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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACSBG2_chr19_6130667_6198091 | 6153889 | GA | G | intron_variant | MODIFIER | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(47): Show |
a0001a0003a0004others(5): Show | a0001c0001a0001c0020a0003c0004others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0020t0001others(12): Show | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(46): Show | 50 | 262 | 0.1908 | -1 | c.386 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6154178 | AG | A | intron_variant | MODIFIER | HG00741.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0011 | a0001c0001t0001a0003c0011t0001 | a0001c0001t0001g0053a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | 262 | 0.0153 | -1 | c.387 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6154432 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
a0001a0003a0018 | a0001c0001a0001c0017a0001c0024others(2): Show | a0001c0001t0001a0001c0017t0001a0001c0024t0001others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | 262 | 0.4008 | -1 | c.387 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6155789 | CA | C | intron_variant | MODIFIER | HG01074.hp1 HG02155.hp2 HG02451.hp2 others(11): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0020a0002c0002others(4): Show | a0001c0001t0001a0001c0020t0001a0002c0002t0001others(4): Show | a0001c0001t0001g0015a0001c0001t0001g0140a0001c0020t0001g0051others(11): Show | 14 | 262 | 0.0534 | -1 | c.387 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6155922 | CA | C | intron_variant | MODIFIER | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(53): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0020a0002c0002others(11): Show | a0001c0001t0001a0001c0001t0003a0001c0020t0001others(14): Show | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(52): Show | 56 | 262 | 0.2137 | -1 | c.387 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6156785 | CA | C | intron_variant | MODIFIER | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
a0001a0003a0004others(3): Show | a0001c0001a0003c0011a0004c0003others(3): Show | a0001c0001t0001a0001c0001t0003a0003c0011t0001others(4): Show | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | 262 | 0.0840 | -1 | c.507 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6156786 | AT | A | intron_variant | MODIFIER | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(29): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0012others(3): Show | a0001c0001t0001a0002c0002t0001a0003c0012t0002others(3): Show | a0001c0001t0001g0033a0001c0001t0001g0055a0001c0001t0001g0056others(29): Show | 32 | 262 | 0.1221 | -1 | c.507 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6156951 | CT | C | intron_variant | MODIFIER | HG00741.hp2 HG01884.hp2 HG01981.hp1 others(20): Show |
a0001a0003a0004others(3): Show | a0001c0001a0003c0011a0004c0003others(3): Show | a0001c0001t0001a0001c0001t0003a0003c0011t0001others(4): Show | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(20): Show | 23 | 262 | 0.0878 | -1 | c.507 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6158060 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
a0001a0003a0004others(7): Show | a0001c0001a0001c0017a0001c0020others(14): Show | a0001c0001t0001a0001c0001t0003a0001c0017t0001others(16): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 166 | 262 | 0.6336 | -1 | c.507 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6160404 | AG | A | intron_variant | MODIFIER | HG00280.hp2 HG01884.hp2 HG01981.hp2 others(31): Show |
a0001a0003a0004others(4): Show | a0001c0001a0001c0020a0003c0004others(8): Show | a0001c0001t0001a0001c0020t0001a0003c0004t0002others(8): Show | a0001c0001t0001g0184a0001c0001t0001g0206a0001c0001t0001g0250others(31): Show | 34 | 262 | 0.1298 | -1 | c.508 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6161329 | AG | A | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
a0001a0003a0004others(4): Show | a0001c0001a0003c0011a0004c0003others(4): Show | a0001c0001t0001a0003c0011t0001a0004c0003t0002others(4): Show | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | 262 | 0.0573 | -1 | c.588 others(7): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6162245 | AC | A | intron_variant | MODIFIER | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | 262 | 0.0267 | -1 | c.588 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6163783 | CA | C | intron_variant | MODIFIER | HG01891.hp2 HG01934.hp1 HG02132.hp1 others(21): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0012others(3): Show | a0001c0001t0001a0002c0002t0001a0003c0012t0002others(3): Show | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(21): Show | 24 | 262 | 0.0916 | -1 | c.589 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6170975 | CT | C | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(18): Show |
a0003a0004a0009others(1): Show | a0003c0004a0003c0012a0004c0003others(3): Show | a0003c0004t0002a0003c0012t0002a0004c0003t0001others(3): Show | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(18): Show | 21 | 262 | 0.0802 | -1 | c.738 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6173937 | AT | A | intron_variant | MODIFIER | HG00741.hp1 HG01256.hp2 HG02258.hp2 others(5): Show |
a0001a0002a0018 | a0001c0001a0002c0002a0018c0015 | a0001c0001t0001a0002c0002t0001a0018c0015t0001 | a0001c0001t0001g0166a0001c0001t0001g0173a0001c0001t0001g0194others(5): Show | 8 | 262 | 0.0305 | -1 | c.739 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6177739 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0020a0002c0002others(17): Show | a0001c0001t0001a0001c0020t0001a0002c0002t0001others(21): Show | a0001c0001t0001g0039a0001c0001t0001g0139a0001c0001t0001g0140others(118): Show | 122 | 262 | 0.4657 | -1 | c.906 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6179293 | AT | A | intron_variant | MODIFIER | HG01256.hp1 HG01515.hp1 HG02965.hp1 others(4): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0011others(1): Show | a0001c0001t0003a0002c0002t0001a0003c0011t0001others(1): Show | a0001c0001t0003g0141a0002c0002t0001g0062a0002c0002t0001g0072others(4): Show | 7 | 262 | 0.0267 | -1 | c.906 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6181044 | TA | T | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(34): Show |
a0002a0003a0004others(5): Show | a0002c0002a0003c0004a0003c0011others(8): Show | a0002c0002t0001a0002c0002t0005a0003c0004t0002others(10): Show | a0002c0002t0001g0074a0002c0002t0005g0116a0003c0004t0002g0006others(34): Show | 37 | 262 | 0.1412 | -1 | c.907 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6181376 | AG | A | intron_variant | MODIFIER | NA18950.hp1 NA18983.hp1 NA19007.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0207others(1): Show | 4 | 262 | 0.0153 | -1 | c.907 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6181813 | GC | G | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(53): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0006c0007others(2): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0005others(4): Show | a0001c0001t0001g0039a0001c0001t0001g0053a0001c0001t0001g0130others(53): Show | 56 | 262 | 0.2137 | -1 | c.907 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6182207 | AT | A | intron_variant | MODIFIER | HG00408.hp1 HG00558.hp2 HG02155.hp2 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0111a0002c0002t0001g0122a0002c0002t0001g0125others(2): Show | 5 | 262 | 0.0191 | -1 | c.907 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6182289 | CT | C | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(29): Show |
a0003a0004a0007others(3): Show | a0003c0004a0003c0012a0004c0003others(5): Show | a0003c0004t0002a0003c0012t0002a0004c0003t0001others(6): Show | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(29): Show | 32 | 262 | 0.1221 | -1 | c.907 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6184832 | GA | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(12): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0007 | a0001c0001t0001a0002c0002t0001a0002c0002t0004others(1): Show | a0001c0001t0001g0038a0001c0001t0001g0171a0001c0001t0001g0174others(12): Show | 15 | 262 | 0.0573 | -1 | c.132 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6186058 | CT | C | intron_variant | MODIFIER | HG01433.hp1 HG01891.hp1 HG02723.hp2 others(10): Show |
a0003a0009a0013others(1): Show | a0003c0005a0003c0011a0009c0010others(2): Show | a0003c0005t0001a0003c0011t0001a0009c0010t0002others(2): Show | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(9): Show | 13 | 262 | 0.0496 | -1 | c.154 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6187002 | GT | G | intron_variant | MODIFIER | HG01433.hp1 HG02145.hp1 HG02572.hp2 others(17): Show |
a0001a0003a0005others(1): Show | a0001c0001a0003c0005a0005c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0003c0005t0001others(2): Show | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(16): Show | 20 | 262 | 0.0763 | -1 | c.154 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6189527 | GT | G | intron_variant | MODIFIER | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
a0003a0009 | a0003c0004a0003c0012a0009c0010 | a0003c0004t0002a0003c0012t0002a0009c0010t0002 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | 262 | 0.0496 | -1 | c.192 others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6189710 | TC | T | intron_variant | MODIFIER | HG02055.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
a0003 | a0003c0004a0003c0012 | a0003c0004t0002a0003c0012t0002 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0009others(5): Show | 8 | 262 | 0.0305 | -1 | c.192 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6191241 | GT | G | intron_variant | MODIFIER | HG01433.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0005others(2): Show | a0001c0001t0001a0002c0002t0001a0003c0005t0001others(2): Show | a0001c0001t0001g0219a0002c0002t0001g0103a0003c0005t0001g0001others(7): Show | 11 | 262 | 0.0420 | -1 | c.*35 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6192071 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0024a0002c0002others(4): Show | a0001c0001t0001a0001c0024t0001a0002c0002t0001others(5): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(99): Show | 102 | 262 | 0.3893 | -1 | c.*36 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6195648 | CA | C | downstream_gene_variant | MODIFIER | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
a0003a0009 | a0003c0004a0003c0012a0009c0010 | a0003c0004t0002a0003c0012t0002a0009c0010t0002 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | 262 | 0.0496 | -1 | c.*30 others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2558 | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6197275 | CA | C | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(66): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0020a0001c0024others(4): Show | a0001c0001t0001a0001c0020t0001a0001c0024t0001others(4): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0033others(66): Show | 69 | 262 | 0.2634 | -1 | c.*46 others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4185 | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6197508 | CT | C | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0017a0001c0020others(6): Show | a0001c0001t0001a0001c0017t0001a0001c0020t0001others(8): Show | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0033others(90): Show | 93 | 262 | 0.3550 | -1 | c.*48 others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4418 | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6197612 | TC | T | downstream_gene_variant | MODIFIER | HG02647.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
a0005 | a0005c0006 | a0005c0006t0001 | a0005c0006t0001g0023a0005c0006t0001g0025a0005c0006t0001g0026others(2): Show | 5 | 262 | 0.0191 | -1 | c.*49 others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4522 | chr19 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50421507 | TA | T | upstream_gene_variant | MODIFIER | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(12): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0059others(11): Show | 15 | 320 | 0.0469 | -1 | c.-47 others(6): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4710 | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50422192 | CT | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(6): Show | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0035others(87): Show | 99 | 320 | 0.3094 | -1 | c.-40 others(6): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4025 | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50439232 | CT | C | intron_variant | MODIFIER | HG01168.hp1 HG01361.hp1 HG01496.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0096others(3): Show | 6 | 320 | 0.0188 | -1 | c.128 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ACSF2_chr17_50421218_50479837 | 50442325 | AT | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 217 | 320 | 0.6781 | -1 | c.128 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ACSF2_chr17_50421218_50479837 | 50450500 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(4): Show | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0129others(84): Show | 101 | 320 | 0.3156 | -1 | c.129 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ACSF2_chr17_50421218_50479837 | 50454169 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(66): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(4): Show | a0001c0001t0001g0069a0001c0001t0001g0197a0001c0001t0001g0229others(57): Show | 69 | 320 | 0.2156 | -1 | c.129 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ACSF2_chr17_50421218_50479837 | 50459398 | AC | A | intron_variant | MODIFIER | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
a0001a0002a0004 | a0001c0002a0001c0009a0002c0004others(1): Show | a0001c0002t0001a0001c0002t0002a0001c0009t0001others(2): Show | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0002g0117others(12): Show | 16 | 320 | 0.0500 | -1 | c.129 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ACSF2_chr17_50421218_50479837 | 50463574 | AC | A | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(4): Show |
a0003 | a0003c0005 | a0003c0005t0002 | a0003c0005t0002g0021a0003c0005t0002g0149a0003c0005t0002g0150others(3): Show | 7 | 320 | 0.0219 | -1 | c.104 others(8): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 8/15 | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50466073 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(6): Show | a0001c0001t0001g0074a0001c0001t0001g0232a0001c0001t0001g0234others(87): Show | 105 | 320 | 0.3281 | -1 | c.121 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ACSF3_chr16_89088852_89161233 | 89092817 | AT | A | upstream_gene_variant | MODIFIER | HG01891.hp2 HG02615.hp1 HG02970.hp1 others(3): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0009 | a0001c0001t0001a0001c0001t0012a0002c0002t0004others(1): Show | a0001c0001t0001g0011a0001c0001t0012g0008a0001c0001t0012g0009others(3): Show | 6 | 368 | 0.0163 | -1 | c.-13 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1034 | chr16 | TogoVar | ||||||
ACSF3_chr16_89088852_89161233 | 89097773 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
a0001a0003a0004others(4): Show | a0001c0001a0001c0005a0001c0014others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(38): Show | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | 368 | 0.6005 | -1 | c.-19 others(9): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | TogoVar | ||||||
ACSF3_chr16_89088852_89161233 | 89099978 | CA | C | intron_variant | MODIFIER | HG01361.hp1 NA18967.hp2 NA18977.hp2 others(3): Show |
a0001a0002a0004 | a0001c0001a0001c0005a0002c0002others(1): Show | a0001c0001t0001a0001c0005t0009a0002c0002t0006others(2): Show | a0001c0001t0001g0356a0001c0005t0009g0309a0002c0002t0006g0151others(3): Show | 6 | 368 | 0.0163 | -1 | c.-20 others(8): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ACSF3_chr16_89088852_89161233 | 89109229 | CA | C | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0005a0002c0003others(5): Show | a0001c0001t0001a0001c0001t0012a0001c0005t0009others(11): Show | a0001c0001t0001g0086a0001c0001t0001g0256a0001c0001t0012g0272others(35): Show | 39 | 368 | 0.1060 | -1 | c.823 others(9): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ACSF3_chr16_89088852_89161233 | 89109403 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0005a0001c0014others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(38): Show | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0085others(187): Show | 194 | 368 | 0.5272 | -1 | c.823 others(9): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ACSF3_chr16_89088852_89161233 | 89122498 | CT | C | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
a0001a0004a0005 | a0001c0005a0004c0004a0005c0009 | a0001c0005t0009a0004c0004t0003a0004c0004t0022others(5): Show | a0001c0005t0009g0296a0001c0005t0009g0297a0004c0004t0003g0005others(33): Show | 37 | 368 | 0.1005 | -1 | c.123 others(10): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | TogoVar | ||||||
ACSF3_chr16_89088852_89161233 | 89124021 | GC | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
a0001a0003a0005others(5): Show | a0001c0001a0001c0005a0001c0014others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(40): Show | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(211): Show | 217 | 368 | 0.5897 | -1 | c.123 others(10): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | TogoVar | ||||||
ACSF3_chr16_89088852_89161233 | 89128972 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0005a0001c0014others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(57): Show | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(287): Show | 294 | 368 | 0.7989 | -1 | c.124 others(10): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |