Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2566 |
| ensemblid | ENSG00000113327.17 |
| hgncid | 4087 |
| symbol | GABRG2 |
| name | gamma-aminobutyric acid type A receptor subunit gamma2 |
| refseq_nuc | NM_198904.4 |
| refseq_prot | NP_944494.1 |
| ensembl_nuc | ENST00000639213.2 |
| ensembl_prot | ENSP00000491909.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 162067773 |
| end | 162155526 |
| strand | + |
| ver | v1.2 |
| region | chr5:162067773-162155526 |
| region5000 | chr5:162062773-162160526 |
| regionname0 | GABRG2_chr5_162067773_162155526 |
| regionname5000 | GABRG2_chr5_162062773_162160526 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 475 | 327 | 84 | 42 | 153 | 12 | 34 | 117 | GABRG2_chr5_162062773_162160526 | GABRG2 | MSSPN others(470): Show |
chr5 | 162062773 | 162160526 |
| a0002 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | MSSPN others(470): Show |
chr5 | 162062773 | 162160526 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1425 | 145 | 34 | 12 | 88 | 5 | 6 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0002 | 1/1 | 1425 | 109 | 38 | 19 | 27 | 5 | 18 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0003 | 0/0 | 1425 | 52 | 0 | 5 | 37 | 2 | 8 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0004 | 0/0 | 1425 | 10 | 8 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0005 | 0/0 | 1425 | 3 | 2 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0006 | 0/0 | 1425 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0008 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0009 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0010 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0011 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0012 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0001c0013 | 0/0 | 1425 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 | ||
| a0002c0007 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | ATGAG others(1420): Show |
chr5 | 162062773 | 162160526 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3813 | 14 | 4 | 2 | 6 | 1 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0001t0002 | 0/0 | 3811 | 78 | 11 | 7 | 53 | 3 | 4 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3806): Show |
chr5 | 162062773 | 162160526 |
| a0001c0001t0003 | 0/0 | 3813 | 27 | 2 | 2 | 22 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0001t0004 | 0/0 | 3813 | 14 | 13 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0001t0008 | 0/0 | 3811 | 3 | 0 | 0 | 3 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3806): Show |
chr5 | 162062773 | 162160526 |
| a0001c0001t0009 | 0/0 | 3811 | 3 | 0 | 0 | 3 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3806): Show |
chr5 | 162062773 | 162160526 |
| a0001c0001t0010 | 0/0 | 3813 | 3 | 3 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0001t0013 | 0/0 | 3811 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3806): Show |
chr5 | 162062773 | 162160526 |
| a0001c0001t0016 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0001t0018 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0002t0001 | 1/0 | 3813 | 67 | 20 | 17 | 14 | 3 | 12 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0002t0002 | 0/0 | 3811 | 9 | 3 | 0 | 4 | 0 | 2 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3806): Show |
chr5 | 162062773 | 162160526 |
| a0001c0002t0003 | 0/0 | 3813 | 8 | 0 | 0 | 4 | 1 | 3 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0002t0004 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0002t0005 | 0/0 | 3813 | 6 | 5 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0002t0006 | 0/0 | 3813 | 6 | 6 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0002t0007 | 0/1 | 3813 | 6 | 0 | 1 | 3 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0002t0011 | 0/0 | 3813 | 3 | 1 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0002t0013 | 0/0 | 3811 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3806): Show |
chr5 | 162062773 | 162160526 |
| a0001c0002t0014 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0003t0001 | 0/0 | 3813 | 30 | 0 | 2 | 21 | 2 | 5 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0003t0002 | 0/0 | 3811 | 6 | 0 | 0 | 6 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3806): Show |
chr5 | 162062773 | 162160526 |
| a0001c0003t0003 | 0/0 | 3813 | 16 | 0 | 3 | 10 | 0 | 3 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0004t0002 | 0/0 | 3811 | 5 | 4 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3806): Show |
chr5 | 162062773 | 162160526 |
| a0001c0004t0005 | 0/0 | 3813 | 4 | 3 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0004t0017 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0005t0003 | 0/0 | 3813 | 2 | 1 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0005t0015 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0006t0012 | 0/0 | 3813 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0008t0001 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0009t0004 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0010t0003 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0011t0003 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0012t0003 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3808): Show |
chr5 | 162062773 | 162160526 |
| a0001c0013t0002 | 0/0 | 3811 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3806): Show |
chr5 | 162062773 | 162160526 |
| a0002c0007t0002 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | GCCAG others(3806): Show |
chr5 | 162062773 | 162160526 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0009g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0010g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0013g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0016g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0001t0018g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0005g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0006g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0007g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0007g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0011g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0011g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0013g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0014g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0002t0014g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0004t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0004t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0004t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0004t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0004t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0004t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0004t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0004t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0004t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0004t0017g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0005t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0005t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0005t0015g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0006t0012g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0008t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0009t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0010t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0011t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0012t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0001c0013t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| a0002c0007t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0178 | EUR | GBR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | GBR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0122 | EUR | GBR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0278 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00639 | hp2 | a0001 | c0004 | t0005 | g0230 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | CHS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01069 | hp1 | a0001 | c0006 | t0012 | g0008 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01071 | hp1 | a0001 | c0006 | t0012 | g0008 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0293 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01243 | hp1 | a0001 | c0004 | t0002 | g0232 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01243 | hp2 | a0001 | c0005 | t0003 | g0033 | AMR | PUR | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0019 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01433 | hp1 | a0001 | c0002 | t0007 | g0079 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0263 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01515 | hp2 | a0001 | c0002 | t0007 | g0086 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0020 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0201 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0020 | EUR | IBS | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01884 | hp1 | a0001 | c0005 | t0003 | g0080 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01884 | hp2 | a0001 | c0002 | t0006 | g0150 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0019 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01952 | hp1 | a0001 | c0013 | t0002 | g0267 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG01981 | hp2 | a0001 | c0002 | t0005 | g0014 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0266 | AMR | PEL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02027 | hp2 | a0001 | c0001 | t0016 | g0120 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02055 | hp1 | a0001 | c0002 | t0005 | g0217 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0265 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0288 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0106 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | KHV | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02145 | hp1 | a0001 | c0002 | t0006 | g0002 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CDX | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | CDX | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | CDX | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02258 | hp1 | a0001 | c0004 | t0002 | g0234 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0303 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02572 | hp2 | a0001 | c0002 | t0014 | g0081 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02647 | hp2 | a0001 | c0004 | t0017 | g0240 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0216 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0268 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02698 | hp2 | a0001 | c0011 | t0003 | g0277 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02735 | hp1 | a0001 | c0010 | t0003 | g0142 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0183 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0204 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0179 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0245 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02818 | hp2 | a0001 | c0004 | t0002 | g0023 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02897 | hp2 | a0001 | c0004 | t0005 | g0231 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0215 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02965 | hp1 | a0001 | c0004 | t0002 | g0235 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0301 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03139 | hp1 | a0001 | c0002 | t0006 | g0149 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03209 | hp1 | a0001 | c0004 | t0005 | g0228 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0249 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03225 | hp2 | a0001 | c0005 | t0015 | g0237 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03453 | hp1 | a0001 | c0002 | t0006 | g0002 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0010 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0010 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0264 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03516 | hp1 | a0001 | c0002 | t0011 | g0090 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03654 | hp1 | a0001 | c0002 | t0013 | g0134 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03669 | hp2 | a0001 | c0003 | t0003 | g0297 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0210 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0273 | SAS | PJL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0131 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0276 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG04184 | hp1 | a0001 | c0003 | t0003 | g0259 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0140 | SAS | BEB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0275 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0024 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | STU | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18522 | hp1 | a0001 | c0008 | t0001 | g0241 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18612 | hp1 | a0001 | c0001 | t0009 | g0211 | EAS | CHB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | CHB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | CHB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18906 | hp1 | a0001 | c0002 | t0006 | g0002 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18943 | hp1 | a0001 | c0003 | t0003 | g0289 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18945 | hp2 | a0001 | c0003 | t0003 | g0112 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18954 | hp1 | a0001 | c0012 | t0003 | g0258 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18954 | hp2 | a0001 | c0001 | t0008 | g0067 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0272 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18959 | hp2 | a0001 | c0002 | t0007 | g0089 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18960 | hp2 | a0001 | c0001 | t0009 | g0196 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18963 | hp2 | a0001 | c0003 | t0003 | g0271 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0292 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18968 | hp2 | a0001 | c0003 | t0003 | g0290 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18969 | hp1 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0291 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0285 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18980 | hp2 | a0001 | c0001 | t0008 | g0073 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0295 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18987 | hp2 | a0001 | c0003 | t0003 | g0270 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18994 | hp1 | a0001 | c0002 | t0007 | g0083 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18994 | hp2 | a0001 | c0003 | t0003 | g0262 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0145 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0279 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18999 | hp1 | a0002 | c0007 | t0002 | g0041 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0287 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0283 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19006 | hp2 | a0001 | c0003 | t0002 | g0260 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19011 | hp2 | a0001 | c0003 | t0003 | g0256 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0280 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0253 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19043 | hp2 | a0001 | c0004 | t0005 | g0229 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19056 | hp1 | a0001 | c0002 | t0011 | g0084 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0300 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19059 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19060 | hp2 | a0001 | c0003 | t0003 | g0257 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0296 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19066 | hp2 | a0001 | c0003 | t0002 | g0274 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19067 | hp1 | a0001 | c0003 | t0002 | g0261 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19067 | hp2 | a0001 | c0002 | t0011 | g0082 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0197 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0281 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19074 | hp2 | a0001 | c0002 | t0007 | g0088 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19076 | hp2 | a0001 | c0003 | t0003 | g0294 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0299 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0097 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0282 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0298 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19088 | hp1 | a0001 | c0003 | t0003 | g0269 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19091 | hp1 | a0001 | c0003 | t0002 | g0286 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA19240 | hp2 | a0001 | c0002 | t0014 | g0085 | AFR | YRI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | ASW | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | ASW | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA20752 | hp1 | a0001 | c0001 | t0013 | g0194 | EUR | TSI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0039 | EUR | TSI | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02109 | hp2 | a0001 | c0002 | t0005 | g0014 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02559 | hp1 | a0001 | c0002 | t0005 | g0218 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0233 | AFR | ACB | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG03471 | hp2 | a0001 | c0009 | t0004 | g0148 | AFR | MSL | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG06807 | hp1 | a0001 | c0002 | t0006 | g0243 | AFR | USA | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | USA | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA20300 | hp1 | a0001 | c0001 | t0018 | g0091 | AFR | USA | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | USA | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0254 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| NA21309 | hp2 | a0001 | c0002 | t0005 | g0214 | AFR | LWK | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0007 | g0087 | REF | REF | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0172 | REF | REF | GABRG2_chr5_162062773_162160526 | GABRG2 | chr5 | 162062773 | 162160526 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:162068051 | G | C | 1 | a0002 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.52G>C | p.Val18Leu | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/10 | 279/3813 | 52/1428 | 18/475 | chr5 | 162068051 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:162095550 | C | T | 4 | a0001c0003 a0001c0011 a0001c0012 others(1): Show |
55 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(52): Show |
synonymous_variant | LOW | c.315C>T | p.Asn105Asn | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/10 | 542/3813 | 315/1428 | 105/475 | chr5 | 162095550 | |||
| chr5:162097664 | G | A | 1 | a0001c0004 | 10 | HG00639.hp2 HG01243.hp1 HG02258.hp1 others(7): Show |
synonymous_variant | LOW | c.354G>A | p.Ala118Ala | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/10 | 581/3813 | 354/1428 | 118/475 | chr5 | 162097664 | |||
| chr5:162097670 | G | A | 2 | a0001c0006 a0001c0008 |
3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.360G>A | p.Thr120Thr | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/10 | 587/3813 | 360/1428 | 120/475 | chr5 | 162097670 | |||
| chr5:162101274 | C | T | 5 | a0001c0001 a0001c0005 a0001c0006 others(2): Show |
152 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(149): Show |
synonymous_variant | LOW | c.588C>T | p.Asn196Asn | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/10 | 815/3813 | 588/1428 | 196/475 | chr5 | 162101274 | |||
| chr5:162103974 | A | G | 1 | a0001c0005 | 3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.717A>G | p.Gln239Gln | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/10 | 944/3813 | 717/1428 | 239/475 | chr5 | 162103974 | |||
| chr5:162104025 | C | T | 1 | a0001c0010 | 1 | HG02735.hp1 | splice_region_variant&synonymous_variant | LOW | c.768C>T | p.Ser256Ser | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/10 | 995/3813 | 768/1428 | 256/475 | chr5 | 162104025 | |||
| chr5:162142192 | T | C | 1 | a0001c0009 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.798T>C | p.Phe266Phe | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/10 | 1025/3813 | 798/1428 | 266/475 | chr5 | 162142192 | |||
| chr5:162142234 | T | C | 1 | a0001c0011 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.840T>C | p.Tyr280Tyr | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/10 | 1067/3813 | 840/1428 | 280/475 | chr5 | 162142234 | |||
| chr5:162153194 | C | T | 1 | a0001c0012 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.1254C>T | p.Asp418Asp | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1481/3813 | 1254/1428 | 418/475 | chr5 | 162153194 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:162067846 | C | T | 4 | a0001c0001t0018 a0001c0002t0007 a0001c0002t0011 others(1): Show |
11 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-154C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/10 | 154 | chr5 | 162067846 | ||||||
| chr5:162153629 | G | A | 1 | a0001c0001t0008 | 3 | NA18954.hp2 NA18969.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*261G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 261 | chr5 | 162153629 | ||||||
| chr5:162153711 | A | G | 2 | a0001c0001t0013 a0001c0002t0013 |
2 | HG03654.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*343A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 343 | chr5 | 162153711 | ||||||
| chr5:162153753 | G | A | 1 | a0001c0006t0012 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 385 | chr5 | 162153753 | ||||||
| chr5:162153977 | C | T | 16 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(13): Show |
129 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*609C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 609 | chr5 | 162153977 | ||||||
| chr5:162154029 | T | A | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(23): Show |
190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*661T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 661 | chr5 | 162154029 | ||||||
| chr5:162154162 | A | G | 1 | a0001c0001t0010 | 3 | HG03471.hp1 NA19030.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*794A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 794 | chr5 | 162154162 | ||||||
| chr5:162154865 | C | T | 3 | a0001c0002t0005 a0001c0002t0014 a0001c0004t0005 |
12 | HG00639.hp2 HG01981.hp2 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1497C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1497 | chr5 | 162154865 | ||||||
| chr5:162154918 | A | G | 1 | a0001c0001t0016 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1550A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1550 | chr5 | 162154918 | ||||||
| chr5:162154925 | A | C | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1557A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1557 | chr5 | 162154925 | ||||||
| chr5:162154928 | C | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1560C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1560 | chr5 | 162154928 | ||||||
| chr5:162154929 | A | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1561A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1561 | chr5 | 162154929 | ||||||
| chr5:162154930 | T | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1562T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1562 | chr5 | 162154930 | ||||||
| chr5:162154933 | T | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1565T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1565 | chr5 | 162154933 | ||||||
| chr5:162154934 | G | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1566G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1566 | chr5 | 162154934 | ||||||
| chr5:162154935 | A | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1567A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1567 | chr5 | 162154935 | ||||||
| chr5:162154937 | T | C | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1569T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1569 | chr5 | 162154937 | ||||||
| chr5:162154940 | A | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1572A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1572 | chr5 | 162154940 | ||||||
| chr5:162154941 | G | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1573G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1573 | chr5 | 162154941 | ||||||
| chr5:162154945 | T | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1577T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1577 | chr5 | 162154945 | ||||||
| chr5:162154948 | C | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1580C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1580 | chr5 | 162154948 | ||||||
| chr5:162154949 | T | C | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1581T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1581 | chr5 | 162154949 | ||||||
| chr5:162154953 | T | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1585T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1585 | chr5 | 162154953 | ||||||
| chr5:162154954 | G | C | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1586G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1586 | chr5 | 162154954 | ||||||
| chr5:162154956 | A | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1588A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1588 | chr5 | 162154956 | ||||||
| chr5:162154957 | C | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1589C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1589 | chr5 | 162154957 | ||||||
| chr5:162154960 | A | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1592A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1592 | chr5 | 162154960 | ||||||
| chr5:162154966 | A | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1598A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1598 | chr5 | 162154966 | ||||||
| chr5:162154967 | A | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1599A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1599 | chr5 | 162154967 | ||||||
| chr5:162154968 | T | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1600T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1600 | chr5 | 162154968 | ||||||
| chr5:162154969 | C | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1601C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1601 | chr5 | 162154969 | ||||||
| chr5:162154975 | T | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1607T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1607 | chr5 | 162154975 | ||||||
| chr5:162154981 | A | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1613A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1613 | chr5 | 162154981 | ||||||
| chr5:162154987 | G | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1619G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1619 | chr5 | 162154987 | ||||||
| chr5:162154988 | C | T | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1620C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1620 | chr5 | 162154988 | ||||||
| chr5:162155068 | A | G | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1700A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1700 | chr5 | 162155068 | ||||||
| chr5:162155129 | C | A | 1 | a0001c0005t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1761C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1761 | chr5 | 162155129 | ||||||
| chr5:162155336 | T | G | 1 | a0001c0004t0017 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1968T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1968 | chr5 | 162155336 | ||||||
| chr5:162155342 | G | A | 1 | a0001c0002t0006 | 6 | HG01884.hp2 HG02145.hp1 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1974G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 1974 | chr5 | 162155342 | ||||||
| chr5:162155463 | C | G | 1 | a0001c0001t0009 | 3 | NA18612.hp1 NA18960.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2095C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 2095 | chr5 | 162155463 | ||||||
| chr5:162155487 | CAT | C | 10 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(7): Show |
108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2120_*2121delAT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 10/10 | 2120 | chr5 | 162155487 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:162068198 | A | G | 1 | a0001c0001t0002g0304 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.107+92A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068198 | |||||||
| chr5:162068217 | G | A | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+111G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068217 | |||||||
| chr5:162068296 | A | G | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107+190A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068296 | |||||||
| chr5:162068329 | T | G | 5 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(2): Show |
5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+223T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068329 | |||||||
| chr5:162068410 | G | T | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+304G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068410 | |||||||
| chr5:162068665 | T | G | 1 | a0001c0003t0001g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.107+559T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068665 | |||||||
| chr5:162068754 | T | C | 1 | a0001c0002t0001g0025 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+648T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068754 | |||||||
| chr5:162068846 | C | T | 50 | a0001c0003t0001g0017 a0001c0003t0001g0018 a0001c0003t0001g0019 others(47): Show |
54 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(51): Show |
intron_variant | MODIFIER | c.107+740C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068846 | |||||||
| chr5:162068949 | G | A | 7 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0029 others(4): Show |
7 | HG00597.hp1 HG01261.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+843G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162068949 | |||||||
| chr5:162069264 | C | G | 1 | a0001c0001t0004g0255 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.107+1158C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069264 | |||||||
| chr5:162069387 | C | T | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+1281C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069387 | |||||||
| chr5:162069663 | T | G | 1 | a0001c0005t0003g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107+1557T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069663 | |||||||
| chr5:162069665 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.107+1559T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069665 | |||||||
| chr5:162069830 | T | C | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.107+1724T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069830 | |||||||
| chr5:162069840 | C | T | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+1734C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069840 | |||||||
| chr5:162069926 | C | G | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+1820C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162069926 | |||||||
| chr5:162070012 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.107+1906T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070012 | |||||||
| chr5:162070044 | T | C | 49 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(46): Show |
54 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.107+1938T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070044 | |||||||
| chr5:162070289 | A | G | 50 | a0001c0003t0001g0017 a0001c0003t0001g0018 a0001c0003t0001g0019 others(47): Show |
54 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(51): Show |
intron_variant | MODIFIER | c.107+2183A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070289 | |||||||
| chr5:162070367 | G | A | 1 | a0001c0002t0007g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.107+2261G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070367 | |||||||
| chr5:162070538 | TA | T | 11 | a0001c0001t0004g0244 a0001c0001t0004g0245 a0001c0001t0004g0246 others(8): Show |
13 | HG01258.hp1 HG01516.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.107+2442delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162070538 | ||||||
| chr5:162070744 | G | C | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+2638G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070744 | |||||||
| chr5:162070828 | T | A | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+2722T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162070828 | |||||||
| chr5:162071011 | C | CAAT | 193 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(190): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.107+2906_107+2908d others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162071011 | ||||||
| chr5:162071075 | A | G | 1 | a0001c0002t0001g0147 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.107+2969A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071075 | |||||||
| chr5:162071092 | A | G | 2 | a0001c0004t0017g0240 a0001c0008t0001g0241 |
2 | HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+2986A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071092 | |||||||
| chr5:162071291 | A | G | 1 | a0001c0002t0001g0146 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.107+3185A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071291 | |||||||
| chr5:162071539 | T | C | 52 | a0001c0003t0001g0017 a0001c0003t0001g0018 a0001c0003t0001g0019 others(49): Show |
56 | HG00558.hp1 HG01074.hp1 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.107+3433T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071539 | |||||||
| chr5:162071682 | A | G | 1 | a0001c0002t0003g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.107+3576A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071682 | |||||||
| chr5:162071731 | T | C | 193 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(190): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.107+3625T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071731 | |||||||
| chr5:162071791 | A | G | 50 | a0001c0003t0001g0017 a0001c0003t0001g0018 a0001c0003t0001g0019 others(47): Show |
54 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(51): Show |
intron_variant | MODIFIER | c.107+3685A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071791 | |||||||
| chr5:162071847 | T | A | 1 | a0001c0003t0003g0256 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.107+3741T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071847 | |||||||
| chr5:162071942 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.107+3836A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162071942 | |||||||
| chr5:162072085 | T | G | 1 | a0001c0006t0012g0008 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.107+3979T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072085 | |||||||
| chr5:162072102 | A | G | 2 | a0001c0001t0001g0238 a0001c0005t0015g0237 |
2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.107+3996A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072102 | |||||||
| chr5:162072303 | T | C | 2 | a0001c0004t0017g0240 a0001c0008t0001g0241 |
2 | HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+4197T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072303 | |||||||
| chr5:162072404 | A | T | 4 | a0001c0003t0001g0018 a0001c0003t0001g0298 a0001c0003t0001g0299 others(1): Show |
5 | NA18969.hp2 NA18999.hp2 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+4298A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072404 | |||||||
| chr5:162072416 | T | C | 2 | a0001c0004t0017g0240 a0001c0008t0001g0241 |
2 | HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+4310T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072416 | |||||||
| chr5:162072449 | T | C | 50 | a0001c0003t0001g0017 a0001c0003t0001g0018 a0001c0003t0001g0019 others(47): Show |
54 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(51): Show |
intron_variant | MODIFIER | c.107+4343T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072449 | |||||||
| chr5:162072522 | A | G | 4 | a0001c0001t0004g0246 a0001c0001t0004g0247 a0001c0001t0004g0248 others(1): Show |
4 | HG02615.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+4416A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072522 | |||||||
| chr5:162072562 | G | A | 4 | a0001c0002t0006g0002 a0001c0002t0006g0149 a0001c0002t0006g0150 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+4456G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072562 | |||||||
| chr5:162072731 | G | T | 2 | a0001c0001t0002g0015 a0001c0001t0003g0236 |
3 | NA18968.hp1 NA19059.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.107+4625G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072731 | |||||||
| chr5:162072736 | C | T | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+4630C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072736 | |||||||
| chr5:162072769 | A | T | 1 | a0001c0001t0002g0032 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.107+4663A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072769 | |||||||
| chr5:162072820 | G | GATA | 63 | a0001c0001t0002g0250 a0001c0001t0004g0022 a0001c0001t0004g0251 others(60): Show |
68 | HG00558.hp1 HG01074.hp1 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.107+4716_107+4717i others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162072820 | ||||||
| chr5:162072831 | A | G | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+4725A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072831 | |||||||
| chr5:162072868 | C | T | 5 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(2): Show |
5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+4762C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072868 | |||||||
| chr5:162072995 | G | A | 2 | a0001c0004t0017g0240 a0001c0008t0001g0241 |
2 | HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+4889G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162072995 | |||||||
| chr5:162073024 | G | A | 11 | a0001c0001t0018g0091 a0001c0002t0007g0079 a0001c0002t0007g0083 others(8): Show |
11 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+4918G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073024 | |||||||
| chr5:162073191 | C | A | 1 | a0001c0012t0003g0258 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.107+5085C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073191 | |||||||
| chr5:162073233 | T | C | 26 | a0001c0001t0002g0095 a0001c0001t0018g0091 a0001c0002t0001g0092 others(23): Show |
27 | HG00673.hp2 HG01069.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.107+5127T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073233 | |||||||
| chr5:162073249 | G | A | 1 | a0001c0002t0003g0106 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.107+5143G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073249 | |||||||
| chr5:162073267 | GT | G | 18 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0036 others(15): Show |
22 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+5171delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162073267 | ||||||
| chr5:162073268 | T | G | 3 | a0001c0004t0002g0232 a0001c0004t0002g0233 a0001c0004t0002g0234 |
3 | HG01243.hp1 HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.107+5162T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073268 | |||||||
| chr5:162073645 | A | T | 10 | a0001c0004t0002g0232 a0001c0004t0002g0233 a0001c0004t0002g0234 others(7): Show |
10 | HG00639.hp2 HG01243.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+5539A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073645 | |||||||
| chr5:162073781 | C | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+5675C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073781 | |||||||
| chr5:162073960 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.107+5854C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162073960 | |||||||
| chr5:162074001 | T | A | 1 | a0001c0003t0003g0259 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.107+5895T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074001 | |||||||
| chr5:162074131 | T | C | 9 | a0001c0001t0004g0244 a0001c0001t0004g0245 a0001c0001t0004g0246 others(6): Show |
9 | HG02572.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+6025T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074131 | |||||||
| chr5:162074203 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+6097C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074203 | |||||||
| chr5:162074255 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.107+6149T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074255 | |||||||
| chr5:162074379 | G | A | 6 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(3): Show |
6 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+6273G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074379 | |||||||
| chr5:162074562 | A | G | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.107+6456A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074562 | |||||||
| chr5:162074605 | A | G | 1 | a0001c0003t0003g0297 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.107+6499A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074605 | |||||||
| chr5:162074641 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG01081.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.107+6535G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074641 | |||||||
| chr5:162074786 | G | C | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107+6680G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074786 | |||||||
| chr5:162074914 | C | CTT | 63 | a0001c0001t0002g0250 a0001c0001t0004g0022 a0001c0001t0004g0251 others(60): Show |
68 | HG00558.hp1 HG01074.hp1 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.107+6812_107+6813d others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162074914 | ||||||
| chr5:162074917 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.107+6811T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162074917 | |||||||
| chr5:162075183 | A | G | 1 | a0001c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.107+7077A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075183 | |||||||
| chr5:162075213 | C | A | 1 | a0001c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.107+7107C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075213 | |||||||
| chr5:162075306 | A | C | 15 | a0001c0002t0001g0216 a0001c0002t0001g0219 a0001c0002t0001g0220 others(12): Show |
16 | HG00735.hp1 HG01081.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.107+7200A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075306 | |||||||
| chr5:162075344 | C | G | 2 | a0001c0005t0003g0033 a0001c0005t0003g0080 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.107+7238C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075344 | |||||||
| chr5:162075372 | C | G | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.107+7266C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075372 | |||||||
| chr5:162075498 | G | C | 1 | a0001c0002t0002g0009 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.107+7392G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075498 | |||||||
| chr5:162075519 | G | T | 8 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(5): Show |
8 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+7413G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075519 | |||||||
| chr5:162075551 | C | T | 1 | a0001c0003t0001g0296 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.107+7445C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075551 | |||||||
| chr5:162075557 | A | G | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+7451A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075557 | |||||||
| chr5:162075583 | C | T | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+7477C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075583 | |||||||
| chr5:162075612 | G | T | 1 | a0001c0002t0001g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.107+7506G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075612 | |||||||
| chr5:162075730 | AG | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(2): Show |
5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+7625delG | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075730 | |||||||
| chr5:162075752 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.107+7646G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075752 | |||||||
| chr5:162075850 | G | A | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.107+7744G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075850 | |||||||
| chr5:162075881 | C | G | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+7775C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075881 | |||||||
| chr5:162075933 | G | A | 2 | a0001c0002t0001g0093 a0001c0002t0001g0094 |
2 | NA18747.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.107+7827G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075933 | |||||||
| chr5:162075972 | G | T | 1 | a0001c0002t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.107+7866G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162075972 | |||||||
| chr5:162075989 | G | GA | 57 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(54): Show |
61 | HG00558.hp1 HG01074.hp1 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.107+7896dupA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162075989 | ||||||
| chr5:162076008 | T | C | 1 | a0001c0001t0002g0304 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.107+7902T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076008 | |||||||
| chr5:162076107 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.107+8001G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076107 | |||||||
| chr5:162076179 | T | C | 2 | a0001c0003t0002g0260 a0001c0003t0002g0261 |
2 | NA19006.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.107+8073T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076179 | |||||||
| chr5:162076335 | C | T | 11 | a0001c0001t0018g0091 a0001c0002t0007g0079 a0001c0002t0007g0083 others(8): Show |
11 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+8229C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076335 | |||||||
| chr5:162076392 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.107+8286C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076392 | |||||||
| chr5:162076399 | T | C | 1 | a0001c0002t0001g0156 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.107+8293T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076399 | |||||||
| chr5:162076504 | C | T | 1 | a0001c0002t0001g0225 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.107+8398C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076504 | |||||||
| chr5:162076736 | G | T | 11 | a0001c0001t0018g0091 a0001c0002t0007g0079 a0001c0002t0007g0083 others(8): Show |
11 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+8630G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076736 | |||||||
| chr5:162076810 | C | G | 2 | a0001c0005t0003g0033 a0001c0005t0003g0080 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.107+8704C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076810 | |||||||
| chr5:162076915 | GT | G | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+8814delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162076915 | ||||||
| chr5:162076989 | T | A | 1 | a0001c0001t0002g0161 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.107+8883T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162076989 | |||||||
| chr5:162077073 | C | CTG | 99 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0238 others(96): Show |
108 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.107+9004_107+9005d others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077073 | C | CTGTG | 26 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0209 others(23): Show |
28 | HG01258.hp1 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.107+9002_107+9005d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077073 | C | CTGTGTG | 8 | a0001c0001t0001g0212 a0001c0003t0001g0292 a0001c0003t0001g0295 others(5): Show |
8 | HG00639.hp2 HG01074.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+9000_107+9005d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077073 | C | CTGTGTGT others(3): Show |
1 | a0001c0004t0002g0232 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.107+8996_107+9005d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077073 | C | CTGTGTGT others(5): Show |
2 | a0001c0004t0002g0233 a0001c0004t0002g0234 |
2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.107+8994_107+9005d others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077073 | C | CTGTGTGT others(7): Show |
2 | a0001c0004t0017g0240 a0001c0008t0001g0241 |
2 | HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+8992_107+9005d others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077073 | CTG | C | 10 | a0001c0001t0003g0004 a0001c0001t0003g0167 a0001c0001t0003g0168 others(7): Show |
12 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+9004_107+9005d others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077073 | CTGTG | C | 13 | a0001c0001t0002g0077 a0001c0001t0004g0244 a0001c0001t0004g0245 others(10): Show |
13 | HG00099.hp2 HG01952.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.107+9002_107+9005d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077073 | CTGTGTG | C | 99 | a0001c0001t0001g0035 a0001c0001t0001g0068 a0001c0001t0001g0111 others(96): Show |
104 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.107+9000_107+9005d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077073 | CTGTGTGT others(1): Show |
C | 6 | a0001c0001t0001g0109 a0001c0001t0002g0042 a0001c0001t0003g0110 others(3): Show |
6 | HG01169.hp1 HG01192.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+8998_107+9005d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077073 | CTGTGTGT others(3): Show |
C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0002t0001g0001 others(2): Show |
7 | HG00140.hp2 HG00735.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+8996_107+9005d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077073 | ||||||
| chr5:162077103 | GTGTGTGT others(2): Show |
G | 5 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(2): Show |
5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+9001_107+9009d others(11): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077103 | ||||||
| chr5:162077109 | GTGA | G | 2 | a0001c0001t0002g0250 a0001c0001t0010g0016 |
3 | HG01109.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+9006_107+9008d others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077109 | ||||||
| chr5:162077159 | T | G | 5 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(2): Show |
5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+9053T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162077159 | |||||||
| chr5:162077161 | ATTC | A | 10 | a0001c0004t0002g0232 a0001c0004t0002g0233 a0001c0004t0002g0234 others(7): Show |
10 | HG00639.hp2 HG01243.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+9063_107+9065d others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162077161 | ||||||
| chr5:162077345 | T | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+9239T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162077345 | |||||||
| chr5:162077751 | T | C | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.107+9645T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162077751 | |||||||
| chr5:162077955 | G | A | 1 | a0001c0002t0003g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.107+9849G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162077955 | |||||||
| chr5:162077959 | G | C | 5 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(2): Show |
5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+9853G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162077959 | |||||||
| chr5:162078219 | G | A | 13 | a0001c0001t0002g0250 a0001c0001t0004g0022 a0001c0001t0004g0251 others(10): Show |
14 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.107+10113G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078219 | |||||||
| chr5:162078266 | T | C | 1 | a0001c0004t0002g0235 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.107+10160T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078266 | |||||||
| chr5:162078369 | C | CTA | 4 | a0001c0002t0007g0079 a0001c0002t0011g0084 a0001c0002t0014g0085 others(1): Show |
4 | HG01433.hp1 NA19056.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+10291_107+1029 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078369 | ||||||
| chr5:162078369 | C | CTATA | 6 | a0001c0002t0001g0102 a0001c0002t0007g0083 a0001c0002t0011g0082 others(3): Show |
6 | HG02572.hp2 NA18994.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+10289_107+1029 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078369 | ||||||
| chr5:162078369 | CTA | C | 38 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0013 others(35): Show |
41 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.107+10291_107+1029 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078369 | ||||||
| chr5:162078369 | CTATA | C | 28 | a0001c0001t0001g0035 a0001c0001t0001g0136 a0001c0001t0002g0006 others(25): Show |
29 | HG00597.hp2 HG00621.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.107+10289_107+1029 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078369 | ||||||
| chr5:162078369 | CTATATA | C | 16 | a0001c0001t0001g0068 a0001c0001t0002g0007 a0001c0001t0002g0069 others(13): Show |
17 | HG00099.hp2 HG00423.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.107+10287_107+1029 others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078369 | ||||||
| chr5:162078388 | TATA | T | 5 | a0001c0001t0004g0246 a0001c0001t0004g0247 a0001c0001t0004g0248 others(2): Show |
5 | HG02615.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+10283_107+1028 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078388 | |||||||
| chr5:162078388 | TATATA | T | 43 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0109 others(40): Show |
46 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.107+10283_107+1028 others(9): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078388 | |||||||
| chr5:162078388 | TATATATA | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0036 a0001c0001t0002g0037 others(1): Show |
5 | NA18979.hp2 NA18993.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+10283_107+1028 others(11): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078388 | |||||||
| chr5:162078390 | TATA | T | 3 | a0001c0001t0002g0184 a0001c0001t0003g0123 a0001c0001t0003g0125 |
3 | HG00438.hp1 HG03041.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.107+10285_107+1028 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078390 | |||||||
| chr5:162078390 | TATATA | T | 3 | a0001c0001t0003g0121 a0001c0002t0001g0130 a0001c0002t0003g0106 |
3 | HG02055.hp2 HG02083.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.107+10285_107+1028 others(9): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078390 | |||||||
| chr5:162078391 | A | T | 3 | a0001c0001t0002g0046 a0001c0001t0003g0059 a0001c0001t0004g0255 |
3 | HG02080.hp2 HG02132.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.107+10285A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078391 | |||||||
| chr5:162078392 | TA | T | 5 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp1 HG03516.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+10287delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078392 | |||||||
| chr5:162078392 | TATA | T | 7 | a0001c0001t0002g0066 a0001c0001t0002g0166 a0001c0002t0001g0223 others(4): Show |
7 | HG00639.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+10287_107+1028 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078392 | |||||||
| chr5:162078393 | A | AT | 3 | a0001c0001t0003g0004 a0001c0002t0001g0189 a0001c0002t0005g0014 |
3 | HG01981.hp2 HG03225.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.107+10288dupT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078393 | ||||||
| chr5:162078393 | A | T | 30 | a0001c0001t0001g0035 a0001c0001t0001g0136 a0001c0001t0001g0238 others(27): Show |
32 | HG00597.hp2 HG00621.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.107+10287A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078393 | |||||||
| chr5:162078394 | TA | T | 16 | a0001c0001t0001g0212 a0001c0001t0002g0015 a0001c0001t0002g0026 others(13): Show |
17 | HG00558.hp2 HG00597.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.107+10289delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078394 | |||||||
| chr5:162078394 | TATA | T | 7 | a0001c0001t0001g0162 a0001c0001t0002g0032 a0001c0001t0002g0045 others(4): Show |
7 | HG00639.hp1 HG01517.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+10289_107+1029 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078394 | |||||||
| chr5:162078395 | A | AT | 4 | a0001c0001t0002g0027 a0001c0001t0002g0195 a0001c0001t0002g0199 others(1): Show |
4 | HG00423.hp2 HG02040.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+10290dupT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078395 | ||||||
| chr5:162078395 | A | T | 133 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(130): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.107+10289A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078395 | |||||||
| chr5:162078397 | A | ATATATAT others(6): Show |
1 | a0001c0001t0004g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.107+10292_107+1029 others(17): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078397 | ||||||
| chr5:162078397 | A | ATATATAT others(3): Show |
1 | a0001c0001t0004g0251 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.107+10292_107+1029 others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078397 | ||||||
| chr5:162078397 | A | ATATTTTT others(3): Show |
2 | a0001c0001t0010g0016 a0001c0001t0010g0253 |
2 | HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.107+10292_107+1029 others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078397 | ||||||
| chr5:162078397 | A | T | 188 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(185): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.107+10291A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078397 | |||||||
| chr5:162078397 | AT | A | 25 | a0001c0002t0001g0011 a0001c0003t0001g0017 a0001c0003t0001g0018 others(22): Show |
27 | HG01074.hp1 HG01074.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.107+10318delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078397 | ||||||
| chr5:162078397 | ATT | A | 6 | a0001c0002t0001g0170 a0001c0002t0001g0227 a0001c0003t0001g0276 others(3): Show |
6 | HG00558.hp1 HG01169.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+10317_107+1031 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162078397 | ||||||
| chr5:162078398 | T | TA | 4 | a0001c0003t0001g0288 a0001c0003t0002g0265 a0001c0003t0003g0256 others(1): Show |
4 | HG02071.hp1 HG02074.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+10292_107+1029 others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078398 | |||||||
| chr5:162078398 | T | TATA | 3 | a0001c0002t0007g0086 a0001c0003t0001g0024 a0001c0006t0012g0008 |
4 | HG01069.hp1 HG01071.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+10292_107+1029 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078398 | |||||||
| chr5:162078398 | T | TATATATA others(12): Show |
1 | a0001c0001t0004g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.107+10292_107+1029 others(23): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078398 | |||||||
| chr5:162078399 | T | A | 24 | a0001c0002t0002g0021 a0001c0002t0007g0083 a0001c0002t0007g0088 others(21): Show |
26 | HG01258.hp1 HG01496.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.107+10293T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078399 | |||||||
| chr5:162078400 | T | A | 32 | a0001c0001t0004g0022 a0001c0002t0007g0089 a0001c0003t0001g0017 others(29): Show |
35 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.107+10294T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078400 | |||||||
| chr5:162078401 | T | A | 24 | a0001c0002t0001g0170 a0001c0002t0002g0021 a0001c0002t0014g0081 others(21): Show |
26 | HG00558.hp1 HG01258.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.107+10295T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078401 | |||||||
| chr5:162078402 | T | A | 29 | a0001c0001t0004g0022 a0001c0003t0001g0017 a0001c0003t0001g0018 others(26): Show |
32 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.107+10296T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078402 | |||||||
| chr5:162078403 | T | A | 20 | a0001c0002t0002g0021 a0001c0003t0001g0019 a0001c0003t0001g0020 others(17): Show |
22 | HG00558.hp1 HG01258.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+10297T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078403 | |||||||
| chr5:162078404 | T | A | 16 | a0001c0003t0001g0018 a0001c0003t0001g0024 a0001c0003t0001g0268 others(13): Show |
18 | HG01069.hp1 HG01071.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.107+10298T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078404 | |||||||
| chr5:162078405 | T | A | 5 | a0001c0002t0002g0021 a0001c0003t0001g0276 a0001c0003t0001g0295 others(2): Show |
5 | HG01891.hp1 HG02698.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+10299T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078405 | |||||||
| chr5:162078406 | T | A | 5 | a0001c0003t0001g0018 a0001c0003t0001g0298 a0001c0003t0001g0299 others(2): Show |
7 | HG01069.hp1 HG01071.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+10300T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078406 | |||||||
| chr5:162078407 | T | A | 1 | a0001c0003t0003g0294 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.107+10301T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078407 | |||||||
| chr5:162078437 | T | C | 230 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(227): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.107+10331T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078437 | |||||||
| chr5:162078450 | G | A | 7 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+10344G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078450 | |||||||
| chr5:162078480 | C | A | 51 | a0001c0002t0002g0021 a0001c0003t0001g0017 a0001c0003t0001g0018 others(48): Show |
55 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(52): Show |
intron_variant | MODIFIER | c.107+10374C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078480 | |||||||
| chr5:162078492 | C | T | 1 | a0001c0003t0001g0300 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.107+10386C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078492 | |||||||
| chr5:162078493 | G | A | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.107+10387G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078493 | |||||||
| chr5:162078518 | A | T | 1 | a0001c0003t0001g0279 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.107+10412A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078518 | |||||||
| chr5:162078576 | T | C | 1 | a0001c0001t0002g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.107+10470T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078576 | |||||||
| chr5:162078637 | C | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG03927.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.107+10531C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078637 | |||||||
| chr5:162078652 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.107+10546G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078652 | |||||||
| chr5:162078754 | A | G | 7 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+10648A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078754 | |||||||
| chr5:162078840 | C | T | 1 | a0001c0002t0002g0009 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.107+10734C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078840 | |||||||
| chr5:162078935 | T | A | 1 | a0001c0001t0002g0213 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.107+10829T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078935 | |||||||
| chr5:162078952 | A | C | 1 | a0001c0001t0002g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.107+10846A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162078952 | |||||||
| chr5:162079015 | T | A | 11 | a0001c0001t0018g0091 a0001c0002t0007g0079 a0001c0002t0007g0083 others(8): Show |
11 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+10909T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079015 | |||||||
| chr5:162079016 | T | C | 11 | a0001c0001t0018g0091 a0001c0002t0007g0079 a0001c0002t0007g0083 others(8): Show |
11 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+10910T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079016 | |||||||
| chr5:162079143 | G | A | 1 | a0001c0002t0001g0204 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.107+11037G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079143 | |||||||
| chr5:162079177 | A | G | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+11071A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079177 | |||||||
| chr5:162079216 | G | C | 1 | a0001c0001t0004g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.107+11110G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079216 | |||||||
| chr5:162079228 | C | A | 1 | a0001c0002t0002g0009 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.107+11122C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079228 | |||||||
| chr5:162079397 | G | A | 1 | a0001c0001t0008g0067 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.107+11291G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079397 | |||||||
| chr5:162079492 | C | T | 1 | a0001c0004t0005g0231 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.107+11386C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079492 | |||||||
| chr5:162079617 | A | T | 1 | a0001c0002t0001g0132 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.107+11511A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079617 | |||||||
| chr5:162079822 | G | A | 2 | a0001c0001t0001g0111 a0001c0002t0001g0108 |
2 | HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+11716G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079822 | |||||||
| chr5:162079889 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.107+11783C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079889 | |||||||
| chr5:162079917 | T | C | 51 | a0001c0002t0002g0021 a0001c0003t0001g0017 a0001c0003t0001g0018 others(48): Show |
55 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(52): Show |
intron_variant | MODIFIER | c.107+11811T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079917 | |||||||
| chr5:162079971 | C | T | 1 | a0001c0001t0003g0180 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.107+11865C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079971 | |||||||
| chr5:162079972 | G | A | 1 | a0001c0001t0004g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107+11866G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162079972 | |||||||
| chr5:162080177 | G | T | 51 | a0001c0002t0002g0021 a0001c0003t0001g0017 a0001c0003t0001g0018 others(48): Show |
55 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(52): Show |
intron_variant | MODIFIER | c.107+12071G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162080177 | |||||||
| chr5:162080355 | A | G | 1 | a0001c0003t0002g0265 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.107+12249A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162080355 | |||||||
| chr5:162080502 | T | C | 1 | a0001c0002t0001g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.107+12396T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162080502 | |||||||
| chr5:162080672 | A | G | 1 | a0001c0012t0003g0258 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.107+12566A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162080672 | |||||||
| chr5:162080769 | G | T | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+12663G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162080769 | |||||||
| chr5:162081093 | T | G | 1 | a0001c0002t0001g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-12735T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081093 | |||||||
| chr5:162081119 | C | T | 1 | a0001c0002t0003g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.108-12709C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081119 | |||||||
| chr5:162081315 | G | T | 1 | a0001c0006t0012g0008 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.108-12513G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081315 | |||||||
| chr5:162081403 | T | A | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-12425T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081403 | |||||||
| chr5:162081497 | A | T | 63 | a0001c0001t0002g0250 a0001c0001t0002g0304 a0001c0001t0004g0022 others(60): Show |
68 | HG00558.hp1 HG01074.hp1 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.108-12331A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081497 | |||||||
| chr5:162081610 | T | C | 12 | a0001c0001t0018g0091 a0001c0002t0007g0079 a0001c0002t0007g0083 others(9): Show |
13 | HG01069.hp1 HG01071.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.108-12218T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081610 | |||||||
| chr5:162081722 | C | T | 128 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(125): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.108-12106C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081722 | |||||||
| chr5:162081727 | A | G | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-12101A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162081727 | |||||||
| chr5:162082310 | G | A | 3 | a0001c0004t0002g0232 a0001c0004t0002g0233 a0001c0004t0002g0234 |
3 | HG01243.hp1 HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.108-11518G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082310 | |||||||
| chr5:162082462 | G | A | 1 | a0001c0002t0005g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.108-11366G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082462 | |||||||
| chr5:162082559 | T | C | 2 | a0001c0005t0003g0033 a0001c0005t0003g0080 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.108-11269T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082559 | |||||||
| chr5:162082679 | A | T | 1 | a0001c0001t0018g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.108-11149A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082679 | |||||||
| chr5:162082692 | A | G | 2 | a0001c0002t0007g0088 a0001c0002t0007g0089 |
2 | NA18959.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.108-11136A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082692 | |||||||
| chr5:162082756 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.108-11072T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082756 | |||||||
| chr5:162082767 | C | T | 1 | a0001c0003t0001g0275 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.108-11061C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082767 | |||||||
| chr5:162082801 | TAAC | T | 14 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0184 others(11): Show |
16 | HG00673.hp1 HG01081.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.108-11021_108-1101 others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162082801 | ||||||
| chr5:162082896 | C | T | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-10932C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082896 | |||||||
| chr5:162082912 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.108-10916G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082912 | |||||||
| chr5:162082969 | A | G | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-10859A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162082969 | |||||||
| chr5:162083013 | C | G | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.108-10815C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083013 | |||||||
| chr5:162083351 | G | T | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-10477G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083351 | |||||||
| chr5:162083449 | T | G | 24 | a0001c0002t0001g0216 a0001c0002t0001g0219 a0001c0002t0001g0220 others(21): Show |
25 | HG00639.hp2 HG00735.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.108-10379T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083449 | |||||||
| chr5:162083458 | A | G | 1 | a0001c0003t0001g0275 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.108-10370A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083458 | |||||||
| chr5:162083601 | A | C | 11 | a0001c0001t0018g0091 a0001c0002t0007g0079 a0001c0002t0007g0083 others(8): Show |
11 | HG01433.hp1 HG01515.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.108-10227A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083601 | |||||||
| chr5:162083685 | A | T | 1 | a0001c0002t0001g0140 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.108-10143A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083685 | |||||||
| chr5:162083693 | G | T | 1 | a0001c0001t0008g0076 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.108-10135G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083693 | |||||||
| chr5:162083790 | T | C | 219 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(216): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.108-10038T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083790 | |||||||
| chr5:162083899 | A | G | 2 | a0001c0002t0014g0081 a0001c0002t0014g0085 |
2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.108-9929A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083899 | |||||||
| chr5:162083933 | A | T | 1 | a0001c0006t0012g0008 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.108-9895A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162083933 | |||||||
| chr5:162084151 | A | C | 1 | a0001c0002t0003g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.108-9677A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084151 | |||||||
| chr5:162084273 | T | TA | 66 | a0001c0001t0001g0068 a0001c0001t0002g0044 a0001c0001t0002g0069 others(63): Show |
71 | HG00423.hp1 HG00558.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.108-9554dupA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162084273 | ||||||
| chr5:162084274 | A | G | 4 | a0001c0004t0005g0228 a0001c0004t0005g0229 a0001c0004t0005g0230 others(1): Show |
4 | HG00639.hp2 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-9554A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084274 | |||||||
| chr5:162084438 | C | T | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-9390C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084438 | |||||||
| chr5:162084560 | T | C | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-9268T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084560 | |||||||
| chr5:162084575 | G | C | 5 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(2): Show |
5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-9253G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084575 | |||||||
| chr5:162084644 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0301 a0001c0001t0004g0302 others(2): Show |
5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-9184G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084644 | |||||||
| chr5:162084848 | A | C | 273 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(270): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.108-8980A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162084848 | |||||||
| chr5:162085015 | G | A | 1 | a0001c0002t0007g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.108-8813G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085015 | |||||||
| chr5:162085095 | C | A | 2 | a0001c0001t0001g0238 a0001c0005t0015g0237 |
2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.108-8733C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085095 | |||||||
| chr5:162085379 | A | G | 4 | a0001c0001t0008g0067 a0001c0001t0008g0073 a0001c0001t0008g0076 others(1): Show |
4 | HG00423.hp1 NA18954.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-8449A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085379 | |||||||
| chr5:162085558 | C | CA | 7 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0183 others(4): Show |
7 | HG01081.hp2 HG01258.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-8270_108-8269i others(3): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085558 | |||||||
| chr5:162085558 | CT | C | 9 | a0001c0001t0001g0238 a0001c0001t0004g0301 a0001c0001t0004g0302 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.108-8259delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162085558 | ||||||
| chr5:162085624 | T | C | 2 | a0001c0005t0003g0033 a0001c0005t0003g0080 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.108-8204T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085624 | |||||||
| chr5:162085655 | G | C | 1 | a0001c0001t0003g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.108-8173G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085655 | |||||||
| chr5:162085712 | G | C | 2 | a0001c0005t0003g0033 a0001c0005t0003g0080 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.108-8116G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085712 | |||||||
| chr5:162085714 | TC | T | 2 | a0001c0006t0012g0008 a0001c0008t0001g0241 |
3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.108-8112delC | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162085714 | ||||||
| chr5:162085914 | G | GT | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-7907dupT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162085914 | ||||||
| chr5:162085951 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.108-7877G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085951 | |||||||
| chr5:162085954 | C | G | 108 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(105): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.108-7874C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162085954 | |||||||
| chr5:162085958 | A | AT | 16 | a0001c0001t0001g0162 a0001c0001t0002g0161 a0001c0001t0002g0163 others(13): Show |
17 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.108-7859dupT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162085958 | ||||||
| chr5:162086045 | C | A | 2 | a0001c0002t0001g0220 a0001c0002t0001g0223 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.108-7783C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086045 | |||||||
| chr5:162086339 | A | G | 2 | a0001c0006t0012g0008 a0001c0008t0001g0241 |
3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.108-7489A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086339 | |||||||
| chr5:162086514 | A | G | 40 | a0001c0001t0001g0238 a0001c0001t0002g0095 a0001c0001t0002g0250 others(37): Show |
44 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.108-7314A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086514 | |||||||
| chr5:162086701 | G | A | 40 | a0001c0001t0001g0238 a0001c0001t0002g0095 a0001c0001t0002g0250 others(37): Show |
44 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.108-7127G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086701 | |||||||
| chr5:162086725 | T | C | 1 | a0001c0002t0013g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.108-7103T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086725 | |||||||
| chr5:162086769 | T | A | 1 | a0001c0009t0004g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.108-7059T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086769 | |||||||
| chr5:162086809 | A | G | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-7019A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162086809 | |||||||
| chr5:162087273 | T | G | 1 | a0001c0003t0001g0276 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.108-6555T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087273 | |||||||
| chr5:162087298 | T | C | 5 | a0001c0001t0002g0034 a0001c0001t0002g0160 a0001c0001t0002g0171 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-6530T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087298 | |||||||
| chr5:162087367 | T | C | 2 | a0001c0003t0003g0266 a0001c0013t0002g0267 |
2 | HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.108-6461T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087367 | |||||||
| chr5:162087508 | A | G | 1 | a0001c0002t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.108-6320A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087508 | |||||||
| chr5:162087508 | A | T | 1 | a0001c0002t0001g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.108-6320A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087508 | |||||||
| chr5:162087509 | TC | T | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-6318delC | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087509 | |||||||
| chr5:162087605 | A | G | 1 | a0001c0001t0004g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.108-6223A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087605 | |||||||
| chr5:162087648 | A | G | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-6180A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087648 | |||||||
| chr5:162087685 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.108-6143C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087685 | |||||||
| chr5:162087705 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.108-6123A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087705 | |||||||
| chr5:162087757 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.108-6071A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087757 | |||||||
| chr5:162087939 | G | A | 5 | a0001c0004t0002g0023 a0001c0004t0002g0232 a0001c0004t0002g0233 others(2): Show |
5 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-5889G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162087939 | |||||||
| chr5:162088014 | C | T | 38 | a0001c0001t0001g0212 a0001c0001t0002g0013 a0001c0001t0002g0015 others(35): Show |
42 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.108-5814C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088014 | |||||||
| chr5:162088043 | C | T | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-5785C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088043 | |||||||
| chr5:162088114 | A | T | 33 | a0001c0001t0001g0212 a0001c0001t0002g0013 a0001c0001t0002g0015 others(30): Show |
37 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.108-5714A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088114 | |||||||
| chr5:162088159 | C | T | 1 | a0001c0002t0006g0243 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.108-5669C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088159 | |||||||
| chr5:162088209 | C | T | 30 | a0001c0001t0001g0238 a0001c0001t0002g0095 a0001c0001t0003g0180 others(27): Show |
33 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.108-5619C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088209 | |||||||
| chr5:162088219 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.108-5609G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088219 | |||||||
| chr5:162088225 | T | C | 8 | a0001c0001t0001g0113 a0001c0002t0001g0025 a0001c0002t0001g0114 others(5): Show |
8 | HG02055.hp2 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-5603T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088225 | |||||||
| chr5:162088273 | C | T | 4 | a0001c0003t0003g0269 a0001c0003t0003g0270 a0001c0003t0003g0271 others(1): Show |
4 | NA18963.hp2 NA18968.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-5555C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088273 | |||||||
| chr5:162088362 | A | G | 5 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-5466A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088362 | |||||||
| chr5:162088382 | G | T | 4 | a0001c0001t0002g0044 a0001c0001t0002g0070 a0001c0001t0002g0071 others(1): Show |
4 | NA18964.hp1 NA19003.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-5446G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088382 | |||||||
| chr5:162088637 | C | T | 1 | a0001c0003t0001g0279 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.108-5191C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088637 | |||||||
| chr5:162088638 | A | C | 1 | a0001c0003t0001g0279 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.108-5190A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088638 | |||||||
| chr5:162088639 | T | A | 1 | a0001c0003t0001g0279 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.108-5189T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088639 | |||||||
| chr5:162088659 | T | C | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-5169T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088659 | |||||||
| chr5:162088787 | T | C | 1 | a0001c0003t0001g0298 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.108-5041T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088787 | |||||||
| chr5:162088847 | A | T | 1 | a0001c0003t0003g0271 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.108-4981A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088847 | |||||||
| chr5:162088860 | A | G | 2 | a0001c0005t0003g0033 a0001c0005t0003g0080 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.108-4968A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088860 | |||||||
| chr5:162088881 | C | T | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-4947C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088881 | |||||||
| chr5:162088900 | G | A | 1 | a0001c0002t0001g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.108-4928G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088900 | |||||||
| chr5:162088908 | C | T | 1 | a0001c0002t0006g0243 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.108-4920C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162088908 | |||||||
| chr5:162089037 | G | T | 1 | a0001c0001t0002g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.108-4791G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089037 | |||||||
| chr5:162089173 | G | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-4655G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089173 | |||||||
| chr5:162089181 | G | C | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.108-4647G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089181 | |||||||
| chr5:162089248 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.108-4580G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089248 | |||||||
| chr5:162089267 | G | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-4561G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089267 | |||||||
| chr5:162089397 | G | A | 36 | a0001c0001t0001g0238 a0001c0001t0002g0095 a0001c0001t0003g0180 others(33): Show |
39 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.108-4431G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089397 | |||||||
| chr5:162089497 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.108-4331T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089497 | |||||||
| chr5:162089640 | T | C | 1 | a0001c0002t0001g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.108-4188T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089640 | |||||||
| chr5:162089837 | C | T | 2 | a0001c0005t0003g0033 a0001c0005t0003g0080 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.108-3991C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162089837 | |||||||
| chr5:162090000 | C | G | 1 | a0001c0003t0001g0020 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.108-3828C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090000 | |||||||
| chr5:162090053 | C | T | 152 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(149): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.108-3775C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090053 | |||||||
| chr5:162090064 | A | C | 1 | a0001c0002t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.108-3764A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090064 | |||||||
| chr5:162090239 | C | T | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-3589C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090239 | |||||||
| chr5:162090246 | A | G | 2 | a0001c0003t0002g0260 a0001c0003t0002g0261 |
2 | NA19006.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.108-3582A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090246 | |||||||
| chr5:162090251 | T | C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | HG02165.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.108-3577T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090251 | |||||||
| chr5:162090325 | C | CCATACA | 104 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0109 others(101): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.108-3478_108-3473d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162090325 | ||||||
| chr5:162090325 | C | CCATACAC others(5): Show |
8 | a0001c0001t0001g0038 a0001c0001t0004g0022 a0001c0001t0004g0244 others(5): Show |
8 | HG00735.hp2 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.108-3484_108-3473d others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162090325 | ||||||
| chr5:162090325 | CCATACA | C | 48 | a0001c0001t0001g0238 a0001c0001t0002g0095 a0001c0001t0002g0250 others(45): Show |
52 | HG00099.hp1 HG00673.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.108-3478_108-3473d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162090325 | ||||||
| chr5:162090343 | A | ACATACAC others(5): Show |
1 | a0001c0001t0004g0249 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.108-3474_108-3473i others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162090343 | ||||||
| chr5:162090564 | C | A | 118 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(115): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.108-3264C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090564 | |||||||
| chr5:162090768 | A | G | 1 | a0001c0009t0004g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.108-3060A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162090768 | |||||||
| chr5:162091222 | T | G | 1 | a0001c0002t0001g0216 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108-2606T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091222 | |||||||
| chr5:162091252 | A | C | 1 | a0001c0001t0002g0036 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.108-2576A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091252 | |||||||
| chr5:162091264 | G | A | 113 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(110): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.108-2564G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091264 | |||||||
| chr5:162091287 | T | C | 2 | a0001c0001t0002g0069 a0001c0001t0003g0043 |
2 | NA18963.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.108-2541T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091287 | |||||||
| chr5:162091531 | A | T | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.108-2297A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091531 | |||||||
| chr5:162091639 | GA | G | 124 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(121): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.108-2180delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 162091639 | ||||||
| chr5:162091878 | A | T | 1 | a0001c0003t0001g0280 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.108-1950A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091878 | |||||||
| chr5:162091940 | A | G | 4 | a0001c0002t0006g0002 a0001c0002t0006g0149 a0001c0002t0006g0150 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-1888A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091940 | |||||||
| chr5:162091978 | A | G | 124 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(121): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.108-1850A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162091978 | |||||||
| chr5:162092239 | C | G | 175 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(172): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.108-1589C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092239 | |||||||
| chr5:162092253 | A | G | 1 | a0001c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.108-1575A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092253 | |||||||
| chr5:162092367 | G | A | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-1461G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092367 | |||||||
| chr5:162092533 | A | C | 4 | a0001c0002t0006g0002 a0001c0002t0006g0149 a0001c0002t0006g0150 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-1295A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092533 | |||||||
| chr5:162092641 | G | A | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-1187G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092641 | |||||||
| chr5:162092751 | A | C | 8 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(5): Show |
9 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.108-1077A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092751 | |||||||
| chr5:162092770 | A | C | 1 | a0001c0003t0001g0279 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.108-1058A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092770 | |||||||
| chr5:162092795 | G | A | 1 | a0001c0002t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.108-1033G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092795 | |||||||
| chr5:162092873 | T | C | 124 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(121): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.108-955T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092873 | |||||||
| chr5:162092949 | C | T | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-879C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092949 | |||||||
| chr5:162092961 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.108-867G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092961 | |||||||
| chr5:162092974 | G | A | 8 | a0001c0001t0004g0022 a0001c0001t0004g0244 a0001c0001t0004g0245 others(5): Show |
8 | HG02572.hp1 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.108-854G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162092974 | |||||||
| chr5:162093070 | G | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0201 |
3 | HG01106.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.108-758G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093070 | |||||||
| chr5:162093147 | G | A | 1 | a0001c0002t0001g0151 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.108-681G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093147 | |||||||
| chr5:162093262 | G | A | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-566G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093262 | |||||||
| chr5:162093263 | C | G | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-565C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093263 | |||||||
| chr5:162093366 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.108-462G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093366 | |||||||
| chr5:162093451 | G | A | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-377G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093451 | |||||||
| chr5:162093497 | T | G | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-331T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093497 | |||||||
| chr5:162093536 | G | C | 2 | a0001c0006t0012g0008 a0001c0008t0001g0241 |
3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.108-292G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093536 | |||||||
| chr5:162093646 | G | A | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.108-182G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093646 | |||||||
| chr5:162093739 | T | A | 2 | a0001c0003t0001g0296 a0001c0003t0003g0294 |
2 | NA19062.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.108-89T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093739 | |||||||
| chr5:162093795 | T | G | 1 | a0001c0002t0001g0216 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108-33T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 1/9 | chr5 | 162093795 | |||||||
| chr5:162094039 | A | T | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.259+60A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094039 | |||||||
| chr5:162094252 | A | G | 2 | a0001c0001t0010g0016 a0001c0001t0010g0253 |
3 | HG03471.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.259+273A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094252 | |||||||
| chr5:162094274 | T | C | 2 | a0001c0006t0012g0008 a0001c0008t0001g0241 |
3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.259+295T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094274 | |||||||
| chr5:162094335 | T | C | 4 | a0001c0001t0008g0067 a0001c0001t0008g0073 a0001c0001t0008g0076 others(1): Show |
4 | HG00423.hp1 NA18954.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+356T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094335 | |||||||
| chr5:162094418 | A | G | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.259+439A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094418 | |||||||
| chr5:162094469 | C | T | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.259+490C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094469 | |||||||
| chr5:162094621 | G | A | 2 | a0001c0001t0010g0016 a0001c0001t0010g0253 |
3 | HG03471.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.259+642G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094621 | |||||||
| chr5:162094685 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.259+706C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094685 | |||||||
| chr5:162094688 | G | C | 1 | a0001c0001t0009g0211 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.259+709G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094688 | |||||||
| chr5:162094985 | T | C | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.260-510T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162094985 | |||||||
| chr5:162095461 | C | G | 1 | a0001c0001t0003g0059 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.260-34C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 2/9 | chr5 | 162095461 | |||||||
| chr5:162095623 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.327+61G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162095623 | |||||||
| chr5:162095628 | G | A | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.327+66G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162095628 | |||||||
| chr5:162095748 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.327+186G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162095748 | |||||||
| chr5:162095870 | A | G | 2 | a0001c0002t0001g0151 a0001c0002t0001g0155 |
2 | HG00673.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.327+308A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162095870 | |||||||
| chr5:162095949 | G | A | 29 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(26): Show |
33 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.327+387G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162095949 | |||||||
| chr5:162096015 | A | G | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+453A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096015 | |||||||
| chr5:162096081 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.327+519A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096081 | |||||||
| chr5:162096195 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.327+633A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096195 | |||||||
| chr5:162096544 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327+982G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096544 | |||||||
| chr5:162096553 | G | T | 2 | a0001c0005t0003g0033 a0001c0005t0003g0080 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.327+991G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096553 | |||||||
| chr5:162096598 | TGAACAAG | T | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.327+1038_328-1032d others(9): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 162096598 | ||||||
| chr5:162096717 | A | G | 107 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(104): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.328-921A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096717 | |||||||
| chr5:162096742 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.328-896G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096742 | |||||||
| chr5:162096769 | G | A | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.328-869G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096769 | |||||||
| chr5:162096788 | T | C | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.328-850T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096788 | |||||||
| chr5:162096864 | G | A | 98 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(95): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.328-774G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096864 | |||||||
| chr5:162096894 | T | C | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.328-744T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162096894 | |||||||
| chr5:162097095 | G | C | 1 | a0001c0001t0002g0046 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.328-543G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162097095 | |||||||
| chr5:162097162 | C | T | 1 | a0001c0003t0001g0287 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.328-476C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162097162 | |||||||
| chr5:162097618 | T | G | 5 | a0001c0002t0005g0014 a0001c0002t0005g0214 a0001c0002t0005g0215 others(2): Show |
6 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-20T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 3/9 | chr5 | 162097618 | |||||||
| chr5:162097984 | A | G | 1 | a0001c0002t0002g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.548+126A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162097984 | |||||||
| chr5:162098047 | T | G | 4 | a0001c0001t0002g0047 a0001c0001t0002g0057 a0001c0001t0002g0077 others(1): Show |
4 | HG00099.hp2 HG01175.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.548+189T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098047 | |||||||
| chr5:162098082 | A | T | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.548+224A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098082 | |||||||
| chr5:162098088 | G | T | 1 | a0001c0011t0003g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.548+230G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098088 | |||||||
| chr5:162098164 | C | T | 1 | a0001c0002t0007g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.548+306C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098164 | |||||||
| chr5:162098376 | C | G | 1 | a0001c0002t0003g0010 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.548+518C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098376 | |||||||
| chr5:162098462 | TAATAA | T | 2 | a0001c0006t0012g0008 a0001c0008t0001g0241 |
3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.548+610_548+614del others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 162098462 | ||||||
| chr5:162098552 | A | G | 3 | a0001c0004t0002g0232 a0001c0004t0002g0233 a0001c0004t0002g0234 |
3 | HG01243.hp1 HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.548+694A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098552 | |||||||
| chr5:162098591 | C | G | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.548+733C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162098591 | |||||||
| chr5:162098826 | GCTGTCCC others(3): Show |
G | 4 | a0001c0004t0005g0228 a0001c0004t0005g0229 a0001c0004t0005g0230 others(1): Show |
4 | HG00639.hp2 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.548+973_548+982del others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 162098826 | ||||||
| chr5:162099009 | T | C | 3 | a0001c0001t0018g0091 a0001c0005t0003g0033 a0001c0005t0003g0080 |
3 | HG01243.hp2 HG01884.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.548+1151T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099009 | |||||||
| chr5:162099201 | A | G | 5 | a0001c0002t0001g0139 a0001c0002t0003g0010 a0001c0002t0003g0106 others(2): Show |
6 | HG00621.hp2 HG02083.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.548+1343A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099201 | |||||||
| chr5:162099256 | G | A | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.548+1398G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099256 | |||||||
| chr5:162099513 | C | A | 1 | a0001c0001t0002g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.548+1655C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099513 | |||||||
| chr5:162099561 | C | A | 1 | a0001c0002t0001g0118 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.549-1674C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099561 | |||||||
| chr5:162099568 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.549-1667C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099568 | |||||||
| chr5:162099571 | A | G | 1 | a0001c0003t0001g0299 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.549-1664A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099571 | |||||||
| chr5:162099720 | T | G | 2 | a0001c0001t0003g0053 a0001c0001t0003g0054 |
2 | NA18944.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.549-1515T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099720 | |||||||
| chr5:162099786 | G | C | 1 | a0001c0001t0002g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.549-1449G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099786 | |||||||
| chr5:162099928 | T | C | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.549-1307T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099928 | |||||||
| chr5:162099948 | T | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549-1287T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162099948 | |||||||
| chr5:162100116 | G | A | 2 | a0001c0006t0012g0008 a0001c0008t0001g0241 |
3 | HG01069.hp1 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.549-1119G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100116 | |||||||
| chr5:162100247 | A | G | 30 | a0001c0001t0002g0095 a0001c0001t0003g0180 a0001c0002t0001g0011 others(27): Show |
33 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.549-988A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100247 | |||||||
| chr5:162100254 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.549-981C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100254 | |||||||
| chr5:162100288 | T | C | 1 | a0001c0011t0003g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.549-947T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100288 | |||||||
| chr5:162100305 | C | T | 1 | a0001c0002t0011g0084 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.549-930C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100305 | |||||||
| chr5:162100316 | A | T | 1 | a0001c0009t0004g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.549-919A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100316 | |||||||
| chr5:162100332 | T | G | 1 | a0001c0001t0002g0188 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.549-903T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100332 | |||||||
| chr5:162100447 | T | C | 6 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(3): Show |
7 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.549-788T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100447 | |||||||
| chr5:162100709 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.549-526C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100709 | |||||||
| chr5:162100775 | A | G | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.549-460A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100775 | |||||||
| chr5:162100837 | A | T | 1 | a0001c0001t0002g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.549-398A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100837 | |||||||
| chr5:162100927 | C | T | 1 | a0001c0003t0003g0289 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.549-308C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162100927 | |||||||
| chr5:162101022 | G | C | 1 | a0001c0001t0004g0251 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.549-213G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 4/9 | chr5 | 162101022 | |||||||
| chr5:162101372 | T | G | 2 | a0001c0003t0003g0293 a0001c0003t0003g0297 |
2 | HG01074.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.631+55T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162101372 | |||||||
| chr5:162101580 | CT | C | 13 | a0001c0001t0002g0070 a0001c0001t0010g0016 a0001c0001t0010g0253 others(10): Show |
17 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.631+275delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 162101580 | ||||||
| chr5:162101853 | A | G | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.631+536A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162101853 | |||||||
| chr5:162101887 | T | C | 9 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 others(6): Show |
9 | HG00639.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+570T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162101887 | |||||||
| chr5:162102051 | A | C | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.631+734A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102051 | |||||||
| chr5:162102090 | G | C | 15 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0002g0250 others(12): Show |
16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.631+773G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102090 | |||||||
| chr5:162102241 | T | C | 3 | a0001c0002t0001g0118 a0001c0002t0001g0119 a0001c0002t0001g0143 |
3 | HG01952.hp2 HG02004.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.631+924T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102241 | |||||||
| chr5:162102262 | A | G | 1 | a0001c0002t0002g0009 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.631+945A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102262 | |||||||
| chr5:162102363 | C | T | 59 | a0001c0001t0001g0068 a0001c0001t0001g0153 a0001c0002t0001g0001 others(56): Show |
66 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.631+1046C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102363 | |||||||
| chr5:162102422 | A | G | 3 | a0001c0001t0004g0144 a0001c0002t0001g0189 a0001c0008t0001g0241 |
3 | HG01192.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.631+1105A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102422 | |||||||
| chr5:162102565 | A | G | 229 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(226): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.631+1248A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102565 | |||||||
| chr5:162102625 | G | T | 29 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(26): Show |
30 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.632-1264G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102625 | |||||||
| chr5:162102627 | C | A | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.632-1262C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102627 | |||||||
| chr5:162102714 | A | G | 199 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(196): Show |
215 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.632-1175A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102714 | |||||||
| chr5:162102725 | G | A | 22 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0039 others(19): Show |
25 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.632-1164G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102725 | |||||||
| chr5:162102802 | C | T | 197 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(194): Show |
213 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.632-1087C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102802 | |||||||
| chr5:162102998 | T | G | 1 | a0001c0002t0001g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.632-891T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162102998 | |||||||
| chr5:162103147 | C | T | 31 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(28): Show |
32 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.632-742C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103147 | |||||||
| chr5:162103262 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.632-627A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103262 | |||||||
| chr5:162103300 | A | G | 1 | a0001c0002t0001g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.632-589A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103300 | |||||||
| chr5:162103379 | T | C | 198 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(195): Show |
214 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.632-510T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103379 | |||||||
| chr5:162103411 | C | T | 229 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(226): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.632-478C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103411 | |||||||
| chr5:162103530 | G | C | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.632-359G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103530 | |||||||
| chr5:162103532 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.632-357G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103532 | |||||||
| chr5:162103597 | G | C | 1 | a0001c0002t0001g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.632-292G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103597 | |||||||
| chr5:162103729 | C | T | 198 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(195): Show |
214 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.632-160C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103729 | |||||||
| chr5:162103818 | T | A | 1 | a0001c0002t0001g0039 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.632-71T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103818 | |||||||
| chr5:162103834 | C | T | 1 | a0001c0003t0002g0274 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.632-55C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103834 | |||||||
| chr5:162103879 | C | A | 1 | a0001c0003t0001g0017 | 2 | NA18980.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.632-10C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 5/9 | chr5 | 162103879 | |||||||
| chr5:162104454 | T | A | 232 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(229): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.769+428T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104454 | |||||||
| chr5:162104675 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.769+649C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104675 | |||||||
| chr5:162104762 | A | ATTTAT | 135 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(132): Show |
147 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.769+740_769+741ins others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162104762 | ||||||
| chr5:162104838 | A | G | 6 | a0001c0001t0002g0012 a0001c0001t0002g0158 a0001c0001t0002g0159 others(3): Show |
7 | NA18945.hp1 NA18953.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+812A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104838 | |||||||
| chr5:162104879 | T | C | 1 | a0001c0002t0007g0086 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.769+853T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104879 | |||||||
| chr5:162104902 | G | C | 3 | a0001c0002t0002g0009 a0001c0002t0004g0254 a0001c0009t0004g0148 |
4 | HG02615.hp1 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+876G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104902 | |||||||
| chr5:162104921 | T | C | 1 | a0001c0002t0002g0105 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.769+895T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162104921 | |||||||
| chr5:162105232 | C | T | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+1206C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105232 | |||||||
| chr5:162105354 | C | T | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+1328C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105354 | |||||||
| chr5:162105380 | T | C | 5 | a0001c0002t0005g0014 a0001c0002t0005g0214 a0001c0002t0005g0215 others(2): Show |
6 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1354T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105380 | |||||||
| chr5:162105397 | C | A | 1 | a0001c0002t0011g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.769+1371C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105397 | |||||||
| chr5:162105423 | T | C | 1 | a0001c0001t0013g0194 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.769+1397T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105423 | |||||||
| chr5:162105432 | C | CTTTTTTT others(1): Show |
68 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0162 others(65): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.769+1414_769+1421d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | ||||||
| chr5:162105432 | C | CTTTTTTT others(2): Show |
59 | a0001c0001t0001g0068 a0001c0001t0001g0153 a0001c0001t0001g0212 others(56): Show |
66 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.769+1413_769+1421d others(11): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | ||||||
| chr5:162105432 | C | CTTTTTTT others(3): Show |
33 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(30): Show |
34 | HG00140.hp1 HG00438.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.769+1412_769+1421d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | ||||||
| chr5:162105432 | C | CTTTTTTT others(4): Show |
7 | a0001c0002t0001g0025 a0001c0002t0001g0103 a0001c0002t0001g0114 others(4): Show |
7 | HG01496.hp1 HG03130.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+1411_769+1421d others(13): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | ||||||
| chr5:162105432 | C | CTTTTTTT others(5): Show |
55 | a0001c0001t0003g0059 a0001c0002t0001g0102 a0001c0002t0001g0104 others(52): Show |
59 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(56): Show |
intron_variant | MODIFIER | c.769+1410_769+1421d others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | ||||||
| chr5:162105432 | C | CTTTTTTT others(6): Show |
2 | a0001c0003t0001g0280 a0001c0003t0002g0260 |
2 | NA19006.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.769+1409_769+1421d others(15): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | ||||||
| chr5:162105432 | C | CTTTTTTT others(8): Show |
1 | a0001c0003t0002g0261 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.769+1407_769+1421d others(17): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105432 | ||||||
| chr5:162105490 | C | T | 1 | a0001c0002t0001g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.769+1464C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105490 | |||||||
| chr5:162105574 | C | T | 1 | a0001c0001t0013g0194 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.769+1548C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105574 | |||||||
| chr5:162105587 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+1561G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105587 | |||||||
| chr5:162105652 | G | A | 3 | a0001c0002t0005g0014 a0001c0002t0005g0215 a0001c0002t0005g0217 |
4 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+1626G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105652 | |||||||
| chr5:162105705 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.769+1679C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105705 | |||||||
| chr5:162105720 | G | A | 6 | a0001c0002t0014g0081 a0001c0002t0014g0085 a0001c0004t0005g0228 others(3): Show |
6 | HG00639.hp2 HG02572.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1694G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105720 | |||||||
| chr5:162105796 | T | C | 9 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 others(6): Show |
9 | HG00639.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+1770T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105796 | |||||||
| chr5:162105814 | T | TAC | 3 | a0001c0001t0002g0052 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | HG02602.hp2 NA18964.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.769+1817_769+1818d others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | ||||||
| chr5:162105814 | T | TACAC | 108 | a0001c0001t0001g0068 a0001c0001t0001g0153 a0001c0001t0018g0091 others(105): Show |
117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.769+1815_769+1818d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | ||||||
| chr5:162105814 | T | TACACAC | 47 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(44): Show |
49 | HG00438.hp1 HG01069.hp2 HG01258.hp1 others(46): Show |
intron_variant | MODIFIER | c.769+1813_769+1818d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | ||||||
| chr5:162105814 | T | TACACACA others(1): Show |
6 | a0001c0001t0001g0238 a0001c0001t0003g0056 a0001c0001t0004g0252 others(3): Show |
7 | HG00140.hp1 HG02622.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+1811_769+1818d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | ||||||
| chr5:162105814 | T | TACACACA others(3): Show |
5 | a0001c0001t0004g0246 a0001c0001t0004g0247 a0001c0001t0004g0248 others(2): Show |
5 | HG02615.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+1809_769+1818d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | ||||||
| chr5:162105814 | T | TACACACA others(5): Show |
6 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0004g0022 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+1807_769+1818d others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | ||||||
| chr5:162105814 | T | TACACACA others(7): Show |
4 | a0001c0001t0002g0250 a0001c0001t0004g0144 a0001c0001t0010g0016 others(1): Show |
5 | HG01109.hp1 HG01192.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+1805_769+1818d others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | ||||||
| chr5:162105814 | TACACAC | T | 45 | a0001c0001t0001g0111 a0001c0001t0001g0212 a0001c0001t0002g0015 others(42): Show |
49 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.769+1813_769+1818d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105814 | ||||||
| chr5:162105834 | C | CACAT | 9 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 others(6): Show |
9 | HG00639.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+1811_769+1812i others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162105834 | ||||||
| chr5:162105976 | T | G | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.769+1950T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162105976 | |||||||
| chr5:162106060 | C | T | 135 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(132): Show |
147 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.769+2034C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106060 | |||||||
| chr5:162106145 | A | G | 1 | a0001c0002t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.769+2119A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106145 | |||||||
| chr5:162106379 | T | C | 3 | a0001c0001t0004g0144 a0001c0002t0001g0189 a0001c0008t0001g0241 |
3 | HG01192.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+2353T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106379 | |||||||
| chr5:162106397 | C | T | 1 | a0001c0001t0018g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.769+2371C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106397 | |||||||
| chr5:162106411 | A | T | 1 | a0001c0003t0003g0297 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.769+2385A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106411 | |||||||
| chr5:162106427 | G | T | 31 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(28): Show |
32 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.769+2401G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106427 | |||||||
| chr5:162106442 | G | C | 229 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(226): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.769+2416G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106442 | |||||||
| chr5:162106490 | C | T | 131 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(128): Show |
143 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.769+2464C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106490 | |||||||
| chr5:162106658 | C | T | 1 | a0001c0004t0002g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.769+2632C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106658 | |||||||
| chr5:162106706 | C | G | 229 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(226): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.769+2680C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106706 | |||||||
| chr5:162106833 | C | T | 1 | a0001c0003t0001g0018 | 2 | NA18969.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.769+2807C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106833 | |||||||
| chr5:162106871 | A | T | 3 | a0001c0001t0004g0144 a0001c0002t0001g0189 a0001c0008t0001g0241 |
3 | HG01192.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+2845A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106871 | |||||||
| chr5:162106891 | T | G | 1 | a0001c0002t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.769+2865T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106891 | |||||||
| chr5:162106916 | G | GGC | 226 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(223): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.769+2891_769+2892i others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162106916 | ||||||
| chr5:162106917 | G | GC | 3 | a0001c0001t0004g0144 a0001c0002t0001g0189 a0001c0008t0001g0241 |
3 | HG01192.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+2891_769+2892i others(3): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106917 | |||||||
| chr5:162106919 | T | C | 226 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(223): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.769+2893T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106919 | |||||||
| chr5:162106919 | T | G | 6 | a0001c0001t0004g0144 a0001c0002t0001g0189 a0001c0002t0002g0009 others(3): Show |
7 | HG01192.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+2893T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106919 | |||||||
| chr5:162106920 | G | A | 5 | a0001c0001t0002g0034 a0001c0001t0002g0160 a0001c0001t0002g0171 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+2894G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106920 | |||||||
| chr5:162106970 | C | T | 229 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(226): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.769+2944C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162106970 | |||||||
| chr5:162107013 | G | A | 31 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(28): Show |
32 | HG00140.hp1 HG00438.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.769+2987G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107013 | |||||||
| chr5:162107079 | C | T | 1 | a0001c0002t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.769+3053C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107079 | |||||||
| chr5:162107087 | C | G | 1 | a0001c0001t0002g0042 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.769+3061C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107087 | |||||||
| chr5:162107140 | G | A | 229 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(226): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.769+3114G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107140 | |||||||
| chr5:162107407 | G | A | 4 | a0001c0001t0001g0238 a0001c0001t0004g0144 a0001c0002t0001g0189 others(1): Show |
4 | HG01192.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+3381G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107407 | |||||||
| chr5:162107496 | A | G | 10 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0004g0022 others(7): Show |
10 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.769+3470A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107496 | |||||||
| chr5:162107622 | G | A | 1 | a0001c0003t0002g0260 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.769+3596G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107622 | |||||||
| chr5:162107630 | G | A | 1 | a0001c0010t0003g0142 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.769+3604G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107630 | |||||||
| chr5:162107675 | T | C | 4 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(1): Show |
4 | HG02622.hp2 HG02723.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+3649T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107675 | |||||||
| chr5:162107787 | C | A | 28 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(25): Show |
29 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.769+3761C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107787 | |||||||
| chr5:162107819 | C | T | 2 | a0001c0002t0001g0189 a0001c0008t0001g0241 |
2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+3793C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107819 | |||||||
| chr5:162107976 | C | T | 30 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(27): Show |
31 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.769+3950C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162107976 | |||||||
| chr5:162108024 | G | A | 131 | a0001c0001t0001g0068 a0001c0001t0001g0153 a0001c0001t0003g0059 others(128): Show |
142 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.769+3998G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108024 | |||||||
| chr5:162108070 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.769+4044A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108070 | |||||||
| chr5:162108113 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.769+4087G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108113 | |||||||
| chr5:162108129 | T | C | 232 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(229): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.769+4103T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108129 | |||||||
| chr5:162108387 | G | A | 2 | a0001c0002t0001g0189 a0001c0008t0001g0241 |
2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+4361G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108387 | |||||||
| chr5:162108666 | T | C | 1 | a0001c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.769+4640T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108666 | |||||||
| chr5:162108749 | C | T | 122 | a0001c0001t0001g0068 a0001c0001t0001g0153 a0001c0001t0003g0059 others(119): Show |
133 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.769+4723C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108749 | |||||||
| chr5:162108926 | C | T | 3 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0200 |
3 | HG02165.hp1 NA19012.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.769+4900C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108926 | |||||||
| chr5:162108956 | C | T | 10 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0004g0022 others(7): Show |
10 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.769+4930C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162108956 | |||||||
| chr5:162109297 | C | T | 1 | a0001c0001t0003g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.769+5271C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109297 | |||||||
| chr5:162109330 | T | A | 31 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(28): Show |
32 | HG00140.hp1 HG00438.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.769+5304T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109330 | |||||||
| chr5:162109356 | C | T | 3 | a0001c0002t0002g0009 a0001c0002t0004g0254 a0001c0009t0004g0148 |
4 | HG02615.hp1 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+5330C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109356 | |||||||
| chr5:162109382 | A | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0153 a0001c0002t0001g0003 others(3): Show |
8 | HG00673.hp1 HG02071.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.769+5356A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109382 | |||||||
| chr5:162109388 | T | TTATATA | 3 | a0001c0001t0001g0113 a0001c0001t0010g0016 a0001c0001t0010g0253 |
4 | HG03471.hp1 HG06807.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+5362_769+5363i others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | |||||||
| chr5:162109388 | T | TTATATAT others(1): Show |
5 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 others(2): Show |
5 | HG00639.hp1 HG02109.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+5362_769+5363i others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | |||||||
| chr5:162109388 | T | TTATATAT others(3): Show |
4 | a0001c0001t0001g0111 a0001c0001t0002g0184 a0001c0001t0002g0190 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+5362_769+5363i others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | |||||||
| chr5:162109388 | T | TTATATAT others(9): Show |
2 | a0001c0001t0002g0161 a0001c0006t0012g0008 |
3 | HG01069.hp1 HG01071.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.769+5362_769+5363i others(18): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | |||||||
| chr5:162109388 | T | TTATATAT others(13): Show |
1 | a0001c0001t0004g0251 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.769+5362_769+5363i others(22): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | |||||||
| chr5:162109388 | TAATATAT others(1): Show |
T | 4 | a0001c0001t0004g0022 a0001c0001t0004g0244 a0001c0001t0004g0245 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+5363_769+5370d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109388 | |||||||
| chr5:162109389 | A | AAT | 33 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(30): Show |
38 | HG00438.hp2 HG00735.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.769+5396_769+5397d others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | AATAT | 18 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0002g0013 others(15): Show |
19 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.769+5394_769+5397d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | AATATAT | 10 | a0001c0001t0001g0040 a0001c0001t0002g0029 a0001c0001t0002g0042 others(7): Show |
10 | HG00597.hp1 HG01081.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.769+5392_769+5397d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | AATATATA others(1): Show |
9 | a0001c0001t0002g0057 a0001c0001t0002g0200 a0001c0001t0008g0067 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.769+5390_769+5397d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | AATATATA others(3): Show |
8 | a0001c0001t0001g0212 a0001c0001t0002g0026 a0001c0001t0002g0031 others(5): Show |
8 | HG01261.hp2 HG02027.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+5388_769+5397d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | AATATATA others(5): Show |
12 | a0001c0001t0002g0176 a0001c0001t0002g0198 a0001c0001t0003g0004 others(9): Show |
14 | HG00558.hp2 HG00621.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+5386_769+5397d others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | AATATATA others(7): Show |
7 | a0001c0001t0002g0160 a0001c0001t0002g0195 a0001c0001t0002g0209 others(4): Show |
7 | HG00423.hp2 HG02080.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+5384_769+5397d others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | AATATATA others(9): Show |
6 | a0001c0001t0002g0030 a0001c0001t0002g0032 a0001c0001t0002g0171 others(3): Show |
6 | HG00639.hp2 HG02717.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+5382_769+5397d others(18): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | AATATATA others(11): Show |
5 | a0001c0001t0002g0015 a0001c0001t0002g0182 a0001c0001t0002g0213 others(2): Show |
6 | HG03195.hp2 NA18747.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+5380_769+5397d others(20): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | AATATATA others(13): Show |
2 | a0001c0001t0002g0034 a0001c0004t0005g0228 |
2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.769+5378_769+5397d others(22): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | AATATATA others(21): Show |
1 | a0001c0001t0002g0027 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.769+5370_769+5397d others(30): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | A | ATATATAT others(6): Show |
1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+5363_769+5364i others(15): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109389 | |||||||
| chr5:162109389 | A | T | 17 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0162 others(14): Show |
19 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.769+5363A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109389 | |||||||
| chr5:162109389 | AATAT | A | 8 | a0001c0002t0001g0099 a0001c0002t0001g0173 a0001c0002t0001g0221 others(5): Show |
8 | HG02486.hp1 HG02486.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+5394_769+5397d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | AATATAT | A | 23 | a0001c0001t0001g0068 a0001c0001t0001g0153 a0001c0001t0004g0144 others(20): Show |
24 | HG00673.hp1 HG01069.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.769+5392_769+5397d others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | AATATATA others(1): Show |
A | 83 | a0001c0001t0003g0059 a0001c0002t0001g0001 a0001c0002t0001g0003 others(80): Show |
92 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.769+5390_769+5397d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109389 | AATATATA others(3): Show |
A | 11 | a0001c0002t0001g0062 a0001c0002t0001g0227 a0001c0002t0007g0083 others(8): Show |
12 | HG01169.hp2 HG01175.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.769+5388_769+5397d others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109389 | ||||||
| chr5:162109412 | A | T | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769+5386A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109412 | |||||||
| chr5:162109416 | A | ATATTTAT others(5): Show |
3 | a0001c0002t0001g0116 a0001c0002t0001g0117 a0001c0002t0001g0135 |
3 | HG02723.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.769+5393_769+5394i others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109416 | ||||||
| chr5:162109416 | A | ATTTATTT others(3): Show |
1 | a0001c0002t0001g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.769+5391_769+5392i others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109416 | ||||||
| chr5:162109416 | A | T | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769+5390A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109416 | |||||||
| chr5:162109420 | A | ATATATAT others(7): Show |
1 | a0001c0009t0004g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.769+5397_769+5398i others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATATATAT others(5): Show |
3 | a0001c0001t0004g0302 a0001c0001t0004g0303 a0001c0001t0018g0091 |
3 | HG02258.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.769+5397_769+5398i others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0136 a0001c0001t0003g0123 |
2 | HG00438.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.769+5397_769+5398i others(22): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATATATAT others(3): Show |
2 | a0001c0001t0004g0301 a0001c0002t0002g0009 |
3 | HG02615.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.769+5397_769+5398i others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.769+5397_769+5398i others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATATATAT others(11): Show |
3 | a0001c0001t0003g0137 a0001c0001t0016g0120 a0001c0002t0003g0122 |
3 | HG00140.hp1 HG02027.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.769+5397_769+5398i others(20): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATATATAT others(9): Show |
10 | a0001c0001t0001g0109 a0001c0001t0001g0152 a0001c0001t0003g0124 others(7): Show |
11 | HG01496.hp2 HG02630.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.769+5397_769+5398i others(18): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATATATAT others(13): Show |
1 | a0001c0008t0001g0241 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.769+5397_769+5398i others(22): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATATATTT others(7): Show |
5 | a0001c0001t0001g0129 a0001c0001t0003g0121 a0001c0001t0003g0127 others(2): Show |
5 | HG01346.hp2 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+5397_769+5398i others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATATATTT others(11): Show |
1 | a0001c0002t0001g0189 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+5397_769+5398i others(20): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATATTTAT others(5): Show |
2 | a0001c0001t0003g0110 a0001c0002t0011g0090 |
2 | HG01433.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.769+5405_769+5406i others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | ATTTATTT others(7): Show |
1 | a0001c0002t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.769+5395_769+5396i others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162109420 | ||||||
| chr5:162109420 | A | T | 8 | a0001c0001t0001g0238 a0001c0001t0004g0144 a0001c0002t0001g0116 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+5394A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109420 | |||||||
| chr5:162109424 | T | A | 2 | a0001c0002t0005g0217 a0002c0007t0002g0041 |
2 | HG02055.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.769+5398T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109424 | |||||||
| chr5:162109466 | C | T | 31 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(28): Show |
32 | HG00140.hp1 HG00438.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.769+5440C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109466 | |||||||
| chr5:162109542 | A | G | 2 | a0001c0004t0002g0023 a0001c0004t0017g0240 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.769+5516A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109542 | |||||||
| chr5:162109578 | A | G | 226 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(223): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.769+5552A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109578 | |||||||
| chr5:162109594 | G | A | 8 | a0001c0002t0001g0102 a0001c0002t0001g0103 a0001c0002t0001g0104 others(5): Show |
9 | NA18941.hp2 NA18962.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+5568G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109594 | |||||||
| chr5:162109775 | G | T | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769+5749G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109775 | |||||||
| chr5:162109922 | A | G | 226 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(223): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.769+5896A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109922 | |||||||
| chr5:162109923 | G | T | 2 | a0001c0003t0003g0112 a0001c0003t0003g0262 |
2 | NA18945.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.769+5897G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109923 | |||||||
| chr5:162109953 | A | G | 1 | a0001c0001t0002g0069 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.769+5927A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162109953 | |||||||
| chr5:162110077 | C | A | 47 | a0001c0001t0001g0111 a0001c0001t0001g0212 a0001c0001t0002g0015 others(44): Show |
51 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.769+6051C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110077 | |||||||
| chr5:162110124 | G | T | 225 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(222): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.769+6098G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110124 | |||||||
| chr5:162110202 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.769+6176G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110202 | |||||||
| chr5:162110416 | T | C | 1 | a0001c0002t0001g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.769+6390T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110416 | |||||||
| chr5:162110526 | G | A | 2 | a0001c0002t0001g0062 a0001c0002t0001g0227 |
2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.769+6500G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110526 | |||||||
| chr5:162110630 | AAAC | A | 32 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(29): Show |
33 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.769+6631_769+6633d others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162110630 | ||||||
| chr5:162110642 | C | T | 9 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 others(6): Show |
9 | HG00639.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+6616C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162110642 | |||||||
| chr5:162111042 | G | A | 1 | a0001c0002t0002g0100 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.769+7016G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111042 | |||||||
| chr5:162111303 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769+7277C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111303 | |||||||
| chr5:162111410 | A | C | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+7384A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111410 | |||||||
| chr5:162111423 | C | T | 1 | a0001c0002t0003g0106 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.769+7397C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111423 | |||||||
| chr5:162111433 | T | G | 1 | a0001c0001t0003g0236 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.769+7407T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111433 | |||||||
| chr5:162111489 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.769+7463A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111489 | |||||||
| chr5:162111514 | G | A | 2 | a0001c0002t0002g0021 a0001c0004t0002g0235 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.769+7488G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111514 | |||||||
| chr5:162111515 | G | T | 1 | a0001c0001t0002g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.769+7489G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111515 | |||||||
| chr5:162111811 | T | C | 2 | a0001c0001t0004g0251 a0001c0001t0004g0252 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.769+7785T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111811 | |||||||
| chr5:162111897 | A | G | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+7871A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162111897 | |||||||
| chr5:162112021 | G | C | 5 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0057 others(2): Show |
6 | HG00099.hp2 HG01106.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+7995G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112021 | |||||||
| chr5:162112128 | G | C | 196 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(193): Show |
212 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.769+8102G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112128 | |||||||
| chr5:162112260 | AT | A | 192 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(189): Show |
206 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.769+8245delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162112260 | ||||||
| chr5:162112331 | G | A | 1 | a0001c0002t0001g0102 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.769+8305G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112331 | |||||||
| chr5:162112351 | T | A | 2 | a0001c0002t0007g0083 a0001c0002t0011g0082 |
2 | NA18994.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.769+8325T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112351 | |||||||
| chr5:162112352 | G | A | 2 | a0001c0002t0007g0083 a0001c0002t0011g0082 |
2 | NA18994.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.769+8326G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112352 | |||||||
| chr5:162112381 | C | A | 1 | a0001c0003t0003g0289 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.769+8355C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112381 | |||||||
| chr5:162112409 | A | AT | 61 | a0001c0001t0003g0059 a0001c0002t0001g0102 a0001c0002t0001g0103 others(58): Show |
65 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(62): Show |
intron_variant | MODIFIER | c.769+8393dupT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162112409 | ||||||
| chr5:162112409 | AT | A | 131 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(128): Show |
143 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.769+8393delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162112409 | ||||||
| chr5:162112427 | C | T | 1 | a0001c0001t0018g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.769+8401C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112427 | |||||||
| chr5:162112638 | G | A | 1 | a0001c0003t0001g0268 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.769+8612G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112638 | |||||||
| chr5:162112876 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.769+8850G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162112876 | |||||||
| chr5:162113001 | G | A | 94 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(91): Show |
99 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.769+8975G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162113001 | |||||||
| chr5:162113283 | C | G | 131 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(128): Show |
143 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.769+9257C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162113283 | |||||||
| chr5:162113633 | A | G | 1 | a0001c0003t0001g0018 | 2 | NA18969.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.769+9607A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162113633 | |||||||
| chr5:162113794 | G | A | 1 | a0001c0001t0003g0167 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.769+9768G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162113794 | |||||||
| chr5:162114026 | C | A | 5 | a0001c0001t0002g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(2): Show |
6 | HG01109.hp1 HG02622.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+10000C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114026 | |||||||
| chr5:162114029 | T | A | 133 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(130): Show |
145 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.769+10003T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114029 | |||||||
| chr5:162114135 | A | T | 133 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(130): Show |
145 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.769+10109A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114135 | |||||||
| chr5:162114192 | C | A | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+10166C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114192 | |||||||
| chr5:162114407 | T | A | 1 | a0001c0003t0002g0281 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.769+10381T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114407 | |||||||
| chr5:162114502 | C | T | 229 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(226): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.769+10476C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114502 | |||||||
| chr5:162114645 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | NA18964.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.769+10619C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114645 | |||||||
| chr5:162114729 | G | T | 133 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(130): Show |
145 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.769+10703G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114729 | |||||||
| chr5:162114788 | T | C | 4 | a0001c0002t0006g0002 a0001c0002t0006g0149 a0001c0002t0006g0150 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+10762T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114788 | |||||||
| chr5:162114925 | C | T | 157 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(154): Show |
168 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.769+10899C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114925 | |||||||
| chr5:162114992 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0004g0144 |
2 | HG01192.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.769+10966C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162114992 | |||||||
| chr5:162115222 | A | G | 1 | a0001c0001t0018g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.769+11196A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115222 | |||||||
| chr5:162115355 | G | A | 1 | a0001c0001t0013g0194 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.769+11329G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115355 | |||||||
| chr5:162115403 | T | A | 2 | a0001c0002t0001g0189 a0001c0008t0001g0241 |
2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+11377T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115403 | |||||||
| chr5:162115603 | A | G | 31 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0136 others(28): Show |
32 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.769+11577A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115603 | |||||||
| chr5:162115805 | G | A | 132 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0113 others(129): Show |
144 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.769+11779G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115805 | |||||||
| chr5:162115844 | A | G | 4 | a0001c0001t0004g0022 a0001c0001t0004g0244 a0001c0001t0004g0245 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+11818A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115844 | |||||||
| chr5:162115849 | G | A | 157 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(154): Show |
168 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.769+11823G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115849 | |||||||
| chr5:162115905 | G | A | 1 | a0001c0002t0007g0083 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.769+11879G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115905 | |||||||
| chr5:162115910 | T | C | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+11884T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162115910 | |||||||
| chr5:162116106 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.769+12080G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116106 | |||||||
| chr5:162116109 | CAT | C | 54 | a0001c0001t0001g0129 a0001c0001t0003g0059 a0001c0001t0003g0180 others(51): Show |
57 | HG00558.hp1 HG01074.hp1 HG01258.hp1 others(54): Show |
intron_variant | MODIFIER | c.769+12084_769+1208 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116109 | |||||||
| chr5:162116109 | CATGT | C | 3 | a0001c0003t0001g0295 a0001c0003t0003g0271 a0001c0012t0003g0258 |
3 | NA18954.hp1 NA18963.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.769+12084_769+1208 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116109 | |||||||
| chr5:162116109 | CATGTGT | C | 3 | a0001c0002t0001g0140 a0001c0003t0003g0264 a0001c0003t0003g0289 |
3 | HG03492.hp2 HG04184.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.769+12084_769+1208 others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116109 | |||||||
| chr5:162116110 | A | ATG | 18 | a0001c0001t0001g0111 a0001c0001t0002g0188 a0001c0001t0003g0167 others(15): Show |
20 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+12120_769+1212 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | ||||||
| chr5:162116110 | A | ATGTG | 44 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0001g0212 others(41): Show |
48 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.769+12118_769+1212 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | ||||||
| chr5:162116110 | A | ATGTGTG | 7 | a0001c0001t0002g0027 a0001c0001t0002g0030 a0001c0001t0002g0032 others(4): Show |
7 | HG01952.hp1 HG03225.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+12116_769+1212 others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | ||||||
| chr5:162116110 | A | ATGTGTGT others(1): Show |
5 | a0001c0001t0002g0029 a0001c0001t0002g0190 a0001c0001t0004g0244 others(2): Show |
5 | HG00597.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+12114_769+1212 others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | ||||||
| chr5:162116110 | A | G | 36 | a0001c0001t0001g0109 a0001c0001t0001g0136 a0001c0001t0001g0152 others(33): Show |
38 | HG00140.hp1 HG00438.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.769+12084A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116110 | |||||||
| chr5:162116110 | ATG | A | 14 | a0001c0001t0001g0038 a0001c0001t0004g0301 a0001c0001t0004g0302 others(11): Show |
16 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.769+12120_769+1212 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | ||||||
| chr5:162116110 | ATGTG | A | 63 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0068 others(60): Show |
69 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.769+12118_769+1212 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116110 | ||||||
| chr5:162116120 | G | A | 30 | a0001c0001t0001g0109 a0001c0001t0001g0136 a0001c0001t0001g0152 others(27): Show |
31 | HG00140.hp1 HG00438.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.769+12094G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116120 | |||||||
| chr5:162116122 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0003g0180 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.769+12096G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116122 | |||||||
| chr5:162116238 | CT | C | 58 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(55): Show |
63 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.769+12213delT | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116238 | |||||||
| chr5:162116288 | ATATAAGT others(570): Show |
A | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+12265_769+1284 others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116288 | ||||||
| chr5:162116290 | A | G | 1 | a0001c0002t0006g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.769+12264A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116290 | |||||||
| chr5:162116348 | C | A | 58 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(55): Show |
63 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.769+12322C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116348 | |||||||
| chr5:162116445 | CAAAAGGG others(1): Show |
C | 58 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(55): Show |
63 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.769+12423_769+1243 others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162116445 | ||||||
| chr5:162116565 | T | C | 158 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(155): Show |
169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.769+12539T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116565 | |||||||
| chr5:162116705 | A | G | 61 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(58): Show |
67 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.769+12679A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116705 | |||||||
| chr5:162116789 | A | G | 2 | a0001c0002t0003g0096 a0001c0002t0003g0097 |
2 | NA19002.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.769+12763A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116789 | |||||||
| chr5:162116846 | G | A | 9 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 others(6): Show |
9 | HG00639.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+12820G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116846 | |||||||
| chr5:162116887 | G | C | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+12861G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116887 | |||||||
| chr5:162116933 | A | G | 1 | a0001c0001t0003g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.769+12907A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116933 | |||||||
| chr5:162116968 | T | C | 61 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(58): Show |
67 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.769+12942T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162116968 | |||||||
| chr5:162117013 | A | G | 159 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(156): Show |
170 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.769+12987A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117013 | |||||||
| chr5:162117015 | A | C | 222 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(219): Show |
238 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.769+12989A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117015 | |||||||
| chr5:162117325 | G | A | 203 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0109 others(200): Show |
218 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.769+13299G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117325 | |||||||
| chr5:162117347 | G | A | 1 | a0001c0003t0003g0269 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.769+13321G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117347 | |||||||
| chr5:162117355 | G | A | 2 | a0001c0002t0001g0189 a0001c0008t0001g0241 |
2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+13329G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117355 | |||||||
| chr5:162117413 | A | G | 1 | a0001c0001t0002g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.769+13387A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117413 | |||||||
| chr5:162117423 | T | C | 1 | a0001c0001t0003g0124 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.769+13397T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117423 | |||||||
| chr5:162117453 | A | G | 2 | a0001c0003t0001g0287 a0001c0003t0001g0292 |
2 | NA18964.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.769+13427A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117453 | |||||||
| chr5:162117492 | A | C | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+13466A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117492 | |||||||
| chr5:162117496 | T | A | 15 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0002g0250 others(12): Show |
16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+13470T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117496 | |||||||
| chr5:162117540 | T | C | 2 | a0001c0002t0002g0021 a0001c0004t0002g0235 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.769+13514T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117540 | |||||||
| chr5:162117665 | A | T | 1 | a0001c0001t0002g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.769+13639A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117665 | |||||||
| chr5:162117878 | A | G | 4 | a0001c0001t0004g0022 a0001c0001t0004g0244 a0001c0001t0004g0245 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+13852A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117878 | |||||||
| chr5:162117958 | G | A | 1 | a0001c0002t0002g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.769+13932G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117958 | |||||||
| chr5:162117959 | C | T | 1 | a0001c0001t0004g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.769+13933C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162117959 | |||||||
| chr5:162118204 | G | GGT | 3 | a0001c0001t0003g0133 a0001c0001t0016g0120 a0001c0001t0018g0091 |
3 | HG02027.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.769+14211_769+1421 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | ||||||
| chr5:162118204 | G | GGTGT | 5 | a0001c0001t0001g0238 a0001c0001t0002g0055 a0001c0001t0004g0301 others(2): Show |
5 | HG02258.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+14209_769+1421 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | ||||||
| chr5:162118204 | G | GGTGTGTG others(3): Show |
1 | a0001c0005t0015g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.769+14203_769+1421 others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | ||||||
| chr5:162118204 | G | GGTGTGTG others(5): Show |
2 | a0001c0005t0003g0033 a0001c0005t0003g0080 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.769+14201_769+1421 others(16): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | ||||||
| chr5:162118204 | GGT | G | 145 | a0001c0001t0001g0038 a0001c0001t0001g0068 a0001c0001t0001g0109 others(142): Show |
159 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.769+14211_769+1421 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | ||||||
| chr5:162118204 | GGTGT | G | 44 | a0001c0001t0001g0212 a0001c0001t0002g0026 a0001c0001t0002g0027 others(41): Show |
46 | HG00597.hp1 HG00639.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.769+14209_769+1421 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162118204 | ||||||
| chr5:162118245 | T | C | 6 | a0001c0002t0002g0009 a0001c0002t0004g0254 a0001c0005t0003g0033 others(3): Show |
7 | HG01243.hp2 HG01884.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+14219T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162118245 | |||||||
| chr5:162118755 | G | A | 2 | a0001c0001t0010g0016 a0001c0001t0010g0253 |
3 | HG03471.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.769+14729G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162118755 | |||||||
| chr5:162118789 | A | G | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+14763A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162118789 | |||||||
| chr5:162118965 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769+14939C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162118965 | |||||||
| chr5:162118987 | T | C | 1 | a0001c0001t0002g0200 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.769+14961T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162118987 | |||||||
| chr5:162119189 | C | T | 1 | a0001c0001t0003g0180 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.769+15163C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162119189 | |||||||
| chr5:162119367 | A | T | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+15341A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162119367 | |||||||
| chr5:162119566 | T | C | 25 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0036 others(22): Show |
27 | HG00438.hp2 HG02135.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.769+15540T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162119566 | |||||||
| chr5:162119815 | T | C | 85 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0001g0238 others(82): Show |
89 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.769+15789T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162119815 | |||||||
| chr5:162119980 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.769+15954C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162119980 | |||||||
| chr5:162120046 | G | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+16020G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120046 | |||||||
| chr5:162120080 | G | A | 1 | a0001c0002t0001g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.769+16054G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120080 | |||||||
| chr5:162120234 | A | T | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+16208A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120234 | |||||||
| chr5:162120376 | C | T | 1 | a0001c0004t0002g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.769+16350C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120376 | |||||||
| chr5:162120594 | C | T | 1 | a0001c0009t0004g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.769+16568C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120594 | |||||||
| chr5:162120598 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.769+16572A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120598 | |||||||
| chr5:162120696 | T | C | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.769+16670T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120696 | |||||||
| chr5:162120704 | C | A | 17 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0001g0238 others(14): Show |
19 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.769+16678C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120704 | |||||||
| chr5:162120917 | T | C | 1 | a0001c0001t0008g0067 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.769+16891T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162120917 | |||||||
| chr5:162121078 | G | A | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.769+17052G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162121078 | |||||||
| chr5:162121137 | G | C | 2 | a0001c0001t0004g0144 a0001c0002t0004g0254 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.769+17111G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162121137 | |||||||
| chr5:162121773 | G | A | 1 | a0001c0002t0006g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.769+17747G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162121773 | |||||||
| chr5:162122279 | A | G | 15 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0002g0250 others(12): Show |
16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+18253A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122279 | |||||||
| chr5:162122310 | C | T | 1 | a0001c0001t0002g0015 | 2 | NA18968.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.769+18284C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122310 | |||||||
| chr5:162122464 | T | C | 5 | a0001c0002t0001g0011 a0001c0002t0001g0173 a0001c0002t0001g0187 others(2): Show |
7 | HG01071.hp2 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+18438T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122464 | |||||||
| chr5:162122606 | C | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+18580C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122606 | |||||||
| chr5:162122757 | G | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+18731G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122757 | |||||||
| chr5:162122888 | A | T | 1 | a0001c0001t0018g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.769+18862A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162122888 | |||||||
| chr5:162123177 | A | G | 1 | a0001c0001t0009g0211 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.770-18987A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123177 | |||||||
| chr5:162123232 | G | C | 22 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(19): Show |
23 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.770-18932G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123232 | |||||||
| chr5:162123379 | A | ATGATTAT others(3): Show |
68 | a0001c0001t0003g0004 a0001c0001t0003g0028 a0001c0001t0003g0043 others(65): Show |
71 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.770-18784_770-1878 others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162123379 | ||||||
| chr5:162123397 | C | T | 1 | a0001c0002t0001g0224 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.770-18767C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123397 | |||||||
| chr5:162123420 | A | G | 22 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(19): Show |
23 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.770-18744A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123420 | |||||||
| chr5:162123551 | G | C | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-18613G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123551 | |||||||
| chr5:162123674 | G | A | 1 | a0001c0002t0007g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.770-18490G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162123674 | |||||||
| chr5:162124185 | C | T | 3 | a0001c0001t0001g0111 a0001c0002t0001g0108 a0001c0002t0001g0147 |
3 | HG01169.hp1 HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.770-17979C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162124185 | |||||||
| chr5:162124364 | A | G | 1 | a0001c0006t0012g0008 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.770-17800A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162124364 | |||||||
| chr5:162124496 | GA | G | 3 | a0001c0002t0001g0074 a0001c0002t0001g0093 a0001c0002t0001g0094 |
3 | HG00423.hp1 NA18747.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.770-17663delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124496 | ||||||
| chr5:162124764 | G | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-17400G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162124764 | |||||||
| chr5:162124774 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.770-17390C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162124774 | |||||||
| chr5:162124958 | A | ATG | 63 | a0001c0001t0001g0035 a0001c0001t0001g0068 a0001c0001t0001g0153 others(60): Show |
68 | HG00639.hp2 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.770-17170_770-1716 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | ||||||
| chr5:162124958 | A | ATGTG | 16 | a0001c0001t0001g0136 a0001c0001t0001g0152 a0001c0001t0003g0180 others(13): Show |
18 | HG01192.hp1 HG02055.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.770-17172_770-1716 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | ||||||
| chr5:162124958 | A | ATGTGTG | 16 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0003g0056 others(13): Show |
17 | HG00140.hp1 HG01074.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.770-17174_770-1716 others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | ||||||
| chr5:162124958 | A | ATGTGTGT others(1): Show |
3 | a0001c0001t0004g0245 a0001c0005t0003g0080 a0001c0009t0004g0148 |
3 | HG01884.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.770-17176_770-1716 others(12): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | ||||||
| chr5:162124958 | A | ATGTGTGT others(3): Show |
5 | a0001c0001t0003g0133 a0001c0002t0001g0157 a0001c0002t0001g0219 others(2): Show |
5 | HG01081.hp1 HG01081.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-17178_770-1716 others(14): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | ||||||
| chr5:162124958 | ATG | A | 31 | a0001c0001t0002g0058 a0001c0001t0002g0070 a0001c0001t0002g0071 others(28): Show |
35 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.770-17170_770-1716 others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | ||||||
| chr5:162124958 | ATGTG | A | 70 | a0001c0001t0001g0111 a0001c0001t0002g0005 a0001c0001t0002g0006 others(67): Show |
76 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.770-17172_770-1716 others(8): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162124958 | ||||||
| chr5:162125161 | A | G | 15 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0002g0250 others(12): Show |
16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-17003A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125161 | |||||||
| chr5:162125207 | T | A | 1 | a0001c0002t0005g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.770-16957T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125207 | |||||||
| chr5:162125219 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.770-16945C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125219 | |||||||
| chr5:162125311 | T | C | 2 | a0001c0002t0002g0021 a0001c0004t0002g0235 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.770-16853T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125311 | |||||||
| chr5:162125362 | C | T | 1 | a0001c0003t0003g0270 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.770-16802C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125362 | |||||||
| chr5:162125401 | CTGGATTC others(130): Show |
C | 6 | a0001c0001t0002g0034 a0001c0001t0002g0160 a0001c0001t0002g0161 others(3): Show |
6 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-16761_770-1662 others(4): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162125401 | ||||||
| chr5:162125405 | A | T | 12 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(9): Show |
13 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.770-16759A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125405 | |||||||
| chr5:162125622 | G | T | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.770-16542G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125622 | |||||||
| chr5:162125710 | A | G | 4 | a0001c0001t0004g0144 a0001c0005t0003g0033 a0001c0005t0003g0080 others(1): Show |
4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-16454A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125710 | |||||||
| chr5:162125833 | G | T | 11 | a0001c0002t0005g0014 a0001c0002t0005g0214 a0001c0002t0005g0215 others(8): Show |
12 | HG00639.hp2 HG01981.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.770-16331G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125833 | |||||||
| chr5:162125941 | T | C | 4 | a0001c0001t0004g0144 a0001c0005t0003g0033 a0001c0005t0003g0080 others(1): Show |
4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-16223T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162125941 | |||||||
| chr5:162126064 | A | T | 1 | a0001c0001t0004g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.770-16100A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162126064 | |||||||
| chr5:162126372 | T | C | 3 | a0001c0001t0008g0067 a0001c0001t0008g0073 a0001c0001t0008g0076 |
3 | NA18954.hp2 NA18969.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.770-15792T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162126372 | |||||||
| chr5:162126447 | T | C | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-15717T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162126447 | |||||||
| chr5:162126516 | T | C | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-15648T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162126516 | |||||||
| chr5:162127138 | T | A | 4 | a0001c0001t0003g0004 a0001c0001t0003g0167 a0001c0001t0003g0168 others(1): Show |
6 | HG02080.hp1 NA18942.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.770-15026T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127138 | |||||||
| chr5:162127180 | T | A | 1 | a0001c0003t0001g0296 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.770-14984T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127180 | |||||||
| chr5:162127276 | T | C | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-14888T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127276 | |||||||
| chr5:162127376 | T | C | 11 | a0001c0001t0001g0129 a0001c0002t0001g0001 a0001c0002t0001g0011 others(8): Show |
15 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.770-14788T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127376 | |||||||
| chr5:162127394 | A | T | 44 | a0001c0001t0003g0004 a0001c0001t0003g0028 a0001c0001t0003g0043 others(41): Show |
46 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(43): Show |
intron_variant | MODIFIER | c.770-14770A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127394 | |||||||
| chr5:162127399 | T | C | 16 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(13): Show |
17 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.770-14765T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127399 | |||||||
| chr5:162127656 | G | A | 2 | a0001c0003t0001g0272 a0001c0003t0001g0291 |
2 | NA18959.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.770-14508G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127656 | |||||||
| chr5:162127657 | T | C | 1 | a0001c0010t0003g0142 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.770-14507T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127657 | |||||||
| chr5:162127675 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-14489G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127675 | |||||||
| chr5:162127749 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.770-14415T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127749 | |||||||
| chr5:162127827 | G | C | 4 | a0001c0001t0004g0144 a0001c0005t0003g0033 a0001c0005t0003g0080 others(1): Show |
4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-14337G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127827 | |||||||
| chr5:162127913 | C | T | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-14251C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127913 | |||||||
| chr5:162127997 | C | T | 2 | a0001c0002t0002g0100 a0001c0002t0002g0101 |
2 | HG00673.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.770-14167C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162127997 | |||||||
| chr5:162128007 | A | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0109 a0001c0002t0001g0074 others(4): Show |
7 | HG00423.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.770-14157A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128007 | |||||||
| chr5:162128192 | C | T | 19 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(16): Show |
20 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.770-13972C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128192 | |||||||
| chr5:162128285 | C | A | 1 | a0001c0001t0002g0048 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.770-13879C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128285 | |||||||
| chr5:162128436 | A | G | 1 | a0001c0003t0003g0269 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.770-13728A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128436 | |||||||
| chr5:162128481 | C | G | 1 | a0001c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.770-13683C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128481 | |||||||
| chr5:162128567 | A | G | 1 | a0001c0002t0001g0189 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.770-13597A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128567 | |||||||
| chr5:162128617 | C | G | 16 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(13): Show |
17 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.770-13547C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128617 | |||||||
| chr5:162128668 | C | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-13496C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128668 | |||||||
| chr5:162128833 | A | G | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-13331A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162128833 | |||||||
| chr5:162129052 | G | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-13112G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129052 | |||||||
| chr5:162129219 | A | G | 15 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0002g0250 others(12): Show |
16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-12945A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129219 | |||||||
| chr5:162129611 | T | C | 1 | a0001c0003t0002g0261 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.770-12553T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129611 | |||||||
| chr5:162129709 | G | T | 1 | a0001c0002t0001g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.770-12455G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129709 | |||||||
| chr5:162129891 | A | C | 2 | a0001c0001t0001g0238 a0001c0006t0012g0008 |
3 | HG01069.hp1 HG01071.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.770-12273A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129891 | |||||||
| chr5:162129988 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.770-12176G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162129988 | |||||||
| chr5:162130232 | G | A | 1 | a0001c0003t0002g0286 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.770-11932G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130232 | |||||||
| chr5:162130450 | C | T | 1 | a0001c0003t0003g0269 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.770-11714C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130450 | |||||||
| chr5:162130471 | A | G | 15 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(12): Show |
16 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-11693A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130471 | |||||||
| chr5:162130733 | T | C | 4 | a0001c0001t0004g0144 a0001c0005t0003g0033 a0001c0005t0003g0080 others(1): Show |
4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-11431T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130733 | |||||||
| chr5:162130734 | G | A | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-11430G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130734 | |||||||
| chr5:162130882 | C | T | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-11282C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130882 | |||||||
| chr5:162130915 | C | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0201 |
4 | HG01106.hp1 HG01346.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-11249C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130915 | |||||||
| chr5:162130947 | A | C | 19 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(16): Show |
20 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.770-11217A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162130947 | |||||||
| chr5:162131058 | A | G | 1 | a0001c0001t0004g0244 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.770-11106A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162131058 | |||||||
| chr5:162131679 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0114 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.770-10485T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162131679 | |||||||
| chr5:162131841 | CTTGGATT others(382): Show |
C | 2 | a0001c0001t0003g0110 a0001c0001t0003g0128 |
2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.770-10321_770-9933 others(3): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162131841 | ||||||
| chr5:162131904 | A | G | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-10260A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162131904 | |||||||
| chr5:162132086 | T | C | 3 | a0001c0002t0001g0074 a0001c0002t0001g0093 a0001c0002t0001g0094 |
3 | HG00423.hp1 NA18747.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.770-10078T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132086 | |||||||
| chr5:162132235 | G | T | 2 | a0001c0001t0003g0110 a0001c0001t0003g0128 |
2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.770-9929G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132235 | |||||||
| chr5:162132236 | T | A | 2 | a0001c0001t0003g0110 a0001c0001t0003g0128 |
2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.770-9928T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132236 | |||||||
| chr5:162132352 | A | G | 2 | a0001c0003t0001g0282 a0001c0003t0001g0285 |
2 | NA18979.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.770-9812A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132352 | |||||||
| chr5:162132396 | C | T | 1 | a0001c0002t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.770-9768C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132396 | |||||||
| chr5:162132549 | G | A | 6 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 others(3): Show |
7 | HG00639.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.770-9615G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132549 | |||||||
| chr5:162132869 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.770-9295C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132869 | |||||||
| chr5:162132875 | A | T | 1 | a0001c0011t0003g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.770-9289A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162132875 | |||||||
| chr5:162133126 | C | G | 41 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0001g0238 others(38): Show |
44 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.770-9038C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133126 | |||||||
| chr5:162133212 | G | A | 1 | a0001c0002t0002g0009 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.770-8952G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133212 | |||||||
| chr5:162133218 | C | A | 1 | a0001c0001t0002g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.770-8946C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133218 | |||||||
| chr5:162133256 | T | C | 45 | a0001c0001t0003g0004 a0001c0001t0003g0028 a0001c0001t0003g0043 others(42): Show |
47 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.770-8908T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133256 | |||||||
| chr5:162133260 | C | T | 15 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0002g0250 others(12): Show |
16 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-8904C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133260 | |||||||
| chr5:162133261 | G | A | 2 | a0001c0003t0003g0293 a0001c0003t0003g0297 |
2 | HG01074.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.770-8903G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133261 | |||||||
| chr5:162133283 | C | T | 12 | a0001c0001t0001g0129 a0001c0002t0001g0001 a0001c0002t0001g0011 others(9): Show |
16 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-8881C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133283 | |||||||
| chr5:162133451 | A | T | 1 | a0001c0001t0001g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.770-8713A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133451 | |||||||
| chr5:162133463 | T | C | 1 | a0001c0001t0002g0208 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.770-8701T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133463 | |||||||
| chr5:162133512 | G | C | 22 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0029 others(19): Show |
22 | HG00558.hp2 HG00597.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.770-8652G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133512 | |||||||
| chr5:162133529 | C | T | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-8635C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133529 | |||||||
| chr5:162133539 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.770-8625A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133539 | |||||||
| chr5:162133784 | G | T | 1 | a0001c0006t0012g0008 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.770-8380G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133784 | |||||||
| chr5:162133972 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.770-8192A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162133972 | |||||||
| chr5:162134090 | TTTTG | T | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0002t0011g0082 others(4): Show |
7 | NA18944.hp1 NA18963.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.770-8066_770-8063d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162134090 | ||||||
| chr5:162134109 | A | T | 1 | a0001c0001t0003g0126 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.770-8055A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134109 | |||||||
| chr5:162134161 | CAGA | C | 22 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0029 others(19): Show |
22 | HG00558.hp2 HG00597.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.770-8000_770-7998d others(5): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162134161 | ||||||
| chr5:162134166 | G | A | 1 | a0001c0003t0001g0298 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.770-7998G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134166 | |||||||
| chr5:162134320 | T | A | 1 | a0001c0001t0002g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.770-7844T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134320 | |||||||
| chr5:162134330 | ATACT | A | 18 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(15): Show |
19 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.770-7831_770-7828d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162134330 | ||||||
| chr5:162134333 | C | T | 120 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0001g0238 others(117): Show |
129 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.770-7831C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134333 | |||||||
| chr5:162134365 | C | G | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-7799C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134365 | |||||||
| chr5:162134673 | A | T | 2 | a0001c0002t0001g0189 a0001c0008t0001g0241 |
2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.770-7491A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134673 | |||||||
| chr5:162134797 | G | T | 168 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(165): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.770-7367G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134797 | |||||||
| chr5:162134895 | C | T | 4 | a0001c0001t0002g0034 a0001c0001t0002g0171 a0001c0001t0002g0182 others(1): Show |
4 | HG02145.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-7269C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134895 | |||||||
| chr5:162134998 | C | T | 59 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(56): Show |
65 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.770-7166C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162134998 | |||||||
| chr5:162135014 | G | A | 1 | a0001c0002t0013g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.770-7150G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135014 | |||||||
| chr5:162135025 | A | G | 1 | a0001c0003t0001g0284 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.770-7139A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135025 | |||||||
| chr5:162135462 | G | T | 1 | a0001c0001t0003g0167 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.770-6702G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135462 | |||||||
| chr5:162135803 | G | A | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-6361G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135803 | |||||||
| chr5:162135833 | A | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0002t0001g0062 others(2): Show |
5 | HG01169.hp2 HG01175.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.770-6331A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135833 | |||||||
| chr5:162135854 | A | T | 1 | a0001c0001t0018g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.770-6310A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135854 | |||||||
| chr5:162135881 | A | AAAAAC | 13 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0004g0022 others(10): Show |
14 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-6265_770-6261d others(7): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162135881 | ||||||
| chr5:162135974 | G | T | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-6190G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162135974 | |||||||
| chr5:162136180 | C | T | 2 | a0001c0002t0001g0130 a0001c0002t0004g0254 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.770-5984C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136180 | |||||||
| chr5:162136275 | A | G | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-5889A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136275 | |||||||
| chr5:162136651 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0162 |
2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.770-5513A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136651 | |||||||
| chr5:162136743 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.770-5421G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136743 | |||||||
| chr5:162136819 | T | G | 1 | a0001c0002t0003g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.770-5345T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136819 | |||||||
| chr5:162136838 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.770-5326T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162136838 | |||||||
| chr5:162137178 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.770-4986G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137178 | |||||||
| chr5:162137298 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.770-4866A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137298 | |||||||
| chr5:162137440 | A | C | 300 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(297): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.770-4724A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137440 | |||||||
| chr5:162137462 | T | C | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-4702T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137462 | |||||||
| chr5:162137475 | A | G | 203 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0001g0238 others(200): Show |
216 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.770-4689A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137475 | |||||||
| chr5:162137854 | G | T | 1 | a0001c0002t0003g0010 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.770-4310G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137854 | |||||||
| chr5:162137960 | A | G | 1 | a0001c0001t0002g0066 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.770-4204A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162137960 | |||||||
| chr5:162138049 | C | T | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-4115C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138049 | |||||||
| chr5:162138134 | A | T | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-4030A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138134 | |||||||
| chr5:162138238 | G | T | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-3926G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138238 | |||||||
| chr5:162138704 | G | A | 15 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(12): Show |
16 | HG00140.hp1 HG01074.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-3460G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138704 | |||||||
| chr5:162138723 | G | C | 1 | a0001c0004t0017g0240 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.770-3441G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138723 | |||||||
| chr5:162138804 | C | T | 1 | a0001c0001t0018g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.770-3360C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138804 | |||||||
| chr5:162138806 | A | C | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-3358A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138806 | |||||||
| chr5:162138886 | G | A | 1 | a0001c0003t0002g0274 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.770-3278G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138886 | |||||||
| chr5:162138986 | C | T | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-3178C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162138986 | |||||||
| chr5:162139009 | C | T | 1 | a0001c0002t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.770-3155C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162139009 | |||||||
| chr5:162139011 | T | TA | 43 | a0001c0001t0003g0004 a0001c0001t0003g0028 a0001c0001t0003g0043 others(40): Show |
45 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.770-3142dupA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 162139011 | ||||||
| chr5:162139560 | C | A | 4 | a0001c0001t0004g0144 a0001c0005t0003g0033 a0001c0005t0003g0080 others(1): Show |
4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-2604C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162139560 | |||||||
| chr5:162140159 | A | G | 1 | a0001c0002t0001g0189 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.770-2005A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162140159 | |||||||
| chr5:162140161 | C | T | 2 | a0001c0001t0002g0057 a0001c0001t0002g0077 |
2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.770-2003C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162140161 | |||||||
| chr5:162140583 | T | G | 1 | a0001c0002t0007g0089 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.770-1581T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162140583 | |||||||
| chr5:162140623 | GAATTTAA others(1): Show |
G | 4 | a0001c0001t0002g0034 a0001c0001t0002g0171 a0001c0001t0002g0182 others(1): Show |
4 | HG02145.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-1540_770-1533d others(10): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162140623 | |||||||
| chr5:162140898 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-1266G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162140898 | |||||||
| chr5:162141061 | G | C | 2 | a0001c0003t0001g0287 a0001c0003t0001g0292 |
2 | NA18964.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.770-1103G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141061 | |||||||
| chr5:162141068 | A | G | 4 | a0001c0001t0004g0144 a0001c0005t0003g0033 a0001c0005t0003g0080 others(1): Show |
4 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-1096A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141068 | |||||||
| chr5:162141105 | C | T | 25 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0015 others(22): Show |
28 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.770-1059C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141105 | |||||||
| chr5:162141185 | C | T | 2 | a0001c0004t0017g0240 a0001c0009t0004g0148 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.770-979C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141185 | |||||||
| chr5:162141239 | G | A | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.770-925G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141239 | |||||||
| chr5:162141279 | C | T | 43 | a0001c0001t0003g0004 a0001c0001t0003g0028 a0001c0001t0003g0043 others(40): Show |
45 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.770-885C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141279 | |||||||
| chr5:162141284 | T | G | 67 | a0001c0001t0003g0004 a0001c0001t0003g0028 a0001c0001t0003g0043 others(64): Show |
70 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.770-880T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141284 | |||||||
| chr5:162141487 | C | G | 2 | a0001c0001t0002g0060 a0001c0001t0002g0065 |
2 | NA19010.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.770-677C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141487 | |||||||
| chr5:162141637 | T | C | 11 | a0001c0001t0001g0129 a0001c0002t0001g0001 a0001c0002t0001g0011 others(8): Show |
15 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.770-527T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141637 | |||||||
| chr5:162141806 | C | T | 3 | a0001c0003t0001g0268 a0001c0003t0001g0273 a0001c0003t0001g0275 |
3 | HG02683.hp2 HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.770-358C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141806 | |||||||
| chr5:162141831 | T | C | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-333T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141831 | |||||||
| chr5:162141934 | A | T | 40 | a0001c0002t0001g0050 a0001c0002t0001g0102 a0001c0002t0001g0103 others(37): Show |
43 | HG00558.hp1 HG00621.hp2 HG01258.hp1 others(40): Show |
intron_variant | MODIFIER | c.770-230A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141934 | |||||||
| chr5:162141941 | C | A | 1 | a0001c0001t0002g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.770-223C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162141941 | |||||||
| chr5:162142083 | A | G | 23 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(20): Show |
24 | HG00140.hp1 HG01074.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.770-81A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 6/9 | chr5 | 162142083 | |||||||
| chr5:162142336 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.922+20G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142336 | |||||||
| chr5:162142424 | A | C | 11 | a0001c0001t0001g0129 a0001c0002t0001g0001 a0001c0002t0001g0011 others(8): Show |
15 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.922+108A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142424 | |||||||
| chr5:162142430 | A | G | 1 | a0001c0002t0005g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.922+114A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142430 | |||||||
| chr5:162142506 | C | T | 43 | a0001c0001t0003g0004 a0001c0001t0003g0028 a0001c0001t0003g0043 others(40): Show |
45 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.922+190C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142506 | |||||||
| chr5:162142642 | C | T | 2 | a0001c0004t0017g0240 a0001c0009t0004g0148 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.922+326C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142642 | |||||||
| chr5:162142655 | A | T | 1 | a0001c0002t0011g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.922+339A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142655 | |||||||
| chr5:162142737 | C | T | 1 | a0001c0002t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.922+421C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142737 | |||||||
| chr5:162142899 | T | TA | 74 | a0001c0001t0001g0162 a0001c0001t0001g0238 a0001c0001t0002g0075 others(71): Show |
79 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.922+597dupA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162142899 | ||||||
| chr5:162142899 | T | TAA | 120 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(117): Show |
128 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.922+596_922+597dup others(2): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162142899 | ||||||
| chr5:162142946 | A | T | 11 | a0001c0002t0005g0014 a0001c0002t0005g0214 a0001c0002t0005g0215 others(8): Show |
12 | HG00639.hp2 HG01981.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.922+630A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162142946 | |||||||
| chr5:162143032 | G | A | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.922+716G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143032 | |||||||
| chr5:162143072 | G | T | 7 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 others(4): Show |
8 | HG00639.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.922+756G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143072 | |||||||
| chr5:162143175 | A | G | 1 | a0001c0001t0008g0073 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.922+859A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143175 | |||||||
| chr5:162143182 | C | T | 1 | a0001c0001t0004g0245 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.922+866C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143182 | |||||||
| chr5:162143227 | C | G | 1 | a0001c0002t0001g0119 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.922+911C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143227 | |||||||
| chr5:162143235 | C | T | 43 | a0001c0001t0003g0004 a0001c0001t0003g0028 a0001c0001t0003g0043 others(40): Show |
45 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.922+919C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143235 | |||||||
| chr5:162143262 | G | A | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.922+946G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143262 | |||||||
| chr5:162143322 | A | G | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG03927.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.922+1006A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143322 | |||||||
| chr5:162143323 | T | A | 1 | a0001c0001t0002g0048 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.922+1007T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143323 | |||||||
| chr5:162143569 | T | C | 4 | a0001c0001t0003g0124 a0001c0001t0003g0127 a0001c0001t0003g0138 others(1): Show |
4 | NA18946.hp1 NA18950.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.922+1253T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143569 | |||||||
| chr5:162143597 | A | G | 2 | a0001c0001t0004g0251 a0001c0001t0004g0252 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.922+1281A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143597 | |||||||
| chr5:162143610 | G | A | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.922+1294G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143610 | |||||||
| chr5:162143684 | A | T | 12 | a0001c0001t0001g0068 a0001c0001t0001g0136 a0001c0001t0001g0152 others(9): Show |
14 | HG00673.hp1 HG02027.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.922+1368A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143684 | |||||||
| chr5:162143745 | A | T | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.922+1429A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143745 | |||||||
| chr5:162143847 | T | C | 1 | a0001c0003t0003g0294 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.922+1531T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143847 | |||||||
| chr5:162143949 | A | G | 1 | a0001c0002t0003g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.922+1633A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162143949 | |||||||
| chr5:162144082 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.922+1766G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144082 | |||||||
| chr5:162144207 | G | C | 4 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0003t0002g0260 others(1): Show |
4 | HG02165.hp1 NA19006.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.922+1891G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144207 | |||||||
| chr5:162144222 | G | A | 1 | a0001c0002t0001g0204 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.922+1906G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144222 | |||||||
| chr5:162144240 | C | T | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.922+1924C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144240 | |||||||
| chr5:162144421 | G | C | 1 | a0001c0002t0001g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.922+2105G>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144421 | |||||||
| chr5:162144431 | A | T | 1 | a0001c0001t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.922+2115A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144431 | |||||||
| chr5:162144638 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.922+2322G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144638 | |||||||
| chr5:162144694 | A | G | 15 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(12): Show |
16 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.922+2378A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144694 | |||||||
| chr5:162144725 | G | T | 15 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(12): Show |
16 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.922+2409G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144725 | |||||||
| chr5:162144907 | C | A | 12 | a0001c0001t0001g0068 a0001c0001t0001g0136 a0001c0001t0001g0152 others(9): Show |
14 | HG00673.hp1 HG02027.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.922+2591C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144907 | |||||||
| chr5:162144941 | A | G | 7 | a0001c0002t0001g0216 a0001c0002t0001g0219 a0001c0002t0001g0220 others(4): Show |
7 | HG00735.hp1 HG01081.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.922+2625A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162144941 | |||||||
| chr5:162145039 | C | T | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.922+2723C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145039 | |||||||
| chr5:162145046 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.922+2730C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145046 | |||||||
| chr5:162145612 | T | G | 15 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(12): Show |
16 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.922+3296T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145612 | |||||||
| chr5:162145618 | A | T | 1 | a0001c0002t0001g0107 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.922+3302A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145618 | |||||||
| chr5:162145674 | A | G | 1 | a0001c0004t0002g0233 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.922+3358A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145674 | |||||||
| chr5:162145731 | A | T | 1 | a0001c0006t0012g0008 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.923-3377A>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145731 | |||||||
| chr5:162145809 | C | T | 1 | a0001c0002t0001g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.923-3299C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162145809 | |||||||
| chr5:162145946 | ATAGAACT others(717): Show |
A | 2 | a0001c0002t0001g0189 a0001c0008t0001g0241 |
2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.923-3157_923-2434d others(2): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162145946 | ||||||
| chr5:162146106 | T | C | 4 | a0001c0002t0001g0170 a0001c0002t0001g0174 a0001c0002t0001g0207 others(1): Show |
4 | HG02630.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.923-3002T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162146106 | |||||||
| chr5:162146486 | C | G | 15 | a0001c0001t0003g0056 a0001c0001t0003g0110 a0001c0001t0003g0128 others(12): Show |
16 | HG00140.hp1 HG01074.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.923-2622C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162146486 | |||||||
| chr5:162146511 | C | A | 1 | a0001c0006t0012g0008 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.923-2597C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162146511 | |||||||
| chr5:162146595 | C | T | 5 | a0001c0001t0004g0144 a0001c0002t0004g0254 a0001c0005t0003g0033 others(2): Show |
5 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.923-2513C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162146595 | |||||||
| chr5:162147195 | CTCTTTCT others(12): Show |
C | 2 | a0001c0004t0017g0240 a0001c0009t0004g0148 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.923-1901_923-1883d others(21): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162147195 | ||||||
| chr5:162147208 | T | C | 1 | a0001c0002t0001g0221 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.923-1900T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147208 | |||||||
| chr5:162147247 | CTTTA | C | 6 | a0001c0001t0002g0034 a0001c0001t0002g0160 a0001c0001t0002g0161 others(3): Show |
6 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.923-1857_923-1854d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162147247 | ||||||
| chr5:162147290 | CCTTT | C | 4 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 others(1): Show |
4 | HG00639.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.923-1805_923-1802d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162147290 | ||||||
| chr5:162147306 | TTTCC | T | 2 | a0001c0001t0001g0238 a0001c0006t0012g0008 |
3 | HG01069.hp1 HG01071.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.923-1783_923-1780d others(6): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162147306 | ||||||
| chr5:162147342 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.923-1766C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147342 | |||||||
| chr5:162147428 | G | T | 3 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 |
3 | HG02258.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.923-1680G>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147428 | |||||||
| chr5:162147458 | G | A | 8 | a0001c0001t0004g0144 a0001c0001t0004g0301 a0001c0001t0004g0302 others(5): Show |
8 | HG01192.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.923-1650G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147458 | |||||||
| chr5:162147518 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.923-1590C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147518 | |||||||
| chr5:162147544 | T | C | 2 | a0001c0001t0003g0110 a0001c0001t0003g0128 |
2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.923-1564T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147544 | |||||||
| chr5:162147552 | G | A | 6 | a0001c0002t0001g0102 a0001c0002t0001g0103 a0001c0002t0001g0104 others(3): Show |
6 | HG02074.hp2 NA18941.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.923-1556G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147552 | |||||||
| chr5:162147657 | C | A | 11 | a0001c0002t0005g0014 a0001c0002t0005g0214 a0001c0002t0005g0215 others(8): Show |
12 | HG00639.hp2 HG01981.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.923-1451C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147657 | |||||||
| chr5:162147940 | T | A | 1 | a0001c0001t0002g0046 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.923-1168T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162147940 | |||||||
| chr5:162148199 | A | C | 1 | a0001c0002t0001g0107 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923-909A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162148199 | |||||||
| chr5:162148219 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.923-889T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162148219 | |||||||
| chr5:162148435 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.923-673A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162148435 | |||||||
| chr5:162148438 | TA | T | 114 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0002g0005 others(111): Show |
122 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.923-665delA | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 162148438 | ||||||
| chr5:162148447 | T | G | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.923-661T>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162148447 | |||||||
| chr5:162148647 | G | A | 139 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0001g0238 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.923-461G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162148647 | |||||||
| chr5:162149013 | A | G | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.923-95A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 7/9 | chr5 | 162149013 | |||||||
| chr5:162149395 | A | C | 1 | a0001c0001t0003g0110 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1128+82A>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162149395 | |||||||
| chr5:162149400 | C | G | 1 | a0001c0003t0002g0286 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1128+87C>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162149400 | |||||||
| chr5:162149412 | C | A | 113 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(110): Show |
121 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1128+99C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162149412 | |||||||
| chr5:162149597 | C | T | 1 | a0001c0002t0003g0097 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1128+284C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162149597 | |||||||
| chr5:162149906 | G | A | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1128+593G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162149906 | |||||||
| chr5:162150069 | G | A | 1 | a0001c0002t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1128+756G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150069 | |||||||
| chr5:162150094 | G | A | 10 | a0001c0001t0004g0022 a0001c0001t0004g0244 a0001c0001t0004g0245 others(7): Show |
11 | HG02572.hp1 HG02615.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1128+781G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150094 | |||||||
| chr5:162150327 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1128+1014G>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150327 | |||||||
| chr5:162150639 | C | T | 1 | a0001c0002t0011g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1129-1091C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150639 | |||||||
| chr5:162150747 | A | G | 1 | a0001c0002t0001g0051 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1129-983A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150747 | |||||||
| chr5:162150896 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1129-834T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162150896 | |||||||
| chr5:162151259 | C | A | 3 | a0001c0005t0003g0033 a0001c0005t0003g0080 a0001c0005t0015g0237 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1129-471C>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162151259 | |||||||
| chr5:162151348 | C | T | 2 | a0001c0004t0005g0228 a0001c0004t0005g0229 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1129-382C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162151348 | |||||||
| chr5:162151359 | T | C | 1 | a0001c0002t0004g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1129-371T>C | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162151359 | |||||||
| chr5:162151593 | A | G | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1129-137A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 8/9 | chr5 | 162151593 | |||||||
| chr5:162151779 | C | T | 1 | a0001c0001t0010g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1152+26C>T | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | chr5 | 162151779 | |||||||
| chr5:162152143 | TACTGTTT others(4): Show |
T | 1 | a0001c0002t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1152+394_1152+404d others(13): Show |
GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 162152143 | ||||||
| chr5:162152144 | A | G | 1 | a0001c0001t0002g0012 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1152+391A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | chr5 | 162152144 | |||||||
| chr5:162152435 | A | G | 193 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(190): Show |
205 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.1153-658A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | chr5 | 162152435 | |||||||
| chr5:162152766 | A | G | 43 | a0001c0001t0003g0004 a0001c0001t0003g0028 a0001c0001t0003g0043 others(40): Show |
45 | HG00438.hp1 HG00621.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.1153-327A>G | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | chr5 | 162152766 | |||||||
| chr5:162152813 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1153-280T>A | GABRG2 | ENSG00000113327.17 | transcript | ENST00000639213.2 | protein_coding | 9/9 | chr5 | 162152813 |