view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TTC27_chr2_32623050_32826051 | 32669883 | C | CAA | intron_variant | MODIFIER | HG01346.hp2 HG02004.hp1 HG03831.hp2 others(5): Show |
a0001a0002a0009 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0002others(1): Show | a0001c0001t0001g0092 a0001c0001t0001g0194 a0001c0001t0001g0202 others(5): Show |
8 | 324 | 0.0247 | 2 | c.940 others(19): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32673225 | A | ATT | intron_variant | MODIFIER | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(6): Show |
a0001a0002a0006 | a0001c0001a0001c0006a0001c0010others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0006t0001others(3): Show | a0001c0001t0001g0051 a0001c0001t0001g0280 a0001c0001t0002g0287 others(6): Show |
9 | 324 | 0.0278 | 2 | c.105 others(19): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32676493 | G | GTT | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp2 HG01069.hp2 others(35): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0006others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(8): Show | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0051 others(35): Show |
38 | 324 | 0.1173 | 2 | c.105 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32676882 | C | CAT | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(32): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(3): Show | a0001c0001t0001g0137 a0001c0001t0001g0165 a0001c0001t0001g0286 others(32): Show |
35 | 324 | 0.1080 | 2 | c.105 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32681980 | A | ATG | intron_variant | MODIFIER | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(23): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0004others(1): Show | a0001c0001t0001g0022 a0001c0001t0001g0109 a0001c0001t0001g0174 others(23): Show |
26 | 324 | 0.0803 | 2 | c.111 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32682668 | C | CTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0006others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(6): Show | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0070 others(95): Show |
98 | 324 | 0.3025 | 2 | c.111 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32682844 | G | GTT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(69): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0006others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0006t0001others(5): Show | a0001c0001t0001g0123 a0001c0001t0001g0150 a0001c0001t0001g0153 others(69): Show |
72 | 324 | 0.2222 | 2 | c.111 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32692036 | G | GTT | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(40): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(3): Show | a0001c0001t0001g0029 a0001c0001t0001g0109 a0001c0001t0001g0127 others(40): Show |
43 | 324 | 0.1327 | 2 | c.112 others(23): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32697191 | C | CAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0005others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(9): Show | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
110 | 324 | 0.3395 | 2 | c.112 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32698482 | C | CTT | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
a0001a0002a0009 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(3): Show | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0070 others(59): Show |
62 | 324 | 0.1914 | 2 | c.112 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32706075 | C | CTT | intron_variant | MODIFIER | HG00639.hp2 HG01361.hp2 HG02004.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0002 a0001c0001t0002g0124 a0001c0001t0002g0182 |
3 | 324 | 0.0093 | 2 | c.123 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32706077 | C | CTT | intron_variant | MODIFIER | HG00597.hp1 HG01192.hp2 HG01361.hp1 others(18): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(3): Show | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0060 others(18): Show |
21 | 324 | 0.0648 | 2 | c.123 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32708304 | G | GTT | intron_variant | MODIFIER | HG00639.hp2 HG01516.hp1 HG02004.hp2 others(9): Show |
a0001a0002 | a0001c0001a0001c0006a0001c0010others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0006t0001others(3): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0051 others(9): Show |
12 | 324 | 0.0370 | 2 | c.123 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32710427 | C | CTT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(103): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0005others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
106 | 324 | 0.3272 | 2 | c.123 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32711116 | C | CAA | intron_variant | MODIFIER | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(12): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0001c0015others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0005t0001others(4): Show | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(12): Show |
15 | 324 | 0.0463 | 2 | c.123 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32745054 | C | CAA | intron_variant | MODIFIER | HG00438.hp1 HG01081.hp1 HG02015.hp2 others(23): Show |
a0001a0002a0008 | a0001c0001a0001c0006a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0006t0001others(3): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0137 others(23): Show |
26 | 324 | 0.0803 | 2 | c.145 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32751258 | C | CCA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
a0001a0004a0008 | a0001c0001a0001c0002a0004c0007others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(4): Show | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0198 others(63): Show |
66 | 324 | 0.2037 | 2 | c.145 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32753429 | C | CTT | intron_variant | MODIFIER | HG00438.hp1 HG01243.hp2 HG02257.hp1 others(12): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0003a0001c0006t0001 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0060 others(12): Show |
15 | 324 | 0.0463 | 2 | c.145 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32762276 | A | AGT | intron_variant | MODIFIER | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(27): Show |
a0001a0003 | a0001c0001a0001c0005a0001c0017others(1): Show | a0001c0001t0001a0001c0005t0001a0001c0017t0001others(1): Show | a0001c0001t0001g0081 a0001c0001t0001g0172 a0001c0001t0001g0174 others(27): Show |
30 | 324 | 0.0926 | 2 | c.168 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32767452 | T | TTG | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(18): Show |
a0001a0004a0008 | a0001c0001a0004c0007a0008c0016 | a0001c0001t0001a0001c0001t0002a0004c0007t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0109 others(18): Show |
21 | 324 | 0.0648 | 2 | c.168 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 13/19 | chr2 | TogoVar | |||||||
TTC27_chr2_32623050_32826051 | 32767453 | G | GTT | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(30): Show |
a0001a0002a0010others(1): Show | a0001c0002a0002c0003a0010c0018others(1): Show | a0001c0002t0001a0002c0003t0001a0002c0003t0002others(2): Show | a0001c0002t0001g0045 a0001c0002t0001g0052 a0001c0002t0001g0059 others(30): Show |
33 | 324 | 0.1019 | 2 | c.168 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32769651 | G | GAA | intron_variant | MODIFIER | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(52): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0003a0005c0008others(2): Show | a0001c0001t0001a0001c0001t0002a0002c0003t0001others(5): Show | a0001c0001t0001g0085 a0001c0001t0001g0217 a0001c0001t0001g0324 others(52): Show |
55 | 324 | 0.1698 | 2 | c.168 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32780850 | G | GTT | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG02257.hp2 others(4): Show |
a0001a0002a0005 | a0001c0001a0002c0003a0005c0008 | a0001c0001t0001a0002c0003t0001a0005c0008t0002 | a0001c0001t0001g0085 a0002c0003t0001g0020 a0002c0003t0001g0021 others(4): Show |
7 | 324 | 0.0216 | 2 | c.178 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32785937 | A | AGT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(154): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0005a0001c0006others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(154): Show |
157 | 324 | 0.4846 | 2 | c.183 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 15/19 | chr2 | TogoVar | |||||||
TTC27_chr2_32623050_32826051 | 32789921 | C | CAA | intron_variant | MODIFIER | HG01175.hp1 HG01243.hp2 HG02055.hp2 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(4): Show | a0001c0001t0001g0005 a0001c0001t0001g0171 a0001c0001t0001g0198 others(9): Show |
12 | 324 | 0.0370 | 2 | c.199 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32798102 | T | TAA | intron_variant | MODIFIER | HG00408.hp1 HG00639.hp2 HG01069.hp2 others(71): Show |
a0001a0002a0005others(3): Show | a0001c0001a0001c0005a0001c0006others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(71): Show |
74 | 324 | 0.2284 | 2 | c.199 others(23): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32807928 | C | CTT | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(63): Show |
a0001a0003a0004 | a0001c0001a0001c0005a0001c0015others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0005t0001others(4): Show | a0001c0001t0001g0022 a0001c0001t0001g0081 a0001c0001t0001g0091 others(63): Show |
66 | 324 | 0.2037 | 2 | c.199 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32810114 | C | CAA | intron_variant | MODIFIER | HG01168.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
a0001a0004a0005 | a0001c0001a0004c0007a0005c0008 | a0001c0001t0001a0001c0001t0002a0004c0007t0001others(1): Show | a0001c0001t0001g0085 a0001c0001t0002g0287 a0001c0001t0002g0288 others(4): Show |
7 | 324 | 0.0216 | 2 | c.199 others(19): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32815080 | G | GTA | intron_variant | MODIFIER | NA18981.hp1 NA19010.hp1 NA19074.hp1 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0301 |
3 | 324 | 0.0093 | 2 | c.230 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC27_chr2_32623050_32826051 | 32815223 | A | ATT | intron_variant | MODIFIER | HG02004.hp1 HG02083.hp1 HG02559.hp1 others(5): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0153 a0001c0001t0001g0196 a0001c0001t0001g0202 others(5): Show |
8 | 324 | 0.0247 | 2 | c.230 others(21): Show |
TTC27 | ENSG00000018699.13 | transcript | ENST00000317907.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TTC28_chr22_27973014_28684840 | 27981230 | A | ATT | 3_prime_UTR_variant | MODIFIER | HG00621.hp1 HG00642.hp1 HG00735.hp2 others(20): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0012others(5): Show | a0001c0001t0006a0001c0001t0009a0001c0001t0013others(10): Show | a0001c0001t0006g0017 a0001c0001t0006g0022 a0001c0001t0006g0046 others(20): Show |
23 | 196 | 0.1174 | 2 | c.*98 others(11): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 23/23 | 990 | chr22 | TogoVar | ||||||
TTC28_chr22_27973014_28684840 | 27981415 | C | CAA | 3_prime_UTR_variant | MODIFIER | HG00621.hp1 HG01175.hp1 HG01255.hp1 others(14): Show |
a0001a0005 | a0001c0002a0001c0027a0001c0030others(1): Show | a0001c0002t0007a0001c0002t0022a0001c0002t0023others(6): Show | a0001c0002t0007g0101 a0001c0002t0007g0102 a0001c0002t0007g0107 others(14): Show |
17 | 196 | 0.0867 | 2 | c.*80 others(11): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 23/23 | 805 | chr22 | TogoVar | ||||||
TTC28_chr22_27973014_28684840 | 27988281 | C | CTT | intron_variant | MODIFIER | HG00280.hp1 HG01257.hp2 HG01943.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0005a0001c0002t0029a0001c0003t0002others(1): Show | a0001c0001t0005g0142 a0001c0002t0029g0080 a0001c0003t0002g0150 others(11): Show |
14 | 196 | 0.0714 | 2 | c.570 others(21): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 21/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 27989228 | C | CCA | intron_variant | MODIFIER | HG00280.hp1 HG01243.hp1 HG01257.hp2 others(26): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0008a0001c0001t0045a0001c0002t0002others(10): Show | a0001c0001t0008g0049 a0001c0001t0045g0030 a0001c0002t0002g0050 others(26): Show |
29 | 196 | 0.1480 | 2 | c.570 others(19): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 21/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 27994450 | G | GTT | intron_variant | MODIFIER | HG02109.hp2 HG02258.hp1 HG02895.hp2 others(2): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0008a0001c0008t0032a0001c0008t0033 | a0001c0001t0008g0170 a0001c0008t0032g0193 a0001c0008t0032g0194 others(2): Show |
5 | 196 | 0.0255 | 2 | c.524 others(19): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 17/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28015419 | T | TAA | intron_variant | MODIFIER | HG00741.hp2 HG02132.hp1 HG02145.hp1 others(3): Show |
a0001a0002 | a0001c0004a0001c0011a0002c0006 | a0001c0004t0001a0001c0011t0018a0001c0011t0025others(1): Show | a0001c0004t0001g0074 a0001c0004t0001g0085 a0001c0011t0018g0009 others(3): Show |
6 | 196 | 0.0306 | 2 | c.407 others(21): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 13/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28018244 | A | AGT | intron_variant | MODIFIER | HG00673.hp1 HG00741.hp2 HG01255.hp2 others(36): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(20): Show | a0001c0001t0003g0029 a0001c0001t0004g0032 a0001c0001t0004g0036 others(36): Show |
39 | 196 | 0.1990 | 2 | c.407 others(21): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 13/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28018306 | C | CGG | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(25): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0003a0001c0004others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | a0001c0001t0001g0103 a0001c0001t0003g0093 a0001c0001t0003g0095 others(25): Show |
28 | 196 | 0.1429 | 2 | c.407 others(21): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 13/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28020778 | A | AAC | intron_variant | MODIFIER | HG00621.hp1 HG00673.hp1 HG01175.hp1 others(46): Show |
a0001a0002a0005others(3): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0003a0001c0001t0008a0001c0001t0019others(29): Show | a0001c0001t0003g0029 a0001c0001t0003g0124 a0001c0001t0003g0126 others(46): Show |
49 | 196 | 0.2500 | 2 | c.407 others(21): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 13/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28020796 | C | CAG | intron_variant | MODIFIER | HG02109.hp2 HG02258.hp1 HG02895.hp2 others(1): Show |
a0001 | a0001c0008 | a0001c0008t0032a0001c0008t0033 | a0001c0008t0032g0193 a0001c0008t0032g0194 a0001c0008t0033g0195 others(1): Show |
4 | 196 | 0.0204 | 2 | c.407 others(21): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 13/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28025162 | G | GTT | intron_variant | MODIFIER | HG00621.hp1 HG00735.hp1 HG00741.hp2 others(35): Show |
a0001a0004a0005others(1): Show | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0003a0001c0002t0007a0001c0002t0022others(15): Show | a0001c0001t0003g0124 a0001c0001t0003g0126 a0001c0002t0007g0101 others(35): Show |
38 | 196 | 0.1939 | 2 | c.407 others(21): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 13/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28032250 | A | AAT | intron_variant | MODIFIER | NA18955.hp1 NA18960.hp1 NA19011.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0094 others(2): Show |
5 | 196 | 0.0255 | 2 | c.393 others(21): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 12/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28032267 | A | AGT | intron_variant | MODIFIER | HG00735.hp2 HG00741.hp1 HG01081.hp1 others(9): Show |
a0001a0003a0008 | a0001c0001a0001c0025a0001c0026others(2): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0009others(7): Show | a0001c0001t0005g0142 a0001c0001t0006g0017 a0001c0001t0009g0140 others(9): Show |
12 | 196 | 0.0612 | 2 | c.393 others(21): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 12/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28032310 | G | GTA | intron_variant | MODIFIER | HG01257.hp2 HG01361.hp2 |
a0001a0003 | a0001c0003a0003c0007 | a0001c0003t0002a0003c0007t0009 | a0001c0003t0002g0165 a0003c0007t0009g0139 |
2 | 196 | 0.0102 | 2 | c.393 others(21): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 12/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28049099 | G | GTC | intron_variant | MODIFIER | HG02723.hp2 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0038a0001c0001t0039 | a0001c0001t0038g0051 a0001c0001t0039g0112 |
2 | 196 | 0.0102 | 2 | c.393 others(23): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 12/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28066274 | C | CTG | intron_variant | MODIFIER | HG00280.hp1 HG01928.hp1 |
a0001 | a0001c0003a0001c0016 | a0001c0003t0002a0001c0016t0002 | a0001c0003t0002g0161 a0001c0016t0002g0160 |
2 | 196 | 0.0102 | 2 | c.393 others(23): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 12/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28066275 | C | CGT | intron_variant | MODIFIER | HG00621.hp1 HG01071.hp1 HG01175.hp1 others(36): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0003g0124 others(36): Show |
39 | 196 | 0.1990 | 2 | c.393 others(23): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 12/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28066304 | G | GGT | intron_variant | MODIFIER | HG01496.hp2 HG02280.hp1 HG02723.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0030 | a0001c0001t0008a0001c0001t0045a0001c0001t0048others(3): Show | a0001c0001t0008g0045 a0001c0001t0008g0049 a0001c0001t0008g0145 others(5): Show |
8 | 196 | 0.0408 | 2 | c.393 others(23): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 12/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28066304 | G | GTT | intron_variant | MODIFIER | HG02717.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
a0001 | a0001c0008a0001c0012a0001c0015 | a0001c0008t0054a0001c0012t0005a0001c0012t0014others(1): Show | a0001c0008t0054g0055 a0001c0012t0005g0146 a0001c0012t0014g0147 others(1): Show |
4 | 196 | 0.0204 | 2 | c.393 others(23): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 12/22 | chr22 | TogoVar | |||||||
TTC28_chr22_27973014_28684840 | 28069925 | A | AAC | intron_variant | MODIFIER | HG00558.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
a0001a0002a0006others(2): Show | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | a0001c0001t0001g0037 a0001c0001t0003g0020 a0001c0001t0003g0071 others(21): Show |
24 | 196 | 0.1225 | 2 | c.393 others(23): Show |
TTC28 | ENSG00000100154.15 | transcript | ENST00000397906.7 | protein_coding | 12/22 | chr22 | TogoVar |