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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
GRHL1_chr2_9946693_10007277 | 9998699 | T | TATATACG others(15): Show |
intron_variant | MODIFIER | NA18999.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0249 | 1 | 418 | 0.0024 | 22 | c.167 others(39): Show |
GRHL1 | ENSG00000134317.18 | transcript | ENST00000324907.14 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GRHL1_chr2_9946693_10007277 | 9998758 | A | ATATATGT others(15): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG02074.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 a0001c0001t0001g0319 |
3 | 418 | 0.0072 | 22 | c.167 others(39): Show |
GRHL1 | ENSG00000134317.18 | transcript | ENST00000324907.14 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GRHL2_chr8_101487439_101674726 | 101559353 | C | CAAAAAAA others(15): Show |
intron_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0122 | 1 | 306 | 0.0033 | 22 | c.678 others(37): Show |
GRHL2 | ENSG00000083307.12 | transcript | ENST00000646743.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
GRHL2_chr8_101487439_101674726 | 101586065 | C | CTTTTTTT others(15): Show |
intron_variant | MODIFIER | HG01928.hp1 HG02080.hp1 HG02738.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0015a0002c0003t0001 | a0001c0001t0001g0235 a0001c0001t0015g0010 a0002c0003t0001g0063 |
3 | 306 | 0.0098 | 22 | c.100 others(41): Show |
GRHL2 | ENSG00000083307.12 | transcript | ENST00000646743.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
GRHL2_chr8_101487439_101674726 | 101623828 | G | GACAGTAC others(15): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(62): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0010a0001c0011others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0137 a0001c0001t0002g0033 a0001c0001t0002g0047 others(62): Show |
65 | 306 | 0.2124 | 22 | c.125 others(41): Show |
GRHL2 | ENSG00000083307.12 | transcript | ENST00000646743.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
GRHL2_chr8_101487439_101674726 | 101624548 | G | GACAGTAC others(15): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0002a0001c0005others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0043 others(214): Show |
217 | 306 | 0.7092 | 22 | c.125 others(41): Show |
GRHL2 | ENSG00000083307.12 | transcript | ENST00000646743.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
GRHL2_chr8_101487439_101674726 | 101656868 | T | TGACACAC others(15): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 | 1 | 306 | 0.0033 | 22 | c.169 others(41): Show |
GRHL2 | ENSG00000083307.12 | transcript | ENST00000646743.1 | protein_coding | 14/15 | chr8 | TogoVar | |||||||
GRHL2_chr8_101487439_101674726 | 101656873 | G | GACACACA others(15): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02723.hp2 NA19079.hp1 |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0005c0008t0001 | a0001c0001t0001g0158 a0001c0001t0001g0284 a0005c0008t0001g0109 |
3 | 306 | 0.0098 | 22 | c.169 others(41): Show |
GRHL2 | ENSG00000083307.12 | transcript | ENST00000646743.1 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
GRIA1_chr5_153485670_153818869 | 153566304 | C | CTTTTTTT others(15): Show |
intron_variant | MODIFIER | HG01256.hp2 HG02698.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0114 a0001c0001t0001g0173 |
2 | 194 | 0.0103 | 22 | c.220 others(41): Show |
GRIA1 | ENSG00000155511.19 | transcript | ENST00000285900.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
GRIA1_chr5_153485670_153818869 | 153607042 | G | GATATATA others(15): Show |
intron_variant | MODIFIER | HG02896.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0038 | 1 | 194 | 0.0052 | 22 | c.221 others(41): Show |
GRIA1 | ENSG00000155511.19 | transcript | ENST00000285900.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
GRIA1_chr5_153485670_153818869 | 153607068 | T | TATATATA others(15): Show |
intron_variant | MODIFIER | HG02698.hp1 HG02698.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0105 a0001c0001t0001g0114 |
2 | 194 | 0.0103 | 22 | c.221 others(41): Show |
GRIA1 | ENSG00000155511.19 | transcript | ENST00000285900.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
GRIA1_chr5_153485670_153818869 | 153656383 | T | TTATATAT others(15): Show |
intron_variant | MODIFIER | HG02055.hp2 HG03098.hp2 HG03654.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0066 a0001c0001t0001g0090 a0001c0001t0001g0104 others(2): Show |
5 | 194 | 0.0258 | 22 | c.699 others(37): Show |
GRIA1 | ENSG00000155511.19 | transcript | ENST00000285900.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
GRIA1_chr5_153485670_153818869 | 153656383 | T | TTTTATAT others(15): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0061 | 1 | 194 | 0.0052 | 22 | c.699 others(37): Show |
GRIA1 | ENSG00000155511.19 | transcript | ENST00000285900.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
GRIA1_chr5_153485670_153818869 | 153701619 | C | CAAAAAAA others(15): Show |
intron_variant | MODIFIER | HG01257.hp2 HG01346.hp1 HG02698.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0055 others(3): Show |
6 | 194 | 0.0309 | 22 | c.145 others(41): Show |
GRIA1 | ENSG00000155511.19 | transcript | ENST00000285900.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
GRIA3_chrX_123179278_123495915 | 123184094 | T | TTCTCTCT others(15): Show |
upstream_gene_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0082 | 1 | 207 | 0.0048 | 22 | c.-44 others(31): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 183 | chrX | TogoVar | |||||||
GRIA3_chrX_123179278_123495915 | 123463627 | A | AGGGAGGG others(15): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0052 | 1 | 207 | 0.0048 | 22 | c.207 others(41): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
GRIA3_chrX_123179278_123495915 | 123463684 | G | GAAAGAAA others(15): Show |
intron_variant | MODIFIER | NA19000.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0101 | 1 | 207 | 0.0048 | 22 | c.207 others(41): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
GRIA3_chrX_123179278_123495915 | 123471990 | C | CATATATA others(15): Show |
intron_variant | MODIFIER | HG01106.hp1 HG01433.hp1 HG02258.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0158 a0001c0001t0002g0027 a0001c0001t0003g0016 others(9): Show |
12 | 207 | 0.0580 | 22 | c.232 others(41): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
GRIA4_chr11_105605073_105987090 | 105829094 | T | TACACACA others(15): Show |
intron_variant | MODIFIER | HG00621.hp1 HG01884.hp1 HG02258.hp1 others(13): Show |
a0001a0002 | a0001c0001a0002c0008 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(11): Show | a0001c0001t0001g0117 a0001c0001t0007g0153 a0001c0001t0009g0159 others(13): Show |
16 | 184 | 0.0870 | 22 | c.488 others(41): Show |
GRIA4 | ENSG00000152578.15 | transcript | ENST00000282499.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRIA4_chr11_105605073_105987090 | 105866549 | G | GTATATAT others(15): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0184 | 1 | 184 | 0.0054 | 22 | c.672 others(39): Show |
GRIA4 | ENSG00000152578.15 | transcript | ENST00000282499.10 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRIA4_chr11_105605073_105987090 | 105866551 | G | GTATATAT others(15): Show |
intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0033 | a0001c0001t0033g0068 | 1 | 184 | 0.0054 | 22 | c.672 others(39): Show |
GRIA4 | ENSG00000152578.15 | transcript | ENST00000282499.10 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRIA4_chr11_105605073_105987090 | 105911775 | A | AATATATA others(15): Show |
intron_variant | MODIFIER | HG00423.hp2 HG02109.hp1 HG02451.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0019others(2): Show | a0001c0001t0002g0176 a0001c0001t0003g0052 a0001c0001t0019g0165 others(2): Show |
5 | 184 | 0.0272 | 22 | c.126 others(41): Show |
GRIA4 | ENSG00000152578.15 | transcript | ENST00000282499.10 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRID1_chr10_85594552_86371795 | 85599802 | A | AAAAAATA others(15): Show |
3_prime_UTR_variant | MODIFIER | HG02735.hp2 | a0001 | a0001c0003 | a0001c0003t0055 | a0001c0003t0055g0044 | 1 | 96 | 0.0104 | 22 | c.*24 others(33): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 16/16 | 2470 | chr10 | TogoVar | ||||||
GRID1_chr10_85594552_86371795 | 85634249 | C | CCTCTCTC others(15): Show |
intron_variant | MODIFIER | HG02809.hp1 HG03017.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0037a0001c0004t0003 | a0001c0001t0037g0033 a0001c0004t0003g0091 |
2 | 96 | 0.0208 | 22 | c.219 others(43): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 13/15 | chr10 | TogoVar | |||||||
GRID1_chr10_85594552_86371795 | 85865904 | C | CATATATA others(15): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0003 | a0001c0003t0025 | a0001c0003t0025g0028 | 1 | 96 | 0.0104 | 22 | c.951 others(39): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 6/15 | chr10 | TogoVar | |||||||
GRID1_chr10_85594552_86371795 | 86145547 | T | TACACACA others(15): Show |
intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG00741.hp2 others(10): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0004others(2): Show | a0001c0002t0029a0001c0003t0001a0001c0003t0007others(10): Show | a0001c0002t0029g0059 a0001c0003t0001g0011 a0001c0003t0007g0007 others(10): Show |
13 | 96 | 0.1354 | 22 | c.521 others(39): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 3/15 | chr10 | TogoVar | |||||||
GRID2IP_chr7_6491778_6556461 | 6539224 | G | GTTCAAGC others(15): Show |
intron_variant | MODIFIER | NA18979.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0099 | 1 | 366 | 0.0027 | 22 | c.584 others(37): Show |
GRID2IP | ENSG00000215045.9 | transcript | ENST00000457091.3 | protein_coding | 2/21 | chr7 | TogoVar | |||||||
GRID2_chr4_92298966_93779566 | 92411655 | G | GTGTGTAT others(15): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 | 1 | 34 | 0.0294 | 22 | c.88+ others(41): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 92460032 | C | CTCTATAT others(15): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0003 | a0003c0007 | a0003c0007t0005 | a0003c0007t0005g0013 | 1 | 34 | 0.0294 | 22 | c.89- others(41): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 92460053 | T | TATATATA others(15): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 | 1 | 34 | 0.0294 | 22 | c.89- others(41): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 92548401 | A | ATTTTTTT others(15): Show |
intron_variant | MODIFIER | HG02615.hp2 HG03098.hp1 NA19030.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0002 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0005t0002g0029 |
3 | 34 | 0.0882 | 22 | c.89- others(39): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 92895384 | C | CATATATA others(15): Show |
intron_variant | MODIFIER | HG01192.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(1): Show |
4 | 34 | 0.1177 | 22 | c.245 others(43): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93115402 | G | GACACACA others(15): Show |
intron_variant | MODIFIER | HG01192.hp2 HG01496.hp2 HG01978.hp1 others(3): Show |
a0001a0003 | a0001c0001a0003c0007 | a0001c0001t0001a0001c0001t0004a0003c0007t0005 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0018 others(3): Show |
6 | 34 | 0.1765 | 22 | c.735 others(39): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93317986 | A | AATATATA others(15): Show |
intron_variant | MODIFIER | HG02922.hp1 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0027 a0001c0001t0003g0032 |
2 | 34 | 0.0588 | 22 | c.124 others(43): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93332295 | T | TGAGAGAG others(15): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 | 1 | 34 | 0.0294 | 22 | c.124 others(43): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93471698 | A | ATTTTTTT others(15): Show |
intron_variant | MODIFIER | NA18950.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 34 | 0.0294 | 22 | c.185 others(43): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93697867 | G | GTATATAT others(15): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 | 1 | 34 | 0.0294 | 22 | c.236 others(43): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93697869 | G | GTATATAT others(15): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0003 | a0003c0007 | a0003c0007t0005 | a0003c0007t0005g0013 | 1 | 34 | 0.0294 | 22 | c.236 others(43): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRIK1_chr21_29531933_29944996 | 29541575 | C | CTTTTTTT others(15): Show |
intron_variant | MODIFIER | HG02132.hp2 NA18983.hp1 |
a0001a0002 | a0001c0004a0002c0010 | a0001c0004t0001a0002c0010t0001 | a0001c0004t0001g0032 a0002c0010t0001g0087 |
2 | 162 | 0.0124 | 22 | c.260 others(41): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 16/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29558376 | T | TCACACAC others(15): Show |
intron_variant | MODIFIER | HG01952.hp1 NA18906.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0067 a0001c0003t0001g0018 |
2 | 162 | 0.0124 | 22 | c.235 others(41): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 15/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29587964 | C | CTTTTTTT others(15): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0055 | 1 | 162 | 0.0062 | 22 | c.157 others(39): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 11/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29888198 | T | TTTCTTTC others(15): Show |
intron_variant | MODIFIER | HG01192.hp2 HG02132.hp2 HG02559.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0002t0001a0001c0004t0001 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0002t0001g0079 others(3): Show |
6 | 162 | 0.0370 | 22 | c.118 others(41): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29913672 | A | AATATATA others(15): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0150 | 1 | 162 | 0.0062 | 22 | c.118 others(41): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
GRIK2_chr6_101388708_102075083 | 101494971 | T | TTATATAT others(15): Show |
intron_variant | MODIFIER | NA18963.hp2 NA20129.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0099 a0001c0001t0002g0032 |
2 | 116 | 0.0172 | 22 | c.115 others(41): Show |
GRIK2 | ENSG00000164418.22 | transcript | ENST00000369134.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
GRIK2_chr6_101388708_102075083 | 101494971 | T | TTTTATAT others(15): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0002 | a0002c0012 | a0002c0012t0003 | a0002c0012t0003g0077 | 1 | 116 | 0.0086 | 22 | c.115 others(41): Show |
GRIK2 | ENSG00000164418.22 | transcript | ENST00000369134.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
GRIK2_chr6_101388708_102075083 | 101556321 | A | ATTTTTTT others(15): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0005 | a0001c0005t0002 | a0001c0005t0002g0022 | 1 | 116 | 0.0086 | 22 | c.116 others(41): Show |
GRIK2 | ENSG00000164418.22 | transcript | ENST00000369134.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
GRIK2_chr6_101388708_102075083 | 101592588 | C | CATATATA others(15): Show |
intron_variant | MODIFIER | HG00544.hp1 HG00735.hp1 HG02647.hp1 |
a0001a0002 | a0001c0001a0002c0012 | a0001c0001t0001a0002c0012t0003 | a0001c0001t0001g0040 a0001c0001t0001g0085 a0002c0012t0003g0077 |
3 | 116 | 0.0259 | 22 | c.116 others(41): Show |
GRIK2 | ENSG00000164418.22 | transcript | ENST00000369134.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
GRIK2_chr6_101388708_102075083 | 101592615 | A | ATATATAT others(15): Show |
intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0028 | 1 | 116 | 0.0086 | 22 | c.116 others(41): Show |
GRIK2 | ENSG00000164418.22 | transcript | ENST00000369134.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
GRIK2_chr6_101388708_102075083 | 101595714 | G | GTATATAT others(15): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0019 | 1 | 116 | 0.0086 | 22 | c.116 others(41): Show |
GRIK2 | ENSG00000164418.22 | transcript | ENST00000369134.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
GRIK2_chr6_101388708_102075083 | 101906366 | C | CTGTGTGT others(15): Show |
intron_variant | MODIFIER | HG02559.hp1 HG02886.hp2 HG02922.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(4): Show | a0001c0001t0001g0017 a0001c0001t0002g0036 a0001c0001t0002g0039 others(6): Show |
9 | 116 | 0.0776 | 22 | c.174 others(43): Show |
GRIK2 | ENSG00000164418.22 | transcript | ENST00000369134.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr6 | TogoVar |