Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79091 |
| ensemblid | ENSG00000067365.15 |
| hgncid | 28368 |
| symbol | METTL22 |
| name | methyltransferase 22, Kin17 lysine |
| refseq_nuc | NM_024109.4 |
| refseq_prot | NP_077014.4 |
| ensembl_nuc | ENST00000381920.8 |
| ensembl_prot | ENSP00000371345.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 8621698 |
| end | 8649654 |
| strand | + |
| ver | v1.2 |
| region | chr16:8621698-8649654 |
| region5000 | chr16:8616698-8654654 |
| regionname0 | METTL22_chr16_8621698_8649654 |
| regionname5000 | METTL22_chr16_8616698_8654654 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 404 | 208 | 75 | 49 | 53 | 7 | 23 | 42 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| a0002 | 0/0 | 404 | 81 | 1 | 11 | 55 | 6 | 8 | 40 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| a0003 | 0/0 | 404 | 78 | 2 | 16 | 45 | 3 | 12 | 33 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| a0004 | 1/0 | 404 | 12 | 11 | 0 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| a0005 | 0/0 | 404 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| a0006 | 0/0 | 404 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| a0007 | 0/0 | 404 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| a0008 | 0/0 | 404 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| a0009 | 0/0 | 404 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| a0010 | 0/0 | 404 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| a0011 | 0/0 | 204 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(199): Show |
chr16 | 8616698 | 8654654 |
| a0012 | 0/0 | 404 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | MVQLA others(399): Show |
chr16 | 8616698 | 8654654 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1212 | 191 | 60 | 47 | 53 | 7 | 23 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0001c0005 | 0/0 | 1212 | 7 | 7 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0001c0006 | 0/0 | 1212 | 5 | 4 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0001c0012 | 0/0 | 1212 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0001c0013 | 0/0 | 1212 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0001c0016 | 0/0 | 1212 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0001c0017 | 0/0 | 1212 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0001c0021 | 0/0 | 1212 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0002c0002 | 0/0 | 1212 | 81 | 1 | 11 | 55 | 6 | 8 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0003c0003 | 0/0 | 1212 | 76 | 2 | 16 | 45 | 3 | 10 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0003c0009 | 0/0 | 1212 | 2 | 0 | 0 | 0 | 0 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0004c0004 | 0/0 | 1212 | 11 | 11 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0004c0018 | 1/0 | 1212 | 1 | 0 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0005c0008 | 0/0 | 1212 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0006c0007 | 0/0 | 1212 | 2 | 0 | 0 | 0 | 0 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0007c0010 | 0/0 | 1212 | 2 | 0 | 0 | 0 | 0 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0008c0020 | 0/0 | 1212 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0009c0011 | 0/0 | 1212 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0010c0014 | 0/0 | 1212 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0011c0019 | 0/0 | 1212 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 | ||
| a0012c0015 | 0/0 | 1212 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | ATGGT others(1207): Show |
chr16 | 8616698 | 8654654 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4973 | 61 | 17 | 16 | 23 | 0 | 5 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0002 | 0/0 | 4973 | 50 | 6 | 14 | 23 | 1 | 6 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0003 | 0/1 | 4973 | 12 | 5 | 2 | 0 | 2 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0004 | 0/0 | 4973 | 9 | 0 | 3 | 0 | 3 | 3 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0005 | 0/0 | 4973 | 9 | 9 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0007 | 0/0 | 4973 | 8 | 2 | 3 | 0 | 1 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0011 | 0/0 | 4973 | 5 | 5 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0012 | 0/0 | 4973 | 4 | 0 | 0 | 4 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0013 | 0/0 | 4973 | 4 | 0 | 3 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0014 | 0/0 | 4973 | 3 | 0 | 2 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0017 | 0/0 | 4973 | 3 | 3 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0022 | 0/0 | 4973 | 2 | 0 | 0 | 2 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0024 | 0/0 | 4973 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0025 | 0/0 | 4976 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4971): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0027 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0028 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0031 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4969): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0032 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0034 | 0/0 | 4973 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0036 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0037 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0042 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0043 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4969): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0048 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4969): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0050 | 0/0 | 4973 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0051 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4969): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0052 | 0/0 | 4973 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0053 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0054 | 0/0 | 4973 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0055 | 0/0 | 4973 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0001t0056 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0005t0009 | 0/0 | 4973 | 6 | 6 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0005t0033 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0006t0010 | 0/0 | 4970 | 5 | 4 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4965): Show |
chr16 | 8616698 | 8654654 |
| a0001c0012t0010 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4965): Show |
chr16 | 8616698 | 8654654 |
| a0001c0013t0026 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4969): Show |
chr16 | 8616698 | 8654654 |
| a0001c0016t0001 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0017t0002 | 0/0 | 4973 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0001c0021t0001 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0002c0002t0001 | 0/0 | 4973 | 66 | 1 | 9 | 43 | 5 | 8 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0002c0002t0008 | 0/0 | 4973 | 8 | 0 | 0 | 8 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0002c0002t0021 | 0/0 | 4973 | 2 | 0 | 1 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0002c0002t0023 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4969): Show |
chr16 | 8616698 | 8654654 |
| a0002c0002t0030 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0002c0002t0035 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0002c0002t0041 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4971): Show |
chr16 | 8616698 | 8654654 |
| a0002c0002t0046 | 0/0 | 4973 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0001 | 0/0 | 4973 | 58 | 2 | 13 | 33 | 2 | 8 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0002 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0015 | 0/0 | 4973 | 3 | 0 | 0 | 3 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0016 | 0/0 | 4973 | 3 | 0 | 0 | 2 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0018 | 0/0 | 4973 | 3 | 0 | 3 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0023 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4969): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0038 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0039 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0040 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0044 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0045 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0047 | 0/0 | 4973 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0003t0049 | 0/0 | 4973 | 1 | 0 | 0 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0003c0009t0001 | 0/0 | 4973 | 2 | 0 | 0 | 0 | 0 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0004c0004t0006 | 0/0 | 4974 | 8 | 8 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4969): Show |
chr16 | 8616698 | 8654654 |
| a0004c0004t0020 | 0/0 | 4972 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4967): Show |
chr16 | 8616698 | 8654654 |
| a0004c0004t0029 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4967): Show |
chr16 | 8616698 | 8654654 |
| a0004c0018t0006 | 1/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4969): Show |
chr16 | 8616698 | 8654654 |
| a0005c0008t0019 | 0/0 | 4973 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0006c0007t0004 | 0/0 | 4973 | 2 | 0 | 0 | 0 | 0 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0007c0010t0001 | 0/0 | 4973 | 2 | 0 | 0 | 0 | 0 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0008c0020t0005 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0009c0011t0001 | 0/0 | 4973 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0010c0014t0001 | 0/0 | 4973 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0011c0019t0001 | 0/0 | 4973 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| a0012c0015t0002 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | AGACC others(4968): Show |
chr16 | 8616698 | 8654654 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0004g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0004g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0007g0012 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0007g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0007g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0011g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0012g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0012g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0013g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0013g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0014g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0014g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0017g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0017g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0017g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0022g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0022g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0024g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0024g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0025g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0027g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0028g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0031g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0032g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0034g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0036g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0037g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0042g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0043g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0048g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0050g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0051g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0052g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0053g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0054g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0055g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0001t0056g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0005t0009g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0005t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0005t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0005t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0005t0033g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0006t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0006t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0006t0010g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0006t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0006t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0012t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0013t0026g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0016t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0017t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0001c0021t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0001 | 0/0 | 15 | 0 | 5 | 7 | 2 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0005 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0008g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0008g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0008g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0021g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0023g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0030g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0035g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0041g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0002c0002t0046g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0002 | 0/0 | 16 | 0 | 5 | 8 | 1 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0015g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0015g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0016g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0018g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0018g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0018g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0023g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0038g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0039g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0040g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0044g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0045g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0047g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0003t0049g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0009t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0003c0009t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0004c0004t0006g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0004c0004t0006g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0004c0004t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0004c0004t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0004c0004t0020g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0004c0004t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0004c0004t0029g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0004c0018t0006g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0005c0008t0019g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0006c0007t0004g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0007c0010t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0007c0010t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0008c0020t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0009c0011t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0010c0014t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0011c0019t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| a0012c0015t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0224 | EUR | GBR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00099 | hp2 | a0003 | c0003 | t0049 | g0126 | EUR | GBR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0025 | EUR | GBR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00140 | hp2 | a0002 | c0002 | t0021 | g0001 | EUR | GBR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0222 | EUR | FIN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00423 | hp2 | a0003 | c0003 | t0001 | g0158 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0125 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0210 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0164 | EAS | CHS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00733 | hp1 | a0002 | c0002 | t0046 | g0001 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00733 | hp2 | a0001 | c0001 | t0014 | g0003 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0139 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00738 | hp1 | a0001 | c0001 | t0014 | g0064 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00741 | hp1 | a0001 | c0017 | t0002 | g0104 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG00741 | hp2 | a0001 | c0001 | t0013 | g0021 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01069 | hp1 | a0003 | c0003 | t0001 | g0009 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01074 | hp2 | a0002 | c0002 | t0021 | g0001 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01167 | hp2 | a0001 | c0001 | t0055 | g0234 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01175 | hp1 | a0001 | c0001 | t0043 | g0143 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01192 | hp2 | a0001 | c0006 | t0010 | g0191 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01255 | hp1 | a0001 | c0001 | t0050 | g0111 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01258 | hp1 | a0001 | c0001 | t0013 | g0021 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0029 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0188 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0237 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0018 | EUR | IBS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0009 | EUR | IBS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0002 | EUR | IBS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0018 | EUR | IBS | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01884 | hp1 | a0008 | c0020 | t0005 | g0251 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01884 | hp2 | a0001 | c0005 | t0033 | g0243 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01891 | hp1 | a0004 | c0004 | t0006 | g0046 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01934 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0029 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01952 | hp2 | a0003 | c0003 | t0018 | g0002 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0197 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01978 | hp2 | a0001 | c0001 | t0013 | g0058 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01981 | hp2 | a0003 | c0003 | t0018 | g0006 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01993 | hp1 | a0001 | c0001 | t0054 | g0181 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02015 | hp1 | a0003 | c0003 | t0044 | g0178 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02055 | hp1 | a0001 | c0001 | t0024 | g0082 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02055 | hp2 | a0001 | c0001 | t0027 | g0250 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0124 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02074 | hp1 | a0003 | c0003 | t0040 | g0132 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02080 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02083 | hp1 | a0003 | c0003 | t0001 | g0148 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02129 | hp1 | a0001 | c0001 | t0022 | g0004 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02135 | hp1 | a0002 | c0002 | t0008 | g0177 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0147 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02145 | hp1 | a0001 | c0006 | t0010 | g0189 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0174 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | CDX | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02257 | hp1 | a0001 | c0001 | t0032 | g0084 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0204 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02280 | hp1 | a0005 | c0008 | t0019 | g0045 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02293 | hp2 | a0003 | c0003 | t0001 | g0155 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02300 | hp1 | a0003 | c0003 | t0018 | g0039 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02451 | hp1 | a0004 | c0004 | t0006 | g0011 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | KHV | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0044 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02572 | hp2 | a0001 | c0005 | t0009 | g0244 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0133 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02615 | hp1 | a0001 | c0001 | t0024 | g0083 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02615 | hp2 | a0004 | c0004 | t0006 | g0215 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02630 | hp2 | a0004 | c0004 | t0020 | g0203 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02698 | hp2 | a0003 | c0009 | t0001 | g0138 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02717 | hp1 | a0001 | c0006 | t0010 | g0193 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02717 | hp2 | a0004 | c0004 | t0020 | g0043 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02723 | hp1 | a0001 | c0016 | t0001 | g0015 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0128 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02735 | hp2 | a0001 | c0001 | t0014 | g0065 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02809 | hp1 | a0001 | c0001 | t0053 | g0048 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02809 | hp2 | a0001 | c0001 | t0025 | g0049 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02895 | hp1 | a0004 | c0004 | t0006 | g0011 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02896 | hp1 | a0004 | c0004 | t0006 | g0011 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0044 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02965 | hp1 | a0001 | c0005 | t0009 | g0019 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0115 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02970 | hp1 | a0001 | c0001 | t0011 | g0205 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02976 | hp1 | a0001 | c0001 | t0025 | g0049 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03098 | hp1 | a0001 | c0005 | t0009 | g0213 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03098 | hp2 | a0001 | c0001 | t0028 | g0089 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03130 | hp2 | a0001 | c0006 | t0010 | g0192 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03139 | hp1 | a0004 | c0004 | t0006 | g0011 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03139 | hp2 | a0001 | c0005 | t0009 | g0019 | AFR | ESN | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03209 | hp1 | a0005 | c0008 | t0019 | g0045 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0099 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03225 | hp1 | a0004 | c0004 | t0006 | g0046 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03225 | hp2 | a0004 | c0004 | t0029 | g0043 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0162 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03239 | hp2 | a0006 | c0007 | t0004 | g0040 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03453 | hp1 | a0001 | c0006 | t0010 | g0190 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03453 | hp2 | a0001 | c0001 | t0037 | g0100 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03490 | hp2 | a0009 | c0011 | t0001 | g0149 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03491 | hp1 | a0007 | c0010 | t0001 | g0135 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03540 | hp1 | a0001 | c0001 | t0048 | g0085 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03540 | hp2 | a0001 | c0012 | t0010 | g0194 | AFR | GWD | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03579 | hp1 | a0004 | c0004 | t0006 | g0214 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03654 | hp1 | a0001 | c0001 | t0034 | g0236 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0002 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03669 | hp1 | a0003 | c0003 | t0016 | g0002 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03688 | hp1 | a0007 | c0010 | t0001 | g0129 | SAS | STU | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0116 | SAS | STU | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0187 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0175 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03831 | hp1 | a0010 | c0014 | t0001 | g0165 | SAS | BEB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03831 | hp2 | a0001 | c0001 | t0052 | g0255 | SAS | BEB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0161 | SAS | BEB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0231 | SAS | BEB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03927 | hp2 | a0001 | c0001 | t0013 | g0059 | SAS | BEB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03942 | hp1 | a0003 | c0003 | t0047 | g0185 | SAS | BEB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03942 | hp2 | a0003 | c0009 | t0001 | g0172 | SAS | BEB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0230 | SAS | STU | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG04184 | hp1 | a0001 | c0001 | t0051 | g0069 | SAS | BEB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | BEB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0109 | SAS | STU | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG04199 | hp2 | a0011 | c0019 | t0001 | g0127 | SAS | STU | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0006 | SAS | STU | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG04228 | hp2 | a0006 | c0007 | t0004 | g0040 | SAS | STU | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | YRI | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18747 | hp1 | a0002 | c0002 | t0030 | g0105 | EAS | CHB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | YRI | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0206 | AFR | YRI | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18942 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18942 | hp2 | a0001 | c0001 | t0012 | g0013 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18943 | hp1 | a0001 | c0001 | t0012 | g0075 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0195 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18947 | hp2 | a0003 | c0003 | t0015 | g0002 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18951 | hp2 | a0001 | c0001 | t0022 | g0120 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18956 | hp2 | a0003 | c0003 | t0039 | g0039 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18957 | hp1 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0110 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18959 | hp2 | a0003 | c0003 | t0016 | g0030 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18960 | hp1 | a0003 | c0003 | t0015 | g0033 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18960 | hp2 | a0001 | c0001 | t0012 | g0013 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18965 | hp2 | a0003 | c0003 | t0001 | g0196 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18971 | hp1 | a0002 | c0002 | t0008 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18973 | hp2 | a0003 | c0003 | t0015 | g0002 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18975 | hp2 | a0012 | c0015 | t0002 | g0068 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18982 | hp2 | a0002 | c0002 | t0008 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18987 | hp1 | a0003 | c0003 | t0038 | g0009 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18994 | hp1 | a0003 | c0003 | t0002 | g0072 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18995 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18999 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA18999 | hp2 | a0002 | c0002 | t0008 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19005 | hp2 | a0002 | c0002 | t0035 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19007 | hp2 | a0002 | c0002 | t0008 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19030 | hp1 | a0001 | c0001 | t0056 | g0170 | AFR | LWK | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19030 | hp2 | a0001 | c0001 | t0017 | g0201 | AFR | LWK | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0228 | AFR | LWK | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | LWK | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19056 | hp1 | a0001 | c0001 | t0012 | g0013 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19057 | hp2 | a0002 | c0002 | t0041 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19060 | hp2 | a0003 | c0003 | t0045 | g0006 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0097 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19066 | hp1 | a0003 | c0003 | t0016 | g0002 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19066 | hp2 | a0002 | c0002 | t0008 | g0154 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19067 | hp1 | a0003 | c0003 | t0001 | g0038 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19068 | hp1 | a0001 | c0001 | t0042 | g0232 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19068 | hp2 | a0002 | c0002 | t0008 | g0005 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19070 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19072 | hp2 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0038 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19086 | hp1 | a0003 | c0003 | t0023 | g0094 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19086 | hp2 | a0002 | c0002 | t0023 | g0091 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19087 | hp2 | a0002 | c0002 | t0008 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19240 | hp1 | a0001 | c0021 | t0001 | g0198 | AFR | YRI | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0245 | AFR | YRI | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | ASW | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0249 | AFR | ASW | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0025 | EUR | TSI | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0012 | EUR | TSI | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0211 | EUR | TSI | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0241 | EUR | TSI | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | GIH | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0131 | SAS | GIH | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0247 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02109 | hp2 | a0001 | c0001 | t0036 | g0096 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0248 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0202 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG02559 | hp2 | a0001 | c0013 | t0026 | g0217 | AFR | ACB | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG03471 | hp2 | a0001 | c0005 | t0009 | g0019 | AFR | MSL | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG06807 | hp1 | a0001 | c0001 | t0031 | g0216 | AFR | USA | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | USA | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0180 | AFR | USA | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA20300 | hp2 | a0001 | c0005 | t0009 | g0242 | AFR | USA | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | LWK | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | LWK | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0219 | REF | REF | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| homoSapiens | grch38p0 | a0004 | c0018 | t0006 | g0057 | REF | REF | METTL22_chr16_8616698_8654654 | METTL22 | chr16 | 8616698 | 8654654 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:8625723 | G | A | 1 | a0009 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.58G>A | p.Val20Met | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/11 | 306/4974 | 58/1215 | 20/404 | chr16 | 8625723 | |||
| chr16:8625786 | G | A | 1 | a0006 | 2 | HG03239.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.121G>A | p.Val41Met | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/11 | 369/4974 | 121/1215 | 41/404 | chr16 | 8625786 | |||
| chr16:8625798 | G | A | 1 | a0005 | 2 | HG02280.hp1 HG03209.hp1 |
missense_variant&splice_region_variant | MODERATE | c.133G>A | p.Val45Ile | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/11 | 381/4974 | 133/1215 | 45/404 | chr16 | 8625798 | |||
| chr16:8628772 | G | C | 2 | a0003 a0007 |
80 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(77): Show |
missense_variant | MODERATE | c.176G>C | p.Trp59Ser | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/11 | 424/4974 | 176/1215 | 59/404 | chr16 | 8628772 | |||
| chr16:8629078 | C | T | 1 | a0008 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.482C>T | p.Ala161Val | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/11 | 730/4974 | 482/1215 | 161/404 | chr16 | 8629078 | |||
| chr16:8635225 | C | T | 1 | a0011 | 1 | HG04199.hp2 | stop_gained | HIGH | c.613C>T | p.Arg205* | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/11 | 861/4974 | 613/1215 | 205/404 | chr16 | 8635225 | |||
| chr16:8635267 | G | A | 3 | a0002 a0010 a0011 |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
missense_variant | MODERATE | c.655G>A | p.Ala219Thr | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/11 | 903/4974 | 655/1215 | 219/404 | chr16 | 8635267 | |||
| chr16:8635278 | C | G | 1 | a0010 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.666C>G | p.Ile222Met | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/11 | 914/4974 | 666/1215 | 222/404 | chr16 | 8635278 | |||
| chr16:8635290 | G | C | 1 | a0010 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.678G>C | p.Met226Ile | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/11 | 926/4974 | 678/1215 | 226/404 | chr16 | 8635290 | |||
| chr16:8635300 | G | A | 1 | a0012 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.688G>A | p.Val230Ile | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/11 | 936/4974 | 688/1215 | 230/404 | chr16 | 8635300 | |||
| chr16:8644642 | G | A | 11 | a0001 a0002 a0003 others(8): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
missense_variant | MODERATE | c.1096G>A | p.Ala366Thr | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/11 | 1344/4974 | 1096/1215 | 366/404 | chr16 | 8644642 | |||
| chr16:8646120 | A | G | 1 | a0007 | 2 | HG03491.hp1 HG03688.hp1 |
missense_variant | MODERATE | c.1192A>G | p.Ile398Val | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1440/4974 | 1192/1215 | 398/404 | chr16 | 8646120 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:8625752 | G | A | 2 | a0001c0005 a0001c0012 |
8 | HG01884.hp2 HG02572.hp2 HG02965.hp1 others(5): Show |
synonymous_variant | LOW | c.87G>A | p.Pro29Pro | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/11 | 335/4974 | 87/1215 | 29/404 | chr16 | 8625752 | |||
| chr16:8628785 | A | G | 2 | a0001c0021 a0004c0004 |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
synonymous_variant | LOW | c.189A>G | p.Gly63Gly | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/11 | 437/4974 | 189/1215 | 63/404 | chr16 | 8628785 | |||
| chr16:8628875 | T | C | 2 | a0001c0021 a0004c0004 |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
synonymous_variant | LOW | c.279T>C | p.His93His | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/11 | 527/4974 | 279/1215 | 93/404 | chr16 | 8628875 | |||
| chr16:8628965 | C | T | 2 | a0001c0006 a0001c0012 |
6 | HG01192.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
synonymous_variant | LOW | c.369C>T | p.Asp123Asp | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/11 | 617/4974 | 369/1215 | 123/404 | chr16 | 8628965 | |||
| chr16:8635260 | G | A | 1 | a0001c0013 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.648G>A | p.Thr216Thr | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/11 | 896/4974 | 648/1215 | 216/404 | chr16 | 8635260 | |||
| chr16:8642171 | T | C | 19 | a0001c0001 a0001c0005 a0001c0006 others(16): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
synonymous_variant | LOW | c.871T>C | p.Leu291Leu | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 8/11 | 1119/4974 | 871/1215 | 291/404 | chr16 | 8642171 | |||
| chr16:8642473 | C | T | 1 | a0001c0017 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.918C>T | p.Asp306Asp | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/11 | 1166/4974 | 918/1215 | 306/404 | chr16 | 8642473 | |||
| chr16:8642503 | G | A | 1 | a0001c0016 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.948G>A | p.Thr316Thr | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/11 | 1196/4974 | 948/1215 | 316/404 | chr16 | 8642503 | |||
| chr16:8642557 | G | A | 1 | a0003c0009 | 2 | HG02698.hp2 HG03942.hp2 |
synonymous_variant | LOW | c.1002G>A | p.Val334Val | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/11 | 1250/4974 | 1002/1215 | 334/404 | chr16 | 8642557 | |||
| chr16:8644570 | T | C | 19 | a0001c0001 a0001c0005 a0001c0006 others(16): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
synonymous_variant | LOW | c.1024T>C | p.Leu342Leu | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/11 | 1272/4974 | 1024/1215 | 342/404 | chr16 | 8644570 | |||
| chr16:8644722 | A | G | 19 | a0001c0001 a0001c0005 a0001c0006 others(16): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
synonymous_variant | LOW | c.1176A>G | p.Gln392Gln | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/11 | 1424/4974 | 1176/1215 | 392/404 | chr16 | 8644722 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:8621766 | C | G | 1 | a0001c0001t0056 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-180C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/11 | 3900 | chr16 | 8621766 | ||||||
| chr16:8625499 | G | T | 1 | a0003c0003t0018 | 3 | HG01952.hp2 HG01981.hp2 HG02300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-167G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/11 | 167 | chr16 | 8625499 | ||||||
| chr16:8625528 | T | C | 8 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(5): Show |
31 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-138T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/11 | 138 | chr16 | 8625528 | ||||||
| chr16:8646149 | C | T | 1 | a0001c0001t0055 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 6 | chr16 | 8646149 | ||||||
| chr16:8646158 | A | C | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*15A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 15 | chr16 | 8646158 | ||||||
| chr16:8646165 | G | A | 1 | a0002c0002t0030 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 22 | chr16 | 8646165 | ||||||
| chr16:8646225 | T | C | 1 | a0002c0002t0021 | 2 | HG00140.hp2 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*82T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 82 | chr16 | 8646225 | ||||||
| chr16:8646294 | G | A | 1 | a0001c0001t0003 | 11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*151G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 151 | chr16 | 8646294 | ||||||
| chr16:8646378 | T | C | 8 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0031 others(5): Show |
28 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*235T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 235 | chr16 | 8646378 | ||||||
| chr16:8646382 | G | A | 1 | a0001c0001t0034 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*239G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 239 | chr16 | 8646382 | ||||||
| chr16:8646435 | C | T | 1 | a0001c0001t0013 | 4 | HG00741.hp2 HG01258.hp1 HG01978.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*292C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 292 | chr16 | 8646435 | ||||||
| chr16:8646473 | G | A | 1 | a0001c0013t0026 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 330 | chr16 | 8646473 | ||||||
| chr16:8646561 | T | C | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(68): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
3_prime_UTR_variant | MODIFIER | c.*418T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 418 | chr16 | 8646561 | ||||||
| chr16:8646565 | G | C | 1 | a0002c0002t0035 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*422G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 422 | chr16 | 8646565 | ||||||
| chr16:8646646 | G | A | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*503G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 503 | chr16 | 8646646 | ||||||
| chr16:8646660 | C | T | 1 | a0001c0001t0012 | 4 | NA18942.hp2 NA18943.hp1 NA18960.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*517C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 517 | chr16 | 8646660 | ||||||
| chr16:8646796 | C | T | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*653C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 653 | chr16 | 8646796 | ||||||
| chr16:8646901 | A | G | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*758A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 758 | chr16 | 8646901 | ||||||
| chr16:8646923 | C | T | 1 | a0001c0001t0054 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*780C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 780 | chr16 | 8646923 | ||||||
| chr16:8646955 | C | A | 1 | a0001c0001t0014 | 3 | HG00733.hp2 HG00738.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*812C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 812 | chr16 | 8646955 | ||||||
| chr16:8646957 | G | C | 1 | a0001c0001t0036 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*814G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 814 | chr16 | 8646957 | ||||||
| chr16:8647024 | T | C | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*881T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 881 | chr16 | 8647024 | ||||||
| chr16:8647028 | C | A | 1 | a0003c0003t0015 | 3 | NA18947.hp2 NA18960.hp1 NA18973.hp2 |
3_prime_UTR_variant | MODIFIER | c.*885C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 885 | chr16 | 8647028 | ||||||
| chr16:8647043 | C | T | 16 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0012 others(13): Show |
89 | HG00438.hp2 HG00639.hp1 HG00642.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*900C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 900 | chr16 | 8647043 | ||||||
| chr16:8647063 | C | T | 4 | a0001c0001t0004 a0001c0001t0053 a0001c0005t0009 others(1): Show |
18 | HG00642.hp1 HG01074.hp1 HG01257.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*920C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 920 | chr16 | 8647063 | ||||||
| chr16:8647081 | G | A | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*938G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 938 | chr16 | 8647081 | ||||||
| chr16:8647139 | C | T | 1 | a0001c0001t0050 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 996 | chr16 | 8647139 | ||||||
| chr16:8647243 | C | G | 1 | a0001c0001t0052 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1100C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1100 | chr16 | 8647243 | ||||||
| chr16:8647243 | C | T | 1 | a0005c0008t0019 | 2 | HG02280.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1100C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1100 | chr16 | 8647243 | ||||||
| chr16:8647260 | G | C | 6 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0031 others(3): Show |
21 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1117G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1117 | chr16 | 8647260 | ||||||
| chr16:8647283 | A | AT | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*1142dupT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1143 | INFO_REALIGN_3_PRIME | chr16 | 8647283 | |||||
| chr16:8647408 | T | C | 1 | a0001c0001t0003 | 11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1265T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1265 | chr16 | 8647408 | ||||||
| chr16:8647510 | C | T | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*1367C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1367 | chr16 | 8647510 | ||||||
| chr16:8647530 | G | A | 1 | a0001c0001t0022 | 2 | HG02129.hp1 NA18951.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1387G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1387 | chr16 | 8647530 | ||||||
| chr16:8647596 | T | TG | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*1453_*1454insG | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1454 | chr16 | 8647596 | ||||||
| chr16:8647603 | G | A | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*1460G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1460 | chr16 | 8647603 | ||||||
| chr16:8647609 | C | A | 1 | a0001c0001t0053 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1466C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1466 | chr16 | 8647609 | ||||||
| chr16:8647647 | C | T | 1 | a0001c0001t0032 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1504C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1504 | chr16 | 8647647 | ||||||
| chr16:8647651 | G | A | 1 | a0003c0003t0016 | 3 | HG03669.hp1 NA18959.hp2 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1508G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1508 | chr16 | 8647651 | ||||||
| chr16:8647882 | C | G | 1 | a0001c0001t0027 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1739C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1739 | chr16 | 8647882 | ||||||
| chr16:8647969 | T | A | 2 | a0004c0004t0020 a0004c0004t0029 |
3 | HG02630.hp2 HG02717.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1826T>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1826 | chr16 | 8647969 | ||||||
| chr16:8647970 | T | C | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*1827T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1827 | chr16 | 8647970 | ||||||
| chr16:8648014 | G | C | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*1871G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1871 | chr16 | 8648014 | ||||||
| chr16:8648074 | G | A | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*1931G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1931 | chr16 | 8648074 | ||||||
| chr16:8648131 | G | T | 2 | a0001c0001t0024 a0001c0001t0025 |
4 | HG02055.hp1 HG02615.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1988G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 1988 | chr16 | 8648131 | ||||||
| chr16:8648199 | G | A | 1 | a0004c0004t0029 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2056G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2056 | chr16 | 8648199 | ||||||
| chr16:8648206 | G | A | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*2063G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2063 | chr16 | 8648206 | ||||||
| chr16:8648257 | C | T | 1 | a0003c0003t0049 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2114C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2114 | chr16 | 8648257 | ||||||
| chr16:8648262 | GTT | G | 2 | a0004c0004t0020 a0004c0004t0029 |
3 | HG02630.hp2 HG02717.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2120_*2121delTT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2120 | chr16 | 8648262 | ||||||
| chr16:8648292 | C | T | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*2149C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2149 | chr16 | 8648292 | ||||||
| chr16:8648294 | C | A | 1 | a0001c0001t0037 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2151C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2151 | chr16 | 8648294 | ||||||
| chr16:8648309 | G | A | 1 | a0003c0003t0038 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2166G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2166 | chr16 | 8648309 | ||||||
| chr16:8648313 | C | A | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*2170C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2170 | chr16 | 8648313 | ||||||
| chr16:8648341 | C | T | 1 | a0001c0001t0048 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2198C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2198 | chr16 | 8648341 | ||||||
| chr16:8648533 | A | G | 1 | a0003c0003t0047 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2390A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2390 | chr16 | 8648533 | ||||||
| chr16:8648580 | C | T | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*2437C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2437 | chr16 | 8648580 | ||||||
| chr16:8648665 | G | C | 1 | a0003c0003t0039 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2522 | chr16 | 8648665 | ||||||
| chr16:8648745 | C | G | 1 | a0002c0002t0046 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2602C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2602 | chr16 | 8648745 | ||||||
| chr16:8648779 | C | A | 1 | a0003c0003t0040 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2636C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2636 | chr16 | 8648779 | ||||||
| chr16:8648788 | A | T | 1 | a0003c0003t0045 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2645A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2645 | chr16 | 8648788 | ||||||
| chr16:8648799 | AAAG | A | 2 | a0001c0006t0010 a0001c0012t0010 |
6 | HG01192.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2657_*2659delAAG | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2657 | chr16 | 8648799 | ||||||
| chr16:8648824 | G | A | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*2681G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2681 | chr16 | 8648824 | ||||||
| chr16:8648853 | C | T | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*2710C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2710 | chr16 | 8648853 | ||||||
| chr16:8648970 | A | G | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*2827A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2827 | chr16 | 8648970 | ||||||
| chr16:8649024 | C | T | 1 | a0003c0003t0044 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2881C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2881 | chr16 | 8649024 | ||||||
| chr16:8649047 | A | C | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*2904A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 2904 | chr16 | 8649047 | ||||||
| chr16:8649158 | G | A | 4 | a0001c0001t0003 a0001c0006t0010 a0001c0012t0010 others(1): Show |
18 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3015G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3015 | chr16 | 8649158 | ||||||
| chr16:8649226 | A | G | 6 | a0001c0001t0004 a0001c0001t0028 a0001c0001t0053 others(3): Show |
20 | HG00642.hp1 HG01074.hp1 HG01257.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3083A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3083 | chr16 | 8649226 | ||||||
| chr16:8649232 | C | T | 2 | a0001c0001t0017 a0001c0001t0043 |
4 | HG01175.hp1 HG02559.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3089C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3089 | chr16 | 8649232 | ||||||
| chr16:8649250 | A | G | 1 | a0002c0002t0008 | 8 | HG02135.hp1 NA18971.hp1 NA18982.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3107A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3107 | chr16 | 8649250 | ||||||
| chr16:8649293 | C | T | 1 | a0001c0001t0042 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3150C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3150 | chr16 | 8649293 | ||||||
| chr16:8649347 | C | T | 3 | a0001c0006t0010 a0001c0012t0010 a0001c0013t0026 |
7 | HG01192.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3204C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3204 | chr16 | 8649347 | ||||||
| chr16:8649370 | T | C | 1 | a0001c0001t0003 | 11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3227T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3227 | chr16 | 8649370 | ||||||
| chr16:8649612 | T | C | 36 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0022 others(33): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*3469T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3469 | chr16 | 8649612 | ||||||
| chr16:8649620 | C | T | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*3477C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3477 | chr16 | 8649620 | ||||||
| chr16:8649637 | CAA | C | 7 | a0001c0001t0031 a0001c0001t0043 a0001c0001t0048 others(4): Show |
7 | HG01175.hp1 HG02559.hp2 HG03540.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3488_*3489delAA | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3488 | INFO_REALIGN_3_PRIME | chr16 | 8649637 | |||||
| chr16:8649637 | CAAA | C | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
3_prime_UTR_variant | MODIFIER | c.*3487_*3489delAAA | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 11/11 | 3487 | INFO_REALIGN_3_PRIME | chr16 | 8649637 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:8621940 | A | G | 3 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0052g0255 |
3 | HG03831.hp2 NA19011.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-171+165A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8621940 | |||||||
| chr16:8622064 | C | G | 9 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(6): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-171+289C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622064 | |||||||
| chr16:8622114 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-171+339G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622114 | |||||||
| chr16:8622179 | C | T | 242 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(239): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-171+404C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622179 | |||||||
| chr16:8622184 | G | T | 242 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(239): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-171+409G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622184 | |||||||
| chr16:8622243 | C | T | 4 | a0001c0005t0009g0019 a0001c0005t0009g0242 a0001c0005t0009g0244 others(1): Show |
6 | HG01884.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-171+468C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622243 | |||||||
| chr16:8622250 | A | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(238): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-171+475A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622250 | |||||||
| chr16:8622271 | A | G | 15 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0002g0235 others(12): Show |
18 | HG01167.hp2 HG01175.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-171+496A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622271 | |||||||
| chr16:8622349 | C | A | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-171+574C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622349 | |||||||
| chr16:8622407 | G | C | 2 | a0001c0001t0024g0082 a0001c0001t0024g0083 |
2 | HG02055.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-171+632G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622407 | |||||||
| chr16:8622442 | A | G | 9 | a0001c0001t0003g0050 a0001c0001t0003g0220 a0001c0001t0003g0221 others(6): Show |
10 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.-171+667A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622442 | |||||||
| chr16:8622458 | A | G | 1 | a0002c0002t0001g0218 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-171+683A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622458 | |||||||
| chr16:8622641 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(239): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-171+866A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622641 | |||||||
| chr16:8622653 | G | A | 2 | a0001c0001t0032g0084 a0001c0001t0048g0085 |
2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-171+878G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622653 | |||||||
| chr16:8622687 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(173): Show |
253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.-171+912T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622687 | |||||||
| chr16:8622698 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-171+923C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622698 | |||||||
| chr16:8622752 | T | C | 9 | a0001c0001t0003g0050 a0001c0001t0003g0220 a0001c0001t0003g0221 others(6): Show |
10 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.-171+977T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622752 | |||||||
| chr16:8622767 | C | T | 242 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(239): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-171+992C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622767 | |||||||
| chr16:8622786 | T | C | 1 | a0002c0002t0001g0086 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-171+1011T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622786 | |||||||
| chr16:8622837 | T | C | 2 | a0002c0002t0001g0087 a0002c0002t0001g0088 |
2 | NA18970.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-171+1062T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622837 | |||||||
| chr16:8622865 | G | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0200 a0001c0001t0017g0201 others(1): Show |
5 | HG02258.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-171+1090G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622865 | |||||||
| chr16:8622980 | A | C | 1 | a0001c0013t0026g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-171+1205A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8622980 | |||||||
| chr16:8623091 | A | G | 1 | a0004c0004t0006g0011 | 4 | HG02451.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-171+1316A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623091 | |||||||
| chr16:8623165 | T | C | 3 | a0001c0001t0028g0089 a0001c0001t0032g0084 a0001c0001t0048g0085 |
3 | HG02257.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-171+1390T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623165 | |||||||
| chr16:8623207 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-171+1432G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623207 | |||||||
| chr16:8623243 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-171+1468G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623243 | |||||||
| chr16:8623255 | G | A | 1 | a0004c0004t0006g0011 | 4 | HG02451.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-171+1480G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623255 | |||||||
| chr16:8623267 | C | T | 1 | a0003c0003t0001g0199 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-171+1492C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623267 | |||||||
| chr16:8623274 | G | A | 1 | a0003c0003t0001g0024 | 2 | NA18957.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-171+1499G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623274 | |||||||
| chr16:8623312 | G | GA | 20 | a0001c0001t0001g0095 a0001c0001t0001g0229 a0001c0001t0002g0052 others(17): Show |
22 | HG01928.hp1 HG02004.hp1 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.-171+1552dupA | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 8623312 | ||||||
| chr16:8623331 | G | T | 1 | a0001c0001t0031g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-171+1556G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623331 | |||||||
| chr16:8623349 | A | G | 3 | a0001c0021t0001g0198 a0004c0004t0006g0214 a0004c0004t0006g0215 |
3 | HG02615.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-171+1574A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623349 | |||||||
| chr16:8623409 | C | T | 1 | a0001c0013t0026g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-171+1634C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623409 | |||||||
| chr16:8623566 | G | A | 1 | a0002c0002t0001g0098 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-171+1791G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623566 | |||||||
| chr16:8623611 | A | G | 1 | a0001c0001t0002g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-171+1836A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623611 | |||||||
| chr16:8623750 | G | A | 9 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(6): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-170-1746G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623750 | |||||||
| chr16:8623909 | C | G | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-170-1587C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8623909 | |||||||
| chr16:8624050 | G | A | 10 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(7): Show |
11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.-170-1446G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624050 | |||||||
| chr16:8624086 | G | A | 9 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(6): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-170-1410G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624086 | |||||||
| chr16:8624163 | C | G | 5 | a0003c0003t0001g0041 a0003c0003t0001g0097 a0003c0003t0001g0195 others(2): Show |
6 | HG01978.hp1 NA18946.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-170-1333C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624163 | |||||||
| chr16:8624208 | C | T | 6 | a0001c0006t0010g0189 a0001c0006t0010g0190 a0001c0006t0010g0191 others(3): Show |
6 | HG01192.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-170-1288C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624208 | |||||||
| chr16:8624363 | CT | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(231): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-170-1117delT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 8624363 | ||||||
| chr16:8624363 | CTT | C | 6 | a0001c0001t0001g0081 a0001c0001t0011g0044 a0002c0002t0001g0001 others(3): Show |
6 | HG00639.hp2 HG01074.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-170-1118_-170-111 others(6): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 8624363 | ||||||
| chr16:8624375 | T | A | 4 | a0001c0005t0009g0019 a0001c0005t0009g0242 a0001c0005t0009g0244 others(1): Show |
6 | HG01884.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-170-1121T>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624375 | |||||||
| chr16:8624478 | C | T | 1 | a0003c0003t0001g0188 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-170-1018C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624478 | |||||||
| chr16:8624551 | A | C | 1 | a0001c0001t0002g0079 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-170-945A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624551 | |||||||
| chr16:8624636 | T | C | 1 | a0001c0001t0017g0099 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-170-860T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624636 | |||||||
| chr16:8624655 | C | G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0023 a0001c0001t0002g0077 others(1): Show |
7 | HG00438.hp2 HG01123.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-170-841C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624655 | |||||||
| chr16:8624664 | G | C | 1 | a0001c0001t0037g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-170-832G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624664 | |||||||
| chr16:8624756 | T | C | 9 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(6): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-170-740T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624756 | |||||||
| chr16:8624757 | G | T | 9 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(6): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-170-739G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8624757 | |||||||
| chr16:8625002 | G | T | 1 | a0001c0001t0002g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-170-494G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8625002 | |||||||
| chr16:8625026 | GA | G | 25 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(22): Show |
30 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-170-462delA | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 8625026 | ||||||
| chr16:8625069 | T | A | 14 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(11): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-170-427T>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8625069 | |||||||
| chr16:8625118 | G | T | 1 | a0002c0002t0001g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-170-378G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8625118 | |||||||
| chr16:8625132 | T | C | 3 | a0002c0002t0001g0025 a0002c0002t0001g0101 a0002c0002t0001g0102 |
4 | HG00140.hp1 HG01168.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-170-364T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8625132 | |||||||
| chr16:8625163 | A | C | 1 | a0001c0001t0002g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-170-333A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8625163 | |||||||
| chr16:8625196 | A | G | 1 | a0006c0007t0004g0040 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-170-300A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8625196 | |||||||
| chr16:8625278 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0186 |
4 | HG02818.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-170-218A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8625278 | |||||||
| chr16:8625346 | A | G | 14 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(11): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-170-150A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8625346 | |||||||
| chr16:8625400 | G | A | 2 | a0001c0001t0002g0103 a0001c0017t0002g0104 |
2 | HG00741.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-170-96G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8625400 | |||||||
| chr16:8625482 | G | A | 3 | a0004c0004t0020g0043 a0004c0004t0020g0203 a0004c0004t0029g0043 |
3 | HG02630.hp2 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-170-14G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1/10 | chr16 | 8625482 | |||||||
| chr16:8625811 | G | A | 1 | a0001c0001t0007g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.133+13G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8625811 | |||||||
| chr16:8625819 | G | A | 2 | a0002c0002t0023g0091 a0002c0002t0030g0105 |
2 | NA18747.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.133+21G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8625819 | |||||||
| chr16:8625881 | G | A | 10 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(7): Show |
11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.133+83G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8625881 | |||||||
| chr16:8625913 | C | T | 1 | a0001c0001t0048g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.133+115C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8625913 | |||||||
| chr16:8625914 | C | T | 1 | a0003c0003t0047g0185 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.133+116C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8625914 | |||||||
| chr16:8626023 | A | G | 7 | a0001c0001t0002g0014 a0001c0001t0002g0023 a0001c0001t0002g0077 others(4): Show |
12 | HG00438.hp2 HG01123.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.133+225A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626023 | |||||||
| chr16:8626035 | C | T | 1 | a0005c0008t0019g0045 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.133+237C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626035 | |||||||
| chr16:8626045 | G | T | 1 | a0005c0008t0019g0045 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.133+247G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626045 | |||||||
| chr16:8626083 | A | G | 1 | a0002c0002t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.133+285A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626083 | |||||||
| chr16:8626093 | C | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
6 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+295C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626093 | |||||||
| chr16:8626183 | G | T | 5 | a0001c0005t0009g0019 a0001c0005t0009g0213 a0001c0005t0009g0242 others(2): Show |
7 | HG01884.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+385G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626183 | |||||||
| chr16:8626307 | T | G | 2 | a0001c0001t0001g0107 a0002c0002t0001g0106 |
2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.133+509T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626307 | |||||||
| chr16:8626324 | A | G | 1 | a0001c0001t0002g0074 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.133+526A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626324 | |||||||
| chr16:8626375 | C | T | 1 | a0001c0001t0003g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.133+577C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626375 | |||||||
| chr16:8626446 | C | CT | 15 | a0001c0001t0001g0107 a0001c0001t0002g0073 a0001c0001t0002g0179 others(12): Show |
15 | HG00741.hp1 HG02071.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+668dupT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 8626446 | ||||||
| chr16:8626446 | CT | C | 16 | a0001c0001t0001g0026 a0001c0001t0001g0108 a0001c0001t0002g0056 others(13): Show |
19 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.133+668delT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 8626446 | ||||||
| chr16:8626446 | CTTT | C | 14 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(11): Show |
19 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.133+666_133+668del others(3): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 8626446 | ||||||
| chr16:8626461 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.133+663T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626461 | |||||||
| chr16:8626479 | C | T | 14 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(11): Show |
18 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.133+681C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626479 | |||||||
| chr16:8626510 | G | A | 1 | a0001c0001t0050g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.133+712G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626510 | |||||||
| chr16:8626691 | C | G | 1 | a0001c0001t0025g0049 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.133+893C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626691 | |||||||
| chr16:8626724 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.133+926C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626724 | |||||||
| chr16:8626749 | C | T | 2 | a0001c0001t0012g0013 a0001c0001t0012g0075 |
4 | NA18942.hp2 NA18943.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+951C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626749 | |||||||
| chr16:8626761 | C | CT | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(156): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.133+986dupT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 8626761 | ||||||
| chr16:8626761 | C | CTT | 33 | a0001c0001t0001g0037 a0001c0001t0001g0107 a0001c0001t0001g0171 others(30): Show |
40 | HG00544.hp2 HG00735.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.133+985_133+986dup others(2): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 8626761 | ||||||
| chr16:8626761 | C | CTTT | 11 | a0001c0001t0003g0050 a0001c0001t0003g0221 a0001c0001t0003g0222 others(8): Show |
12 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+984_133+986dup others(3): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 8626761 | ||||||
| chr16:8626815 | A | G | 8 | a0001c0001t0004g0018 a0001c0001t0004g0047 a0001c0001t0004g0048 others(5): Show |
12 | HG00642.hp1 HG01074.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+1017A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626815 | |||||||
| chr16:8626818 | G | C | 8 | a0001c0001t0004g0018 a0001c0001t0004g0047 a0001c0001t0004g0048 others(5): Show |
12 | HG00642.hp1 HG01074.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+1020G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626818 | |||||||
| chr16:8626825 | CAT | C | 8 | a0001c0001t0004g0018 a0001c0001t0004g0047 a0001c0001t0004g0048 others(5): Show |
12 | HG00642.hp1 HG01074.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+1028_133+1029d others(4): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626825 | |||||||
| chr16:8626835 | C | T | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+1037C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626835 | |||||||
| chr16:8626859 | C | T | 1 | a0003c0003t0001g0110 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.133+1061C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8626859 | |||||||
| chr16:8627012 | G | A | 1 | a0001c0001t0005g0245 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.133+1214G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627012 | |||||||
| chr16:8627038 | C | G | 1 | a0004c0004t0006g0011 | 4 | HG02451.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+1240C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627038 | |||||||
| chr16:8627193 | A | C | 9 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(6): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.133+1395A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627193 | |||||||
| chr16:8627224 | G | A | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+1426G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627224 | |||||||
| chr16:8627234 | G | C | 5 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(2): Show |
9 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.133+1436G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627234 | |||||||
| chr16:8627255 | G | C | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+1457G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627255 | |||||||
| chr16:8627504 | A | G | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.134-1226A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627504 | |||||||
| chr16:8627540 | A | C | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-1190A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627540 | |||||||
| chr16:8627668 | G | A | 10 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(7): Show |
11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.134-1062G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627668 | |||||||
| chr16:8627680 | C | G | 1 | a0008c0020t0005g0251 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.134-1050C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627680 | |||||||
| chr16:8627682 | G | A | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-1048G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627682 | |||||||
| chr16:8627727 | A | G | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-1003A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627727 | |||||||
| chr16:8627734 | C | G | 1 | a0001c0001t0056g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.134-996C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627734 | |||||||
| chr16:8627770 | G | A | 1 | a0003c0003t0001g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.134-960G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627770 | |||||||
| chr16:8627772 | G | T | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-958G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627772 | |||||||
| chr16:8627777 | A | T | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-953A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627777 | |||||||
| chr16:8627800 | C | T | 9 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0238 others(6): Show |
10 | HG02055.hp1 HG02615.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-930C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627800 | |||||||
| chr16:8627801 | G | A | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-929G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627801 | |||||||
| chr16:8627885 | T | G | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-845T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627885 | |||||||
| chr16:8627927 | A | G | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-803A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8627927 | |||||||
| chr16:8628073 | T | C | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-657T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8628073 | |||||||
| chr16:8628139 | C | T | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-591C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8628139 | |||||||
| chr16:8628152 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.134-578C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8628152 | |||||||
| chr16:8628193 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.134-537C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8628193 | |||||||
| chr16:8628195 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(224): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.134-535A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8628195 | |||||||
| chr16:8628196 | A | G | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-534A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8628196 | |||||||
| chr16:8628466 | A | G | 6 | a0001c0006t0010g0189 a0001c0006t0010g0190 a0001c0006t0010g0191 others(3): Show |
6 | HG01192.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-264A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8628466 | |||||||
| chr16:8628494 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.134-236G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8628494 | |||||||
| chr16:8628526 | G | A | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-204G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8628526 | |||||||
| chr16:8628703 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.134-27C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 2/10 | chr16 | 8628703 | |||||||
| chr16:8629126 | A | G | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.514+16A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629126 | |||||||
| chr16:8629149 | C | T | 1 | a0003c0003t0044g0178 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.514+39C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629149 | |||||||
| chr16:8629191 | C | T | 3 | a0001c0006t0010g0192 a0001c0006t0010g0193 a0001c0012t0010g0194 |
3 | HG02717.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.514+81C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629191 | |||||||
| chr16:8629283 | C | A | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | NA18969.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.514+173C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629283 | |||||||
| chr16:8629341 | G | A | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.514+231G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629341 | |||||||
| chr16:8629375 | T | C | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.514+265T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629375 | |||||||
| chr16:8629418 | C | G | 10 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(7): Show |
11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.514+308C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629418 | |||||||
| chr16:8629487 | G | C | 1 | a0001c0001t0028g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.514+377G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629487 | |||||||
| chr16:8629608 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0027 others(5): Show |
17 | HG00423.hp1 HG01099.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.514+498G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629608 | |||||||
| chr16:8629626 | G | A | 1 | a0008c0020t0005g0251 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.514+516G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629626 | |||||||
| chr16:8629646 | G | A | 1 | a0002c0002t0001g0121 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.514+536G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629646 | |||||||
| chr16:8629693 | C | G | 8 | a0001c0021t0001g0198 a0004c0004t0006g0011 a0004c0004t0006g0046 others(5): Show |
12 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.514+583C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629693 | |||||||
| chr16:8629723 | C | G | 15 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(12): Show |
19 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.514+613C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629723 | |||||||
| chr16:8629776 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(237): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.514+666A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629776 | |||||||
| chr16:8629834 | G | C | 8 | a0001c0001t0005g0020 a0001c0001t0005g0246 a0001c0001t0005g0247 others(5): Show |
10 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.514+724G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629834 | |||||||
| chr16:8629881 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.514+771G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629881 | |||||||
| chr16:8629881 | G | C | 1 | a0001c0001t0031g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.514+771G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629881 | |||||||
| chr16:8629900 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+790A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629900 | |||||||
| chr16:8629920 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+810T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629920 | |||||||
| chr16:8629923 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.514+813A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8629923 | |||||||
| chr16:8630027 | AT | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+920delT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 8630027 | ||||||
| chr16:8630200 | GCAAA | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(237): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.514+1093_514+1096d others(6): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 8630200 | ||||||
| chr16:8630235 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.514+1125A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630235 | |||||||
| chr16:8630294 | G | A | 1 | a0001c0013t0026g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.514+1184G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630294 | |||||||
| chr16:8630316 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+1206C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630316 | |||||||
| chr16:8630381 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.514+1271G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630381 | |||||||
| chr16:8630384 | C | T | 1 | a0001c0001t0037g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.514+1274C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630384 | |||||||
| chr16:8630417 | G | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+1307G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630417 | |||||||
| chr16:8630462 | G | A | 3 | a0001c0001t0013g0021 a0001c0001t0013g0058 a0001c0001t0013g0059 |
4 | HG00741.hp2 HG01258.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.514+1352G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630462 | |||||||
| chr16:8630546 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.514+1436C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630546 | |||||||
| chr16:8630650 | T | A | 1 | a0001c0001t0031g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.514+1540T>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630650 | |||||||
| chr16:8630652 | C | G | 1 | a0001c0013t0026g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.514+1542C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630652 | |||||||
| chr16:8630715 | A | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+1605A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630715 | |||||||
| chr16:8630720 | C | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+1610C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630720 | |||||||
| chr16:8630733 | G | A | 1 | a0003c0003t0001g0195 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.514+1623G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630733 | |||||||
| chr16:8630814 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.514+1704C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630814 | |||||||
| chr16:8630843 | A | G | 10 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(7): Show |
11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.514+1733A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630843 | |||||||
| chr16:8630925 | A | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+1815A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630925 | |||||||
| chr16:8630926 | G | A | 1 | a0001c0001t0032g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.514+1816G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630926 | |||||||
| chr16:8630938 | G | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+1828G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8630938 | |||||||
| chr16:8631078 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+1968C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631078 | |||||||
| chr16:8631255 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+2145C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631255 | |||||||
| chr16:8631302 | C | G | 1 | a0004c0004t0006g0011 | 4 | HG02451.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+2192C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631302 | |||||||
| chr16:8631370 | G | A | 1 | a0001c0001t0024g0082 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.514+2260G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631370 | |||||||
| chr16:8631414 | G | A | 1 | a0001c0001t0031g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.514+2304G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631414 | |||||||
| chr16:8631468 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+2358C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631468 | |||||||
| chr16:8631541 | G | A | 8 | a0001c0001t0004g0018 a0001c0001t0004g0047 a0001c0001t0004g0048 others(5): Show |
12 | HG00642.hp1 HG01074.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.514+2431G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631541 | |||||||
| chr16:8631543 | G | A | 1 | a0001c0001t0028g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.514+2433G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631543 | |||||||
| chr16:8631571 | G | A | 2 | a0001c0001t0032g0084 a0001c0001t0048g0085 |
2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.514+2461G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631571 | |||||||
| chr16:8631596 | A | G | 1 | a0001c0013t0026g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.514+2486A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631596 | |||||||
| chr16:8631625 | G | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+2515G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631625 | |||||||
| chr16:8631641 | G | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+2531G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631641 | |||||||
| chr16:8631737 | A | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG00738.hp2 HG01346.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.514+2627A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631737 | |||||||
| chr16:8631795 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+2685C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631795 | |||||||
| chr16:8631848 | G | A | 1 | a0001c0001t0051g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.514+2738G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631848 | |||||||
| chr16:8631869 | T | G | 1 | a0001c0001t0003g0050 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.514+2759T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631869 | |||||||
| chr16:8631892 | G | T | 1 | a0001c0001t0011g0205 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.514+2782G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631892 | |||||||
| chr16:8631942 | T | G | 10 | a0001c0001t0004g0047 a0001c0001t0004g0048 a0001c0001t0004g0212 others(7): Show |
14 | HG01257.hp2 HG01884.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.514+2832T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631942 | |||||||
| chr16:8631949 | C | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.514+2839C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631949 | |||||||
| chr16:8631954 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(265): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.514+2844G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8631954 | |||||||
| chr16:8632076 | C | T | 1 | a0010c0014t0001g0165 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.515-2963C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632076 | |||||||
| chr16:8632096 | G | A | 1 | a0002c0002t0001g0123 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.515-2943G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632096 | |||||||
| chr16:8632101 | C | T | 1 | a0002c0002t0001g0119 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.515-2938C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632101 | |||||||
| chr16:8632153 | G | C | 2 | a0003c0003t0001g0124 a0003c0003t0001g0125 |
2 | HG00544.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.515-2886G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632153 | |||||||
| chr16:8632201 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-2838T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632201 | |||||||
| chr16:8632321 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-2718C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632321 | |||||||
| chr16:8632327 | C | G | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.515-2712C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632327 | |||||||
| chr16:8632387 | A | T | 6 | a0001c0006t0010g0189 a0001c0006t0010g0190 a0001c0006t0010g0191 others(3): Show |
6 | HG01192.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.515-2652A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632387 | |||||||
| chr16:8632407 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-2632C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632407 | |||||||
| chr16:8632455 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-2584T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632455 | |||||||
| chr16:8632511 | C | T | 1 | a0001c0001t0037g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.515-2528C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632511 | |||||||
| chr16:8632566 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-2473T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632566 | |||||||
| chr16:8632567 | G | T | 1 | a0012c0015t0002g0068 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.515-2472G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632567 | |||||||
| chr16:8632629 | A | G | 28 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(25): Show |
33 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.515-2410A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632629 | |||||||
| chr16:8632629 | A | T | 241 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(238): Show |
343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.515-2410A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632629 | |||||||
| chr16:8632816 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-2223C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632816 | |||||||
| chr16:8632849 | C | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.515-2190C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632849 | |||||||
| chr16:8632896 | C | G | 1 | a0001c0001t0002g0103 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.515-2143C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632896 | |||||||
| chr16:8632957 | G | A | 4 | a0001c0001t0002g0092 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | NA18957.hp2 NA18980.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.515-2082G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8632957 | |||||||
| chr16:8633006 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-2033T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633006 | |||||||
| chr16:8633225 | C | T | 1 | a0003c0003t0001g0164 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.515-1814C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633225 | |||||||
| chr16:8633245 | C | A | 1 | a0003c0003t0044g0178 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.515-1794C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633245 | |||||||
| chr16:8633343 | A | G | 5 | a0002c0002t0001g0035 a0002c0002t0001g0118 a0002c0002t0001g0119 others(2): Show |
6 | HG02135.hp1 NA18948.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.515-1696A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633343 | |||||||
| chr16:8633355 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-1684T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633355 | |||||||
| chr16:8633399 | C | A | 1 | a0001c0001t0002g0179 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.515-1640C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633399 | |||||||
| chr16:8633499 | G | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(254): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.515-1540G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633499 | |||||||
| chr16:8633515 | A | C | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.515-1524A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633515 | |||||||
| chr16:8633721 | A | G | 2 | a0002c0002t0001g0161 a0002c0002t0001g0162 |
2 | HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.515-1318A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633721 | |||||||
| chr16:8633733 | G | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-1306G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633733 | |||||||
| chr16:8633826 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-1213A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633826 | |||||||
| chr16:8633911 | T | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-1128T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633911 | |||||||
| chr16:8633958 | C | G | 1 | a0001c0013t0026g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.515-1081C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8633958 | |||||||
| chr16:8634073 | G | A | 3 | a0004c0004t0020g0043 a0004c0004t0020g0203 a0004c0004t0029g0043 |
3 | HG02630.hp2 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.515-966G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634073 | |||||||
| chr16:8634205 | A | G | 1 | a0001c0001t0034g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.515-834A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634205 | |||||||
| chr16:8634230 | G | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-809G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634230 | |||||||
| chr16:8634248 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-791A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634248 | |||||||
| chr16:8634259 | G | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-780G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634259 | |||||||
| chr16:8634278 | C | T | 1 | a0001c0013t0026g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.515-761C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634278 | |||||||
| chr16:8634281 | T | C | 1 | a0001c0017t0002g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.515-758T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634281 | |||||||
| chr16:8634404 | C | G | 1 | a0002c0002t0001g0098 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.515-635C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634404 | |||||||
| chr16:8634431 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-608C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634431 | |||||||
| chr16:8634435 | C | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-604C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634435 | |||||||
| chr16:8634553 | A | AT | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.515-479dupT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 8634553 | ||||||
| chr16:8634748 | C | T | 6 | a0001c0006t0010g0189 a0001c0006t0010g0190 a0001c0006t0010g0191 others(3): Show |
6 | HG01192.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.515-291C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634748 | |||||||
| chr16:8634761 | T | C | 9 | a0001c0001t0005g0020 a0001c0001t0005g0245 a0001c0001t0005g0246 others(6): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.515-278T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634761 | |||||||
| chr16:8634814 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-225A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634814 | |||||||
| chr16:8634907 | C | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(240): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.515-132C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634907 | |||||||
| chr16:8634915 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.515-124C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634915 | |||||||
| chr16:8634961 | C | T | 2 | a0002c0002t0001g0159 a0002c0002t0001g0160 |
2 | NA18949.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.515-78C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8634961 | |||||||
| chr16:8635008 | G | A | 1 | a0001c0001t0050g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.515-31G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3/10 | chr16 | 8635008 | |||||||
| chr16:8635096 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.555+17C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 4/10 | chr16 | 8635096 | |||||||
| chr16:8635142 | G | A | 1 | a0003c0003t0049g0126 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.556-26G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 4/10 | chr16 | 8635142 | |||||||
| chr16:8635154 | C | T | 3 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0001t0003g0227 |
3 | HG00099.hp1 HG00642.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.556-14C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 4/10 | chr16 | 8635154 | |||||||
| chr16:8635363 | A | G | 7 | a0001c0001t0004g0018 a0001c0001t0004g0047 a0001c0001t0004g0048 others(4): Show |
10 | HG00642.hp1 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.700+51A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8635363 | |||||||
| chr16:8635397 | C | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.700+85C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8635397 | |||||||
| chr16:8635418 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.700+106T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8635418 | |||||||
| chr16:8635466 | A | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.700+154A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8635466 | |||||||
| chr16:8635499 | C | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.700+187C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8635499 | |||||||
| chr16:8635670 | T | A | 1 | a0011c0019t0001g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.700+358T>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8635670 | |||||||
| chr16:8635685 | C | G | 1 | a0003c0003t0001g0158 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.700+373C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8635685 | |||||||
| chr16:8635701 | T | C | 2 | a0002c0002t0023g0091 a0003c0003t0023g0094 |
2 | NA19086.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.700+389T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8635701 | |||||||
| chr16:8635906 | C | G | 1 | a0001c0001t0032g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.700+594C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8635906 | |||||||
| chr16:8636116 | C | G | 2 | a0001c0001t0001g0095 a0001c0001t0036g0096 |
2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.700+804C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636116 | |||||||
| chr16:8636180 | G | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.700+868G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636180 | |||||||
| chr16:8636226 | C | G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0023 a0001c0001t0002g0077 others(1): Show |
7 | HG00438.hp2 HG01123.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.700+914C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636226 | |||||||
| chr16:8636262 | C | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
6 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.700+950C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636262 | |||||||
| chr16:8636420 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.700+1108C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636420 | |||||||
| chr16:8636424 | G | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG00738.hp2 HG01346.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.700+1112G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636424 | |||||||
| chr16:8636532 | A | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0027 others(68): Show |
103 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.700+1220A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636532 | |||||||
| chr16:8636536 | AAAAC | A | 14 | a0001c0001t0003g0050 a0001c0001t0003g0220 a0001c0001t0003g0221 others(11): Show |
15 | HG00323.hp2 HG00642.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.700+1229_700+1232d others(6): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 8636536 | ||||||
| chr16:8636537 | AAAC | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(242): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.700+1228_700+1230d others(5): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 8636537 | ||||||
| chr16:8636538 | AAC | A | 14 | a0001c0001t0001g0026 a0001c0001t0002g0208 a0001c0001t0002g0209 others(11): Show |
14 | HG02145.hp1 HG02559.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.700+1228_700+1229d others(4): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 8636538 | ||||||
| chr16:8636553 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(265): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.700+1241T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636553 | |||||||
| chr16:8636625 | C | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.700+1313C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636625 | |||||||
| chr16:8636649 | T | G | 1 | a0001c0001t0031g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.700+1337T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636649 | |||||||
| chr16:8636652 | G | GT | 250 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(247): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.700+1349dupT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 8636652 | ||||||
| chr16:8636652 | G | GTT | 19 | a0001c0001t0001g0168 a0001c0001t0001g0176 a0001c0001t0002g0073 others(16): Show |
19 | HG00438.hp2 HG00544.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.700+1348_700+1349d others(4): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 8636652 | ||||||
| chr16:8636721 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.700+1409A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636721 | |||||||
| chr16:8636815 | G | A | 1 | a0001c0013t0026g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.700+1503G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636815 | |||||||
| chr16:8636835 | G | C | 1 | a0001c0001t0002g0208 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.700+1523G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636835 | |||||||
| chr16:8636928 | T | C | 1 | a0001c0001t0031g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.700+1616T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636928 | |||||||
| chr16:8636929 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.700+1617A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636929 | |||||||
| chr16:8636957 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0182 others(2): Show |
8 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+1645A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8636957 | |||||||
| chr16:8637013 | T | C | 1 | a0001c0001t0028g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.700+1701T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637013 | |||||||
| chr16:8637088 | C | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.700+1776C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637088 | |||||||
| chr16:8637188 | C | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.700+1876C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637188 | |||||||
| chr16:8637343 | T | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(265): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.701-1748T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637343 | |||||||
| chr16:8637369 | G | A | 2 | a0002c0002t0001g0161 a0002c0002t0001g0162 |
2 | HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.701-1722G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637369 | |||||||
| chr16:8637384 | T | C | 23 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(20): Show |
28 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.701-1707T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637384 | |||||||
| chr16:8637392 | A | T | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.701-1699A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637392 | |||||||
| chr16:8637394 | TAGCAGAC others(4): Show |
T | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.701-1695_701-1685d others(13): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 8637394 | ||||||
| chr16:8637406 | A | T | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.701-1685A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637406 | |||||||
| chr16:8637496 | T | C | 11 | a0001c0001t0005g0020 a0001c0001t0005g0246 a0001c0001t0005g0247 others(8): Show |
15 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.701-1595T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637496 | |||||||
| chr16:8637686 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.701-1405T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637686 | |||||||
| chr16:8637763 | C | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-1328C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637763 | |||||||
| chr16:8637775 | G | C | 1 | a0001c0001t0056g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-1316G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637775 | |||||||
| chr16:8637784 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-1307C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637784 | |||||||
| chr16:8637864 | G | A | 1 | a0002c0002t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.701-1227G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637864 | |||||||
| chr16:8637874 | A | G | 23 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(20): Show |
28 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.701-1217A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637874 | |||||||
| chr16:8637950 | C | T | 6 | a0001c0006t0010g0189 a0001c0006t0010g0190 a0001c0006t0010g0191 others(3): Show |
6 | HG01192.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.701-1141C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637950 | |||||||
| chr16:8637955 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-1136C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637955 | |||||||
| chr16:8637968 | T | G | 1 | a0001c0001t0007g0231 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.701-1123T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8637968 | |||||||
| chr16:8637983 | C | CAA | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(260): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.701-1095_701-1094d others(4): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 8637983 | ||||||
| chr16:8638114 | T | A | 1 | a0003c0003t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.701-977T>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638114 | |||||||
| chr16:8638118 | G | GC | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-973_701-972ins others(1): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638118 | |||||||
| chr16:8638168 | G | A | 3 | a0001c0001t0024g0082 a0001c0001t0024g0083 a0001c0001t0025g0049 |
4 | HG02055.hp1 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-923G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638168 | |||||||
| chr16:8638210 | G | T | 1 | a0001c0001t0001g0254 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.701-881G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638210 | |||||||
| chr16:8638226 | C | T | 2 | a0002c0002t0001g0159 a0002c0002t0001g0160 |
2 | NA18949.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.701-865C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638226 | |||||||
| chr16:8638237 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-854A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638237 | |||||||
| chr16:8638265 | C | G | 1 | a0003c0003t0001g0164 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.701-826C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638265 | |||||||
| chr16:8638360 | C | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-731C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638360 | |||||||
| chr16:8638375 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-716T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638375 | |||||||
| chr16:8638462 | A | G | 1 | a0001c0001t0028g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.701-629A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638462 | |||||||
| chr16:8638538 | C | G | 1 | a0006c0007t0004g0040 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.701-553C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638538 | |||||||
| chr16:8638610 | G | A | 1 | a0002c0002t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.701-481G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638610 | |||||||
| chr16:8638705 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-386A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638705 | |||||||
| chr16:8638767 | T | C | 1 | a0002c0002t0001g0151 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.701-324T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638767 | |||||||
| chr16:8638771 | T | G | 1 | a0003c0003t0001g0110 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.701-320T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638771 | |||||||
| chr16:8638813 | T | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-278T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638813 | |||||||
| chr16:8638822 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-269T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638822 | |||||||
| chr16:8638823 | G | A | 1 | a0001c0005t0009g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.701-268G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638823 | |||||||
| chr16:8638848 | C | G | 1 | a0001c0001t0004g0211 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.701-243C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638848 | |||||||
| chr16:8638876 | C | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-215C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | chr16 | 8638876 | |||||||
| chr16:8639025 | CA | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.701-60delA | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 8639025 | ||||||
| chr16:8639214 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.772+52A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639214 | |||||||
| chr16:8639297 | G | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.772+135G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639297 | |||||||
| chr16:8639317 | C | T | 1 | a0001c0001t0048g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.772+155C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639317 | |||||||
| chr16:8639335 | G | C | 8 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0238 others(5): Show |
9 | HG02055.hp1 HG02615.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.772+173G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639335 | |||||||
| chr16:8639338 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.772+176C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639338 | |||||||
| chr16:8639343 | G | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.772+181G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639343 | |||||||
| chr16:8639409 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.772+247C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639409 | |||||||
| chr16:8639455 | A | G | 1 | a0003c0003t0001g0158 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.772+293A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639455 | |||||||
| chr16:8639508 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.772+346A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639508 | |||||||
| chr16:8639518 | C | G | 10 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(7): Show |
11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.772+356C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639518 | |||||||
| chr16:8639570 | C | T | 1 | a0011c0019t0001g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.772+408C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639570 | |||||||
| chr16:8639601 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.772+439C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639601 | |||||||
| chr16:8639607 | G | T | 1 | a0003c0003t0001g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.772+445G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639607 | |||||||
| chr16:8639657 | C | T | 1 | a0003c0003t0001g0032 | 2 | NA18988.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.772+495C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639657 | |||||||
| chr16:8639699 | G | GC | 41 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0002g0061 others(38): Show |
44 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.772+539dupC | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8639699 | ||||||
| chr16:8639702 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.772+540T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639702 | |||||||
| chr16:8639705 | G | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.772+543G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639705 | |||||||
| chr16:8639706 | C | G | 8 | a0001c0001t0002g0014 a0001c0001t0002g0023 a0001c0001t0002g0056 others(5): Show |
13 | HG00438.hp2 HG01123.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.772+544C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639706 | |||||||
| chr16:8639737 | C | T | 1 | a0001c0001t0032g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.772+575C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639737 | |||||||
| chr16:8639770 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.772+608C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639770 | |||||||
| chr16:8639770 | C | T | 1 | a0001c0001t0017g0099 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.772+608C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639770 | |||||||
| chr16:8639771 | G | A | 1 | a0003c0003t0001g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.772+609G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639771 | |||||||
| chr16:8639833 | A | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.772+671A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639833 | |||||||
| chr16:8639879 | G | A | 1 | a0002c0002t0001g0134 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.772+717G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639879 | |||||||
| chr16:8639884 | G | A | 1 | a0003c0003t0001g0158 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.772+722G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639884 | |||||||
| chr16:8639884 | G | GC | 23 | a0001c0001t0001g0145 a0001c0001t0001g0156 a0001c0001t0001g0168 others(20): Show |
23 | HG00738.hp2 HG01192.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.772+728dupC | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8639884 | ||||||
| chr16:8639886 | C | G | 1 | a0001c0001t0002g0067 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.772+724C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639886 | |||||||
| chr16:8639891 | A | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(260): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.772+729A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639891 | |||||||
| chr16:8639891 | A | G | 6 | a0001c0001t0005g0020 a0001c0001t0005g0246 a0001c0001t0005g0247 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.772+729A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639891 | |||||||
| chr16:8639904 | G | A | 3 | a0004c0004t0020g0043 a0004c0004t0020g0203 a0004c0004t0029g0043 |
3 | HG02630.hp2 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.772+742G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639904 | |||||||
| chr16:8639961 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(265): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.772+799T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639961 | |||||||
| chr16:8639978 | G | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.772+816G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8639978 | |||||||
| chr16:8640093 | C | T | 1 | a0006c0007t0004g0040 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.772+931C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640093 | |||||||
| chr16:8640107 | T | C | 1 | a0004c0004t0006g0011 | 4 | HG02451.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.772+945T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640107 | |||||||
| chr16:8640128 | G | A | 2 | a0007c0010t0001g0129 a0007c0010t0001g0135 |
2 | HG03491.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.772+966G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640128 | |||||||
| chr16:8640185 | A | C | 5 | a0001c0001t0005g0020 a0001c0001t0005g0246 a0001c0001t0005g0247 others(2): Show |
7 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.773-946A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640185 | |||||||
| chr16:8640246 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.773-885A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640246 | |||||||
| chr16:8640250 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.773-881T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640250 | |||||||
| chr16:8640307 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.773-824T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640307 | |||||||
| chr16:8640353 | C | T | 1 | a0001c0001t0048g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.773-778C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640353 | |||||||
| chr16:8640354 | G | A | 1 | a0003c0003t0001g0029 | 2 | HG01346.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.773-777G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640354 | |||||||
| chr16:8640430 | T | C | 1 | a0001c0001t0032g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773-701T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640430 | |||||||
| chr16:8640477 | C | G | 1 | a0001c0013t0026g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.773-654C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640477 | |||||||
| chr16:8640496 | G | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(256): Show |
365 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.773-635G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640496 | |||||||
| chr16:8640527 | G | T | 1 | a0002c0002t0001g0151 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.773-604G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640527 | |||||||
| chr16:8640530 | G | GAGA | 272 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(269): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.773-599_773-598ins others(3): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640530 | ||||||
| chr16:8640607 | AGGATGGA others(1): Show |
A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(266): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.773-508_773-501del others(8): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640607 | ||||||
| chr16:8640678 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.773-453A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640678 | |||||||
| chr16:8640716 | G | C | 2 | a0002c0002t0001g0035 a0002c0002t0001g0163 |
3 | NA18948.hp2 NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.773-415G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640716 | |||||||
| chr16:8640773 | G | A | 1 | a0001c0001t0032g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773-358G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640773 | |||||||
| chr16:8640828 | AGATGGAT others(1): Show |
A | 18 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(15): Show |
21 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.773-287_773-280del others(8): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640828 | ||||||
| chr16:8640836 | G | GGATGGAT others(274): Show |
1 | a0001c0001t0001g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.773-288_773-287ins others(281): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640836 | G | GGATGGAT others(125): Show |
1 | a0001c0001t0048g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.773-288_773-287ins others(132): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640836 | G | GGATGGAT others(201): Show |
4 | a0001c0001t0001g0254 a0002c0002t0001g0001 a0002c0002t0001g0028 others(1): Show |
4 | HG02083.hp1 HG02602.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.773-288_773-287ins others(208): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640836 | G | GGATGGAT others(129): Show |
1 | a0001c0001t0002g0053 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.773-288_773-287ins others(136): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640836 | G | GGATGGAT others(257): Show |
1 | a0001c0001t0054g0181 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.773-288_773-287ins others(264): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640836 | G | GGATGGAT others(261): Show |
1 | a0002c0002t0021g0001 | 2 | HG00140.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.773-288_773-287ins others(268): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640836 | G | GGATGGAT others(201): Show |
29 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0238 others(26): Show |
39 | HG00639.hp2 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.773-288_773-287ins others(208): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640836 | G | GGATGGAT others(273): Show |
173 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(170): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.773-288_773-287ins others(280): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640836 | G | GGATGGAT others(345): Show |
1 | a0003c0003t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.773-288_773-287ins others(352): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640836 | G | GGATGGAT others(277): Show |
1 | a0002c0002t0001g0007 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.773-288_773-287ins others(284): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640836 | G | GGATGGAT others(201): Show |
43 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0014 others(40): Show |
59 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.773-288_773-287ins others(208): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640836 | ||||||
| chr16:8640882 | G | GTGGGTGG others(5): Show |
154 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(151): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.773-239_773-238ins others(12): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640882 | ||||||
| chr16:8640890 | G | GTGGTTGG others(9): Show |
55 | a0001c0001t0001g0107 a0001c0001t0001g0117 a0001c0001t0001g0122 others(52): Show |
68 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.773-239_773-238ins others(16): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640890 | ||||||
| chr16:8640890 | G | GTGGTTGG others(13): Show |
32 | a0001c0001t0001g0090 a0001c0001t0001g0136 a0001c0001t0001g0229 others(29): Show |
43 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.773-239_773-238ins others(20): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640890 | ||||||
| chr16:8640890 | G | GTGGTTGG others(17): Show |
11 | a0001c0001t0002g0008 a0001c0001t0002g0023 a0001c0001t0002g0055 others(8): Show |
15 | HG01433.hp2 HG01975.hp1 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.773-239_773-238ins others(24): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640890 | ||||||
| chr16:8640890 | G | GTGGTTGG others(21): Show |
3 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0076 |
3 | HG01255.hp2 HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.773-239_773-238ins others(28): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640890 | ||||||
| chr16:8640890 | G | GTGGTTGG others(9): Show |
2 | a0001c0005t0009g0019 a0001c0005t0033g0243 |
4 | HG01884.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.773-239_773-238ins others(16): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640890 | ||||||
| chr16:8640890 | GTGAA | G | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.773-238_773-235del others(4): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640890 | ||||||
| chr16:8640893 | A | G | 120 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0001g0117 others(117): Show |
154 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.773-238A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640893 | |||||||
| chr16:8640894 | A | G | 1 | a0001c0001t0004g0212 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.773-237A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640894 | |||||||
| chr16:8640894 | A | T | 6 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0031g0216 others(3): Show |
6 | HG02559.hp2 HG02723.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.773-237A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640894 | |||||||
| chr16:8640898 | A | G | 4 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0037g0100 others(1): Show |
4 | HG02559.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.773-233A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640898 | |||||||
| chr16:8640898 | A | T | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.773-233A>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640898 | |||||||
| chr16:8640902 | A | G | 7 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(4): Show |
9 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.773-229A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640902 | |||||||
| chr16:8640905 | G | A | 2 | a0001c0001t0037g0100 a0001c0013t0026g0217 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.773-226G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640905 | |||||||
| chr16:8640906 | A | G | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.773-225A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640906 | |||||||
| chr16:8640909 | G | A | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.773-222G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640909 | |||||||
| chr16:8640942 | A | ATGGATGG others(1): Show |
5 | a0004c0004t0006g0011 a0004c0004t0006g0214 a0004c0004t0020g0043 others(2): Show |
8 | HG02451.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.773-186_773-185ins others(8): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640942 | ||||||
| chr16:8640942 | A | C | 8 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(5): Show |
9 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.773-189A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640942 | |||||||
| chr16:8640942 | A | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0200 others(2): Show |
6 | HG02258.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.773-189A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640942 | |||||||
| chr16:8640946 | G | A | 189 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0016 others(186): Show |
258 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.773-185G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640946 | |||||||
| chr16:8640946 | G | C | 9 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(6): Show |
10 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.773-185G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640946 | |||||||
| chr16:8640950 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(76): Show |
118 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.773-181G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640950 | |||||||
| chr16:8640950 | G | C | 18 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0200 others(15): Show |
20 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.773-181G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640950 | |||||||
| chr16:8640954 | A | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(88): Show |
130 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.773-177A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640954 | |||||||
| chr16:8640969 | G | GCTGGCTG others(5): Show |
10 | a0001c0001t0001g0136 a0001c0001t0001g0229 a0001c0001t0001g0233 others(7): Show |
10 | HG01167.hp2 HG02602.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.773-151_773-150ins others(12): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640969 | ||||||
| chr16:8640973 | G | GCTGGCTG others(13): Show |
1 | a0001c0001t0003g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.773-146_773-145ins others(20): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640973 | ||||||
| chr16:8640973 | G | GCTGGCTG others(1): Show |
163 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0016 others(160): Show |
228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.773-151_773-150ins others(8): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640973 | ||||||
| chr16:8640973 | G | GCTGGCTG others(9): Show |
1 | a0001c0001t0003g0221 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.773-151_773-150ins others(16): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640973 | ||||||
| chr16:8640973 | G | GCTGT | 72 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(69): Show |
110 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.773-155_773-154ins others(4): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640973 | ||||||
| chr16:8640973 | G | GCTGTCTG others(5): Show |
7 | a0001c0001t0003g0050 a0001c0001t0003g0220 a0001c0001t0003g0222 others(4): Show |
8 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.773-155_773-154ins others(12): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 8640973 | ||||||
| chr16:8640973 | G | T | 14 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0200 others(11): Show |
17 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.773-158G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8640973 | |||||||
| chr16:8641004 | A | C | 2 | a0001c0006t0010g0189 a0001c0006t0010g0190 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.773-127A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 6/10 | chr16 | 8641004 | |||||||
| chr16:8641239 | C | A | 2 | a0001c0001t0001g0095 a0001c0001t0036g0096 |
2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.826+55C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641239 | |||||||
| chr16:8641254 | C | G | 1 | a0004c0004t0006g0011 | 4 | HG02451.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+70C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641254 | |||||||
| chr16:8641263 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(249): Show |
356 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(353): Show |
intron_variant | MODIFIER | c.826+79T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641263 | |||||||
| chr16:8641307 | G | A | 6 | a0001c0001t0001g0254 a0001c0001t0011g0044 a0001c0001t0011g0204 others(3): Show |
8 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.826+123G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641307 | |||||||
| chr16:8641343 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(249): Show |
356 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(353): Show |
intron_variant | MODIFIER | c.826+159G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641343 | |||||||
| chr16:8641355 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.826+171T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641355 | |||||||
| chr16:8641388 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.826+204C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641388 | |||||||
| chr16:8641498 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.826+314A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641498 | |||||||
| chr16:8641581 | C | A | 1 | a0003c0003t0049g0126 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.826+397C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641581 | |||||||
| chr16:8641626 | T | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
6 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+442T>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641626 | |||||||
| chr16:8641643 | CT | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(259): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.826+470delT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 8641643 | ||||||
| chr16:8641724 | G | A | 251 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(248): Show |
355 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.827-403G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641724 | |||||||
| chr16:8641745 | A | G | 1 | a0001c0001t0014g0065 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.827-382A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641745 | |||||||
| chr16:8641805 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.827-322C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641805 | |||||||
| chr16:8641839 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.827-288T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641839 | |||||||
| chr16:8641842 | C | A | 1 | a0002c0002t0001g0218 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.827-285C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641842 | |||||||
| chr16:8641858 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.827-269G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641858 | |||||||
| chr16:8641886 | C | T | 1 | a0001c0001t0056g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.827-241C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641886 | |||||||
| chr16:8641918 | A | G | 2 | a0007c0010t0001g0129 a0007c0010t0001g0135 |
2 | HG03491.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.827-209A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641918 | |||||||
| chr16:8641956 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(253): Show |
361 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(358): Show |
intron_variant | MODIFIER | c.827-171G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8641956 | |||||||
| chr16:8642055 | G | A | 1 | a0001c0001t0032g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.827-72G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 7/10 | chr16 | 8642055 | |||||||
| chr16:8642262 | T | C | 6 | a0001c0006t0010g0189 a0001c0006t0010g0190 a0001c0006t0010g0191 others(3): Show |
6 | HG01192.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.907+55T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 8/10 | chr16 | 8642262 | |||||||
| chr16:8642293 | A | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.907+86A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 8/10 | chr16 | 8642293 | |||||||
| chr16:8642389 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.908-74G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 8/10 | chr16 | 8642389 | |||||||
| chr16:8642406 | C | T | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.908-57C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 8/10 | chr16 | 8642406 | |||||||
| chr16:8642407 | G | A | 44 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0014 others(41): Show |
60 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.908-56G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 8/10 | chr16 | 8642407 | |||||||
| chr16:8642414 | G | A | 1 | a0001c0001t0048g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.908-49G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 8/10 | chr16 | 8642414 | |||||||
| chr16:8642642 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1010+77C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642642 | |||||||
| chr16:8642714 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1010+149T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642714 | |||||||
| chr16:8642759 | G | A | 1 | a0001c0001t0003g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1010+194G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642759 | |||||||
| chr16:8642761 | G | A | 1 | a0003c0003t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1010+196G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642761 | |||||||
| chr16:8642761 | G | T | 1 | a0001c0001t0005g0245 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1010+196G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642761 | |||||||
| chr16:8642800 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1010+235G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642800 | |||||||
| chr16:8642832 | A | G | 6 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(3): Show |
8 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1010+267A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642832 | |||||||
| chr16:8642881 | G | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1010+316G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642881 | |||||||
| chr16:8642884 | T | G | 1 | a0001c0001t0002g0092 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1010+319T>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642884 | |||||||
| chr16:8642885 | G | T | 1 | a0001c0001t0002g0092 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1010+320G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642885 | |||||||
| chr16:8642901 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1010+336T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642901 | |||||||
| chr16:8642985 | A | G | 1 | a0001c0001t0007g0231 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1010+420A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8642985 | |||||||
| chr16:8643134 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1010+569C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643134 | |||||||
| chr16:8643206 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1010+641C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643206 | |||||||
| chr16:8643261 | T | C | 1 | a0001c0001t0004g0047 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1010+696T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643261 | |||||||
| chr16:8643266 | A | G | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1010+701A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643266 | |||||||
| chr16:8643359 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1010+794C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643359 | |||||||
| chr16:8643438 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1010+873T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643438 | |||||||
| chr16:8643470 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1010+905G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643470 | |||||||
| chr16:8643534 | G | T | 1 | a0001c0001t0002g0063 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1010+969G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643534 | |||||||
| chr16:8643614 | G | GT | 5 | a0001c0001t0002g0067 a0001c0001t0013g0058 a0001c0001t0024g0083 others(2): Show |
5 | HG01168.hp2 HG01978.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1011-935dupT | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 8643614 | ||||||
| chr16:8643652 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1011-905A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643652 | |||||||
| chr16:8643697 | G | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(261): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1011-860G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643697 | |||||||
| chr16:8643717 | C | T | 1 | a0001c0006t0010g0190 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1011-840C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643717 | |||||||
| chr16:8643737 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1011-820C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643737 | |||||||
| chr16:8643757 | G | T | 1 | a0001c0001t0032g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1011-800G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643757 | |||||||
| chr16:8643785 | T | C | 1 | a0004c0004t0020g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1011-772T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643785 | |||||||
| chr16:8643802 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1011-755C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643802 | |||||||
| chr16:8643818 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1011-739C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643818 | |||||||
| chr16:8643874 | A | C | 13 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0007g0012 others(10): Show |
16 | HG01167.hp2 HG01175.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1011-683A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8643874 | |||||||
| chr16:8644041 | C | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1011-516C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8644041 | |||||||
| chr16:8644119 | TTC | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1011-432_1011-431d others(4): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 8644119 | ||||||
| chr16:8644177 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1011-380A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8644177 | |||||||
| chr16:8644179 | T | C | 13 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0007g0012 others(10): Show |
16 | HG01167.hp2 HG01175.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1011-378T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8644179 | |||||||
| chr16:8644213 | G | A | 1 | a0001c0001t0032g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1011-344G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8644213 | |||||||
| chr16:8644229 | C | G | 1 | a0001c0001t0007g0231 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1011-328C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8644229 | |||||||
| chr16:8644337 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1011-220G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8644337 | |||||||
| chr16:8644356 | G | C | 52 | a0001c0001t0001g0031 a0001c0001t0001g0136 a0001c0001t0001g0166 others(49): Show |
81 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1011-201G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8644356 | |||||||
| chr16:8644448 | G | A | 1 | a0005c0008t0019g0045 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1011-109G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8644448 | |||||||
| chr16:8644493 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(234): Show |
337 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.1011-64C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8644493 | |||||||
| chr16:8644541 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1011-16A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 9/10 | chr16 | 8644541 | |||||||
| chr16:8644765 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1179+40C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8644765 | |||||||
| chr16:8644768 | T | C | 12 | a0001c0001t0001g0095 a0001c0001t0005g0020 a0001c0001t0005g0245 others(9): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1179+43T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8644768 | |||||||
| chr16:8644784 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1179+59A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8644784 | |||||||
| chr16:8644840 | A | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0186 others(1): Show |
6 | HG02818.hp1 HG02896.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1179+115A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8644840 | |||||||
| chr16:8644851 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1179+126C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8644851 | |||||||
| chr16:8644969 | A | G | 1 | a0002c0002t0001g0152 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1179+244A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8644969 | |||||||
| chr16:8644980 | G | T | 1 | a0001c0013t0026g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1179+255G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8644980 | |||||||
| chr16:8644997 | C | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1179+272C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8644997 | |||||||
| chr16:8645160 | C | G | 6 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(3): Show |
8 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1179+435C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645160 | |||||||
| chr16:8645221 | T | C | 2 | a0002c0002t0001g0035 a0002c0002t0001g0163 |
3 | NA18948.hp2 NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1179+496T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645221 | |||||||
| chr16:8645253 | G | A | 45 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0014 others(42): Show |
61 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1179+528G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645253 | |||||||
| chr16:8645309 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1179+584T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645309 | |||||||
| chr16:8645321 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1179+596C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645321 | |||||||
| chr16:8645323 | C | T | 1 | a0002c0002t0001g0137 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1179+598C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645323 | |||||||
| chr16:8645372 | G | T | 1 | a0001c0001t0052g0255 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1179+647G>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645372 | |||||||
| chr16:8645416 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1179+691G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645416 | |||||||
| chr16:8645426 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-682A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645426 | |||||||
| chr16:8645453 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-655G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645453 | |||||||
| chr16:8645483 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-625C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645483 | |||||||
| chr16:8645503 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(63): Show |
103 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1180-605C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645503 | |||||||
| chr16:8645532 | C | G | 1 | a0001c0001t0050g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1180-576C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645532 | |||||||
| chr16:8645543 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-565T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645543 | |||||||
| chr16:8645590 | T | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-518T>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645590 | |||||||
| chr16:8645618 | GA | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-482delA | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 8645618 | ||||||
| chr16:8645634 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-474T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645634 | |||||||
| chr16:8645637 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-471A>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645637 | |||||||
| chr16:8645791 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-317T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645791 | |||||||
| chr16:8645821 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-287C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645821 | |||||||
| chr16:8645874 | A | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-234A>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645874 | |||||||
| chr16:8645904 | C | G | 1 | a0003c0003t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1180-204C>G | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645904 | |||||||
| chr16:8645927 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-181T>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645927 | |||||||
| chr16:8645965 | C | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(250): Show |
357 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.1180-143C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645965 | |||||||
| chr16:8645974 | C | T | 1 | a0001c0001t0007g0231 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1180-134C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645974 | |||||||
| chr16:8645975 | C | T | 10 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(7): Show |
11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.1180-133C>T | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645975 | |||||||
| chr16:8645983 | G | A | 5 | a0001c0001t0011g0044 a0001c0001t0011g0204 a0001c0001t0011g0205 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-125G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645983 | |||||||
| chr16:8645984 | C | A | 1 | a0001c0001t0002g0235 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1180-124C>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8645984 | |||||||
| chr16:8645986 | C | CGCCTGCT others(73): Show |
17 | a0001c0001t0003g0050 a0001c0001t0003g0207 a0001c0001t0003g0220 others(14): Show |
20 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.1180-104_1180-103i others(82): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 8645986 | ||||||
| chr16:8645986 | C | CGCCTGCT others(73): Show |
245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(242): Show |
349 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.1180-81_1180-80ins others(80): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 8645986 | ||||||
| chr16:8645986 | C | CGCCTGCT others(113): Show |
5 | a0003c0003t0001g0124 a0003c0003t0001g0125 a0003c0003t0001g0140 others(2): Show |
5 | HG00544.hp1 HG02015.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-81_1180-80ins others(120): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 8645986 | ||||||
| chr16:8646004 | C | CGTGTTGT others(73): Show |
3 | a0001c0001t0002g0238 a0001c0001t0002g0239 a0001c0001t0002g0240 |
3 | HG02895.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1180-81_1180-80ins others(80): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 8646004 | ||||||
| chr16:8646064 | G | C | 3 | a0004c0004t0020g0043 a0004c0004t0020g0203 a0004c0004t0029g0043 |
3 | HG02630.hp2 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1180-44G>C | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8646064 | |||||||
| chr16:8646097 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(267): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1180-11G>A | METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 10/10 | chr16 | 8646097 |