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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SNX2_chr5_122770080_122839543 | 122831009 | CA | C | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0012a0001c0001t0023others(9): Show | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
86 | 372 | 0.2312 | -1 | c.*13 others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1385 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
SNX2_chr5_122770080_122839543 | 122831488 | TA | T | 3_prime_UTR_variant | MODIFIER | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0026a0001c0001t0034a0001c0001t0072 | a0001c0001t0026g0086 a0001c0001t0026g0087 a0001c0001t0026g0242 others(3): Show |
6 | 372 | 0.0161 | -1 | c.*18 others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1848 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
SNX2_chr5_122770080_122839543 | 122833487 | AG | A | 3_prime_UTR_variant | MODIFIER | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0015a0001c0006t0015 | a0001c0001t0015g0012 a0001c0001t0015g0270 a0001c0001t0015g0271 others(2): Show |
5 | 372 | 0.0134 | -1 | c.*38 others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 3840 | chr5 | TogoVar | ||||||
SNX2_chr5_122770080_122839543 | 122839204 | GA | G | downstream_gene_variant | MODIFIER | NA18975.hp1 NA19012.hp1 NA19058.hp2 |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0052 | a0001c0001t0008g0036 a0001c0001t0008g0053 a0001c0001t0052g0043 |
3 | 372 | 0.0081 | -1 | c.*95 others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 4662 | chr5 | TogoVar | |||||||
SNX30_chr9_112745760_112879987 | 112746591 | CA | C | upstream_gene_variant | MODIFIER | HG00423.hp2 HG00621.hp1 HG00673.hp2 others(25): Show |
a0001a0003 | a0001c0002a0001c0004a0003c0007 | a0001c0002t0001a0001c0002t0003a0001c0002t0004others(9): Show | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(25): Show |
28 | 338 | 0.0828 | -1 | c.-44 others(6): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 4168 | chr9 | TogoVar | |||||||
SNX30_chr9_112745760_112879987 | 112748067 | GA | G | upstream_gene_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(71): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0133 others(71): Show |
74 | 338 | 0.2189 | -1 | c.-29 others(6): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2692 | chr9 | TogoVar | |||||||
SNX30_chr9_112745760_112879987 | 112748085 | AC | A | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(44): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0248 a0001c0001t0001g0250 a0001c0001t0001g0260 others(44): Show |
47 | 338 | 0.1391 | -1 | c.-29 others(6): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2674 | chr9 | TogoVar | |||||||
SNX30_chr9_112745760_112879987 | 112750421 | GC | G | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
a0001a0002 | a0001c0001a0002c0003a0002c0010 | a0001c0001t0002a0002c0003t0002a0002c0003t0004others(5): Show | a0001c0001t0002g0025 a0002c0003t0002g0009 a0002c0003t0004g0002 others(22): Show |
25 | 338 | 0.0740 | -1 | c.-58 others(5): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 338 | chr9 | TogoVar | |||||||
SNX30_chr9_112745760_112879987 | 112752304 | AG | A | intron_variant | MODIFIER | HG02135.hp1 NA18954.hp2 NA18957.hp1 others(4): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(4): Show |
7 | 338 | 0.0207 | -1 | c.156 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112756223 | AG | A | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(3): Show |
a0002 | a0002c0003a0002c0010 | a0002c0003t0004a0002c0010t0001 | a0002c0003t0004g0003 a0002c0003t0004g0004 a0002c0003t0004g0005 others(3): Show |
6 | 338 | 0.0178 | -1 | c.156 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112756435 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0248 a0001c0001t0001g0250 a0001c0001t0002g0124 others(49): Show |
52 | 338 | 0.1539 | -1 | c.156 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112759727 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(68): Show | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0069 others(328): Show |
331 | 338 | 0.9793 | -1 | c.156 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112761906 | AG | A | intron_variant | MODIFIER | HG00099.hp2 HG00597.hp2 HG00735.hp2 others(47): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0083 a0001c0001t0002g0033 a0001c0001t0002g0043 others(47): Show |
50 | 338 | 0.1479 | -1 | c.156 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112763360 | CT | C | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG01106.hp2 others(36): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0250 a0001c0001t0001g0291 a0001c0001t0001g0310 others(36): Show |
39 | 338 | 0.1154 | -1 | c.156 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112763846 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(21): Show | a0001c0001t0002g0025 a0001c0001t0002g0109 a0001c0001t0003g0050 others(52): Show |
55 | 338 | 0.1627 | -1 | c.156 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112767123 | TA | T | intron_variant | MODIFIER | HG02109.hp2 HG02818.hp1 NA20300.hp1 |
a0001 | a0001c0002 | a0001c0002t0025a0001c0002t0050 | a0001c0002t0025g0217 a0001c0002t0025g0218 a0001c0002t0050g0197 |
3 | 338 | 0.0089 | -1 | c.156 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | chr9 | TogoVar | |||||||
SNX30_chr9_112745760_112879987 | 112774844 | CT | C | intron_variant | MODIFIER | HG02040.hp2 HG02735.hp2 NA18941.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(3): Show | a0001c0001t0002g0087 a0001c0001t0005g0194 a0001c0001t0010g0244 others(3): Show |
6 | 338 | 0.0178 | -1 | c.156 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112775154 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0133 a0001c0001t0001g0233 a0001c0001t0001g0260 others(57): Show |
60 | 338 | 0.1775 | -1 | c.156 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112775781 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(35): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0174 others(35): Show |
38 | 338 | 0.1124 | -1 | c.156 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112778891 | TG | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(247): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0069 others(247): Show |
250 | 338 | 0.7396 | -1 | c.157 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112785383 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0069 others(275): Show |
278 | 338 | 0.8225 | -1 | c.157 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112786117 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(42): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0141 a0001c0001t0002g0025 a0001c0001t0003g0306 others(42): Show |
45 | 338 | 0.1331 | -1 | c.157 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112793804 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
a0001a0002 | a0001c0001a0002c0003a0002c0010 | a0001c0001t0002a0001c0001t0004a0002c0003t0002others(5): Show | a0001c0001t0002g0025 a0001c0001t0004g0312 a0002c0003t0002g0009 others(22): Show |
25 | 338 | 0.0740 | -1 | c.157 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112797873 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0002a0001c0002t0001a0001c0002t0003others(20): Show | a0001c0001t0002g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 others(66): Show |
69 | 338 | 0.2041 | -1 | c.157 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112798121 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0024others(14): Show | a0001c0001t0001g0281 a0001c0001t0003g0257 a0001c0001t0003g0258 others(39): Show |
42 | 338 | 0.1243 | -1 | c.157 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112805222 | AT | A | intron_variant | MODIFIER | HG00423.hp2 HG00621.hp1 HG00673.hp2 others(44): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0003c0007others(1): Show | a0001c0001t0012a0001c0002t0001a0001c0002t0003others(13): Show | a0001c0001t0012g0321 a0001c0001t0012g0322 a0001c0001t0012g0323 others(44): Show |
47 | 338 | 0.1391 | -1 | c.348 others(8): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112805475 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(21): Show |
a0002 | a0002c0003a0002c0010 | a0002c0003t0002a0002c0003t0004a0002c0003t0010others(4): Show | a0002c0003t0002g0009 a0002c0003t0004g0002 a0002c0003t0004g0003 others(21): Show |
24 | 338 | 0.0710 | -1 | c.348 others(8): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112807052 | CT | C | intron_variant | MODIFIER | HG00621.hp1 HG00673.hp2 HG01952.hp2 others(18): Show |
a0001a0003 | a0001c0002a0001c0004a0003c0007 | a0001c0002t0001a0001c0002t0003a0001c0002t0004others(8): Show | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(18): Show |
21 | 338 | 0.0621 | -1 | c.348 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112813300 | CA | C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(58): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(7): Show | a0001c0001t0001g0248 a0001c0001t0001g0250 a0001c0001t0001g0260 others(58): Show |
61 | 338 | 0.1805 | -1 | c.349 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112813469 | AT | A | intron_variant | MODIFIER | HG00423.hp2 HG00621.hp1 HG00673.hp2 others(25): Show |
a0001a0002a0003 | a0001c0002a0002c0003a0003c0007 | a0001c0002t0001a0001c0002t0003a0001c0002t0004others(9): Show | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0029 others(25): Show |
28 | 338 | 0.0828 | -1 | c.349 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112813786 | TA | T | intron_variant | MODIFIER | HG00280.hp2 HG01123.hp1 HG01167.hp2 others(6): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
9 | 338 | 0.0266 | -1 | c.349 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112815359 | CT | C | intron_variant | MODIFIER | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(51): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0130 a0001c0001t0001g0153 a0001c0001t0002g0097 others(51): Show |
54 | 338 | 0.1598 | -1 | c.349 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112817383 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(297): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0069 others(297): Show |
300 | 338 | 0.8876 | -1 | c.349 others(8): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112818199 | CT | C | intron_variant | MODIFIER | HG00423.hp2 HG00621.hp1 HG00673.hp2 others(44): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0056a0001c0002t0001others(15): Show | a0001c0001t0001g0167 a0001c0001t0001g0178 a0001c0001t0001g0266 others(44): Show |
47 | 338 | 0.1391 | -1 | c.459 others(8): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112822540 | TG | T | intron_variant | MODIFIER | HG00621.hp1 HG00673.hp2 HG01952.hp2 others(22): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0007 | a0001c0001t0004a0001c0001t0009a0001c0002t0001others(10): Show | a0001c0001t0004g0312 a0001c0001t0009g0241 a0001c0002t0001g0201 others(22): Show |
25 | 338 | 0.0740 | -1 | c.459 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 3/8 | chr9 | TogoVar | |||||||
SNX30_chr9_112745760_112879987 | 112824334 | AT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(173): Show |
a0001a0002a0005 | a0001c0001a0001c0006a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0069 others(173): Show |
176 | 338 | 0.5207 | -1 | c.460 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112829250 | AT | A | intron_variant | MODIFIER | HG01515.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005a0001c0001t0041 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0057 others(4): Show |
7 | 338 | 0.0207 | -1 | c.460 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112831139 | TA | T | intron_variant | MODIFIER | HG01168.hp1 HG01256.hp2 HG01515.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0166 a0001c0001t0002g0105 a0001c0001t0003g0284 others(4): Show |
7 | 338 | 0.0207 | -1 | c.618 others(8): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112832509 | AG | A | intron_variant | MODIFIER | HG00621.hp1 HG00639.hp1 HG00673.hp2 others(35): Show |
a0001a0002a0003others(1): Show | a0001c0002a0002c0003a0003c0007others(1): Show | a0001c0002t0001a0001c0002t0004a0001c0002t0005others(14): Show | a0001c0002t0001g0201 a0001c0002t0004g0127 a0001c0002t0004g0219 others(35): Show |
38 | 338 | 0.1124 | -1 | c.618 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 4/8 | chr9 | TogoVar | |||||||
SNX30_chr9_112745760_112879987 | 112835438 | TG | T | intron_variant | MODIFIER | HG01884.hp2 HG02257.hp2 HG02486.hp2 others(5): Show |
a0001 | a0001c0002 | a0001c0002t0007a0001c0002t0015a0001c0002t0029others(1): Show | a0001c0002t0007g0320 a0001c0002t0007g0325 a0001c0002t0007g0326 others(5): Show |
8 | 338 | 0.0237 | -1 | c.619 others(8): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112835472 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(28): Show | a0001c0001t0001g0174 a0001c0002t0001g0026 a0001c0002t0001g0027 others(71): Show |
74 | 338 | 0.2189 | -1 | c.619 others(8): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112835907 | TA | T | intron_variant | MODIFIER | HG02257.hp2 HG02886.hp2 HG02970.hp1 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0007a0001c0002t0015 | a0001c0002t0007g0325 a0001c0002t0007g0326 a0001c0002t0007g0327 others(2): Show |
5 | 338 | 0.0148 | -1 | c.619 others(8): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112837887 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0069 others(205): Show |
208 | 338 | 0.6154 | -1 | c.815 others(8): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112847446 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(167): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0069 others(167): Show |
170 | 338 | 0.5030 | -1 | c.101 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112851762 | AG | A | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(46): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0019others(5): Show | a0001c0001t0001g0141 a0001c0001t0001g0158 a0001c0001t0003g0135 others(46): Show |
49 | 338 | 0.1450 | -1 | c.110 others(9): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112859893 | AC | A | intron_variant | MODIFIER | HG00423.hp2 HG00621.hp1 HG00673.hp2 others(15): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0007 | a0001c0001t0013a0001c0002t0006a0001c0002t0013others(4): Show | a0001c0001t0013g0184 a0001c0002t0006g0200 a0001c0002t0006g0202 others(15): Show |
18 | 338 | 0.0533 | -1 | c.110 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 7/8 | chr9 | TogoVar | |||||||
SNX30_chr9_112745760_112879987 | 112867392 | AC | A | intron_variant | MODIFIER | HG00140.hp1 HG00735.hp1 HG02300.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0045 | a0001c0001t0003g0249 a0001c0001t0003g0263 a0001c0001t0003g0273 others(4): Show |
7 | 338 | 0.0207 | -1 | c.125 others(10): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112869615 | TG | T | 3_prime_UTR_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(81): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0010 | a0001c0001t0001a0001c0001t0017a0001c0001t0028others(4): Show | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0069 others(81): Show |
84 | 338 | 0.2485 | -1 | c.*77 others(5): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 9/9 | 774 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
SNX30_chr9_112745760_112879987 | 112873637 | CT | C | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(27): Show | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0069 others(185): Show |
188 | 338 | 0.5562 | -1 | c.*48 others(6): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 9/9 | 4808 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
SNX30_chr9_112745760_112879987 | 112874013 | GT | G | 3_prime_UTR_variant | MODIFIER | NA18941.hp2 NA18979.hp2 NA18992.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0014a0001c0002t0014a0001c0002t0052 | a0001c0001t0014g0075 a0001c0001t0014g0114 a0001c0002t0014g0203 others(1): Show |
4 | 338 | 0.0118 | -1 | c.*51 others(6): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 9/9 | 5171 | chr9 | TogoVar |