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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
GPR88_chr1_100533139_100547021 | 100538629 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | HG02135.hp1 HG03831.hp2 NA18963.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 | 3 | 426 | 0.0070 | 30 | c.-74 others(45): Show |
GPR88 | ENSG00000181656.7 | transcript | ENST00000315033.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
GPR88_chr1_100533139_100547021 | 100538629 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | NA18970.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0076 | 1 | 426 | 0.0024 | 30 | c.-74 others(45): Show |
GPR88 | ENSG00000181656.7 | transcript | ENST00000315033.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
GPR88_chr1_100533139_100547021 | 100538629 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0002 | a0002c0002 | a0002c0002t0006 | a0002c0002t0006g0078 | 1 | 426 | 0.0024 | 30 | c.-74 others(45): Show |
GPR88 | ENSG00000181656.7 | transcript | ENST00000315033.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
GPRC5B_chr16_19851691_19889848 | 19880428 | T | TAAATAAA others(23): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00733.hp1 HG02257.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0018others(2): Show | a0001c0001t0001g0269 a0001c0001t0004g0215 a0001c0001t0004g0216 others(5): Show |
10 | 408 | 0.0245 | 30 | c.-2+ others(45): Show |
GPRC5B | ENSG00000167191.12 | transcript | ENST00000300571.7 | protein_coding | 1/3 | chr16 | TogoVar | |||||||
GPRC5D_chr12_12935575_12957170 | 12955975 | T | TCTTTTTC others(23): Show |
upstream_gene_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069 | 1 | 406 | 0.0025 | 30 | c.-39 others(41): Show |
GPRC5D | ENSG00000111291.9 | transcript | ENST00000228887.6 | protein_coding | 3806 | chr12 | TogoVar | |||||||
GPRC5D_chr12_12935575_12957170 | 12956155 | T | TTTTCTTT others(23): Show |
upstream_gene_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0382 | 1 | 406 | 0.0025 | 30 | c.-40 others(41): Show |
GPRC5D | ENSG00000111291.9 | transcript | ENST00000228887.6 | protein_coding | 3986 | chr12 | TogoVar | |||||||
GPRC5D_chr12_12935575_12957170 | 12956448 | T | TCCTTCCT others(23): Show |
upstream_gene_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0129 | 1 | 406 | 0.0025 | 30 | c.-43 others(41): Show |
GPRC5D | ENSG00000111291.9 | transcript | ENST00000228887.6 | protein_coding | 4279 | chr12 | TogoVar | |||||||
GPRC5D_chr12_12935575_12957170 | 12956450 | C | CTTCCTTC others(23): Show |
upstream_gene_variant | MODIFIER | HG01952.hp2 NA19000.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 a0001c0001t0001g0192 |
2 | 406 | 0.0049 | 30 | c.-43 others(41): Show |
GPRC5D | ENSG00000111291.9 | transcript | ENST00000228887.6 | protein_coding | 4281 | chr12 | TogoVar | |||||||
GPSM2_chr1_108871985_108939545 | 108908728 | A | AACACACA others(23): Show |
intron_variant | MODIFIER | HG01099.hp1 HG01099.hp2 HG01516.hp1 others(11): Show |
a0002a0004 | a0002c0002a0004c0004 | a0002c0002t0009a0002c0002t0011a0002c0002t0019others(2): Show | a0002c0002t0009g0033 a0002c0002t0009g0036 a0002c0002t0009g0038 others(11): Show |
14 | 260 | 0.0539 | 30 | c.119 others(49): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
GPSM2_chr1_108871985_108939545 | 108917611 | C | CACACACA others(23): Show |
intron_variant | MODIFIER | NA19068.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0072 | 1 | 260 | 0.0039 | 30 | c.126 others(49): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
GPT_chr8_144499140_144512172 | 144510901 | C | CAGGTGAG others(23): Show |
downstream_gene_variant | MODIFIER | HG02300.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0001 | 1 | 386 | 0.0026 | 30 | c.*39 others(41): Show |
GPT | ENSG00000167701.14 | transcript | ENST00000394955.3 | protein_coding | 3730 | chr8 | TogoVar | |||||||
GRAMD1B_chr11_123425269_123632767 | 123449714 | C | CTTTTTTT others(23): Show |
intron_variant | MODIFIER | HG00544.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0102 | 1 | 282 | 0.0036 | 30 | c.374 others(49): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRAMD1B_chr11_123425269_123632767 | 123467821 | C | CTTTTCTT others(23): Show |
intron_variant | MODIFIER | HG01070.hp1 HG02683.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0005 | a0001c0001t0004g0199 a0001c0002t0005g0173 |
2 | 282 | 0.0071 | 30 | c.375 others(49): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 1/19 | chr11 | TogoVar | |||||||
GRAMD1B_chr11_123425269_123632767 | 123469766 | T | TCCTTCCT others(23): Show |
intron_variant | MODIFIER | HG01952.hp2 HG02300.hp2 |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0077 | a0001c0001t0007g0054 a0001c0001t0077g0070 |
2 | 282 | 0.0071 | 30 | c.375 others(49): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 1/19 | chr11 | TogoVar | |||||||
GRAMD1B_chr11_123425269_123632767 | 123524318 | T | TTTTTATT others(23): Show |
intron_variant | MODIFIER | HG01109.hp2 HG01257.hp1 HG02135.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(6): Show | a0001c0001t0001g0128 a0001c0001t0001g0256 a0001c0001t0002g0180 others(9): Show |
12 | 282 | 0.0426 | 30 | c.452 others(49): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRAMD1B_chr11_123425269_123632767 | 123548325 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | NA18950.hp2 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0141 | 1 | 282 | 0.0036 | 30 | c.453 others(49): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRAMD1B_chr11_123425269_123632767 | 123589612 | T | TTATATAT others(23): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0094 | a0001c0001t0094g0039 | 1 | 282 | 0.0036 | 30 | c.685 others(47): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRAMD1B_chr11_123425269_123632767 | 123589614 | T | TTTTATAT others(23): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0062 | 1 | 282 | 0.0036 | 30 | c.685 others(47): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GREB1_chr2_11529045_11647788 | 11539017 | C | CCTTCTCT others(23): Show |
intron_variant | MODIFIER | HG02559.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
a0002a0006a0007others(1): Show | a0002c0007a0006c0033a0007c0060others(1): Show | a0002c0007t0020a0006c0033t0034a0007c0060t0061others(1): Show | a0002c0007t0020g0307 a0006c0033t0034g0302 a0007c0060t0061g0305 others(1): Show |
4 | 308 | 0.0130 | 30 | c.-16 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GREB1_chr2_11529045_11647788 | 11539062 | T | TCTTCTCT others(23): Show |
intron_variant | MODIFIER | HG03041.hp2 HG03209.hp2 NA18522.hp2 |
a0002a0008a0013 | a0002c0007a0008c0015a0013c0018 | a0002c0007t0037a0008c0015t0027a0013c0018t0022 | a0002c0007t0037g0023 a0008c0015t0027g0004 a0013c0018t0022g0030 |
3 | 308 | 0.0097 | 30 | c.-16 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GREB1_chr2_11529045_11647788 | 11546641 | G | GGTTCTGG others(23): Show |
intron_variant | MODIFIER | NA19086.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0222 | 1 | 308 | 0.0033 | 30 | c.-16 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GREB1_chr2_11529045_11647788 | 11587741 | A | ACACACAC others(23): Show |
intron_variant | MODIFIER | HG02004.hp2 | a0002 | a0002c0011 | a0002c0011t0005 | a0002c0011t0005g0135 | 1 | 308 | 0.0033 | 30 | c.116 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GREB1_chr2_11529045_11647788 | 11587741 | A | ACACACAC others(23): Show |
intron_variant | MODIFIER | HG02273.hp2 | a0005 | a0005c0002 | a0005c0002t0001 | a0005c0002t0001g0142 | 1 | 308 | 0.0033 | 30 | c.116 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GREB1_chr2_11529045_11647788 | 11587741 | A | ACACACAC others(23): Show |
intron_variant | MODIFIER | NA18612.hp2 | a0046 | a0046c0087 | a0046c0087t0004 | a0046c0087t0004g0172 | 1 | 308 | 0.0033 | 30 | c.116 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GREM2_chr1_240484573_240617155 | 240547532 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0072 | 1 | 376 | 0.0027 | 30 | c.-1- others(47): Show |
GREM2 | ENSG00000180875.5 | transcript | ENST00000318160.5 | protein_coding | 1/1 | chr1 | TogoVar | |||||||
GRHL1_chr2_9946693_10007277 | 9979151 | C | CAAAAAAA others(23): Show |
intron_variant | MODIFIER | HG01258.hp1 HG01516.hp2 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0165 a0002c0002t0002g0190 |
2 | 418 | 0.0048 | 30 | c.111 others(49): Show |
GRHL1 | ENSG00000134317.18 | transcript | ENST00000324907.14 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GRHL1_chr2_9946693_10007277 | 9998679 | T | TATACATA others(23): Show |
intron_variant | MODIFIER | NA18960.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0193 | 1 | 418 | 0.0024 | 30 | c.167 others(47): Show |
GRHL1 | ENSG00000134317.18 | transcript | ENST00000324907.14 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GRHL1_chr2_9946693_10007277 | 9998887 | T | TATACATA others(23): Show |
intron_variant | MODIFIER | HG01243.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0054 a0002c0002t0002g0181 a0002c0002t0002g0190 others(6): Show |
9 | 418 | 0.0215 | 30 | c.167 others(45): Show |
GRHL1 | ENSG00000134317.18 | transcript | ENST00000324907.14 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
GRHL2_chr8_101487439_101674726 | 101522721 | T | TTATACAT others(23): Show |
intron_variant | MODIFIER | HG02723.hp2 HG03139.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 a0001c0001t0001g0284 |
2 | 306 | 0.0065 | 30 | c.21- others(47): Show |
GRHL2 | ENSG00000083307.12 | transcript | ENST00000646743.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
GRHL2_chr8_101487439_101674726 | 101656873 | G | GACACACA others(23): Show |
intron_variant | MODIFIER | HG03225.hp2 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0049 a0001c0001t0007g0231 |
2 | 306 | 0.0065 | 30 | c.169 others(49): Show |
GRHL2 | ENSG00000083307.12 | transcript | ENST00000646743.1 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
GRHL2_chr8_101487439_101674726 | 101662860 | C | CATATATA others(23): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0105 | 1 | 306 | 0.0033 | 30 | c.169 others(49): 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(23): Show |
intron_variant | MODIFIER | HG01993.hp1 HG03486.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0005a0001c0006t0001 | a0001c0001t0005g0193 a0001c0006t0001g0192 |
2 | 194 | 0.0103 | 30 | c.220 others(49): Show |
GRIA1 | ENSG00000155511.19 | transcript | ENST00000285900.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
GRIA1_chr5_153485670_153818869 | 153701619 | C | CAAAAAAA others(23): Show |
intron_variant | MODIFIER | NA18972.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0066 | 1 | 194 | 0.0052 | 30 | c.145 others(49): Show |
GRIA1 | ENSG00000155511.19 | transcript | ENST00000285900.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
GRIA2_chr4_157215728_157371075 | 157277882 | G | GTATATAT others(23): Show |
intron_variant | MODIFIER | NA18977.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0159 | 1 | 216 | 0.0046 | 30 | c.230 others(49): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRIA3_chrX_123179278_123495915 | 123471990 | C | CATATATA others(23): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0005a0001c0002t0002others(2): Show | a0001c0001t0003g0115 a0001c0001t0005g0128 a0001c0002t0002g0085 others(4): Show |
7 | 207 | 0.0338 | 30 | c.232 others(49): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
GRIA4_chr11_105605073_105987090 | 105911775 | A | AATATATA others(23): Show |
intron_variant | MODIFIER | HG02129.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(1): Show | a0001c0001t0002g0106 a0001c0001t0003g0158 a0001c0001t0005g0017 others(1): Show |
4 | 184 | 0.0217 | 30 | c.126 others(49): Show |
GRIA4 | ENSG00000152578.15 | transcript | ENST00000282499.10 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GRID1_chr10_85594552_86371795 | 85599802 | A | AAAAAAAA others(23): Show |
3_prime_UTR_variant | MODIFIER | HG01891.hp2 | a0002 | a0002c0007 | a0002c0007t0028 | a0002c0007t0028g0051 | 1 | 96 | 0.0104 | 30 | c.*24 others(41): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 16/16 | 2470 | chr10 | TogoVar | ||||||
GRID1_chr10_85594552_86371795 | 85737645 | G | GATATATA others(23): Show |
intron_variant | MODIFIER | HG00642.hp1 HG04199.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0029a0001c0004t0031 | a0001c0002t0029g0059 a0001c0004t0031g0074 |
2 | 96 | 0.0208 | 30 | c.123 others(49): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 8/15 | chr10 | TogoVar | |||||||
GRID1_chr10_85594552_86371795 | 85737673 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG01069.hp2 HG01071.hp1 HG02897.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0014a0001c0004t0007 | a0001c0001t0014g0049 a0001c0004t0007g0065 a0001c0004t0007g0066 |
3 | 96 | 0.0313 | 30 | c.123 others(49): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 8/15 | chr10 | TogoVar | |||||||
GRID1_chr10_85594552_86371795 | 85865916 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0084 | 1 | 96 | 0.0104 | 30 | c.951 others(47): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 6/15 | chr10 | TogoVar | |||||||
GRID2_chr4_92298966_93779566 | 92384609 | A | ATATATGT others(23): Show |
intron_variant | MODIFIER | HG01978.hp2 HG02055.hp2 HG03041.hp1 others(3): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0007 | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0003g0032 others(3): Show |
6 | 34 | 0.1765 | 30 | c.88+ others(47): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 92460032 | C | CTATATAT others(23): Show |
intron_variant | MODIFIER | HG02698.hp2 NA20129.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0007 | a0001c0002t0001g0007 a0001c0004t0007g0028 |
2 | 34 | 0.0588 | 30 | c.89- others(49): 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(23): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 | 1 | 34 | 0.0294 | 30 | c.89- others(49): 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(23): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 34 | 0.0294 | 30 | c.89- others(47): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93398133 | G | GTGTGTGT others(23): Show |
intron_variant | MODIFIER | HG01192.hp1 HG03195.hp2 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 |
3 | 34 | 0.0882 | 30 | c.134 others(49): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93697869 | G | GTATATAT others(23): Show |
intron_variant | MODIFIER | HG01496.hp1 HG02698.hp2 NA20129.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0007 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0004t0007g0028 |
3 | 34 | 0.0882 | 30 | c.236 others(51): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 93697869 | G | GTGTATAT others(23): Show |
intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018 | 1 | 34 | 0.0294 | 30 | c.236 others(51): 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(23): Show |
intron_variant | MODIFIER | HG02145.hp2 HG03579.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0088 a0001c0002t0001g0097 |
2 | 162 | 0.0124 | 30 | c.260 others(49): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 16/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29560364 | T | TTTCTTTC others(23): Show |
intron_variant | MODIFIER | NA18968.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0121 | 1 | 162 | 0.0062 | 30 | c.235 others(49): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 15/17 | chr21 | TogoVar | |||||||
GRIK1_chr21_29531933_29944996 | 29848779 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0137 | 1 | 162 | 0.0062 | 30 | c.118 others(49): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar |