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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM177_chr2_119674201_119687118 | 119678651 | GGT | G | upstream_gene_variant | MODIFIER | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(51): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0006 | a0001c0001t0001a0002c0002t0002a0004c0006t0002 | a0001c0001t0001g0001a0002c0002t0002g0001a0004c0006t0002g0001 | 54 | 376 | 0.1436 | -2 | c.-64 others(11): Show |
TMEM177 | ENSG00000144120.13 | transcript | ENST00000272521.7 | protein_coding | 549 | chr2 | TogoVar | ||||||
TMEM177_chr2_119674201_119687118 | 119678692 | GGT | G | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(260): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0005a0001c0009others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(13): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 263 | 376 | 0.6995 | -2 | c.-60 others(11): Show |
TMEM177 | ENSG00000144120.13 | transcript | ENST00000272521.7 | protein_coding | 508 | chr2 | TogoVar | ||||||
TMEM177_chr2_119674201_119687118 | 119685212 | GCC | G | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0005a0001c0009others(8): Show | a0001c0001t0001a0001c0001t0005a0001c0005t0001others(10): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(14): Show | 219 | 376 | 0.5825 | -2 | c.*34 others(13): Show |
TMEM177 | ENSG00000144120.13 | transcript | ENST00000272521.7 | protein_coding | 3095 | chr2 | TogoVar | ||||||
TMEM177_chr2_119674201_119687118 | 119687064 | GAT | G | downstream_gene_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01346.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 3 | 376 | 0.0080 | -2 | c.*52 others(13): Show |
TMEM177 | ENSG00000144120.13 | transcript | ENST00000272521.7 | protein_coding | 4947 | chr2 | TogoVar | ||||||
TMEM178A_chr2_39660917_39722963 | 39667335 | ATT | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(120): Show | 146 | 296 | 0.4932 | -2 | c.400 others(17): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TMEM178A_chr2_39660917_39722963 | 39681164 | CTT | C | intron_variant | MODIFIER | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0053others(5): Show | 12 | 296 | 0.0405 | -2 | c.400 others(21): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TMEM178A_chr2_39660917_39722963 | 39686963 | ATG | A | intron_variant | MODIFIER | HG00140.hp2 HG01123.hp2 HG01516.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0103others(3): Show | 6 | 296 | 0.0203 | -2 | c.401 others(21): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TMEM178A_chr2_39660917_39722963 | 39712041 | TTG | T | intron_variant | MODIFIER | HG02630.hp2 HG02717.hp2 HG02897.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0007 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(10): Show | 13 | 296 | 0.0439 | -2 | c.652 others(19): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TMEM178A_chr2_39660917_39722963 | 39721985 | CAA | C | downstream_gene_variant | MODIFIER | HG00408.hp2 HG01081.hp1 HG01167.hp1 others(16): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(14): Show | 19 | 296 | 0.0642 | -2 | c.*47 others(13): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4023 | chr2 | TogoVar | ||||||
TMEM178B_chr7_141069064_141485380 | 141069101 | ATT | A | upstream_gene_variant | MODIFIER | HG00544.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0002g0019others(18): Show | 21 | 80 | 0.2625 | -2 | c.-52 others(13): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4962 | chr7 | TogoVar | ||||||
TMEM178B_chr7_141069064_141485380 | 141071481 | GGA | G | upstream_gene_variant | MODIFIER | HG00544.hp2 HG01106.hp1 HG01106.hp2 others(70): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(53): Show | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(70): Show | 73 | 80 | 0.9125 | -2 | c.-28 others(13): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2582 | chr7 | TogoVar | ||||||
TMEM178B_chr7_141069064_141485380 | 141085150 | ATT | A | intron_variant | MODIFIER | HG01243.hp1 HG01256.hp2 HG02027.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(12): Show | a0001c0001t0001g0035a0001c0001t0004g0029a0001c0001t0008g0030others(13): Show | 16 | 80 | 0.2000 | -2 | c.382 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141097089 | CAA | C | intron_variant | MODIFIER | HG01884.hp2 HG01952.hp2 HG02258.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(7): Show | 10 | 80 | 0.1250 | -2 | c.382 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141097365 | CAA | C | intron_variant | MODIFIER | HG00544.hp1 HG01891.hp1 HG02630.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(3): Show | a0001c0001t0001g0080a0001c0001t0002g0019a0001c0001t0008g0030others(3): Show | 6 | 80 | 0.0750 | -2 | c.382 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141101908 | CGT | C | intron_variant | MODIFIER | HG03139.hp2 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0008 | a0001c0001t0005g0014a0001c0001t0008g0004 | 2 | 80 | 0.0250 | -2 | c.382 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141126856 | AGT | A | intron_variant | MODIFIER | HG01891.hp2 HG02027.hp1 HG02083.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(11): Show | a0001c0001t0002g0019a0001c0001t0003g0007a0001c0001t0005g0014others(11): Show | 14 | 80 | 0.1750 | -2 | c.382 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141139386 | GTT | G | intron_variant | MODIFIER | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0008a0001c0001t0014a0001c0001t0016others(7): Show | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | 80 | 0.1375 | -2 | c.382 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141142146 | AGT | A | intron_variant | MODIFIER | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0008a0001c0001t0014a0001c0001t0016others(7): Show | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | 80 | 0.1375 | -2 | c.382 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141157427 | GCA | G | intron_variant | MODIFIER | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0008a0001c0001t0014a0001c0001t0016others(5): Show | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | 80 | 0.1125 | -2 | c.383 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141160055 | AAT | A | intron_variant | MODIFIER | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | 80 | 0.7000 | -2 | c.383 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141161959 | TGA | T | intron_variant | MODIFIER | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | 80 | 0.7000 | -2 | c.383 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141180463 | CAA | C | intron_variant | MODIFIER | HG01891.hp1 HG01952.hp2 HG02109.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(8): Show | a0001c0001t0001g0035a0001c0001t0004g0023a0001c0001t0008g0030others(8): Show | 11 | 80 | 0.1375 | -2 | c.383 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141192490 | CTT | C | intron_variant | MODIFIER | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | 80 | 0.7000 | -2 | c.383 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141223479 | CTT | C | intron_variant | MODIFIER | HG01255.hp1 HG01261.hp1 HG01884.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0022a0001c0001t0023a0001c0002t0001others(3): Show | a0001c0001t0022g0013a0001c0001t0023g0018a0001c0002t0001g0057others(4): Show | 7 | 80 | 0.0875 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141225429 | ATT | A | intron_variant | MODIFIER | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(8): Show | a0001c0001t0002g0027a0001c0001t0004g0029a0001c0001t0005g0014others(8): Show | 11 | 80 | 0.1375 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141226873 | AAG | A | intron_variant | MODIFIER | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(48): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(48): Show | 51 | 80 | 0.6375 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141229013 | CTT | C | intron_variant | MODIFIER | HG00544.hp1 HG01243.hp2 HG01255.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(11): Show | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(13): Show | 16 | 80 | 0.2000 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141229100 | GGT | G | intron_variant | MODIFIER | HG00544.hp2 HG03704.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0007a0001c0002t0013 | a0001c0001t0007g0011a0001c0002t0013g0047 | 2 | 80 | 0.0250 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141240996 | CTT | C | intron_variant | MODIFIER | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0001g0015a0001c0001t0003g0007a0001c0001t0004g0024others(14): Show | 17 | 80 | 0.2125 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141242148 | CTT | C | intron_variant | MODIFIER | HG01243.hp1 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0014a0001c0001t0028 | a0001c0001t0014g0033a0001c0001t0028g0022 | 2 | 80 | 0.0250 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141242477 | AGT | A | intron_variant | MODIFIER | HG01952.hp1 HG01978.hp2 HG02258.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(7): Show | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0008g0030others(9): Show | 12 | 80 | 0.1500 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141247204 | TAC | T | intron_variant | MODIFIER | HG01884.hp1 HG02258.hp1 HG03540.hp1 |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0035a0001c0002t0017a0001c0003t0019 | a0001c0001t0035g0079a0001c0002t0017g0062a0001c0003t0019g0070 | 3 | 80 | 0.0375 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141258161 | CAT | C | intron_variant | MODIFIER | HG01106.hp2 HG01891.hp1 HG01952.hp1 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(11): Show | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0005g0014others(12): Show | 15 | 80 | 0.1875 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141262474 | AAT | A | intron_variant | MODIFIER | HG01106.hp1 HG01243.hp1 HG01952.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0006a0001c0001t0011a0001c0001t0012others(8): Show | a0001c0001t0006g0017a0001c0001t0011g0016a0001c0001t0012g0036others(9): Show | 12 | 80 | 0.1500 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141285152 | TTC | T | intron_variant | MODIFIER | HG00544.hp2 HG01243.hp1 HG01243.hp2 others(20): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(17): Show | a0001c0001t0001g0015a0001c0001t0003g0020a0001c0001t0005g0008others(20): Show | 23 | 80 | 0.2875 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141288195 | CTT | C | intron_variant | MODIFIER | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | 80 | 0.1875 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141291926 | ATT | A | intron_variant | MODIFIER | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(25): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(20): Show | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(25): Show | 28 | 80 | 0.3500 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141293615 | ATG | A | intron_variant | MODIFIER | HG02258.hp2 HG02572.hp2 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0011 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016 | 3 | 80 | 0.0375 | -2 | c.496 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141322363 | TAA | T | intron_variant | MODIFIER | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(19): Show | a0001c0001t0001g0012a0001c0001t0004g0023a0001c0001t0005g0008others(19): Show | 22 | 80 | 0.2750 | -2 | c.496 others(23): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141324416 | GTT | G | intron_variant | MODIFIER | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0014others(2): Show | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0004g0029others(4): Show | 7 | 80 | 0.0875 | -2 | c.496 others(23): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141343525 | CTT | C | intron_variant | MODIFIER | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(3): Show | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0009g0078others(3): Show | 6 | 80 | 0.0750 | -2 | c.497 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141364659 | CAA | C | intron_variant | MODIFIER | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(11): Show | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0008g0030others(11): Show | 14 | 80 | 0.1750 | -2 | c.497 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141369316 | CGT | C | intron_variant | MODIFIER | HG01255.hp2 HG01256.hp1 HG01256.hp2 others(15): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(14): Show | a0001c0001t0004g0023a0001c0001t0004g0029a0001c0001t0005g0014others(15): Show | 18 | 80 | 0.2250 | -2 | c.497 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141369357 | GTA | G | intron_variant | MODIFIER | HG00544.hp2 HG03704.hp2 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0013a0001c0005t0001 | a0001c0002t0013g0047a0001c0005t0001g0005 | 2 | 80 | 0.0250 | -2 | c.497 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141370116 | AGT | A | intron_variant | MODIFIER | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(36): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(31): Show | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(36): Show | 39 | 80 | 0.4875 | -2 | c.497 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141383162 | TTC | T | intron_variant | MODIFIER | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0008a0001c0001t0035others(6): Show | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(7): Show | 10 | 80 | 0.1250 | -2 | c.497 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141388676 | ACC | A | intron_variant | MODIFIER | HG01891.hp2 HG02109.hp1 HG03225.hp2 |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0015a0001c0002t0030 | a0001c0002t0003g0052a0001c0002t0015g0056a0001c0002t0030g0067 | 3 | 80 | 0.0375 | -2 | c.497 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | TogoVar | ||||||
TMEM178B_chr7_141069064_141485380 | 141396529 | CAG | C | intron_variant | MODIFIER | HG01106.hp2 HG01243.hp2 HG01255.hp2 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(21): Show | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0002g0019others(24): Show | 27 | 80 | 0.3375 | -2 | c.497 others(21): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141428383 | AAG | A | intron_variant | MODIFIER | HG02602.hp1 HG02602.hp2 HG03225.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0006 | a0001c0001t0007a0001c0001t0044a0001c0002t0007others(2): Show | a0001c0001t0007g0011a0001c0001t0044g0001a0001c0002t0007g0053others(3): Show | 6 | 80 | 0.0750 | -2 | c.497 others(19): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141429308 | TAC | T | intron_variant | MODIFIER | HG02922.hp1 HG03453.hp1 HG03540.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0038a0001c0001t0044a0001c0002t0027 | a0001c0001t0038g0034a0001c0001t0044g0001a0001c0002t0027g0051 | 3 | 80 | 0.0375 | -2 | c.497 others(19): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |