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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TBL1X_chrX_9460058_9724740 | 9475553 | G | GTT | intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0001 | a0001c0001t0037 | a0001c0001t0037g0128 | 1 | 199 | 0.0050 | 2 | c.-20 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9479938 | A | ATG | intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0001 | a0001c0001t0032 | a0001c0001t0032g0121 | 1 | 199 | 0.0050 | 2 | c.-20 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9480757 | A | ACC | intron_variant | MODIFIER | HG00738.hp1 HG01433.hp1 HG01934.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(3): Show | a0001c0001t0001g0082a0001c0001t0001g0090a0001c0001t0005g0167others(5): Show | 8 | 199 | 0.0402 | 2 | c.-20 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9484317 | T | TAC | intron_variant | MODIFIER | HG01257.hp1 HG02647.hp1 HG04228.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0010 | a0001c0001t0002g0129a0001c0001t0003g0170a0001c0001t0010g0086 | 3 | 199 | 0.0151 | 2 | c.-20 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9484916 | T | TAA | intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0195 | 1 | 199 | 0.0050 | 2 | c.-20 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9486239 | C | CTT | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0012 | a0001c0001t0005g0109a0001c0001t0012g0108 | 2 | 199 | 0.0101 | 2 | c.-20 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9491306 | T | TTA | intron_variant | MODIFIER | HG00140.hp1 HG01175.hp2 HG01192.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0019others(1): Show | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(7): Show | 10 | 199 | 0.0503 | 2 | c.-20 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9491336 | A | ATT | intron_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0151 | 1 | 199 | 0.0050 | 2 | c.-20 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9491338 | A | ATT | intron_variant | MODIFIER | HG01169.hp2 HG01255.hp1 HG01515.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0089a0001c0001t0001g0113a0001c0001t0001g0177others(5): Show | 8 | 199 | 0.0402 | 2 | c.-20 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9492838 | G | GGT | intron_variant | MODIFIER | HG01081.hp1 NA18960.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0089a0001c0001t0008g0103 | 2 | 199 | 0.0101 | 2 | c.-20 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9492894 | T | TAG | intron_variant | MODIFIER | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(4): Show | a0001c0001t0002g0024a0001c0001t0006g0140a0001c0001t0007g0193others(4): Show | 7 | 199 | 0.0352 | 2 | c.-20 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | chrX | TogoVar | ||||||
TBL1X_chrX_9460058_9724740 | 9492894 | T | TGG | intron_variant | MODIFIER | HG02129.hp1 HG03688.hp1 NA19009.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0087a0001c0001t0001g0101a0001c0001t0002g0114 | 3 | 199 | 0.0151 | 2 | c.-20 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9497408 | C | CAA | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(63): Show | 66 | 199 | 0.3317 | 2 | c.-20 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9497769 | C | CCT | intron_variant | MODIFIER | HG02257.hp2 HG02630.hp1 HG02809.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0037 | a0001c0001t0003g0127a0001c0001t0007g0134a0001c0001t0037g0128 | 3 | 199 | 0.0151 | 2 | c.-20 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9500276 | C | CAA | intron_variant | MODIFIER | HG00673.hp1 HG02717.hp1 NA18961.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0002g0028others(4): Show | 7 | 199 | 0.0352 | 2 | c.-20 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9500301 | G | GAA | intron_variant | MODIFIER | HG01256.hp1 HG02258.hp1 HG02280.hp1 others(9): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0008 | a0001c0001t0004a0001c0001t0007a0001c0001t0009others(7): Show | a0001c0001t0004g0072a0001c0001t0007g0198a0001c0001t0009g0194others(9): Show | 12 | 199 | 0.0603 | 2 | c.-20 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9504602 | C | CAT | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG01071.hp2 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0012 | a0001c0001t0005g0098a0001c0001t0005g0109a0001c0001t0012g0108 | 3 | 199 | 0.0151 | 2 | c.-13 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9509365 | C | CAA | intron_variant | MODIFIER | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(15): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0004a0001c0001t0007a0001c0001t0009others(12): Show | a0001c0001t0004g0158a0001c0001t0007g0193a0001c0001t0007g0198others(15): Show | 18 | 199 | 0.0905 | 2 | c.-13 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9509482 | C | CTT | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(66): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0029others(66): Show | 69 | 199 | 0.3467 | 2 | c.-13 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9512514 | G | GTT | intron_variant | MODIFIER | HG02738.hp1 NA18982.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0115a0001c0001t0004g0015 | 2 | 199 | 0.0101 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9514334 | G | GTT | intron_variant | MODIFIER | HG02970.hp2 NA21309.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0016a0001c0003t0018 | a0001c0002t0016g0186a0001c0003t0018g0199 | 2 | 199 | 0.0101 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9523960 | C | CTT | intron_variant | MODIFIER | HG02572.hp1 HG03579.hp1 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0014a0001c0001t0022 | a0001c0001t0006g0065a0001c0001t0014g0168a0001c0001t0022g0021 | 3 | 199 | 0.0151 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9531352 | A | AGG | intron_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143 | 1 | 199 | 0.0050 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9531354 | G | GGT | intron_variant | MODIFIER | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
a0001a0005 | a0001c0001a0005c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(6): Show | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0045others(18): Show | 21 | 199 | 0.1055 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9545000 | C | CTT | intron_variant | MODIFIER | HG00642.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(8): Show | a0001c0001t0001g0161a0001c0001t0006g0140a0001c0001t0007g0193others(8): Show | 11 | 199 | 0.0553 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9546803 | A | ATT | intron_variant | MODIFIER | HG00280.hp1 HG01081.hp1 HG01099.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0027others(7): Show | 10 | 199 | 0.0503 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9556814 | G | GTT | intron_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0151 | 1 | 199 | 0.0050 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9560596 | T | TAA | intron_variant | MODIFIER | HG02055.hp1 HG02647.hp1 HG02723.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0007a0001c0001t0009a0001c0001t0010others(7): Show | a0001c0001t0007g0134a0001c0001t0007g0198a0001c0001t0009g0194others(10): Show | 13 | 199 | 0.0653 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9564731 | C | CAA | intron_variant | MODIFIER | HG02055.hp1 HG03486.hp2 NA19240.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0011a0001c0002t0009a0001c0002t0035others(1): Show | a0001c0001t0011g0135a0001c0002t0009g0077a0001c0002t0035g0069others(1): Show | 4 | 199 | 0.0201 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9569063 | C | CTA | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(110): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0033others(110): Show | 113 | 199 | 0.5678 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9574459 | G | GAA | intron_variant | MODIFIER | HG02071.hp1 HG03195.hp1 HG03654.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006a0001c0001t0043 | a0001c0001t0002g0187a0001c0001t0006g0083a0001c0001t0043g0074 | 3 | 199 | 0.0151 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9576695 | T | TAA | intron_variant | MODIFIER | HG00738.hp1 HG01346.hp1 HG02071.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0090a0001c0001t0002g0187a0001c0001t0003g0175others(6): Show | 9 | 199 | 0.0452 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9585340 | T | TCC | intron_variant | MODIFIER | HG00621.hp1 HG01099.hp1 HG01192.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0045others(21): Show | 24 | 199 | 0.1206 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9588607 | A | ATT | intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0031 | a0001c0001t0031g0183 | 1 | 199 | 0.0050 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9591947 | T | TGA | intron_variant | MODIFIER | NA18943.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 199 | 0.0050 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9597353 | T | TGG | intron_variant | MODIFIER | NA19076.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0005 | 1 | 199 | 0.0050 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | chrX | TogoVar | ||||||
TBL1X_chrX_9460058_9724740 | 9598957 | T | TTC | intron_variant | MODIFIER | NA19076.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0005 | 1 | 199 | 0.0050 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9600469 | C | CGG | intron_variant | MODIFIER | HG01167.hp1 HG01952.hp1 HG02738.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(1): Show | a0001c0001t0001g0152a0001c0001t0002g0115a0001c0001t0007g0073others(1): Show | 4 | 199 | 0.0201 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9600470 | G | GGT | intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0125 | 1 | 199 | 0.0050 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9600472 | G | GGC | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp2 HG02965.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0005a0001c0001t0009a0001c0001t0011others(2): Show | a0001c0001t0005g0098a0001c0001t0005g0109a0001c0001t0009g0191others(3): Show | 6 | 199 | 0.0302 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9600475 | G | GGA | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG00673.hp1 others(83): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 86 | 199 | 0.4322 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9607964 | A | ATT | intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0137 | 1 | 199 | 0.0050 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9609336 | G | GGT | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(13): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0003c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0119a0001c0001t0002g0179a0001c0001t0003g0017others(13): Show | 16 | 199 | 0.0804 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9609411 | G | GGT | intron_variant | MODIFIER | HG00741.hp1 HG01169.hp2 HG01361.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0070a0001c0001t0001g0177a0001c0001t0002g0187others(10): Show | 13 | 199 | 0.0653 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9613985 | C | CAA | intron_variant | MODIFIER | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(32): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(20): Show | a0001c0001t0001g0048a0001c0001t0003g0142a0001c0001t0003g0156others(32): Show | 35 | 199 | 0.1759 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9613999 | A | AAG | intron_variant | MODIFIER | NA18967.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029 | 1 | 199 | 0.0050 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9616406 | G | GAA | intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0002 | a0001c0002t0016 | a0001c0002t0016g0186 | 1 | 199 | 0.0050 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9628158 | A | AAG | intron_variant | MODIFIER | HG02486.hp1 HG02723.hp1 HG02809.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0007a0001c0001t0024 | a0001c0001t0004g0072a0001c0001t0007g0193a0001c0001t0024g0066 | 3 | 199 | 0.0151 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9628554 | C | CTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(32): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0082a0001c0001t0002g0148a0001c0001t0002g0154others(32): Show | 35 | 199 | 0.1759 | 2 | c.-13 others(23): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TBL1X_chrX_9460058_9724740 | 9630999 | A | AAT | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0003 | a0001c0003t0018 | a0001c0003t0018g0199 | 1 | 199 | 0.0050 | 2 | c.-13 others(21): Show |
TBL1X | ENSG00000101849.18 | transcript | ENST00000645353.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | TogoVar |