regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
GRAMD1B_chr11_123425269_123632767 | 123469772 | T | TTTCCTTC others(25): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0034 | a0001c0001t0034g0036 | 1 | 282 | 0.0036 | 32 | c.375 others(51): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GRAMD1B_chr11_123425269_123632767 | 123513605 | C | CCTTTCTT others(25): Show |
intron_variant | MODIFIER | HG01123.hp1 HG01975.hp1 HG02155.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0001t0004a0001c0002t0014others(1): Show | a0001c0001t0001g0098a0001c0001t0004g0052a0001c0002t0014g0107others(1): Show | 4 | 282 | 0.0142 | 32 | c.452 others(51): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GRAMD1B_chr11_123425269_123632767 | 123513609 | C | CCTTTCTT others(25): Show |
intron_variant | MODIFIER | HG01952.hp2 | a0001 | a0001c0001 | a0001c0001t0077 | a0001c0001t0077g0070 | 1 | 282 | 0.0036 | 32 | c.452 others(51): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GRAMD1B_chr11_123425269_123632767 | 123513613 | C | CCTTTCTT others(25): Show |
intron_variant | MODIFIER | HG02083.hp2 HG02132.hp1 HG04115.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0012a0001c0001t0013a0001c0002t0051 | a0001c0001t0012g0066a0001c0001t0013g0115a0001c0002t0051g0189 | 3 | 282 | 0.0106 | 32 | c.452 others(51): 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(25): Show |
intron_variant | MODIFIER | HG01496.hp1 NA18983.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0007a0001c0002t0023 | a0001c0001t0007g0201a0001c0002t0023g0068 | 2 | 282 | 0.0071 | 32 | c.452 others(51): 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(25): Show |
intron_variant | MODIFIER | HG02683.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0196 | 1 | 282 | 0.0036 | 32 | c.452 others(51): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GRAMD1B_chr11_123425269_123632767 | 123513617 | C | CCTTTCTT others(25): Show |
intron_variant | MODIFIER | HG01361.hp1 HG01496.hp2 HG01515.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0261others(1): Show | 4 | 282 | 0.0142 | 32 | c.452 others(51): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GRAMD1B_chr11_123425269_123632767 | 123513623 | T | TTTCTTCT others(25): Show |
intron_variant | MODIFIER | NA18999.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 | 1 | 282 | 0.0036 | 32 | c.452 others(51): 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(25): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0020a0001c0001t0037a0001c0001t0071others(1): Show | a0001c0001t0020g0230a0001c0001t0037g0025a0001c0001t0071g0022others(1): Show | 4 | 282 | 0.0142 | 32 | c.685 others(49): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GRAMD1C_chr3_113833788_113952174 | 113849964 | G | GCGGGGGG others(25): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(39): Show | 42 | 324 | 0.1296 | 32 | c.174 others(49): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
GRAMD4_chr22_46615386_46684785 | 46648911 | G | GATGGATG others(25): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0049 | 1 | 328 | 0.0031 | 32 | c.284 others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
GREB1L_chr18_21237232_21531112 | 21429129 | T | TCCTTCCT others(25): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0142 | 1 | 148 | 0.0068 | 32 | c.833 others(51): Show |
GREB1L | ENSG00000141449.16 | transcript | ENST00000424526.7 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
GREB1_chr2_11529045_11647788 | 11539027 | T | TCTTCTCT others(25): Show |
intron_variant | MODIFIER | HG01261.hp1 HG02572.hp2 |
a0018a0037 | a0018c0037a0037c0067 | a0018c0037t0053a0037c0067t0021 | a0018c0037t0053g0067a0037c0067t0021g0070 | 2 | 308 | 0.0065 | 32 | c.-16 others(51): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GREB1_chr2_11529045_11647788 | 11539032 | T | TCTTCTCT others(25): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
a0005a0007a0010others(3): Show | a0005c0066a0007c0015a0010c0032others(3): Show | a0005c0066t0022a0007c0015t0021a0010c0032t0028others(3): Show | a0005c0066t0022g0072a0007c0015t0021g0069a0010c0032t0028g0007others(4): Show | 7 | 308 | 0.0227 | 32 | c.-16 others(51): 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(25): Show |
intron_variant | MODIFIER | HG01993.hp2 NA18989.hp2 NA19002.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0002a0003c0003t0001a0003c0003t0005 | a0001c0001t0002g0192a0003c0003t0001g0155a0003c0003t0005g0113 | 3 | 308 | 0.0097 | 32 | c.116 others(51): 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(25): Show |
intron_variant | MODIFIER | NA18941.hp1 | a0005 | a0005c0002 | a0005c0002t0003 | a0005c0002t0003g0098 | 1 | 308 | 0.0033 | 32 | c.116 others(51): 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(25): Show |
intron_variant | MODIFIER | HG03669.hp2 | a0025 | a0025c0093 | a0025c0093t0002 | a0025c0093t0002g0178 | 1 | 308 | 0.0033 | 32 | c.116 others(51): 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(25): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0002 | a0002c0007 | a0002c0007t0020 | a0002c0007t0020g0307 | 1 | 308 | 0.0033 | 32 | c.116 others(51): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GREB1_chr2_11529045_11647788 | 11618128 | A | AGATGGGC others(25): Show |
intron_variant | MODIFIER | NA18981.hp1 NA19060.hp1 |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0073a0004c0004t0004 | a0001c0001t0073g0253a0004c0004t0004g0289 | 2 | 308 | 0.0065 | 32 | c.341 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GREB1_chr2_11529045_11647788 | 11618136 | C | CACTCCTG others(25): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG01109.hp2 others(16): Show |
a0001a0002a0003others(8): Show | a0001c0001a0002c0005a0002c0007others(11): Show | a0001c0001t0002a0001c0001t0069a0002c0005t0001others(15): Show | a0001c0001t0002g0207a0001c0001t0002g0252a0001c0001t0069g0288others(16): Show | 19 | 308 | 0.0617 | 32 | c.341 others(47): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GREB1_chr2_11529045_11647788 | 11618160 | G | GGATGGGC others(25): Show |
intron_variant | MODIFIER | HG02083.hp1 | a0004 | a0004c0004 | a0004c0004t0008 | a0004c0004t0008g0273 | 1 | 308 | 0.0033 | 32 | c.341 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GREB1_chr2_11529045_11647788 | 11618167 | T | TGACTCCT others(25): Show |
intron_variant | MODIFIER | HG04199.hp1 | a0002 | a0002c0005 | a0002c0005t0011 | a0002c0005t0011g0250 | 1 | 308 | 0.0033 | 32 | c.341 others(47): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GREB1_chr2_11529045_11647788 | 11618168 | G | GACTCCTG others(25): Show |
intron_variant | MODIFIER | HG01192.hp2 | a0008 | a0008c0006 | a0008c0006t0005 | a0008c0006t0005g0121 | 1 | 308 | 0.0033 | 32 | c.341 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GREB1_chr2_11529045_11647788 | 11618192 | G | GGATGGGC others(25): Show |
intron_variant | MODIFIER | HG02083.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0138 | 1 | 308 | 0.0033 | 32 | c.341 others(47): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GRHL1_chr2_9946693_10007277 | 9979151 | C | CAAAAAAA others(25): Show |
intron_variant | MODIFIER | HG03688.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0163 | 1 | 418 | 0.0024 | 32 | c.111 others(51): Show |
GRHL1 | ENSG00000134317.18 | transcript | ENST00000324907.14 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GRHL3_chr1_24314357_24360318 | 24326389 | T | TCCTCCAC others(25): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0236 | 1 | 372 | 0.0027 | 32 | c.18- others(47): Show |
GRHL3 | ENSG00000158055.17 | transcript | ENST00000361548.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
GRHL3_chr1_24314357_24360318 | 24345043 | C | CCTCCACA others(25): Show |
intron_variant | MODIFIER | HG02027.hp2 NA18943.hp2 NA18997.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0102a0001c0002t0001g0167a0001c0002t0001g0172 | 3 | 372 | 0.0081 | 32 | c.145 others(49): Show |
GRHL3 | ENSG00000158055.17 | transcript | ENST00000361548.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
GRHL3_chr1_24314357_24360318 | 24345157 | C | CCCCTCCA others(25): Show |
intron_variant | MODIFIER | NA19055.hp2 | a0002 | a0002c0006 | a0002c0006t0001 | a0002c0006t0001g0292 | 1 | 372 | 0.0027 | 32 | c.145 others(49): Show |
GRHL3 | ENSG00000158055.17 | transcript | ENST00000361548.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
GRIA1_chr5_153485670_153818869 | 153566304 | C | CTTTTTTT others(25): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(1): Show | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0040others(9): Show | 12 | 194 | 0.0619 | 32 | c.220 others(51): Show |
GRIA1 | ENSG00000155511.19 | transcript | ENST00000285900.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
GRIA2_chr4_157215728_157371075 | 157356121 | A | ATATTTAT others(25): Show |
intron_variant | MODIFIER | HG01168.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0127 | 1 | 216 | 0.0046 | 32 | c.204 others(51): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRIA2_chr4_157215728_157371075 | 157356149 | T | TTATTTAT others(25): Show |
intron_variant | MODIFIER | HG02071.hp1 HG02109.hp1 |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0014 | a0001c0001t0011g0014a0001c0001t0014g0035 | 2 | 216 | 0.0093 | 32 | c.204 others(51): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRIA2_chr4_157215728_157371075 | 157356163 | A | ATATTTAT others(25): Show |
intron_variant | MODIFIER | NA19003.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0165 | 1 | 216 | 0.0046 | 32 | c.204 others(51): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRIA3_chrX_123179278_123495915 | 123260457 | A | AAAGAAAG others(25): Show |
intron_variant | MODIFIER | NA18972.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0034 | 1 | 207 | 0.0048 | 32 | c.508 others(49): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
GRIA3_chrX_123179278_123495915 | 123260457 | A | AAAGAAAG others(25): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02698.hp1 HG03688.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0088a0001c0001t0002g0027a0001c0001t0002g0135 | 3 | 207 | 0.0145 | 32 | c.508 others(49): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
GRIA3_chrX_123179278_123495915 | 123260457 | A | AAAGAAAG others(25): Show |
intron_variant | MODIFIER | HG01496.hp2 HG02622.hp1 HG04204.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0051a0001c0001t0001g0198a0001c0002t0001g0175 | 3 | 207 | 0.0145 | 32 | c.508 others(49): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
GRIA3_chrX_123179278_123495915 | 123260457 | A | AAAGAAAG others(25): Show |
intron_variant | MODIFIER | HG01258.hp1 HG01433.hp1 HG02071.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0009g0083a0001c0002t0001g0084a0001c0002t0002g0021others(2): Show | 5 | 207 | 0.0242 | 32 | c.508 others(49): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
GRIA3_chrX_123179278_123495915 | 123260457 | A | AAAGAAAG others(25): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01169.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0057a0001c0001t0002g0065 | 2 | 207 | 0.0097 | 32 | c.508 others(49): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
GRIA3_chrX_123179278_123495915 | 123463550 | C | CGAAGGAA others(25): Show |
intron_variant | MODIFIER | HG01496.hp1 HG02886.hp2 |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0006 | a0001c0002t0002g0134a0001c0002t0006g0133 | 2 | 207 | 0.0097 | 32 | c.207 others(51): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
GRIA3_chrX_123179278_123495915 | 123463576 | A | AAGGAAGG others(25): Show |
intron_variant | MODIFIER | HG02895.hp1 HG02897.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0186a0001c0001t0005g0187 | 2 | 207 | 0.0097 | 32 | c.207 others(51): 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(25): Show |
intron_variant | MODIFIER | HG02257.hp2 NA19085.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0004 | a0001c0001t0002g0060a0001c0002t0004g0036 | 2 | 207 | 0.0097 | 32 | c.232 others(51): Show |
GRIA3 | ENSG00000125675.20 | transcript | ENST00000620443.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
GRIA4_chr11_105605073_105987090 | 105911775 | A | AATACATA others(25): Show |
intron_variant | MODIFIER | HG01346.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0107 | 1 | 184 | 0.0054 | 32 | c.126 others(51): Show |
GRIA4 | ENSG00000152578.15 | transcript | ENST00000282499.10 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GRIA4_chr11_105605073_105987090 | 105911775 | A | AATATATA others(25): Show |
intron_variant | MODIFIER | HG01071.hp1 HG01109.hp1 HG02922.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(3): Show | a0001c0001t0002g0048a0001c0001t0002g0148a0001c0001t0005g0065others(4): Show | 7 | 184 | 0.0380 | 32 | c.126 others(51): Show |
GRIA4 | ENSG00000152578.15 | transcript | ENST00000282499.10 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GRID1_chr10_85594552_86371795 | 85737673 | T | TATATATA others(25): Show |
intron_variant | MODIFIER | HG00639.hp2 HG02622.hp2 HG02922.hp1 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0005a0001c0004t0015 | a0001c0002t0005g0090a0001c0002t0005g0092a0001c0004t0015g0094 | 3 | 96 | 0.0313 | 32 | c.123 others(51): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 8/15 | chr10 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 92411655 | G | GTGTGTGT others(25): Show |
intron_variant | MODIFIER | HG02922.hp2 NA19030.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0034a0002c0003t0001g0033 | 2 | 34 | 0.0588 | 32 | c.88+ others(51): 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(25): Show |
intron_variant | MODIFIER | HG02922.hp1 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010a0001c0001t0001g0027 | 2 | 34 | 0.0588 | 32 | c.89- others(51): 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(25): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0030 | 1 | 34 | 0.0294 | 32 | 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 | 93078779 | G | GTATATAC others(25): Show |
intron_variant | MODIFIER | HG01192.hp2 HG01496.hp1 HG01496.hp2 others(13): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(2): Show | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(13): Show | 16 | 34 | 0.4706 | 32 | c.245 others(49): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRID2_chr4_92298966_93779566 | 93264709 | G | GATATATA others(25): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0004 | a0001c0004t0007 | a0001c0004t0007g0028 | 1 | 34 | 0.0294 | 32 | c.124 others(53): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRID2_chr4_92298966_93779566 | 93697869 | G | GTATATAT others(25): Show |
intron_variant | MODIFIER | NA18942.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0002 | 1 | 34 | 0.0294 | 32 | c.236 others(53): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRIK1_chr21_29531933_29944996 | 29559669 | G | GGGTCTAT others(25): Show |
intron_variant | MODIFIER | HG00738.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0143 | 1 | 162 | 0.0062 | 32 | c.235 others(51): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 15/17 | chr21 | TogoVar |