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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SNX10_chr7_26286862_26379383 | 26307680 | CT | C | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(122): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0021others(122): Show | 125 | 390 | 0.3205 | -1 | c.-24 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26309368 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 96 | 390 | 0.2462 | -1 | c.-24 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26310683 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 278 | 390 | 0.7128 | -1 | c.-24 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26314156 | TA | T | intron_variant | MODIFIER | NA18946.hp2 NA18951.hp2 NA18985.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0242a0001c0001t0003g0071a0001c0001t0003g0095 | 3 | 390 | 0.0077 | -1 | c.-24 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26314264 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 249 | 390 | 0.6385 | -1 | c.-24 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26316181 | CA | C | intron_variant | MODIFIER | HG00738.hp1 HG01106.hp2 HG01258.hp2 others(32): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0080others(32): Show | 35 | 390 | 0.0897 | -1 | c.-24 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26317659 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 189 | 390 | 0.4846 | -1 | c.-24 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26322578 | AT | A | intron_variant | MODIFIER | HG03209.hp2 HG03540.hp1 NA18988.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013 | a0001c0001t0001g0308a0001c0001t0013g0371a0001c0001t0013g0372 | 3 | 390 | 0.0077 | -1 | c.-23 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26325731 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 223 | 390 | 0.5718 | -1 | c.-23 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26326949 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(213): Show | 218 | 390 | 0.5590 | -1 | c.-23 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26327726 | CT | C | intron_variant | MODIFIER | HG01099.hp1 HG01516.hp1 HG02165.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010a0001c0001t0015 | a0001c0001t0001g0289a0001c0001t0001g0312a0001c0001t0001g0330others(4): Show | 7 | 390 | 0.0180 | -1 | c.-23 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26331167 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(67): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0062others(66): Show | 70 | 390 | 0.1795 | -1 | c.-23 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26335735 | CT | C | intron_variant | MODIFIER | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(36): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0137a0001c0001t0001g0226a0001c0001t0001g0231others(35): Show | 39 | 390 | 0.1000 | -1 | c.-23 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26336372 | TA | T | intron_variant | MODIFIER | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(32): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0021a0001c0001t0001g0235a0001c0001t0002g0004others(31): Show | 35 | 390 | 0.0897 | -1 | c.-23 others(10): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26338110 | CT | C | intron_variant | MODIFIER | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(13): Show | 16 | 390 | 0.0410 | -1 | c.-23 others(9): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26339543 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(153): Show | 158 | 390 | 0.4051 | -1 | c.-23 others(9): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26339850 | CT | C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(143): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0162others(142): Show | 146 | 390 | 0.3744 | -1 | c.-23 others(9): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26341499 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 159 | 390 | 0.4077 | -1 | c.-23 others(9): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26342028 | CT | C | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0014a0001c0001t0024others(1): Show | a0001c0001t0001g0105a0001c0001t0001g0137a0001c0001t0001g0155others(6): Show | 9 | 390 | 0.0231 | -1 | c.-23 others(9): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26349681 | CT | C | intron_variant | MODIFIER | HG01099.hp1 HG01891.hp1 HG02258.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0180others(7): Show | 10 | 390 | 0.0256 | -1 | c.24+ others(8): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 2/6 | chr7 | TogoVar | |||||||
SNX10_chr7_26286862_26379383 | 26351658 | TG | T | intron_variant | MODIFIER | HG00621.hp1 HG01255.hp2 HG01346.hp1 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0102a0001c0001t0001g0110a0001c0001t0001g0111others(18): Show | 21 | 390 | 0.0539 | -1 | c.24+ others(8): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 2/6 | chr7 | TogoVar | |||||||
SNX10_chr7_26286862_26379383 | 26353437 | CT | C | intron_variant | MODIFIER | HG01081.hp2 HG01099.hp1 HG02109.hp1 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0082others(17): Show | 20 | 390 | 0.0513 | -1 | c.24+ others(8): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26354690 | GT | G | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp2 HG00741.hp1 others(52): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0180others(51): Show | 55 | 390 | 0.1410 | -1 | c.25- others(8): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26354699 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 240 | 390 | 0.6154 | -1 | c.25- others(8): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26357327 | TA | T | intron_variant | MODIFIER | HG00323.hp2 HG01167.hp1 HG01257.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0017 | a0001c0001t0001g0065a0001c0001t0001g0265a0001c0001t0001g0266others(6): Show | 9 | 390 | 0.0231 | -1 | c.25- others(8): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26359515 | TA | T | intron_variant | MODIFIER | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0007a0001c0001t0001g0089a0001c0001t0001g0094others(24): Show | 27 | 390 | 0.0692 | -1 | c.25- others(8): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26379087 | TG | T | downstream_gene_variant | MODIFIER | HG01081.hp2 HG01243.hp1 HG01361.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(1): Show | a0001c0001t0001g0006a0001c0001t0001g0077a0001c0001t0001g0080others(13): Show | 16 | 390 | 0.0410 | -1 | c.*65 others(6): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 4705 | chr7 | TogoVar | |||||||
SNX11_chr17_48102766_48128601 | 48104073 | TG | T | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 310 | 416 | 0.7452 | -1 | c.-37 others(6): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 3692 | chr17 | TogoVar | |||||||
SNX11_chr17_48102766_48128601 | 48104652 | AT | A | upstream_gene_variant | MODIFIER | HG01257.hp1 HG02630.hp2 HG02735.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0084others(10): Show | 16 | 416 | 0.0385 | -1 | c.-31 others(6): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 3113 | chr17 | TogoVar | |||||||
SNX11_chr17_48102766_48128601 | 48112731 | CT | C | intron_variant | MODIFIER | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(31): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0007 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 34 | 416 | 0.0817 | -1 | c.129 others(7): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
SNX11_chr17_48102766_48128601 | 48114168 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 306 | 416 | 0.7356 | -1 | c.230 others(8): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
SNX11_chr17_48102766_48128601 | 48114457 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 104 | 416 | 0.2500 | -1 | c.230 others(9): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
SNX11_chr17_48102766_48128601 | 48115943 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(126): Show | 266 | 416 | 0.6394 | -1 | c.230 others(9): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
SNX11_chr17_48102766_48128601 | 48117258 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 412 | 416 | 0.9904 | -1 | c.231 others(9): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
SNX11_chr17_48102766_48128601 | 48120201 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00741.hp2 others(46): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0034others(26): Show | 49 | 416 | 0.1178 | -1 | c.540 others(9): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
SNX11_chr17_48102766_48128601 | 48125131 | CT | C | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(40): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0017others(17): Show | 43 | 416 | 0.1034 | -1 | c.*36 others(6): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 1531 | chr17 | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71054787 | TA | T | downstream_gene_variant | MODIFIER | NA18989.hp1 NA18991.hp2 NA19054.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0001a0001c0001t0002g0004 | 3 | 309 | 0.0097 | -1 | c.*62 others(6): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 4459 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71055021 | TA | T | downstream_gene_variant | MODIFIER | NA19089.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0042 | 1 | 309 | 0.0032 | -1 | c.*59 others(6): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 4225 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71056012 | TA | T | downstream_gene_variant | MODIFIER | NA19054.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0001 | 1 | 309 | 0.0032 | -1 | c.*50 others(6): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 3234 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71056168 | AG | A | downstream_gene_variant | MODIFIER | NA19054.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0001 | 1 | 309 | 0.0032 | -1 | c.*48 others(6): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 3078 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71057846 | AT | A | downstream_gene_variant | MODIFIER | HG01257.hp2 HG01496.hp1 HG01975.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0076 | 3 | 309 | 0.0097 | -1 | c.*31 others(6): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 1400 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71058388 | CT | C | downstream_gene_variant | MODIFIER | NA18960.hp1 NA18969.hp2 NA19082.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0009 | 3 | 309 | 0.0097 | -1 | c.*26 others(6): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 858 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71058616 | TA | T | downstream_gene_variant | MODIFIER | NA19089.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0042 | 1 | 309 | 0.0032 | -1 | c.*23 others(6): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 630 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71059120 | TA | T | downstream_gene_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0004 | 1 | 309 | 0.0032 | -1 | c.*18 others(6): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 126 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71059962 | CA | C | 3_prime_UTR_variant | MODIFIER | NA19089.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0042 | 1 | 309 | 0.0032 | -1 | c.*10 others(6): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 4/4 | 1053 | chrX | TogoVar | ||||||
SNX12_chrX_71054247_71073334 | 71061150 | AT | A | intron_variant | MODIFIER | NA19089.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0042 | 1 | 309 | 0.0032 | -1 | c.387 others(7): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 3/3 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71062146 | GT | G | intron_variant | MODIFIER | NA18988.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0091 | 1 | 309 | 0.0032 | -1 | c.262 others(8): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 2/3 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71062368 | CT | C | intron_variant | MODIFIER | HG01168.hp2 HG01257.hp2 HG02258.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0076others(6): Show | 9 | 309 | 0.0291 | -1 | c.262 others(8): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 2/3 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71062525 | AC | A | intron_variant | MODIFIER | HG02155.hp2 HG02165.hp2 HG02523.hp1 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 21 | 309 | 0.0680 | -1 | c.261 others(8): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 2/3 | chrX | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71062620 | GC | G | intron_variant | MODIFIER | NA18988.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0091 | 1 | 309 | 0.0032 | -1 | c.261 others(8): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 2/3 | chrX | TogoVar |