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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SMS_chrX_21935709_21999837 | 21941486 | CG | C | intron_variant | MODIFIER | NA18972.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 1 | 298 | 0.0034 | -1 | c.49+ others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21941548 | AG | A | intron_variant | MODIFIER | NA18972.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 1 | 298 | 0.0034 | -1 | c.49+ others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21941573 | AC | A | intron_variant | MODIFIER | NA19082.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0286 | 1 | 298 | 0.0034 | -1 | c.49+ others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21941657 | CG | C | intron_variant | MODIFIER | NA18972.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 1 | 298 | 0.0034 | -1 | c.49+ others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21941839 | CG | C | intron_variant | MODIFIER | NA18972.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 1 | 298 | 0.0034 | -1 | c.49+ others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | TogoVar | ||||||
SMS_chrX_21935709_21999837 | 21941884 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG01169.hp2 others(26): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0006 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0084others(26): Show | 29 | 298 | 0.0973 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21942829 | CT | C | intron_variant | MODIFIER | HG00597.hp2 HG01168.hp2 HG02280.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0080others(11): Show | 14 | 298 | 0.0470 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21943006 | AT | A | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21943053 | GC | G | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21943232 | TC | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21943284 | GT | G | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21943308 | GA | G | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21943524 | AG | A | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21944047 | CT | C | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21944102 | AC | A | intron_variant | MODIFIER | NA19001.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0297 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21944229 | GA | G | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21944522 | CA | C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(57): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0037a0001c0001t0001g0061a0001c0001t0001g0100others(57): Show | 60 | 298 | 0.2013 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21944589 | TC | T | intron_variant | MODIFIER | NA19006.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0026 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21945511 | AC | A | intron_variant | MODIFIER | NA19006.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0026 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21945634 | TC | T | intron_variant | MODIFIER | HG00673.hp1 HG02080.hp2 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0015 | a0001c0001t0005g0261a0001c0001t0015g0004 | 2 | 298 | 0.0067 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21945714 | TC | T | intron_variant | MODIFIER | NA18963.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21946148 | GT | G | intron_variant | MODIFIER | NA19006.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0026 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21946427 | AT | A | intron_variant | MODIFIER | NA19058.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0245 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21948439 | CT | C | intron_variant | MODIFIER | HG00280.hp1 HG02698.hp1 HG02735.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0009 | a0001c0001t0001g0027a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | 298 | 0.0201 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21948512 | TC | T | intron_variant | MODIFIER | NA18951.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0194 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21948894 | CT | C | intron_variant | MODIFIER | NA18951.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0194 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21949072 | TC | T | intron_variant | MODIFIER | NA18951.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0194 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21949229 | TC | T | intron_variant | MODIFIER | NA18978.hp2 | a0004 | a0004c0004 | a0004c0004t0013 | a0004c0004t0013g0293 | 1 | 298 | 0.0034 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21949950 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(164): Show | 167 | 298 | 0.5604 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21950433 | CT | C | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(4): Show | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(31): Show | 34 | 298 | 0.1141 | -1 | c.49+ others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21951736 | CT | C | intron_variant | MODIFIER | HG02723.hp1 HG02735.hp1 HG02809.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0011 | a0001c0001t0001g0087a0001c0001t0003g0115a0001c0001t0011g0139 | 3 | 298 | 0.0101 | -1 | c.49+ others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21952421 | GT | G | intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0087 | 1 | 298 | 0.0034 | -1 | c.49+ others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21952749 | GT | G | intron_variant | MODIFIER | HG02280.hp2 HG02451.hp1 HG02970.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0002g0123a0001c0001t0003g0271a0001c0001t0004g0043others(2): Show | 5 | 298 | 0.0168 | -1 | c.49+ others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21953662 | TG | T | intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0239 | 1 | 298 | 0.0034 | -1 | c.49+ others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | TogoVar | ||||||
SMS_chrX_21935709_21999837 | 21953890 | AT | A | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(28): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(3): Show | a0001c0001t0002g0267a0001c0001t0002g0276a0001c0001t0002g0277others(28): Show | 31 | 298 | 0.1040 | -1 | c.49+ others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21954730 | TA | T | intron_variant | MODIFIER | HG02109.hp1 HG02809.hp2 HG03453.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0005 | a0001c0001t0002g0007a0001c0001t0003g0012a0001c0001t0003g0115others(1): Show | 4 | 298 | 0.0134 | -1 | c.50- others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | TogoVar | ||||||
SMS_chrX_21935709_21999837 | 21957153 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(153): Show | 156 | 298 | 0.5235 | -1 | c.50- others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21957310 | AT | A | intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0047 | 1 | 298 | 0.0034 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21957959 | GT | G | intron_variant | MODIFIER | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(43): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0117a0001c0001t0002g0112a0001c0001t0002g0114others(43): Show | 46 | 298 | 0.1544 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21960399 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(153): Show | 156 | 298 | 0.5235 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21961034 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(80): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0070others(80): Show | 83 | 298 | 0.2785 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21963092 | AT | A | intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0199 | 1 | 298 | 0.0034 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21964062 | AT | A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01081.hp1 others(23): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0039a0001c0001t0001g0057a0001c0001t0001g0140others(23): Show | 26 | 298 | 0.0873 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21964556 | TC | T | intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0199 | 1 | 298 | 0.0034 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21964936 | GC | G | intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0199 | 1 | 298 | 0.0034 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21964960 | AG | A | intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0199 | 1 | 298 | 0.0034 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21965501 | TG | T | intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0199 | 1 | 298 | 0.0034 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21965783 | TA | T | intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0215 | 1 | 298 | 0.0034 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21965962 | TA | T | intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0199 | 1 | 298 | 0.0034 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21966144 | TG | T | intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0047 | 1 | 298 | 0.0034 | -1 | c.50- others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar |