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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CYP4F11_chr19_15907377_15939529 | 15931568 | A | AGGAATGA others(7): Show |
intron_variant | MODIFIER | NA18991.hp1 | a0002 | a0002c0001 | a0002c0001t0013 | a0002c0001t0013g0373 | 1 | 386 | 0.0026 | 14 | c.199 others(31): Show |
CYP4F11 | ENSG00000171903.17 | transcript | ENST00000402119.9 | protein_coding | 1/11 | chr19 | TogoVar | ||||||
CYP4F11_chr19_15907377_15939529 | 15938221 | G | GCACACAC others(7): Show |
upstream_gene_variant | MODIFIER | HG03209.hp2 NA19056.hp1 |
a0002 | a0002c0001 | a0002c0001t0010a0002c0001t0094 | a0002c0001t0010g0142a0002c0001t0094g0202 | 2 | 386 | 0.0052 | 14 | c.-38 others(25): Show |
CYP4F11 | ENSG00000171903.17 | transcript | ENST00000402119.9 | protein_coding | 3693 | chr19 | TogoVar | ||||||
CYP4F12_chr19_15668087_15702174 | 15677824 | A | ATTCCTCT others(7): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02622.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | 410 | 0.0049 | 14 | c.199 others(29): Show |
CYP4F12 | ENSG00000186204.15 | transcript | ENST00000550308.6 | protein_coding | 2/12 | chr19 | TogoVar | ||||||
CYP4F12_chr19_15668087_15702174 | 15678846 | G | GCCAGCTC others(7): Show |
intron_variant | MODIFIER | HG01099.hp2 | a0013 | a0013c0015 | a0013c0015t0001 | a0013c0015t0001g0204 | 1 | 410 | 0.0024 | 14 | c.343 others(29): Show |
CYP4F12 | ENSG00000186204.15 | transcript | ENST00000550308.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F12_chr19_15668087_15702174 | 15684756 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02486.hp1 HG03098.hp1 others(1): Show |
a0005a0012a0018 | a0005c0007a0012c0022a0018c0012 | a0005c0007t0004a0012c0022t0007a0018c0012t0002 | a0005c0007t0004g0207a0005c0007t0004g0211a0012c0022t0007g0205others(1): Show | 4 | 410 | 0.0098 | 14 | c.919 others(27): Show |
CYP4F12 | ENSG00000186204.15 | transcript | ENST00000550308.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F22_chr19_15503525_15557317 | 15508598 | G | GGTGAGGG others(7): Show |
intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(5): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0003a0003c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0373others(5): Show | 8 | 384 | 0.0208 | 14 | c.-10 others(29): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F22_chr19_15503525_15557317 | 15509900 | C | CTTCTTTC others(7): Show |
intron_variant | MODIFIER | NA20752.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0246 | 1 | 384 | 0.0026 | 14 | c.-10 others(33): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | TogoVar | ||||||
CYP4F22_chr19_15503525_15557317 | 15510966 | A | ATATATAT others(7): Show |
intron_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0011 | 1 | 384 | 0.0026 | 14 | c.-10 others(33): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F22_chr19_15503525_15557317 | 15510966 | A | ATATTTTT others(7): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0008 | a0008c0018 | a0008c0018t0002 | a0008c0018t0002g0379 | 1 | 384 | 0.0026 | 14 | c.-10 others(33): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F22_chr19_15503525_15557317 | 15545648 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(2): Show |
a0001a0002a0006 | a0001c0001a0002c0003a0006c0017 | a0001c0001t0002a0002c0003t0002a0002c0003t0003others(1): Show | a0001c0001t0002g0075a0002c0003t0002g0006a0002c0003t0002g0007others(2): Show | 5 | 384 | 0.0130 | 14 | c.113 others(33): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F22_chr19_15503525_15557317 | 15547018 | G | GTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00558.hp1 HG02055.hp2 others(27): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(2): Show | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0022others(27): Show | 30 | 384 | 0.0781 | 14 | c.113 others(33): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F22_chr19_15503525_15557317 | 15555144 | C | CGCGTGTG others(7): Show |
downstream_gene_variant | MODIFIER | HG03927.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0102 | 1 | 384 | 0.0026 | 14 | c.*36 others(25): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2828 | chr19 | TogoVar | ||||||
CYP4F22_chr19_15503525_15557317 | 15555144 | C | CGTGTGTG others(7): Show |
downstream_gene_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0110 | 1 | 384 | 0.0026 | 14 | c.*36 others(25): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2828 | chr19 | TogoVar | ||||||
CYP4F3_chr19_15635897_15667825 | 15650722 | T | TTCTCTCT others(7): Show |
intron_variant | MODIFIER | HG01099.hp2 | a0001 | a0001c0005 | a0001c0005t0004 | a0001c0005t0004g0028 | 1 | 424 | 0.0024 | 14 | c.918 others(29): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F3_chr19_15635897_15667825 | 15650806 | T | TTCTCTCT others(7): Show |
intron_variant | MODIFIER | NA18989.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0250 | 1 | 424 | 0.0024 | 14 | c.918 others(29): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F3_chr19_15635897_15667825 | 15650808 | C | CTTTCTCT others(7): Show |
intron_variant | MODIFIER | HG03471.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0157a0001c0001t0009g0203 | 2 | 424 | 0.0047 | 14 | c.918 others(29): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F3_chr19_15635897_15667825 | 15650860 | T | TTCTCTCT others(7): Show |
intron_variant | MODIFIER | HG04184.hp1 NA19055.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0225a0001c0001t0002g0245 | 2 | 424 | 0.0047 | 14 | c.918 others(29): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F3_chr19_15635897_15667825 | 15650864 | T | TTCTCTCT others(7): Show |
intron_variant | MODIFIER | HG02809.hp2 HG02970.hp2 |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0055 | a0001c0001t0010g0187a0001c0001t0055g0196 | 2 | 424 | 0.0047 | 14 | c.918 others(29): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F3_chr19_15635897_15667825 | 15650868 | T | TTCTCTCT others(7): Show |
intron_variant | MODIFIER | HG02165.hp2 HG02683.hp2 HG03471.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0009a0001c0001t0025others(1): Show | a0001c0001t0002g0261a0001c0001t0009g0157a0001c0001t0025g0175others(1): Show | 4 | 424 | 0.0094 | 14 | c.918 others(29): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F3_chr19_15635897_15667825 | 15653735 | G | GGAGAGAG others(7): Show |
intron_variant | MODIFIER | HG03130.hp1 HG03225.hp2 |
a0001 | a0001c0002 | a0001c0002t0023a0001c0002t0045 | a0001c0002t0023g0376a0001c0002t0045g0377 | 2 | 424 | 0.0047 | 14 | c.111 others(31): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F3_chr19_15635897_15667825 | 15653773 | A | AGAGAGAG others(7): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0004 | a0001c0004t0075 | a0001c0004t0075g0038 | 1 | 424 | 0.0024 | 14 | c.111 others(31): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CYP4F3_chr19_15635897_15667825 | 15662270 | C | CAAAAAAA others(7): Show |
3_prime_UTR_variant | MODIFIER | HG02559.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0162a0001c0001t0016g0184a0001c0001t0016g0209others(1): Show | 4 | 424 | 0.0094 | 14 | c.*28 others(25): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | TogoVar | |||||
CYP4F3_chr19_15635897_15667825 | 15662272 | C | CAAAAAAA others(7): Show |
3_prime_UTR_variant | MODIFIER | HG03831.hp2 HG03834.hp1 HG03834.hp2 others(3): Show |
a0001 | a0001c0004 | a0001c0004t0011a0001c0004t0037 | a0001c0004t0011g0054a0001c0004t0011g0064a0001c0004t0011g0071others(3): Show | 6 | 424 | 0.0142 | 14 | c.*28 others(25): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||
CYP4V2_chr4_186186567_186218463 | 186211664 | T | TACATACA others(7): Show |
3_prime_UTR_variant | MODIFIER | HG03669.hp1 HG04199.hp1 |
a0002 | a0002c0001 | a0002c0001t0048 | a0002c0001t0048g0216a0002c0001t0048g0224 | 2 | 452 | 0.0044 | 14 | c.*10 others(25): Show |
CYP4V2 | ENSG00000145476.16 | transcript | ENST00000378802.5 | protein_coding | 11/11 | 1027 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||
CYP4V2_chr4_186186567_186218463 | 186211694 | C | CACACACA others(7): Show |
3_prime_UTR_variant | MODIFIER | HG00423.hp2 HG01168.hp1 HG01884.hp1 others(17): Show |
a0001a0002a0003others(2): Show | a0001c0002a0002c0001a0003c0006others(2): Show | a0001c0002t0019a0002c0001t0019a0002c0001t0046others(8): Show | a0001c0002t0019g0006a0001c0002t0019g0208a0002c0001t0019g0001others(16): Show | 20 | 452 | 0.0443 | 14 | c.*10 others(25): Show |
CYP4V2 | ENSG00000145476.16 | transcript | ENST00000378802.5 | protein_coding | 11/11 | 1057 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||
CYP4X1_chr1_47018669_47055751 | 47021142 | C | CAAAAAAA others(7): Show |
upstream_gene_variant | MODIFIER | HG01257.hp2 HG01258.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 | 2 | 350 | 0.0057 | 14 | c.-26 others(25): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2526 | chr1 | TogoVar | ||||||
CYP4X1_chr1_47018669_47055751 | 47036368 | T | TTATATAT others(7): Show |
intron_variant | MODIFIER | HG03139.hp1 NA18970.hp1 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0116 | 3 | 350 | 0.0086 | 14 | c.775 others(29): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CYP4X1_chr1_47018669_47055751 | 47036370 | T | TTATATAT others(7): Show |
intron_variant | MODIFIER | HG01074.hp2 HG01109.hp2 HG01928.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 | 7 | 350 | 0.0200 | 14 | c.775 others(29): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CYP4Z1_chr1_47062231_47123318 | 47076844 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | NA18941.hp2 NA18952.hp1 NA18990.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0040a0001c0001t0001g0185 | 3 | 318 | 0.0094 | 14 | c.320 others(31): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CYP51A1_chr7_92107153_92139477 | 92128428 | C | CTCTGTGT others(7): Show |
intron_variant | MODIFIER | HG00738.hp1 HG02109.hp2 HG02717.hp2 others(8): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0012 | a0001c0002t0002g0010a0001c0002t0002g0025a0001c0002t0002g0112others(1): Show | 11 | 392 | 0.0281 | 14 | c.468 others(29): Show |
CYP51A1 | ENSG00000001630.18 | transcript | ENST00000003100.13 | protein_coding | 3/9 | chr7 | TogoVar | ||||||
CYP51A1_chr7_92107153_92139477 | 92128428 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | NA18940.hp2 NA19063.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0151a0001c0001t0003g0152 | 2 | 392 | 0.0051 | 14 | c.468 others(29): Show |
CYP51A1 | ENSG00000001630.18 | transcript | ENST00000003100.13 | protein_coding | 3/9 | chr7 | TogoVar | ||||||
CYP51A1_chr7_92107153_92139477 | 92128455 | T | TGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG00673.hp1 HG01123.hp2 HG01261.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0015a0001c0001t0003g0173 | 6 | 392 | 0.0153 | 14 | c.468 others(29): Show |
CYP51A1 | ENSG00000001630.18 | transcript | ENST00000003100.13 | protein_coding | 3/9 | chr7 | TogoVar | ||||||
CYP7B1_chr8_64585851_64803737 | 64618570 | T | TTCTCTCT others(7): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0069 | 1 | 258 | 0.0039 | 14 | c.260 others(31): Show |
CYP7B1 | ENSG00000172817.4 | transcript | ENST00000310193.4 | protein_coding | 2/5 | chr8 | TogoVar | ||||||
CYP7B1_chr8_64585851_64803737 | 64624951 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0113 | 1 | 258 | 0.0039 | 14 | c.123 others(29): Show |
CYP7B1 | ENSG00000172817.4 | transcript | ENST00000310193.4 | protein_coding | 1/5 | chr8 | TogoVar | ||||||
CYP7B1_chr8_64585851_64803737 | 64730751 | G | GCACACAC others(7): Show |
intron_variant | MODIFIER | HG02572.hp2 HG03130.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0009a0002c0002t0009 | a0001c0001t0009g0230a0002c0002t0009g0003 | 2 | 258 | 0.0078 | 14 | c.122 others(33): Show |
CYP7B1 | ENSG00000172817.4 | transcript | ENST00000310193.4 | protein_coding | 1/5 | chr8 | TogoVar | ||||||
CYP7B1_chr8_64585851_64803737 | 64778174 | A | AATATATA others(7): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00558.hp2 HG01167.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(4): Show | a0001c0001t0003g0216a0001c0001t0004g0202a0001c0001t0004g0204others(12): Show | 15 | 258 | 0.0581 | 14 | c.122 others(33): Show |
CYP7B1 | ENSG00000172817.4 | transcript | ENST00000310193.4 | protein_coding | 1/5 | chr8 | TogoVar | ||||||
CYP7B1_chr8_64585851_64803737 | 64794195 | G | GAAAAGAA others(7): Show |
intron_variant | MODIFIER | NA19075.hp2 | a0001 | a0001c0001 | a0001c0001t0053 | a0001c0001t0053g0190 | 1 | 258 | 0.0039 | 14 | c.122 others(31): Show |
CYP7B1 | ENSG00000172817.4 | transcript | ENST00000310193.4 | protein_coding | 1/5 | chr8 | TogoVar | ||||||
CYREN_chr7_135160785_135175707 | 135168291 | A | ACCCCCCC others(7): Show |
intron_variant | MODIFIER | NA18949.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0111 | 1 | 406 | 0.0025 | 14 | c.138 others(29): Show |
CYREN | ENSG00000122783.17 | transcript | ENST00000393114.8 | protein_coding | 2/3 | chr7 | TogoVar | ||||||
CYRIA_chr2_16544459_16670834 | 16610897 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(8): Show | a0001c0001t0001g0086a0001c0001t0001g0109a0001c0001t0001g0114others(18): Show | 21 | 290 | 0.0724 | 14 | c.-11 others(33): Show |
CYRIA | ENSG00000197872.11 | transcript | ENST00000381323.7 | protein_coding | 2/11 | chr2 | TogoVar | ||||||
CYRIB_chr8_129834593_130021560 | 129965248 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG01243.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009 | a0001c0001t0001g0255a0001c0001t0009g0191 | 2 | 288 | 0.0069 | 14 | c.-13 others(33): Show |
CYRIB | ENSG00000153310.22 | transcript | ENST00000694912.1 | protein_coding | 2/13 | chr8 | TogoVar | ||||||
CYRIB_chr8_129834593_130021560 | 129991971 | A | AAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01255.hp1 HG03017.hp2 NA20805.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013a0001c0001t0029 | a0001c0001t0001g0222a0001c0001t0013g0287a0001c0001t0029g0288 | 3 | 288 | 0.0104 | 14 | c.-18 others(35): Show |
CYRIB | ENSG00000153310.22 | transcript | ENST00000694912.1 | protein_coding | 1/13 | chr8 | TogoVar | ||||||
CYRIB_chr8_129834593_130021560 | 129997115 | A | AGGAGGAG others(7): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0279 | 1 | 288 | 0.0035 | 14 | c.-19 others(35): Show |
CYRIB | ENSG00000153310.22 | transcript | ENST00000694912.1 | protein_coding | 1/13 | chr8 | TogoVar | ||||||
CYRIB_chr8_129834593_130021560 | 129997119 | A | AGGAGGAG others(7): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00733.hp2 HG01074.hp1 others(13): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0097a0001c0001t0001g0235a0001c0001t0001g0238others(13): Show | 16 | 288 | 0.0556 | 14 | c.-19 others(35): Show |
CYRIB | ENSG00000153310.22 | transcript | ENST00000694912.1 | protein_coding | 1/13 | chr8 | TogoVar | ||||||
CYSLTR2_chr13_48648929_48716226 | 48695068 | A | ATTTTTTT others(7): Show |
intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0157 | 1 | 318 | 0.0031 | 14 | c.-10 others(33): Show |
CYSLTR2 | ENSG00000152207.8 | transcript | ENST00000682523.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
CYSTM1_chr5_140170188_140248789 | 140177078 | A | AAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG00621.hp1 HG01175.hp2 HG01261.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0111others(12): Show | 15 | 324 | 0.0463 | 14 | c.-21 others(31): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CYSTM1_chr5_140170188_140248789 | 140178441 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00558.hp2 HG01070.hp2 HG02602.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0002g0126others(5): Show | 8 | 324 | 0.0247 | 14 | c.-21 others(31): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CYSTM1_chr5_140170188_140248789 | 140200557 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019 | 1 | 324 | 0.0031 | 14 | c.187 others(31): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CYSTM1_chr5_140170188_140248789 | 140212983 | G | GTGTATAT others(7): Show |
intron_variant | MODIFIER | HG02129.hp2 HG02622.hp1 HG03098.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0084others(3): Show | 6 | 324 | 0.0185 | 14 | c.187 others(33): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CYSTM1_chr5_140170188_140248789 | 140226586 | T | TTATATAT others(7): Show |
intron_variant | MODIFIER | HG01074.hp2 HG01257.hp2 HG01261.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0056others(9): Show | 13 | 324 | 0.0401 | 14 | c.188 others(33): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CYTH1_chr17_78669048_78787273 | 78690393 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02080.hp1 NA18971.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0006 | a0001c0001t0003g0071a0001c0001t0006g0347 | 2 | 378 | 0.0053 | 14 | c.891 others(31): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | TogoVar |