Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 65983 |
| ensemblid | ENSG00000155324.10 |
| hgncid | 24911 |
| symbol | GRAMD2B |
| name | GRAM domain containing 2B |
| refseq_nuc | NM_023927.4 |
| refseq_prot | NP_076416.2 |
| ensembl_nuc | ENST00000285689.8 |
| ensembl_prot | ENSP00000285689.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 126423409 |
| end | 126494364 |
| strand | + |
| ver | v1.2 |
| region | chr5:126423409-126494364 |
| region5000 | chr5:126418409-126499364 |
| regionname0 | GRAMD2B_chr5_126423409_126494364 |
| regionname5000 | GRAMD2B_chr5_126418409_126499364 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 432 | 331 | 90 | 71 | 116 | 18 | 34 | 76 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | MTELQ others(427): Show |
chr5 | 126418409 | 126499364 |
| a0002 | 0/0 | 432 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | MTELQ others(427): Show |
chr5 | 126418409 | 126499364 |
| a0003 | 0/0 | 432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | MTELQ others(427): Show |
chr5 | 126418409 | 126499364 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1296 | 326 | 86 | 71 | 115 | 18 | 34 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | ATGAC others(1291): Show |
chr5 | 126418409 | 126499364 | ||
| a0001c0002 | 0/0 | 1296 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | ATGAC others(1291): Show |
chr5 | 126418409 | 126499364 | ||
| a0001c0004 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | ATGAC others(1291): Show |
chr5 | 126418409 | 126499364 | ||
| a0001c0006 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | ATGAC others(1291): Show |
chr5 | 126418409 | 126499364 | ||
| a0002c0003 | 0/0 | 1296 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | ATGAC others(1291): Show |
chr5 | 126418409 | 126499364 | ||
| a0003c0005 | 0/0 | 1296 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | ATGAC others(1291): Show |
chr5 | 126418409 | 126499364 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2905 | 181 | 33 | 23 | 93 | 9 | 22 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0002 | 1/0 | 2905 | 55 | 12 | 22 | 9 | 5 | 6 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0003 | 0/0 | 2906 | 50 | 15 | 17 | 10 | 4 | 4 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2901): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0004 | 0/0 | 2905 | 11 | 10 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0005 | 0/0 | 2905 | 8 | 4 | 3 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0006 | 0/0 | 2905 | 4 | 4 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0007 | 0/0 | 2906 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2901): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0008 | 0/0 | 2905 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0009 | 0/0 | 2906 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2901): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0010 | 0/0 | 2905 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0011 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0012 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0013 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0014 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0015 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0016 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0017 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0001t0018 | 0/0 | 2873 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2868): Show |
chr5 | 126418409 | 126499364 |
| a0001c0002t0001 | 0/0 | 2905 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0004t0001 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0001c0006t0001 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0002c0003t0001 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| a0002c0003t0003 | 0/0 | 2906 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2901): Show |
chr5 | 126418409 | 126499364 |
| a0003c0005t0002 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | AATCG others(2900): Show |
chr5 | 126418409 | 126499364 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0006g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0009g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0011g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0012g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0013g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0014g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0015g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0016g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0017g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0018g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0006t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0002c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0002c0003t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0003c0005t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0306 | EUR | GBR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0108 | EUR | GBR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | GBR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | FIN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0078 | EUR | FIN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0098 | EUR | FIN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0269 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00738 | hp1 | a0001 | c0001 | t0009 | g0008 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00738 | hp2 | a0001 | c0001 | t0016 | g0027 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0188 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0189 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0008 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0025 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0268 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0304 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0312 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0015 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0315 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01981 | hp2 | a0001 | c0001 | t0013 | g0053 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0254 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0319 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02074 | hp1 | a0001 | c0001 | t0010 | g0168 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02135 | hp1 | a0001 | c0006 | t0001 | g0060 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02257 | hp2 | a0002 | c0003 | t0003 | g0283 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02273 | hp1 | a0003 | c0005 | t0002 | g0217 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0294 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0293 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0137 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0292 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0303 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0287 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0320 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0179 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0321 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0177 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0214 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03942 | hp2 | a0001 | c0001 | t0014 | g0034 | SAS | BEB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0296 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0182 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19066 | hp2 | a0001 | c0001 | t0010 | g0126 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19084 | hp2 | a0001 | c0001 | t0018 | g0198 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | ASW | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ASW | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | TSI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | TSI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | TSI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | GIH | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | GIH | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0274 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0113 | AFR | USA | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | USA | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | USA | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | USA | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0014 | REF | REF | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0172 | REF | REF | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126485737 | C | T | 1 | a0003 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.1022C>T | p.Pro341Leu | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/14 | 1220/2905 | 1022/1299 | 341/432 | chr5 | 126485737 | |||
| chr5:126488806 | G | A | 1 | a0002 | 2 | HG02257.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.1171G>A | p.Ala391Thr | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/14 | 1369/2905 | 1171/1299 | 391/432 | chr5 | 126488806 | |||
| chr5:126494364 | A | G | 1 | a0001 | 11 | HG00642.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
splice_region_variant | LOW | c.*1408A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | chr5 | 126494364 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126477712 | G | A | 1 | a0001c0004 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.507G>A | p.Ser169Ser | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/14 | 705/2905 | 507/1299 | 169/432 | chr5 | 126477712 | |||
| chr5:126477730 | A | G | 1 | a0001c0002 | 3 | HG02055.hp1 HG02976.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.525A>G | p.Lys175Lys | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/14 | 723/2905 | 525/1299 | 175/432 | chr5 | 126477730 | |||
| chr5:126484424 | A | G | 1 | a0001c0006 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.870A>G | p.Gln290Gln | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/14 | 1068/2905 | 870/1299 | 290/432 | chr5 | 126484424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126423439 | G | C | 1 | a0001c0001t0011 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-168G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/14 | 168 | chr5 | 126423439 | ||||||
| chr5:126423478 | TGGGCGGA others(26): Show |
T | 1 | a0001c0001t0018 | 1 | NA19084.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128_-96delGGGCGGA others(26): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/14 | 96 | chr5 | 126423478 | ||||||
| chr5:126423533 | A | C | 1 | a0001c0001t0017 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/14 | 74 | chr5 | 126423533 | ||||||
| chr5:126423537 | A | G | 1 | a0001c0001t0016 | 1 | HG00738.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/14 | chr5 | 126423537 | |||||||
| chr5:126423553 | C | A | 2 | a0001c0001t0008 a0001c0001t0012 |
3 | HG01243.hp2 HG03540.hp1 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-54C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/14 | 54 | chr5 | 126423553 | ||||||
| chr5:126493111 | A | G | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(17): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*155A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 155 | chr5 | 126493111 | ||||||
| chr5:126493231 | C | T | 1 | a0001c0001t0010 | 2 | HG02074.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*275C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 275 | chr5 | 126493231 | ||||||
| chr5:126493337 | C | T | 1 | a0001c0001t0013 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*381C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 381 | chr5 | 126493337 | ||||||
| chr5:126493392 | A | G | 1 | a0001c0001t0015 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 436 | chr5 | 126493392 | ||||||
| chr5:126493429 | C | T | 1 | a0001c0001t0005 | 8 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*473C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 473 | chr5 | 126493429 | ||||||
| chr5:126493487 | C | T | 2 | a0001c0001t0006 a0001c0001t0012 |
5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*531C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 531 | chr5 | 126493487 | ||||||
| chr5:126493535 | C | A | 1 | a0001c0001t0009 | 2 | HG00738.hp1 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*579C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 579 | chr5 | 126493535 | ||||||
| chr5:126493600 | G | A | 1 | a0001c0001t0007 | 3 | HG02615.hp2 HG03225.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*644G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 644 | chr5 | 126493600 | ||||||
| chr5:126493720 | A | C | 1 | a0001c0001t0014 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*764A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 764 | chr5 | 126493720 | ||||||
| chr5:126493738 | T | G | 1 | a0001c0001t0014 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*782T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 782 | chr5 | 126493738 | ||||||
| chr5:126493812 | T | G | 2 | a0001c0001t0006 a0001c0001t0012 |
5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*856T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 856 | chr5 | 126493812 | ||||||
| chr5:126494320 | A | C | 1 | a0001c0001t0004 | 11 | HG00642.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1364A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 1364 | chr5 | 126494320 | ||||||
| chr5:126494322 | C | T | 1 | a0001c0001t0004 | 11 | HG00642.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1366C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 1366 | chr5 | 126494322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126423832 | A | ACT | 110 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(107): Show |
114 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.83+154_83+155dupCT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126423832 | ||||||
| chr5:126424245 | T | C | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
48 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.83+556T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424245 | |||||||
| chr5:126424278 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.83+589T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424278 | |||||||
| chr5:126424330 | C | T | 35 | a0001c0001t0001g0115 a0001c0001t0001g0295 a0001c0001t0001g0297 others(32): Show |
37 | HG00099.hp1 HG00733.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.83+641C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424330 | |||||||
| chr5:126424350 | CT | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(6): Show |
10 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.83+662delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424350 | |||||||
| chr5:126424472 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.83+783G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424472 | |||||||
| chr5:126424474 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0004g0161 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.83+785T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424474 | |||||||
| chr5:126424557 | G | A | 3 | a0001c0001t0008g0023 a0001c0001t0008g0024 a0001c0001t0012g0025 |
3 | HG01243.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.83+868G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424557 | |||||||
| chr5:126424626 | A | G | 3 | a0001c0001t0007g0293 a0001c0001t0017g0294 a0001c0004t0001g0292 |
3 | HG02451.hp2 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.83+937A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424626 | |||||||
| chr5:126424696 | A | G | 276 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(273): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.83+1007A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424696 | |||||||
| chr5:126425030 | T | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0026 others(72): Show |
76 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.83+1341T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425030 | |||||||
| chr5:126425038 | G | T | 9 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(6): Show |
9 | HG02257.hp2 HG02280.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+1349G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425038 | |||||||
| chr5:126425087 | A | C | 17 | a0001c0001t0001g0159 a0001c0001t0001g0279 a0001c0001t0001g0280 others(14): Show |
17 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+1398A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425087 | |||||||
| chr5:126425117 | T | C | 1 | a0001c0001t0007g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.83+1428T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425117 | |||||||
| chr5:126425131 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83+1442A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425131 | |||||||
| chr5:126425348 | C | T | 18 | a0001c0001t0001g0159 a0001c0001t0001g0279 a0001c0001t0001g0280 others(15): Show |
18 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.83+1659C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425348 | |||||||
| chr5:126425533 | G | A | 74 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0026 others(71): Show |
75 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.83+1844G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425533 | |||||||
| chr5:126425543 | G | A | 18 | a0001c0001t0001g0121 a0001c0001t0001g0159 a0001c0001t0001g0279 others(15): Show |
18 | HG00621.hp1 HG02109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.83+1854G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425543 | |||||||
| chr5:126425875 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.83+2186G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425875 | |||||||
| chr5:126425898 | G | A | 1 | a0001c0001t0006g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.83+2209G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425898 | |||||||
| chr5:126425985 | T | A | 270 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(267): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.83+2296T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425985 | |||||||
| chr5:126426332 | A | G | 13 | a0001c0001t0001g0121 a0001c0001t0001g0159 a0001c0001t0001g0272 others(10): Show |
14 | HG00621.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.83+2643A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426332 | |||||||
| chr5:126426455 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0002g0281 a0001c0001t0002g0291 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+2766C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426455 | |||||||
| chr5:126426608 | A | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(10): Show |
14 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.83+2919A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426608 | |||||||
| chr5:126426757 | T | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(155): Show |
162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.83+3068T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426757 | |||||||
| chr5:126426795 | C | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(8): Show |
12 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.83+3106C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426795 | |||||||
| chr5:126426826 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.83+3137C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426826 | |||||||
| chr5:126426880 | C | T | 5 | a0001c0001t0003g0140 a0001c0001t0003g0142 a0001c0001t0008g0024 others(2): Show |
5 | HG01243.hp2 HG02055.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+3191C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426880 | |||||||
| chr5:126426933 | A | T | 10 | a0001c0001t0001g0230 a0001c0001t0001g0263 a0001c0001t0001g0284 others(7): Show |
10 | HG01255.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.83+3244A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426933 | |||||||
| chr5:126426937 | A | C | 1 | a0001c0001t0001g0227 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.83+3248A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426937 | |||||||
| chr5:126426944 | G | A | 1 | a0001c0001t0006g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.83+3255G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426944 | |||||||
| chr5:126427039 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.83+3350C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427039 | |||||||
| chr5:126427045 | G | A | 111 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0017 others(108): Show |
113 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.83+3356G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427045 | |||||||
| chr5:126427159 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0004g0161 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.83+3470C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427159 | |||||||
| chr5:126427231 | A | G | 80 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(77): Show |
81 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.83+3542A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427231 | |||||||
| chr5:126427387 | G | GA | 176 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(173): Show |
181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.83+3699dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126427387 | ||||||
| chr5:126427437 | C | T | 14 | a0001c0001t0001g0230 a0001c0001t0001g0235 a0001c0001t0001g0263 others(11): Show |
14 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.83+3748C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427437 | |||||||
| chr5:126427498 | A | G | 2 | a0001c0001t0007g0293 a0001c0004t0001g0292 |
2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.83+3809A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427498 | |||||||
| chr5:126427859 | T | G | 2 | a0001c0001t0001g0033 a0001c0001t0014g0034 |
2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.83+4170T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427859 | |||||||
| chr5:126428094 | G | C | 2 | a0001c0001t0003g0143 a0001c0001t0003g0144 |
2 | NA18940.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.83+4405G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428094 | |||||||
| chr5:126428220 | A | G | 3 | a0001c0001t0001g0322 a0001c0001t0003g0158 a0001c0001t0003g0232 |
3 | HG01106.hp2 HG02257.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.83+4531A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428220 | |||||||
| chr5:126428447 | G | T | 74 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(71): Show |
75 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.83+4758G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428447 | |||||||
| chr5:126428471 | A | G | 79 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(76): Show |
80 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.83+4782A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428471 | |||||||
| chr5:126428482 | T | G | 6 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0282 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+4793T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428482 | |||||||
| chr5:126428729 | G | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(44): Show |
49 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.83+5040G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428729 | |||||||
| chr5:126428810 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(145): Show |
151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.83+5121G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428810 | |||||||
| chr5:126428815 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(53): Show |
58 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.83+5126G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428815 | |||||||
| chr5:126428911 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0003g0236 a0001c0001t0003g0237 |
3 | HG01069.hp1 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.83+5222A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428911 | |||||||
| chr5:126428934 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.83+5245T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428934 | |||||||
| chr5:126428936 | C | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(132): Show |
138 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.83+5247C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428936 | |||||||
| chr5:126428959 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.83+5270C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428959 | |||||||
| chr5:126429078 | A | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0270 a0001c0001t0003g0325 |
3 | HG02155.hp1 NA18973.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.83+5389A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429078 | |||||||
| chr5:126429119 | A | G | 1 | a0001c0001t0008g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.83+5430A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429119 | |||||||
| chr5:126429286 | A | C | 15 | a0001c0001t0001g0120 a0001c0001t0001g0276 a0001c0001t0001g0288 others(12): Show |
16 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.83+5597A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429286 | |||||||
| chr5:126429333 | T | G | 3 | a0001c0001t0001g0235 a0001c0001t0003g0236 a0001c0001t0003g0237 |
3 | HG01069.hp1 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.83+5644T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429333 | |||||||
| chr5:126429506 | A | G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(18): Show |
22 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.83+5817A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429506 | |||||||
| chr5:126429647 | T | C | 3 | a0001c0001t0001g0235 a0001c0001t0003g0236 a0001c0001t0003g0237 |
3 | HG01069.hp1 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.83+5958T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429647 | |||||||
| chr5:126429726 | C | T | 7 | a0001c0001t0001g0159 a0001c0001t0001g0279 a0001c0001t0001g0280 others(4): Show |
7 | HG02280.hp2 HG02970.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+6037C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429726 | |||||||
| chr5:126429906 | A | C | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+6217A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429906 | |||||||
| chr5:126430031 | C | G | 1 | a0001c0001t0002g0004 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.83+6342C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430031 | |||||||
| chr5:126430203 | G | A | 65 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0033 others(62): Show |
66 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.83+6514G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430203 | |||||||
| chr5:126430342 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.83+6653G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430342 | |||||||
| chr5:126430487 | T | G | 198 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(195): Show |
204 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.83+6798T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430487 | |||||||
| chr5:126430656 | C | T | 157 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(154): Show |
162 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.83+6967C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430656 | |||||||
| chr5:126430665 | C | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(44): Show |
48 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.83+6976C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430665 | |||||||
| chr5:126430671 | A | G | 1 | a0001c0001t0003g0321 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.83+6982A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430671 | |||||||
| chr5:126430722 | G | A | 5 | a0001c0001t0001g0117 a0001c0001t0001g0125 a0001c0001t0001g0127 others(2): Show |
5 | HG00621.hp2 HG02056.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+7033G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430722 | |||||||
| chr5:126430729 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.83+7040A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430729 | |||||||
| chr5:126430738 | G | A | 10 | a0001c0001t0001g0118 a0001c0001t0001g0181 a0001c0001t0001g0282 others(7): Show |
10 | HG02109.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+7049G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430738 | |||||||
| chr5:126430741 | T | A | 10 | a0001c0001t0001g0118 a0001c0001t0001g0181 a0001c0001t0001g0282 others(7): Show |
10 | HG02109.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+7052T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430741 | |||||||
| chr5:126430803 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.83+7114T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430803 | |||||||
| chr5:126430925 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.83+7236T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430925 | |||||||
| chr5:126431051 | C | T | 10 | a0001c0001t0001g0118 a0001c0001t0001g0181 a0001c0001t0001g0282 others(7): Show |
10 | HG02109.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+7362C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431051 | |||||||
| chr5:126431108 | C | G | 10 | a0001c0001t0001g0118 a0001c0001t0001g0181 a0001c0001t0001g0282 others(7): Show |
10 | HG02109.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+7419C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431108 | |||||||
| chr5:126431133 | C | A | 1 | a0001c0001t0007g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+7444C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431133 | |||||||
| chr5:126431134 | G | T | 1 | a0001c0001t0001g0318 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.83+7445G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431134 | |||||||
| chr5:126431424 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
85 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.83+7735T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431424 | |||||||
| chr5:126431432 | T | C | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+7743T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431432 | |||||||
| chr5:126431494 | C | T | 17 | a0001c0001t0001g0230 a0001c0001t0001g0263 a0001c0001t0001g0265 others(14): Show |
17 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+7805C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431494 | |||||||
| chr5:126431553 | C | G | 10 | a0001c0001t0001g0118 a0001c0001t0001g0181 a0001c0001t0001g0282 others(7): Show |
10 | HG02109.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+7864C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431553 | |||||||
| chr5:126431603 | A | G | 1 | a0001c0001t0007g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+7914A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431603 | |||||||
| chr5:126431623 | G | A | 2 | a0001c0001t0001g0282 a0001c0001t0002g0281 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.83+7934G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431623 | |||||||
| chr5:126431773 | G | GA | 50 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(47): Show |
52 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.83+8092dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126431773 | ||||||
| chr5:126431913 | C | T | 1 | a0001c0001t0003g0296 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.83+8224C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431913 | |||||||
| chr5:126432089 | T | C | 4 | a0001c0001t0001g0129 a0001c0001t0002g0132 a0001c0001t0004g0130 others(1): Show |
4 | HG02886.hp1 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+8400T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432089 | |||||||
| chr5:126432129 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0005g0139 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+8440A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432129 | |||||||
| chr5:126432156 | T | G | 98 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(95): Show |
102 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.83+8467T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432156 | |||||||
| chr5:126432221 | A | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(197): Show |
207 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.83+8532A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432221 | |||||||
| chr5:126432328 | C | T | 95 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(92): Show |
97 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.83+8639C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432328 | |||||||
| chr5:126432559 | C | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(45): Show |
50 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.83+8870C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432559 | |||||||
| chr5:126432608 | T | G | 1 | a0001c0001t0003g0184 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.83+8919T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432608 | |||||||
| chr5:126432715 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0005g0139 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+9026C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432715 | |||||||
| chr5:126432775 | G | T | 2 | a0001c0001t0001g0175 a0001c0001t0005g0139 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+9086G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432775 | |||||||
| chr5:126432790 | A | G | 1 | a0001c0001t0003g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.83+9101A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432790 | |||||||
| chr5:126432808 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.83+9119G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432808 | |||||||
| chr5:126432838 | A | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(46): Show |
51 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.83+9149A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432838 | |||||||
| chr5:126433084 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG00280.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.83+9395G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433084 | |||||||
| chr5:126433104 | T | C | 2 | a0001c0001t0003g0015 a0001c0001t0003g0016 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.83+9415T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433104 | |||||||
| chr5:126433207 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(46): Show |
51 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.83+9518G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433207 | |||||||
| chr5:126433358 | A | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(8): Show |
12 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.83+9669A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433358 | |||||||
| chr5:126433423 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.83+9734C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433423 | |||||||
| chr5:126433468 | G | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(181): Show |
189 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.83+9779G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433468 | |||||||
| chr5:126433685 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83+9996C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433685 | |||||||
| chr5:126433987 | C | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(189): Show |
198 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.83+10298C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433987 | |||||||
| chr5:126434066 | A | G | 1 | a0001c0001t0002g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.83+10377A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434066 | |||||||
| chr5:126434284 | T | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(184): Show |
192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.83+10595T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434284 | |||||||
| chr5:126434287 | A | G | 4 | a0001c0001t0003g0102 a0001c0001t0004g0269 a0001c0001t0005g0268 others(1): Show |
4 | HG00642.hp1 HG01257.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+10598A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434287 | |||||||
| chr5:126434377 | A | G | 7 | a0001c0001t0001g0273 a0001c0001t0002g0291 a0001c0001t0003g0102 others(4): Show |
7 | HG00642.hp1 HG01257.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+10688A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434377 | |||||||
| chr5:126434386 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.83+10697T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434386 | |||||||
| chr5:126434387 | A | G | 3 | a0001c0001t0001g0300 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | HG00642.hp2 HG01070.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.83+10698A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434387 | |||||||
| chr5:126434424 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.83+10735A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434424 | |||||||
| chr5:126434492 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(44): Show |
49 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.83+10803C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434492 | |||||||
| chr5:126434508 | T | TTTTTTA | 20 | a0001c0001t0001g0118 a0001c0001t0001g0230 a0001c0001t0001g0263 others(17): Show |
20 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.83+10837_83+10842d others(8): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126434508 | ||||||
| chr5:126434531 | T | G | 2 | a0001c0001t0001g0136 a0001c0001t0005g0137 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.83+10842T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434531 | |||||||
| chr5:126434626 | A | T | 7 | a0001c0001t0001g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(4): Show |
7 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+10937A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434626 | |||||||
| chr5:126434731 | A | G | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(10): Show |
14 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.83+11042A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434731 | |||||||
| chr5:126434807 | G | A | 33 | a0001c0001t0001g0011 a0001c0001t0001g0129 a0001c0001t0001g0136 others(30): Show |
33 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.83+11118G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434807 | |||||||
| chr5:126435141 | G | T | 53 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(50): Show |
56 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.83+11452G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435141 | |||||||
| chr5:126435260 | T | G | 1 | a0001c0001t0004g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.83+11571T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435260 | |||||||
| chr5:126435506 | C | T | 5 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG00621.hp2 NA18965.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+11817C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435506 | |||||||
| chr5:126435547 | C | G | 53 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(50): Show |
56 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.83+11858C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435547 | |||||||
| chr5:126435623 | T | C | 1 | a0001c0001t0007g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+11934T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435623 | |||||||
| chr5:126435811 | C | G | 25 | a0001c0001t0001g0011 a0001c0001t0001g0129 a0001c0001t0001g0136 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.83+12122C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435811 | |||||||
| chr5:126435813 | T | C | 22 | a0001c0001t0001g0120 a0001c0001t0001g0276 a0001c0001t0001g0284 others(19): Show |
24 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.83+12124T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435813 | |||||||
| chr5:126435922 | G | C | 43 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0230 others(40): Show |
45 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(42): Show |
intron_variant | MODIFIER | c.83+12233G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435922 | |||||||
| chr5:126435947 | C | A | 1 | a0001c0001t0003g0278 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.83+12258C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435947 | |||||||
| chr5:126435989 | T | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(10): Show |
14 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.83+12300T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435989 | |||||||
| chr5:126436070 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.83+12381A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436070 | |||||||
| chr5:126436153 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.83+12464A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436153 | |||||||
| chr5:126436190 | A | G | 9 | a0001c0001t0001g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(6): Show |
9 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+12501A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436190 | |||||||
| chr5:126436358 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83+12669A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436358 | |||||||
| chr5:126436459 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0077 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.83+12770G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436459 | |||||||
| chr5:126436601 | C | G | 5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+12912C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436601 | |||||||
| chr5:126437015 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83+13326G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437015 | |||||||
| chr5:126437016 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83+13327C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437016 | |||||||
| chr5:126437146 | G | A | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0190 others(8): Show |
11 | HG00280.hp1 HG00558.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+13457G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437146 | |||||||
| chr5:126437309 | G | A | 8 | a0001c0001t0001g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(5): Show |
8 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+13620G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437309 | |||||||
| chr5:126437313 | T | C | 1 | a0001c0001t0003g0325 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.83+13624T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437313 | |||||||
| chr5:126437317 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.83+13628T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437317 | |||||||
| chr5:126437325 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.83+13636G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437325 | |||||||
| chr5:126437472 | A | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(45): Show |
50 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.83+13783A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437472 | |||||||
| chr5:126437639 | A | C | 210 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(207): Show |
216 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.83+13950A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437639 | |||||||
| chr5:126437641 | C | T | 8 | a0001c0001t0001g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(5): Show |
8 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+13952C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437641 | |||||||
| chr5:126437696 | A | T | 9 | a0001c0001t0001g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(6): Show |
9 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+14007A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437696 | |||||||
| chr5:126437763 | G | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0324 |
3 | NA18965.hp1 NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.83+14074G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437763 | |||||||
| chr5:126437817 | C | G | 29 | a0001c0001t0001g0011 a0001c0001t0001g0129 a0001c0001t0001g0136 others(26): Show |
30 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.83+14128C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437817 | |||||||
| chr5:126437878 | G | A | 50 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(47): Show |
52 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.83+14189G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437878 | |||||||
| chr5:126438463 | G | A | 64 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0033 others(61): Show |
65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.83+14774G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126438463 | |||||||
| chr5:126438780 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.83+15091T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126438780 | |||||||
| chr5:126438783 | T | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(9): Show |
13 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.83+15094T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126438783 | |||||||
| chr5:126438830 | A | G | 88 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(85): Show |
91 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(88): Show |
intron_variant | MODIFIER | c.83+15141A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126438830 | |||||||
| chr5:126439009 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(9): Show |
13 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.83+15320G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439009 | |||||||
| chr5:126439078 | A | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+15389A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439078 | |||||||
| chr5:126439328 | C | CT | 15 | a0001c0001t0001g0012 a0001c0001t0001g0071 a0001c0001t0001g0263 others(12): Show |
15 | HG00735.hp2 HG01109.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.83+15656dupT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126439328 | ||||||
| chr5:126439328 | C | CTTTTT | 26 | a0001c0001t0001g0265 a0001c0001t0001g0276 a0001c0001t0001g0284 others(23): Show |
27 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.83+15652_83+15656d others(7): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126439328 | ||||||
| chr5:126439328 | C | CTTTTTT | 24 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0138 others(21): Show |
24 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.83+15651_83+15656d others(8): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126439328 | ||||||
| chr5:126439372 | G | A | 4 | a0001c0001t0003g0102 a0001c0001t0004g0269 a0001c0001t0005g0268 others(1): Show |
4 | HG00642.hp1 HG01257.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+15683G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439372 | |||||||
| chr5:126439374 | T | G | 1 | a0001c0001t0003g0074 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.83+15685T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439374 | |||||||
| chr5:126439378 | G | A | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+15689G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439378 | |||||||
| chr5:126439540 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.83+15851G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439540 | |||||||
| chr5:126439559 | C | A | 1 | a0001c0001t0002g0194 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.83+15870C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439559 | |||||||
| chr5:126439748 | T | C | 88 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(85): Show |
91 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(88): Show |
intron_variant | MODIFIER | c.83+16059T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439748 | |||||||
| chr5:126439785 | C | T | 20 | a0001c0001t0001g0120 a0001c0001t0001g0276 a0001c0001t0001g0284 others(17): Show |
21 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.83+16096C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439785 | |||||||
| chr5:126440058 | T | C | 9 | a0001c0001t0001g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(6): Show |
9 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+16369T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440058 | |||||||
| chr5:126440244 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(43): Show |
48 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.83+16555G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440244 | |||||||
| chr5:126440270 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.83+16581T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440270 | |||||||
| chr5:126440376 | T | C | 9 | a0001c0001t0001g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(6): Show |
9 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+16687T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440376 | |||||||
| chr5:126440483 | T | C | 31 | a0001c0001t0001g0120 a0001c0001t0001g0265 a0001c0001t0001g0276 others(28): Show |
33 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.83+16794T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440483 | |||||||
| chr5:126440494 | A | AT | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+16809dupT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126440494 | ||||||
| chr5:126440574 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+16885G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440574 | |||||||
| chr5:126440596 | CA | C | 8 | a0001c0001t0001g0230 a0001c0001t0001g0263 a0001c0001t0001g0273 others(5): Show |
8 | HG01255.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+16909delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126440596 | ||||||
| chr5:126440658 | A | G | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+16969A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440658 | |||||||
| chr5:126440660 | T | C | 1 | a0002c0003t0003g0283 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.83+16971T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440660 | |||||||
| chr5:126440733 | A | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(9): Show |
13 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.83+17044A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440733 | |||||||
| chr5:126440735 | T | C | 31 | a0001c0001t0001g0120 a0001c0001t0001g0265 a0001c0001t0001g0276 others(28): Show |
33 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.83+17046T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440735 | |||||||
| chr5:126440766 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.83+17077A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440766 | |||||||
| chr5:126440794 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(43): Show |
48 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.83+17105G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440794 | |||||||
| chr5:126440871 | C | T | 2 | a0001c0001t0003g0015 a0001c0001t0003g0016 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.83+17182C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440871 | |||||||
| chr5:126440930 | A | G | 31 | a0001c0001t0001g0120 a0001c0001t0001g0265 a0001c0001t0001g0276 others(28): Show |
33 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.83+17241A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440930 | |||||||
| chr5:126441115 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.83+17426G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441115 | |||||||
| chr5:126441119 | G | A | 5 | a0001c0001t0001g0230 a0001c0001t0001g0263 a0001c0001t0001g0295 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+17430G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441119 | |||||||
| chr5:126441670 | A | G | 2 | a0001c0001t0001g0317 a0001c0001t0003g0109 |
2 | HG00735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.83+17981A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441670 | |||||||
| chr5:126441795 | C | T | 5 | a0001c0001t0001g0230 a0001c0001t0001g0263 a0001c0001t0001g0295 others(2): Show |
5 | HG01255.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+18106C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441795 | |||||||
| chr5:126441834 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.83+18145T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441834 | |||||||
| chr5:126441884 | T | C | 2 | a0001c0001t0002g0291 a0001c0001t0017g0294 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.83+18195T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441884 | |||||||
| chr5:126441991 | G | A | 1 | a0001c0001t0005g0268 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.83+18302G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441991 | |||||||
| chr5:126442293 | CT | C | 61 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(58): Show |
63 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.83+18617delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126442293 | ||||||
| chr5:126442321 | C | A | 1 | a0001c0001t0006g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.83+18632C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442321 | |||||||
| chr5:126442400 | C | T | 1 | a0002c0003t0001g0182 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.83+18711C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442400 | |||||||
| chr5:126442437 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.83+18748G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442437 | |||||||
| chr5:126442454 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83+18765G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442454 | |||||||
| chr5:126442506 | A | G | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+18817A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442506 | |||||||
| chr5:126442572 | G | A | 1 | a0001c0001t0006g0255 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.83+18883G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442572 | |||||||
| chr5:126442719 | G | A | 4 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(1): Show |
4 | NA18981.hp1 NA19072.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+19030G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442719 | |||||||
| chr5:126442857 | A | T | 9 | a0001c0001t0001g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(6): Show |
9 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+19168A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442857 | |||||||
| chr5:126442859 | A | C | 1 | a0001c0001t0002g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.83+19170A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442859 | |||||||
| chr5:126443002 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0252 a0001c0001t0003g0251 others(1): Show |
4 | HG01884.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+19313C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443002 | |||||||
| chr5:126443096 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+19407G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443096 | |||||||
| chr5:126443243 | T | C | 63 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(60): Show |
66 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.83+19554T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443243 | |||||||
| chr5:126443263 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.83+19574G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443263 | |||||||
| chr5:126443339 | A | G | 15 | a0001c0001t0001g0120 a0001c0001t0001g0276 a0001c0001t0001g0288 others(12): Show |
16 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.83+19650A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443339 | |||||||
| chr5:126443417 | T | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+19728T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443417 | |||||||
| chr5:126443488 | A | C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(45): Show |
50 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.83+19799A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443488 | |||||||
| chr5:126443659 | A | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+19970A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443659 | |||||||
| chr5:126443663 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+19974C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443663 | |||||||
| chr5:126443795 | A | T | 47 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(44): Show |
50 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.83+20106A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443795 | |||||||
| chr5:126443847 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+20158C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443847 | |||||||
| chr5:126443953 | G | A | 10 | a0001c0001t0001g0118 a0001c0001t0001g0272 a0001c0001t0001g0282 others(7): Show |
10 | HG02109.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.83+20264G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443953 | |||||||
| chr5:126443962 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.83+20273G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443962 | |||||||
| chr5:126444072 | G | T | 1 | a0001c0001t0003g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.83+20383G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444072 | |||||||
| chr5:126444173 | T | C | 25 | a0001c0001t0001g0011 a0001c0001t0001g0129 a0001c0001t0001g0136 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.83+20484T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444173 | |||||||
| chr5:126444268 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.83+20579C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444268 | |||||||
| chr5:126444400 | G | A | 11 | a0001c0001t0001g0129 a0001c0001t0001g0136 a0001c0001t0001g0138 others(8): Show |
11 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.83+20711G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444400 | |||||||
| chr5:126444422 | T | C | 88 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(85): Show |
91 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(88): Show |
intron_variant | MODIFIER | c.83+20733T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444422 | |||||||
| chr5:126444440 | T | G | 47 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(44): Show |
50 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.83+20751T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444440 | |||||||
| chr5:126444493 | T | C | 49 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(46): Show |
52 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.83+20804T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444493 | |||||||
| chr5:126444758 | G | A | 33 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0230 others(30): Show |
34 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.84-20668G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444758 | |||||||
| chr5:126444760 | C | T | 15 | a0001c0001t0001g0120 a0001c0001t0001g0276 a0001c0001t0001g0288 others(12): Show |
16 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-20666C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444760 | |||||||
| chr5:126444782 | C | A | 33 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0230 others(30): Show |
34 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.84-20644C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444782 | |||||||
| chr5:126444943 | C | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18954.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.84-20483C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444943 | |||||||
| chr5:126444943 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.84-20483C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444943 | |||||||
| chr5:126444944 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.84-20482G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444944 | |||||||
| chr5:126444974 | G | A | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-20452G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444974 | |||||||
| chr5:126444985 | A | G | 8 | a0001c0001t0001g0230 a0001c0001t0001g0263 a0001c0001t0001g0273 others(5): Show |
8 | HG01255.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-20441A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444985 | |||||||
| chr5:126445046 | C | T | 1 | a0001c0001t0003g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.84-20380C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445046 | |||||||
| chr5:126445101 | T | C | 47 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(44): Show |
50 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.84-20325T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445101 | |||||||
| chr5:126445120 | C | T | 1 | a0001c0001t0002g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.84-20306C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445120 | |||||||
| chr5:126445227 | T | A | 1 | a0001c0001t0007g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-20199T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445227 | |||||||
| chr5:126445268 | G | T | 10 | a0001c0001t0001g0118 a0001c0001t0001g0272 a0001c0001t0001g0282 others(7): Show |
10 | HG02109.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.84-20158G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445268 | |||||||
| chr5:126445519 | C | A | 1 | a0001c0001t0001g0106 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.84-19907C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445519 | |||||||
| chr5:126445522 | A | C | 53 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(50): Show |
56 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.84-19904A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445522 | |||||||
| chr5:126445995 | C | G | 109 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(106): Show |
110 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.84-19431C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445995 | |||||||
| chr5:126446062 | C | T | 1 | a0001c0001t0007g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-19364C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446062 | |||||||
| chr5:126446136 | T | A | 116 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(113): Show |
117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.84-19290T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446136 | |||||||
| chr5:126446137 | A | T | 15 | a0001c0001t0001g0120 a0001c0001t0001g0276 a0001c0001t0001g0288 others(12): Show |
16 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-19289A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446137 | |||||||
| chr5:126446195 | C | T | 9 | a0001c0001t0001g0118 a0001c0001t0001g0272 a0001c0001t0001g0282 others(6): Show |
9 | HG02109.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.84-19231C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446195 | |||||||
| chr5:126446230 | A | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(9): Show |
13 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.84-19196A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446230 | |||||||
| chr5:126446346 | A | G | 47 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(44): Show |
50 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.84-19080A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446346 | |||||||
| chr5:126446433 | C | A | 10 | a0001c0001t0001g0230 a0001c0001t0001g0263 a0001c0001t0001g0273 others(7): Show |
11 | HG01255.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.84-18993C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446433 | |||||||
| chr5:126446532 | T | G | 2 | a0001c0001t0002g0075 a0001c0001t0003g0074 |
2 | HG01074.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.84-18894T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446532 | |||||||
| chr5:126446594 | T | C | 316 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(313): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.84-18832T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446594 | |||||||
| chr5:126446620 | T | TA | 10 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0201 others(7): Show |
10 | HG00438.hp1 HG01255.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.84-18786dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126446620 | ||||||
| chr5:126446620 | TA | T | 102 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(99): Show |
103 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.84-18786delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126446620 | ||||||
| chr5:126446620 | TAA | T | 45 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(42): Show |
47 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.84-18787_84-18786d others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126446620 | ||||||
| chr5:126446620 | TAAA | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(41): Show |
46 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.84-18788_84-18786d others(5): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126446620 | ||||||
| chr5:126446634 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0008g0023 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.84-18792A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446634 | |||||||
| chr5:126446724 | G | A | 2 | a0001c0001t0001g0280 a0001c0004t0001g0292 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.84-18702G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446724 | |||||||
| chr5:126446976 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.84-18450C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446976 | |||||||
| chr5:126447104 | C | A | 24 | a0001c0001t0001g0120 a0001c0001t0001g0230 a0001c0001t0001g0263 others(21): Show |
25 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.84-18322C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447104 | |||||||
| chr5:126447166 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(42): Show |
47 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.84-18260G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447166 | |||||||
| chr5:126447189 | C | T | 9 | a0001c0001t0001g0118 a0001c0001t0001g0272 a0001c0001t0001g0282 others(6): Show |
9 | HG02109.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.84-18237C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447189 | |||||||
| chr5:126447385 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(44): Show |
49 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.84-18041G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447385 | |||||||
| chr5:126447453 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.84-17973A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447453 | |||||||
| chr5:126447458 | T | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.84-17968T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447458 | |||||||
| chr5:126447478 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.84-17948C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447478 | |||||||
| chr5:126447525 | G | A | 125 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(122): Show |
126 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.84-17901G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447525 | |||||||
| chr5:126447551 | C | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
61 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.84-17875C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447551 | |||||||
| chr5:126447557 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.84-17869A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447557 | |||||||
| chr5:126447613 | G | A | 122 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(119): Show |
123 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.84-17813G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447613 | |||||||
| chr5:126447630 | C | G | 2 | a0001c0001t0002g0291 a0001c0001t0017g0294 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84-17796C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447630 | |||||||
| chr5:126447642 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.84-17784C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447642 | |||||||
| chr5:126447650 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.84-17776C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447650 | |||||||
| chr5:126447651 | A | G | 1 | a0001c0001t0002g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.84-17775A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447651 | |||||||
| chr5:126447658 | C | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(41): Show |
46 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.84-17768C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447658 | |||||||
| chr5:126447671 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.84-17755G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447671 | |||||||
| chr5:126447671 | G | GA | 122 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(119): Show |
123 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.84-17740dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126447671 | ||||||
| chr5:126447671 | G | GAAA | 35 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(32): Show |
38 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.84-17742_84-17740d others(5): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126447671 | ||||||
| chr5:126447687 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.84-17739G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447687 | |||||||
| chr5:126447698 | G | C | 2 | a0001c0001t0001g0280 a0001c0004t0001g0292 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.84-17728G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447698 | |||||||
| chr5:126447703 | C | T | 5 | a0001c0001t0001g0262 a0001c0001t0002g0308 a0001c0001t0002g0310 others(2): Show |
5 | HG00140.hp2 HG01109.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-17723C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447703 | |||||||
| chr5:126447754 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0022 others(1): Show |
5 | HG01069.hp2 HG01106.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-17672T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447754 | |||||||
| chr5:126447761 | T | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-17665T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447761 | |||||||
| chr5:126447873 | TTTAA | T | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(10): Show |
14 | HG00558.hp1 HG01069.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.84-17552_84-17549d others(6): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447873 | |||||||
| chr5:126447874 | TTAA | T | 24 | a0001c0001t0001g0120 a0001c0001t0001g0230 a0001c0001t0001g0263 others(21): Show |
25 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.84-17551_84-17549d others(5): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447874 | |||||||
| chr5:126447875 | TA | T | 5 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0002g0056 others(2): Show |
6 | HG02735.hp1 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.84-17545delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126447875 | ||||||
| chr5:126447875 | TAA | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(43): Show |
48 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.84-17546_84-17545d others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126447875 | ||||||
| chr5:126447876 | A | T | 113 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(110): Show |
114 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.84-17550A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447876 | |||||||
| chr5:126447877 | A | T | 3 | a0001c0001t0002g0070 a0001c0001t0003g0162 a0001c0001t0006g0006 |
4 | HG02300.hp1 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-17549A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447877 | |||||||
| chr5:126447882 | T | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-17544T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447882 | |||||||
| chr5:126447920 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-17506C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447920 | |||||||
| chr5:126447927 | T | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-17499T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447927 | |||||||
| chr5:126447948 | C | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(41): Show |
46 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.84-17478C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447948 | |||||||
| chr5:126448000 | C | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-17426C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448000 | |||||||
| chr5:126448006 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0302 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.84-17420T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448006 | |||||||
| chr5:126448034 | AT | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-17386delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126448034 | ||||||
| chr5:126448063 | G | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-17363G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448063 | |||||||
| chr5:126448133 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-17293A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448133 | |||||||
| chr5:126448185 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-17241C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448185 | |||||||
| chr5:126448278 | A | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
89 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.84-17148A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448278 | |||||||
| chr5:126448357 | G | A | 2 | a0001c0001t0002g0305 a0001c0001t0003g0304 |
2 | HG01074.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.84-17069G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448357 | |||||||
| chr5:126448509 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0002g0205 |
2 | HG02602.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.84-16917G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448509 | |||||||
| chr5:126448539 | T | C | 4 | a0001c0001t0003g0140 a0001c0001t0003g0142 a0001c0001t0003g0319 others(1): Show |
4 | HG01243.hp2 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-16887T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448539 | |||||||
| chr5:126448590 | G | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(8): Show |
12 | HG00558.hp1 HG01069.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.84-16836G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448590 | |||||||
| chr5:126448596 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(83): Show |
91 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.84-16830A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448596 | |||||||
| chr5:126448667 | C | G | 1 | a0001c0001t0003g0074 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.84-16759C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448667 | |||||||
| chr5:126448766 | G | A | 1 | a0001c0001t0007g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-16660G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448766 | |||||||
| chr5:126448800 | T | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
89 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.84-16626T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448800 | |||||||
| chr5:126448839 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.84-16587T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448839 | |||||||
| chr5:126448840 | G | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(45): Show |
50 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.84-16586G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448840 | |||||||
| chr5:126448844 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
89 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.84-16582C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448844 | |||||||
| chr5:126449071 | G | A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0081 others(36): Show |
41 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.84-16355G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449071 | |||||||
| chr5:126449073 | T | A | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-16353T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449073 | |||||||
| chr5:126449075 | C | T | 92 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(89): Show |
93 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.84-16351C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449075 | |||||||
| chr5:126449090 | T | G | 36 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(33): Show |
38 | HG00558.hp1 HG01069.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.84-16336T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449090 | |||||||
| chr5:126449424 | C | G | 2 | a0001c0001t0003g0015 a0001c0001t0003g0016 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.84-16002C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449424 | |||||||
| chr5:126449522 | AT | A | 130 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(127): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.84-15899delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126449522 | ||||||
| chr5:126449546 | G | A | 153 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0032 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.84-15880G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449546 | |||||||
| chr5:126449568 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.84-15858C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449568 | |||||||
| chr5:126449720 | G | T | 23 | a0001c0001t0001g0118 a0001c0001t0001g0175 a0001c0001t0001g0235 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.84-15706G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449720 | |||||||
| chr5:126449743 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18965.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.84-15683A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449743 | |||||||
| chr5:126449760 | G | T | 4 | a0001c0001t0001g0032 a0001c0001t0002g0064 a0001c0001t0002g0065 others(1): Show |
4 | HG00735.hp1 HG01934.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-15666G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449760 | |||||||
| chr5:126449889 | A | C | 1 | a0001c0001t0001g0222 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.84-15537A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449889 | |||||||
| chr5:126449921 | G | A | 6 | a0001c0001t0002g0233 a0001c0001t0003g0140 a0001c0001t0003g0142 others(3): Show |
6 | HG02055.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-15505G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449921 | |||||||
| chr5:126449957 | C | G | 26 | a0001c0001t0001g0032 a0001c0001t0001g0059 a0001c0001t0001g0061 others(23): Show |
26 | HG00438.hp2 HG00642.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.84-15469C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449957 | |||||||
| chr5:126450068 | T | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0302 a0001c0001t0002g0298 |
3 | HG03239.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.84-15358T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450068 | |||||||
| chr5:126450191 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.84-15235A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450191 | |||||||
| chr5:126450221 | G | C | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.84-15205G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450221 | |||||||
| chr5:126450325 | C | G | 1 | a0001c0001t0001g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.84-15101C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450325 | |||||||
| chr5:126450340 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.84-15086A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450340 | |||||||
| chr5:126450420 | C | T | 1 | a0001c0004t0001g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84-15006C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450420 | |||||||
| chr5:126450588 | T | C | 318 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(315): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.84-14838T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450588 | |||||||
| chr5:126450613 | T | G | 198 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(195): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.84-14813T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450613 | |||||||
| chr5:126450652 | T | TA | 119 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(116): Show |
123 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.84-14748dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | ||||||
| chr5:126450652 | T | TAA | 19 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0049 others(16): Show |
19 | HG00639.hp1 HG00642.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.84-14749_84-14748d others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | ||||||
| chr5:126450652 | TA | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0080 a0001c0001t0001g0094 others(9): Show |
12 | HG00140.hp2 HG01258.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.84-14748delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | ||||||
| chr5:126450652 | TAA | T | 89 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0026 others(86): Show |
92 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.84-14749_84-14748d others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | ||||||
| chr5:126450652 | TAAA | T | 25 | a0001c0001t0001g0010 a0001c0001t0001g0044 a0001c0001t0001g0045 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.84-14750_84-14748d others(5): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | ||||||
| chr5:126450652 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0147 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.84-14758_84-14748d others(13): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | ||||||
| chr5:126450652 | TAAAAAAA others(5): Show |
T | 4 | a0001c0001t0001g0159 a0001c0001t0002g0132 a0001c0001t0007g0293 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-14759_84-14748d others(14): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | ||||||
| chr5:126450689 | T | C | 2 | a0001c0001t0002g0075 a0001c0001t0003g0259 |
2 | HG01261.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.84-14737T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450689 | |||||||
| chr5:126450695 | C | T | 1 | a0001c0004t0001g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84-14731C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450695 | |||||||
| chr5:126450707 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.84-14719G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450707 | |||||||
| chr5:126450899 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.84-14527C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450899 | |||||||
| chr5:126450905 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.84-14521G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450905 | |||||||
| chr5:126450907 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.84-14519G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450907 | |||||||
| chr5:126450908 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(119): Show |
126 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.84-14518C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450908 | |||||||
| chr5:126450912 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0067 a0001c0001t0001g0192 others(5): Show |
8 | HG00280.hp1 HG01074.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-14514G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450912 | |||||||
| chr5:126450969 | C | T | 4 | a0001c0001t0002g0312 a0001c0001t0003g0086 a0001c0001t0003g0102 others(1): Show |
4 | HG00741.hp2 HG01255.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-14457C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450969 | |||||||
| chr5:126450987 | C | G | 1 | a0001c0004t0001g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84-14439C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450987 | |||||||
| chr5:126451119 | C | T | 8 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(5): Show |
8 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-14307C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451119 | |||||||
| chr5:126451161 | C | T | 143 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(140): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.84-14265C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451161 | |||||||
| chr5:126451162 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0252 a0001c0001t0004g0253 |
3 | HG02809.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.84-14264G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451162 | |||||||
| chr5:126451171 | G | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(106): Show |
113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.84-14255G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451171 | |||||||
| chr5:126451178 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.84-14248A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451178 | |||||||
| chr5:126451244 | A | C | 7 | a0001c0001t0001g0159 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-14182A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451244 | |||||||
| chr5:126451249 | C | T | 5 | a0001c0001t0001g0276 a0001c0001t0001g0280 a0001c0002t0001g0116 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-14177C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451249 | |||||||
| chr5:126451369 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.84-14057G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451369 | |||||||
| chr5:126451442 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0005g0139 |
2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.84-13984G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451442 | |||||||
| chr5:126451590 | C | T | 299 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(296): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.84-13836C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451590 | |||||||
| chr5:126451681 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0004t0001g0292 |
3 | HG00673.hp2 HG02886.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.84-13745G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451681 | |||||||
| chr5:126451693 | G | T | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.84-13733G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451693 | |||||||
| chr5:126451699 | G | A | 8 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(5): Show |
8 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-13727G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451699 | |||||||
| chr5:126451749 | G | T | 1 | a0001c0001t0003g0158 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.84-13677G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451749 | |||||||
| chr5:126451798 | G | A | 154 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.84-13628G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451798 | |||||||
| chr5:126451890 | G | T | 139 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(136): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.84-13536G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451890 | |||||||
| chr5:126451927 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.84-13499C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451927 | |||||||
| chr5:126452021 | A | C | 7 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0175 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-13405A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452021 | |||||||
| chr5:126452156 | G | A | 7 | a0001c0001t0001g0135 a0001c0001t0001g0160 a0001c0001t0001g0273 others(4): Show |
7 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-13270G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452156 | |||||||
| chr5:126452161 | T | G | 1 | a0001c0001t0002g0314 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.84-13265T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452161 | |||||||
| chr5:126452271 | G | T | 17 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0093 others(14): Show |
17 | HG00408.hp1 HG00423.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.84-13155G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452271 | |||||||
| chr5:126452320 | C | T | 5 | a0001c0001t0001g0276 a0001c0001t0001g0280 a0001c0002t0001g0116 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-13106C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452320 | |||||||
| chr5:126452333 | A | G | 1 | a0001c0001t0004g0253 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.84-13093A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452333 | |||||||
| chr5:126452369 | C | T | 20 | a0001c0001t0001g0136 a0001c0001t0001g0230 a0001c0001t0001g0238 others(17): Show |
21 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.84-13057C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452369 | |||||||
| chr5:126452446 | A | G | 5 | a0001c0001t0001g0276 a0001c0001t0001g0280 a0001c0002t0001g0116 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-12980A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452446 | |||||||
| chr5:126452501 | T | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(127): Show |
134 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.84-12925T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452501 | |||||||
| chr5:126452580 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0118 others(4): Show |
7 | HG00642.hp1 HG01891.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-12846G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452580 | |||||||
| chr5:126452679 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0252 a0001c0001t0004g0253 |
3 | HG02809.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.84-12747G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452679 | |||||||
| chr5:126452833 | A | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(118): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.84-12593A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452833 | |||||||
| chr5:126453174 | A | G | 1 | a0001c0001t0004g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.84-12252A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126453174 | |||||||
| chr5:126453348 | G | GA | 7 | a0001c0001t0001g0276 a0001c0001t0001g0280 a0001c0001t0003g0162 others(4): Show |
8 | HG02055.hp1 HG02451.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-12059dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126453348 | ||||||
| chr5:126453348 | GA | G | 163 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(160): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.84-12059delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126453348 | ||||||
| chr5:126453348 | GAAAA | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(121): Show |
128 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.84-12062_84-12059d others(6): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126453348 | ||||||
| chr5:126453516 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(123): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-11910A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126453516 | |||||||
| chr5:126453812 | C | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0004g0269 others(1): Show |
4 | HG00642.hp1 HG01891.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-11614C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126453812 | |||||||
| chr5:126453974 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.84-11452T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126453974 | |||||||
| chr5:126454029 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(123): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-11397A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454029 | |||||||
| chr5:126454133 | C | T | 1 | a0001c0001t0002g0004 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.84-11293C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454133 | |||||||
| chr5:126454160 | C | A | 1 | a0001c0001t0003g0162 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.84-11266C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454160 | |||||||
| chr5:126454172 | A | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(123): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-11254A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454172 | |||||||
| chr5:126454291 | C | T | 6 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-11135C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454291 | |||||||
| chr5:126454311 | T | C | 3 | a0001c0001t0001g0235 a0001c0001t0003g0236 a0001c0001t0003g0237 |
3 | HG01069.hp1 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.84-11115T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454311 | |||||||
| chr5:126454476 | G | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(123): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-10950G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454476 | |||||||
| chr5:126454809 | G | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(118): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.84-10617G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454809 | |||||||
| chr5:126454868 | T | C | 34 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0136 others(31): Show |
35 | HG00099.hp2 HG00642.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.84-10558T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454868 | |||||||
| chr5:126454895 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.84-10531T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454895 | |||||||
| chr5:126455029 | C | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(123): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-10397C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455029 | |||||||
| chr5:126455076 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(119): Show |
126 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.84-10350G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455076 | |||||||
| chr5:126455118 | T | A | 1 | a0001c0001t0003g0278 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.84-10308T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455118 | |||||||
| chr5:126455178 | C | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(123): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-10248C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455178 | |||||||
| chr5:126455180 | T | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(123): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-10246T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455180 | |||||||
| chr5:126455327 | T | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(123): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-10099T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455327 | |||||||
| chr5:126455403 | T | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(121): Show |
128 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.84-10023T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455403 | |||||||
| chr5:126455448 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(123): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-9978A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455448 | |||||||
| chr5:126455591 | A | C | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-9835A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455591 | |||||||
| chr5:126455598 | T | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(123): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-9828T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455598 | |||||||
| chr5:126455599 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(119): Show |
126 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.84-9827G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455599 | |||||||
| chr5:126455625 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(129): Show |
136 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.84-9801A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455625 | |||||||
| chr5:126455782 | G | A | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-9644G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455782 | |||||||
| chr5:126455784 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.84-9642A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455784 | |||||||
| chr5:126455919 | T | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(125): Show |
133 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.84-9507T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455919 | |||||||
| chr5:126455947 | T | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(125): Show |
133 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.84-9479T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455947 | |||||||
| chr5:126455981 | G | C | 24 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0136 others(21): Show |
25 | HG00099.hp2 HG00642.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.84-9445G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455981 | |||||||
| chr5:126456138 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.84-9288A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456138 | |||||||
| chr5:126456200 | C | G | 1 | a0001c0001t0003g0119 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.84-9226C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456200 | |||||||
| chr5:126456267 | G | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(121): Show |
128 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.84-9159G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456267 | |||||||
| chr5:126456279 | C | T | 177 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.84-9147C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456279 | |||||||
| chr5:126456280 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(125): Show |
133 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.84-9146G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456280 | |||||||
| chr5:126456355 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(130): Show |
138 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.84-9071T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456355 | |||||||
| chr5:126456385 | GT | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(132): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.84-9032delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126456385 | ||||||
| chr5:126456386 | T | G | 21 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0136 others(18): Show |
22 | HG00642.hp1 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.84-9040T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456386 | |||||||
| chr5:126456445 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.84-8981C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456445 | |||||||
| chr5:126456452 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.84-8974T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456452 | |||||||
| chr5:126456502 | T | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(157): Show |
167 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.84-8924T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456502 | |||||||
| chr5:126456625 | T | C | 1 | a0001c0004t0001g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84-8801T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456625 | |||||||
| chr5:126456808 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.84-8618A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456808 | |||||||
| chr5:126456812 | G | T | 8 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(5): Show |
8 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-8614G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456812 | |||||||
| chr5:126456813 | C | T | 8 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(5): Show |
8 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-8613C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456813 | |||||||
| chr5:126456856 | G | T | 298 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(295): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.84-8570G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456856 | |||||||
| chr5:126456914 | C | T | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-8512C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456914 | |||||||
| chr5:126456917 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.84-8509A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456917 | |||||||
| chr5:126456956 | G | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(261): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.84-8470G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456956 | |||||||
| chr5:126456959 | A | G | 306 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(303): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.84-8467A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456959 | |||||||
| chr5:126456989 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.84-8437A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456989 | |||||||
| chr5:126457008 | C | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.84-8418C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457008 | |||||||
| chr5:126457065 | G | A | 8 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(5): Show |
8 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-8361G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457065 | |||||||
| chr5:126457097 | C | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.84-8329C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457097 | |||||||
| chr5:126457114 | T | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.84-8312T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457114 | |||||||
| chr5:126457115 | G | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.84-8311G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457115 | |||||||
| chr5:126457146 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.84-8280C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457146 | |||||||
| chr5:126457147 | G | A | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-8279G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457147 | |||||||
| chr5:126457162 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.84-8264A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457162 | |||||||
| chr5:126457173 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.84-8253C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457173 | |||||||
| chr5:126457187 | G | A | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-8239G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457187 | |||||||
| chr5:126457191 | C | CA | 6 | a0001c0001t0001g0120 a0001c0001t0001g0160 a0001c0001t0001g0181 others(3): Show |
6 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-8205dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | ||||||
| chr5:126457191 | CAAAAAA | C | 31 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0097 others(28): Show |
33 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.84-8210_84-8205del others(6): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | ||||||
| chr5:126457191 | CAAAAAAA | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(242): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.84-8211_84-8205del others(7): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | ||||||
| chr5:126457191 | CAAAAAAA others(1): Show |
C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0185 others(6): Show |
9 | HG01074.hp1 HG01257.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.84-8212_84-8205del others(8): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | ||||||
| chr5:126457191 | CAAAAAAA others(4): Show |
C | 1 | a0001c0004t0001g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84-8215_84-8205del others(11): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | ||||||
| chr5:126457191 | CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-8217_84-8205del others(13): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | ||||||
| chr5:126457191 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0005g0189 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.84-8218_84-8205del others(14): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | ||||||
| chr5:126457219 | A | G | 17 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0136 others(14): Show |
18 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.84-8207A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457219 | |||||||
| chr5:126457222 | G | A | 1 | a0001c0001t0004g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.84-8204G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457222 | |||||||
| chr5:126457248 | T | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.84-8178T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457248 | |||||||
| chr5:126457298 | A | G | 125 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(122): Show |
129 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.84-8128A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457298 | |||||||
| chr5:126457432 | A | G | 269 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(266): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.84-7994A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457432 | |||||||
| chr5:126457563 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84-7863G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457563 | |||||||
| chr5:126457586 | G | T | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-7840G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457586 | |||||||
| chr5:126457631 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0272 a0001c0001t0002g0233 |
3 | HG02622.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.84-7795G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457631 | |||||||
| chr5:126457642 | A | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(278): Show |
288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.84-7784A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457642 | |||||||
| chr5:126457729 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.84-7697G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457729 | |||||||
| chr5:126457761 | TG | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(261): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.84-7660delG | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457761 | ||||||
| chr5:126457812 | C | T | 17 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0136 others(14): Show |
18 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.84-7614C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457812 | |||||||
| chr5:126457836 | T | C | 1 | a0001c0001t0004g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.84-7590T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457836 | |||||||
| chr5:126457895 | G | A | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-7531G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457895 | |||||||
| chr5:126458156 | C | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(258): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.84-7270C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458156 | |||||||
| chr5:126458157 | A | G | 285 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(282): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.84-7269A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458157 | |||||||
| chr5:126458263 | T | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0272 a0001c0001t0002g0233 |
3 | HG02622.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.84-7163T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458263 | |||||||
| chr5:126458264 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.84-7162G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458264 | |||||||
| chr5:126458378 | C | T | 300 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(297): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.84-7048C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458378 | |||||||
| chr5:126458427 | A | G | 304 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(301): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.84-6999A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458427 | |||||||
| chr5:126458444 | CA | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0117 a0001c0001t0001g0249 others(3): Show |
6 | HG00544.hp2 HG00621.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-6969delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126458444 | ||||||
| chr5:126458448 | A | AC | 13 | a0001c0001t0001g0138 a0001c0001t0001g0175 a0001c0001t0001g0238 others(10): Show |
13 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.84-6978_84-6977ins others(1): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458448 | |||||||
| chr5:126458448 | A | C | 3 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0003g0313 |
3 | HG00733.hp1 HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.84-6978A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458448 | |||||||
| chr5:126458449 | A | C | 2 | a0001c0001t0001g0125 a0001c0001t0003g0202 |
2 | HG00438.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.84-6977A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458449 | |||||||
| chr5:126458616 | G | A | 282 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(279): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.84-6810G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458616 | |||||||
| chr5:126458674 | G | A | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-6752G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458674 | |||||||
| chr5:126458746 | C | G | 16 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0136 others(13): Show |
17 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.84-6680C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458746 | |||||||
| chr5:126458751 | C | A | 299 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(296): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.84-6675C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458751 | |||||||
| chr5:126458812 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.84-6614C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458812 | |||||||
| chr5:126458965 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.84-6461C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458965 | |||||||
| chr5:126458966 | G | A | 1 | a0001c0001t0003g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.84-6460G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458966 | |||||||
| chr5:126459033 | C | T | 1 | a0001c0001t0007g0177 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.84-6393C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459033 | |||||||
| chr5:126459075 | T | C | 12 | a0001c0001t0001g0136 a0001c0001t0001g0230 a0001c0001t0001g0263 others(9): Show |
13 | HG01255.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.84-6351T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459075 | |||||||
| chr5:126459119 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.84-6307C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459119 | |||||||
| chr5:126459130 | G | A | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-6296G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459130 | |||||||
| chr5:126459230 | A | G | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-6196A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459230 | |||||||
| chr5:126459318 | A | C | 7 | a0001c0001t0001g0050 a0001c0001t0001g0057 a0001c0001t0001g0122 others(4): Show |
7 | NA18960.hp2 NA18964.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-6108A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459318 | |||||||
| chr5:126459346 | C | G | 283 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(280): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.84-6080C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459346 | |||||||
| chr5:126459484 | A | T | 298 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(295): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.84-5942A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459484 | |||||||
| chr5:126459533 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(265): Show |
274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.84-5893A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459533 | |||||||
| chr5:126459613 | A | G | 314 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(311): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.84-5813A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459613 | |||||||
| chr5:126459719 | C | T | 20 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0129 others(17): Show |
21 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.84-5707C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459719 | |||||||
| chr5:126459823 | A | G | 278 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(275): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.84-5603A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459823 | |||||||
| chr5:126459849 | C | T | 12 | a0001c0001t0001g0138 a0001c0001t0001g0175 a0001c0001t0001g0238 others(9): Show |
12 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.84-5577C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459849 | |||||||
| chr5:126459871 | T | G | 61 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0037 others(58): Show |
63 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.84-5555T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459871 | |||||||
| chr5:126459888 | A | AT | 5 | a0001c0001t0001g0138 a0001c0001t0001g0175 a0001c0001t0001g0282 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-5532dupT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126459888 | ||||||
| chr5:126459890 | T | C | 284 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(281): Show |
291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.84-5536T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459890 | |||||||
| chr5:126459913 | C | T | 282 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(279): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.84-5513C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459913 | |||||||
| chr5:126460059 | G | A | 296 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(293): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.84-5367G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460059 | |||||||
| chr5:126460071 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0004g0303 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.84-5355T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460071 | |||||||
| chr5:126460105 | G | T | 1 | a0001c0001t0001g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.84-5321G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460105 | |||||||
| chr5:126460127 | A | C | 283 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(280): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.84-5299A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460127 | |||||||
| chr5:126460153 | C | T | 301 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(298): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.84-5273C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460153 | |||||||
| chr5:126460206 | C | T | 283 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(280): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.84-5220C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460206 | |||||||
| chr5:126460216 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0072 others(1): Show |
4 | HG01256.hp2 HG01496.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-5210C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460216 | |||||||
| chr5:126460285 | A | C | 5 | a0001c0001t0001g0138 a0001c0001t0001g0175 a0001c0001t0001g0282 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-5141A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460285 | |||||||
| chr5:126460476 | G | T | 1 | a0001c0001t0007g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-4950G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460476 | |||||||
| chr5:126460725 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0003g0162 a0001c0001t0006g0006 |
4 | HG02896.hp1 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-4701G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460725 | |||||||
| chr5:126460766 | T | C | 16 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0136 others(13): Show |
17 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.84-4660T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460766 | |||||||
| chr5:126460973 | T | C | 1 | a0001c0001t0005g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.84-4453T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460973 | |||||||
| chr5:126461158 | T | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(289): Show |
299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.84-4268T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461158 | |||||||
| chr5:126461175 | C | T | 300 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(297): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.84-4251C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461175 | |||||||
| chr5:126461211 | TC | T | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-4212delC | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126461211 | ||||||
| chr5:126461284 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.84-4142G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461284 | |||||||
| chr5:126461379 | T | G | 301 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(298): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.84-4047T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461379 | |||||||
| chr5:126461411 | T | C | 1 | a0001c0001t0007g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-4015T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461411 | |||||||
| chr5:126461419 | G | T | 1 | a0001c0001t0003g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.84-4007G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461419 | |||||||
| chr5:126461422 | C | G | 2 | a0001c0001t0003g0162 a0001c0001t0006g0006 |
3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-4004C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461422 | |||||||
| chr5:126461500 | T | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0295 a0001c0001t0004g0303 |
3 | HG02922.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.84-3926T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461500 | |||||||
| chr5:126461629 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(122): Show |
129 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.84-3797G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461629 | |||||||
| chr5:126461692 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0159 |
2 | NA19091.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-3734C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461692 | |||||||
| chr5:126461757 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0295 a0001c0001t0004g0303 |
3 | HG02922.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.84-3669G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461757 | |||||||
| chr5:126461823 | A | G | 6 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-3603A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461823 | |||||||
| chr5:126461854 | G | A | 1 | a0001c0001t0010g0168 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.84-3572G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461854 | |||||||
| chr5:126461921 | A | G | 2 | a0001c0001t0003g0009 a0001c0001t0004g0264 |
3 | HG02622.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.84-3505A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461921 | |||||||
| chr5:126461939 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.84-3487A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461939 | |||||||
| chr5:126462259 | G | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(257): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.84-3167G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462259 | |||||||
| chr5:126462407 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.84-3019A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462407 | |||||||
| chr5:126462581 | A | G | 17 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0136 others(14): Show |
18 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.84-2845A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462581 | |||||||
| chr5:126462717 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.84-2709C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462717 | |||||||
| chr5:126462774 | A | G | 5 | a0001c0001t0001g0276 a0001c0001t0005g0139 a0001c0002t0001g0116 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-2652A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462774 | |||||||
| chr5:126462879 | G | A | 6 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-2547G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462879 | |||||||
| chr5:126462922 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84-2504T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462922 | |||||||
| chr5:126462945 | A | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0175 a0001c0001t0001g0282 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-2481A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462945 | |||||||
| chr5:126463196 | C | G | 2 | a0001c0001t0004g0180 a0001c0001t0008g0024 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.84-2230C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463196 | |||||||
| chr5:126463337 | G | A | 6 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0095 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-2089G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463337 | |||||||
| chr5:126463450 | A | G | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | HG00642.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.84-1976A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463450 | |||||||
| chr5:126463509 | T | C | 22 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0136 others(19): Show |
23 | HG00642.hp1 HG01243.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.84-1917T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463509 | |||||||
| chr5:126463525 | G | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0272 a0001c0001t0002g0233 |
3 | HG02622.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.84-1901G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463525 | |||||||
| chr5:126463620 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.84-1806C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463620 | |||||||
| chr5:126463681 | T | C | 137 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.84-1745T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463681 | |||||||
| chr5:126463756 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.84-1670C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463756 | |||||||
| chr5:126463854 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.84-1572A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463854 | |||||||
| chr5:126463983 | G | A | 4 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0070 others(1): Show |
4 | HG01928.hp2 HG01943.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-1443G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463983 | |||||||
| chr5:126463985 | G | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(120): Show |
127 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.84-1441G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463985 | |||||||
| chr5:126464024 | A | G | 1 | a0001c0001t0001g0243 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.84-1402A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464024 | |||||||
| chr5:126464028 | C | CA | 7 | a0001c0001t0001g0151 a0001c0001t0001g0176 a0001c0001t0003g0178 others(4): Show |
7 | HG02486.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-1384dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126464028 | ||||||
| chr5:126464141 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(135): Show |
143 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.84-1285A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464141 | |||||||
| chr5:126464165 | T | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0272 a0001c0001t0002g0233 |
3 | HG02622.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.84-1261T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464165 | |||||||
| chr5:126464278 | C | G | 3 | a0001c0001t0003g0140 a0001c0001t0003g0142 a0001c0001t0003g0319 |
3 | HG02055.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.84-1148C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464278 | |||||||
| chr5:126464331 | T | G | 22 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0136 others(19): Show |
23 | HG00642.hp1 HG01243.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.84-1095T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464331 | |||||||
| chr5:126464473 | C | G | 3 | a0001c0001t0003g0140 a0001c0001t0003g0142 a0001c0001t0003g0319 |
3 | HG02055.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.84-953C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464473 | |||||||
| chr5:126464493 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0252 a0001c0001t0004g0253 |
3 | HG02809.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.84-933G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464493 | |||||||
| chr5:126464658 | A | G | 14 | a0001c0001t0001g0120 a0001c0001t0001g0160 a0001c0001t0001g0235 others(11): Show |
14 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.84-768A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464658 | |||||||
| chr5:126464709 | T | C | 10 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0135 others(7): Show |
10 | HG00642.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.84-717T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464709 | |||||||
| chr5:126464874 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84-552C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464874 | |||||||
| chr5:126464954 | T | C | 134 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0018 others(131): Show |
138 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.84-472T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464954 | |||||||
| chr5:126464992 | A | G | 1 | a0001c0001t0005g0214 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.84-434A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464992 | |||||||
| chr5:126465105 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0273 a0001c0001t0004g0103 others(2): Show |
5 | HG02922.hp2 HG03130.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-321C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465105 | |||||||
| chr5:126465144 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0018 others(105): Show |
112 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.84-282C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465144 | |||||||
| chr5:126465155 | A | C | 1 | a0001c0001t0001g0055 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.84-271A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465155 | |||||||
| chr5:126465233 | G | T | 1 | a0001c0001t0004g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.84-193G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465233 | |||||||
| chr5:126465237 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.84-189C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465237 | |||||||
| chr5:126465242 | G | T | 1 | a0001c0001t0002g0267 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.84-184G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465242 | |||||||
| chr5:126465363 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.84-63C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465363 | |||||||
| chr5:126465631 | T | C | 1 | a0001c0001t0011g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.203+86T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465631 | |||||||
| chr5:126465702 | T | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(223): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.203+157T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465702 | |||||||
| chr5:126465722 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.203+177T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465722 | |||||||
| chr5:126465724 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0017 others(104): Show |
111 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.203+179C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465724 | |||||||
| chr5:126465898 | G | A | 1 | a0001c0001t0007g0177 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.203+353G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465898 | |||||||
| chr5:126465960 | T | G | 1 | a0001c0001t0006g0255 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.203+415T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465960 | |||||||
| chr5:126466123 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.203+578C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466123 | |||||||
| chr5:126466184 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0005g0139 |
3 | HG02922.hp1 NA18973.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.203+639T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466184 | |||||||
| chr5:126466335 | G | A | 68 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0062 others(65): Show |
69 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.203+790G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466335 | |||||||
| chr5:126466355 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0107 |
2 | HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.203+810C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466355 | |||||||
| chr5:126466430 | CT | C | 23 | a0001c0001t0001g0011 a0001c0001t0001g0136 a0001c0001t0001g0138 others(20): Show |
24 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.203+897delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 126466430 | ||||||
| chr5:126466443 | C | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(22): Show |
26 | HG00558.hp1 HG00609.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.203+898C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466443 | |||||||
| chr5:126466460 | C | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0252 a0001c0001t0007g0177 |
3 | HG02809.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.203+915C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466460 | |||||||
| chr5:126466559 | G | A | 5 | a0001c0001t0001g0138 a0001c0001t0001g0175 a0001c0001t0001g0282 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+1014G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466559 | |||||||
| chr5:126466667 | C | T | 1 | a0001c0001t0014g0034 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.203+1122C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466667 | |||||||
| chr5:126466712 | T | C | 10 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0175 others(7): Show |
11 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.203+1167T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466712 | |||||||
| chr5:126466729 | G | T | 1 | a0001c0001t0002g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.203+1184G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466729 | |||||||
| chr5:126466776 | G | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0230 a0001c0001t0001g0263 others(3): Show |
7 | HG02055.hp2 HG02615.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+1231G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466776 | |||||||
| chr5:126466809 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0230 a0001c0001t0001g0263 others(2): Show |
6 | HG02055.hp2 HG02615.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.203+1264G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466809 | |||||||
| chr5:126466914 | T | C | 5 | a0001c0001t0004g0130 a0001c0001t0004g0131 a0001c0001t0004g0253 others(2): Show |
5 | HG02886.hp1 HG03471.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+1369T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466914 | |||||||
| chr5:126466986 | C | G | 7 | a0001c0001t0001g0097 a0001c0001t0001g0279 a0001c0001t0003g0167 others(4): Show |
7 | HG00642.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.203+1441C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466986 | |||||||
| chr5:126466993 | A | C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0118 others(18): Show |
21 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.203+1448A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466993 | |||||||
| chr5:126467012 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
294 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.203+1467A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467012 | |||||||
| chr5:126467110 | T | C | 48 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0062 others(45): Show |
49 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.203+1565T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467110 | |||||||
| chr5:126467224 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(26): Show |
30 | HG00558.hp1 HG02040.hp2 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.203+1679G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467224 | |||||||
| chr5:126467427 | G | A | 97 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0043 others(94): Show |
100 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.203+1882G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467427 | |||||||
| chr5:126467503 | A | G | 4 | a0001c0001t0001g0276 a0001c0002t0001g0116 a0001c0002t0001g0141 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+1958A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467503 | |||||||
| chr5:126467526 | C | G | 1 | a0001c0004t0001g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.203+1981C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467526 | |||||||
| chr5:126467614 | G | C | 1 | a0001c0001t0014g0034 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.204-2063G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467614 | |||||||
| chr5:126467628 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0183 |
2 | HG02015.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.204-2049A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467628 | |||||||
| chr5:126467648 | T | C | 2 | a0001c0001t0003g0114 a0001c0001t0003g0142 |
2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.204-2029T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467648 | |||||||
| chr5:126467890 | T | C | 2 | a0001c0001t0003g0009 a0001c0001t0003g0319 |
3 | HG02055.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.204-1787T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467890 | |||||||
| chr5:126467966 | C | G | 3 | a0001c0001t0004g0130 a0001c0001t0004g0131 a0001c0001t0004g0274 |
3 | HG02886.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.204-1711C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467966 | |||||||
| chr5:126468073 | G | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(313): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.204-1604G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468073 | |||||||
| chr5:126468079 | C | T | 5 | a0001c0001t0001g0169 a0001c0001t0002g0233 a0001c0001t0002g0291 others(2): Show |
5 | HG02622.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-1598C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468079 | |||||||
| chr5:126468187 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0014g0034 |
2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.204-1490C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468187 | |||||||
| chr5:126468469 | T | G | 1 | a0001c0004t0001g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.204-1208T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468469 | |||||||
| chr5:126468677 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.204-1000G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468677 | |||||||
| chr5:126468730 | C | T | 22 | a0001c0001t0001g0063 a0001c0001t0001g0136 a0001c0001t0001g0145 others(19): Show |
23 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.204-947C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468730 | |||||||
| chr5:126468935 | A | G | 1 | a0001c0001t0002g0314 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.204-742A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468935 | |||||||
| chr5:126469053 | T | C | 24 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0252 others(21): Show |
25 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.204-624T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469053 | |||||||
| chr5:126469119 | A | C | 52 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0062 others(49): Show |
53 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.204-558A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469119 | |||||||
| chr5:126469267 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.204-410A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469267 | |||||||
| chr5:126469277 | G | GA | 5 | a0001c0001t0001g0169 a0001c0001t0002g0233 a0001c0001t0002g0291 others(2): Show |
5 | HG02622.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-395dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 126469277 | ||||||
| chr5:126469365 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0067 a0001c0001t0001g0271 others(2): Show |
5 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-312G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469365 | |||||||
| chr5:126469546 | G | A | 1 | a0001c0001t0008g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.204-131G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469546 | |||||||
| chr5:126469583 | C | T | 3 | a0001c0002t0001g0116 a0001c0002t0001g0141 a0001c0002t0001g0320 |
3 | HG02055.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.204-94C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469583 | |||||||
| chr5:126469620 | G | T | 1 | a0001c0001t0010g0126 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.204-57G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469620 | |||||||
| chr5:126469641 | ATTATC | A | 10 | a0001c0001t0003g0114 a0001c0001t0003g0142 a0001c0001t0003g0236 others(7): Show |
10 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.204-31_204-27delCT others(3): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 126469641 | ||||||
| chr5:126469886 | A | G | 24 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0252 others(21): Show |
25 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.315+98A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126469886 | |||||||
| chr5:126469917 | T | G | 2 | a0001c0001t0003g0167 a0001c0001t0003g0321 |
2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.315+129T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126469917 | |||||||
| chr5:126469929 | C | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0252 a0001c0001t0001g0265 |
3 | HG02809.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.315+141C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126469929 | |||||||
| chr5:126470060 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.315+272C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470060 | |||||||
| chr5:126470062 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.315+274C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470062 | |||||||
| chr5:126470237 | T | C | 24 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0252 others(21): Show |
25 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.315+449T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470237 | |||||||
| chr5:126470385 | C | A | 1 | a0001c0001t0001g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.315+597C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470385 | |||||||
| chr5:126470556 | A | G | 19 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0001g0165 others(16): Show |
19 | HG00639.hp2 HG02280.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.315+768A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470556 | |||||||
| chr5:126470709 | C | T | 22 | a0001c0001t0001g0063 a0001c0001t0001g0136 a0001c0001t0001g0145 others(19): Show |
23 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.315+921C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470709 | |||||||
| chr5:126470786 | T | G | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | HG00642.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.315+998T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470786 | |||||||
| chr5:126470842 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.315+1054G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470842 | |||||||
| chr5:126470931 | C | T | 1 | a0001c0001t0004g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.315+1143C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470931 | |||||||
| chr5:126471170 | A | G | 12 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0273 others(9): Show |
12 | HG00639.hp2 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.316-1068A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471170 | |||||||
| chr5:126471192 | T | A | 1 | a0001c0001t0014g0034 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.316-1046T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471192 | |||||||
| chr5:126471334 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(137): Show |
144 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.316-904C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471334 | |||||||
| chr5:126471555 | T | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG00609.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.316-683T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471555 | |||||||
| chr5:126471665 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.316-573A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471665 | |||||||
| chr5:126471946 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.316-292C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471946 | |||||||
| chr5:126472145 | A | G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0118 a0001c0001t0001g0160 others(18): Show |
21 | HG00639.hp2 HG02280.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.316-93A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126472145 | |||||||
| chr5:126472219 | T | C | 22 | a0001c0001t0001g0063 a0001c0001t0001g0136 a0001c0001t0001g0145 others(19): Show |
23 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.316-19T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126472219 | |||||||
| chr5:126472228 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.316-10C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126472228 | |||||||
| chr5:126472577 | C | T | 10 | a0001c0001t0003g0114 a0001c0001t0003g0142 a0001c0001t0003g0236 others(7): Show |
10 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.382+273C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 4/13 | chr5 | 126472577 | |||||||
| chr5:126472662 | CCTT | C | 43 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0062 others(40): Show |
44 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.382+359_382+361del others(3): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 4/13 | chr5 | 126472662 | |||||||
| chr5:126472750 | C | A | 2 | a0001c0001t0002g0260 a0001c0001t0008g0024 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.382+446C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 4/13 | chr5 | 126472750 | |||||||
| chr5:126473060 | T | A | 2 | a0001c0001t0001g0036 a0001c0001t0014g0034 |
2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.383-205T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 4/13 | chr5 | 126473060 | |||||||
| chr5:126473253 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0014g0034 |
2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.383-12A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 4/13 | chr5 | 126473253 | |||||||
| chr5:126473453 | G | A | 97 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0043 others(94): Show |
100 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.486+85G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126473453 | |||||||
| chr5:126473457 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.486+89A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126473457 | |||||||
| chr5:126473689 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0123 |
2 | HG02040.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.486+321T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126473689 | |||||||
| chr5:126473791 | G | A | 54 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0062 others(51): Show |
55 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.486+423G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126473791 | |||||||
| chr5:126473868 | G | A | 96 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0043 others(93): Show |
99 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.486+500G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126473868 | |||||||
| chr5:126474004 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0014g0034 |
2 | HG03516.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.486+636G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474004 | |||||||
| chr5:126474046 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0014g0034 a0002c0003t0003g0283 |
3 | HG02257.hp2 HG03942.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.486+678C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474046 | |||||||
| chr5:126474066 | A | G | 1 | a0001c0001t0003g0074 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.486+698A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474066 | |||||||
| chr5:126474480 | T | A | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.486+1112T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474480 | |||||||
| chr5:126474606 | T | A | 1 | a0001c0001t0017g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486+1238T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474606 | |||||||
| chr5:126474616 | A | T | 8 | a0001c0001t0001g0097 a0001c0001t0001g0160 a0001c0001t0001g0165 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.486+1248A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474616 | |||||||
| chr5:126474903 | A | G | 4 | a0001c0001t0003g0114 a0001c0001t0003g0142 a0001c0001t0004g0161 others(1): Show |
4 | HG02145.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+1535A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474903 | |||||||
| chr5:126474996 | A | G | 54 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0036 others(51): Show |
54 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.486+1628A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474996 | |||||||
| chr5:126475081 | C | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0273 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+1713C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475081 | |||||||
| chr5:126475085 | T | C | 74 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(71): Show |
78 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.486+1717T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475085 | |||||||
| chr5:126475165 | T | A | 6 | a0001c0001t0001g0118 a0001c0001t0001g0276 a0001c0001t0014g0034 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+1797T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475165 | |||||||
| chr5:126475173 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.486+1805C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475173 | |||||||
| chr5:126475444 | G | A | 2 | a0002c0003t0001g0182 a0002c0003t0003g0283 |
2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.486+2076G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475444 | |||||||
| chr5:126475498 | G | A | 52 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0038 others(49): Show |
53 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.486+2130G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475498 | |||||||
| chr5:126475673 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.487-2019G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475673 | |||||||
| chr5:126475735 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.487-1957C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475735 | |||||||
| chr5:126475754 | C | T | 9 | a0001c0001t0001g0318 a0001c0001t0002g0260 a0001c0001t0003g0015 others(6): Show |
9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-1938C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475754 | |||||||
| chr5:126475758 | C | A | 153 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(150): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.487-1934C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475758 | |||||||
| chr5:126475834 | C | T | 9 | a0001c0001t0001g0118 a0001c0001t0004g0103 a0001c0001t0004g0130 others(6): Show |
9 | HG02257.hp2 HG02886.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-1858C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475834 | |||||||
| chr5:126475835 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0252 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.487-1857G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475835 | |||||||
| chr5:126475846 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.487-1846C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475846 | |||||||
| chr5:126475971 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.487-1721G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475971 | |||||||
| chr5:126476095 | C | T | 99 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0057 others(96): Show |
102 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.487-1597C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476095 | |||||||
| chr5:126476199 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.487-1493G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476199 | |||||||
| chr5:126476203 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.487-1489A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476203 | |||||||
| chr5:126476758 | T | A | 1 | a0001c0001t0003g0304 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.487-934T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476758 | |||||||
| chr5:126476852 | A | T | 321 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(318): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.487-840A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476852 | |||||||
| chr5:126476970 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.487-722G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476970 | |||||||
| chr5:126477067 | C | T | 10 | a0001c0001t0003g0114 a0001c0001t0004g0161 a0001c0001t0004g0180 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.487-625C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126477067 | |||||||
| chr5:126477109 | T | C | 1 | a0001c0001t0003g0296 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.487-583T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126477109 | |||||||
| chr5:126477423 | T | A | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.487-269T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126477423 | |||||||
| chr5:126477673 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0134 others(1): Show |
4 | HG00408.hp1 NA18949.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-19C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126477673 | |||||||
| chr5:126477823 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.582+36G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126477823 | |||||||
| chr5:126477912 | G | T | 2 | a0001c0001t0001g0036 a0001c0001t0014g0034 |
2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.582+125G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126477912 | |||||||
| chr5:126477982 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0118 a0001c0001t0001g0252 |
3 | HG02809.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.582+195A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126477982 | |||||||
| chr5:126477984 | A | G | 305 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(302): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.582+197A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126477984 | |||||||
| chr5:126478140 | G | GA | 160 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(157): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.582+372dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 126478140 | ||||||
| chr5:126478140 | G | GAA | 76 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0050 others(73): Show |
78 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.582+371_582+372dup others(2): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 126478140 | ||||||
| chr5:126478314 | T | A | 1 | a0001c0001t0001g0174 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.582+527T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478314 | |||||||
| chr5:126478363 | A | G | 11 | a0001c0001t0001g0192 a0001c0001t0001g0306 a0001c0001t0001g0318 others(8): Show |
11 | HG00099.hp1 HG00280.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.582+576A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478363 | |||||||
| chr5:126478424 | A | C | 305 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(302): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.582+637A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478424 | |||||||
| chr5:126478430 | C | A | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.582+643C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478430 | |||||||
| chr5:126478561 | T | C | 156 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(153): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.582+774T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478561 | |||||||
| chr5:126478583 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.582+796A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478583 | |||||||
| chr5:126478679 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0262 |
2 | HG00140.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.582+892T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478679 | |||||||
| chr5:126478692 | G | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.582+905G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478692 | |||||||
| chr5:126478729 | C | T | 34 | a0001c0001t0001g0062 a0001c0001t0001g0157 a0001c0001t0001g0199 others(31): Show |
35 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.582+942C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478729 | |||||||
| chr5:126478978 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.582+1191A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478978 | |||||||
| chr5:126479444 | T | C | 2 | a0002c0003t0001g0182 a0002c0003t0003g0283 |
2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.583-1012T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126479444 | |||||||
| chr5:126479616 | TAGTA | T | 5 | a0001c0001t0001g0118 a0001c0001t0004g0103 a0001c0001t0004g0130 others(2): Show |
5 | HG02886.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-836_583-833del others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 126479616 | ||||||
| chr5:126479780 | C | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0091 |
2 | NA18999.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.583-676C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126479780 | |||||||
| chr5:126479791 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.583-665A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126479791 | |||||||
| chr5:126479903 | C | T | 1 | a0001c0001t0002g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.583-553C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126479903 | |||||||
| chr5:126479910 | A | G | 151 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0012 others(148): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.583-546A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126479910 | |||||||
| chr5:126480047 | G | A | 85 | a0001c0001t0001g0007 a0001c0001t0001g0057 a0001c0001t0001g0061 others(82): Show |
88 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.583-409G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126480047 | |||||||
| chr5:126480054 | C | T | 3 | a0001c0001t0006g0006 a0001c0001t0006g0234 a0001c0001t0012g0025 |
4 | HG01243.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-402C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126480054 | |||||||
| chr5:126480072 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.583-384C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126480072 | |||||||
| chr5:126480238 | G | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0270 a0001c0001t0001g0289 others(1): Show |
4 | HG02080.hp1 HG02155.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-218G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126480238 | |||||||
| chr5:126480257 | TTTTATGG others(12): Show |
T | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.583-193_583-175del others(19): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 126480257 | ||||||
| chr5:126480545 | G | A | 3 | a0001c0001t0006g0006 a0001c0001t0006g0234 a0001c0001t0012g0025 |
4 | HG01243.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+18G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 7/13 | chr5 | 126480545 | |||||||
| chr5:126480549 | C | T | 3 | a0001c0001t0006g0006 a0001c0001t0006g0234 a0001c0001t0012g0025 |
4 | HG01243.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+22C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 7/13 | chr5 | 126480549 | |||||||
| chr5:126480765 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.735+58C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126480765 | |||||||
| chr5:126480807 | G | A | 10 | a0001c0001t0003g0009 a0001c0001t0003g0142 a0001c0001t0003g0162 others(7): Show |
11 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+100G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126480807 | |||||||
| chr5:126481031 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.735+324T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481031 | |||||||
| chr5:126481148 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.735+441C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481148 | |||||||
| chr5:126481170 | G | C | 1 | a0001c0001t0003g0184 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.735+463G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481170 | |||||||
| chr5:126481202 | AAAAAGAA others(14): Show |
A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0284 a0001c0001t0001g0286 others(1): Show |
4 | HG02896.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+499_735+519del others(21): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481202 | ||||||
| chr5:126481203 | A | AAAAGAAA others(5): Show |
2 | a0001c0001t0004g0264 a0001c0001t0006g0255 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.735+532_735+543dup others(12): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | ||||||
| chr5:126481203 | A | AAAAGAAA others(9): Show |
1 | a0001c0001t0008g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.735+528_735+543dup others(16): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | ||||||
| chr5:126481203 | AAAAG | A | 7 | a0001c0001t0001g0285 a0001c0001t0002g0005 a0001c0001t0002g0132 others(4): Show |
7 | HG00639.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+540_735+543del others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | ||||||
| chr5:126481203 | AAAAGAAA others(1): Show |
A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0067 others(8): Show |
11 | HG00280.hp1 HG01167.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+536_735+543del others(8): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | ||||||
| chr5:126481203 | AAAAGAAA others(5): Show |
A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0012 others(132): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.735+532_735+543del others(12): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | ||||||
| chr5:126481203 | AAAAGAAA others(9): Show |
A | 50 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0038 others(47): Show |
51 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.735+528_735+543del others(16): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | ||||||
| chr5:126481203 | AAAAGAAA others(13): Show |
A | 1 | a0001c0001t0001g0221 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.735+524_735+543del others(20): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | ||||||
| chr5:126481203 | AAAAGAAA others(17): Show |
A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0277 a0001c0001t0003g0078 |
3 | HG00323.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.735+520_735+543del others(24): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | ||||||
| chr5:126481203 | AAAAGAAA others(21): Show |
A | 4 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0273 others(1): Show |
4 | HG02486.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+516_735+543del others(28): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | ||||||
| chr5:126481204 | AAAGAAAG others(4): Show |
A | 2 | a0001c0001t0001g0115 a0001c0001t0002g0066 |
2 | HG01934.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.735+500_735+510del others(11): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481204 | ||||||
| chr5:126481204 | AAAGAAAG others(8): Show |
A | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.735+500_735+514del others(15): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481204 | ||||||
| chr5:126481204 | AAAGAAAG others(16): Show |
A | 81 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0057 others(78): Show |
84 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.735+500_735+522del others(23): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481204 | ||||||
| chr5:126481205 | AAGAAAGA others(7): Show |
A | 9 | a0001c0001t0001g0318 a0001c0001t0002g0260 a0001c0001t0003g0015 others(6): Show |
9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+500_735+513del others(14): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481205 | ||||||
| chr5:126481205 | AAGAAAGA others(15): Show |
A | 1 | a0001c0001t0003g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.735+500_735+521del others(22): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481205 | ||||||
| chr5:126481223 | G | A | 9 | a0001c0001t0001g0318 a0001c0001t0002g0260 a0001c0001t0003g0015 others(6): Show |
9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+516G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481223 | |||||||
| chr5:126481231 | G | A | 83 | a0001c0001t0001g0007 a0001c0001t0001g0057 a0001c0001t0001g0061 others(80): Show |
86 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.735+524G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481231 | |||||||
| chr5:126481237 | A | G | 51 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0038 others(48): Show |
52 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.735+530A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481237 | |||||||
| chr5:126481529 | G | A | 3 | a0001c0002t0001g0116 a0001c0002t0001g0141 a0001c0002t0001g0320 |
3 | HG02055.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.735+822G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481529 | |||||||
| chr5:126481531 | T | G | 9 | a0001c0001t0001g0318 a0001c0001t0002g0260 a0001c0001t0003g0015 others(6): Show |
9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+824T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481531 | |||||||
| chr5:126481622 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.735+915G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481622 | |||||||
| chr5:126481776 | G | T | 10 | a0001c0001t0003g0009 a0001c0001t0003g0142 a0001c0001t0003g0162 others(7): Show |
11 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+1069G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481776 | |||||||
| chr5:126481782 | A | G | 9 | a0001c0001t0001g0318 a0001c0001t0002g0260 a0001c0001t0003g0015 others(6): Show |
9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+1075A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481782 | |||||||
| chr5:126481836 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0279 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.735+1129C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481836 | |||||||
| chr5:126481868 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0295 a0001c0001t0001g0297 |
3 | HG02280.hp2 NA18949.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.735+1161C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481868 | |||||||
| chr5:126481869 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.735+1162G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481869 | |||||||
| chr5:126481927 | C | T | 53 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0037 others(50): Show |
54 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.735+1220C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481927 | |||||||
| chr5:126481970 | CA | C | 52 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0038 others(49): Show |
53 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.735+1279delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481970 | ||||||
| chr5:126481985 | AAG | A | 93 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0057 others(90): Show |
96 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.735+1279_735+1280d others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481985 | |||||||
| chr5:126481986 | A | G | 17 | a0001c0001t0001g0258 a0001c0001t0001g0324 a0001c0001t0003g0114 others(14): Show |
18 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.735+1279A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481986 | |||||||
| chr5:126482373 | G | A | 94 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0057 others(91): Show |
97 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.736-1090G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482373 | |||||||
| chr5:126482604 | G | C | 4 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0001c0001t0002g0312 others(1): Show |
4 | HG00733.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-859G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482604 | |||||||
| chr5:126482620 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.736-843A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482620 | |||||||
| chr5:126482761 | T | G | 1 | a0001c0001t0003g0301 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.736-702T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482761 | |||||||
| chr5:126482853 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.736-610A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482853 | |||||||
| chr5:126482926 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0279 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.736-537A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482926 | |||||||
| chr5:126483006 | C | T | 149 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(146): Show |
153 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.736-457C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483006 | |||||||
| chr5:126483035 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.736-428T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483035 | |||||||
| chr5:126483062 | TTC | T | 53 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0038 others(50): Show |
54 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.736-395_736-394del others(2): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126483062 | ||||||
| chr5:126483062 | TTCTC | T | 10 | a0001c0001t0003g0009 a0001c0001t0003g0142 a0001c0001t0003g0162 others(7): Show |
11 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.736-397_736-394del others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126483062 | ||||||
| chr5:126483139 | T | G | 1 | a0001c0001t0001g0030 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.736-324T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483139 | |||||||
| chr5:126483159 | A | G | 3 | a0001c0001t0006g0006 a0001c0001t0006g0234 a0001c0001t0012g0025 |
4 | HG01243.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-304A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483159 | |||||||
| chr5:126483180 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0235 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.736-283C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483180 | |||||||
| chr5:126483217 | C | T | 153 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(150): Show |
157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.736-246C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483217 | |||||||
| chr5:126483292 | A | C | 10 | a0001c0001t0003g0114 a0001c0001t0004g0161 a0001c0001t0004g0180 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.736-171A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483292 | |||||||
| chr5:126483731 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0252 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.847+157G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 9/13 | chr5 | 126483731 | |||||||
| chr5:126483914 | C | T | 10 | a0001c0001t0003g0009 a0001c0001t0003g0142 a0001c0001t0003g0162 others(7): Show |
11 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.847+340C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 9/13 | chr5 | 126483914 | |||||||
| chr5:126483919 | C | A | 1 | a0001c0001t0002g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.847+345C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 9/13 | chr5 | 126483919 | |||||||
| chr5:126484018 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.848-384C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 9/13 | chr5 | 126484018 | |||||||
| chr5:126484584 | CT | C | 11 | a0001c0001t0001g0061 a0001c0001t0003g0114 a0001c0001t0004g0161 others(8): Show |
12 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.970+75delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 126484584 | ||||||
| chr5:126484651 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0252 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.970+127T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126484651 | |||||||
| chr5:126484762 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.970+238T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126484762 | |||||||
| chr5:126484804 | G | A | 4 | a0001c0001t0003g0009 a0001c0001t0003g0142 a0001c0001t0003g0162 others(1): Show |
5 | HG02055.hp2 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+280G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126484804 | |||||||
| chr5:126484975 | T | A | 11 | a0001c0001t0001g0295 a0001c0001t0001g0297 a0001c0001t0001g0318 others(8): Show |
11 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.970+451T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126484975 | |||||||
| chr5:126485031 | C | T | 7 | a0001c0001t0004g0103 a0001c0001t0004g0130 a0001c0001t0004g0131 others(4): Show |
7 | HG02257.hp2 HG02886.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.970+507C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485031 | |||||||
| chr5:126485120 | C | A | 151 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(148): Show |
155 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.971-566C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485120 | |||||||
| chr5:126485131 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.971-555T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485131 | |||||||
| chr5:126485205 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0197 |
2 | NA19005.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.971-481T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485205 | |||||||
| chr5:126485300 | G | A | 9 | a0001c0001t0004g0161 a0001c0001t0004g0180 a0001c0001t0005g0139 others(6): Show |
10 | HG01243.hp2 HG02055.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.971-386G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485300 | |||||||
| chr5:126485308 | G | A | 11 | a0001c0001t0003g0009 a0001c0001t0003g0114 a0001c0001t0003g0142 others(8): Show |
12 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.971-378G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485308 | |||||||
| chr5:126485404 | C | G | 7 | a0001c0001t0004g0103 a0001c0001t0004g0130 a0001c0001t0004g0131 others(4): Show |
7 | HG02257.hp2 HG02886.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.971-282C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485404 | |||||||
| chr5:126485413 | C | T | 9 | a0001c0001t0001g0318 a0001c0001t0002g0260 a0001c0001t0003g0015 others(6): Show |
9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.971-273C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485413 | |||||||
| chr5:126485451 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0176 |
2 | NA18964.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.971-235T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485451 | |||||||
| chr5:126485520 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0252 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.971-166A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485520 | |||||||
| chr5:126485595 | T | C | 5 | a0001c0001t0003g0078 a0001c0001t0003g0095 a0001c0001t0003g0191 others(2): Show |
5 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-91T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485595 | |||||||
| chr5:126485602 | T | G | 8 | a0001c0001t0003g0009 a0001c0001t0003g0114 a0001c0001t0003g0142 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.971-84T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485602 | |||||||
| chr5:126485663 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.971-23G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485663 | |||||||
| chr5:126485849 | A | G | 4 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0273 others(1): Show |
4 | HG02486.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+76A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126485849 | |||||||
| chr5:126485916 | C | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0279 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1058+143C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126485916 | |||||||
| chr5:126486057 | T | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0273 others(1): Show |
4 | HG02486.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+284T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486057 | |||||||
| chr5:126486151 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1058+378C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486151 | |||||||
| chr5:126486169 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1058+396A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486169 | |||||||
| chr5:126486264 | A | G | 54 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0038 others(51): Show |
54 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1058+491A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486264 | |||||||
| chr5:126486313 | G | T | 65 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0057 others(62): Show |
67 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.1058+540G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486313 | |||||||
| chr5:126486651 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059-222T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486651 | |||||||
| chr5:126486654 | C | T | 1 | a0001c0001t0005g0268 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1059-219C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486654 | |||||||
| chr5:126486749 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1059-124C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486749 | |||||||
| chr5:126486835 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0284 a0001c0001t0001g0286 others(1): Show |
4 | HG02896.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-38G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486835 | |||||||
| chr5:126487066 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0014g0034 |
2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1163+89T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487066 | |||||||
| chr5:126487382 | T | G | 2 | a0001c0001t0001g0036 a0001c0001t0014g0034 |
2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1163+405T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487382 | |||||||
| chr5:126487634 | G | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0279 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1163+657G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487634 | |||||||
| chr5:126487665 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0279 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1163+688A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487665 | |||||||
| chr5:126487699 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1163+722G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487699 | |||||||
| chr5:126487743 | G | A | 1 | a0001c0001t0003g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1163+766G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487743 | |||||||
| chr5:126487787 | T | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0273 others(1): Show |
4 | HG02486.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163+810T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487787 | |||||||
| chr5:126487825 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1163+848T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487825 | |||||||
| chr5:126487892 | G | A | 255 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(252): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1164-907G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487892 | |||||||
| chr5:126487902 | G | T | 12 | a0001c0001t0001g0277 a0001c0001t0003g0009 a0001c0001t0003g0114 others(9): Show |
13 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1164-897G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487902 | |||||||
| chr5:126488122 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0297 |
2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1164-677G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126488122 | |||||||
| chr5:126488163 | A | G | 1 | a0001c0001t0003g0184 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1164-636A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126488163 | |||||||
| chr5:126488260 | G | T | 3 | a0001c0001t0004g0161 a0001c0001t0004g0180 a0001c0001t0005g0139 |
3 | HG02922.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1164-539G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126488260 | |||||||
| chr5:126488357 | G | A | 255 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(252): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1164-442G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126488357 | |||||||
| chr5:126488597 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1164-202G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126488597 | |||||||
| chr5:126488994 | G | A | 3 | a0001c0001t0004g0161 a0001c0001t0004g0180 a0001c0001t0005g0139 |
3 | HG02922.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1257+102G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126488994 | |||||||
| chr5:126489018 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1257+126T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489018 | |||||||
| chr5:126489117 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1257+225G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489117 | |||||||
| chr5:126489127 | C | T | 255 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(252): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1257+235C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489127 | |||||||
| chr5:126489182 | T | C | 255 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(252): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1257+290T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489182 | |||||||
| chr5:126489186 | G | A | 9 | a0001c0001t0001g0318 a0001c0001t0002g0260 a0001c0001t0003g0015 others(6): Show |
9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1257+294G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489186 | |||||||
| chr5:126489208 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1257+316A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489208 | |||||||
| chr5:126489324 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1257+432C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489324 | |||||||
| chr5:126489387 | C | G | 262 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(259): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1257+495C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489387 | |||||||
| chr5:126489403 | C | T | 1 | a0002c0003t0001g0182 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1257+511C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489403 | |||||||
| chr5:126489422 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1257+530C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489422 | |||||||
| chr5:126489427 | G | A | 9 | a0001c0001t0001g0318 a0001c0001t0002g0260 a0001c0001t0003g0015 others(6): Show |
9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1257+535G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489427 | |||||||
| chr5:126489615 | C | T | 3 | a0001c0001t0004g0103 a0001c0001t0004g0131 a0001c0001t0004g0274 |
3 | HG03130.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1257+723C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489615 | |||||||
| chr5:126489630 | A | T | 255 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(252): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1257+738A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489630 | |||||||
| chr5:126489800 | G | GAGA | 255 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(252): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1257+910_1257+912d others(5): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr5 | 126489800 | ||||||
| chr5:126489997 | A | G | 4 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0273 others(1): Show |
4 | HG02486.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257+1105A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489997 | |||||||
| chr5:126490030 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1257+1138T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490030 | |||||||
| chr5:126490132 | A | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(254): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1257+1240A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490132 | |||||||
| chr5:126490184 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1257+1292G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490184 | |||||||
| chr5:126490240 | A | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(254): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1257+1348A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490240 | |||||||
| chr5:126490258 | A | G | 1 | a0001c0001t0004g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1257+1366A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490258 | |||||||
| chr5:126490349 | G | A | 1 | a0001c0001t0015g0287 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1257+1457G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490349 | |||||||
| chr5:126490351 | TG | T | 252 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(249): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.1257+1462delG | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr5 | 126490351 | ||||||
| chr5:126490362 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1257+1470G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490362 | |||||||
| chr5:126490397 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1257+1505A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490397 | |||||||
| chr5:126490469 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0295 |
2 | HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1257+1577G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490469 | |||||||
| chr5:126490499 | T | C | 273 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1257+1607T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490499 | |||||||
| chr5:126490532 | A | G | 1 | a0002c0003t0003g0283 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1257+1640A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490532 | |||||||
| chr5:126490544 | G | A | 1 | a0001c0001t0003g0245 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1257+1652G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490544 | |||||||
| chr5:126490556 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0252 a0001c0001t0001g0277 others(12): Show |
16 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1257+1664C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490556 | |||||||
| chr5:126490557 | G | A | 1 | a0001c0001t0006g0255 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1257+1665G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490557 | |||||||
| chr5:126490593 | A | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0279 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1257+1701A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490593 | |||||||
| chr5:126490634 | C | A | 5 | a0001c0001t0001g0318 a0001c0001t0002g0260 a0001c0001t0005g0188 others(2): Show |
5 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257+1742C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490634 | |||||||
| chr5:126490637 | C | T | 5 | a0001c0001t0001g0285 a0001c0001t0002g0005 a0001c0001t0002g0166 others(2): Show |
5 | HG00639.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257+1745C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490637 | |||||||
| chr5:126490642 | G | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0159 others(15): Show |
19 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1257+1750G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490642 | |||||||
| chr5:126490708 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1257+1816C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490708 | |||||||
| chr5:126490732 | T | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0017 others(150): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1257+1840T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490732 | |||||||
| chr5:126490839 | C | T | 1 | a0001c0001t0005g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1257+1947C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490839 | |||||||
| chr5:126490953 | C | T | 1 | a0001c0001t0004g0253 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1258-1962C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490953 | |||||||
| chr5:126491080 | A | C | 1 | a0001c0001t0001g0288 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1258-1835A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491080 | |||||||
| chr5:126491097 | T | C | 270 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(267): Show |
276 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1258-1818T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491097 | |||||||
| chr5:126491148 | T | C | 1 | a0001c0001t0014g0034 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1258-1767T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491148 | |||||||
| chr5:126491332 | G | A | 127 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0012 others(124): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1258-1583G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491332 | |||||||
| chr5:126491427 | T | C | 6 | a0001c0001t0001g0118 a0001c0001t0001g0318 a0001c0001t0006g0006 others(3): Show |
7 | HG01243.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1258-1488T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491427 | |||||||
| chr5:126491538 | C | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(80): Show |
85 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1258-1377C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491538 | |||||||
| chr5:126491542 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1258-1373G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491542 | |||||||
| chr5:126491591 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1258-1324T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491591 | |||||||
| chr5:126491606 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1258-1309C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491606 | |||||||
| chr5:126491645 | T | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0318 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1258-1270T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491645 | |||||||
| chr5:126491647 | T | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0318 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1258-1268T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491647 | |||||||
| chr5:126491689 | G | T | 4 | a0001c0001t0006g0006 a0001c0001t0006g0234 a0001c0001t0006g0255 others(1): Show |
5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-1226G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491689 | |||||||
| chr5:126491827 | A | G | 4 | a0001c0001t0006g0006 a0001c0001t0006g0234 a0001c0001t0006g0255 others(1): Show |
5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-1088A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491827 | |||||||
| chr5:126492130 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0212 a0001c0001t0001g0243 others(1): Show |
4 | HG02165.hp1 NA18984.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1258-785G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492130 | |||||||
| chr5:126492210 | GTTAAACA others(13): Show |
G | 4 | a0001c0001t0006g0006 a0001c0001t0006g0234 a0001c0001t0006g0255 others(1): Show |
5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-702_1258-683d others(22): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr5 | 126492210 | ||||||
| chr5:126492224 | T | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(262): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1258-691T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492224 | |||||||
| chr5:126492229 | G | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(262): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1258-686G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492229 | |||||||
| chr5:126492392 | T | C | 1 | a0002c0003t0003g0283 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1258-523T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492392 | |||||||
| chr5:126492411 | G | A | 4 | a0001c0001t0006g0006 a0001c0001t0006g0234 a0001c0001t0006g0255 others(1): Show |
5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-504G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492411 | |||||||
| chr5:126492477 | T | C | 2 | a0001c0001t0001g0280 a0001c0004t0001g0292 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1258-438T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492477 | |||||||
| chr5:126492484 | G | C | 2 | a0001c0001t0002g0082 a0001c0001t0002g0315 |
2 | HG01891.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1258-431G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492484 | |||||||
| chr5:126492512 | G | C | 6 | a0001c0001t0003g0078 a0001c0001t0003g0095 a0001c0001t0003g0158 others(3): Show |
6 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1258-403G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492512 | |||||||
| chr5:126492556 | A | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0012 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1258-359A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492556 | |||||||
| chr5:126492769 | A | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0279 a0001c0002t0001g0116 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258-146A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492769 |