Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9402 |
| ensemblid | ENSG00000100351.17 |
| hgncid | 4563 |
| symbol | GRAP2 |
| name | GRB2 related adaptor protein 2 |
| refseq_nuc | NM_004810.4 |
| refseq_prot | NP_004801.1 |
| ensembl_nuc | ENST00000344138.9 |
| ensembl_prot | ENSP00000339186.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 39901084 |
| end | 39973721 |
| strand | + |
| ver | v1.2 |
| region | chr22:39901084-39973721 |
| region5000 | chr22:39896084-39978721 |
| regionname0 | GRAP2_chr22_39901084_39973721 |
| regionname5000 | GRAP2_chr22_39896084_39978721 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 330 | 302 | 71 | 76 | 99 | 16 | 38 | 73 | GRAP2_chr22_39896084_39978721 | GRAP2 | MEAVA others(325): Show |
chr22 | 39896084 | 39978721 |
| a0002 | 0/0 | 330 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | MEAVA others(325): Show |
chr22 | 39896084 | 39978721 |
| a0003 | 0/0 | 330 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | MEAVA others(325): Show |
chr22 | 39896084 | 39978721 |
| a0004 | 0/0 | 330 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | MEAVA others(325): Show |
chr22 | 39896084 | 39978721 |
| a0005 | 0/0 | 330 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | MEAVA others(325): Show |
chr22 | 39896084 | 39978721 |
| a0006 | 0/0 | 330 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | MEAVA others(325): Show |
chr22 | 39896084 | 39978721 |
| a0007 | 0/0 | 330 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | MEAVA others(325): Show |
chr22 | 39896084 | 39978721 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 990 | 294 | 71 | 76 | 91 | 16 | 38 | GRAP2_chr22_39896084_39978721 | GRAP2 | ATGGA others(985): Show |
chr22 | 39896084 | 39978721 | ||
| a0001c0002 | 0/0 | 990 | 8 | 0 | 0 | 8 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | ATGGA others(985): Show |
chr22 | 39896084 | 39978721 | ||
| a0002c0003 | 0/0 | 990 | 5 | 5 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | ATGGA others(985): Show |
chr22 | 39896084 | 39978721 | ||
| a0003c0004 | 0/0 | 990 | 4 | 3 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | ATGGA others(985): Show |
chr22 | 39896084 | 39978721 | ||
| a0004c0005 | 0/0 | 990 | 2 | 0 | 1 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | ATGGA others(985): Show |
chr22 | 39896084 | 39978721 | ||
| a0005c0006 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | ATGGA others(985): Show |
chr22 | 39896084 | 39978721 | ||
| a0006c0008 | 0/0 | 990 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | ATGGA others(985): Show |
chr22 | 39896084 | 39978721 | ||
| a0007c0007 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | ATGGA others(985): Show |
chr22 | 39896084 | 39978721 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3891 | 173 | 43 | 51 | 45 | 11 | 22 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0002 | 1/0 | 3891 | 79 | 4 | 21 | 38 | 4 | 11 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0003 | 0/0 | 3891 | 6 | 5 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0004 | 0/0 | 3891 | 6 | 5 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0005 | 0/0 | 3891 | 4 | 4 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0008 | 0/0 | 3891 | 3 | 0 | 0 | 0 | 0 | 3 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0009 | 0/0 | 3891 | 3 | 2 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0010 | 0/0 | 3891 | 3 | 0 | 0 | 3 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0011 | 0/0 | 3891 | 2 | 0 | 0 | 0 | 0 | 2 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0012 | 0/0 | 3891 | 2 | 0 | 0 | 2 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0013 | 0/0 | 3891 | 2 | 2 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0014 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0015 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0016 | 0/0 | 3891 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0017 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0018 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0019 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0020 | 0/0 | 3891 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0021 | 0/0 | 3891 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0022 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3887): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0023 | 0/0 | 3891 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0001t0024 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0001c0002t0002 | 0/0 | 3891 | 8 | 0 | 0 | 8 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0002c0003t0007 | 0/0 | 3891 | 4 | 4 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0002c0003t0025 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0003c0004t0006 | 0/0 | 3891 | 4 | 3 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0004c0005t0002 | 0/0 | 3891 | 2 | 0 | 1 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0005c0006t0002 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0006c0008t0002 | 0/0 | 3891 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| a0007c0007t0001 | 0/0 | 3891 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | AGACT others(3886): Show |
chr22 | 39896084 | 39978721 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0004g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0009g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0009g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0010g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0010g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0010g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0011g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0011g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0012g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0014g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0015g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0016g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0017g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0018g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0019g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0020g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0021g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0022g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0023g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0001t0024g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0002c0003t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0002c0003t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0002c0003t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0002c0003t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0002c0003t0025g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0003c0004t0006g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0003c0004t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0003c0004t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0003c0004t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0004c0005t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0004c0005t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0005c0006t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0006c0008t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| a0007c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0065 | EUR | GBR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0200 | EUR | FIN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01243 | hp1 | a0003 | c0004 | t0006 | g0122 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01261 | hp1 | a0004 | c0005 | t0002 | g0220 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01358 | hp1 | a0001 | c0001 | t0023 | g0012 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0236 | EUR | IBS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | IBS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01516 | hp2 | a0001 | c0001 | t0021 | g0176 | EUR | IBS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0232 | EUR | IBS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01891 | hp1 | a0001 | c0001 | t0015 | g0134 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01891 | hp2 | a0005 | c0006 | t0002 | g0156 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01978 | hp1 | a0001 | c0001 | t0016 | g0074 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02145 | hp2 | a0002 | c0003 | t0025 | g0186 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | CDX | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02622 | hp2 | a0002 | c0003 | t0007 | g0123 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02630 | hp2 | a0002 | c0003 | t0007 | g0121 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02647 | hp1 | a0003 | c0004 | t0006 | g0125 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02717 | hp2 | a0003 | c0004 | t0006 | g0124 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0049 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02809 | hp1 | a0002 | c0003 | t0007 | g0158 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02818 | hp1 | a0001 | c0001 | t0017 | g0286 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03017 | hp1 | a0004 | c0005 | t0002 | g0150 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | MSL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0161 | AFR | ESN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0284 | AFR | ESN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0287 | AFR | ESN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ESN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03225 | hp1 | a0002 | c0003 | t0007 | g0126 | AFR | MSL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0036 | AFR | MSL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0051 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03239 | hp2 | a0006 | c0008 | t0002 | g0217 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0281 | AFR | ESN | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | GWD | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0159 | AFR | MSL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03688 | hp1 | a0001 | c0001 | t0011 | g0034 | SAS | STU | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03834 | hp1 | a0001 | c0001 | t0008 | g0050 | SAS | BEB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0033 | SAS | STU | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | BEB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | STU | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | STU | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | YRI | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | YRI | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18942 | hp2 | a0001 | c0001 | t0010 | g0084 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18963 | hp2 | a0001 | c0001 | t0022 | g0064 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18972 | hp2 | a0001 | c0001 | t0010 | g0136 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18979 | hp1 | a0001 | c0001 | t0012 | g0141 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18992 | hp1 | a0001 | c0001 | t0009 | g0180 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19002 | hp1 | a0001 | c0001 | t0020 | g0108 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19043 | hp2 | a0001 | c0001 | t0024 | g0023 | AFR | LWK | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19070 | hp2 | a0001 | c0001 | t0012 | g0031 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19083 | hp1 | a0007 | c0007 | t0001 | g0098 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0275 | AFR | YRI | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ASW | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ASW | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | GIH | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | GIH | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0276 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02486 | hp1 | a0001 | c0001 | t0019 | g0253 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0277 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG03471 | hp2 | a0003 | c0004 | t0006 | g0128 | AFR | MSL | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | USA | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0283 | AFR | USA | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18955 | hp1 | a0001 | c0001 | t0010 | g0076 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | USA | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | USA | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0094 | REF | REF | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0066 | REF | REF | GRAP2_chr22_39896084_39978721 | GRAP2 | chr22 | 39896084 | 39978721 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39960157 | C | A | 1 | a0005 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.273C>A | p.Asp91Glu | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/8 | 534/3891 | 273/993 | 91/330 | chr22 | 39960157 | |||
| chr22:39968048 | C | T | 1 | a0003 | 4 | HG01243.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
missense_variant | MODERATE | c.466C>T | p.Arg156Trp | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/8 | 727/3891 | 466/993 | 156/330 | chr22 | 39968048 | |||
| chr22:39968118 | G | A | 1 | a0004 | 2 | HG01261.hp1 HG03017.hp1 |
missense_variant | MODERATE | c.536G>A | p.Arg179Gln | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/8 | 797/3891 | 536/993 | 179/330 | chr22 | 39968118 | |||
| chr22:39969459 | G | A | 1 | a0002 | 5 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.739G>A | p.Gly247Ser | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/8 | 1000/3891 | 739/993 | 247/330 | chr22 | 39969459 | |||
| chr22:39970921 | G | A | 1 | a0007 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.830G>A | p.Arg277Gln | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 1091/3891 | 830/993 | 277/330 | chr22 | 39970921 | |||
| chr22:39970968 | C | T | 1 | a0006 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.877C>T | p.His293Tyr | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 1138/3891 | 877/993 | 293/330 | chr22 | 39970968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39969521 | C | G | 1 | a0001c0002 | 8 | HG02027.hp2 HG02083.hp1 HG02165.hp2 others(5): Show |
synonymous_variant | LOW | c.801C>G | p.Leu267Leu | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/8 | 1062/3891 | 801/993 | 267/330 | chr22 | 39969521 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39901155 | G | A | 1 | a0001c0001t0014 | 1 | HG03195.hp1 | 5_prime_UTR_variant | MODIFIER | c.-190G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/8 | 45952 | chr22 | 39901155 | ||||||
| chr22:39901175 | C | T | 3 | a0001c0001t0013 a0001c0001t0024 a0002c0003t0025 |
4 | HG02145.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-170C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/8 | 45932 | chr22 | 39901175 | ||||||
| chr22:39971125 | C | T | 1 | a0001c0001t0023 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*41C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 41 | chr22 | 39971125 | ||||||
| chr22:39971150 | C | A | 1 | a0001c0001t0015 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 66 | chr22 | 39971150 | ||||||
| chr22:39971167 | A | G | 1 | a0001c0001t0004 | 6 | HG01109.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*83A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 83 | chr22 | 39971167 | ||||||
| chr22:39971216 | T | A | 1 | a0001c0001t0016 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 132 | chr22 | 39971216 | ||||||
| chr22:39971251 | G | GTTGATGC others(24): Show |
1 | a0001c0001t0022 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168_*198dupTTGATG others(25): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 199 | INFO_REALIGN_3_PRIME | chr22 | 39971251 | |||||
| chr22:39971294 | T | C | 1 | a0001c0001t0022 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 210 | chr22 | 39971294 | ||||||
| chr22:39971296 | C | T | 1 | a0001c0001t0022 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*212C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 212 | chr22 | 39971296 | ||||||
| chr22:39971301 | C | T | 1 | a0001c0001t0022 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*217C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 217 | chr22 | 39971301 | ||||||
| chr22:39971302 | T | C | 1 | a0001c0001t0022 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*218T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 218 | chr22 | 39971302 | ||||||
| chr22:39971308 | CCTCAGGG others(23): Show |
C | 1 | a0001c0001t0022 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225_*254delCTCAGG others(24): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 225 | chr22 | 39971308 | ||||||
| chr22:39971491 | T | C | 1 | a0001c0001t0017 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*407T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 407 | chr22 | 39971491 | ||||||
| chr22:39971522 | G | A | 1 | a0001c0001t0011 | 2 | HG03688.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*438G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 438 | chr22 | 39971522 | ||||||
| chr22:39971539 | G | A | 1 | a0001c0001t0018 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*455G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 455 | chr22 | 39971539 | ||||||
| chr22:39971540 | C | A | 1 | a0001c0001t0018 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*456C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 456 | chr22 | 39971540 | ||||||
| chr22:39971543 | A | G | 1 | a0001c0001t0003 | 6 | HG01243.hp2 HG02055.hp2 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*459A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 459 | chr22 | 39971543 | ||||||
| chr22:39971947 | A | G | 3 | a0002c0003t0007 a0002c0003t0025 a0003c0004t0006 |
9 | HG01243.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*863A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 863 | chr22 | 39971947 | ||||||
| chr22:39972171 | C | T | 3 | a0002c0003t0007 a0002c0003t0025 a0003c0004t0006 |
9 | HG01243.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1087C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 1087 | chr22 | 39972171 | ||||||
| chr22:39972225 | T | C | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*1141T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 1141 | chr22 | 39972225 | ||||||
| chr22:39972423 | A | C | 2 | a0002c0003t0007 a0002c0003t0025 |
5 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1339A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 1339 | chr22 | 39972423 | ||||||
| chr22:39972463 | G | A | 1 | a0001c0001t0020 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1379G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 1379 | chr22 | 39972463 | ||||||
| chr22:39972474 | C | T | 1 | a0001c0001t0010 | 3 | NA18942.hp2 NA18955.hp1 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1390C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 1390 | chr22 | 39972474 | ||||||
| chr22:39972475 | G | A | 3 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0017 |
6 | HG01891.hp1 HG02257.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1391G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 1391 | chr22 | 39972475 | ||||||
| chr22:39972604 | G | A | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(17): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1520G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 1520 | chr22 | 39972604 | ||||||
| chr22:39973069 | G | A | 1 | a0001c0001t0021 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1985G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 1985 | chr22 | 39973069 | ||||||
| chr22:39973297 | G | T | 1 | a0001c0001t0008 | 3 | HG02738.hp1 HG03239.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2213G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 2213 | chr22 | 39973297 | ||||||
| chr22:39973439 | C | T | 2 | a0002c0003t0007 a0002c0003t0025 |
5 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2355C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 2355 | chr22 | 39973439 | ||||||
| chr22:39973540 | A | T | 1 | a0001c0001t0012 | 2 | NA18979.hp1 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2456A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 2456 | chr22 | 39973540 | ||||||
| chr22:39973645 | C | G | 1 | a0001c0001t0019 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2561C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 8/8 | 2561 | chr22 | 39973645 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39901415 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-15+85T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39901415 | |||||||
| chr22:39901548 | C | T | 3 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0004g0290 |
3 | HG02258.hp2 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-15+218C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39901548 | |||||||
| chr22:39901805 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-15+475C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39901805 | |||||||
| chr22:39902004 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-15+674A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39902004 | |||||||
| chr22:39902178 | A | G | 3 | a0001c0001t0001g0288 a0001c0001t0014g0287 a0001c0001t0017g0286 |
3 | HG02622.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15+848A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39902178 | |||||||
| chr22:39902563 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0005g0019 |
2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-15+1233G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39902563 | |||||||
| chr22:39902710 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+1380T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39902710 | |||||||
| chr22:39902727 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+1397A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39902727 | |||||||
| chr22:39902940 | C | T | 1 | a0001c0001t0002g0279 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-15+1610C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39902940 | |||||||
| chr22:39903119 | G | C | 1 | a0001c0001t0002g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+1789G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39903119 | |||||||
| chr22:39903154 | A | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(153): Show |
172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.-15+1824A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39903154 | |||||||
| chr22:39903475 | C | CT | 107 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(104): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-15+2165dupT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39903475 | ||||||
| chr22:39903475 | C | CTT | 16 | a0001c0001t0001g0020 a0001c0001t0001g0142 a0001c0001t0001g0268 others(13): Show |
17 | HG02055.hp1 HG02083.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-15+2164_-15+2165d others(4): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39903475 | ||||||
| chr22:39903475 | CT | C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
12 | HG01069.hp2 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-15+2165delT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39903475 | ||||||
| chr22:39903499 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-15+2169A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39903499 | |||||||
| chr22:39903740 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-15+2410G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39903740 | |||||||
| chr22:39903874 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-15+2544G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39903874 | |||||||
| chr22:39904900 | C | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG02523.hp2 NA19004.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+3570C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39904900 | |||||||
| chr22:39904904 | C | G | 11 | a0001c0001t0001g0145 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
12 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-15+3574C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39904904 | |||||||
| chr22:39904909 | T | G | 1 | a0001c0001t0005g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15+3579T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39904909 | |||||||
| chr22:39904964 | C | T | 13 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(10): Show |
13 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+3634C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39904964 | |||||||
| chr22:39905140 | C | G | 1 | a0002c0003t0025g0186 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-15+3810C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905140 | |||||||
| chr22:39905145 | G | C | 2 | a0001c0001t0001g0029 a0001c0001t0002g0030 |
2 | NA18984.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-15+3815G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905145 | |||||||
| chr22:39905151 | T | C | 3 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0004g0290 |
3 | HG02258.hp2 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-15+3821T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905151 | |||||||
| chr22:39905170 | A | G | 9 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0259 others(6): Show |
9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+3840A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905170 | |||||||
| chr22:39905219 | G | A | 1 | a0001c0001t0003g0280 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-15+3889G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905219 | |||||||
| chr22:39905462 | G | C | 2 | a0001c0001t0012g0031 a0001c0001t0012g0141 |
2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-15+4132G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905462 | |||||||
| chr22:39905476 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(199): Show |
219 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-15+4146G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905476 | |||||||
| chr22:39905541 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-15+4211G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905541 | |||||||
| chr22:39905596 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-15+4266C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905596 | |||||||
| chr22:39905741 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-15+4411G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905741 | |||||||
| chr22:39905873 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+4543C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905873 | |||||||
| chr22:39905917 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+4587T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905917 | |||||||
| chr22:39905980 | G | T | 1 | a0001c0001t0001g0258 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-15+4650G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39905980 | |||||||
| chr22:39906014 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-15+4684G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39906014 | |||||||
| chr22:39906234 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-15+4904C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39906234 | |||||||
| chr22:39906257 | A | G | 1 | a0001c0001t0015g0134 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-15+4927A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39906257 | |||||||
| chr22:39906723 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-15+5393G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39906723 | |||||||
| chr22:39906924 | T | C | 1 | a0001c0001t0002g0279 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-15+5594T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39906924 | |||||||
| chr22:39907003 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-15+5673A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39907003 | |||||||
| chr22:39907038 | C | T | 5 | a0001c0001t0001g0273 a0001c0001t0005g0274 a0001c0001t0009g0276 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+5708C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39907038 | |||||||
| chr22:39907221 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-15+5891G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39907221 | |||||||
| chr22:39907560 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-15+6230G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39907560 | |||||||
| chr22:39907823 | T | A | 2 | a0001c0001t0001g0020 a0001c0001t0005g0019 |
2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-15+6493T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39907823 | |||||||
| chr22:39907907 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-15+6577G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39907907 | |||||||
| chr22:39907918 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-15+6588C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39907918 | |||||||
| chr22:39907930 | C | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0168 others(11): Show |
15 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15+6600C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39907930 | |||||||
| chr22:39908262 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-15+6932C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39908262 | |||||||
| chr22:39908577 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(177): Show |
197 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-15+7247C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39908577 | |||||||
| chr22:39909639 | C | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0111 others(17): Show |
20 | HG00280.hp1 HG01081.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15+8309C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39909639 | |||||||
| chr22:39909660 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-15+8330G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39909660 | |||||||
| chr22:39909701 | C | A | 1 | a0001c0001t0005g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-15+8371C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39909701 | |||||||
| chr22:39909922 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+8592G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39909922 | |||||||
| chr22:39910189 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(196): Show |
216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.-15+8859C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39910189 | |||||||
| chr22:39910294 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-15+8964T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39910294 | |||||||
| chr22:39910499 | C | T | 1 | a0001c0001t0005g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15+9169C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39910499 | |||||||
| chr22:39910597 | C | T | 1 | a0001c0001t0005g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15+9267C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39910597 | |||||||
| chr22:39910649 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-15+9319C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39910649 | |||||||
| chr22:39910650 | G | A | 71 | a0001c0001t0001g0013 a0001c0001t0001g0198 a0001c0001t0001g0199 others(68): Show |
76 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.-15+9320G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39910650 | |||||||
| chr22:39910741 | T | TA | 32 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0035 others(29): Show |
34 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-15+9426dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39910741 | ||||||
| chr22:39911207 | G | C | 1 | a0001c0001t0002g0201 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-15+9877G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911207 | |||||||
| chr22:39911287 | G | A | 2 | a0001c0001t0002g0120 a0002c0003t0007g0121 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-15+9957G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911287 | |||||||
| chr22:39911293 | C | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0167 a0001c0001t0001g0196 |
4 | HG02145.hp1 HG02717.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+9963C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911293 | |||||||
| chr22:39911333 | C | A | 17 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(14): Show |
17 | HG00280.hp1 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-15+10003C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911333 | |||||||
| chr22:39911383 | A | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(200): Show |
220 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-15+10053A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911383 | |||||||
| chr22:39911440 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-15+10110A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911440 | |||||||
| chr22:39911528 | C | G | 74 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0198 others(71): Show |
77 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-15+10198C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911528 | |||||||
| chr22:39911537 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+10207G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911537 | |||||||
| chr22:39911755 | C | T | 1 | a0001c0001t0019g0253 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-15+10425C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911755 | |||||||
| chr22:39911832 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-15+10502G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911832 | |||||||
| chr22:39911890 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(139): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-15+10560C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39911890 | |||||||
| chr22:39912013 | C | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG01109.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-15+10683C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39912013 | |||||||
| chr22:39912249 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-15+10919C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39912249 | |||||||
| chr22:39912281 | A | G | 17 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(14): Show |
17 | HG00280.hp1 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-15+10951A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39912281 | |||||||
| chr22:39912333 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
8 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+11003A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39912333 | |||||||
| chr22:39912424 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(195): Show |
215 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.-15+11094G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39912424 | |||||||
| chr22:39912647 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-15+11317T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39912647 | |||||||
| chr22:39912742 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-15+11412T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39912742 | |||||||
| chr22:39912914 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(141): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.-15+11584C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39912914 | |||||||
| chr22:39912921 | G | C | 1 | a0001c0001t0005g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15+11591G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39912921 | |||||||
| chr22:39912933 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-15+11603C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39912933 | |||||||
| chr22:39913049 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-15+11719T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39913049 | |||||||
| chr22:39913062 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-15+11732G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39913062 | |||||||
| chr22:39913100 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-15+11770G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39913100 | |||||||
| chr22:39913192 | C | CA | 8 | a0001c0001t0001g0040 a0001c0001t0001g0184 a0001c0001t0001g0197 others(5): Show |
8 | HG00323.hp2 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+11881dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39913192 | ||||||
| chr22:39913192 | C | CAA | 17 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(14): Show |
17 | HG00280.hp1 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-15+11880_-15+1188 others(6): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39913192 | ||||||
| chr22:39913192 | CA | C | 12 | a0001c0001t0001g0144 a0001c0001t0001g0165 a0001c0001t0001g0166 others(9): Show |
12 | HG01070.hp1 HG01168.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-15+11881delA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39913192 | ||||||
| chr22:39913326 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0152 others(3): Show |
11 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+11996G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39913326 | |||||||
| chr22:39913506 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(202): Show |
222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-15+12176T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39913506 | |||||||
| chr22:39913514 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-15+12184C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39913514 | |||||||
| chr22:39913852 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(195): Show |
215 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.-15+12522G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39913852 | |||||||
| chr22:39913929 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-15+12599G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39913929 | |||||||
| chr22:39914013 | A | T | 1 | a0001c0001t0002g0246 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-15+12683A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39914013 | |||||||
| chr22:39914082 | T | C | 2 | a0001c0001t0002g0272 a0001c0002t0002g0208 |
2 | NA19003.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-15+12752T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39914082 | |||||||
| chr22:39914149 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+12819G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39914149 | |||||||
| chr22:39914310 | A | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0040 others(13): Show |
18 | HG00621.hp1 HG02027.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-15+12980A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39914310 | |||||||
| chr22:39914482 | ATT | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(195): Show |
215 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.-15+13156_-15+1315 others(6): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39914482 | ||||||
| chr22:39914579 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-15+13249A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39914579 | |||||||
| chr22:39914687 | A | G | 2 | a0001c0001t0009g0276 a0001c0001t0009g0277 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-15+13357A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39914687 | |||||||
| chr22:39914791 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0252 a0001c0001t0001g0257 others(1): Show |
5 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+13461G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39914791 | |||||||
| chr22:39914828 | T | A | 17 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(14): Show |
17 | HG00280.hp1 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-15+13498T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39914828 | |||||||
| chr22:39915069 | A | C | 1 | a0001c0001t0001g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-15+13739A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39915069 | |||||||
| chr22:39915095 | G | A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0127 others(22): Show |
26 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-15+13765G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39915095 | |||||||
| chr22:39915188 | C | CA | 24 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0042 others(21): Show |
25 | HG00140.hp1 HG00741.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-15+13875dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39915188 | ||||||
| chr22:39915642 | C | G | 2 | a0001c0001t0013g0036 a0001c0001t0024g0023 |
2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-15+14312C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39915642 | |||||||
| chr22:39915650 | G | A | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG00639.hp2 HG01175.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+14320G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39915650 | |||||||
| chr22:39915651 | G | C | 18 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0038 others(15): Show |
18 | HG00423.hp1 HG00438.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.-15+14321G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39915651 | |||||||
| chr22:39915770 | C | A | 2 | a0001c0001t0002g0209 a0001c0001t0002g0247 |
2 | NA18954.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.-15+14440C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39915770 | |||||||
| chr22:39915779 | A | G | 1 | a0001c0001t0002g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-15+14449A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39915779 | |||||||
| chr22:39915875 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(140): Show |
158 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.-15+14545G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39915875 | |||||||
| chr22:39915878 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0252 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-15+14548C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39915878 | |||||||
| chr22:39916069 | C | T | 1 | a0001c0001t0004g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-15+14739C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39916069 | |||||||
| chr22:39916289 | A | G | 1 | a0001c0001t0002g0243 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-15+14959A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39916289 | |||||||
| chr22:39916323 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+14993C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39916323 | |||||||
| chr22:39916837 | C | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0252 a0001c0001t0001g0257 others(5): Show |
9 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+15507C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39916837 | |||||||
| chr22:39916870 | AT | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0252 a0001c0001t0001g0257 others(5): Show |
9 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+15550delT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39916870 | ||||||
| chr22:39916946 | T | A | 1 | a0001c0001t0005g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-15+15616T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39916946 | |||||||
| chr22:39916958 | T | A | 2 | a0001c0001t0002g0120 a0002c0003t0007g0121 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-15+15628T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39916958 | |||||||
| chr22:39916959 | T | G | 2 | a0001c0001t0002g0120 a0002c0003t0007g0121 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-15+15629T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39916959 | |||||||
| chr22:39917120 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+15790T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39917120 | |||||||
| chr22:39917244 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-15+15914C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39917244 | |||||||
| chr22:39917352 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(199): Show |
219 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-15+16022T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39917352 | |||||||
| chr22:39917365 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-15+16035C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39917365 | |||||||
| chr22:39917366 | A | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-15+16036A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39917366 | |||||||
| chr22:39917495 | G | A | 1 | a0002c0003t0007g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-15+16165G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39917495 | |||||||
| chr22:39917672 | A | T | 1 | a0001c0001t0002g0097 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-15+16342A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39917672 | |||||||
| chr22:39917877 | G | A | 3 | a0001c0001t0013g0036 a0001c0001t0024g0023 a0002c0003t0025g0186 |
3 | HG02145.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-15+16547G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39917877 | |||||||
| chr22:39918007 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+16677C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39918007 | |||||||
| chr22:39918021 | A | G | 3 | a0001c0001t0001g0288 a0001c0001t0014g0287 a0001c0001t0017g0286 |
3 | HG02622.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15+16691A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39918021 | |||||||
| chr22:39918048 | T | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(198): Show |
218 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.-15+16718T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39918048 | |||||||
| chr22:39918156 | C | T | 98 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0035 others(95): Show |
104 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-15+16826C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39918156 | |||||||
| chr22:39918231 | A | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0152 others(3): Show |
11 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+16901A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39918231 | |||||||
| chr22:39918541 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-15+17211A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39918541 | |||||||
| chr22:39919006 | C | T | 3 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG02738.hp1 HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-15+17676C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39919006 | |||||||
| chr22:39919090 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+17760G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39919090 | |||||||
| chr22:39919099 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0152 others(3): Show |
11 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+17769C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39919099 | |||||||
| chr22:39919183 | C | A | 16 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(13): Show |
16 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15+17853C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39919183 | |||||||
| chr22:39919306 | A | G | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+17976A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39919306 | |||||||
| chr22:39919483 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-15+18153C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39919483 | |||||||
| chr22:39919662 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15+18332G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39919662 | |||||||
| chr22:39920042 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-15+18712A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39920042 | |||||||
| chr22:39920214 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-15+18884G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39920214 | |||||||
| chr22:39920344 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-15+19014C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39920344 | |||||||
| chr22:39920719 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-15+19389G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39920719 | |||||||
| chr22:39920767 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-15+19437C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39920767 | |||||||
| chr22:39920923 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-15+19593G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39920923 | |||||||
| chr22:39920943 | G | GAC | 10 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0102 others(7): Show |
11 | HG01361.hp1 HG02135.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+19659_-15+1966 others(6): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | G | GACAC | 7 | a0001c0001t0001g0198 a0001c0001t0001g0241 a0001c0001t0002g0139 others(4): Show |
7 | HG00621.hp2 HG01928.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+19657_-15+1966 others(8): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | G | GACACAC | 2 | a0001c0001t0002g0015 a0001c0001t0002g0095 |
3 | HG01981.hp1 NA18963.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-15+19655_-15+1966 others(10): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | G | GACACACA others(3): Show |
1 | a0001c0001t0001g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-15+19651_-15+1966 others(14): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | GAC | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-15+19659_-15+1966 others(6): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | GACAC | G | 24 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(21): Show |
25 | HG00323.hp1 HG00639.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-15+19657_-15+1966 others(8): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | GACACAC | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0069 a0001c0001t0001g0129 others(18): Show |
22 | HG00733.hp2 HG01099.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.-15+19655_-15+1966 others(10): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | GACACACA others(1): Show |
G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0111 others(31): Show |
41 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-15+19653_-15+1966 others(12): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | GACACACA others(3): Show |
G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0154 others(15): Show |
20 | HG00642.hp2 HG02109.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15+19651_-15+1966 others(14): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | GACACACA others(5): Show |
G | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0018 others(26): Show |
32 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.-15+19649_-15+1966 others(16): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | GACACACA others(7): Show |
G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0022 |
3 | HG02698.hp2 HG02922.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-15+19647_-15+1966 others(18): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | GACACACA others(9): Show |
G | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-15+19645_-15+1966 others(20): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920943 | GACACACA others(11): Show |
G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0255 |
2 | HG02074.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-15+19643_-15+1966 others(22): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39920943 | ||||||
| chr22:39920999 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-15+19669T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39920999 | |||||||
| chr22:39921031 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-15+19701A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921031 | |||||||
| chr22:39921055 | G | T | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-15+19725G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921055 | |||||||
| chr22:39921122 | C | A | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(77): Show |
86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.-15+19792C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921122 | |||||||
| chr22:39921218 | G | A | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0020g0108 |
3 | NA19002.hp1 NA19010.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-15+19888G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921218 | |||||||
| chr22:39921270 | T | G | 2 | a0001c0001t0001g0020 a0001c0001t0005g0019 |
2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-15+19940T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921270 | |||||||
| chr22:39921332 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-15+20002T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921332 | |||||||
| chr22:39921356 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-15+20026A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921356 | |||||||
| chr22:39921359 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+20029T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921359 | |||||||
| chr22:39921551 | G | A | 1 | a0001c0001t0004g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-15+20221G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921551 | |||||||
| chr22:39921623 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(176): Show |
195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.-15+20293T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921623 | |||||||
| chr22:39921725 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-15+20395A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921725 | |||||||
| chr22:39921891 | G | A | 1 | a0001c0001t0004g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-15+20561G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39921891 | |||||||
| chr22:39922194 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(171): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-15+20864A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39922194 | |||||||
| chr22:39922382 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-15+21052A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39922382 | |||||||
| chr22:39922449 | T | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0162 a0001c0001t0001g0163 others(4): Show |
9 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+21119T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39922449 | |||||||
| chr22:39922719 | G | A | 2 | a0001c0001t0013g0036 a0002c0003t0025g0186 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-15+21389G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39922719 | |||||||
| chr22:39922797 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-15+21467C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39922797 | |||||||
| chr22:39922806 | G | A | 1 | a0005c0006t0002g0156 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-15+21476G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39922806 | |||||||
| chr22:39922871 | C | T | 1 | a0001c0001t0013g0161 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-15+21541C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39922871 | |||||||
| chr22:39923039 | T | TA | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(56): Show |
69 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-15+21726dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39923039 | ||||||
| chr22:39923039 | TA | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0037 others(13): Show |
19 | HG00323.hp1 HG01256.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15+21726delA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39923039 | ||||||
| chr22:39923673 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-15+22343T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39923673 | |||||||
| chr22:39924011 | G | A | 9 | a0001c0001t0001g0127 a0001c0001t0002g0120 a0002c0003t0007g0121 others(6): Show |
9 | HG01243.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+22681G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39924011 | |||||||
| chr22:39924057 | A | T | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-15+22727A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39924057 | |||||||
| chr22:39924205 | G | A | 2 | a0001c0001t0013g0161 a0002c0003t0007g0158 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-15+22875G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39924205 | |||||||
| chr22:39924357 | C | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(173): Show |
192 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.-14-22736C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39924357 | |||||||
| chr22:39924722 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-14-22371A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39924722 | |||||||
| chr22:39924754 | A | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(179): Show |
198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.-14-22339A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39924754 | |||||||
| chr22:39924936 | A | G | 1 | a0001c0001t0013g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-14-22157A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39924936 | |||||||
| chr22:39925340 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-14-21753A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39925340 | |||||||
| chr22:39925583 | G | A | 3 | a0001c0001t0001g0288 a0001c0001t0014g0287 a0001c0001t0017g0286 |
3 | HG02622.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-14-21510G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39925583 | |||||||
| chr22:39925611 | T | G | 1 | a0001c0001t0001g0259 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-14-21482T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39925611 | |||||||
| chr22:39925658 | T | A | 1 | a0001c0001t0002g0240 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-14-21435T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39925658 | |||||||
| chr22:39926621 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-14-20472G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39926621 | |||||||
| chr22:39926621 | G | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0199 a0001c0001t0001g0250 |
3 | HG01975.hp1 HG01981.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-14-20472G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39926621 | |||||||
| chr22:39926680 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(170): Show |
189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.-14-20413G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39926680 | |||||||
| chr22:39926747 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-20346C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39926747 | |||||||
| chr22:39926867 | T | C | 2 | a0001c0001t0002g0027 a0001c0001t0002g0109 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-14-20226T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39926867 | |||||||
| chr22:39926875 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-14-20218G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39926875 | |||||||
| chr22:39926964 | G | T | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-14-20129G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39926964 | |||||||
| chr22:39927061 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(36): Show |
48 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-14-20032G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39927061 | |||||||
| chr22:39927227 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0131 a0001c0001t0001g0142 |
4 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-19866G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39927227 | |||||||
| chr22:39927267 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-14-19826C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39927267 | |||||||
| chr22:39927652 | G | T | 5 | a0001c0001t0001g0255 a0001c0001t0004g0010 a0001c0001t0004g0192 others(2): Show |
6 | HG01109.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-19441G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39927652 | |||||||
| chr22:39927689 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-14-19404G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39927689 | |||||||
| chr22:39927775 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14-19318G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39927775 | |||||||
| chr22:39928069 | T | C | 2 | a0001c0001t0005g0147 a0001c0001t0005g0159 |
2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-14-19024T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39928069 | |||||||
| chr22:39928479 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-14-18614G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39928479 | |||||||
| chr22:39928531 | A | C | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-14-18562A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39928531 | |||||||
| chr22:39928548 | G | A | 2 | a0001c0001t0001g0138 a0007c0007t0001g0098 |
2 | NA18991.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-14-18545G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39928548 | |||||||
| chr22:39928694 | G | C | 3 | a0001c0001t0001g0288 a0001c0001t0014g0287 a0001c0001t0017g0286 |
3 | HG02622.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-14-18399G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39928694 | |||||||
| chr22:39928906 | C | A | 1 | a0001c0001t0001g0018 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-14-18187C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39928906 | |||||||
| chr22:39929157 | C | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
56 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-14-17936C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39929157 | |||||||
| chr22:39929253 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-14-17840C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39929253 | |||||||
| chr22:39929401 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14-17692G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39929401 | |||||||
| chr22:39929599 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-14-17494A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39929599 | |||||||
| chr22:39929714 | A | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0255 a0001c0001t0004g0010 others(3): Show |
7 | HG01109.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-17379A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39929714 | |||||||
| chr22:39929848 | A | T | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14-17245A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39929848 | |||||||
| chr22:39929869 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | HG02135.hp2 HG02165.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-17224C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39929869 | |||||||
| chr22:39930170 | A | G | 116 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0035 others(113): Show |
122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.-14-16923A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39930170 | |||||||
| chr22:39930172 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-14-16921G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39930172 | |||||||
| chr22:39930730 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-14-16363G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39930730 | |||||||
| chr22:39930831 | C | G | 96 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0111 others(93): Show |
102 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-14-16262C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39930831 | |||||||
| chr22:39931084 | A | G | 1 | a0001c0001t0004g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14-16009A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39931084 | |||||||
| chr22:39931165 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-14-15928C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39931165 | |||||||
| chr22:39931185 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-14-15908A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39931185 | |||||||
| chr22:39931202 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0144 a0001c0001t0001g0174 others(5): Show |
9 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-15891A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39931202 | |||||||
| chr22:39931209 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-14-15884G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39931209 | |||||||
| chr22:39931740 | G | A | 5 | a0001c0001t0001g0255 a0001c0001t0004g0010 a0001c0001t0004g0192 others(2): Show |
6 | HG01109.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-15353G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39931740 | |||||||
| chr22:39931957 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-14-15136G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39931957 | |||||||
| chr22:39932046 | A | C | 10 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0002g0212 others(7): Show |
10 | HG00438.hp2 HG01099.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-15047A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39932046 | |||||||
| chr22:39932434 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-14-14659G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39932434 | |||||||
| chr22:39932513 | T | C | 1 | a0001c0001t0005g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-14-14580T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39932513 | |||||||
| chr22:39932548 | C | CA | 42 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(39): Show |
44 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.-14-14522dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39932548 | ||||||
| chr22:39932548 | CA | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(38): Show |
46 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-14-14522delA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39932548 | ||||||
| chr22:39932711 | T | A | 1 | a0001c0001t0001g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-14-14382T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39932711 | |||||||
| chr22:39932716 | C | CA | 49 | a0001c0001t0001g0007 a0001c0001t0001g0067 a0001c0001t0001g0129 others(46): Show |
52 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14-14360dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39932716 | ||||||
| chr22:39932987 | C | T | 52 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(49): Show |
56 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-14-14106C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39932987 | |||||||
| chr22:39933144 | G | GT | 58 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
63 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.-14-13948dupT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39933144 | ||||||
| chr22:39933210 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-14-13883C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39933210 | |||||||
| chr22:39933254 | C | G | 2 | a0001c0001t0002g0227 a0001c0001t0002g0229 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-14-13839C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39933254 | |||||||
| chr22:39933415 | T | A | 1 | a0001c0001t0019g0253 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-14-13678T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39933415 | |||||||
| chr22:39933563 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-14-13530G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39933563 | |||||||
| chr22:39933578 | C | T | 6 | a0001c0001t0002g0120 a0002c0003t0007g0121 a0003c0004t0006g0122 others(3): Show |
6 | HG01243.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-13515C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39933578 | |||||||
| chr22:39933600 | G | A | 2 | a0001c0001t0004g0290 a0005c0006t0002g0156 |
2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-14-13493G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39933600 | |||||||
| chr22:39933798 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0252 a0001c0001t0001g0257 others(1): Show |
5 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-13295G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39933798 | |||||||
| chr22:39934763 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-14-12330C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39934763 | |||||||
| chr22:39934764 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14-12329G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39934764 | |||||||
| chr22:39935086 | A | T | 1 | a0001c0001t0004g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14-12007A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39935086 | |||||||
| chr22:39935403 | TA | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01069.hp2 HG01099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-14-11689delA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39935403 | |||||||
| chr22:39935530 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14-11563A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39935530 | |||||||
| chr22:39936597 | C | G | 4 | a0001c0001t0001g0216 a0001c0001t0002g0218 a0001c0001t0002g0232 others(1): Show |
4 | HG01256.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-10496C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39936597 | |||||||
| chr22:39936628 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-14-10465G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39936628 | |||||||
| chr22:39936719 | G | A | 3 | a0001c0001t0002g0160 a0001c0001t0005g0147 a0001c0001t0005g0159 |
3 | HG03098.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-10374G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39936719 | |||||||
| chr22:39936771 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0167 a0001c0001t0001g0196 |
4 | HG02145.hp1 HG02717.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-10322G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39936771 | |||||||
| chr22:39936840 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-14-10253G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39936840 | |||||||
| chr22:39936840 | G | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | HG02135.hp2 HG02165.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-10253G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39936840 | |||||||
| chr22:39937125 | G | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(168): Show |
183 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-14-9968G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39937125 | |||||||
| chr22:39937156 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-14-9937G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39937156 | |||||||
| chr22:39937272 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-14-9821G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39937272 | |||||||
| chr22:39937528 | G | A | 1 | a0002c0003t0025g0186 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-14-9565G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39937528 | |||||||
| chr22:39937836 | C | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0040 others(9): Show |
14 | HG00621.hp1 HG02074.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-9257C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39937836 | |||||||
| chr22:39938018 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-14-9075G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39938018 | |||||||
| chr22:39938037 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-14-9056G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39938037 | |||||||
| chr22:39938049 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-14-9044G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39938049 | |||||||
| chr22:39938111 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-14-8982G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39938111 | |||||||
| chr22:39938364 | G | C | 1 | a0001c0001t0001g0003 | 3 | HG02109.hp2 HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-14-8729G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39938364 | |||||||
| chr22:39938389 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-14-8704T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39938389 | |||||||
| chr22:39938424 | C | T | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-14-8669C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39938424 | |||||||
| chr22:39938677 | G | A | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | NA18969.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-14-8416G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39938677 | |||||||
| chr22:39938892 | C | A | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-14-8201C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39938892 | |||||||
| chr22:39938923 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(214): Show |
238 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-14-8170A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39938923 | |||||||
| chr22:39939300 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-14-7793C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39939300 | |||||||
| chr22:39939379 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-14-7714G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39939379 | |||||||
| chr22:39939420 | G | A | 1 | a0001c0001t0021g0176 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-14-7673G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39939420 | |||||||
| chr22:39939551 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-14-7542G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39939551 | |||||||
| chr22:39939561 | C | CA | 22 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0025 others(19): Show |
23 | HG00438.hp1 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-14-7511dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39939561 | ||||||
| chr22:39939561 | C | CAA | 158 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-14-7512_-14-7511d others(4): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39939561 | ||||||
| chr22:39939561 | C | CAAA | 7 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0188 others(4): Show |
7 | HG01175.hp1 HG01175.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-7513_-14-7511d others(5): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39939561 | ||||||
| chr22:39939613 | T | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-7480T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39939613 | |||||||
| chr22:39939679 | G | C | 116 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0073 others(113): Show |
121 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-14-7414G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39939679 | |||||||
| chr22:39939773 | G | T | 1 | a0001c0001t0015g0134 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-14-7320G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39939773 | |||||||
| chr22:39940285 | T | A | 1 | a0001c0001t0015g0134 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-14-6808T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39940285 | |||||||
| chr22:39940383 | GT | G | 174 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
182 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.-14-6694delT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39940383 | ||||||
| chr22:39940385 | T | G | 1 | a0003c0004t0006g0125 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-14-6708T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39940385 | |||||||
| chr22:39940413 | T | C | 2 | a0001c0001t0001g0273 a0001c0001t0018g0275 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-14-6680T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39940413 | |||||||
| chr22:39940737 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-14-6356G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39940737 | |||||||
| chr22:39940817 | G | A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0130 a0001c0001t0001g0144 others(8): Show |
12 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-6276G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39940817 | |||||||
| chr22:39940841 | T | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
72 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-14-6252T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39940841 | |||||||
| chr22:39940940 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14-6153T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39940940 | |||||||
| chr22:39941431 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-14-5662T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39941431 | |||||||
| chr22:39941530 | G | T | 1 | a0001c0001t0009g0277 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-14-5563G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39941530 | |||||||
| chr22:39941569 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-14-5524T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39941569 | |||||||
| chr22:39941701 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01069.hp2 HG01099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-14-5392C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39941701 | |||||||
| chr22:39942280 | C | A | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(242): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-14-4813C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39942280 | |||||||
| chr22:39942338 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0005g0147 a0001c0001t0005g0159 |
3 | HG02976.hp2 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-14-4755G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39942338 | |||||||
| chr22:39942400 | C | A | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-14-4693C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39942400 | |||||||
| chr22:39942602 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-14-4491T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39942602 | |||||||
| chr22:39942616 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-14-4477T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39942616 | |||||||
| chr22:39942623 | C | CA | 6 | a0001c0001t0001g0112 a0001c0001t0001g0146 a0001c0001t0005g0019 others(3): Show |
6 | HG01934.hp1 HG03139.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-4453dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39942623 | ||||||
| chr22:39942728 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-14-4365G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39942728 | |||||||
| chr22:39942908 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0014g0287 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-14-4185A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39942908 | |||||||
| chr22:39943376 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-14-3717G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39943376 | |||||||
| chr22:39943547 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-14-3546G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39943547 | |||||||
| chr22:39943575 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-14-3518G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39943575 | |||||||
| chr22:39943614 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-14-3479T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39943614 | |||||||
| chr22:39943720 | C | CT | 7 | a0001c0001t0001g0009 a0001c0001t0001g0146 a0001c0001t0001g0175 others(4): Show |
8 | HG00099.hp1 HG00280.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-3355dupT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39943720 | ||||||
| chr22:39943720 | CT | C | 13 | a0001c0001t0001g0044 a0001c0001t0001g0078 a0001c0001t0001g0127 others(10): Show |
13 | HG01256.hp1 HG01517.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-3355delT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 39943720 | ||||||
| chr22:39943839 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-14-3254C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39943839 | |||||||
| chr22:39943927 | G | T | 1 | a0003c0004t0006g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-14-3166G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39943927 | |||||||
| chr22:39944086 | G | T | 76 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0087 others(73): Show |
80 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.-14-3007G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944086 | |||||||
| chr22:39944101 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-14-2992C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944101 | |||||||
| chr22:39944180 | A | G | 6 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0183 others(3): Show |
7 | HG01358.hp1 HG01361.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-2913A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944180 | |||||||
| chr22:39944236 | C | A | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-14-2857C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944236 | |||||||
| chr22:39944441 | C | A | 1 | a0001c0001t0002g0116 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-14-2652C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944441 | |||||||
| chr22:39944511 | C | T | 6 | a0001c0001t0001g0035 a0001c0001t0005g0019 a0001c0001t0013g0161 others(3): Show |
6 | HG02622.hp2 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-2582C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944511 | |||||||
| chr22:39944559 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-14-2534T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944559 | |||||||
| chr22:39944589 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-14-2504A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944589 | |||||||
| chr22:39944743 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-14-2350C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944743 | |||||||
| chr22:39944771 | T | C | 67 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(64): Show |
72 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-14-2322T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944771 | |||||||
| chr22:39944874 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-14-2219A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944874 | |||||||
| chr22:39944910 | A | C | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14-2183A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944910 | |||||||
| chr22:39944951 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-14-2142G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39944951 | |||||||
| chr22:39945307 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0014g0287 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-14-1786A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39945307 | |||||||
| chr22:39945357 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-14-1736G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39945357 | |||||||
| chr22:39945390 | C | G | 1 | a0001c0001t0002g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-14-1703C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39945390 | |||||||
| chr22:39945481 | T | A | 1 | a0001c0001t0005g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-14-1612T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39945481 | |||||||
| chr22:39945530 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-14-1563C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39945530 | |||||||
| chr22:39945612 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-14-1481A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39945612 | |||||||
| chr22:39945667 | G | A | 2 | a0001c0001t0002g0148 a0001c0001t0002g0149 |
2 | NA18979.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-14-1426G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39945667 | |||||||
| chr22:39945848 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0002c0003t0025g0186 |
4 | HG02145.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1245A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39945848 | |||||||
| chr22:39946053 | G | T | 1 | a0001c0001t0022g0064 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-14-1040G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39946053 | |||||||
| chr22:39946113 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0005g0147 a0001c0001t0005g0159 |
3 | HG02976.hp2 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-14-980G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39946113 | |||||||
| chr22:39946135 | A | G | 1 | a0001c0001t0015g0134 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-14-958A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39946135 | |||||||
| chr22:39946285 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-14-808C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39946285 | |||||||
| chr22:39946482 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0168 |
2 | HG01109.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-14-611G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39946482 | |||||||
| chr22:39946700 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0199 a0001c0001t0001g0250 |
3 | HG01975.hp1 HG01981.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-14-393G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39946700 | |||||||
| chr22:39946762 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-14-331C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39946762 | |||||||
| chr22:39946845 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0014g0287 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-14-248G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39946845 | |||||||
| chr22:39947045 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-14-48C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 1/7 | chr22 | 39947045 | |||||||
| chr22:39947223 | T | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0288 a0001c0001t0014g0287 |
3 | HG02055.hp1 HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.78+39T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39947223 | |||||||
| chr22:39947365 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.78+181C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39947365 | |||||||
| chr22:39947793 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0002c0003t0025g0186 |
4 | HG02145.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+609G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39947793 | |||||||
| chr22:39947879 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0131 |
3 | HG00323.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.78+695T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39947879 | |||||||
| chr22:39948004 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.78+820C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39948004 | |||||||
| chr22:39948039 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(180): Show |
195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.78+855A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39948039 | |||||||
| chr22:39948058 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.78+874C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39948058 | |||||||
| chr22:39948203 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.78+1019G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39948203 | |||||||
| chr22:39948209 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.78+1025T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39948209 | |||||||
| chr22:39948398 | G | A | 1 | a0001c0001t0002g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.78+1214G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39948398 | |||||||
| chr22:39948525 | GA | G | 97 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0111 others(94): Show |
102 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.78+1355delA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 39948525 | ||||||
| chr22:39948693 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.78+1509A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39948693 | |||||||
| chr22:39948770 | A | G | 97 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 others(94): Show |
102 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.78+1586A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39948770 | |||||||
| chr22:39949784 | G | A | 5 | a0001c0001t0001g0255 a0001c0001t0004g0010 a0001c0001t0004g0192 others(2): Show |
6 | HG01109.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+2600G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39949784 | |||||||
| chr22:39949838 | A | G | 4 | a0001c0001t0002g0239 a0001c0001t0002g0246 a0001c0001t0002g0248 others(1): Show |
4 | HG02735.hp2 HG03239.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+2654A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39949838 | |||||||
| chr22:39950026 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0252 a0001c0001t0001g0257 others(1): Show |
5 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+2842T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39950026 | |||||||
| chr22:39950066 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.78+2882C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39950066 | |||||||
| chr22:39950254 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.78+3070C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39950254 | |||||||
| chr22:39950472 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0080 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.78+3288C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39950472 | |||||||
| chr22:39950971 | A | G | 5 | a0001c0001t0001g0255 a0001c0001t0004g0010 a0001c0001t0004g0192 others(2): Show |
6 | HG01109.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+3787A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39950971 | |||||||
| chr22:39951088 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.78+3904A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39951088 | |||||||
| chr22:39951202 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.78+4018C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39951202 | |||||||
| chr22:39951381 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.78+4197C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39951381 | |||||||
| chr22:39951479 | TA | T | 95 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 others(92): Show |
100 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.78+4299delA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 39951479 | ||||||
| chr22:39951485 | C | G | 95 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 others(92): Show |
100 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.78+4301C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39951485 | |||||||
| chr22:39951812 | A | T | 30 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0035 others(27): Show |
32 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.79-4007A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39951812 | |||||||
| chr22:39951902 | C | T | 23 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0132 others(20): Show |
23 | HG00639.hp2 HG00733.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.79-3917C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39951902 | |||||||
| chr22:39951922 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79-3897T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39951922 | |||||||
| chr22:39952019 | G | GT | 13 | a0001c0001t0001g0032 a0001c0001t0001g0060 a0001c0001t0001g0099 others(10): Show |
13 | HG00735.hp1 HG02055.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-3781dupT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 39952019 | ||||||
| chr22:39952019 | GT | G | 12 | a0001c0001t0001g0093 a0001c0001t0001g0188 a0001c0001t0001g0256 others(9): Show |
12 | HG01175.hp1 HG01516.hp1 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-3781delT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 39952019 | ||||||
| chr22:39952026 | T | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(49): Show |
57 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.79-3793T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39952026 | |||||||
| chr22:39952192 | A | G | 136 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(133): Show |
146 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.79-3627A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39952192 | |||||||
| chr22:39952332 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0014g0287 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.79-3487G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39952332 | |||||||
| chr22:39952468 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.79-3351G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39952468 | |||||||
| chr22:39952497 | T | G | 11 | a0001c0001t0001g0146 a0001c0001t0001g0190 a0001c0001t0001g0196 others(8): Show |
11 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-3322T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39952497 | |||||||
| chr22:39952515 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79-3304C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39952515 | |||||||
| chr22:39952516 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0039 others(37): Show |
43 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.79-3303G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39952516 | |||||||
| chr22:39953086 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.79-2733T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953086 | |||||||
| chr22:39953252 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0090 |
2 | NA18978.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.79-2567G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953252 | |||||||
| chr22:39953349 | G | A | 22 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0057 others(19): Show |
24 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.79-2470G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953349 | |||||||
| chr22:39953377 | G | C | 1 | a0001c0001t0009g0180 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.79-2442G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953377 | |||||||
| chr22:39953427 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.79-2392G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953427 | |||||||
| chr22:39953483 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.79-2336C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953483 | |||||||
| chr22:39953569 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0129 a0001c0001t0001g0132 |
3 | HG00733.hp2 HG01261.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.79-2250A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953569 | |||||||
| chr22:39953598 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.79-2221C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953598 | |||||||
| chr22:39953705 | G | A | 1 | a0001c0001t0003g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.79-2114G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953705 | |||||||
| chr22:39953723 | C | T | 3 | a0001c0001t0010g0076 a0001c0001t0010g0084 a0001c0001t0010g0136 |
3 | NA18942.hp2 NA18955.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.79-2096C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953723 | |||||||
| chr22:39953796 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0019g0253 |
3 | HG02486.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.79-2023T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39953796 | |||||||
| chr22:39954312 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.79-1507G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39954312 | |||||||
| chr22:39954480 | T | C | 4 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-1339T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39954480 | |||||||
| chr22:39954646 | T | C | 4 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-1173T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39954646 | |||||||
| chr22:39954722 | G | A | 9 | a0001c0001t0005g0019 a0001c0001t0005g0147 a0001c0001t0005g0159 others(6): Show |
9 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.79-1097G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39954722 | |||||||
| chr22:39955043 | A | G | 9 | a0001c0001t0005g0019 a0001c0001t0005g0147 a0001c0001t0005g0159 others(6): Show |
9 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.79-776A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39955043 | |||||||
| chr22:39955064 | T | G | 2 | a0001c0001t0002g0148 a0001c0001t0002g0149 |
2 | NA18979.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.79-755T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39955064 | |||||||
| chr22:39955154 | C | T | 4 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-665C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39955154 | |||||||
| chr22:39955364 | C | T | 10 | a0001c0001t0001g0288 a0001c0001t0005g0019 a0001c0001t0005g0147 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-455C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39955364 | |||||||
| chr22:39955414 | G | GA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.79-394dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 39955414 | ||||||
| chr22:39955434 | G | A | 41 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(38): Show |
44 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.79-385G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39955434 | |||||||
| chr22:39955454 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.79-365T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39955454 | |||||||
| chr22:39955491 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.79-328T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39955491 | |||||||
| chr22:39955676 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.79-143C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39955676 | |||||||
| chr22:39955742 | T | TGA | 4 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-77_79-76insGA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39955742 | |||||||
| chr22:39955743 | T | A | 4 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-76T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 2/7 | chr22 | 39955743 | |||||||
| chr22:39955963 | A | G | 26 | a0001c0001t0001g0016 a0001c0001t0001g0135 a0001c0001t0001g0143 others(23): Show |
27 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.170+53A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39955963 | |||||||
| chr22:39956080 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.170+170G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956080 | |||||||
| chr22:39956132 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.170+222A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956132 | |||||||
| chr22:39956156 | C | CT | 9 | a0001c0001t0001g0262 a0001c0001t0001g0265 a0001c0001t0001g0269 others(6): Show |
9 | HG01070.hp1 HG01192.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.170+263dupT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 39956156 | ||||||
| chr22:39956284 | A | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0174 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.170+374A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956284 | |||||||
| chr22:39956301 | G | A | 4 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.170+391G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956301 | |||||||
| chr22:39956369 | G | A | 4 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.170+459G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956369 | |||||||
| chr22:39956404 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.170+494G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956404 | |||||||
| chr22:39956465 | G | GTTTTGGG others(3): Show |
5 | a0001c0001t0001g0006 a0001c0001t0001g0060 a0001c0001t0001g0102 others(2): Show |
6 | HG02135.hp1 NA18941.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.170+562_170+563ins others(10): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 39956465 | ||||||
| chr22:39956519 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.170+609A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956519 | |||||||
| chr22:39956634 | A | G | 2 | a0001c0001t0002g0223 a0001c0001t0020g0108 |
2 | NA19002.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.170+724A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956634 | |||||||
| chr22:39956636 | C | CTTTTTTT others(176): Show |
1 | a0001c0001t0002g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.170+730_170+731ins others(183): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 39956636 | ||||||
| chr22:39956636 | C | CTTTTTTT others(177): Show |
1 | a0001c0001t0002g0151 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.170+730_170+731ins others(184): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 39956636 | ||||||
| chr22:39956680 | G | A | 7 | a0001c0001t0001g0135 a0001c0001t0001g0143 a0001c0001t0001g0189 others(4): Show |
7 | HG00639.hp2 HG01496.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+770G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956680 | |||||||
| chr22:39956755 | C | G | 1 | a0001c0001t0002g0202 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.170+845C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956755 | |||||||
| chr22:39956813 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.170+903A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956813 | |||||||
| chr22:39956952 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.170+1042A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39956952 | |||||||
| chr22:39957315 | G | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.170+1405G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39957315 | |||||||
| chr22:39957517 | A | G | 2 | a0001c0001t0002g0228 a0001c0001t0002g0251 |
2 | NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.170+1607A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39957517 | |||||||
| chr22:39957630 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.170+1720C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39957630 | |||||||
| chr22:39957965 | A | C | 1 | a0001c0001t0003g0280 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.170+2055A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39957965 | |||||||
| chr22:39958067 | C | G | 2 | a0001c0001t0002g0052 a0001c0001t0002g0272 |
2 | NA19003.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.171-1988C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39958067 | |||||||
| chr22:39958187 | C | T | 1 | a0001c0001t0005g0159 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.171-1868C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39958187 | |||||||
| chr22:39958434 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.171-1621C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39958434 | |||||||
| chr22:39958545 | T | G | 1 | a0001c0001t0002g0182 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.171-1510T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39958545 | |||||||
| chr22:39958545 | T | TTGAA | 65 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.171-1489_171-1486d others(6): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 39958545 | ||||||
| chr22:39958581 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171-1474G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39958581 | |||||||
| chr22:39958590 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171-1465A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39958590 | |||||||
| chr22:39958977 | T | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.171-1078T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39958977 | |||||||
| chr22:39959016 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.171-1039G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959016 | |||||||
| chr22:39959039 | G | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02258.hp2 HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.171-1016G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959039 | |||||||
| chr22:39959054 | A | C | 7 | a0001c0001t0001g0135 a0001c0001t0001g0143 a0001c0001t0001g0189 others(4): Show |
7 | HG00639.hp2 HG01496.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-1001A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959054 | |||||||
| chr22:39959268 | A | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0278 a0001c0001t0001g0288 others(3): Show |
6 | HG02622.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.171-787A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959268 | |||||||
| chr22:39959399 | A | G | 5 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.171-656A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959399 | |||||||
| chr22:39959417 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.171-638C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959417 | |||||||
| chr22:39959563 | A | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0273 a0001c0001t0001g0278 others(4): Show |
7 | HG02622.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-492A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959563 | |||||||
| chr22:39959631 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.171-424C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959631 | |||||||
| chr22:39959725 | T | C | 4 | a0001c0001t0002g0218 a0001c0001t0002g0232 a0001c0001t0002g0236 others(1): Show |
4 | HG01256.hp1 HG01515.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-330T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959725 | |||||||
| chr22:39959729 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.171-326G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959729 | |||||||
| chr22:39959904 | T | C | 1 | a0001c0001t0015g0134 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.171-151T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959904 | |||||||
| chr22:39959994 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.171-61G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 3/7 | chr22 | 39959994 | |||||||
| chr22:39960416 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.290+242C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39960416 | |||||||
| chr22:39960464 | T | C | 5 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+290T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39960464 | |||||||
| chr22:39960862 | A | T | 4 | a0001c0001t0001g0157 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG01175.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+688A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39960862 | |||||||
| chr22:39960953 | C | CT | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.290+797dupT | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | 39960953 | ||||||
| chr22:39961379 | G | C | 4 | a0003c0004t0006g0122 a0003c0004t0006g0124 a0003c0004t0006g0125 others(1): Show |
4 | HG01243.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+1205G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39961379 | |||||||
| chr22:39961383 | G | A | 1 | a0001c0001t0002g0272 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.290+1209G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39961383 | |||||||
| chr22:39961663 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0129 a0001c0001t0001g0132 |
3 | HG00733.hp2 HG01261.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.290+1489G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39961663 | |||||||
| chr22:39961964 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.290+1790C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39961964 | |||||||
| chr22:39962144 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
127 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.290+1970C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962144 | |||||||
| chr22:39962145 | G | A | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.290+1971G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962145 | |||||||
| chr22:39962173 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290+1999A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962173 | |||||||
| chr22:39962176 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.290+2002A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962176 | |||||||
| chr22:39962179 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
128 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.290+2005T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962179 | |||||||
| chr22:39962237 | A | G | 7 | a0001c0001t0001g0135 a0001c0001t0001g0143 a0001c0001t0001g0189 others(4): Show |
7 | HG00639.hp2 HG01496.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+2063A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962237 | |||||||
| chr22:39962380 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.290+2206G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962380 | |||||||
| chr22:39962385 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.290+2211A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962385 | |||||||
| chr22:39962688 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290+2514C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962688 | |||||||
| chr22:39962838 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.290+2664T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962838 | |||||||
| chr22:39962866 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.290+2692G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962866 | |||||||
| chr22:39962905 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+2731G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962905 | |||||||
| chr22:39962984 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.290+2810A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39962984 | |||||||
| chr22:39963036 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.290+2862C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963036 | |||||||
| chr22:39963091 | C | T | 3 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG02738.hp1 HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.291-2899C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963091 | |||||||
| chr22:39963302 | C | A | 1 | a0001c0001t0014g0287 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.291-2688C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963302 | |||||||
| chr22:39963386 | G | C | 7 | a0001c0001t0001g0135 a0001c0001t0001g0143 a0001c0001t0001g0189 others(4): Show |
7 | HG00639.hp2 HG01496.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-2604G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963386 | |||||||
| chr22:39963503 | G | A | 1 | a0001c0001t0024g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.291-2487G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963503 | |||||||
| chr22:39963668 | A | G | 5 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-2322A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963668 | |||||||
| chr22:39963744 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.291-2246G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963744 | |||||||
| chr22:39963873 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0041 others(37): Show |
43 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.291-2117G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963873 | |||||||
| chr22:39963889 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.291-2101G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963889 | |||||||
| chr22:39963950 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.291-2040T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963950 | |||||||
| chr22:39963999 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291-1991G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39963999 | |||||||
| chr22:39964059 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.291-1931G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39964059 | |||||||
| chr22:39964509 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.291-1481G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39964509 | |||||||
| chr22:39964509 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.291-1481G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39964509 | |||||||
| chr22:39964593 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.291-1397C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39964593 | |||||||
| chr22:39964715 | T | TA | 7 | a0001c0001t0001g0090 a0001c0001t0001g0252 a0001c0001t0002g0100 others(4): Show |
7 | HG00621.hp1 HG02630.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-1256dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | 39964715 | ||||||
| chr22:39964715 | T | TAAA | 33 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0029 others(30): Show |
34 | HG00621.hp2 HG00639.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.291-1258_291-1256d others(5): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | 39964715 | ||||||
| chr22:39964715 | T | TAAAA | 45 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0016 others(42): Show |
48 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.291-1259_291-1256d others(6): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | 39964715 | ||||||
| chr22:39964715 | T | TAAAAA | 5 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0043 others(2): Show |
6 | HG02055.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-1260_291-1256d others(7): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | 39964715 | ||||||
| chr22:39964771 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0172 |
2 | HG02523.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.291-1219C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39964771 | |||||||
| chr22:39964928 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0133 |
3 | HG01256.hp2 HG01258.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.291-1062G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39964928 | |||||||
| chr22:39965003 | G | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0192 a0001c0001t0004g0193 others(2): Show |
6 | HG01109.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-987G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39965003 | |||||||
| chr22:39965115 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.291-875C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39965115 | |||||||
| chr22:39965487 | A | G | 1 | a0001c0001t0001g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.291-503A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39965487 | |||||||
| chr22:39965505 | G | GA | 6 | a0001c0001t0002g0015 a0001c0001t0002g0202 a0001c0001t0002g0234 others(3): Show |
7 | HG01928.hp1 HG01952.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-479dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | 39965505 | ||||||
| chr22:39965672 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.291-318G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39965672 | |||||||
| chr22:39965914 | TC | T | 9 | a0001c0001t0005g0019 a0001c0001t0005g0147 a0001c0001t0005g0159 others(6): Show |
9 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.291-73delC | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | 39965914 | ||||||
| chr22:39965954 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.291-36G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 4/7 | chr22 | 39965954 | |||||||
| chr22:39966336 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.459+178G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | chr22 | 39966336 | |||||||
| chr22:39966345 | G | A | 1 | a0001c0001t0012g0031 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.459+187G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | chr22 | 39966345 | |||||||
| chr22:39966537 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.459+379A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | chr22 | 39966537 | |||||||
| chr22:39966942 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.459+784A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | chr22 | 39966942 | |||||||
| chr22:39966996 | TCA | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
201 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.459+856_459+857del others(2): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr22 | 39966996 | ||||||
| chr22:39966996 | TCACACA | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0096 a0001c0001t0001g0130 others(8): Show |
12 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+852_459+857del others(6): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr22 | 39966996 | ||||||
| chr22:39967185 | C | T | 1 | a0004c0005t0002g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.460-857C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | chr22 | 39967185 | |||||||
| chr22:39967379 | A | G | 3 | a0001c0001t0010g0076 a0001c0001t0010g0084 a0001c0001t0010g0136 |
3 | NA18942.hp2 NA18955.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.460-663A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | chr22 | 39967379 | |||||||
| chr22:39967429 | A | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0020 others(15): Show |
20 | HG01175.hp1 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.460-613A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | chr22 | 39967429 | |||||||
| chr22:39967544 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
112 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.460-498C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | chr22 | 39967544 | |||||||
| chr22:39967546 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.460-496T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | chr22 | 39967546 | |||||||
| chr22:39967774 | G | A | 198 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(195): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.460-268G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 5/7 | chr22 | 39967774 | |||||||
| chr22:39968303 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.690+31C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968303 | |||||||
| chr22:39968367 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.690+95C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968367 | |||||||
| chr22:39968390 | C | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(129): Show |
143 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.690+118C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968390 | |||||||
| chr22:39968411 | A | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.690+139A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968411 | |||||||
| chr22:39968458 | A | AAC | 7 | a0001c0001t0001g0135 a0001c0001t0001g0288 a0001c0001t0009g0276 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+207_690+208dup others(2): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 39968458 | ||||||
| chr22:39968458 | AAC | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.690+207_690+208del others(2): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 39968458 | ||||||
| chr22:39968458 | AACACACA others(1): Show |
A | 5 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+201_690+208del others(8): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 39968458 | ||||||
| chr22:39968479 | A | T | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.690+207A>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968479 | |||||||
| chr22:39968480 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.690+208C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968480 | |||||||
| chr22:39968482 | G | C | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.690+210G>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968482 | |||||||
| chr22:39968485 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.690+213T>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968485 | |||||||
| chr22:39968612 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.690+340C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968612 | |||||||
| chr22:39968616 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.690+344T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968616 | |||||||
| chr22:39968617 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.690+345C>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968617 | |||||||
| chr22:39968886 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.691-525G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968886 | |||||||
| chr22:39968912 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.691-499G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968912 | |||||||
| chr22:39968914 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0018g0275 |
2 | HG03490.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.691-497C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968914 | |||||||
| chr22:39968923 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.691-488G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39968923 | |||||||
| chr22:39969119 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0257 a0001c0001t0001g0273 others(3): Show |
7 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-292G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39969119 | |||||||
| chr22:39969299 | A | C | 1 | a0001c0001t0002g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.691-112A>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39969299 | |||||||
| chr22:39969357 | C | T | 13 | a0001c0001t0001g0278 a0001c0001t0002g0002 a0001c0001t0002g0027 others(10): Show |
16 | HG00423.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.691-54C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39969357 | |||||||
| chr22:39969387 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.691-24C>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 6/7 | chr22 | 39969387 | |||||||
| chr22:39969625 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.813+92C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39969625 | |||||||
| chr22:39969823 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.813+290A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39969823 | |||||||
| chr22:39969870 | C | T | 4 | a0001c0001t0001g0190 a0001c0001t0002g0011 a0001c0001t0002g0012 others(1): Show |
5 | HG00639.hp2 HG01358.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+337C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39969870 | |||||||
| chr22:39969910 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.813+377G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39969910 | |||||||
| chr22:39969911 | T | C | 5 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+378T>C | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39969911 | |||||||
| chr22:39969916 | AAAAACAA others(3): Show |
A | 1 | a0001c0001t0001g0127 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.813+398_813+407del others(10): Show |
GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr22 | 39969916 | ||||||
| chr22:39970531 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0014g0287 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.814-374A>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39970531 | |||||||
| chr22:39970535 | C | T | 4 | a0003c0004t0006g0122 a0003c0004t0006g0124 a0003c0004t0006g0125 others(1): Show |
4 | HG01243.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.814-370C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39970535 | |||||||
| chr22:39970600 | G | A | 3 | a0001c0001t0010g0076 a0001c0001t0010g0084 a0001c0001t0010g0136 |
3 | NA18942.hp2 NA18955.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.814-305G>A | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39970600 | |||||||
| chr22:39970642 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0002g0028 |
2 | HG03579.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.814-263C>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39970642 | |||||||
| chr22:39970757 | C | CA | 5 | a0002c0003t0007g0121 a0002c0003t0007g0123 a0002c0003t0007g0126 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-141dupA | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr22 | 39970757 | ||||||
| chr22:39970785 | G | T | 1 | a0001c0001t0002g0151 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.814-120G>T | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39970785 | |||||||
| chr22:39970794 | T | G | 6 | a0001c0001t0018g0275 a0002c0003t0007g0121 a0002c0003t0007g0123 others(3): Show |
6 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.814-111T>G | GRAP2 | ENSG00000100351.17 | transcript | ENST00000344138.9 | protein_coding | 7/7 | chr22 | 39970794 |