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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACER3_chr11_76855918_77031797 | 76891115 | TA | T | intron_variant | MODIFIER | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(80): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(35): Show | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0023others(80): Show | 83 | 346 | 0.2399 | -1 | c.103 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76897707 | CT | C | intron_variant | MODIFIER | HG01261.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
a0001 | a0001c0003 | a0001c0003t0026a0001c0003t0137a0001c0003t0139others(3): Show | a0001c0003t0026g0114a0001c0003t0026g0115a0001c0003t0026g0117others(5): Show | 8 | 346 | 0.0231 | -1 | c.104 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76898727 | AC | A | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(23): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(69): Show | 72 | 346 | 0.2081 | -1 | c.104 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76898903 | CA | C | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(70): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0002 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(32): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(70): Show | 73 | 346 | 0.2110 | -1 | c.104 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76901270 | TA | T | intron_variant | MODIFIER | HG01099.hp2 HG01891.hp1 HG02145.hp1 others(12): Show |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0011a0001c0003t0016a0001c0003t0138others(3): Show | a0001c0003t0011g0101a0001c0003t0011g0103a0001c0003t0011g0104others(12): Show | 15 | 346 | 0.0434 | -1 | c.104 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76902048 | AT | A | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
a0001a0002 | a0001c0001a0001c0005a0001c0007others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(76): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(182): Show | 185 | 346 | 0.5347 | -1 | c.104 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76903494 | AG | A | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(104): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(223): Show | 226 | 346 | 0.6532 | -1 | c.104 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76907355 | TG | T | intron_variant | MODIFIER | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(81): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(35): Show | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0023others(81): Show | 84 | 346 | 0.2428 | -1 | c.104 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | chr11 | TogoVar | ||||||
ACER3_chr11_76855918_77031797 | 76913540 | TC | T | intron_variant | MODIFIER | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(81): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(35): Show | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0023others(81): Show | 84 | 346 | 0.2428 | -1 | c.104 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76916533 | GT | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(78): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(184): Show | 187 | 346 | 0.5405 | -1 | c.104 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76917859 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0002others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(74): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(186): Show | 189 | 346 | 0.5462 | -1 | c.104 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76920634 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(119): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0007others(2): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(66): Show | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0023others(119): Show | 122 | 346 | 0.3526 | -1 | c.104 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76930659 | GT | G | intron_variant | MODIFIER | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(13): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0014a0001c0001t0017a0001c0001t0029others(5): Show | a0001c0001t0014g0199a0001c0001t0014g0205a0001c0001t0014g0206others(13): Show | 16 | 346 | 0.0462 | -1 | c.214 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76931953 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(159): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(85): Show | a0001c0001t0002g0161a0001c0001t0003g0020a0001c0001t0003g0021others(159): Show | 162 | 346 | 0.4682 | -1 | c.214 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76933240 | CT | C | intron_variant | MODIFIER | HG01081.hp1 HG01261.hp2 HG01884.hp1 others(55): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0007others(1): Show | a0001c0001t0005a0001c0001t0071a0001c0003t0011others(37): Show | a0001c0001t0005g0147a0001c0001t0071g0138a0001c0003t0011g0101others(55): Show | 58 | 346 | 0.1676 | -1 | c.214 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76933330 | AG | A | intron_variant | MODIFIER | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0014a0001c0001t0029a0001c0001t0070others(3): Show | a0001c0001t0014g0199a0001c0001t0014g0205a0001c0001t0014g0206others(8): Show | 11 | 346 | 0.0318 | -1 | c.214 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76935190 | AT | A | intron_variant | MODIFIER | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(38): Show |
a0001 | a0001c0003 | a0001c0003t0011a0001c0003t0016a0001c0003t0026others(25): Show | a0001c0003t0011g0101a0001c0003t0011g0103a0001c0003t0011g0104others(38): Show | 41 | 346 | 0.1185 | -1 | c.214 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76940889 | GA | G | intron_variant | MODIFIER | HG03041.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0037a0001c0001t0074a0001c0001t0088 | a0001c0001t0037g0099a0001c0001t0037g0128a0001c0001t0074g0129others(1): Show | 4 | 346 | 0.0116 | -1 | c.214 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76941010 | TA | T | intron_variant | MODIFIER | HG03209.hp1 HG03209.hp2 NA19090.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0033a0001c0003t0026a0001c0003t0150 | a0001c0001t0033g0024a0001c0003t0026g0115a0001c0003t0150g0339 | 3 | 346 | 0.0087 | -1 | c.214 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76943749 | AC | A | intron_variant | MODIFIER | HG01346.hp2 HG02109.hp2 HG02486.hp2 others(11): Show |
a0002 | a0002c0002 | a0002c0002t0020a0002c0002t0025a0002c0002t0098others(6): Show | a0002c0002t0020g0214a0002c0002t0020g0215a0002c0002t0020g0217others(11): Show | 14 | 346 | 0.0405 | -1 | c.215 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76943913 | CT | C | intron_variant | MODIFIER | HG00597.hp2 HG00621.hp2 HG01167.hp2 others(52): Show |
a0001a0002 | a0001c0003a0002c0002a0002c0004 | a0001c0003t0026a0001c0003t0130a0001c0003t0131others(31): Show | a0001c0003t0026g0115a0001c0003t0130g0346a0001c0003t0131g0342others(52): Show | 55 | 346 | 0.1590 | -1 | c.215 others(10): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76949600 | CA | C | intron_variant | MODIFIER | HG02258.hp2 HG02486.hp1 HG02922.hp1 others(6): Show |
a0002 | a0002c0002 | a0002c0002t0021a0002c0002t0045a0002c0002t0121others(2): Show | a0002c0002t0021g0006a0002c0002t0021g0008a0002c0002t0021g0011others(6): Show | 9 | 346 | 0.0260 | -1 | c.215 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76950410 | TA | T | intron_variant | MODIFIER | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(11): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(8): Show | a0001c0001t0002g0166a0001c0001t0004g0077a0001c0001t0004g0078others(11): Show | 14 | 346 | 0.0405 | -1 | c.215 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76952668 | CT | C | intron_variant | MODIFIER | HG01256.hp1 HG01261.hp2 HG01884.hp1 others(43): Show |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0011a0001c0003t0016a0001c0003t0026others(29): Show | a0001c0003t0011g0101a0001c0003t0011g0103a0001c0003t0011g0104others(43): Show | 46 | 346 | 0.1330 | -1 | c.215 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76953947 | CT | C | intron_variant | MODIFIER | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(54): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0002a0001c0003t0011a0001c0003t0016others(36): Show | a0001c0001t0002g0192a0001c0003t0011g0101a0001c0003t0011g0103others(54): Show | 57 | 346 | 0.1647 | -1 | c.215 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76954591 | GT | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
a0001 | a0001c0001a0001c0005a0001c0007 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(69): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(169): Show | 172 | 346 | 0.4971 | -1 | c.215 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76956684 | CT | C | intron_variant | MODIFIER | HG01975.hp2 HG04228.hp1 NA18942.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0005a0002c0002t0001a0002c0002t0010others(3): Show | a0001c0001t0005g0160a0002c0002t0001g0247a0002c0002t0001g0252others(4): Show | 7 | 346 | 0.0202 | -1 | c.215 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76958183 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG01496.hp2 HG02145.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0003a0001c0001t0059a0001c0003t0138others(2): Show | a0001c0001t0003g0032a0001c0001t0003g0036a0001c0001t0003g0096others(4): Show | 7 | 346 | 0.0202 | -1 | c.215 others(8): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76972280 | TC | T | intron_variant | MODIFIER | HG01081.hp2 HG01099.hp2 HG01175.hp2 others(11): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0010a0002c0002t0043others(7): Show | a0002c0002t0001g0228a0002c0002t0010g0248a0002c0002t0010g0277others(11): Show | 14 | 346 | 0.0405 | -1 | c.268 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 3/10 | chr11 | TogoVar | ||||||
ACER3_chr11_76855918_77031797 | 76972550 | CT | C | intron_variant | MODIFIER | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0014a0001c0001t0017a0001c0001t0029others(4): Show | a0001c0001t0014g0199a0001c0001t0014g0205a0001c0001t0014g0206others(12): Show | 15 | 346 | 0.0434 | -1 | c.268 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76972786 | CA | C | intron_variant | MODIFIER | HG01074.hp2 HG02630.hp1 HG02717.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0195a0001c0001t0017g0196a0001c0001t0017g0197others(1): Show | 4 | 346 | 0.0116 | -1 | c.268 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 3/10 | chr11 | TogoVar | ||||||
ACER3_chr11_76855918_77031797 | 76974776 | TA | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(98): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(212): Show | 215 | 346 | 0.6214 | -1 | c.268 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76974785 | AG | A | intron_variant | MODIFIER | HG00597.hp2 HG00621.hp2 HG01167.hp2 others(13): Show |
a0002 | a0002c0004 | a0002c0004t0006a0002c0004t0015a0002c0004t0087others(2): Show | a0002c0004t0006g0304a0002c0004t0006g0305a0002c0004t0006g0306others(13): Show | 16 | 346 | 0.0462 | -1 | c.268 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76975874 | CT | C | intron_variant | MODIFIER | HG00597.hp2 HG00621.hp2 HG00673.hp2 others(18): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0002others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0068others(10): Show | a0001c0001t0002g0181a0001c0001t0004g0056a0001c0001t0004g0077others(18): Show | 21 | 346 | 0.0607 | -1 | c.268 others(8): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76983796 | AT | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(67): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(142): Show | 145 | 346 | 0.4191 | -1 | c.321 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76989035 | TA | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(73): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(185): Show | 188 | 346 | 0.5434 | -1 | c.403 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76991815 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
a0001a0002a0003 | a0001c0005a0002c0002a0003c0006 | a0001c0005t0047a0002c0002t0001a0002c0002t0009others(47): Show | a0001c0005t0047g0005a0002c0002t0001g0002a0002c0002t0001g0003others(107): Show | 110 | 346 | 0.3179 | -1 | c.438 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76992874 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(95): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(216): Show | 219 | 346 | 0.6330 | -1 | c.438 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 76994136 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(102): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(227): Show | 230 | 346 | 0.6647 | -1 | c.438 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 77002160 | TA | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(103): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(228): Show | 231 | 346 | 0.6676 | -1 | c.497 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 77005990 | TA | T | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp2 HG00738.hp1 others(14): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0002a0001c0001t0012a0001c0003t0131others(7): Show | a0001c0001t0002g0144a0001c0001t0012g0143a0001c0003t0131g0342others(14): Show | 17 | 346 | 0.0491 | -1 | c.497 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 7/10 | chr11 | TogoVar | ||||||
ACER3_chr11_76855918_77031797 | 77005991 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0006 | a0001c0001t0007a0002c0002t0001a0002c0002t0009others(21): Show | a0001c0001t0007g0150a0002c0002t0001g0003a0002c0002t0001g0004others(48): Show | 51 | 346 | 0.1474 | -1 | c.497 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 77010431 | CA | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(66): Show | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0140others(143): Show | 146 | 346 | 0.4220 | -1 | c.498 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 77012416 | CA | C | intron_variant | MODIFIER | HG01081.hp1 HG01256.hp1 HG01256.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0003a0001c0001t0032a0001c0007t0064others(5): Show | a0001c0001t0003g0039a0001c0001t0032g0066a0001c0007t0064g0126others(7): Show | 10 | 346 | 0.0289 | -1 | c.498 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 77016822 | GT | G | intron_variant | MODIFIER | HG01081.hp1 HG01261.hp2 HG01884.hp1 others(61): Show |
a0001a0002 | a0001c0003a0001c0005a0001c0007others(1): Show | a0001c0003t0011a0001c0003t0016a0001c0003t0026others(39): Show | a0001c0003t0011g0101a0001c0003t0011g0103a0001c0003t0011g0104others(61): Show | 64 | 346 | 0.1850 | -1 | c.704 others(7): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 77017940 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(82): Show | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0023others(176): Show | 179 | 346 | 0.5173 | -1 | c.704 others(9): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACER3_chr11_76855918_77031797 | 77020589 | CA | C | 3_prime_UTR_variant | MODIFIER | HG01106.hp1 HG01167.hp1 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0001 | a0001c0001t0127a0001c0001t0128a0001c0001t0129 | a0001c0001t0127g0046a0001c0001t0128g0072a0001c0001t0129g0071 | 3 | 346 | 0.0087 | -1 | c.*26 others(5): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 11/11 | 265 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||
ACER3_chr11_76855918_77031797 | 77022868 | CA | C | 3_prime_UTR_variant | MODIFIER | HG01081.hp2 HG01943.hp2 HG02523.hp1 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0043a0002c0002t0112a0002c0002t0115others(2): Show | a0002c0002t0043g0227a0002c0002t0043g0322a0002c0002t0112g0320others(3): Show | 6 | 346 | 0.0173 | -1 | c.*25 others(6): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 11/11 | 2565 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||
ACER3_chr11_76855918_77031797 | 77024073 | CA | C | 3_prime_UTR_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(51): Show | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0023others(129): Show | 132 | 346 | 0.3815 | -1 | c.*37 others(6): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 11/11 | 3774 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||
ACER3_chr11_76855918_77031797 | 77024156 | GA | G | 3_prime_UTR_variant | MODIFIER | HG01261.hp2 HG01884.hp2 HG02258.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0075a0001c0003t0027a0001c0003t0137others(1): Show | a0001c0001t0075g0200a0001c0003t0027g0118a0001c0003t0027g0119others(3): Show | 6 | 346 | 0.0173 | -1 | c.*38 others(6): Show |
ACER3 | ENSG00000078124.13 | transcript | ENST00000532485.6 | protein_coding | 11/11 | 3845 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |