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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
GPR137B_chr1_236137539_236213907 | 236169172 | C | CTGCAGGT others(35): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0141 | 1 | 386 | 0.0026 | 42 | c.464 others(57): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
GPR146_chr7_1039546_1064261 | 1044867 | G | GGGGGCGG others(35): Show |
intron_variant | MODIFIER | HG03490.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0235 | 1 | 434 | 0.0023 | 42 | c.-25 others(57): Show |
GPR146 | ENSG00000164849.10 | transcript | ENST00000444847.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
GPR157_chr1_9095305_9134102 | 9123552 | A | AATATATA others(35): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(82): Show |
a0001a0005a0007others(1): Show | a0001c0001a0001c0010a0001c0011others(5): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(28): Show | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0005g0007others(80): Show | 85 | 404 | 0.2104 | 42 | c.383 others(59): Show |
GPR157 | ENSG00000180758.12 | transcript | ENST00000377411.5 | protein_coding | 1/3 | chr1 | TogoVar | ||||||
GPR157_chr1_9095305_9134102 | 9123565 | A | ATATATCT others(35): Show |
intron_variant | MODIFIER | HG02109.hp1 | a0003 | a0003c0007 | a0003c0007t0014 | a0003c0007t0014g0323 | 1 | 404 | 0.0025 | 42 | c.383 others(59): Show |
GPR157 | ENSG00000180758.12 | transcript | ENST00000377411.5 | protein_coding | 1/3 | chr1 | TogoVar | ||||||
GPR158_chr10_25170001_25607229 | 25241372 | C | CTCTTCTC others(35): Show |
intron_variant | MODIFIER | HG02132.hp1 | a0004 | a0004c0004 | a0004c0004t0003 | a0004c0004t0003g0121 | 1 | 162 | 0.0062 | 42 | c.100 others(63): Show |
GPR158 | ENSG00000151025.11 | transcript | ENST00000376351.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
GPR161_chr1_168074542_168141930 | 168119229 | T | TATATATA others(35): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0176 | 1 | 340 | 0.0029 | 42 | c.-44 others(61): Show |
GPR161 | ENSG00000143147.15 | transcript | ENST00000682931.1 | protein_coding | 1/5 | chr1 | TogoVar | ||||||
GPR22_chr7_107465057_107480684 | 107476183 | T | TAAAAAAA others(35): Show |
downstream_gene_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 412 | 0.0024 | 42 | c.*82 others(51): Show |
GPR22 | ENSG00000172209.6 | transcript | ENST00000304402.6 | protein_coding | 500 | chr7 | TogoVar | ||||||
GPR26_chr10_123661355_123702399 | 123675833 | C | CGTGTGTG others(35): Show |
intron_variant | MODIFIER | HG02080.hp2 NA19063.hp1 |
a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0081a0001c0002t0003g0154 | 2 | 412 | 0.0049 | 42 | c.782 others(57): Show |
GPR26 | ENSG00000154478.4 | transcript | ENST00000284674.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
GPR42_chr19_35366068_35377962 | 35375461 | G | GGAAAGAA others(35): Show |
downstream_gene_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG01192.hp2 others(22): Show |
a0001a0007a0008others(1): Show | a0001c0001a0007c0008a0008c0027others(1): Show | a0001c0001t0001a0001c0001t0010a0007c0008t0001others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0010g0003others(3): Show | 25 | 399 | 0.0627 | 42 | c.*30 others(53): Show |
GPR42 | ENSG00000126251.7 | transcript | ENST00000454971.3 | protein_coding | 2500 | chr19 | TogoVar | ||||||
GPR42_chr19_35366068_35377962 | 35375461 | G | GGAAAGAA others(35): Show |
downstream_gene_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 399 | 0.0025 | 42 | c.*30 others(53): Show |
GPR42 | ENSG00000126251.7 | transcript | ENST00000454971.3 | protein_coding | 2500 | chr19 | TogoVar | ||||||
GPRC5A_chr12_12886562_12922937 | 12914594 | T | TTCTTTCT others(35): Show |
3_prime_UTR_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0002 | a0001c0002t0231 | a0001c0002t0231g0372 | 1 | 396 | 0.0025 | 42 | c.*20 others(53): Show |
GPRC5A | ENSG00000013588.10 | transcript | ENST00000014914.6 | protein_coding | 4/4 | 2059 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||
GPRC5A_chr12_12886562_12922937 | 12914594 | T | TTCTTTCT others(35): Show |
3_prime_UTR_variant | MODIFIER | HG01109.hp2 | a0001 | a0001c0002 | a0001c0002t0234 | a0001c0002t0234g0348 | 1 | 396 | 0.0025 | 42 | c.*20 others(53): Show |
GPRC5A | ENSG00000013588.10 | transcript | ENST00000014914.6 | protein_coding | 4/4 | 2059 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||
GPRC5D_chr12_12935575_12957170 | 12956446 | T | TTTCCTTC others(35): Show |
upstream_gene_variant | MODIFIER | HG00140.hp2 HG01257.hp1 HG01261.hp2 others(4): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0082a0001c0002t0001g0087a0001c0002t0001g0088others(4): Show | 7 | 406 | 0.0172 | 42 | c.-43 others(53): Show |
GPRC5D | ENSG00000111291.9 | transcript | ENST00000228887.6 | protein_coding | 4277 | chr12 | TogoVar | ||||||
GPRC5D_chr12_12935575_12957170 | 12956446 | T | TTTCCTTC others(35): Show |
upstream_gene_variant | MODIFIER | HG01106.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0010a0001c0001t0001g0174a0001c0001t0001g0181others(2): Show | 6 | 406 | 0.0148 | 42 | c.-43 others(53): Show |
GPRC5D | ENSG00000111291.9 | transcript | ENST00000228887.6 | protein_coding | 4277 | chr12 | TogoVar | ||||||
GPSM1_chr9_136322539_136364601 | 136355043 | G | GAGGGGTA others(35): Show |
intron_variant | MODIFIER | HG02083.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0309 | 1 | 400 | 0.0025 | 42 | c.145 others(59): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
GPSM1_chr9_136322539_136364601 | 136355126 | T | TAGGGGTA others(35): Show |
intron_variant | MODIFIER | HG02015.hp2 HG02257.hp1 HG03017.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0002c0002t0002 | a0001c0001t0004g0071a0001c0001t0004g0072a0001c0001t0004g0239others(3): Show | 6 | 400 | 0.0150 | 42 | c.145 others(59): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
GPSM2_chr1_108871985_108939545 | 108908728 | A | AACACACA others(35): Show |
intron_variant | MODIFIER | HG03130.hp2 NA18906.hp1 |
a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0236a0003c0003t0003g0245 | 2 | 260 | 0.0077 | 42 | c.119 others(61): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
GPT_chr8_144499140_144512172 | 144505490 | G | GTGCGTTC others(35): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0004 | a0004c0011 | a0004c0011t0005 | a0004c0011t0005g0027 | 1 | 386 | 0.0026 | 42 | c.739 others(55): Show |
GPT | ENSG00000167701.14 | transcript | ENST00000394955.3 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
GPT_chr8_144499140_144512172 | 144505532 | T | TTGCGTTC others(35): Show |
intron_variant | MODIFIER | NA19079.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0016 | 1 | 386 | 0.0026 | 42 | c.739 others(57): Show |
GPT | ENSG00000167701.14 | transcript | ENST00000394955.3 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
GPT_chr8_144499140_144512172 | 144505646 | C | CCCGCGCC others(35): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0004 | a0004c0011 | a0004c0011t0005 | a0004c0011t0005g0027 | 1 | 386 | 0.0026 | 42 | c.740 others(57): Show |
GPT | ENSG00000167701.14 | transcript | ENST00000394955.3 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
GRAMD1B_chr11_123425269_123632767 | 123513644 | T | TTCTTTCT others(35): Show |
intron_variant | MODIFIER | HG01106.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 | 1 | 282 | 0.0036 | 42 | c.452 others(61): 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(35): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0001 | a0001c0001t0020 | a0001c0001t0020g0003 | 1 | 282 | 0.0036 | 42 | c.685 others(59): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GRAMD1B_chr11_123425269_123632767 | 123621913 | T | TTTTCTTC others(35): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0003a0001c0004others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(167): Show | 170 | 282 | 0.6028 | 42 | c.254 others(59): Show |
GRAMD1B | ENSG00000023171.20 | transcript | ENST00000635736.2 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GREB1_chr2_11529045_11647788 | 11539022 | T | TCTTCTCT others(35): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0019 | a0019c0036 | a0019c0036t0001 | a0019c0036t0001g0299 | 1 | 308 | 0.0033 | 42 | c.-16 others(61): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GRHL1_chr2_9946693_10007277 | 9998461 | T | TATATATA others(35): Show |
intron_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0144 | 1 | 418 | 0.0024 | 42 | c.167 others(59): Show |
GRHL1 | ENSG00000134317.18 | transcript | ENST00000324907.14 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GRHL1_chr2_9946693_10007277 | 9998577 | C | CATATATA others(35): Show |
intron_variant | MODIFIER | NA18986.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0123 | 1 | 418 | 0.0024 | 42 | c.167 others(59): Show |
GRHL1 | ENSG00000134317.18 | transcript | ENST00000324907.14 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GRHL1_chr2_9946693_10007277 | 9998612 | A | ATATATAT others(35): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0277 | 1 | 418 | 0.0024 | 42 | c.167 others(59): Show |
GRHL1 | ENSG00000134317.18 | transcript | ENST00000324907.14 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GRIA1_chr5_153485670_153818869 | 153566304 | C | CTTTTTTT others(35): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0150 | 1 | 194 | 0.0052 | 42 | c.220 others(61): Show |
GRIA1 | ENSG00000155511.19 | transcript | ENST00000285900.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
GRIA2_chr4_157215728_157371075 | 157256238 | A | ATATTACA others(35): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(56): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(54): Show | 59 | 216 | 0.2732 | 42 | c.229 others(61): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRIA2_chr4_157215728_157371075 | 157356079 | T | TTATTTAT others(35): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0002others(3): Show | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(65): Show | 69 | 216 | 0.3194 | 42 | c.204 others(61): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRIA3_chrX_123179278_123495915 | 123471990 | C | CATATATA others(35): Show |
intron_variant | MODIFIER | HG01070.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0173 | 1 | 207 | 0.0048 | 42 | c.232 others(61): 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(35): Show |
intron_variant | MODIFIER | HG01257.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0020 | 1 | 184 | 0.0054 | 42 | c.126 others(61): Show |
GRIA4 | ENSG00000152578.15 | transcript | ENST00000282499.10 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
GRID1_chr10_85594552_86371795 | 85865916 | T | TATATATA others(35): Show |
intron_variant | MODIFIER | NA18981.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0032 | 1 | 96 | 0.0104 | 42 | c.951 others(59): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 6/15 | chr10 | TogoVar | ||||||
GRID1_chr10_85594552_86371795 | 86250557 | C | CTGGGGGG others(35): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0052 | 1 | 96 | 0.0104 | 42 | c.236 others(61): Show |
GRID1 | ENSG00000182771.19 | transcript | ENST00000327946.12 | protein_coding | 2/15 | chr10 | TogoVar | ||||||
GRID2_chr4_92298966_93779566 | 92460032 | C | CTATATAT others(35): Show |
intron_variant | MODIFIER | HG01978.hp1 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | 34 | 0.0588 | 42 | c.89- others(61): 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(35): Show |
intron_variant | MODIFIER | HG02922.hp2 HG03225.hp2 |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0012a0002c0003t0001g0033 | 2 | 34 | 0.0588 | 42 | c.134 others(61): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRID2_chr4_92298966_93779566 | 93448886 | T | TCCCCTTC others(35): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019 | 1 | 34 | 0.0294 | 42 | c.154 others(61): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRID2_chr4_92298966_93779566 | 93697869 | G | GTATATAT others(35): Show |
intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0031 | 1 | 34 | 0.0294 | 42 | c.236 others(63): Show |
GRID2 | ENSG00000152208.13 | transcript | ENST00000282020.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRIK1_chr21_29531933_29944996 | 29888197 | C | CTTTCTTT others(35): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0137 | 1 | 162 | 0.0062 | 42 | c.118 others(61): Show |
GRIK1 | ENSG00000171189.18 | transcript | ENST00000327783.9 | protein_coding | 1/17 | chr21 | TogoVar | ||||||
GRIN2B_chr12_13532337_13986602 | 13605551 | T | TCTCTCTC others(35): Show |
intron_variant | MODIFIER | HG01099.hp2 | a0001 | a0001c0002 | a0001c0002t0032 | a0001c0002t0032g0131 | 1 | 194 | 0.0052 | 42 | c.201 others(61): Show |
GRIN2B | ENSG00000273079.7 | transcript | ENST00000609686.4 | protein_coding | 10/13 | chr12 | TogoVar | ||||||
GRIN2B_chr12_13532337_13986602 | 13954811 | G | GAAAAAAA others(35): Show |
intron_variant | MODIFIER | NA19091.hp2 | a0001 | a0001c0003 | a0001c0003t0010 | a0001c0003t0010g0085 | 1 | 194 | 0.0052 | 42 | c.-19 others(61): Show |
GRIN2B | ENSG00000273079.7 | transcript | ENST00000609686.4 | protein_coding | 2/13 | chr12 | TogoVar | ||||||
GRK4_chr4_2958571_3045760 | 3001089 | A | ATATATAT others(35): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0008 | a0008c0008 | a0008c0008t0004 | a0008c0008t0004g0010 | 1 | 268 | 0.0037 | 42 | c.340 others(59): Show |
GRK4 | ENSG00000125388.20 | transcript | ENST00000398052.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
GRK5_chr10_119202571_119464745 | 119313146 | G | GTGATGGT others(35): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0002 | a0002c0003 | a0002c0003t0012 | a0002c0003t0012g0184 | 1 | 202 | 0.0050 | 42 | c.53- others(59): Show |
GRK5 | ENSG00000198873.12 | transcript | ENST00000392870.3 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
GRK5_chr10_119202571_119464745 | 119394632 | T | TCGGTGTG others(35): Show |
intron_variant | MODIFIER | NA18944.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0088 | 1 | 202 | 0.0050 | 42 | c.262 others(59): Show |
GRK5 | ENSG00000198873.12 | transcript | ENST00000392870.3 | protein_coding | 3/15 | chr10 | TogoVar | ||||||
GRM1_chr6_146024062_146442601 | 146043796 | T | TATATATA others(35): Show |
intron_variant | MODIFIER | NA18991.hp2 | a0006 | a0006c0013 | a0006c0013t0004 | a0006c0013t0004g0142 | 1 | 158 | 0.0063 | 42 | c.700 others(61): Show |
GRM1 | ENSG00000152822.15 | transcript | ENST00000282753.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
GRM3_chr7_86638909_86869879 | 86698520 | T | TTATATAT others(35): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0089 | 1 | 216 | 0.0046 | 42 | c.-14 others(63): Show |
GRM3 | ENSG00000198822.11 | transcript | ENST00000361669.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
GRM5_chr11_88499642_89070982 | 88919238 | C | CTATATAT others(35): Show |
intron_variant | MODIFIER | HG02148.hp1 HG02976.hp1 NA19079.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0038a0001c0001t0001g0055a0001c0001t0002g0026 | 3 | 184 | 0.0163 | 42 | c.662 others(61): Show |
GRM5 | ENSG00000168959.15 | transcript | ENST00000305447.5 | protein_coding | 2/9 | chr11 | TogoVar | ||||||
GRM7_chr3_6856115_7746533 | 7064469 | T | TATATATA others(35): Show |
intron_variant | MODIFIER | HG02897.hp2 HG06807.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0005a0001c0002t0006 | a0001c0001t0005g0072a0001c0002t0006g0014 | 2 | 80 | 0.0250 | 42 | c.520 others(61): Show |
GRM7 | ENSG00000196277.17 | transcript | ENST00000357716.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
GRM7_chr3_6856115_7746533 | 7064479 | T | TATATATA others(35): Show |
intron_variant | MODIFIER | HG03710.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0032 | 1 | 80 | 0.0125 | 42 | c.520 others(61): Show |
GRM7 | ENSG00000196277.17 | transcript | ENST00000357716.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
GRM8_chr7_126433598_127257941 | 126788420 | A | AAAAAAAA others(35): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0078 | 1 | 108 | 0.0093 | 42 | c.115 others(63): Show |
GRM8 | ENSG00000179603.19 | transcript | ENST00000339582.7 | protein_coding | 6/10 | chr7 | TogoVar |