a0007c0006 | a0007c0006t0004a0007c0006t0035 | a0007c0006t0004g0176a0007c0006t0035g0163 | 2 | 284 | 0.0070 | 30 | c.145 others(47): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | TogoVar | |||||||
COL4A4_chr2_226997714_227169205 | 227138133 | A | AAATAATA others(23): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0070 | a0001c0070t0039 | a0001c0070t0039g0204 | 1 | 284 | 0.0035 | 30 | c.192 others(47): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | TogoVar | |||||||
COL5A1_chr9_134636803_134849843 | 134669212 | T | TTTCCCTT others(23): Show |
intron_variant | MODIFIER | NA19074.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0077 | 1 | 272 | 0.0037 | 30 | c.110 others(49): Show |
COL5A1 | ENSG00000130635.17 | transcript | ENST00000371817.8 | protein_coding | 1/65 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
COL5A1_chr9_134636803_134849843 | 134669235 | T | TCCTTCCC others(23): Show |
intron_variant | MODIFIER | NA19057.hp1 | a0002 | a0002c0013 | a0002c0013t0003 | a0002c0013t0003g0076 | 1 | 272 | 0.0037 | 30 | c.110 others(49): Show |
COL5A1 | ENSG00000130635.17 | transcript | ENST00000371817.8 | protein_coding | 1/65 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
COL5A1_chr9_134636803_134849843 | 134705457 | G | GCTGTCCC others(23): Show |
intron_variant | MODIFIER | NA18999.hp1 | a0004 | a0004c0029 | a0004c0029t0005 | a0004c0029t0005g0100 | 1 | 272 | 0.0037 | 30 | c.654 others(47): Show |
COL5A1 | ENSG00000130635.17 | transcript | ENST00000371817.8 | protein_coding | 4/65 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
COL5A1_chr9_134636803_134849843 | 134712040 | T | TTCCCCCC others(23): Show |
intron_variant | MODIFIER | HG02970.hp1 NA18906.hp1 |
a0001 | a0001c0003a0001c0064 | a0001c0003t0004a0001c0064t0019 | a0001c0003t0004g0038a0001c0064t0019g0010 | 2 | 272 | 0.0074 | 30 | c.654 others(49): Show |
COL5A1 | ENSG00000130635.17 | transcript | ENST00000371817.8 | protein_coding | 4/65 | chr9 | TogoVar | |||||||
COL5A1_chr9_134636803_134849843 | 134712166 | T | TCTTCTTC others(23): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0003others(39): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(97): Show | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0041others(165): Show | 168 | 272 | 0.6177 | 30 | c.654 others(49): Show |
COL5A1 | ENSG00000130635.17 | transcript | ENST00000371817.8 | protein_coding | 4/65 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
COL5A1_chr9_134636803_134849843 | 134751123 | G | GCCCCGAG others(23): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(46): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(13): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(25): Show | a0001c0001t0002g0023a0001c0001t0002g0069a0001c0001t0002g0073others(46): Show | 49 | 272 | 0.1802 | 30 | c.166 others(47): Show |
COL5A1 | ENSG00000130635.17 | transcript | ENST00000371817.8 | protein_coding | 13/65 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
COL5A2_chr2_189026898_189184761 | 189094588 | G | GACACACA others(23): Show |
intron_variant | MODIFIER | HG01517.hp2 HG02258.hp1 HG02818.hp1 others(2): Show |
a0001 | a0001c0001a0001c0007a0001c0028 | a0001c0001t0001a0001c0007t0005a0001c0028t0012 | a0001c0001t0001g0070a0001c0001t0001g0107a0001c0007t0005g0006others(2): Show | 5 | 248 | 0.0202 | 30 | c.457 others(47): Show |
COL5A2 | ENSG00000204262.14 | transcript | ENST00000374866.9 | protein_coding | 6/53 | chr2 | TogoVar | |||||||
COL5A2_chr2_189026898_189184761 | 189157133 | T | TATAGATA others(23): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00597.hp1 HG01106.hp2 others(19): Show |
a0001a0006a0015 | a0001c0001a0001c0002a0006c0009others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0020others(2): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0030others(19): Show | 22 | 248 | 0.0887 | 30 | c.97+ others(47): Show |
COL5A2 | ENSG00000204262.14 | transcript | ENST00000374866.9 | protein_coding | 1/53 | chr2 | TogoVar | |||||||
COL5A3_chr19_9954561_10015504 | 9988855 | A | AAAAAAAA others(23): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0034 | a0034c0078 | a0034c0078t0001 | a0034c0078t0001g0389 | 1 | 412 | 0.0024 | 30 | c.214 others(47): Show |
COL5A3 | ENSG00000080573.7 | transcript | ENST00000264828.4 | protein_coding | 27/66 | chr19 | TogoVar | |||||||
COL6A1_chr21_45976770_46010048 | 45978248 | C | CGTGAGAG others(23): Show |
upstream_gene_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(89): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0003a0001c0010others(26): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(37): Show | a0001c0001t0001g0065a0001c0001t0002g0004a0001c0001t0002g0007others(89): Show | 92 | 128 | 0.7188 | 30 | c.-36 others(41): Show |
COL6A1 | ENSG00000142156.16 | transcript | ENST00000361866.8 | protein_coding | 3521 | chr21 | TogoVar | |||||||
COL6A1_chr21_45976770_46010048 | 45978261 | A | AGGGGGAG others(23): Show |
upstream_gene_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0124 | 1 | 128 | 0.0078 | 30 | c.-35 others(41): Show |
COL6A1 | ENSG00000142156.16 | transcript | ENST00000361866.8 | protein_coding | 3508 | chr21 | TogoVar | |||||||
COL6A1_chr21_45976770_46010048 | 45978267 | A | AGGAGTGA others(23): Show |
upstream_gene_variant | MODIFIER | HG02602.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0125 | 1 | 128 | 0.0078 | 30 | c.-35 others(41): Show |
COL6A1 | ENSG00000142156.16 | transcript | ENST00000361866.8 | protein_coding | 3502 | chr21 | TogoVar | |||||||
COL6A1_chr21_45976770_46010048 | 45981603 | G | GCCCCCTC others(23): Show |
upstream_gene_variant | MODIFIER | NA18983.hp1 | a0004 | a0004c0030 | a0004c0030t0001 | a0004c0030t0001g0085 | 1 | 128 | 0.0078 | 30 | c.-24 others(39): Show |
COL6A1 | ENSG00000142156.16 | transcript | ENST00000361866.8 | protein_coding | 166 | chr21 | TogoVar | |||||||
COL6A1_chr21_45976770_46010048 | 45981603 | G | GCCCCTCC others(23): Show |
upstream_gene_variant | MODIFIER | HG01978.hp1 | a0006 | a0006c0011 | a0006c0011t0002 | a0006c0011t0002g0097 | 1 | 128 | 0.0078 | 30 | c.-24 others(39): Show |
COL6A1 | ENSG00000142156.16 | transcript | ENST00000361866.8 | protein_coding | 166 | chr21 | TogoVar | |||||||
COL6A1_chr21_45976770_46010048 | 45981618 | T | TCCCGCCC others(23): Show |
upstream_gene_variant | MODIFIER | HG00423.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0111 | 1 | 128 | 0.0078 | 30 | c.-23 others(39): Show |
COL6A1 | ENSG00000142156.16 | transcript | ENST00000361866.8 | protein_coding | 151 | chr21 | TogoVar | |||||||
COL6A1_chr21_45976770_46010048 | 45981618 | T | TCCCGCCC others(23): Show |
upstream_gene_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0106 | 1 | 128 | 0.0078 | 30 | c.-23 others(39): Show |
COL6A1 | ENSG00000142156.16 | transcript | ENST00000361866.8 | protein_coding | 151 | chr21 | TogoVar |