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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
GPRC5D_chr12_12935575_12957170 | 12956468 | T | TTTTCCTC others(41): Show |
upstream_gene_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0192 | 1 | 363 | 0.0028 | 48 | c.-44 others(59): Show |
GPRC5D | ENSG00000111291.9 | transcript | ENST00000228887.6 | protein_coding | 4299 | chr12 | TogoVar | |||||||
GPSM2_chr1_108871985_108939545 | 108874386 | T | TGGGGAAA others(41): Show |
upstream_gene_variant | MODIFIER | NA20905.hp2 | a0004 | a0004c0004 | a0004c0004t0004 | a0004c0004t0004g0181 | 1 | 258 | 0.0039 | 48 | c.-30 others(59): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2598 | chr1 | TogoVar | |||||||
GPSM2_chr1_108871985_108939545 | 108908728 | A | AACACACA others(41): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02895.hp2 |
a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0214 a0003c0003t0003g0221 |
2 | 160 | 0.0125 | 48 | c.119 others(67): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
GRAMD1B_chr11_123425269_123632767 | 123457117 | A | AAAAGAAA others(41): Show |
intron_variant | MODIFIER | HG01109.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0001g0084 a0001c0001t0001g0093 a0001c0001t0001g0178 others(5): Show |
8 | 126 | 0.0635 | 48 | c.375 others(67): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRAMD1B_chr11_123425269_123632767 | 123513609 | C | CCTTTCTT others(41): Show |
intron_variant | MODIFIER | NA19087.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0156 | 1 | 211 | 0.0047 | 48 | c.452 others(67): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRAMD1B_chr11_123425269_123632767 | 123513617 | C | CCTTCCTT others(41): Show |
intron_variant | MODIFIER | HG03688.hp1 HG03942.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0082 a0001c0001t0004g0111 |
2 | 84 | 0.0238 | 48 | c.452 others(67): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRAMD1B_chr11_123425269_123632767 | 123513617 | C | CCTTCCTT others(41): Show |
intron_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0077 | 1 | 83 | 0.0120 | 48 | c.452 others(67): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46648847 | C | CATGGATG others(41): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0027 | a0001c0001t0027g0055 | 1 | 308 | 0.0032 | 48 | c.284 others(65): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRHL2_chr8_101487439_101674726 | 101509141 | C | CCTTTCTT others(41): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0240 | 1 | 271 | 0.0037 | 48 | c.20+ others(65): Show |
GRHL2 | ENSG00000083307.12 | transcript | ENST00000646743.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
GRIA2_chr4_157215728_157371075 | 157248568 | T | TGTGTATA others(41): Show |
intron_variant | MODIFIER | HG00639.hp1 HG02698.hp1 HG02698.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0205 a0001c0002t0002g0122 a0001c0002t0002g0152 |
3 | 7 | 0.4286 | 48 | c.229 others(67): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRIA2_chr4_157215728_157371075 | 157277882 | G | GTATATAT others(41): Show |
intron_variant | MODIFIER | NA19063.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0064 | 1 | 214 | 0.0047 | 48 | c.230 others(67): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRIA3_chrX_123179278_123495915 | 123260457 | A | AAAGAAAG others(41): Show |
intron_variant | MODIFIER | NA18950.hp1 | a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0096 | 1 | 89 | 0.0112 | 48 | c.508 others(65): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
GRIA3_chrX_123179278_123495915 | 123463576 | A | AAGGAAGG others(41): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0046 | 1 | 110 | 0.0091 | 48 | c.207 others(67): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93398133 | G | GTGTGTGT others(41): Show |
intron_variant | MODIFIER | NA18950.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 20 | 0.0500 | 48 | c.134 others(67): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93518002 | T | TATGTATG others(41): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0003 | a0003c0007 | a0003c0007t0005 | a0003c0007t0005g0013 | 1 | 22 | 0.0455 | 48 | c.219 others(67): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRIK1_chr21_29531933_29944996 | 29707430 | T | TCCTCCCT others(41): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0077 | 1 | 157 | 0.0064 | 48 | c.119 others(67): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29707434 | C | CCCTCCCT others(41): Show |
intron_variant | MODIFIER | HG03209.hp2 NA18612.hp1 NA18944.hp2 others(7): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0009others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(3): Show | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0107 others(7): Show |
10 | 159 | 0.0629 | 48 | c.119 others(67): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29707438 | C | CCCTCCCT others(41): Show |
intron_variant | MODIFIER | HG02970.hp2 HG03130.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0046 a0001c0001t0004g0001 |
2 | 157 | 0.0127 | 48 | c.119 others(67): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29707442 | C | CCCTCCCT others(41): Show |
intron_variant | MODIFIER | NA18957.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0102 | 1 | 142 | 0.0070 | 48 | c.119 others(67): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29707446 | C | CCCTCCCT others(41): Show |
intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0129 | 1 | 53 | 0.0189 | 48 | c.119 others(67): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29707446 | C | CCCTCCCT others(41): Show |
intron_variant | MODIFIER | HG00741.hp2 HG02055.hp2 HG02451.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001a0001c0003t0002 | a0001c0001t0001g0042 a0001c0001t0001g0083 a0001c0003t0001g0119 others(3): Show |
6 | 58 | 0.1034 | 48 | c.119 others(67): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29707450 | C | CCCTCCCT others(41): Show |
intron_variant | MODIFIER | HG02132.hp2 NA18980.hp2 NA19060.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0001 | a0001c0002t0001g0062 a0001c0004t0001g0032 a0001c0004t0001g0060 |
3 | 124 | 0.0242 | 48 | c.119 others(67): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29888161 | T | TTTTCTTT others(41): Show |
intron_variant | MODIFIER | HG00639.hp1 HG02886.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011 a0001c0001t0001g0156 |
2 | 100 | 0.0200 | 48 | c.118 others(67): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29888180 | T | TCTTTCTT others(41): Show |
intron_variant | MODIFIER | HG03471.hp1 HG03486.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001 | a0001c0001t0002g0090 a0001c0002t0001g0091 |
2 | 159 | 0.0126 | 48 | c.118 others(67): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29888180 | T | TCTTTCTT others(41): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0150 | 1 | 158 | 0.0063 | 48 | c.118 others(67): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK2_chr6_101388708_102075083 | 101760695 | T | TATATATT others(41): Show |
intron_variant | MODIFIER | HG02056.hp1 HG03017.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0045 a0001c0001t0003g0029 |
2 | 65 | 0.0308 | 48 | c.952 others(67): Show |
GRIK2 | ENSG00000164418.22 | transcript | ENST00000369134.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
GRK3_chr22_25559675_25734294 | 25698103 | G | GAGGGAGG others(41): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0156 | 1 | 174 | 0.0057 | 48 | c.116 others(67): Show |
GRK3 | ENSG00000100077.16 | transcript | ENST00000324198.11 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRK5_chr10_119202571_119464745 | 119261070 | G | GGCCGGGC others(41): Show |
intron_variant | MODIFIER | HG04199.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0159 | 1 | 12 | 0.0833 | 48 | c.52+ others(65): Show |
GRK5 | ENSG00000198873.12 | transcript | ENST00000392870.3 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
GRK5_chr10_119202571_119464745 | 119292152 | C | CTCCTCCT others(41): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0201 | 1 | 200 | 0.0050 | 48 | c.53- others(65): Show |
GRK5 | ENSG00000198873.12 | transcript | ENST00000392870.3 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
GRK5_chr10_119202571_119464745 | 119312939 | A | ATGGTGGT others(41): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(155): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0010others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(91): Show | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(155): Show |
158 | 177 | 0.8927 | 48 | c.53- others(65): Show |
GRK5 | ENSG00000198873.12 | transcript | ENST00000392870.3 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
GRK5_chr10_119202571_119464745 | 119312939 | A | ATGGTGGT others(41): Show |
intron_variant | MODIFIER | NA19070.hp1 | a0003 | a0003c0002 | a0003c0002t0003 | a0003c0002t0003g0167 | 1 | 20 | 0.0500 | 48 | c.53- others(65): Show |
GRK5 | ENSG00000198873.12 | transcript | ENST00000392870.3 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
GRK5_chr10_119202571_119464745 | 119312945 | G | GTAATGGT others(41): Show |
intron_variant | MODIFIER | HG02451.hp2 | a0002 | a0002c0003 | a0002c0003t0065 | a0002c0003t0065g0139 | 1 | 200 | 0.0050 | 48 | c.53- others(65): Show |
GRK5 | ENSG00000198873.12 | transcript | ENST00000392870.3 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
GRP_chr18_59215158_59235771 | 59226992 | C | CCTTCCTT others(41): Show |
intron_variant | MODIFIER | HG01433.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0065 | 1 | 160 | 0.0063 | 48 | c.382 others(65): Show |
GRP | ENSG00000134443.10 | transcript | ENST00000256857.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
GRP_chr18_59215158_59235771 | 59227000 | T | TCTTTCTT others(41): Show |
intron_variant | MODIFIER | NA19079.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 | 1 | 403 | 0.0025 | 48 | c.382 others(65): Show |
GRP | ENSG00000134443.10 | transcript | ENST00000256857.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
GRP_chr18_59215158_59235771 | 59227012 | T | TCTTTCTT others(41): Show |
intron_variant | MODIFIER | HG01168.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0079 | 1 | 392 | 0.0026 | 48 | c.382 others(65): Show |
GRP | ENSG00000134443.10 | transcript | ENST00000256857.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
GRP_chr18_59215158_59235771 | 59227020 | T | TCTTTCTT others(41): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 | 1 | 395 | 0.0025 | 48 | c.382 others(65): Show |
GRP | ENSG00000134443.10 | transcript | ENST00000256857.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
GRP_chr18_59215158_59235771 | 59233812 | A | AACATGAT others(41): Show |
downstream_gene_variant | MODIFIER | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 7 | 405 | 0.0173 | 48 | c.*33 others(59): Show |
GRP | ENSG00000134443.10 | transcript | ENST00000256857.7 | protein_coding | 3042 | chr18 | TogoVar | |||||||
GRTP1_chr13_113319163_113369130 | 113367844 | G | GGTCACCA others(41): Show |
upstream_gene_variant | MODIFIER | HG02129.hp1 NA18612.hp1 NA18747.hp1 others(4): Show |
a0001a0003a0004 | a0001c0001a0003c0004a0004c0003 | a0001c0001t0001a0003c0004t0001a0004c0003t0001others(1): Show | a0001c0001t0001g0064 a0001c0001t0001g0105 a0003c0004t0001g0063 others(4): Show |
7 | 284 | 0.0246 | 48 | c.-37 others(59): Show |
GRTP1 | ENSG00000139835.14 | transcript | ENST00000375431.9 | protein_coding | 3715 | chr13 | TogoVar | |||||||
GRTP1_chr13_113319163_113369130 | 113367844 | G | GGTGACCA others(41): Show |
upstream_gene_variant | MODIFIER | HG03486.hp1 | a0010 | a0010c0011 | a0010c0011t0001 | a0010c0011t0001g0271 | 1 | 278 | 0.0036 | 48 | c.-37 others(59): Show |
GRTP1 | ENSG00000139835.14 | transcript | ENST00000375431.9 | protein_coding | 3715 | chr13 | TogoVar | |||||||
GRTP1_chr13_113319163_113369130 | 113367884 | G | GTGGGCCC others(41): Show |
upstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0002c0014others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(181): Show |
185 | 276 | 0.6703 | 48 | c.-38 others(59): Show |
GRTP1 | ENSG00000139835.14 | transcript | ENST00000375431.9 | protein_coding | 3755 | chr13 | TogoVar | |||||||
GRTP1_chr13_113319163_113369130 | 113367927 | T | TGACCATG others(41): Show |
upstream_gene_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0237 | 1 | 286 | 0.0035 | 48 | c.-38 others(59): Show |
GRTP1 | ENSG00000139835.14 | transcript | ENST00000375431.9 | protein_coding | 3798 | chr13 | TogoVar | |||||||
GRXCR1_chr4_42887713_43035658 | 42987222 | T | TATTATAT others(41): Show |
intron_variant | MODIFIER | HG02165.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0217 | 1 | 155 | 0.0065 | 48 | c.627 others(67): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | TogoVar | |||||||
GSE1_chr16_85608322_85681200 | 85653223 | T | TCCCCCCT others(41): Show |
intron_variant | MODIFIER | HG01257.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0136 | 1 | 243 | 0.0041 | 48 | c.427 others(65): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
GSG1L_chr16_27782528_28068714 | 27979642 | G | GGAAAGAA others(41): Show |
intron_variant | MODIFIER | HG00621.hp1 NA20129.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0030a0001c0002t0002 | a0001c0001t0030g0034 a0001c0002t0002g0170 |
2 | 220 | 0.0091 | 48 | c.350 others(67): Show |
GSG1L | ENSG00000169181.13 | transcript | ENST00000447459.7 | protein_coding | 1/6 | chr16 | TogoVar | |||||||
GSG1L_chr16_27782528_28068714 | 27979697 | A | AAGAAAGA others(41): Show |
intron_variant | MODIFIER | HG01496.hp1 HG01884.hp1 HG03540.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0042a0001c0002t0032 | a0001c0001t0002g0027 a0001c0001t0042g0111 a0001c0002t0032g0229 |
3 | 236 | 0.0127 | 48 | c.350 others(67): Show |
GSG1L | ENSG00000169181.13 | transcript | ENST00000447459.7 | protein_coding | 1/6 | chr16 | TogoVar | |||||||
GSG1L_chr16_27782528_28068714 | 27979726 | G | GGAAGGAA others(41): Show |
intron_variant | MODIFIER | NA18995.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0239 | 1 | 67 | 0.0149 | 48 | c.350 others(67): Show |
GSG1L | ENSG00000169181.13 | transcript | ENST00000447459.7 | protein_coding | 1/6 | chr16 | TogoVar | |||||||
GSS_chr20_34923432_34960806 | 34950020 | C | CACACACA others(41): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054 | 1 | 283 | 0.0035 | 48 | c.129 others(65): Show |
GSS | ENSG00000100983.12 | transcript | ENST00000651619.1 | protein_coding | 2/12 | chr20 | TogoVar | |||||||
GSTM2_chr1_109663057_109680286 | 109670103 | A | AGGGGAGG others(41): Show |
intron_variant | MODIFIER | HG03654.hp1 NA18969.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0076 a0001c0001t0001g0112 |
2 | 195 | 0.0103 | 48 | c.360 others(63): Show |
GSTM2 | ENSG00000213366.13 | transcript | ENST00000241337.9 | protein_coding | 5/7 | chr1 | TogoVar | |||||||
GTF2F2_chr13_45115510_45289893 | 45212520 | C | CTCTTTCT others(41): Show |
intron_variant | MODIFIER | HG01123.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0102 | 1 | 155 | 0.0065 | 48 | c.386 others(65): Show |
GTF2F2 | ENSG00000188342.13 | transcript | ENST00000340473.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
GTF2F2_chr13_45115510_45289893 | 45228283 | C | CTTTTTTT others(41): Show |
intron_variant | MODIFIER | HG00558.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0060 | 1 | 101 | 0.0099 | 48 | c.386 others(67): Show |
GTF2F2 | ENSG00000188342.13 | transcript | ENST00000340473.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | TogoVar |