Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8731 |
| ensemblid | ENSG00000101654.18 |
| hgncid | 10075 |
| symbol | RNMT |
| name | RNA guanine-7 methyltransferase |
| refseq_nuc | NM_003799.3 |
| refseq_prot | NP_003790.1 |
| ensembl_nuc | ENST00000383314.7 |
| ensembl_prot | ENSP00000372804.2 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 13726673 |
| end | 13764556 |
| strand | + |
| ver | v1.2 |
| region | chr18:13726673-13764556 |
| region5000 | chr18:13721673-13769556 |
| regionname0 | RNMT_chr18_13726673_13764556 |
| regionname5000 | RNMT_chr18_13721673_13769556 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 476 | 368 | 83 | 70 | 157 | 14 | 42 | 122 | RNMT_chr18_13721673_13769556 | RNMT | MANSA others(471): Show |
chr18 | 13721673 | 13769556 |
| a0002 | 0/0 | 476 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | MANSA others(471): Show |
chr18 | 13721673 | 13769556 |
| a0003 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | MANSA others(471): Show |
chr18 | 13721673 | 13769556 |
| a0004 | 0/0 | 476 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RNMT_chr18_13721673_13769556 | RNMT | MANSA others(471): Show |
chr18 | 13721673 | 13769556 |
| a0005 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | MANSA others(471): Show |
chr18 | 13721673 | 13769556 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1428 | 367 | 83 | 69 | 157 | 14 | 42 | RNMT_chr18_13721673_13769556 | RNMT | ATGGC others(1423): Show |
chr18 | 13721673 | 13769556 | ||
| a0001c0006 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | ATGGC others(1423): Show |
chr18 | 13721673 | 13769556 | ||
| a0002c0002 | 0/0 | 1428 | 3 | 3 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | ATGGC others(1423): Show |
chr18 | 13721673 | 13769556 | ||
| a0003c0003 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | ATGGC others(1423): Show |
chr18 | 13721673 | 13769556 | ||
| a0004c0004 | 0/0 | 1428 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | ATGGC others(1423): Show |
chr18 | 13721673 | 13769556 | ||
| a0005c0005 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | ATGGC others(1423): Show |
chr18 | 13721673 | 13769556 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6236 | 183 | 18 | 29 | 109 | 7 | 19 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0002 | 0/0 | 6236 | 51 | 10 | 13 | 16 | 6 | 6 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0003 | 1/0 | 6236 | 25 | 7 | 5 | 5 | 0 | 7 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0004 | 0/0 | 6236 | 10 | 10 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0005 | 0/0 | 6236 | 10 | 10 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0006 | 0/0 | 6236 | 10 | 0 | 8 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0007 | 0/0 | 6236 | 9 | 1 | 4 | 0 | 0 | 4 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0008 | 0/0 | 6236 | 9 | 9 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0009 | 0/0 | 6236 | 6 | 0 | 6 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0010 | 0/0 | 6236 | 6 | 2 | 0 | 2 | 0 | 2 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0011 | 0/0 | 6236 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0012 | 0/0 | 6236 | 3 | 0 | 0 | 3 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0013 | 0/0 | 6236 | 3 | 0 | 0 | 3 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0014 | 0/0 | 6236 | 3 | 0 | 0 | 3 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0015 | 0/0 | 6236 | 3 | 1 | 0 | 0 | 0 | 2 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0016 | 0/0 | 6236 | 3 | 3 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0018 | 0/0 | 6236 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0019 | 0/0 | 6236 | 2 | 0 | 0 | 0 | 0 | 2 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0020 | 0/0 | 6236 | 2 | 1 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0021 | 0/0 | 6236 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0022 | 0/0 | 6236 | 2 | 0 | 2 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0023 | 0/0 | 6236 | 2 | 2 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0024 | 0/0 | 6236 | 2 | 2 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0025 | 0/0 | 6236 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0026 | 0/0 | 6236 | 1 | 0 | 0 | 0 | 1 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0027 | 0/0 | 6236 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0028 | 0/0 | 6236 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0029 | 0/0 | 6236 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0030 | 0/0 | 6236 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0031 | 0/0 | 6236 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0032 | 0/0 | 6236 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0033 | 0/0 | 6236 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0034 | 0/0 | 6236 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0035 | 0/0 | 6236 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0036 | 0/0 | 6236 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0037 | 0/0 | 6236 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0038 | 0/0 | 6236 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0039 | 0/0 | 6236 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0040 | 0/0 | 6236 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0001t0041 | 0/0 | 6236 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0001c0006t0009 | 0/0 | 6236 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0002c0002t0017 | 0/0 | 6236 | 3 | 3 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0003c0003t0011 | 0/0 | 6236 | 2 | 2 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0004c0004t0002 | 0/0 | 6236 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| a0005c0005t0001 | 0/0 | 6236 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | AGACA others(6231): Show |
chr18 | 13721673 | 13769556 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 1 | 11 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0002 | 0/0 | 10 | 1 | 3 | 3 | 2 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0004 | 1/0 | 8 | 0 | 1 | 1 | 0 | 5 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0005g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0005g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0006g0007 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0007g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0008g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0009g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0009g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0010g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0010g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0011g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0012g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0013g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0013g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0013g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0014g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0014g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0014g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0015g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0015g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0015g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0016g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0016g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0016g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0018g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0019g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0019g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0020g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0020g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0021g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0022g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0023g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0023g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0024g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0025g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0026g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0027g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0028g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0029g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0030g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0031g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0032g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0033g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0034g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0035g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0036g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0037g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0038g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0039g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0040g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0001t0041g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0001c0006t0009g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0002c0002t0017g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0002c0002t0017g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0002c0002t0017g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0003c0003t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0003c0003t0011g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0004c0004t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| a0005c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0076 | EUR | GBR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | FIN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00408 | hp1 | a0001 | c0001 | t0030 | g0038 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00408 | hp2 | a0001 | c0001 | t0037 | g0009 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00558 | hp1 | a0001 | c0001 | t0039 | g0017 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00621 | hp2 | a0001 | c0001 | t0014 | g0174 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00738 | hp1 | a0001 | c0006 | t0009 | g0005 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01074 | hp2 | a0001 | c0001 | t0020 | g0251 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01167 | hp2 | a0001 | c0001 | t0022 | g0030 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0133 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01169 | hp1 | a0001 | c0001 | t0022 | g0030 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0015 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01243 | hp2 | a0001 | c0001 | t0041 | g0250 | AMR | PUR | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0138 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0130 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0074 | EUR | IBS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01516 | hp1 | a0001 | c0001 | t0026 | g0125 | EUR | IBS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0028 | EUR | IBS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0028 | EUR | IBS | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0104 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0228 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01952 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0135 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0139 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02004 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0012 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02040 | hp1 | a0001 | c0001 | t0013 | g0234 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02055 | hp1 | a0001 | c0001 | t0024 | g0044 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02083 | hp1 | a0001 | c0001 | t0029 | g0001 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0118 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02148 | hp1 | a0001 | c0001 | t0009 | g0019 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02155 | hp1 | a0005 | c0005 | t0001 | g0193 | EAS | CDX | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02155 | hp2 | a0001 | c0001 | t0013 | g0238 | EAS | CDX | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02257 | hp1 | a0003 | c0003 | t0011 | g0021 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02257 | hp2 | a0001 | c0001 | t0038 | g0117 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02258 | hp1 | a0001 | c0001 | t0025 | g0085 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02280 | hp1 | a0001 | c0001 | t0024 | g0044 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0003 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02300 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02451 | hp2 | a0001 | c0001 | t0023 | g0115 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0096 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0102 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02735 | hp1 | a0001 | c0001 | t0015 | g0218 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02818 | hp1 | a0001 | c0001 | t0028 | g0048 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02818 | hp2 | a0002 | c0002 | t0017 | g0152 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02886 | hp1 | a0001 | c0001 | t0031 | g0241 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0091 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03017 | hp2 | a0001 | c0001 | t0015 | g0121 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03098 | hp2 | a0001 | c0001 | t0020 | g0252 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03130 | hp2 | a0001 | c0001 | t0036 | g0217 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03195 | hp2 | a0002 | c0002 | t0017 | g0154 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0050 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0134 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0227 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03491 | hp1 | a0001 | c0001 | t0019 | g0080 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03516 | hp1 | a0001 | c0001 | t0040 | g0100 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | ESN | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03540 | hp1 | a0001 | c0001 | t0027 | g0101 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0087 | AFR | GWD | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03579 | hp2 | a0003 | c0003 | t0011 | g0259 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0015 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03688 | hp1 | a0001 | c0001 | t0010 | g0023 | SAS | STU | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | STU | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03704 | hp1 | a0001 | c0001 | t0019 | g0081 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0015 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0132 | SAS | BEB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG04184 | hp2 | a0001 | c0001 | t0010 | g0023 | SAS | BEB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | STU | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | STU | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | YRI | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | YRI | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18906 | hp1 | a0001 | c0001 | t0023 | g0116 | AFR | YRI | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18906 | hp2 | a0001 | c0001 | t0015 | g0219 | AFR | YRI | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18942 | hp1 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18944 | hp1 | a0001 | c0001 | t0021 | g0035 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18949 | hp2 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18950 | hp2 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18951 | hp2 | a0001 | c0001 | t0014 | g0175 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18953 | hp2 | a0001 | c0001 | t0010 | g0022 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18969 | hp1 | a0001 | c0001 | t0035 | g0140 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18975 | hp2 | a0001 | c0001 | t0012 | g0079 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18986 | hp2 | a0001 | c0001 | t0012 | g0051 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18989 | hp1 | a0001 | c0001 | t0032 | g0003 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18992 | hp2 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18993 | hp1 | a0001 | c0001 | t0012 | g0073 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18993 | hp2 | a0001 | c0001 | t0010 | g0022 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18999 | hp2 | a0004 | c0004 | t0002 | g0024 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19006 | hp2 | a0001 | c0001 | t0021 | g0035 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | LWK | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | LWK | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19054 | hp1 | a0001 | c0001 | t0014 | g0230 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19065 | hp1 | a0001 | c0001 | t0033 | g0159 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19068 | hp2 | a0001 | c0001 | t0034 | g0236 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19078 | hp2 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19081 | hp1 | a0004 | c0004 | t0002 | g0024 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19240 | hp1 | a0001 | c0001 | t0016 | g0103 | AFR | YRI | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0049 | AFR | YRI | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0029 | EUR | TSI | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | GIH | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01123 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0090 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG02559 | hp2 | a0002 | c0002 | t0017 | g0153 | AFR | ACB | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | USA | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| HG06807 | hp2 | a0001 | c0001 | t0016 | g0105 | AFR | USA | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0131 | AFR | USA | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | USA | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | LWK | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0088 | REF | REF | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0004 | REF | REF | RNMT_chr18_13721673_13769556 | RNMT | chr18 | 13721673 | 13769556 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:13731545 | T | C | 1 | a0002 | 3 | HG02559.hp2 HG02818.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.28T>C | p.Tyr10His | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/12 | 256/6236 | 28/1431 | 10/476 | chr18 | 13731545 | |||
| chr18:13731575 | G | C | 1 | a0003 | 2 | HG02257.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.58G>C | p.Ala20Pro | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/12 | 286/6236 | 58/1431 | 20/476 | chr18 | 13731575 | |||
| chr18:13740226 | C | T | 1 | a0004 | 2 | NA18999.hp2 NA19081.hp1 |
missense_variant | MODERATE | c.739C>T | p.Arg247Cys | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/12 | 967/6236 | 739/1431 | 247/476 | chr18 | 13740226 | |||
| chr18:13741532 | G | A | 1 | a0005 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.815G>A | p.Arg272His | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/12 | 1043/6236 | 815/1431 | 272/476 | chr18 | 13741532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:13740174 | C | T | 1 | a0001c0006 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.687C>T | p.Ala229Ala | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/12 | 915/6236 | 687/1431 | 229/476 | chr18 | 13740174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:13726683 | G | C | 4 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0025 others(1): Show |
21 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-218G>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/12 | 4835 | chr18 | 13726683 | ||||||
| chr18:13730637 | C | T | 1 | a0001c0001t0041 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-161C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 2/12 | 881 | chr18 | 13730637 | ||||||
| chr18:13760009 | T | C | 1 | a0001c0001t0027 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 30 | chr18 | 13760009 | ||||||
| chr18:13760083 | A | C | 1 | a0002c0002t0017 | 3 | HG02559.hp2 HG02818.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*104A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 104 | chr18 | 13760083 | ||||||
| chr18:13760116 | A | C | 4 | a0001c0001t0008 a0001c0001t0016 a0001c0001t0027 others(1): Show |
14 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*137A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 137 | chr18 | 13760116 | ||||||
| chr18:13760159 | G | A | 1 | a0001c0001t0018 | 2 | NA18942.hp1 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*180G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 180 | chr18 | 13760159 | ||||||
| chr18:13760291 | T | C | 8 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(5): Show |
68 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*312T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 312 | chr18 | 13760291 | ||||||
| chr18:13760372 | A | G | 1 | a0001c0001t0024 | 2 | HG02055.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 393 | chr18 | 13760372 | ||||||
| chr18:13760389 | A | G | 1 | a0001c0001t0039 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 410 | chr18 | 13760389 | ||||||
| chr18:13760500 | T | C | 1 | a0001c0001t0029 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 521 | chr18 | 13760500 | ||||||
| chr18:13760657 | G | C | 1 | a0001c0001t0040 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*678G>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 678 | chr18 | 13760657 | ||||||
| chr18:13760862 | T | C | 1 | a0001c0001t0021 | 2 | NA18944.hp1 NA19006.hp2 |
3_prime_UTR_variant | MODIFIER | c.*883T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 883 | chr18 | 13760862 | ||||||
| chr18:13760955 | T | C | 7 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0013 others(4): Show |
64 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*976T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 976 | chr18 | 13760955 | ||||||
| chr18:13761043 | C | T | 1 | a0001c0001t0038 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1064C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 1064 | chr18 | 13761043 | ||||||
| chr18:13761154 | T | G | 1 | a0001c0001t0019 | 2 | HG03491.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1175T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 1175 | chr18 | 13761154 | ||||||
| chr18:13761155 | C | T | 1 | a0001c0001t0019 | 2 | HG03491.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1176C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 1176 | chr18 | 13761155 | ||||||
| chr18:13761343 | A | T | 2 | a0001c0001t0011 a0003c0003t0011 |
4 | HG02257.hp1 HG03579.hp2 NA18949.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1364A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 1364 | chr18 | 13761343 | ||||||
| chr18:13761648 | C | G | 1 | a0001c0001t0012 | 3 | NA18975.hp2 NA18986.hp2 NA18993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1669C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 1669 | chr18 | 13761648 | ||||||
| chr18:13761663 | A | C | 1 | a0001c0001t0037 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 1684 | chr18 | 13761663 | ||||||
| chr18:13761810 | C | T | 1 | a0001c0001t0036 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1831C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 1831 | chr18 | 13761810 | ||||||
| chr18:13761856 | C | T | 1 | a0001c0001t0015 | 3 | HG02735.hp1 HG03017.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1877C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 1877 | chr18 | 13761856 | ||||||
| chr18:13761927 | G | T | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0026 |
20 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1948G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 1948 | chr18 | 13761927 | ||||||
| chr18:13762012 | C | A | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(40): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*2033C>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 2033 | chr18 | 13762012 | ||||||
| chr18:13762207 | C | T | 2 | a0001c0001t0009 a0001c0006t0009 |
7 | HG00738.hp1 HG01123.hp1 HG01952.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2228C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 2228 | chr18 | 13762207 | ||||||
| chr18:13762298 | A | G | 1 | a0001c0001t0028 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2319A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 2319 | chr18 | 13762298 | ||||||
| chr18:13762314 | T | C | 1 | a0001c0001t0014 | 3 | HG00621.hp2 NA18951.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2335T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 2335 | chr18 | 13762314 | ||||||
| chr18:13762370 | C | T | 2 | a0001c0001t0006 a0001c0001t0035 |
11 | HG01255.hp2 HG01258.hp2 HG01261.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2391C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 2391 | chr18 | 13762370 | ||||||
| chr18:13762459 | A | G | 1 | a0001c0001t0035 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2480A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 2480 | chr18 | 13762459 | ||||||
| chr18:13762871 | G | A | 1 | a0001c0001t0030 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2892G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 2892 | chr18 | 13762871 | ||||||
| chr18:13763112 | C | G | 1 | a0001c0001t0034 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3133C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3133 | chr18 | 13763112 | ||||||
| chr18:13763115 | T | C | 2 | a0001c0001t0007 a0001c0001t0026 |
10 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3136T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3136 | chr18 | 13763115 | ||||||
| chr18:13763138 | G | A | 2 | a0001c0001t0031 a0001c0001t0038 |
2 | HG02257.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3159G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3159 | chr18 | 13763138 | ||||||
| chr18:13763341 | G | A | 1 | a0001c0001t0022 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3362G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3362 | chr18 | 13763341 | ||||||
| chr18:13763392 | C | A | 2 | a0001c0001t0010 a0001c0001t0028 |
7 | HG02818.hp1 HG03225.hp1 HG03688.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3413C>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3413 | chr18 | 13763392 | ||||||
| chr18:13763411 | C | T | 1 | a0001c0001t0020 | 2 | HG01074.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3432C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3432 | chr18 | 13763411 | ||||||
| chr18:13763425 | A | T | 1 | a0001c0001t0016 | 3 | HG02622.hp2 HG06807.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3446A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3446 | chr18 | 13763425 | ||||||
| chr18:13763439 | C | T | 1 | a0001c0001t0038 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3460C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3460 | chr18 | 13763439 | ||||||
| chr18:13763630 | T | C | 1 | a0001c0001t0005 | 10 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3651T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3651 | chr18 | 13763630 | ||||||
| chr18:13763636 | T | A | 1 | a0001c0001t0032 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3657T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3657 | chr18 | 13763636 | ||||||
| chr18:13763639 | T | C | 1 | a0001c0001t0026 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3660T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3660 | chr18 | 13763639 | ||||||
| chr18:13763654 | G | A | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(40): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*3675G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3675 | chr18 | 13763654 | ||||||
| chr18:13763657 | A | T | 1 | a0001c0001t0023 | 2 | HG02451.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3678A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3678 | chr18 | 13763657 | ||||||
| chr18:13763938 | G | A | 1 | a0001c0001t0015 | 3 | HG02735.hp1 HG03017.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3959G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 3959 | chr18 | 13763938 | ||||||
| chr18:13764017 | A | T | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(29): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*4038A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 4038 | chr18 | 13764017 | ||||||
| chr18:13764094 | A | T | 1 | a0002c0002t0017 | 3 | HG02559.hp2 HG02818.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4115A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 4115 | chr18 | 13764094 | ||||||
| chr18:13764372 | C | T | 1 | a0001c0001t0033 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4393C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 12/12 | 4393 | chr18 | 13764372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:13726772 | T | G | 5 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(2): Show |
7 | HG02818.hp1 HG03225.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-172+43T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13726772 | |||||||
| chr18:13726817 | C | A | 41 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(38): Show |
49 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-172+88C>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13726817 | |||||||
| chr18:13726827 | G | A | 1 | a0001c0001t0025g0085 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-172+98G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13726827 | |||||||
| chr18:13726836 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-172+107G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13726836 | |||||||
| chr18:13726874 | A | G | 3 | a0001c0001t0011g0021 a0003c0003t0011g0021 a0003c0003t0011g0259 |
4 | HG02257.hp1 HG03579.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+145A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13726874 | |||||||
| chr18:13726904 | T | C | 1 | a0001c0001t0003g0086 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-172+175T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13726904 | |||||||
| chr18:13727156 | C | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG02258.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-172+427C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13727156 | |||||||
| chr18:13727489 | T | C | 1 | a0001c0001t0005g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-172+760T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13727489 | |||||||
| chr18:13727967 | A | G | 53 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(50): Show |
61 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.-172+1238A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13727967 | |||||||
| chr18:13728081 | G | T | 1 | a0001c0001t0031g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-172+1352G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728081 | |||||||
| chr18:13728260 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-172+1531A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728260 | |||||||
| chr18:13728299 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-172+1570T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728299 | |||||||
| chr18:13728319 | TTTTTTTT others(18): Show |
T | 39 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(36): Show |
46 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-172+1592_-172+161 others(29): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728319 | ||||||
| chr18:13728320 | TTTTTTTT others(17): Show |
T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0120 a0001c0001t0002g0077 others(4): Show |
7 | HG01433.hp2 HG02738.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.-172+1593_-172+161 others(28): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728320 | ||||||
| chr18:13728321 | TTTTTTTT others(16): Show |
T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.-172+1594_-172+161 others(27): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728321 | ||||||
| chr18:13728321 | TTTTTTTT others(18): Show |
T | 6 | a0001c0001t0001g0220 a0001c0001t0002g0029 a0001c0001t0002g0075 others(3): Show |
7 | HG00099.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-172+1594_-172+161 others(29): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728321 | ||||||
| chr18:13728322 | TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0028g0048 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-172+1595_-172+160 others(16): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728322 | ||||||
| chr18:13728322 | TTTTTTTT others(15): Show |
T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(10): Show |
18 | HG00621.hp2 HG01255.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-172+1595_-172+161 others(26): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728322 | ||||||
| chr18:13728322 | TTTTTTTT others(17): Show |
T | 10 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0258 others(7): Show |
12 | HG01891.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+1595_-172+161 others(28): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728322 | ||||||
| chr18:13728323 | TTTTTTTT others(16): Show |
T | 24 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0093 others(21): Show |
27 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-172+1596_-172+161 others(27): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728323 | ||||||
| chr18:13728324 | TTTTTTTT others(5): Show |
T | 4 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(1): Show |
6 | HG03225.hp1 HG03688.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.-172+1597_-172+160 others(16): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728324 | ||||||
| chr18:13728324 | TTTTTTTT others(9): Show |
T | 1 | a0001c0001t0011g0021 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-172+1597_-172+161 others(20): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728324 | ||||||
| chr18:13728324 | TTTTTTTT others(11): Show |
T | 2 | a0003c0003t0011g0021 a0003c0003t0011g0259 |
2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-172+1597_-172+161 others(22): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728324 | ||||||
| chr18:13728324 | TTTTTTTT others(15): Show |
T | 8 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0015g0219 others(5): Show |
8 | HG01074.hp2 HG01516.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-172+1597_-172+161 others(26): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728324 | ||||||
| chr18:13728325 | TTTTTTTG others(10): Show |
T | 1 | a0001c0001t0011g0021 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-172+1598_-172+161 others(21): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728325 | ||||||
| chr18:13728325 | TTTTTTTG others(12): Show |
T | 2 | a0001c0001t0019g0080 a0001c0001t0019g0081 |
2 | HG03491.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-172+1598_-172+161 others(23): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728325 | ||||||
| chr18:13728325 | TTTTTTTG others(14): Show |
T | 17 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(14): Show |
19 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.-172+1598_-172+161 others(25): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728325 | ||||||
| chr18:13728326 | TTTTTTGT others(13): Show |
T | 11 | a0001c0001t0001g0216 a0001c0001t0004g0126 a0001c0001t0004g0127 others(8): Show |
11 | HG00741.hp2 HG01978.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-172+1599_-172+161 others(24): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13728326 | ||||||
| chr18:13728328 | T | G | 1 | a0001c0001t0003g0110 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-172+1599T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728328 | |||||||
| chr18:13728330 | T | G | 5 | a0001c0001t0003g0033 a0001c0001t0003g0110 a0001c0001t0003g0111 others(2): Show |
6 | HG01361.hp1 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-172+1601T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728330 | |||||||
| chr18:13728375 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0022g0030 |
3 | HG01167.hp2 HG01169.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-172+1646G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728375 | |||||||
| chr18:13728402 | C | T | 5 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(2): Show |
7 | HG02818.hp1 HG03225.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-172+1673C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728402 | |||||||
| chr18:13728439 | G | A | 18 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
20 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.-172+1710G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728439 | |||||||
| chr18:13728471 | G | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-172+1742G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728471 | |||||||
| chr18:13728480 | C | T | 51 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(48): Show |
59 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-172+1751C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728480 | |||||||
| chr18:13728626 | G | A | 2 | a0001c0001t0031g0241 a0001c0001t0038g0117 |
2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-172+1897G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728626 | |||||||
| chr18:13728872 | G | A | 3 | a0001c0001t0011g0021 a0003c0003t0011g0021 a0003c0003t0011g0259 |
4 | HG02257.hp1 HG03579.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.-171-1755G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728872 | |||||||
| chr18:13728921 | C | A | 1 | a0001c0001t0006g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-171-1706C>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13728921 | |||||||
| chr18:13729343 | G | A | 1 | a0001c0001t0012g0051 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-171-1284G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13729343 | |||||||
| chr18:13729466 | T | A | 1 | a0001c0001t0008g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-171-1161T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13729466 | |||||||
| chr18:13729503 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-171-1124G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13729503 | |||||||
| chr18:13729592 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-171-1035T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13729592 | |||||||
| chr18:13729767 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-171-860A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13729767 | |||||||
| chr18:13729768 | C | CT | 5 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(2): Show |
7 | HG02818.hp1 HG03225.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-171-849dupT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 13729768 | ||||||
| chr18:13729800 | G | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0232 others(7): Show |
13 | HG00597.hp1 HG02015.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.-171-827G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13729800 | |||||||
| chr18:13730009 | C | T | 1 | a0001c0001t0038g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-171-618C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13730009 | |||||||
| chr18:13730094 | C | T | 2 | a0001c0001t0020g0251 a0001c0001t0020g0252 |
2 | HG01074.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-171-533C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13730094 | |||||||
| chr18:13730182 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-171-445T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13730182 | |||||||
| chr18:13730311 | G | T | 2 | a0001c0001t0020g0251 a0001c0001t0020g0252 |
2 | HG01074.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-171-316G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13730311 | |||||||
| chr18:13730348 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-171-279A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 1/11 | chr18 | 13730348 | |||||||
| chr18:13730810 | T | G | 1 | a0001c0001t0021g0035 | 2 | NA18944.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-43+55T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 2/11 | chr18 | 13730810 | |||||||
| chr18:13731144 | C | T | 1 | a0001c0001t0014g0230 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-42-332C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 2/11 | chr18 | 13731144 | |||||||
| chr18:13731145 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-42-331G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 2/11 | chr18 | 13731145 | |||||||
| chr18:13731173 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.-42-303A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 2/11 | chr18 | 13731173 | |||||||
| chr18:13731216 | G | A | 1 | a0001c0001t0008g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-42-260G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 2/11 | chr18 | 13731216 | |||||||
| chr18:13731236 | G | A | 1 | a0001c0001t0015g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-42-240G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 2/11 | chr18 | 13731236 | |||||||
| chr18:13731236 | G | T | 2 | a0001c0001t0023g0115 a0001c0001t0023g0116 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-42-240G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 2/11 | chr18 | 13731236 | |||||||
| chr18:13731314 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-42-162G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 2/11 | chr18 | 13731314 | |||||||
| chr18:13731408 | C | CA | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.-42-54dupA | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 13731408 | ||||||
| chr18:13731964 | A | T | 8 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0087 others(5): Show |
10 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.417+30A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13731964 | |||||||
| chr18:13732054 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.417+120A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732054 | |||||||
| chr18:13732060 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.417+126C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732060 | |||||||
| chr18:13732074 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.417+140G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732074 | |||||||
| chr18:13732203 | C | CT | 9 | a0001c0001t0008g0032 a0001c0001t0008g0090 a0001c0001t0008g0091 others(6): Show |
10 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.417+277dupT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 13732203 | ||||||
| chr18:13732229 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.417+295A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732229 | |||||||
| chr18:13732272 | T | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01167.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.417+338T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732272 | |||||||
| chr18:13732364 | T | A | 1 | a0001c0001t0005g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.417+430T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732364 | |||||||
| chr18:13732380 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | NA18612.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.417+446C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732380 | |||||||
| chr18:13732385 | T | G | 12 | a0001c0001t0004g0126 a0001c0001t0004g0127 a0001c0001t0004g0128 others(9): Show |
14 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.417+451T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732385 | |||||||
| chr18:13732455 | A | G | 20 | a0001c0001t0001g0089 a0001c0001t0001g0220 a0001c0001t0001g0254 others(17): Show |
23 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.417+521A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732455 | |||||||
| chr18:13732553 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0136 a0001c0001t0001g0137 |
4 | HG01109.hp2 HG01981.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.417+619T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732553 | |||||||
| chr18:13732735 | GC | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
246 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.417+808delC | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 13732735 | ||||||
| chr18:13732735 | GCC | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
7 | HG00280.hp1 HG01361.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.417+807_417+808del others(2): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 13732735 | ||||||
| chr18:13732736 | C | T | 2 | a0001c0001t0003g0112 a0001c0001t0003g0113 |
2 | HG01361.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.417+802C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732736 | |||||||
| chr18:13732741 | C | CT | 8 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(5): Show |
11 | HG02257.hp1 HG02818.hp1 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.417+807_417+808ins others(1): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732741 | |||||||
| chr18:13732741 | C | T | 63 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(60): Show |
72 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.417+807C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732741 | |||||||
| chr18:13732742 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.417+808C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732742 | |||||||
| chr18:13732762 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.417+828T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732762 | |||||||
| chr18:13732762 | T | TC | 45 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(42): Show |
53 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.417+828_417+829ins others(1): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732762 | |||||||
| chr18:13732762 | T | TTC | 6 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0083 others(3): Show |
6 | HG01175.hp2 HG02738.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.417+828_417+829ins others(2): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732762 | |||||||
| chr18:13732767 | A | C | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.417+833A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732767 | |||||||
| chr18:13732815 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.417+881G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732815 | |||||||
| chr18:13732855 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG02615.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.417+921G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732855 | |||||||
| chr18:13732865 | G | A | 20 | a0001c0001t0001g0089 a0001c0001t0001g0220 a0001c0001t0001g0254 others(17): Show |
23 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.417+931G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732865 | |||||||
| chr18:13732886 | C | T | 18 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
20 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.417+952C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732886 | |||||||
| chr18:13732915 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.417+981C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732915 | |||||||
| chr18:13732936 | G | GT | 5 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(2): Show |
7 | HG02818.hp1 HG03225.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.417+1008dupT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 13732936 | ||||||
| chr18:13732981 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.417+1047T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13732981 | |||||||
| chr18:13733143 | C | G | 3 | a0001c0001t0011g0021 a0003c0003t0011g0021 a0003c0003t0011g0259 |
4 | HG02257.hp1 HG03579.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.417+1209C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13733143 | |||||||
| chr18:13733258 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.418-1206G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13733258 | |||||||
| chr18:13733373 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.418-1091A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13733373 | |||||||
| chr18:13733433 | G | A | 1 | a0001c0001t0007g0135 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.418-1031G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13733433 | |||||||
| chr18:13733479 | G | A | 2 | a0001c0001t0020g0251 a0001c0001t0020g0252 |
2 | HG01074.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.418-985G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13733479 | |||||||
| chr18:13733480 | C | T | 1 | a0001c0001t0015g0219 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.418-984C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13733480 | |||||||
| chr18:13733528 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG02602.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.418-936C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13733528 | |||||||
| chr18:13733856 | A | G | 1 | a0001c0001t0038g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.418-608A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13733856 | |||||||
| chr18:13733874 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG02258.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.418-590A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13733874 | |||||||
| chr18:13733974 | A | G | 6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG00741.hp2 HG02040.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.418-490A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13733974 | |||||||
| chr18:13734092 | G | A | 13 | a0001c0001t0001g0089 a0001c0001t0001g0220 a0001c0001t0004g0147 others(10): Show |
14 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.418-372G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13734092 | |||||||
| chr18:13734131 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.418-333C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13734131 | |||||||
| chr18:13734240 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.418-224C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13734240 | |||||||
| chr18:13734251 | T | C | 1 | a0001c0001t0036g0217 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.418-213T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 3/11 | chr18 | 13734251 | |||||||
| chr18:13734655 | A | G | 1 | a0001c0001t0010g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.553+56A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13734655 | |||||||
| chr18:13734749 | G | T | 8 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0087 others(5): Show |
10 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.553+150G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13734749 | |||||||
| chr18:13734782 | G | A | 5 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(2): Show |
7 | HG02818.hp1 HG03225.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.553+183G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13734782 | |||||||
| chr18:13734793 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18747.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.553+194T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13734793 | |||||||
| chr18:13734898 | A | G | 18 | a0001c0001t0004g0126 a0001c0001t0004g0127 a0001c0001t0004g0128 others(15): Show |
20 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.553+299A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13734898 | |||||||
| chr18:13734905 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.553+306C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13734905 | |||||||
| chr18:13735444 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.553+845T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13735444 | |||||||
| chr18:13735500 | C | CT | 22 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0120 others(19): Show |
26 | HG00323.hp2 HG01515.hp2 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.553+918dupT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 13735500 | ||||||
| chr18:13735500 | C | CTT | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.553+917_553+918dup others(2): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 13735500 | ||||||
| chr18:13735500 | C | CTTT | 19 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(16): Show |
23 | HG01074.hp2 HG01891.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.553+916_553+918dup others(3): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 13735500 | ||||||
| chr18:13735663 | A | G | 2 | a0001c0001t0002g0249 a0001c0001t0041g0250 |
2 | HG01243.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.553+1064A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13735663 | |||||||
| chr18:13735716 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.553+1117A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13735716 | |||||||
| chr18:13735814 | C | G | 2 | a0001c0001t0023g0115 a0001c0001t0023g0116 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.554-1196C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13735814 | |||||||
| chr18:13735817 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(259): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.554-1193T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13735817 | |||||||
| chr18:13735880 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG02258.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.554-1130A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13735880 | |||||||
| chr18:13735995 | A | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0001c0001t0001g0200 others(2): Show |
6 | HG01358.hp2 HG01928.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.554-1015A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13735995 | |||||||
| chr18:13736079 | G | T | 3 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 |
3 | HG00735.hp1 HG01255.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.554-931G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13736079 | |||||||
| chr18:13736097 | T | C | 2 | a0001c0001t0010g0022 a0001c0001t0010g0023 |
4 | HG03688.hp1 HG04184.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.554-913T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13736097 | |||||||
| chr18:13736217 | A | T | 1 | a0001c0001t0001g0041 | 2 | NA19057.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.554-793A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13736217 | |||||||
| chr18:13736369 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.554-641C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13736369 | |||||||
| chr18:13736494 | CT | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0199 others(5): Show |
11 | HG01358.hp2 HG01928.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.554-505delT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 13736494 | ||||||
| chr18:13736635 | CA | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(9): Show |
20 | HG00738.hp1 HG01123.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.554-366delA | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 13736635 | ||||||
| chr18:13736985 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.554-25A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 4/11 | chr18 | 13736985 | |||||||
| chr18:13737233 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.679+98T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13737233 | |||||||
| chr18:13737270 | C | T | 18 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
20 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.679+135C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13737270 | |||||||
| chr18:13737361 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01167.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.679+226G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13737361 | |||||||
| chr18:13737453 | G | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.679+318G>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13737453 | |||||||
| chr18:13737462 | T | C | 1 | a0001c0001t0028g0048 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.679+327T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13737462 | |||||||
| chr18:13737474 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(35): Show |
64 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.679+339T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13737474 | |||||||
| chr18:13737584 | A | C | 1 | a0001c0001t0003g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.679+449A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13737584 | |||||||
| chr18:13737628 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.679+493G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13737628 | |||||||
| chr18:13737646 | T | G | 3 | a0001c0001t0014g0174 a0001c0001t0014g0175 a0001c0001t0014g0230 |
3 | HG00621.hp2 NA18951.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.679+511T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13737646 | |||||||
| chr18:13737803 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.679+668T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13737803 | |||||||
| chr18:13738029 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.679+894C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738029 | |||||||
| chr18:13738369 | C | G | 1 | a0001c0001t0002g0082 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.679+1234C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738369 | |||||||
| chr18:13738469 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.679+1334T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738469 | |||||||
| chr18:13738530 | A | G | 3 | a0001c0001t0011g0021 a0003c0003t0011g0021 a0003c0003t0011g0259 |
4 | HG02257.hp1 HG03579.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+1395A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738530 | |||||||
| chr18:13738568 | T | C | 1 | a0001c0001t0002g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.679+1433T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738568 | |||||||
| chr18:13738782 | A | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(60): Show |
92 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.680-1385A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738782 | |||||||
| chr18:13738877 | T | C | 1 | a0001c0001t0024g0044 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.680-1290T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738877 | |||||||
| chr18:13738945 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.680-1222G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738945 | |||||||
| chr18:13738953 | C | A | 51 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(48): Show |
59 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.680-1214C>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738953 | |||||||
| chr18:13738955 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.680-1212T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738955 | |||||||
| chr18:13738983 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01081.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.680-1184T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13738983 | |||||||
| chr18:13739027 | G | A | 1 | a0001c0001t0038g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.680-1140G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739027 | |||||||
| chr18:13739123 | AG | A | 6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG00741.hp2 HG02040.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-1043delG | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739123 | |||||||
| chr18:13739152 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.680-1015A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739152 | |||||||
| chr18:13739270 | C | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.680-897C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739270 | |||||||
| chr18:13739273 | C | G | 8 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0087 others(5): Show |
10 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.680-894C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739273 | |||||||
| chr18:13739543 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.680-624G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739543 | |||||||
| chr18:13739563 | A | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(59): Show |
107 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.680-604A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739563 | |||||||
| chr18:13739585 | C | T | 1 | a0001c0001t0003g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.680-582C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739585 | |||||||
| chr18:13739807 | G | A | 5 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(2): Show |
7 | HG02818.hp1 HG03225.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-360G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739807 | |||||||
| chr18:13739862 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.680-305T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739862 | |||||||
| chr18:13739960 | C | T | 51 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(48): Show |
59 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.680-207C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13739960 | |||||||
| chr18:13739966 | TATTGAGA others(20): Show |
T | 1 | a0001c0001t0001g0120 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.680-199_680-173del others(27): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 13739966 | ||||||
| chr18:13740012 | G | A | 6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG00741.hp2 HG02040.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-155G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13740012 | |||||||
| chr18:13740039 | T | C | 24 | a0001c0001t0001g0089 a0001c0001t0001g0220 a0001c0001t0001g0254 others(21): Show |
27 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.680-128T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 5/11 | chr18 | 13740039 | |||||||
| chr18:13740343 | T | C | 7 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0224 others(4): Show |
9 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.792+64T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13740343 | |||||||
| chr18:13740496 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.792+217G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13740496 | |||||||
| chr18:13740782 | T | G | 1 | a0001c0001t0005g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.792+503T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13740782 | |||||||
| chr18:13740824 | T | C | 18 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
20 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.792+545T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13740824 | |||||||
| chr18:13740913 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.793-597G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13740913 | |||||||
| chr18:13740995 | G | T | 1 | a0001c0001t0023g0116 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-515G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13740995 | |||||||
| chr18:13741008 | C | T | 5 | a0001c0001t0004g0148 a0001c0001t0004g0149 a0001c0001t0004g0150 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-502C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13741008 | |||||||
| chr18:13741009 | A | G | 18 | a0001c0001t0004g0126 a0001c0001t0004g0127 a0001c0001t0004g0128 others(15): Show |
20 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.793-501A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13741009 | |||||||
| chr18:13741096 | G | T | 1 | a0001c0001t0003g0034 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.793-414G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13741096 | |||||||
| chr18:13741178 | G | T | 1 | a0001c0001t0024g0044 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.793-332G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13741178 | |||||||
| chr18:13741205 | GT | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.793-303delT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr18 | 13741205 | ||||||
| chr18:13741330 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.793-180G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13741330 | |||||||
| chr18:13741338 | A | G | 1 | a0001c0001t0006g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.793-172A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13741338 | |||||||
| chr18:13741450 | A | G | 3 | a0001c0001t0011g0021 a0003c0003t0011g0021 a0003c0003t0011g0259 |
4 | HG02257.hp1 HG03579.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-60A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 6/11 | chr18 | 13741450 | |||||||
| chr18:13741789 | CTT | C | 51 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(48): Show |
59 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.974+99_974+100delT others(1): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/11 | chr18 | 13741789 | |||||||
| chr18:13741798 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0001c0001t0001g0200 others(2): Show |
6 | HG01358.hp2 HG01928.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.974+107G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/11 | chr18 | 13741798 | |||||||
| chr18:13741963 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.974+272C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/11 | chr18 | 13741963 | |||||||
| chr18:13742258 | C | T | 2 | a0001c0001t0031g0241 a0001c0001t0038g0117 |
2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.975-230C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/11 | chr18 | 13742258 | |||||||
| chr18:13742265 | T | G | 1 | a0001c0001t0013g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.975-223T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/11 | chr18 | 13742265 | |||||||
| chr18:13742337 | T | TA | 11 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.975-135dupA | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 13742337 | ||||||
| chr18:13742337 | TA | T | 10 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0136 others(7): Show |
10 | HG01167.hp1 HG01169.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-135delA | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 13742337 | ||||||
| chr18:13742366 | A | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(259): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.975-122A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/11 | chr18 | 13742366 | |||||||
| chr18:13742395 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.975-93A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/11 | chr18 | 13742395 | |||||||
| chr18:13742428 | T | G | 2 | a0001c0001t0002g0249 a0001c0001t0041g0250 |
2 | HG01243.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.975-60T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 7/11 | chr18 | 13742428 | |||||||
| chr18:13742794 | T | A | 1 | a0001c0001t0002g0247 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1139+142T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13742794 | |||||||
| chr18:13742794 | T | TA | 5 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
6 | HG00597.hp1 HG01167.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1139+154dupA | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13742794 | ||||||
| chr18:13742795 | A | T | 9 | a0001c0001t0001g0220 a0001c0001t0002g0249 a0001c0001t0004g0148 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1139+143A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13742795 | |||||||
| chr18:13742803 | AAAAC | A | 6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG00741.hp2 HG02040.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1139+155_1139+158d others(6): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13742803 | ||||||
| chr18:13742811 | A | G | 2 | a0001c0001t0002g0028 a0001c0001t0002g0067 |
3 | HG01069.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1139+159A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13742811 | |||||||
| chr18:13742895 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1139+243T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13742895 | |||||||
| chr18:13742902 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1139+250G>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13742902 | |||||||
| chr18:13742968 | A | G | 1 | a0001c0001t0004g0151 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1139+316A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13742968 | |||||||
| chr18:13742971 | G | GT | 28 | a0001c0001t0001g0089 a0001c0001t0001g0173 a0001c0001t0001g0202 others(25): Show |
31 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1139+335dupT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13742971 | ||||||
| chr18:13743099 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1139+447C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743099 | |||||||
| chr18:13743106 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1139+454T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743106 | |||||||
| chr18:13743191 | C | T | 10 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(7): Show |
13 | HG02257.hp1 HG02451.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1139+539C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743191 | |||||||
| chr18:13743195 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1139+543C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743195 | |||||||
| chr18:13743213 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1139+561C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743213 | |||||||
| chr18:13743223 | T | C | 5 | a0001c0001t0001g0089 a0001c0001t0015g0121 a0001c0001t0015g0218 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1139+571T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743223 | |||||||
| chr18:13743280 | G | A | 6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG00741.hp2 HG02040.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1139+628G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743280 | |||||||
| chr18:13743326 | AAAAAAAT others(4): Show |
A | 8 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0087 others(5): Show |
10 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1139+678_1139+688d others(13): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13743326 | ||||||
| chr18:13743329 | A | T | 1 | a0001c0001t0003g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1139+677A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743329 | |||||||
| chr18:13743329 | AAAATAAA others(1): Show |
A | 30 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0183 others(27): Show |
30 | HG00741.hp2 HG01168.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.1139+714_1139+721d others(10): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13743329 | ||||||
| chr18:13743330 | AAAT | A | 6 | a0001c0001t0001g0089 a0001c0001t0001g0255 a0001c0001t0001g0256 others(3): Show |
7 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1139+681_1139+683d others(5): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13743330 | ||||||
| chr18:13743330 | AAATAAAT | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1139+681_1139+687d others(9): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13743330 | ||||||
| chr18:13743330 | AAATAAAT others(4): Show |
A | 1 | a0001c0001t0002g0069 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1139+681_1139+691d others(13): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13743330 | ||||||
| chr18:13743331 | AATAAAT | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0002g0025 others(4): Show |
7 | HG01256.hp1 HG02027.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1139+681_1139+686d others(8): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13743331 | ||||||
| chr18:13743332 | AT | A | 11 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0110 others(8): Show |
15 | HG00673.hp1 HG02257.hp1 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1139+681delT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743332 | |||||||
| chr18:13743333 | T | A | 11 | a0001c0001t0003g0033 a0001c0001t0003g0086 a0001c0001t0003g0106 others(8): Show |
12 | HG01074.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1139+681T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743333 | |||||||
| chr18:13743337 | T | A | 11 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(8): Show |
13 | HG02258.hp1 HG02258.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1139+685T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743337 | |||||||
| chr18:13743339 | AAT | A | 7 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(4): Show |
10 | HG02257.hp1 HG02818.hp1 HG03579.hp2 others(7): Show |
intron_variant | MODIFIER | c.1139+689_1139+690d others(4): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13743339 | ||||||
| chr18:13743341 | T | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.1139+689T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743341 | |||||||
| chr18:13743345 | T | A | 67 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(64): Show |
80 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1139+693T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743345 | |||||||
| chr18:13743349 | T | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0198 a0001c0001t0002g0025 others(6): Show |
10 | HG02572.hp2 HG02683.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1139+697T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743349 | |||||||
| chr18:13743370 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0203 |
6 | HG00673.hp2 HG02015.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1139+718A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743370 | |||||||
| chr18:13743443 | C | G | 1 | a0001c0001t0001g0183 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1139+791C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743443 | |||||||
| chr18:13743551 | G | T | 2 | a0001c0001t0003g0112 a0001c0001t0003g0113 |
2 | HG01361.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1139+899G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743551 | |||||||
| chr18:13743670 | T | C | 1 | a0001c0001t0024g0044 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1139+1018T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743670 | |||||||
| chr18:13743762 | C | G | 1 | a0001c0001t0014g0230 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1139+1110C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743762 | |||||||
| chr18:13743837 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1139+1185G>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743837 | |||||||
| chr18:13743860 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0215 |
3 | HG00280.hp2 HG00733.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1139+1208C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13743860 | |||||||
| chr18:13744078 | C | T | 1 | a0001c0001t0002g0249 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1139+1426C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13744078 | |||||||
| chr18:13744156 | C | CTTTTTTT others(3): Show |
2 | a0002c0002t0017g0152 a0002c0002t0017g0153 |
2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1139+1506_1139+150 others(14): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744156 | ||||||
| chr18:13744156 | C | CTTTTTTT others(4): Show |
1 | a0002c0002t0017g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1139+1506_1139+150 others(15): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744156 | ||||||
| chr18:13744156 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0038g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1139+1506_1139+150 others(27): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744156 | ||||||
| chr18:13744159 | C | CT | 11 | a0001c0001t0001g0099 a0001c0001t0003g0111 a0001c0001t0008g0032 others(8): Show |
13 | HG01884.hp1 HG01952.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1139+1533dupT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | C | CTTTTTTT others(3): Show |
18 | a0001c0001t0002g0027 a0001c0001t0002g0057 a0001c0001t0002g0061 others(15): Show |
21 | HG01255.hp1 HG01433.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.1139+1524_1139+153 others(14): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | C | CTTTTTTT others(4): Show |
18 | a0001c0001t0001g0089 a0001c0001t0002g0025 a0001c0001t0002g0028 others(15): Show |
22 | HG00735.hp1 HG00738.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.1139+1523_1139+153 others(15): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | C | CTTTTTTT others(5): Show |
16 | a0001c0001t0001g0206 a0001c0001t0002g0013 a0001c0001t0002g0026 others(13): Show |
22 | HG00323.hp2 HG00639.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.1139+1522_1139+153 others(16): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | C | CTTTTTTT others(6): Show |
7 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0066 others(4): Show |
7 | HG01081.hp1 HG01175.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1139+1521_1139+153 others(17): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | C | CTTTTTTT others(7): Show |
12 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0207 others(9): Show |
12 | HG02040.hp2 HG03195.hp1 HG03225.hp2 others(9): Show |
intron_variant | MODIFIER | c.1139+1520_1139+153 others(18): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | C | CTTTTTTT others(8): Show |
6 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0002g0248 others(3): Show |
6 | HG01168.hp1 HG02055.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1139+1519_1139+153 others(19): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0004g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1139+1512_1139+153 others(26): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0255 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1139+1509_1139+153 others(29): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1139+1533_1139+153 others(35): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | C | T | 4 | a0001c0001t0038g0117 a0002c0002t0017g0152 a0002c0002t0017g0153 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1139+1507C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13744159 | |||||||
| chr18:13744159 | CT | C | 9 | a0001c0001t0003g0014 a0001c0001t0003g0033 a0001c0001t0003g0106 others(6): Show |
14 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1139+1533delT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | CTTTTT | C | 6 | a0001c0001t0002g0056 a0001c0001t0004g0147 a0001c0001t0004g0149 others(3): Show |
6 | HG01243.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1139+1529_1139+153 others(9): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0249 a0001c0001t0041g0250 |
2 | HG01243.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1139+1522_1139+153 others(16): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | CTTTTTTT others(6): Show |
C | 1 | a0005c0005t0001g0193 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1139+1521_1139+153 others(17): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | CTTTTTTT others(7): Show |
C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1139+1520_1139+153 others(18): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744159 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0142 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1139+1519_1139+153 others(19): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13744159 | ||||||
| chr18:13744377 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1139+1725T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13744377 | |||||||
| chr18:13744815 | T | G | 5 | a0001c0001t0004g0148 a0001c0001t0004g0149 a0001c0001t0004g0150 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140-1405T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13744815 | |||||||
| chr18:13744905 | C | G | 1 | a0001c0001t0024g0044 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1140-1315C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13744905 | |||||||
| chr18:13744954 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG02602.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1140-1266G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13744954 | |||||||
| chr18:13744969 | T | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1140-1251T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13744969 | |||||||
| chr18:13744985 | G | T | 18 | a0001c0001t0004g0126 a0001c0001t0004g0127 a0001c0001t0004g0128 others(15): Show |
20 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1140-1235G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13744985 | |||||||
| chr18:13745056 | G | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(34): Show |
63 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1140-1164G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745056 | |||||||
| chr18:13745168 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1140-1052T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745168 | |||||||
| chr18:13745179 | G | A | 1 | a0001c0001t0007g0133 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1140-1041G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745179 | |||||||
| chr18:13745218 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0260 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1140-1002G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745218 | |||||||
| chr18:13745224 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1140-996T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745224 | |||||||
| chr18:13745434 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0166 |
2 | NA19070.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1140-786T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745434 | |||||||
| chr18:13745520 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1140-700G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745520 | |||||||
| chr18:13745667 | C | G | 1 | a0001c0001t0028g0048 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1140-553C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745667 | |||||||
| chr18:13745706 | GTACTC | G | 51 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(48): Show |
59 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1140-510_1140-506d others(7): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13745706 | ||||||
| chr18:13745765 | GA | G | 27 | a0001c0001t0001g0192 a0001c0001t0001g0204 a0001c0001t0001g0205 others(24): Show |
29 | HG00741.hp1 HG00741.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1140-443delA | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 13745765 | ||||||
| chr18:13745906 | T | C | 18 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
20 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1140-314T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745906 | |||||||
| chr18:13745936 | T | G | 51 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(48): Show |
59 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1140-284T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745936 | |||||||
| chr18:13745938 | C | T | 1 | a0001c0001t0024g0044 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1140-282C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13745938 | |||||||
| chr18:13746024 | C | G | 24 | a0001c0001t0001g0089 a0001c0001t0001g0220 a0001c0001t0001g0254 others(21): Show |
27 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.1140-196C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13746024 | |||||||
| chr18:13746112 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1140-108G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13746112 | |||||||
| chr18:13746144 | T | C | 1 | a0001c0001t0002g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1140-76T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13746144 | |||||||
| chr18:13746145 | C | T | 2 | a0001c0001t0023g0115 a0001c0001t0023g0116 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1140-75C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13746145 | |||||||
| chr18:13746150 | C | G | 1 | a0001c0001t0007g0133 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1140-70C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13746150 | |||||||
| chr18:13746197 | A | G | 4 | a0001c0001t0020g0251 a0001c0001t0020g0252 a0001c0001t0031g0241 others(1): Show |
4 | HG01074.hp2 HG02257.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140-23A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 8/11 | chr18 | 13746197 | |||||||
| chr18:13746976 | A | G | 1 | a0001c0001t0026g0125 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1257+639A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13746976 | |||||||
| chr18:13746993 | T | G | 49 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(46): Show |
57 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1257+656T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13746993 | |||||||
| chr18:13747078 | A | C | 1 | a0001c0001t0002g0068 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1257+741A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747078 | |||||||
| chr18:13747219 | AT | A | 9 | a0001c0001t0001g0182 a0001c0001t0010g0022 a0001c0001t0010g0023 others(6): Show |
12 | HG02257.hp1 HG02818.hp1 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.1257+895delT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 13747219 | ||||||
| chr18:13747232 | TG | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1257+896delG | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747232 | |||||||
| chr18:13747233 | G | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(26): Show |
34 | HG00323.hp1 HG00639.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1257+896G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747233 | |||||||
| chr18:13747249 | T | C | 2 | a0001c0001t0023g0115 a0001c0001t0023g0116 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1257+912T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747249 | |||||||
| chr18:13747252 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0034g0236 |
2 | HG02074.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1257+915C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747252 | |||||||
| chr18:13747362 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0042 others(9): Show |
15 | HG00408.hp1 HG01358.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.1257+1025G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747362 | |||||||
| chr18:13747424 | G | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1257+1087G>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747424 | |||||||
| chr18:13747532 | T | G | 5 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(2): Show |
7 | HG02818.hp1 HG03225.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1257+1195T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747532 | |||||||
| chr18:13747818 | T | C | 1 | a0001c0001t0002g0059 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1257+1481T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747818 | |||||||
| chr18:13747826 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0041g0250 |
2 | HG01243.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1257+1489G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747826 | |||||||
| chr18:13747866 | A | G | 1 | a0001c0001t0004g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1257+1529A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13747866 | |||||||
| chr18:13748089 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1257+1752C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13748089 | |||||||
| chr18:13748138 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1257+1801G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13748138 | |||||||
| chr18:13748225 | T | TTCTTCAG others(3): Show |
1 | a0001c0001t0016g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1257+1894_1257+190 others(14): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 13748225 | ||||||
| chr18:13748371 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1257+2034G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13748371 | |||||||
| chr18:13748412 | A | C | 1 | a0001c0001t0015g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1257+2075A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13748412 | |||||||
| chr18:13748435 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1257+2098A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13748435 | |||||||
| chr18:13748634 | C | T | 8 | a0001c0001t0002g0249 a0001c0001t0010g0022 a0001c0001t0010g0023 others(5): Show |
10 | HG01243.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1257+2297C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13748634 | |||||||
| chr18:13748639 | G | T | 6 | a0001c0001t0006g0007 a0001c0001t0006g0118 a0001c0001t0006g0138 others(3): Show |
11 | HG01255.hp2 HG01258.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1257+2302G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13748639 | |||||||
| chr18:13748642 | CAGAG | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0183 others(4): Show |
11 | HG00408.hp2 HG02083.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1257+2309_1257+231 others(8): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 13748642 | ||||||
| chr18:13748803 | G | A | 1 | a0001c0001t0031g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1257+2466G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13748803 | |||||||
| chr18:13748846 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1257+2509A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13748846 | |||||||
| chr18:13749060 | C | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG02258.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257+2723C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749060 | |||||||
| chr18:13749284 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG02258.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257+2947A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749284 | |||||||
| chr18:13749316 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1257+2979C>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749316 | |||||||
| chr18:13749357 | T | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1258-2969T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749357 | |||||||
| chr18:13749358 | T | A | 2 | a0001c0001t0002g0249 a0001c0001t0041g0250 |
2 | HG01243.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1258-2968T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749358 | |||||||
| chr18:13749499 | A | G | 2 | a0001c0001t0020g0251 a0001c0001t0020g0252 |
2 | HG01074.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1258-2827A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749499 | |||||||
| chr18:13749505 | G | A | 1 | a0001c0001t0004g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1258-2821G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749505 | |||||||
| chr18:13749603 | CAAAGAAT others(3): Show |
C | 1 | a0001c0001t0015g0218 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1258-2709_1258-270 others(14): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 13749603 | ||||||
| chr18:13749673 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1258-2653A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749673 | |||||||
| chr18:13749692 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1258-2634A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749692 | |||||||
| chr18:13749732 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1258-2594A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749732 | |||||||
| chr18:13749745 | C | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(55): Show |
102 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1258-2581C>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749745 | |||||||
| chr18:13749783 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | NA18612.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1258-2543C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749783 | |||||||
| chr18:13749786 | C | A | 2 | a0001c0001t0020g0251 a0001c0001t0020g0252 |
2 | HG01074.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1258-2540C>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749786 | |||||||
| chr18:13749977 | C | T | 1 | a0001c0001t0007g0133 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1258-2349C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13749977 | |||||||
| chr18:13750014 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1258-2312T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750014 | |||||||
| chr18:13750049 | G | A | 7 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0224 others(4): Show |
9 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1258-2277G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750049 | |||||||
| chr18:13750232 | T | G | 53 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(50): Show |
61 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1258-2094T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750232 | |||||||
| chr18:13750261 | C | T | 5 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | NA18954.hp2 NA18959.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-2065C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750261 | |||||||
| chr18:13750269 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1258-2057G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750269 | |||||||
| chr18:13750326 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1258-2000T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750326 | |||||||
| chr18:13750392 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1258-1934T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750392 | |||||||
| chr18:13750444 | T | C | 6 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG01884.hp2 HG01891.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1258-1882T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750444 | |||||||
| chr18:13750552 | C | T | 3 | a0001c0001t0011g0021 a0003c0003t0011g0021 a0003c0003t0011g0259 |
4 | HG02257.hp1 HG03579.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1258-1774C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750552 | |||||||
| chr18:13750667 | T | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG00621.hp1 HG02135.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1258-1659T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750667 | |||||||
| chr18:13750676 | C | T | 3 | a0002c0002t0017g0152 a0002c0002t0017g0153 a0002c0002t0017g0154 |
3 | HG02559.hp2 HG02818.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1258-1650C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750676 | |||||||
| chr18:13750742 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.1258-1584A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750742 | |||||||
| chr18:13750990 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1258-1336A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13750990 | |||||||
| chr18:13751062 | C | T | 1 | a0001c0001t0002g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1258-1264C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751062 | |||||||
| chr18:13751357 | A | G | 1 | a0001c0001t0003g0110 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1258-969A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751357 | |||||||
| chr18:13751501 | G | A | 10 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(7): Show |
13 | HG02257.hp1 HG02451.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1258-825G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751501 | |||||||
| chr18:13751603 | A | C | 2 | a0001c0001t0023g0115 a0001c0001t0023g0116 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1258-723A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751603 | |||||||
| chr18:13751619 | G | A | 2 | a0001c0001t0023g0115 a0001c0001t0023g0116 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1258-707G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751619 | |||||||
| chr18:13751633 | T | C | 2 | a0001c0001t0023g0115 a0001c0001t0023g0116 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1258-693T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751633 | |||||||
| chr18:13751693 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1258-633C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751693 | |||||||
| chr18:13751704 | AC | A | 10 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(7): Show |
13 | HG02257.hp1 HG02451.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1258-621delC | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751704 | |||||||
| chr18:13751731 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1258-595A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751731 | |||||||
| chr18:13751773 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1258-553G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751773 | |||||||
| chr18:13751914 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1258-412G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751914 | |||||||
| chr18:13751924 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1258-402C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751924 | |||||||
| chr18:13751935 | A | G | 1 | a0001c0001t0010g0022 | 2 | NA18953.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1258-391A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13751935 | |||||||
| chr18:13752096 | G | A | 3 | a0002c0002t0017g0152 a0002c0002t0017g0153 a0002c0002t0017g0154 |
3 | HG02559.hp2 HG02818.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1258-230G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13752096 | |||||||
| chr18:13752129 | T | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1258-197T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13752129 | |||||||
| chr18:13752168 | T | A | 2 | a0001c0001t0001g0178 a0001c0001t0002g0061 |
2 | NA18954.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1258-158T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 9/11 | chr18 | 13752168 | |||||||
| chr18:13752431 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG00738.hp2 | splice_region_variant&intron_variant | LOW | c.1359+4A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13752431 | |||||||
| chr18:13752740 | A | G | 2 | a0001c0001t0023g0115 a0001c0001t0023g0116 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1359+313A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13752740 | |||||||
| chr18:13752868 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0002g0242 |
2 | NA19063.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1359+441A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13752868 | |||||||
| chr18:13753226 | T | C | 1 | a0001c0001t0007g0135 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1359+799T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13753226 | |||||||
| chr18:13753265 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1359+838G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13753265 | |||||||
| chr18:13753359 | T | G | 3 | a0001c0001t0004g0148 a0001c0001t0004g0149 a0001c0001t0004g0151 |
3 | HG02109.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1360-755T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13753359 | |||||||
| chr18:13753419 | C | T | 1 | a0001c0001t0007g0133 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1360-695C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13753419 | |||||||
| chr18:13753500 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG02258.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1360-614A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13753500 | |||||||
| chr18:13753749 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1360-365C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13753749 | |||||||
| chr18:13753778 | G | GA | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
250 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1360-326dupA | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753778 | ||||||
| chr18:13753789 | T | A | 1 | a0001c0001t0001g0235 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1360-325T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13753789 | |||||||
| chr18:13753816 | T | TAC | 15 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0141 others(12): Show |
26 | HG00280.hp1 HG00673.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1360-264_1360-263d others(4): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | T | TACAC | 16 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0098 others(13): Show |
19 | HG00621.hp1 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1360-266_1360-263d others(6): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | T | TACACAC | 13 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0001g0099 others(10): Show |
14 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360-268_1360-263d others(8): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | T | TACACACA others(1): Show |
18 | a0001c0001t0001g0089 a0001c0001t0001g0254 a0001c0001t0001g0255 others(15): Show |
22 | HG01123.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1360-270_1360-263d others(10): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | T | TACACACA others(3): Show |
33 | a0001c0001t0001g0220 a0001c0001t0002g0013 a0001c0001t0002g0025 others(30): Show |
39 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1360-272_1360-263d others(12): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | T | TACACACA others(5): Show |
11 | a0001c0001t0001g0257 a0001c0001t0002g0028 a0001c0001t0002g0060 others(8): Show |
12 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1360-274_1360-263d others(14): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | T | TACACACA others(7): Show |
4 | a0001c0001t0002g0055 a0001c0001t0002g0062 a0001c0001t0002g0064 others(1): Show |
4 | HG00639.hp1 HG01081.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1360-276_1360-263d others(16): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | T | TACACACA others(9): Show |
1 | a0001c0001t0019g0081 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1360-278_1360-263d others(18): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | T | TACACACA others(11): Show |
2 | a0001c0001t0002g0244 a0001c0001t0002g0253 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1360-280_1360-263d others(20): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | TAC | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(66): Show |
102 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1360-264_1360-263d others(4): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | TACAC | T | 17 | a0001c0001t0001g0039 a0001c0001t0001g0181 a0001c0001t0001g0183 others(14): Show |
18 | HG00741.hp2 HG01516.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1360-266_1360-263d others(6): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | TACACACA others(5): Show |
T | 1 | a0003c0003t0011g0259 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1360-274_1360-263d others(14): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753816 | TACACACA others(7): Show |
T | 2 | a0001c0001t0011g0021 a0003c0003t0011g0021 |
3 | HG02257.hp1 NA18949.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1360-276_1360-263d others(16): Show |
RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 13753816 | ||||||
| chr18:13753896 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1360-218A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13753896 | |||||||
| chr18:13753974 | A | G | 2 | a0001c0001t0023g0115 a0001c0001t0023g0116 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1360-140A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 10/11 | chr18 | 13753974 | |||||||
| chr18:13754211 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1393+64A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13754211 | |||||||
| chr18:13754309 | C | T | 5 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(2): Show |
7 | HG02818.hp1 HG03225.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1393+162C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13754309 | |||||||
| chr18:13754493 | C | T | 1 | a0001c0001t0003g0107 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1393+346C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13754493 | |||||||
| chr18:13754521 | T | G | 2 | a0001c0001t0023g0115 a0001c0001t0023g0116 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1393+374T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13754521 | |||||||
| chr18:13754522 | T | C | 5 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0049 others(2): Show |
7 | HG02818.hp1 HG03225.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1393+375T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13754522 | |||||||
| chr18:13754721 | C | T | 12 | a0001c0001t0004g0126 a0001c0001t0004g0127 a0001c0001t0004g0128 others(9): Show |
14 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1393+574C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13754721 | |||||||
| chr18:13754755 | C | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1393+608C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13754755 | |||||||
| chr18:13754787 | T | C | 51 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(48): Show |
60 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1393+640T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13754787 | |||||||
| chr18:13754848 | A | G | 4 | a0001c0001t0008g0031 a0001c0001t0011g0021 a0003c0003t0011g0021 others(1): Show |
6 | HG02257.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1393+701A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13754848 | |||||||
| chr18:13754939 | A | C | 1 | a0001c0001t0002g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1393+792A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13754939 | |||||||
| chr18:13755111 | A | T | 53 | a0001c0001t0002g0013 a0001c0001t0002g0025 a0001c0001t0002g0026 others(50): Show |
61 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1393+964A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13755111 | |||||||
| chr18:13755121 | G | C | 2 | a0001c0001t0002g0249 a0001c0001t0041g0250 |
2 | HG01243.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1393+974G>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13755121 | |||||||
| chr18:13755275 | G | A | 2 | a0001c0001t0020g0251 a0001c0001t0020g0252 |
2 | HG01074.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1393+1128G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13755275 | |||||||
| chr18:13755359 | G | A | 8 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0087 others(5): Show |
10 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1393+1212G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13755359 | |||||||
| chr18:13755381 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1393+1234C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13755381 | |||||||
| chr18:13755402 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1393+1255T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13755402 | |||||||
| chr18:13755488 | C | A | 1 | a0001c0001t0002g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1393+1341C>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13755488 | |||||||
| chr18:13755773 | T | G | 1 | a0001c0001t0003g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1393+1626T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13755773 | |||||||
| chr18:13755975 | C | T | 1 | a0001c0001t0024g0044 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1393+1828C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13755975 | |||||||
| chr18:13756194 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1393+2047T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13756194 | |||||||
| chr18:13756256 | C | T | 3 | a0001c0001t0003g0033 a0001c0001t0003g0106 a0001c0001t0003g0107 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1393+2109C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13756256 | |||||||
| chr18:13756287 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1393+2140T>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13756287 | |||||||
| chr18:13756548 | G | T | 1 | a0001c0001t0004g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1393+2401G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13756548 | |||||||
| chr18:13756605 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1393+2458T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13756605 | |||||||
| chr18:13756715 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1393+2568G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13756715 | |||||||
| chr18:13756886 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1393+2739C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13756886 | |||||||
| chr18:13757047 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1394-2895T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757047 | |||||||
| chr18:13757117 | C | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1394-2825C>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757117 | |||||||
| chr18:13757118 | A | G | 7 | a0001c0001t0001g0089 a0001c0001t0001g0220 a0001c0001t0015g0121 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394-2824A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757118 | |||||||
| chr18:13757127 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0197 |
4 | NA18966.hp1 NA19072.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394-2815C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757127 | |||||||
| chr18:13757139 | A | C | 1 | a0001c0001t0010g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1394-2803A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757139 | |||||||
| chr18:13757152 | T | TA | 12 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0090 others(9): Show |
14 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1394-2783dupA | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 13757152 | ||||||
| chr18:13757208 | G | C | 1 | a0001c0001t0024g0044 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1394-2734G>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757208 | |||||||
| chr18:13757331 | AT | A | 3 | a0001c0001t0003g0033 a0001c0001t0003g0106 a0001c0001t0003g0107 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1394-2608delT | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 13757331 | ||||||
| chr18:13757548 | G | C | 18 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
20 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1394-2394G>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757548 | |||||||
| chr18:13757554 | G | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1394-2388G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757554 | |||||||
| chr18:13757653 | A | C | 1 | a0001c0001t0002g0076 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1394-2289A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757653 | |||||||
| chr18:13757757 | A | T | 14 | a0001c0001t0001g0089 a0001c0001t0001g0220 a0001c0001t0001g0254 others(11): Show |
15 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1394-2185A>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757757 | |||||||
| chr18:13757770 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1394-2172T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757770 | |||||||
| chr18:13757778 | G | C | 1 | a0001c0001t0005g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1394-2164G>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757778 | |||||||
| chr18:13757842 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1394-2100A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757842 | |||||||
| chr18:13757851 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1394-2091A>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13757851 | |||||||
| chr18:13758019 | G | A | 1 | a0001c0001t0004g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1394-1923G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13758019 | |||||||
| chr18:13758171 | T | A | 1 | a0001c0001t0014g0174 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1394-1771T>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13758171 | |||||||
| chr18:13758256 | C | T | 18 | a0001c0001t0004g0126 a0001c0001t0004g0127 a0001c0001t0004g0128 others(15): Show |
20 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1394-1686C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13758256 | |||||||
| chr18:13758387 | A | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0136 |
3 | HG01981.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1394-1555A>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13758387 | |||||||
| chr18:13758622 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0181 |
3 | NA18974.hp2 NA18982.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1394-1320T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13758622 | |||||||
| chr18:13758853 | C | G | 1 | a0001c0001t0005g0228 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1394-1089C>G | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13758853 | |||||||
| chr18:13759147 | C | T | 18 | a0001c0001t0004g0126 a0001c0001t0004g0127 a0001c0001t0004g0128 others(15): Show |
20 | HG01168.hp1 HG01175.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1394-795C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13759147 | |||||||
| chr18:13759421 | G | A | 20 | a0001c0001t0001g0089 a0001c0001t0001g0220 a0001c0001t0001g0254 others(17): Show |
23 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1394-521G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13759421 | |||||||
| chr18:13759429 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1394-513G>A | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13759429 | |||||||
| chr18:13759817 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1394-125T>C | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13759817 | |||||||
| chr18:13759821 | G | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1394-121G>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13759821 | |||||||
| chr18:13759828 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0022g0030 |
3 | HG01167.hp2 HG01169.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1394-114C>T | RNMT | ENSG00000101654.18 | transcript | ENST00000383314.7 | protein_coding | 11/11 | chr18 | 13759828 |