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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ATP2B3_chrX_153512642_153587929 | 153542168 | TCC | T | intron_variant | MODIFIER | NA18962.hp1 | a0007 | a0007c0023 | a0007c0023t0001 | a0007c0023t0001g0097 | 1 | 267 | 0.0038 | -2 | c.665 others(17): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ATP2B3_chrX_153512642_153587929 | 153545092 | CGG | C | intron_variant | MODIFIER | HG02258.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0035 | 1 | 267 | 0.0038 | -2 | c.917 others(17): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ATP2B3_chrX_153512642_153587929 | 153559707 | GGT | G | intron_variant | MODIFIER | HG03453.hp1 NA18906.hp1 |
a0001 | a0001c0005 | a0001c0005t0007 | a0001c0005t0007g0016 | 2 | 267 | 0.0075 | -2 | c.262 others(17): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ATP2B3_chrX_153512642_153587929 | 153571003 | TAC | T | intron_variant | MODIFIER | HG00639.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0020others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0020t0009others(1): Show | a0001c0001t0001g0161a0001c0001t0001g0206a0001c0001t0001g0208others(3): Show | 6 | 267 | 0.0225 | -2 | c.334 others(21): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ATP2B3_chrX_153512642_153587929 | 153572628 | CAT | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(261): Show |
a0000a0001a0002others(5): Show | a0000c0008a0000c0013a0000c0018others(21): Show | a0000c0008t0021a0000c0013t0041a0000c0018t0013others(77): Show | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(243): Show | 264 | 267 | 0.9888 | -2 | c.334 others(21): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ATP2B3_chrX_153512642_153587929 | 153587651 | GCA | G | downstream_gene_variant | MODIFIER | HG01433.hp1 HG02004.hp1 NA18950.hp2 others(3): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0014a0001c0002t0029others(1): Show | a0001c0002t0002g0012a0001c0002t0002g0169a0001c0002t0014g0012others(3): Show | 6 | 267 | 0.0225 | -2 | c.*73 others(13): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 4723 | chrX | TogoVar | ||||||
ATP2B4_chr1_203621832_203749081 | 203626272 | GGT | G | upstream_gene_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(58): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0082others(58): Show | 61 | 318 | 0.1918 | -2 | c.-14 others(13): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 559 | chr1 | TogoVar | ||||||
ATP2B4_chr1_203621832_203749081 | 203627674 | GAA | G | intron_variant | MODIFIER | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0012a0001c0001t0014a0001c0002t0008others(2): Show | a0001c0001t0012g0311a0001c0001t0014g0315a0001c0001t0014g0316others(4): Show | 7 | 318 | 0.0220 | -2 | c.-46 others(19): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203630347 | TTC | T | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp1 HG02258.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0006a0002c0005 | a0001c0001t0002a0001c0001t0015a0001c0001t0030others(2): Show | a0001c0001t0002g0051a0001c0001t0015g0034a0001c0001t0015g0035others(4): Show | 7 | 318 | 0.0220 | -2 | c.-46 others(21): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203637435 | CAA | C | intron_variant | MODIFIER | HG01109.hp2 HG02451.hp1 HG02572.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0002a0001c0001t0014a0001c0001t0043others(3): Show | a0001c0001t0002g0153a0001c0001t0014g0315a0001c0001t0014g0316others(5): Show | 8 | 318 | 0.0252 | -2 | c.-46 others(23): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203644249 | TAA | T | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(85): Show |
a0001a0006a0008 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(85): Show | 88 | 318 | 0.2767 | -2 | c.-46 others(23): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203670168 | ACT | A | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0055others(193): Show | 197 | 318 | 0.6195 | -2 | c.-46 others(23): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203672324 | CTT | C | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(71): Show |
a0001a0009 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0039others(71): Show | 74 | 318 | 0.2327 | -2 | c.-46 others(23): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203675771 | AAG | A | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(29): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0041a0001c0001t0001g0076a0001c0001t0001g0116others(29): Show | 32 | 318 | 0.1006 | -2 | c.-46 others(21): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203680060 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0003a0001c0004others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0055others(127): Show | 130 | 318 | 0.4088 | -2 | c.-46 others(21): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203683666 | CTT | C | intron_variant | MODIFIER | HG01496.hp1 HG02109.hp1 HG02896.hp2 others(3): Show |
a0001 | a0001c0001a0001c0011a0001c0012 | a0001c0001t0001a0001c0001t0003a0001c0011t0012others(2): Show | a0001c0001t0001g0072a0001c0001t0003g0194a0001c0011t0012g0284others(3): Show | 6 | 318 | 0.0189 | -2 | c.193 others(17): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203685540 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0003a0001c0004others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(71): Show | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0016others(281): Show | 285 | 318 | 0.8962 | -2 | c.193 others(19): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203703164 | CGA | C | intron_variant | MODIFIER | HG00558.hp2 HG00621.hp1 HG02148.hp2 others(10): Show |
a0001 | a0001c0001a0001c0003a0001c0023 | a0001c0001t0001a0001c0001t0003a0001c0001t0026others(6): Show | a0001c0001t0001g0083a0001c0001t0003g0246a0001c0001t0026g0257others(10): Show | 13 | 318 | 0.0409 | -2 | c.938 others(17): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203704467 | CTT | C | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp2 HG01109.hp2 others(36): Show |
a0001 | a0001c0001a0001c0008a0001c0019 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(36): Show | 39 | 318 | 0.1226 | -2 | c.109 others(19): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203717441 | CAA | C | intron_variant | MODIFIER | HG01243.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0006a0001c0009 | a0001c0006t0002a0001c0006t0006a0001c0006t0039others(1): Show | a0001c0006t0002g0317a0001c0006t0006g0066a0001c0006t0039g0018others(2): Show | 5 | 318 | 0.0157 | -2 | c.240 others(21): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203723392 | GTT | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(96): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0003a0001c0016others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0002g0051others(95): Show | 99 | 318 | 0.3113 | -2 | c.302 others(19): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203723420 | ATC | A | intron_variant | MODIFIER | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
a0001 | a0001c0001a0001c0006a0001c0009 | a0001c0001t0028a0001c0001t0048a0001c0006t0002others(2): Show | a0001c0001t0028g0010a0001c0001t0048g0213a0001c0006t0002g0317others(3): Show | 6 | 318 | 0.0189 | -2 | c.302 others(19): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203734705 | CAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(103): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(33): Show | a0001c0001t0002g0153a0001c0001t0004g0045a0001c0001t0004g0047others(103): Show | 106 | 318 | 0.3333 | -2 | c.331 others(21): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ATP2B4_chr1_203621832_203749081 | 203740441 | CTT | C | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(34): Show | a0001c0001t0002g0044a0001c0001t0002g0046a0001c0001t0002g0049others(109): Show | 112 | 318 | 0.3522 | -2 | c.*60 others(11): Show |
ATP2B4 | ENSG00000058668.16 | transcript | ENST00000357681.10 | protein_coding | 21/21 | 604 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||
ATP2C1_chr3_130889084_131008150 | 130907079 | TAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | 382 | 0.1309 | -2 | c.6+1 others(17): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ATP2C1_chr3_130889084_131008150 | 130921227 | GCC | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | 382 | 0.1309 | -2 | c.7-9 others(15): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | TogoVar | ||||||
ATP2C1_chr3_130889084_131008150 | 130941223 | AGT | A | intron_variant | MODIFIER | HG00741.hp2 HG01884.hp2 HG01943.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | 382 | 0.0471 | -2 | c.423 others(17): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ATP2C1_chr3_130889084_131008150 | 130961250 | GTT | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(154): Show |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(154): Show | 157 | 382 | 0.4110 | -2 | c.899 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ATP2C1_chr3_130889084_131008150 | 130962715 | TAA | T | intron_variant | MODIFIER | HG01243.hp1 HG02258.hp1 HG02809.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0006a0001c0003t0001 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | 382 | 0.0157 | -2 | c.900 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ATP2C1_chr3_130889084_131008150 | 130967821 | CTT | C | intron_variant | MODIFIER | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0370a0001c0003t0001g0371a0001c0003t0001g0372others(2): Show | 5 | 382 | 0.0131 | -2 | c.130 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ATP2C1_chr3_130889084_131008150 | 130970369 | TAC | T | intron_variant | MODIFIER | HG01943.hp2 HG02040.hp2 HG02145.hp2 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0009a0001c0002t0001 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 17 | 382 | 0.0445 | -2 | c.141 others(21): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ATP2C1_chr3_130889084_131008150 | 131006635 | TTG | T | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(35): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 38 | 382 | 0.0995 | -2 | c.*52 others(13): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3486 | chr3 | TogoVar | ||||||
ATP2C2_chr16_84363538_84469187 | 84364781 | TAA | T | upstream_gene_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
a0001a0002a0004others(3): Show | a0001c0002a0001c0003a0001c0010others(11): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(17): Show | a0001c0002t0001g0259a0001c0002t0001g0267a0001c0002t0001g0268others(57): Show | 60 | 432 | 0.1389 | -2 | c.-38 others(13): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 3756 | chr16 | TogoVar | ||||||
ATP2C2_chr16_84363538_84469187 | 84364956 | CAA | C | upstream_gene_variant | MODIFIER | HG02280.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0009others(4): Show | a0001c0002t0002a0001c0003t0001a0001c0009t0001others(4): Show | a0001c0002t0002g0068a0001c0003t0001g0065a0001c0009t0001g0286others(6): Show | 9 | 432 | 0.0208 | -2 | c.-36 others(13): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 3581 | chr16 | TogoVar | ||||||
ATP2C2_chr16_84363538_84469187 | 84365297 | ATT | A | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0003a0001c0005others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0411a0001c0001t0002g0007a0001c0001t0002g0397others(47): Show | 50 | 432 | 0.1157 | -2 | c.-33 others(13): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 3240 | chr16 | TogoVar | ||||||
ATP2C2_chr16_84363538_84469187 | 84375540 | CAA | C | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(183): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0002a0001c0003others(40): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | a0001c0001t0001g0078a0001c0001t0001g0313a0001c0001t0001g0329others(183): Show | 186 | 432 | 0.4306 | -2 | c.99+ others(17): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84389720 | CTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00621.hp1 HG00621.hp2 others(65): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(21): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0419a0001c0001t0002g0007a0001c0001t0002g0312others(65): Show | 68 | 432 | 0.1574 | -2 | c.100 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84396223 | CGT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0001c0003others(51): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(70): Show | a0001c0001t0001g0329a0001c0001t0001g0334a0001c0001t0002g0186others(234): Show | 237 | 432 | 0.5486 | -2 | c.100 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84396549 | CAA | C | intron_variant | MODIFIER | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(21): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0001c0005others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(14): Show | a0001c0001t0001g0391a0001c0001t0002g0216a0001c0003t0001g0048others(21): Show | 24 | 432 | 0.0556 | -2 | c.100 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84404809 | CTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(27): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0003a0001c0005others(13): Show | a0001c0001t0002a0001c0001t0003a0001c0003t0001others(15): Show | a0001c0001t0002g0071a0001c0001t0002g0198a0001c0001t0003g0226others(27): Show | 30 | 432 | 0.0694 | -2 | c.211 others(17): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84412252 | GTA | G | intron_variant | MODIFIER | HG01243.hp2 HG02818.hp1 HG03130.hp2 |
a0001a0004a0015 | a0001c0005a0004c0013a0015c0078 | a0001c0005t0002a0004c0013t0001a0015c0078t0001 | a0001c0005t0002g0392a0004c0013t0001g0077a0015c0078t0001g0001 | 3 | 432 | 0.0069 | -2 | c.515 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84412290 | ATG | A | intron_variant | MODIFIER | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(2): Show |
a0001a0002 | a0001c0015a0002c0007a0002c0008 | a0001c0015t0001a0002c0007t0001a0002c0008t0001 | a0001c0015t0001g0088a0002c0007t0001g0293a0002c0008t0001g0049others(2): Show | 5 | 432 | 0.0116 | -2 | c.515 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84412382 | GTA | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0003others(37): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | a0001c0001t0001g0078a0001c0001t0001g0313a0001c0001t0001g0391others(170): Show | 173 | 432 | 0.4005 | -2 | c.515 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84412452 | CTG | C | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(18): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0329a0001c0001t0001g0419a0001c0001t0002g0071others(81): Show | 84 | 432 | 0.1944 | -2 | c.515 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84412508 | CTG | C | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(108): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0003others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(37): Show | a0001c0001t0001g0334a0001c0001t0002g0228a0001c0001t0002g0229others(108): Show | 111 | 432 | 0.2569 | -2 | c.515 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84412547 | CGT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(259): Show |
a0001a0002a0003others(17): Show | a0001c0001a0001c0002a0001c0003others(51): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | a0001c0001t0001g0329a0001c0001t0001g0334a0001c0001t0001g0419others(259): Show | 262 | 432 | 0.6065 | -2 | c.515 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84413098 | CAA | C | intron_variant | MODIFIER | HG00544.hp1 HG00597.hp2 HG00733.hp1 others(72): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0001c0003others(19): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | a0001c0001t0001g0313a0001c0001t0001g0391a0001c0001t0001g0411others(72): Show | 75 | 432 | 0.1736 | -2 | c.515 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ATP2C2_chr16_84363538_84469187 | 84413769 | CAG | C | intron_variant | MODIFIER | HG02055.hp2 HG03098.hp2 HG03139.hp1 others(1): Show |
a0001a0002 | a0001c0003a0002c0004a0002c0006 | a0001c0003t0001a0002c0004t0001a0002c0006t0001 | a0001c0003t0001g0048a0002c0004t0001g0223a0002c0006t0001g0069others(1): Show | 4 | 432 | 0.0093 | -2 | c.516 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 6/26 | chr16 | TogoVar | ||||||
ATP2C2_chr16_84363538_84469187 | 84416930 | CAG | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0002a0001c0003others(45): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | a0001c0001t0001g0078a0001c0001t0001g0313a0001c0001t0001g0391others(202): Show | 205 | 432 | 0.4745 | -2 | c.624 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 7/26 | chr16 | TogoVar | ||||||
ATP2C2_chr16_84363538_84469187 | 84419208 | TAA | T | intron_variant | MODIFIER | HG01192.hp1 HG02040.hp1 HG02280.hp2 others(12): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0002a0001c0002t0001a0001c0003t0001others(11): Show | a0001c0001t0002g0071a0001c0002t0001g0267a0001c0003t0001g0170others(12): Show | 15 | 432 | 0.0347 | -2 | c.625 others(19): Show |
ATP2C2 | ENSG00000064270.13 | transcript | ENST00000262429.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |