Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 196074 |
| ensemblid | ENSG00000169519.21 |
| hgncid | 26606 |
| symbol | METTL15 |
| name | methyltransferase 15, mitochondrial 12S rRNA N4-cytidine |
| refseq_nuc | NM_001113528.2 |
| refseq_prot | NP_001107000.1 |
| ensembl_nuc | ENST00000407364.8 |
| ensembl_prot | ENSP00000384369.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 28108388 |
| end | 28333507 |
| strand | + |
| ver | v1.2 |
| region | chr11:28108388-28333507 |
| region5000 | chr11:28103388-28338507 |
| regionname0 | METTL15_chr11_28108388_28333507 |
| regionname5000 | METTL15_chr11_28103388_28338507 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 407 | 225 | 55 | 21 | 125 | 3 | 20 | 101 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| a0002 | 1/0 | 407 | 85 | 10 | 17 | 40 | 1 | 16 | 31 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| a0003 | 0/0 | 407 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| a0004 | 0/0 | 407 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| a0005 | 0/0 | 407 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| a0006 | 0/0 | 407 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| a0007 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| a0008 | 0/0 | 407 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| a0009 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| a0010 | 0/0 | 407 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| a0011 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | MLRYP others(402): Show |
chr11 | 28103388 | 28338507 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1221 | 222 | 53 | 21 | 124 | 3 | 20 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0001c0007 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0001c0008 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0001c0014 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0002c0002 | 1/0 | 1221 | 85 | 10 | 17 | 40 | 1 | 16 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0003c0004 | 0/0 | 1221 | 6 | 6 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0004c0003 | 0/0 | 1221 | 6 | 6 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0005c0005 | 0/0 | 1221 | 3 | 3 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0006c0006 | 0/0 | 1221 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0007c0009 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0008c0013 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0009c0010 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0010c0011 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 | ||
| a0011c0012 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | ATGCT others(1216): Show |
chr11 | 28103388 | 28338507 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4208 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4203): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0002 | 0/0 | 4209 | 64 | 1 | 11 | 45 | 2 | 5 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCG others(4204): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0003 | 0/0 | 4213 | 52 | 1 | 1 | 42 | 0 | 8 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4208): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0004 | 0/0 | 4216 | 35 | 15 | 5 | 10 | 1 | 4 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4211): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0005 | 0/0 | 4214 | 12 | 2 | 0 | 9 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4209): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0006 | 0/0 | 4215 | 12 | 9 | 0 | 3 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4210): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0007 | 0/0 | 4217 | 10 | 2 | 1 | 6 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4212): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0008 | 0/0 | 4216 | 7 | 6 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4211): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0009 | 0/0 | 4218 | 6 | 4 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4213): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0010 | 0/0 | 4208 | 5 | 2 | 0 | 3 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCG others(4203): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0011 | 0/0 | 4208 | 4 | 4 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4203): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0012 | 0/0 | 4213 | 3 | 3 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4208): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0013 | 0/0 | 4215 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4210): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0016 | 0/0 | 4214 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4209): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0017 | 0/0 | 4215 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4210): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0018 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4207): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0019 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4211): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0022 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4211): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0023 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4209): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0024 | 0/0 | 4216 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4211): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0028 | 0/0 | 4209 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCG others(4204): Show |
chr11 | 28103388 | 28338507 |
| a0001c0001t0029 | 0/1 | 4209 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCG others(4204): Show |
chr11 | 28103388 | 28338507 |
| a0001c0007t0003 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4208): Show |
chr11 | 28103388 | 28338507 |
| a0001c0008t0020 | 0/0 | 4217 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4212): Show |
chr11 | 28103388 | 28338507 |
| a0001c0014t0021 | 0/0 | 4208 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4203): Show |
chr11 | 28103388 | 28338507 |
| a0002c0002t0001 | 1/0 | 4208 | 82 | 10 | 17 | 37 | 1 | 16 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4203): Show |
chr11 | 28103388 | 28338507 |
| a0002c0002t0015 | 0/0 | 4208 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4203): Show |
chr11 | 28103388 | 28338507 |
| a0002c0002t0026 | 0/0 | 4208 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4203): Show |
chr11 | 28103388 | 28338507 |
| a0003c0004t0001 | 0/0 | 4208 | 5 | 5 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4203): Show |
chr11 | 28103388 | 28338507 |
| a0003c0004t0027 | 0/0 | 4208 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4203): Show |
chr11 | 28103388 | 28338507 |
| a0004c0003t0002 | 0/0 | 4209 | 6 | 6 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCG others(4204): Show |
chr11 | 28103388 | 28338507 |
| a0005c0005t0014 | 0/0 | 4214 | 2 | 2 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4209): Show |
chr11 | 28103388 | 28338507 |
| a0005c0005t0025 | 0/0 | 4215 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4210): Show |
chr11 | 28103388 | 28338507 |
| a0006c0006t0003 | 0/0 | 4213 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4208): Show |
chr11 | 28103388 | 28338507 |
| a0007c0009t0003 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4208): Show |
chr11 | 28103388 | 28338507 |
| a0008c0013t0004 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4211): Show |
chr11 | 28103388 | 28338507 |
| a0009c0010t0002 | 0/0 | 4209 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCG others(4204): Show |
chr11 | 28103388 | 28338507 |
| a0010c0011t0003 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4208): Show |
chr11 | 28103388 | 28338507 |
| a0011c0012t0003 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | AGCCA others(4208): Show |
chr11 | 28103388 | 28338507 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0009g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0009g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0010g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0010g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0010g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0010g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0011g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0011g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0011g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0011g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0013g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0013g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0016g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0017g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0019g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0022g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0023g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0024g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0028g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0029g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0007t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0008t0020g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0014t0021g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0015g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0015g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0026g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0004t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0004t0027g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0003t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0003t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0005c0005t0014g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0005c0005t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0005c0005t0025g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0006c0006t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0006c0006t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0007c0009t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0008c0013t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0009c0010t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0010c0011t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0011c0012t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00423 | hp1 | a0007 | c0009 | t0003 | g0023 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0237 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0072 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0322 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00673 | hp2 | a0001 | c0007 | t0003 | g0057 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0200 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0279 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0177 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0323 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0297 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0280 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0310 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0202 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0168 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0206 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0314 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0303 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01361 | hp2 | a0001 | c0001 | t0016 | g0020 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0327 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | IBS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0304 | EUR | IBS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0238 | EUR | IBS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0128 | EUR | IBS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01891 | hp2 | a0003 | c0004 | t0001 | g0296 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0201 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0185 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | CDX | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CDX | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0194 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0216 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0328 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02258 | hp2 | a0001 | c0001 | t0019 | g0208 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0074 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0165 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02572 | hp1 | a0004 | c0003 | t0002 | g0111 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0263 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0209 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02622 | hp1 | a0005 | c0005 | t0014 | g0079 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02630 | hp2 | a0004 | c0003 | t0002 | g0086 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02647 | hp1 | a0004 | c0003 | t0002 | g0112 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0242 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0283 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0228 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02717 | hp1 | a0004 | c0003 | t0002 | g0110 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0043 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0281 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0301 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0198 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0195 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0073 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0221 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0192 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02886 | hp1 | a0001 | c0001 | t0023 | g0037 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0210 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0240 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0241 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0207 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0193 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0315 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0316 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0167 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02976 | hp1 | a0003 | c0004 | t0001 | g0313 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0064 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0075 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0277 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0219 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0317 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03209 | hp1 | a0003 | c0004 | t0001 | g0285 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0212 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0220 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0291 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03453 | hp1 | a0001 | c0014 | t0021 | g0229 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03453 | hp2 | a0003 | c0004 | t0027 | g0284 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0215 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03486 | hp2 | a0004 | c0003 | t0002 | g0109 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0300 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0282 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0179 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0324 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03540 | hp1 | a0001 | c0001 | t0022 | g0157 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0224 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0169 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03579 | hp2 | a0003 | c0004 | t0001 | g0305 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0254 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0187 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | STU | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0275 | SAS | STU | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0307 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0158 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0325 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0249 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03927 | hp2 | a0001 | c0001 | t0028 | g0149 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0252 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0046 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0251 | SAS | STU | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | STU | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0270 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | YRI | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | YRI | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | CHB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | CHB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | CHB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | CHB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18906 | hp1 | a0008 | c0013 | t0004 | g0172 | AFR | YRI | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0166 | AFR | YRI | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18948 | hp2 | a0001 | c0001 | t0010 | g0118 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18957 | hp1 | a0002 | c0002 | t0015 | g0318 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18961 | hp2 | a0001 | c0001 | t0010 | g0117 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18963 | hp1 | a0001 | c0001 | t0007 | g0236 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18967 | hp1 | a0001 | c0001 | t0010 | g0087 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18968 | hp2 | a0001 | c0001 | t0013 | g0055 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18973 | hp2 | a0001 | c0001 | t0007 | g0233 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18978 | hp2 | a0001 | c0001 | t0013 | g0035 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0234 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18982 | hp1 | a0002 | c0002 | t0026 | g0326 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18982 | hp2 | a0001 | c0001 | t0024 | g0184 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18992 | hp2 | a0001 | c0001 | t0009 | g0235 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18995 | hp2 | a0006 | c0006 | t0003 | g0052 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19000 | hp2 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19005 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19012 | hp2 | a0009 | c0010 | t0002 | g0101 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0321 | AFR | LWK | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19030 | hp2 | a0010 | c0011 | t0003 | g0217 | AFR | LWK | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19043 | hp1 | a0004 | c0003 | t0002 | g0113 | AFR | LWK | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0227 | AFR | LWK | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19056 | hp1 | a0001 | c0001 | t0007 | g0189 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19060 | hp2 | a0011 | c0012 | t0003 | g0071 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19068 | hp2 | a0001 | c0001 | t0007 | g0231 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19074 | hp1 | a0002 | c0002 | t0015 | g0319 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19077 | hp2 | a0006 | c0006 | t0003 | g0054 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA20129 | hp1 | a0005 | c0005 | t0014 | g0080 | AFR | ASW | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | ASW | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0186 | SAS | GIH | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0248 | SAS | GIH | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0312 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0205 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0083 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0295 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0226 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02559 | hp2 | a0005 | c0005 | t0025 | g0081 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0223 | AFR | USA | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0244 | AFR | USA | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA20300 | hp1 | a0001 | c0008 | t0020 | g0211 | AFR | USA | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0311 | AFR | USA | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0222 | AFR | LWK | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | LWK | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0029 | g0156 | REF | REF | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0159 | REF | REF | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:28113427 | C | A | 9 | a0001 a0004 a0005 others(6): Show |
240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): Show |
missense_variant | MODERATE | c.93C>A | p.Asn31Lys | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/7 | 411/4208 | 93/1224 | 31/407 | chr11 | 28113427 | |||
| chr11:28113470 | C | T | 1 | a0008 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.136C>T | p.Arg46Trp | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/7 | 454/4208 | 136/1224 | 46/407 | chr11 | 28113470 | |||
| chr11:28113533 | A | G | 1 | a0011 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.199A>G | p.Thr67Ala | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/7 | 517/4208 | 199/1224 | 67/407 | chr11 | 28113533 | |||
| chr11:28290243 | G | A | 1 | a0003 | 6 | HG01891.hp2 HG02109.hp2 HG02976.hp1 others(3): Show |
missense_variant | MODERATE | c.445G>A | p.Ala149Thr | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/7 | 763/4208 | 445/1224 | 149/407 | chr11 | 28290243 | |||
| chr11:28330416 | A | T | 1 | a0004 | 6 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
missense_variant | MODERATE | c.799A>T | p.Ile267Phe | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1117/4208 | 799/1224 | 267/407 | chr11 | 28330416 | |||
| chr11:28330446 | T | A | 1 | a0006 | 2 | NA18995.hp2 NA19077.hp2 |
missense_variant | MODERATE | c.829T>A | p.Ser277Thr | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1147/4208 | 829/1224 | 277/407 | chr11 | 28330446 | |||
| chr11:28330450 | C | G | 1 | a0010 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.833C>G | p.Thr278Ser | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1151/4208 | 833/1224 | 278/407 | chr11 | 28330450 | |||
| chr11:28330482 | C | T | 1 | a0009 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.865C>T | p.Arg289Cys | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1183/4208 | 865/1224 | 289/407 | chr11 | 28330482 | |||
| chr11:28330629 | A | T | 1 | a0007 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.1012A>T | p.Met338Leu | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1330/4208 | 1012/1224 | 338/407 | chr11 | 28330629 | |||
| chr11:28330807 | G | A | 2 | a0005 a0010 |
4 | HG02559.hp2 HG02622.hp1 NA19030.hp2 others(1): Show |
missense_variant | MODERATE | c.1190G>A | p.Arg397His | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1508/4208 | 1190/1224 | 397/407 | chr11 | 28330807 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:28113382 | A | C | 1 | a0001c0014 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.48A>C | p.Ser16Ser | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/7 | 366/4208 | 48/1224 | 16/407 | chr11 | 28113382 | |||
| chr11:28330682 | A | G | 1 | a0001c0008 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1065A>G | p.Gln355Gln | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1383/4208 | 1065/1224 | 355/407 | chr11 | 28330682 | |||
| chr11:28330697 | C | T | 1 | a0001c0007 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.1080C>T | p.His360His | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1398/4208 | 1080/1224 | 360/407 | chr11 | 28330697 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:28108392 | A | G | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0028 others(2): Show |
77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-314A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/7 | 4943 | chr11 | 28108392 | ||||||
| chr11:28108435 | C | A | 27 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(24): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
5_prime_UTR_variant | MODIFIER | c.-271C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/7 | 4900 | chr11 | 28108435 | ||||||
| chr11:28110169 | A | G | 2 | a0005c0005t0014 a0005c0005t0025 |
3 | HG02559.hp2 HG02622.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-250A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/7 | 3166 | chr11 | 28110169 | ||||||
| chr11:28331126 | T | C | 1 | a0001c0001t0016 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*285T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 285 | chr11 | 28331126 | ||||||
| chr11:28331221 | A | T | 1 | a0001c0001t0024 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*380A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 380 | chr11 | 28331221 | ||||||
| chr11:28331254 | A | G | 4 | a0001c0001t0012 a0001c0001t0023 a0005c0005t0014 others(1): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*413A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 413 | chr11 | 28331254 | ||||||
| chr11:28331505 | T | C | 1 | a0001c0001t0017 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*664T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 664 | chr11 | 28331505 | ||||||
| chr11:28332080 | AATAG | A | 14 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0012 others(11): Show |
81 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1245_*1248delTAGA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1245 | INFO_REALIGN_3_PRIME | chr11 | 28332080 | |||||
| chr11:28332201 | C | G | 1 | a0002c0002t0015 | 2 | NA18957.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1360C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1360 | chr11 | 28332201 | ||||||
| chr11:28332555 | T | A | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(25): Show |
163 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1714T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1714 | chr11 | 28332555 | ||||||
| chr11:28332579 | G | C | 1 | a0001c0001t0019 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1738G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1738 | chr11 | 28332579 | ||||||
| chr11:28332676 | G | C | 1 | a0002c0002t0026 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1835G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 1835 | chr11 | 28332676 | ||||||
| chr11:28332923 | C | T | 1 | a0001c0001t0022 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2082C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2082 | chr11 | 28332923 | ||||||
| chr11:28332936 | C | CAAAAAAA | 2 | a0001c0001t0006 a0001c0001t0017 |
13 | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2106_*2112dupAAAA others(3): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2113 | INFO_REALIGN_3_PRIME | chr11 | 28332936 | |||||
| chr11:28332936 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0018 others(4): Show |
47 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2105_*2112dupAAAA others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2113 | INFO_REALIGN_3_PRIME | chr11 | 28332936 | |||||
| chr11:28332936 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0012 others(6): Show |
72 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2104_*2112dupAAAA others(5): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2113 | INFO_REALIGN_3_PRIME | chr11 | 28332936 | |||||
| chr11:28332936 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0016 others(2): Show |
22 | HG00544.hp2 HG00621.hp2 HG01361.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2103_*2112dupAAAA others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2113 | INFO_REALIGN_3_PRIME | chr11 | 28332936 | |||||
| chr11:28332936 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0013 a0005c0005t0025 |
3 | HG02559.hp2 NA18968.hp2 NA18978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2102_*2112dupAAAA others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2113 | INFO_REALIGN_3_PRIME | chr11 | 28332936 | |||||
| chr11:28332953 | A | AG | 4 | a0001c0001t0002 a0001c0001t0028 a0004c0003t0002 others(1): Show |
72 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2114dupG | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2115 | INFO_REALIGN_3_PRIME | chr11 | 28332953 | |||||
| chr11:28332954 | G | A | 1 | a0001c0014t0021 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2113G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2113 | chr11 | 28332954 | ||||||
| chr11:28333239 | C | G | 1 | a0001c0014t0021 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2398C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2398 | chr11 | 28333239 | ||||||
| chr11:28333365 | A | G | 1 | a0003c0004t0027 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2524A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2524 | chr11 | 28333365 | ||||||
| chr11:28333441 | C | T | 3 | a0001c0001t0008 a0001c0001t0019 a0001c0008t0020 |
9 | HG00735.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2600C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2600 | chr11 | 28333441 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:28108561 | T | A | 2 | a0001c0001t0002g0005 a0001c0001t0002g0006 |
2 | HG01952.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-254+109T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28108561 | |||||||
| chr11:28108587 | T | C | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.-254+135T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28108587 | |||||||
| chr11:28108928 | A | C | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-254+476A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28108928 | |||||||
| chr11:28109071 | A | G | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.-254+619A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28109071 | |||||||
| chr11:28109110 | C | T | 3 | a0001c0001t0007g0240 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-254+658C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28109110 | |||||||
| chr11:28109691 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-253-475A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28109691 | |||||||
| chr11:28109773 | T | C | 1 | a0001c0001t0008g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-253-393T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28109773 | |||||||
| chr11:28109900 | A | G | 1 | a0001c0001t0004g0238 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-253-266A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28109900 | |||||||
| chr11:28109912 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-253-254G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28109912 | |||||||
| chr11:28109969 | C | T | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-253-197C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28109969 | |||||||
| chr11:28110134 | G | A | 1 | a0002c0002t0001g0243 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-253-32G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 1/6 | chr11 | 28110134 | |||||||
| chr11:28110562 | C | T | 8 | a0001c0001t0004g0232 a0001c0001t0006g0230 a0001c0001t0007g0231 others(5): Show |
8 | HG00621.hp1 HG00673.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+161C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28110562 | |||||||
| chr11:28110624 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-18+223T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28110624 | |||||||
| chr11:28110721 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-18+320A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28110721 | |||||||
| chr11:28110825 | A | G | 1 | a0001c0001t0003g0082 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-18+424A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28110825 | |||||||
| chr11:28110853 | A | G | 1 | a0002c0002t0026g0326 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-18+452A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28110853 | |||||||
| chr11:28110979 | C | G | 1 | a0001c0001t0004g0228 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18+578C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28110979 | |||||||
| chr11:28111200 | A | G | 10 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(7): Show |
10 | HG02559.hp1 HG02818.hp1 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+799A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28111200 | |||||||
| chr11:28111249 | G | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18+848G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28111249 | |||||||
| chr11:28111257 | T | C | 1 | a0002c0002t0001g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+856T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28111257 | |||||||
| chr11:28111277 | T | C | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.-18+876T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28111277 | |||||||
| chr11:28111593 | T | C | 1 | a0004c0003t0002g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-18+1192T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28111593 | |||||||
| chr11:28111873 | A | G | 42 | a0001c0001t0002g0085 a0001c0001t0002g0115 a0001c0001t0002g0116 others(39): Show |
42 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-17-1445A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28111873 | |||||||
| chr11:28111964 | C | T | 1 | a0002c0002t0001g0325 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-17-1354C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28111964 | |||||||
| chr11:28112298 | A | G | 1 | a0002c0002t0001g0324 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-17-1020A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28112298 | |||||||
| chr11:28112390 | G | A | 1 | a0001c0001t0022g0157 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-17-928G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28112390 | |||||||
| chr11:28112405 | T | G | 1 | a0001c0001t0004g0158 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-17-913T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28112405 | |||||||
| chr11:28112752 | A | C | 3 | a0002c0002t0001g0004 a0002c0002t0001g0322 a0002c0002t0001g0323 |
4 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-566A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28112752 | |||||||
| chr11:28112802 | C | T | 3 | a0005c0005t0014g0079 a0005c0005t0014g0080 a0005c0005t0025g0081 |
3 | HG02559.hp2 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-17-516C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28112802 | |||||||
| chr11:28112825 | C | G | 2 | a0002c0002t0001g0320 a0002c0002t0001g0321 |
2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-17-493C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28112825 | |||||||
| chr11:28112980 | C | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-17-338C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 2/6 | chr11 | 28112980 | |||||||
| chr11:28113621 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.270+17T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28113621 | |||||||
| chr11:28113808 | G | T | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+204G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28113808 | |||||||
| chr11:28113898 | C | T | 1 | a0001c0001t0002g0114 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.270+294C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28113898 | |||||||
| chr11:28114274 | T | A | 1 | a0001c0001t0002g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.270+670T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28114274 | |||||||
| chr11:28114381 | G | C | 1 | a0002c0002t0001g0246 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.270+777G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28114381 | |||||||
| chr11:28114709 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+1105C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28114709 | |||||||
| chr11:28114886 | A | G | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+1282A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28114886 | |||||||
| chr11:28114991 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270+1387G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28114991 | |||||||
| chr11:28115199 | A | G | 62 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(59): Show |
62 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.270+1595A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28115199 | |||||||
| chr11:28115264 | C | CT | 7 | a0001c0001t0002g0239 a0004c0003t0002g0086 a0004c0003t0002g0109 others(4): Show |
7 | HG00642.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1671dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28115264 | ||||||
| chr11:28115278 | G | A | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+1674G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28115278 | |||||||
| chr11:28115301 | C | G | 2 | a0002c0002t0015g0318 a0002c0002t0015g0319 |
2 | NA18957.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.270+1697C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28115301 | |||||||
| chr11:28115588 | T | G | 5 | a0001c0001t0007g0168 a0001c0001t0009g0165 a0001c0001t0009g0166 others(2): Show |
5 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+1984T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28115588 | |||||||
| chr11:28115661 | T | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.270+2057T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28115661 | |||||||
| chr11:28115809 | G | A | 1 | a0002c0002t0001g0247 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.270+2205G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28115809 | |||||||
| chr11:28115935 | T | TAC | 164 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0085 others(161): Show |
166 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.270+2361_270+2362d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28115935 | ||||||
| chr11:28115935 | T | TACAC | 18 | a0001c0001t0002g0084 a0001c0001t0002g0097 a0001c0001t0002g0104 others(15): Show |
18 | HG01433.hp2 HG02027.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.270+2359_270+2362d others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28115935 | ||||||
| chr11:28115935 | T | TACACACA others(1): Show |
4 | a0001c0001t0007g0240 a0001c0001t0011g0241 a0001c0001t0011g0242 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+2355_270+2362d others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28115935 | ||||||
| chr11:28115935 | TAC | T | 4 | a0001c0001t0001g0214 a0001c0001t0003g0008 a0002c0002t0001g0264 others(1): Show |
4 | HG01496.hp1 HG02602.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+2361_270+2362d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28115935 | ||||||
| chr11:28115953 | C | G | 1 | a0005c0005t0025g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.270+2349C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28115953 | |||||||
| chr11:28116246 | T | C | 1 | a0001c0001t0010g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.270+2642T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28116246 | |||||||
| chr11:28116292 | C | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.270+2688C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28116292 | |||||||
| chr11:28116406 | T | C | 90 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(87): Show |
92 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.270+2802T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28116406 | |||||||
| chr11:28116495 | G | A | 1 | a0002c0002t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.270+2891G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28116495 | |||||||
| chr11:28116664 | A | T | 1 | a0001c0001t0004g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.270+3060A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28116664 | |||||||
| chr11:28116667 | C | T | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+3063C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28116667 | |||||||
| chr11:28116763 | A | T | 1 | a0004c0003t0002g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.270+3159A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28116763 | |||||||
| chr11:28117201 | G | A | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+3597G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117201 | |||||||
| chr11:28117204 | T | C | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 |
3 | NA18981.hp1 NA18994.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.270+3600T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117204 | |||||||
| chr11:28117225 | CTATA | C | 29 | a0001c0001t0004g0158 a0001c0001t0004g0199 a0001c0001t0004g0200 others(26): Show |
29 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.270+3625_270+3628d others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117225 | ||||||
| chr11:28117229 | A | G | 51 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(48): Show |
51 | HG00735.hp1 HG01243.hp2 HG01517.hp1 others(48): Show |
intron_variant | MODIFIER | c.270+3625A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117229 | |||||||
| chr11:28117233 | GTA | G | 17 | a0001c0001t0004g0164 a0001c0001t0004g0174 a0001c0001t0004g0188 others(14): Show |
17 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+3631_270+3632d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117233 | ||||||
| chr11:28117235 | A | ATG | 20 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(17): Show |
21 | HG00423.hp1 HG00544.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.270+3655_270+3656d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117235 | ||||||
| chr11:28117235 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0003g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.270+3645_270+3656d others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117235 | ||||||
| chr11:28117235 | A | G | 113 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(110): Show |
113 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.270+3631A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117235 | |||||||
| chr11:28117243 | G | T | 33 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(30): Show |
33 | HG00735.hp1 HG01517.hp1 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.270+3639G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117243 | |||||||
| chr11:28117245 | G | T | 17 | a0001c0001t0004g0164 a0001c0001t0004g0174 a0001c0001t0004g0188 others(14): Show |
17 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+3641G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117245 | |||||||
| chr11:28117247 | G | T | 29 | a0001c0001t0004g0158 a0001c0001t0004g0199 a0001c0001t0004g0200 others(26): Show |
29 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.270+3643G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117247 | |||||||
| chr11:28117259 | GTA | G | 20 | a0001c0001t0003g0039 a0001c0001t0003g0045 a0001c0001t0003g0046 others(17): Show |
20 | HG00621.hp2 HG02451.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+3695_270+3696d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117259 | ||||||
| chr11:28117259 | GTATA | G | 17 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0047 others(14): Show |
18 | HG02735.hp1 HG06807.hp2 NA18612.hp2 others(15): Show |
intron_variant | MODIFIER | c.270+3693_270+3696d others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117259 | ||||||
| chr11:28117259 | GTATATA | G | 34 | a0001c0001t0002g0085 a0001c0001t0003g0041 a0001c0001t0003g0042 others(31): Show |
34 | HG00673.hp2 HG01517.hp1 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+3691_270+3696d others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117259 | ||||||
| chr11:28117259 | GTATATAT others(1): Show |
G | 37 | a0001c0001t0002g0106 a0001c0001t0004g0186 a0001c0001t0004g0187 others(34): Show |
38 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3689_270+3696d others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117259 | ||||||
| chr11:28117259 | GTATATAT others(3): Show |
G | 58 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0115 others(55): Show |
59 | HG00423.hp2 HG00609.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.270+3687_270+3696d others(12): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117259 | ||||||
| chr11:28117259 | GTATATAT others(5): Show |
G | 46 | a0001c0001t0002g0084 a0001c0001t0002g0090 a0001c0001t0002g0099 others(43): Show |
46 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.270+3685_270+3696d others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117259 | ||||||
| chr11:28117259 | GTATATAT others(7): Show |
G | 11 | a0001c0001t0001g0214 a0001c0001t0002g0088 a0001c0001t0002g0089 others(8): Show |
11 | HG01496.hp1 HG02165.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.270+3683_270+3696d others(16): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117259 | ||||||
| chr11:28117259 | GTATATAT others(9): Show |
G | 11 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(8): Show |
11 | HG00544.hp1 HG00642.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.270+3681_270+3696d others(18): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28117259 | ||||||
| chr11:28117261 | A | G | 91 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(88): Show |
92 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.270+3657A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117261 | |||||||
| chr11:28117263 | A | G | 110 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0009 others(107): Show |
111 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.270+3659A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117263 | |||||||
| chr11:28117265 | A | G | 118 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(115): Show |
120 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.270+3661A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117265 | |||||||
| chr11:28117267 | A | G | 137 | a0001c0001t0002g0085 a0001c0001t0003g0001 a0001c0001t0003g0002 others(134): Show |
139 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.270+3663A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117267 | |||||||
| chr11:28117269 | A | G | 144 | a0001c0001t0002g0085 a0001c0001t0002g0106 a0001c0001t0003g0001 others(141): Show |
147 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.270+3665A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117269 | |||||||
| chr11:28117271 | A | G | 158 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0085 others(155): Show |
161 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.270+3667A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117271 | |||||||
| chr11:28117273 | A | G | 182 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(179): Show |
185 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.270+3669A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117273 | |||||||
| chr11:28117275 | A | G | 121 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(118): Show |
121 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.270+3671A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117275 | |||||||
| chr11:28117277 | A | G | 82 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(79): Show |
82 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.270+3673A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117277 | |||||||
| chr11:28117279 | A | G | 80 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
80 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.270+3675A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117279 | |||||||
| chr11:28117281 | A | G | 78 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+3677A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117281 | |||||||
| chr11:28117283 | A | G | 74 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(71): Show |
74 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.270+3679A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117283 | |||||||
| chr11:28117285 | A | G | 30 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0088 others(27): Show |
30 | HG00544.hp1 HG01952.hp2 HG01993.hp1 others(27): Show |
intron_variant | MODIFIER | c.270+3681A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117285 | |||||||
| chr11:28117287 | A | G | 10 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(7): Show |
10 | HG00544.hp1 HG02040.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.270+3683A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117287 | |||||||
| chr11:28117299 | A | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+3695A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117299 | |||||||
| chr11:28117463 | A | C | 1 | a0001c0001t0003g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.270+3859A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117463 | |||||||
| chr11:28117468 | T | C | 1 | a0002c0002t0001g0278 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.270+3864T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117468 | |||||||
| chr11:28117489 | A | T | 1 | a0001c0001t0002g0239 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.270+3885A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117489 | |||||||
| chr11:28117558 | A | G | 2 | a0002c0002t0015g0318 a0002c0002t0015g0319 |
2 | NA18957.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.270+3954A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117558 | |||||||
| chr11:28117677 | C | T | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+4073C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117677 | |||||||
| chr11:28117835 | T | C | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+4231T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117835 | |||||||
| chr11:28118012 | T | G | 1 | a0002c0002t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.270+4408T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118012 | |||||||
| chr11:28118041 | C | T | 1 | a0002c0002t0001g0311 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.270+4437C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118041 | |||||||
| chr11:28118072 | A | G | 238 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(235): Show |
240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.270+4468A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118072 | |||||||
| chr11:28118207 | A | G | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+4603A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118207 | |||||||
| chr11:28118340 | T | C | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+4736T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118340 | |||||||
| chr11:28118494 | T | C | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.270+4890T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118494 | |||||||
| chr11:28118573 | A | G | 3 | a0002c0002t0001g0004 a0002c0002t0001g0322 a0002c0002t0001g0323 |
4 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+4969A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118573 | |||||||
| chr11:28119455 | G | A | 62 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(59): Show |
62 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.270+5851G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28119455 | |||||||
| chr11:28119494 | GA | G | 5 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0143 others(2): Show |
5 | HG00609.hp1 HG02523.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+5896delA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28119494 | ||||||
| chr11:28119539 | G | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.270+5935G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28119539 | |||||||
| chr11:28119612 | T | C | 1 | a0001c0001t0002g0122 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.270+6008T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28119612 | |||||||
| chr11:28119763 | G | A | 1 | a0002c0002t0001g0320 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.270+6159G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28119763 | |||||||
| chr11:28119814 | A | G | 2 | a0002c0002t0001g0276 a0002c0002t0001g0277 |
2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.270+6210A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28119814 | |||||||
| chr11:28119861 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.270+6257A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28119861 | |||||||
| chr11:28119934 | A | G | 1 | a0001c0001t0012g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.270+6330A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28119934 | |||||||
| chr11:28120078 | A | C | 1 | a0002c0002t0015g0319 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.270+6474A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28120078 | |||||||
| chr11:28120146 | G | A | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.270+6542G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28120146 | |||||||
| chr11:28120251 | C | CT | 6 | a0001c0001t0002g0122 a0001c0001t0002g0155 a0001c0001t0003g0026 others(3): Show |
6 | HG00544.hp2 HG00621.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+6662dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28120251 | ||||||
| chr11:28120251 | CT | C | 6 | a0001c0001t0003g0027 a0001c0001t0004g0161 a0001c0001t0004g0162 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+6662delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28120251 | ||||||
| chr11:28120413 | T | C | 5 | a0002c0002t0001g0279 a0002c0002t0001g0280 a0002c0002t0001g0281 others(2): Show |
5 | HG00733.hp2 HG01081.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+6809T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28120413 | |||||||
| chr11:28120556 | T | G | 1 | a0001c0001t0002g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.270+6952T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28120556 | |||||||
| chr11:28120591 | G | A | 1 | a0005c0005t0025g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.270+6987G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28120591 | |||||||
| chr11:28120834 | T | G | 3 | a0001c0001t0007g0240 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.270+7230T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28120834 | |||||||
| chr11:28120860 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.270+7256C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28120860 | |||||||
| chr11:28120861 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.270+7257C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28120861 | |||||||
| chr11:28120867 | T | A | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.270+7263T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28120867 | |||||||
| chr11:28120940 | C | T | 1 | a0002c0002t0001g0325 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.270+7336C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28120940 | |||||||
| chr11:28121126 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+7522C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28121126 | |||||||
| chr11:28121567 | C | A | 62 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(59): Show |
62 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.270+7963C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28121567 | |||||||
| chr11:28121765 | A | G | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.270+8161A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28121765 | |||||||
| chr11:28121775 | TATGTGTT others(10): Show |
T | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.270+8174_270+8190d others(19): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28121775 | ||||||
| chr11:28122185 | A | G | 18 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0212 others(15): Show |
18 | HG00735.hp1 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.270+8581A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122185 | |||||||
| chr11:28122247 | A | G | 1 | a0002c0002t0001g0310 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.270+8643A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122247 | |||||||
| chr11:28122329 | G | GTA | 28 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(25): Show |
28 | HG00544.hp1 HG00642.hp2 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.270+8729_270+8730d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122329 | ||||||
| chr11:28122333 | A | ATATG | 24 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0103 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.270+8730_270+8731i others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122333 | ||||||
| chr11:28122333 | A | ATATGTG | 4 | a0001c0001t0002g0121 a0001c0001t0002g0143 a0001c0001t0002g0144 others(1): Show |
4 | HG00609.hp1 HG03927.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+8730_270+8731i others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122333 | ||||||
| chr11:28122333 | A | ATG | 49 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0244 others(46): Show |
51 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.270+8767_270+8768d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122333 | ||||||
| chr11:28122333 | A | ATGTG | 20 | a0001c0001t0002g0085 a0002c0002t0001g0246 a0002c0002t0001g0251 others(17): Show |
20 | HG02602.hp1 HG02698.hp1 HG02976.hp1 others(17): Show |
intron_variant | MODIFIER | c.270+8765_270+8768d others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122333 | ||||||
| chr11:28122333 | A | ATGTGTG | 3 | a0002c0002t0001g0272 a0002c0002t0001g0273 a0002c0002t0001g0274 |
3 | HG02056.hp1 NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.270+8763_270+8768d others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122333 | ||||||
| chr11:28122333 | ATG | A | 4 | a0002c0002t0001g0243 a0002c0002t0001g0275 a0002c0002t0001g0311 others(1): Show |
4 | HG00597.hp1 HG03453.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+8767_270+8768d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122333 | ||||||
| chr11:28122333 | ATGTGTGT others(3): Show |
A | 5 | a0001c0001t0003g0002 a0001c0001t0003g0047 a0001c0001t0003g0049 others(2): Show |
6 | NA18964.hp2 NA18983.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+8759_270+8768d others(12): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122333 | ||||||
| chr11:28122333 | ATGTGTGT others(7): Show |
A | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+8755_270+8768d others(16): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122333 | ||||||
| chr11:28122335 | G | A | 171 | a0001c0001t0001g0214 a0001c0001t0002g0095 a0001c0001t0002g0115 others(168): Show |
172 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.270+8731G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122335 | |||||||
| chr11:28122336 | T | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.270+8732T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122336 | |||||||
| chr11:28122345 | G | A | 5 | a0001c0001t0003g0002 a0001c0001t0003g0047 a0001c0001t0003g0049 others(2): Show |
6 | NA18964.hp2 NA18983.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+8741G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122345 | |||||||
| chr11:28122349 | G | A | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+8745G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122349 | |||||||
| chr11:28122359 | GTGTGTGT others(7): Show |
G | 56 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(53): Show |
56 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.270+8757_270+8770d others(16): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122359 | ||||||
| chr11:28122361 | GTGTGTGT others(5): Show |
G | 63 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0011 others(60): Show |
64 | HG00544.hp2 HG00621.hp2 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.270+8759_270+8770d others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122361 | ||||||
| chr11:28122361 | GTGTGTGT others(7): Show |
G | 16 | a0001c0001t0004g0176 a0001c0001t0004g0180 a0001c0001t0004g0207 others(13): Show |
16 | HG02559.hp1 HG02818.hp1 HG02922.hp1 others(13): Show |
intron_variant | MODIFIER | c.270+8759_270+8772d others(16): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122361 | ||||||
| chr11:28122363 | GTGTGTGT others(3): Show |
G | 16 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0026 others(13): Show |
16 | HG00423.hp1 HG01361.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+8761_270+8770d others(12): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122363 | ||||||
| chr11:28122363 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.270+8761_270+8772d others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122363 | ||||||
| chr11:28122371 | GTA | G | 11 | a0001c0001t0002g0116 a0001c0001t0002g0125 a0001c0001t0002g0126 others(8): Show |
11 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.270+8784_270+8785d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28122371 | ||||||
| chr11:28122373 | A | G | 68 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
68 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.270+8769A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122373 | |||||||
| chr11:28122375 | A | G | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.270+8771A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122375 | |||||||
| chr11:28122377 | A | G | 20 | a0001c0001t0002g0116 a0001c0001t0002g0123 a0001c0001t0002g0124 others(17): Show |
20 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.270+8773A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122377 | |||||||
| chr11:28122379 | A | G | 2 | a0001c0001t0002g0123 a0004c0003t0002g0111 |
2 | HG02572.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.270+8775A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122379 | |||||||
| chr11:28122477 | A | G | 1 | a0001c0001t0003g0025 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.270+8873A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122477 | |||||||
| chr11:28122764 | G | C | 1 | a0001c0001t0003g0076 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.270+9160G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122764 | |||||||
| chr11:28123027 | G | A | 1 | a0002c0002t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.270+9423G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28123027 | |||||||
| chr11:28123038 | A | G | 1 | a0001c0001t0002g0106 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.270+9434A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28123038 | |||||||
| chr11:28123071 | T | C | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.270+9467T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28123071 | |||||||
| chr11:28123199 | C | T | 1 | a0001c0001t0004g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.270+9595C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28123199 | |||||||
| chr11:28123568 | A | ATATCATT | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.270+9966_270+9967i others(9): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28123568 | ||||||
| chr11:28123734 | A | T | 6 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+10130A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28123734 | |||||||
| chr11:28123778 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.270+10174A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28123778 | |||||||
| chr11:28123963 | A | G | 1 | a0004c0003t0002g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.270+10359A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28123963 | |||||||
| chr11:28124210 | T | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
2 | HG00738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.270+10606T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28124210 | |||||||
| chr11:28124222 | C | G | 159 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(156): Show |
161 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.270+10618C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28124222 | |||||||
| chr11:28124239 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270+10635A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28124239 | |||||||
| chr11:28124524 | T | G | 6 | a0001c0001t0003g0058 a0001c0001t0003g0059 a0001c0001t0003g0060 others(3): Show |
6 | HG00673.hp2 HG02040.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+10920T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28124524 | |||||||
| chr11:28124556 | C | T | 1 | a0001c0001t0008g0195 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.270+10952C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28124556 | |||||||
| chr11:28124570 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270+10966A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28124570 | |||||||
| chr11:28124589 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.270+10985G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28124589 | |||||||
| chr11:28124729 | G | T | 1 | a0002c0002t0001g0308 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.270+11125G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28124729 | |||||||
| chr11:28125301 | A | G | 1 | a0001c0001t0003g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.270+11697A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28125301 | |||||||
| chr11:28125380 | GAAATCTG others(3): Show |
G | 2 | a0001c0001t0004g0176 a0001c0001t0004g0207 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.270+11778_270+1178 others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28125380 | ||||||
| chr11:28125509 | G | A | 4 | a0002c0002t0001g0004 a0002c0002t0001g0275 a0002c0002t0001g0322 others(1): Show |
5 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+11905G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28125509 | |||||||
| chr11:28125511 | GTATTC | G | 4 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(1): Show |
4 | HG00544.hp1 HG02040.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+11914_270+1191 others(9): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28125511 | ||||||
| chr11:28125675 | A | T | 8 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(5): Show |
8 | HG02717.hp2 HG02886.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.270+12071A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28125675 | |||||||
| chr11:28125683 | C | T | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.270+12079C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28125683 | |||||||
| chr11:28125859 | C | T | 3 | a0001c0001t0007g0240 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.270+12255C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28125859 | |||||||
| chr11:28126043 | C | T | 31 | a0001c0001t0004g0158 a0001c0001t0004g0175 a0001c0001t0004g0178 others(28): Show |
31 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.270+12439C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28126043 | |||||||
| chr11:28126044 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+12440G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28126044 | |||||||
| chr11:28126091 | G | A | 1 | a0001c0001t0023g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.270+12487G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28126091 | |||||||
| chr11:28126220 | C | G | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.270+12616C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28126220 | |||||||
| chr11:28126375 | C | A | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+12771C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28126375 | |||||||
| chr11:28126443 | C | T | 2 | a0002c0002t0001g0320 a0002c0002t0001g0321 |
2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.270+12839C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28126443 | |||||||
| chr11:28126477 | C | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+12873C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28126477 | |||||||
| chr11:28126546 | T | C | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+12942T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28126546 | |||||||
| chr11:28126709 | A | G | 1 | a0002c0002t0001g0307 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.270+13105A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28126709 | |||||||
| chr11:28126771 | G | T | 1 | a0002c0002t0026g0326 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.270+13167G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28126771 | |||||||
| chr11:28127007 | C | G | 2 | a0001c0001t0004g0176 a0001c0001t0004g0207 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.270+13403C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28127007 | |||||||
| chr11:28127429 | TC | T | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.270+13827delC | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28127429 | ||||||
| chr11:28127462 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.270+13858A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28127462 | |||||||
| chr11:28127530 | G | T | 69 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(66): Show |
69 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.270+13926G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28127530 | |||||||
| chr11:28128679 | C | G | 1 | a0001c0001t0002g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.270+15075C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28128679 | |||||||
| chr11:28128888 | T | C | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+15284T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28128888 | |||||||
| chr11:28128962 | A | T | 1 | a0002c0002t0001g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.270+15358A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28128962 | |||||||
| chr11:28129407 | CT | C | 81 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(78): Show |
81 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.270+15818delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28129407 | ||||||
| chr11:28129433 | G | A | 1 | a0003c0004t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+15829G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28129433 | |||||||
| chr11:28129490 | A | G | 4 | a0002c0002t0001g0003 a0002c0002t0001g0245 a0002c0002t0001g0306 others(1): Show |
5 | HG02132.hp2 NA18979.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+15886A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28129490 | |||||||
| chr11:28129651 | C | T | 1 | a0001c0001t0004g0228 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.270+16047C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28129651 | |||||||
| chr11:28129657 | G | C | 3 | a0001c0001t0007g0240 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.270+16053G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28129657 | |||||||
| chr11:28129770 | A | G | 1 | a0002c0002t0001g0245 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.270+16166A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28129770 | |||||||
| chr11:28129823 | T | A | 1 | a0001c0001t0007g0231 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.270+16219T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28129823 | |||||||
| chr11:28129866 | A | G | 2 | a0001c0001t0002g0121 a0001c0001t0002g0155 |
2 | NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.270+16262A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28129866 | |||||||
| chr11:28129949 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+16345C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28129949 | |||||||
| chr11:28130021 | C | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+16417C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28130021 | |||||||
| chr11:28130062 | C | A | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.270+16458C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28130062 | |||||||
| chr11:28130107 | C | T | 1 | a0001c0001t0003g0039 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.270+16503C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28130107 | |||||||
| chr11:28130316 | A | C | 1 | a0002c0002t0001g0325 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.270+16712A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28130316 | |||||||
| chr11:28130491 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.270+16887A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28130491 | |||||||
| chr11:28130605 | CTG | C | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.270+17002_270+1700 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28130605 | |||||||
| chr11:28130619 | G | A | 1 | a0001c0001t0003g0051 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.270+17015G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28130619 | |||||||
| chr11:28130675 | C | T | 1 | a0001c0001t0005g0056 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.270+17071C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28130675 | |||||||
| chr11:28130740 | A | T | 1 | a0004c0003t0002g0113 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.270+17136A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28130740 | |||||||
| chr11:28130849 | G | A | 3 | a0005c0005t0014g0079 a0005c0005t0014g0080 a0005c0005t0025g0081 |
3 | HG02559.hp2 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.270+17245G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28130849 | |||||||
| chr11:28131044 | C | T | 1 | a0001c0001t0004g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.270+17440C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28131044 | |||||||
| chr11:28131075 | T | A | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+17471T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28131075 | |||||||
| chr11:28131193 | A | G | 1 | a0002c0002t0001g0262 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.270+17589A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28131193 | |||||||
| chr11:28131299 | A | G | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.270+17695A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28131299 | |||||||
| chr11:28131382 | G | T | 1 | a0001c0001t0002g0006 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.270+17778G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28131382 | |||||||
| chr11:28131428 | G | C | 3 | a0005c0005t0014g0079 a0005c0005t0014g0080 a0005c0005t0025g0081 |
3 | HG02559.hp2 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.270+17824G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28131428 | |||||||
| chr11:28131501 | A | AT | 146 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(143): Show |
148 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.270+17917dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28131501 | ||||||
| chr11:28131501 | A | ATT | 21 | a0001c0001t0002g0090 a0001c0001t0002g0102 a0001c0001t0002g0108 others(18): Show |
21 | HG00597.hp2 HG01123.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.270+17916_270+1791 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28131501 | ||||||
| chr11:28131501 | AT | A | 71 | a0001c0001t0004g0158 a0001c0001t0004g0164 a0001c0001t0004g0170 others(68): Show |
71 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.270+17917delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28131501 | ||||||
| chr11:28131537 | T | C | 1 | a0002c0002t0001g0291 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.270+17933T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28131537 | |||||||
| chr11:28131564 | G | A | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+17960G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28131564 | |||||||
| chr11:28131887 | T | C | 1 | a0001c0001t0003g0021 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.270+18283T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28131887 | |||||||
| chr11:28132298 | A | G | 1 | a0001c0007t0003g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.270+18694A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28132298 | |||||||
| chr11:28132424 | A | G | 1 | a0002c0002t0001g0250 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.270+18820A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28132424 | |||||||
| chr11:28132499 | TTC | T | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.270+18905_270+1890 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28132499 | ||||||
| chr11:28132547 | C | G | 1 | a0001c0001t0005g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.270+18943C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28132547 | |||||||
| chr11:28132585 | G | A | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+18981G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28132585 | |||||||
| chr11:28132602 | A | G | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.270+18998A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28132602 | |||||||
| chr11:28133005 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+19401C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133005 | |||||||
| chr11:28133124 | C | T | 1 | a0001c0001t0004g0174 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.270+19520C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133124 | |||||||
| chr11:28133145 | A | T | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.270+19541A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133145 | |||||||
| chr11:28133394 | A | G | 2 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
2 | HG00738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.270+19790A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133394 | |||||||
| chr11:28133602 | G | C | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+19998G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133602 | |||||||
| chr11:28133643 | G | T | 1 | a0002c0002t0001g0314 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.270+20039G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133643 | |||||||
| chr11:28133709 | C | T | 1 | a0001c0001t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.270+20105C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133709 | |||||||
| chr11:28133768 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.270+20164T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133768 | |||||||
| chr11:28133778 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.270+20174C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133778 | |||||||
| chr11:28133982 | T | C | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.270+20378T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133982 | |||||||
| chr11:28134202 | G | A | 1 | a0002c0002t0001g0250 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.270+20598G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28134202 | |||||||
| chr11:28134621 | A | C | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+21017A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28134621 | |||||||
| chr11:28134661 | C | T | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.270+21057C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28134661 | |||||||
| chr11:28134771 | C | T | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+21167C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28134771 | |||||||
| chr11:28134782 | G | C | 3 | a0001c0001t0004g0158 a0001c0001t0004g0199 a0001c0001t0007g0198 |
3 | HG02074.hp1 HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.270+21178G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28134782 | |||||||
| chr11:28134852 | T | C | 1 | a0002c0002t0001g0293 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.270+21248T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28134852 | |||||||
| chr11:28134889 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.270+21285G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28134889 | |||||||
| chr11:28135035 | A | G | 1 | a0003c0004t0001g0305 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.270+21431A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28135035 | |||||||
| chr11:28135051 | T | C | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.270+21447T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28135051 | |||||||
| chr11:28135162 | T | C | 2 | a0001c0001t0004g0186 a0001c0001t0004g0187 |
2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.270+21558T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28135162 | |||||||
| chr11:28135564 | G | T | 1 | a0002c0002t0001g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.270+21960G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28135564 | |||||||
| chr11:28135566 | T | C | 7 | a0001c0001t0002g0239 a0004c0003t0002g0086 a0004c0003t0002g0109 others(4): Show |
7 | HG00642.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+21962T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28135566 | |||||||
| chr11:28135661 | T | C | 71 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(68): Show |
73 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.270+22057T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28135661 | |||||||
| chr11:28135691 | C | T | 1 | a0003c0004t0001g0305 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.270+22087C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28135691 | |||||||
| chr11:28135742 | C | T | 71 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(68): Show |
73 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.270+22138C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28135742 | |||||||
| chr11:28136320 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.270+22716C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28136320 | |||||||
| chr11:28136555 | A | C | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+22951A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28136555 | |||||||
| chr11:28136557 | C | T | 1 | a0002c0002t0001g0278 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.270+22953C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28136557 | |||||||
| chr11:28137060 | A | G | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+23456A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28137060 | |||||||
| chr11:28137180 | G | A | 3 | a0001c0001t0002g0119 a0001c0001t0010g0117 a0001c0001t0010g0118 |
3 | NA18948.hp2 NA18961.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.270+23576G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28137180 | |||||||
| chr11:28137240 | A | G | 1 | a0001c0001t0004g0158 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+23636A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28137240 | |||||||
| chr11:28137788 | A | T | 77 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(74): Show |
79 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.270+24184A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28137788 | |||||||
| chr11:28137793 | T | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0151 |
2 | HG02523.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.270+24189T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28137793 | |||||||
| chr11:28137800 | T | C | 76 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(73): Show |
78 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+24196T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28137800 | |||||||
| chr11:28137852 | G | A | 1 | a0002c0002t0001g0246 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.270+24248G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28137852 | |||||||
| chr11:28138116 | A | AT | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.270+24524dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28138116 | ||||||
| chr11:28138408 | G | A | 2 | a0001c0001t0004g0176 a0001c0001t0004g0207 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.270+24804G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28138408 | |||||||
| chr11:28138614 | T | C | 1 | a0001c0001t0003g0045 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.270+25010T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28138614 | |||||||
| chr11:28138667 | G | A | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.270+25063G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28138667 | |||||||
| chr11:28138776 | G | A | 1 | a0001c0001t0005g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.270+25172G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28138776 | |||||||
| chr11:28138788 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.270+25184G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28138788 | |||||||
| chr11:28138941 | C | G | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.270+25337C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28138941 | |||||||
| chr11:28139354 | C | A | 6 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+25750C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28139354 | |||||||
| chr11:28139521 | G | A | 1 | a0001c0001t0003g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.270+25917G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28139521 | |||||||
| chr11:28139765 | A | C | 1 | a0001c0001t0002g0106 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.270+26161A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28139765 | |||||||
| chr11:28140096 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.270+26492C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28140096 | |||||||
| chr11:28140103 | C | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0140 |
2 | NA18993.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.270+26499C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28140103 | |||||||
| chr11:28140304 | A | G | 1 | a0001c0001t0005g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.270+26700A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28140304 | |||||||
| chr11:28140356 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.270+26752C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28140356 | |||||||
| chr11:28140434 | T | C | 1 | a0002c0002t0001g0294 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.270+26830T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28140434 | |||||||
| chr11:28140737 | C | T | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.270+27133C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28140737 | |||||||
| chr11:28140771 | A | G | 2 | a0001c0001t0012g0074 a0001c0001t0023g0037 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.270+27167A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28140771 | |||||||
| chr11:28140862 | C | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+27258C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28140862 | |||||||
| chr11:28140867 | C | T | 2 | a0001c0001t0004g0213 a0002c0002t0001g0270 |
2 | HG04184.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.270+27263C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28140867 | |||||||
| chr11:28141035 | T | C | 2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
2 | NA18612.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.270+27431T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28141035 | |||||||
| chr11:28141055 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270+27451G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28141055 | |||||||
| chr11:28141129 | G | C | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.270+27525G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28141129 | |||||||
| chr11:28141155 | G | A | 1 | a0005c0005t0014g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.270+27551G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28141155 | |||||||
| chr11:28141365 | T | C | 1 | a0001c0001t0003g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.270+27761T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28141365 | |||||||
| chr11:28141385 | T | C | 1 | a0001c0001t0004g0199 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.270+27781T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28141385 | |||||||
| chr11:28141399 | A | G | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+27795A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28141399 | |||||||
| chr11:28142080 | A | G | 1 | a0001c0001t0007g0237 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.270+28476A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28142080 | |||||||
| chr11:28142263 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.270+28659G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28142263 | |||||||
| chr11:28142394 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+28790G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28142394 | |||||||
| chr11:28142523 | T | C | 1 | a0001c0001t0003g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.270+28919T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28142523 | |||||||
| chr11:28142583 | A | C | 1 | a0002c0002t0001g0247 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.270+28979A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28142583 | |||||||
| chr11:28142612 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.270+29008A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28142612 | |||||||
| chr11:28142615 | G | A | 2 | a0001c0001t0006g0218 a0001c0001t0011g0219 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.270+29011G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28142615 | |||||||
| chr11:28142646 | C | G | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.270+29042C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28142646 | |||||||
| chr11:28142882 | A | G | 1 | a0002c0002t0001g0304 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.270+29278A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28142882 | |||||||
| chr11:28142910 | G | A | 1 | a0001c0001t0004g0238 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.270+29306G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28142910 | |||||||
| chr11:28143072 | C | T | 5 | a0001c0001t0003g0044 a0001c0001t0003g0069 a0001c0001t0003g0070 others(2): Show |
5 | HG00621.hp2 HG02132.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+29468C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28143072 | |||||||
| chr11:28143308 | A | C | 5 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0143 others(2): Show |
5 | HG00609.hp1 HG02523.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+29704A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28143308 | |||||||
| chr11:28143314 | A | G | 86 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(83): Show |
88 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.270+29710A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28143314 | |||||||
| chr11:28143562 | G | A | 1 | a0002c0002t0001g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.270+29958G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28143562 | |||||||
| chr11:28143768 | C | A | 1 | a0001c0001t0003g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.270+30164C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28143768 | |||||||
| chr11:28143783 | C | G | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.270+30179C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28143783 | |||||||
| chr11:28143893 | C | A | 1 | a0001c0001t0010g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.270+30289C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28143893 | |||||||
| chr11:28144110 | A | G | 2 | a0001c0001t0002g0104 a0001c0001t0002g0114 |
2 | NA18965.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.270+30506A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28144110 | |||||||
| chr11:28144132 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.270+30528G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28144132 | |||||||
| chr11:28144725 | G | T | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.270+31121G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28144725 | |||||||
| chr11:28144869 | A | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+31265A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28144869 | |||||||
| chr11:28144949 | C | G | 1 | a0002c0002t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.270+31345C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28144949 | |||||||
| chr11:28144957 | C | T | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.270+31353C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28144957 | |||||||
| chr11:28145075 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.270+31471G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28145075 | |||||||
| chr11:28145086 | A | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
2 | HG00738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.270+31482A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28145086 | |||||||
| chr11:28145127 | A | G | 1 | a0002c0002t0001g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.270+31523A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28145127 | |||||||
| chr11:28145217 | G | A | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.270+31613G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28145217 | |||||||
| chr11:28145537 | T | C | 1 | a0001c0001t0003g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.270+31933T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28145537 | |||||||
| chr11:28145600 | C | T | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.270+31996C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28145600 | |||||||
| chr11:28145777 | A | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+32173A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28145777 | |||||||
| chr11:28145902 | G | C | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+32298G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28145902 | |||||||
| chr11:28146273 | C | T | 2 | a0001c0001t0005g0034 a0001c0001t0013g0035 |
2 | NA18947.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.270+32669C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28146273 | |||||||
| chr11:28146351 | T | G | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.270+32747T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28146351 | |||||||
| chr11:28146435 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.270+32831C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28146435 | |||||||
| chr11:28146679 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.270+33075A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28146679 | |||||||
| chr11:28146745 | A | T | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+33141A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28146745 | |||||||
| chr11:28146972 | G | T | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.270+33368G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28146972 | |||||||
| chr11:28147360 | A | C | 2 | a0001c0001t0010g0117 a0001c0001t0010g0118 |
2 | NA18948.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.270+33756A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28147360 | |||||||
| chr11:28147507 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+33903A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28147507 | |||||||
| chr11:28147810 | A | G | 1 | a0001c0001t0008g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.270+34206A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28147810 | |||||||
| chr11:28147957 | C | G | 2 | a0002c0002t0001g0301 a0002c0002t0001g0310 |
2 | HG01099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.270+34353C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28147957 | |||||||
| chr11:28148726 | G | A | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+35122G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28148726 | |||||||
| chr11:28148787 | T | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.270+35183T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28148787 | |||||||
| chr11:28148858 | A | G | 1 | a0002c0002t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.270+35254A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28148858 | |||||||
| chr11:28149188 | A | AT | 58 | a0001c0001t0002g0122 a0001c0001t0002g0133 a0001c0001t0002g0135 others(55): Show |
60 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.270+35600dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28149188 | ||||||
| chr11:28149188 | AT | A | 8 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 others(5): Show |
8 | HG02572.hp2 NA18947.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.270+35600delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28149188 | ||||||
| chr11:28149228 | T | G | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.270+35624T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28149228 | |||||||
| chr11:28149231 | G | A | 1 | a0002c0002t0001g0325 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.270+35627G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28149231 | |||||||
| chr11:28149352 | G | T | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.270+35748G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28149352 | |||||||
| chr11:28149549 | G | A | 1 | a0002c0002t0001g0325 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.270+35945G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28149549 | |||||||
| chr11:28149843 | A | G | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.270+36239A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28149843 | |||||||
| chr11:28150020 | C | T | 2 | a0002c0002t0001g0300 a0002c0002t0001g0307 |
2 | HG03491.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.270+36416C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28150020 | |||||||
| chr11:28150118 | G | A | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+36514G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28150118 | |||||||
| chr11:28150162 | CT | C | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.270+36562delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28150162 | ||||||
| chr11:28150369 | T | C | 2 | a0001c0001t0004g0180 a0001c0001t0007g0179 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.270+36765T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28150369 | |||||||
| chr11:28150531 | T | C | 1 | a0002c0002t0015g0319 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.270+36927T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28150531 | |||||||
| chr11:28150633 | G | GA | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.270+37037dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28150633 | ||||||
| chr11:28150692 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.270+37088C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28150692 | |||||||
| chr11:28151004 | A | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+37400A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28151004 | |||||||
| chr11:28151006 | C | CA | 156 | a0001c0001t0002g0133 a0001c0001t0003g0001 a0001c0001t0003g0002 others(153): Show |
158 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(155): Show |
intron_variant | MODIFIER | c.270+37421dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28151006 | ||||||
| chr11:28151465 | C | A | 1 | a0001c0001t0003g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.270+37861C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28151465 | |||||||
| chr11:28151578 | C | G | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.270+37974C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28151578 | |||||||
| chr11:28151615 | C | G | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.270+38011C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28151615 | |||||||
| chr11:28151728 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+38124A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28151728 | |||||||
| chr11:28151948 | G | T | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.270+38344G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28151948 | |||||||
| chr11:28152023 | TTATAC | T | 6 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+38424_270+3842 others(9): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28152023 | ||||||
| chr11:28152087 | T | C | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.270+38483T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28152087 | |||||||
| chr11:28152114 | C | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+38510C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28152114 | |||||||
| chr11:28152137 | A | T | 1 | a0001c0001t0024g0184 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.270+38533A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28152137 | |||||||
| chr11:28152782 | T | TA | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.270+39182dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28152782 | ||||||
| chr11:28152922 | C | A | 2 | a0001c0001t0003g0041 a0001c0001t0003g0042 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.270+39318C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28152922 | |||||||
| chr11:28153081 | G | A | 1 | a0002c0002t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.270+39477G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28153081 | |||||||
| chr11:28153084 | A | G | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.270+39480A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28153084 | |||||||
| chr11:28153266 | A | G | 40 | a0002c0002t0001g0003 a0002c0002t0001g0245 a0002c0002t0001g0247 others(37): Show |
41 | HG00423.hp2 HG00609.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.270+39662A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28153266 | |||||||
| chr11:28153286 | C | T | 1 | a0001c0001t0004g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.270+39682C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28153286 | |||||||
| chr11:28153319 | T | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.270+39715T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28153319 | |||||||
| chr11:28153328 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270+39724A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28153328 | |||||||
| chr11:28153498 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270+39894A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28153498 | |||||||
| chr11:28153698 | G | T | 62 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(59): Show |
62 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.270+40094G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28153698 | |||||||
| chr11:28154336 | T | C | 1 | a0002c0002t0001g0286 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.270+40732T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28154336 | |||||||
| chr11:28154391 | G | C | 1 | a0001c0001t0002g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.270+40787G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28154391 | |||||||
| chr11:28154735 | T | C | 6 | a0001c0001t0007g0168 a0001c0001t0007g0240 a0001c0001t0009g0165 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+41131T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28154735 | |||||||
| chr11:28155865 | A | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.270+42261A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28155865 | |||||||
| chr11:28155909 | G | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.270+42305G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28155909 | |||||||
| chr11:28155995 | C | G | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.270+42391C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28155995 | |||||||
| chr11:28156056 | A | T | 1 | a0001c0001t0004g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.270+42452A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28156056 | |||||||
| chr11:28156148 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270+42544A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28156148 | |||||||
| chr11:28156176 | A | G | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.270+42572A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28156176 | |||||||
| chr11:28156282 | A | G | 1 | a0001c0001t0006g0191 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.270+42678A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28156282 | |||||||
| chr11:28156332 | A | C | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.270+42728A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28156332 | |||||||
| chr11:28156450 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270+42846C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28156450 | |||||||
| chr11:28156469 | C | A | 1 | a0001c0001t0016g0020 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.270+42865C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28156469 | |||||||
| chr11:28156610 | T | G | 11 | a0001c0001t0006g0160 a0001c0001t0006g0218 a0001c0001t0006g0220 others(8): Show |
11 | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.270+43006T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28156610 | |||||||
| chr11:28157001 | A | G | 1 | a0001c0001t0008g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.270+43397A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28157001 | |||||||
| chr11:28157272 | T | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.270+43668T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28157272 | |||||||
| chr11:28157355 | C | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+43751C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28157355 | |||||||
| chr11:28157470 | C | T | 1 | a0007c0009t0003g0023 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.270+43866C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28157470 | |||||||
| chr11:28157699 | C | T | 1 | a0001c0001t0003g0078 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.270+44095C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28157699 | |||||||
| chr11:28157712 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.270+44108G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28157712 | |||||||
| chr11:28157751 | T | G | 1 | a0001c0001t0003g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.270+44147T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28157751 | |||||||
| chr11:28157966 | G | A | 1 | a0001c0001t0010g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.270+44362G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28157966 | |||||||
| chr11:28158427 | A | G | 1 | a0001c0001t0003g0060 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.270+44823A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28158427 | |||||||
| chr11:28158561 | T | C | 5 | a0002c0002t0001g0247 a0002c0002t0001g0286 a0002c0002t0001g0287 others(2): Show |
5 | HG00609.hp2 NA18950.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+44957T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28158561 | |||||||
| chr11:28158815 | T | C | 1 | a0001c0001t0005g0007 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.270+45211T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28158815 | |||||||
| chr11:28158925 | C | T | 53 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0009 others(50): Show |
55 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.270+45321C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28158925 | |||||||
| chr11:28159310 | A | G | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.270+45706A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28159310 | |||||||
| chr11:28159311 | G | A | 1 | a0002c0002t0001g0252 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.270+45707G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28159311 | |||||||
| chr11:28159447 | G | GA | 13 | a0001c0001t0002g0085 a0001c0001t0002g0106 a0001c0001t0003g0022 others(10): Show |
13 | HG00673.hp2 HG00733.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.270+45856dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28159447 | ||||||
| chr11:28159584 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+45980G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28159584 | |||||||
| chr11:28159677 | C | T | 6 | a0001c0001t0007g0168 a0001c0001t0007g0240 a0001c0001t0009g0165 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+46073C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28159677 | |||||||
| chr11:28160156 | T | A | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.270+46552T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28160156 | |||||||
| chr11:28160181 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.270+46577G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28160181 | |||||||
| chr11:28160182 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.270+46578C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28160182 | |||||||
| chr11:28160395 | T | C | 1 | a0003c0004t0001g0313 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.270+46791T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28160395 | |||||||
| chr11:28160398 | T | C | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.270+46794T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28160398 | |||||||
| chr11:28160428 | G | T | 1 | a0002c0002t0001g0243 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.270+46824G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28160428 | |||||||
| chr11:28160620 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+47016A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28160620 | |||||||
| chr11:28160899 | A | G | 1 | a0002c0002t0001g0294 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.270+47295A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28160899 | |||||||
| chr11:28161034 | A | G | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.270+47430A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28161034 | |||||||
| chr11:28161107 | C | CT | 7 | a0001c0001t0001g0214 a0002c0002t0001g0244 a0002c0002t0001g0255 others(4): Show |
7 | HG01496.hp1 HG02630.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+47522dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28161107 | ||||||
| chr11:28161107 | C | CTT | 80 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(77): Show |
82 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.270+47521_270+4752 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28161107 | ||||||
| chr11:28161107 | CT | C | 66 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(63): Show |
66 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.270+47522delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28161107 | ||||||
| chr11:28161107 | CTTTTTTT | C | 157 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(154): Show |
159 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.270+47516_270+4752 others(11): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28161107 | ||||||
| chr11:28161120 | T | G | 1 | a0002c0002t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.270+47516T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28161120 | |||||||
| chr11:28161127 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270+47523G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28161127 | |||||||
| chr11:28161146 | T | A | 1 | a0002c0002t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.270+47542T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28161146 | |||||||
| chr11:28161360 | T | C | 18 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0212 others(15): Show |
18 | HG00735.hp1 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.270+47756T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28161360 | |||||||
| chr11:28161732 | GA | G | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.270+48135delA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28161732 | ||||||
| chr11:28161904 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+48300C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28161904 | |||||||
| chr11:28162147 | A | G | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.270+48543A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28162147 | |||||||
| chr11:28162709 | T | G | 1 | a0001c0001t0010g0117 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.271-48353T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28162709 | |||||||
| chr11:28162866 | T | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-48196T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28162866 | |||||||
| chr11:28163154 | G | GA | 89 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(86): Show |
91 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.271-47902dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28163154 | ||||||
| chr11:28163410 | T | C | 2 | a0002c0002t0001g0320 a0002c0002t0001g0321 |
2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.271-47652T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163410 | |||||||
| chr11:28163465 | C | G | 1 | a0001c0001t0003g0076 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.271-47597C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163465 | |||||||
| chr11:28163470 | C | G | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.271-47592C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163470 | |||||||
| chr11:28163478 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.271-47584C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163478 | |||||||
| chr11:28163529 | A | ATC | 3 | a0001c0001t0004g0180 a0001c0001t0005g0043 a0001c0001t0007g0179 |
3 | HG02735.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.271-47511_271-4751 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28163529 | ||||||
| chr11:28163543 | C | G | 1 | a0002c0002t0001g0259 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.271-47519C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163543 | |||||||
| chr11:28163551 | C | G | 11 | a0001c0001t0006g0160 a0001c0001t0006g0218 a0001c0001t0006g0220 others(8): Show |
11 | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-47511C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163551 | |||||||
| chr11:28163553 | G | C | 77 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(74): Show |
77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.271-47509G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163553 | |||||||
| chr11:28163706 | T | A | 1 | a0001c0001t0002g0145 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.271-47356T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163706 | |||||||
| chr11:28163780 | T | C | 1 | a0001c0001t0003g0065 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.271-47282T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163780 | |||||||
| chr11:28163806 | G | A | 1 | a0001c0001t0003g0065 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.271-47256G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163806 | |||||||
| chr11:28163989 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.271-47073A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28163989 | |||||||
| chr11:28164112 | C | T | 6 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-46950C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28164112 | |||||||
| chr11:28164173 | A | G | 1 | a0002c0002t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.271-46889A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28164173 | |||||||
| chr11:28164298 | A | T | 1 | a0001c0001t0005g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.271-46764A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28164298 | |||||||
| chr11:28164385 | C | T | 7 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0137 others(4): Show |
7 | HG00408.hp2 HG00597.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-46677C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28164385 | |||||||
| chr11:28164407 | G | T | 1 | a0001c0001t0002g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.271-46655G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28164407 | |||||||
| chr11:28164459 | T | A | 2 | a0001c0001t0004g0196 a0001c0001t0004g0197 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.271-46603T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28164459 | |||||||
| chr11:28164636 | A | G | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.271-46426A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28164636 | |||||||
| chr11:28165465 | A | G | 1 | a0002c0002t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271-45597A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28165465 | |||||||
| chr11:28165561 | C | T | 2 | a0001c0001t0004g0176 a0001c0001t0004g0207 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.271-45501C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28165561 | |||||||
| chr11:28165573 | T | C | 3 | a0001c0001t0002g0119 a0001c0001t0010g0117 a0001c0001t0010g0118 |
3 | NA18948.hp2 NA18961.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.271-45489T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28165573 | |||||||
| chr11:28165713 | TA | T | 87 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(84): Show |
89 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.271-45339delA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28165713 | ||||||
| chr11:28165863 | C | T | 4 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 others(1): Show |
4 | NA18949.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-45199C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28165863 | |||||||
| chr11:28165906 | G | C | 1 | a0001c0001t0003g0045 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.271-45156G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28165906 | |||||||
| chr11:28166026 | G | C | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.271-45036G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28166026 | |||||||
| chr11:28166074 | A | T | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.271-44988A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28166074 | |||||||
| chr11:28166565 | C | T | 1 | a0001c0001t0008g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.271-44497C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28166565 | |||||||
| chr11:28166880 | T | C | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 |
3 | NA18981.hp1 NA18994.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.271-44182T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28166880 | |||||||
| chr11:28167389 | G | A | 1 | a0001c0001t0004g0228 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.271-43673G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28167389 | |||||||
| chr11:28167665 | G | C | 1 | a0002c0002t0001g0325 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.271-43397G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28167665 | |||||||
| chr11:28167666 | C | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-43396C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28167666 | |||||||
| chr11:28167717 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.271-43345T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28167717 | |||||||
| chr11:28167745 | C | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.271-43317C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28167745 | |||||||
| chr11:28168010 | G | A | 2 | a0001c0001t0003g0041 a0001c0001t0003g0042 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.271-43052G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28168010 | |||||||
| chr11:28168092 | A | G | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.271-42970A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28168092 | |||||||
| chr11:28168217 | A | G | 1 | a0001c0001t0004g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.271-42845A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28168217 | |||||||
| chr11:28168220 | A | G | 1 | a0002c0002t0001g0279 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.271-42842A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28168220 | |||||||
| chr11:28168518 | C | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-42544C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28168518 | |||||||
| chr11:28168611 | T | TC | 165 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0103 others(162): Show |
167 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(164): Show |
intron_variant | MODIFIER | c.271-42446dupC | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28168611 | ||||||
| chr11:28168633 | C | G | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.271-42429C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28168633 | |||||||
| chr11:28168851 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-42211A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28168851 | |||||||
| chr11:28168882 | G | T | 1 | a0002c0002t0001g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.271-42180G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28168882 | |||||||
| chr11:28168953 | C | G | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.271-42109C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28168953 | |||||||
| chr11:28169200 | G | A | 4 | a0001c0001t0004g0200 a0001c0001t0004g0201 a0001c0001t0004g0202 others(1): Show |
4 | HG00733.hp1 HG01106.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-41862G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28169200 | |||||||
| chr11:28169285 | A | G | 1 | a0002c0002t0001g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.271-41777A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28169285 | |||||||
| chr11:28169296 | G | A | 1 | a0001c0001t0008g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.271-41766G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28169296 | |||||||
| chr11:28169415 | TATA | T | 11 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.271-41643_271-4164 others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28169415 | ||||||
| chr11:28169461 | A | G | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.271-41601A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28169461 | |||||||
| chr11:28169483 | G | A | 6 | a0002c0002t0001g0250 a0002c0002t0001g0256 a0002c0002t0001g0257 others(3): Show |
6 | HG02056.hp1 NA18971.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-41579G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28169483 | |||||||
| chr11:28169707 | C | T | 1 | a0001c0001t0028g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.271-41355C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28169707 | |||||||
| chr11:28169718 | A | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-41344A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28169718 | |||||||
| chr11:28169809 | TC | T | 62 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(59): Show |
62 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.271-41251delC | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28169809 | ||||||
| chr11:28170218 | T | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-40844T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28170218 | |||||||
| chr11:28171660 | G | A | 7 | a0001c0001t0012g0073 a0001c0001t0012g0074 a0001c0001t0012g0075 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-39402G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28171660 | |||||||
| chr11:28171691 | T | A | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.271-39371T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28171691 | |||||||
| chr11:28172415 | G | A | 1 | a0001c0001t0004g0182 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.271-38647G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28172415 | |||||||
| chr11:28172562 | G | A | 1 | a0002c0002t0001g0246 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.271-38500G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28172562 | |||||||
| chr11:28172588 | C | T | 2 | a0006c0006t0003g0052 a0006c0006t0003g0054 |
2 | NA18995.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.271-38474C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28172588 | |||||||
| chr11:28172631 | T | A | 1 | a0002c0002t0001g0250 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.271-38431T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28172631 | |||||||
| chr11:28172742 | A | G | 6 | a0003c0004t0001g0285 a0003c0004t0001g0295 a0003c0004t0001g0296 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-38320A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28172742 | |||||||
| chr11:28173018 | T | A | 1 | a0002c0002t0001g0265 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.271-38044T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28173018 | |||||||
| chr11:28173021 | A | G | 1 | a0002c0002t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.271-38041A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28173021 | |||||||
| chr11:28173100 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-37962A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28173100 | |||||||
| chr11:28173148 | A | G | 238 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(235): Show |
240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.271-37914A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28173148 | |||||||
| chr11:28173176 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.271-37886C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28173176 | |||||||
| chr11:28173306 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.271-37756G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28173306 | |||||||
| chr11:28173436 | T | C | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.271-37626T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28173436 | |||||||
| chr11:28173709 | A | C | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.271-37353A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28173709 | |||||||
| chr11:28173899 | G | A | 1 | a0002c0002t0001g0324 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.271-37163G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28173899 | |||||||
| chr11:28174065 | C | G | 1 | a0001c0001t0003g0027 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.271-36997C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174065 | |||||||
| chr11:28174228 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-36834A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174228 | |||||||
| chr11:28174298 | ATAGT | A | 159 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(156): Show |
161 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.271-36759_271-3675 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28174298 | ||||||
| chr11:28174442 | A | C | 1 | a0001c0001t0003g0060 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.271-36620A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174442 | |||||||
| chr11:28174474 | G | C | 2 | a0001c0001t0012g0074 a0001c0001t0023g0037 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.271-36588G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174474 | |||||||
| chr11:28174597 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-36465G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174597 | |||||||
| chr11:28174642 | G | A | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.271-36420G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174642 | |||||||
| chr11:28174670 | C | T | 1 | a0002c0002t0001g0264 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.271-36392C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174670 | |||||||
| chr11:28174705 | C | G | 1 | a0001c0001t0002g0131 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.271-36357C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174705 | |||||||
| chr11:28174710 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.271-36352G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174710 | |||||||
| chr11:28174739 | C | T | 1 | a0001c0001t0003g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.271-36323C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174739 | |||||||
| chr11:28174740 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.271-36322G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174740 | |||||||
| chr11:28174801 | C | T | 1 | a0001c0001t0022g0157 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.271-36261C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174801 | |||||||
| chr11:28174814 | C | CA | 139 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(136): Show |
139 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.271-36232dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28174814 | ||||||
| chr11:28174820 | AAAAAAAA others(4): Show |
A | 1 | a0002c0002t0001g0252 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.271-36240_271-3623 others(15): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28174820 | ||||||
| chr11:28174824 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-36238A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174824 | |||||||
| chr11:28174830 | AC | A | 79 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(76): Show |
80 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.271-36231delC | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174830 | |||||||
| chr11:28174900 | A | T | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.271-36162A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174900 | |||||||
| chr11:28174941 | T | A | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.271-36121T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174941 | |||||||
| chr11:28174944 | TTTA | T | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.271-36109_271-3610 others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28174944 | ||||||
| chr11:28175254 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.271-35808A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28175254 | |||||||
| chr11:28175281 | CT | C | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.271-35774delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28175281 | ||||||
| chr11:28175409 | C | T | 1 | a0001c0001t0004g0174 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.271-35653C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28175409 | |||||||
| chr11:28175740 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-35322A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28175740 | |||||||
| chr11:28175910 | A | AAT | 10 | a0001c0001t0006g0160 a0001c0001t0006g0218 a0001c0001t0006g0221 others(7): Show |
10 | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-35137_271-3513 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28175910 | ||||||
| chr11:28176014 | A | G | 39 | a0001c0001t0002g0116 a0001c0001t0002g0119 a0001c0001t0002g0121 others(36): Show |
39 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.271-35048A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28176014 | |||||||
| chr11:28176288 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-34774A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28176288 | |||||||
| chr11:28176523 | G | T | 6 | a0001c0001t0002g0122 a0001c0001t0002g0133 a0001c0001t0002g0135 others(3): Show |
6 | NA18973.hp1 NA18993.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-34539G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28176523 | |||||||
| chr11:28176802 | G | A | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.271-34260G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28176802 | |||||||
| chr11:28177519 | T | C | 1 | a0001c0001t0003g0047 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.271-33543T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28177519 | |||||||
| chr11:28177535 | A | G | 1 | a0001c0001t0004g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.271-33527A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28177535 | |||||||
| chr11:28177680 | T | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-33382T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28177680 | |||||||
| chr11:28178118 | C | T | 4 | a0002c0002t0001g0291 a0002c0002t0001g0294 a0002c0002t0001g0303 others(1): Show |
4 | HG01361.hp1 HG01993.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-32944C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28178118 | |||||||
| chr11:28178869 | A | C | 1 | a0001c0001t0003g0008 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.271-32193A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28178869 | |||||||
| chr11:28179293 | G | T | 1 | a0001c0001t0005g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.271-31769G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28179293 | |||||||
| chr11:28179800 | T | G | 9 | a0002c0002t0001g0243 a0002c0002t0001g0264 a0002c0002t0001g0266 others(6): Show |
9 | HG00597.hp1 NA18965.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.271-31262T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28179800 | |||||||
| chr11:28179839 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-31223G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28179839 | |||||||
| chr11:28179852 | T | G | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.271-31210T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28179852 | |||||||
| chr11:28179903 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.271-31159A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28179903 | |||||||
| chr11:28180203 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-30859G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28180203 | |||||||
| chr11:28181259 | A | ATTTTTT | 71 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(68): Show |
71 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.271-29794_271-2978 others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28181259 | ||||||
| chr11:28181259 | A | ATTTTTTT | 91 | a0001c0001t0002g0120 a0001c0001t0002g0122 a0001c0001t0002g0133 others(88): Show |
93 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.271-29795_271-2978 others(11): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28181259 | ||||||
| chr11:28181333 | G | A | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.271-29729G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28181333 | |||||||
| chr11:28181401 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-29661T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28181401 | |||||||
| chr11:28181422 | G | T | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.271-29640G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28181422 | |||||||
| chr11:28181592 | AT | A | 166 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(163): Show |
168 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.271-29464delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28181592 | ||||||
| chr11:28181684 | C | G | 62 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(59): Show |
62 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.271-29378C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28181684 | |||||||
| chr11:28181718 | CGT | C | 168 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(165): Show |
170 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.271-29338_271-2933 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28181718 | ||||||
| chr11:28181815 | T | A | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.271-29247T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28181815 | |||||||
| chr11:28182073 | T | C | 3 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0005g0072 |
3 | HG00621.hp2 NA18943.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.271-28989T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182073 | |||||||
| chr11:28182075 | T | C | 3 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0005g0072 |
3 | HG00621.hp2 NA18943.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.271-28987T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182075 | |||||||
| chr11:28182078 | A | G | 3 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0005g0072 |
3 | HG00621.hp2 NA18943.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.271-28984A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182078 | |||||||
| chr11:28182084 | T | C | 3 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0005g0072 |
3 | HG00621.hp2 NA18943.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.271-28978T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182084 | |||||||
| chr11:28182100 | G | A | 4 | a0001c0001t0004g0200 a0001c0001t0004g0201 a0001c0001t0004g0202 others(1): Show |
4 | HG00733.hp1 HG01106.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-28962G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182100 | |||||||
| chr11:28182107 | T | C | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-28955T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182107 | |||||||
| chr11:28182110 | T | C | 1 | a0001c0001t0003g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.271-28952T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182110 | |||||||
| chr11:28182306 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-28756T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182306 | |||||||
| chr11:28182617 | A | G | 8 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0007g0168 others(5): Show |
8 | HG01243.hp2 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-28445A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182617 | |||||||
| chr11:28182706 | T | A | 1 | a0002c0002t0001g0321 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.271-28356T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182706 | |||||||
| chr11:28182838 | A | G | 1 | a0002c0002t0001g0276 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.271-28224A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182838 | |||||||
| chr11:28182853 | G | T | 1 | a0001c0001t0002g0093 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.271-28209G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182853 | |||||||
| chr11:28183205 | A | G | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.271-27857A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183205 | |||||||
| chr11:28183326 | G | T | 1 | a0002c0002t0001g0278 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.271-27736G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183326 | |||||||
| chr11:28183490 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-27572G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183490 | |||||||
| chr11:28183546 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.271-27516G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183546 | |||||||
| chr11:28183575 | T | C | 4 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 others(1): Show |
4 | NA18949.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-27487T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183575 | |||||||
| chr11:28183621 | G | T | 1 | a0001c0001t0002g0121 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.271-27441G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183621 | |||||||
| chr11:28183635 | C | T | 42 | a0002c0002t0001g0004 a0002c0002t0001g0243 a0002c0002t0001g0246 others(39): Show |
43 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-27427C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183635 | |||||||
| chr11:28183682 | G | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-27380G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183682 | |||||||
| chr11:28183805 | T | C | 1 | a0002c0002t0001g0312 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.271-27257T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183805 | |||||||
| chr11:28183871 | G | T | 1 | a0003c0004t0001g0296 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.271-27191G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183871 | |||||||
| chr11:28183904 | G | A | 1 | a0002c0002t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271-27158G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183904 | |||||||
| chr11:28183988 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-27074G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183988 | |||||||
| chr11:28184174 | G | A | 18 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0212 others(15): Show |
18 | HG00735.hp1 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.271-26888G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28184174 | |||||||
| chr11:28184264 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.271-26798T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28184264 | |||||||
| chr11:28184372 | T | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-26690T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28184372 | |||||||
| chr11:28184377 | G | A | 1 | a0001c0001t0010g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.271-26685G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28184377 | |||||||
| chr11:28184472 | T | G | 1 | a0002c0002t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.271-26590T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28184472 | |||||||
| chr11:28184566 | A | G | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.271-26496A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28184566 | |||||||
| chr11:28184697 | T | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-26365T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28184697 | |||||||
| chr11:28185295 | T | A | 1 | a0001c0001t0003g0060 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.271-25767T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28185295 | |||||||
| chr11:28185343 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-25719A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28185343 | |||||||
| chr11:28185571 | C | G | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.271-25491C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28185571 | |||||||
| chr11:28186031 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.271-25031A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186031 | |||||||
| chr11:28186085 | G | A | 2 | a0001c0001t0002g0152 a0001c0001t0002g0153 |
2 | NA18956.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.271-24977G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186085 | |||||||
| chr11:28186437 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24625T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186437 | |||||||
| chr11:28186442 | G | C | 5 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0258 others(2): Show |
5 | HG02056.hp1 NA18971.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-24620G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186442 | |||||||
| chr11:28186454 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24608T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186454 | |||||||
| chr11:28186456 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24606A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186456 | |||||||
| chr11:28186458 | G | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24604G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186458 | |||||||
| chr11:28186459 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24603A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186459 | |||||||
| chr11:28186465 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24597A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186465 | |||||||
| chr11:28186467 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24595T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186467 | |||||||
| chr11:28186468 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24594T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186468 | |||||||
| chr11:28186469 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24593T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186469 | |||||||
| chr11:28186470 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24592T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186470 | |||||||
| chr11:28186474 | G | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24588G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186474 | |||||||
| chr11:28186476 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24586T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186476 | |||||||
| chr11:28186477 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24585A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186477 | |||||||
| chr11:28186492 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24570T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186492 | |||||||
| chr11:28186493 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24569T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186493 | |||||||
| chr11:28186496 | T | G | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24566T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186496 | |||||||
| chr11:28186498 | G | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24564G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186498 | |||||||
| chr11:28186508 | T | G | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24554T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186508 | |||||||
| chr11:28186510 | G | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24552G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186510 | |||||||
| chr11:28186511 | G | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24551G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186511 | |||||||
| chr11:28186513 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24549T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186513 | |||||||
| chr11:28186518 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24544A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186518 | |||||||
| chr11:28186520 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24542A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186520 | |||||||
| chr11:28186527 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24535T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186527 | |||||||
| chr11:28186528 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24534T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186528 | |||||||
| chr11:28186530 | A | T | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24532A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186530 | |||||||
| chr11:28186544 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24518A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186544 | |||||||
| chr11:28186553 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24509T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186553 | |||||||
| chr11:28186554 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24508A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186554 | |||||||
| chr11:28186555 | G | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24507G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186555 | |||||||
| chr11:28186556 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24506A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186556 | |||||||
| chr11:28186564 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24498A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186564 | |||||||
| chr11:28186575 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24487T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186575 | |||||||
| chr11:28186577 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24485T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186577 | |||||||
| chr11:28186584 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24478T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186584 | |||||||
| chr11:28186586 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24476T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186586 | |||||||
| chr11:28186589 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24473A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186589 | |||||||
| chr11:28186591 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24471A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186591 | |||||||
| chr11:28186593 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24469A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186593 | |||||||
| chr11:28186594 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24468T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186594 | |||||||
| chr11:28186596 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24466T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186596 | |||||||
| chr11:28186600 | G | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24462G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186600 | |||||||
| chr11:28186601 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24461T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186601 | |||||||
| chr11:28186605 | G | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24457G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186605 | |||||||
| chr11:28186606 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24456T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186606 | |||||||
| chr11:28186607 | G | T | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24455G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186607 | |||||||
| chr11:28186608 | T | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24454T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186608 | |||||||
| chr11:28186610 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24452A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186610 | |||||||
| chr11:28186640 | A | G | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-24422A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186640 | |||||||
| chr11:28186645 | A | T | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24417A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186645 | |||||||
| chr11:28186655 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24407A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186655 | |||||||
| chr11:28186678 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24384A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186678 | |||||||
| chr11:28186693 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24369T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186693 | |||||||
| chr11:28186761 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24301A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186761 | |||||||
| chr11:28186771 | T | A | 1 | a0002c0002t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-24291T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186771 | |||||||
| chr11:28186776 | A | T | 2 | a0001c0001t0006g0218 a0001c0001t0011g0219 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.271-24286A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186776 | |||||||
| chr11:28187351 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.271-23711A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28187351 | |||||||
| chr11:28187411 | T | C | 1 | a0001c0001t0003g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.271-23651T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28187411 | |||||||
| chr11:28187474 | A | T | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.271-23588A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28187474 | |||||||
| chr11:28187517 | G | A | 3 | a0001c0001t0004g0158 a0001c0001t0004g0199 a0001c0001t0007g0198 |
3 | HG02074.hp1 HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.271-23545G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28187517 | |||||||
| chr11:28187524 | C | CT | 80 | a0001c0001t0003g0060 a0001c0001t0004g0158 a0001c0001t0004g0161 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.271-23522dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28187524 | ||||||
| chr11:28187614 | T | G | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.271-23448T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28187614 | |||||||
| chr11:28187692 | A | G | 1 | a0001c0001t0008g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.271-23370A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28187692 | |||||||
| chr11:28187707 | A | G | 1 | a0001c0001t0003g0029 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.271-23355A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28187707 | |||||||
| chr11:28188317 | A | G | 1 | a0001c0001t0005g0007 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.271-22745A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28188317 | |||||||
| chr11:28188434 | T | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-22628T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28188434 | |||||||
| chr11:28188506 | C | A | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.271-22556C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28188506 | |||||||
| chr11:28188698 | G | A | 23 | a0001c0001t0004g0176 a0001c0001t0004g0180 a0001c0001t0004g0196 others(20): Show |
23 | HG00735.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.271-22364G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28188698 | |||||||
| chr11:28188732 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-22330C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28188732 | |||||||
| chr11:28188888 | T | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-22174T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28188888 | |||||||
| chr11:28189015 | T | C | 5 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0138 others(2): Show |
5 | HG00408.hp2 NA18999.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-22047T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28189015 | |||||||
| chr11:28189821 | C | A | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.271-21241C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28189821 | |||||||
| chr11:28189881 | T | C | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.271-21181T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28189881 | |||||||
| chr11:28190311 | A | G | 1 | a0001c0001t0006g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-20751A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28190311 | |||||||
| chr11:28190331 | T | C | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.271-20731T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28190331 | |||||||
| chr11:28190767 | TTAGA | T | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.271-20290_271-2028 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28190767 | ||||||
| chr11:28190799 | A | G | 62 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(59): Show |
62 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.271-20263A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28190799 | |||||||
| chr11:28190828 | A | G | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.271-20234A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28190828 | |||||||
| chr11:28190874 | C | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.271-20188C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28190874 | |||||||
| chr11:28190960 | T | C | 1 | a0001c0001t0006g0230 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.271-20102T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28190960 | |||||||
| chr11:28191173 | C | G | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.271-19889C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28191173 | |||||||
| chr11:28191207 | A | T | 5 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0224 others(2): Show |
5 | HG02559.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-19855A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28191207 | |||||||
| chr11:28191634 | A | T | 1 | a0001c0001t0003g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.271-19428A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28191634 | |||||||
| chr11:28191837 | A | G | 1 | a0001c0001t0004g0232 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.271-19225A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28191837 | |||||||
| chr11:28192047 | A | C | 1 | a0001c0001t0008g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.271-19015A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28192047 | |||||||
| chr11:28192082 | A | G | 1 | a0001c0001t0006g0191 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.271-18980A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28192082 | |||||||
| chr11:28192148 | C | T | 1 | a0001c0001t0006g0230 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.271-18914C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28192148 | |||||||
| chr11:28192372 | T | G | 1 | a0009c0010t0002g0101 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.271-18690T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28192372 | |||||||
| chr11:28192633 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.271-18429A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28192633 | |||||||
| chr11:28193190 | A | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.271-17872A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28193190 | |||||||
| chr11:28193310 | G | A | 2 | a0002c0002t0001g0276 a0002c0002t0001g0277 |
2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.271-17752G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28193310 | |||||||
| chr11:28193311 | C | T | 5 | a0001c0001t0004g0175 a0001c0001t0004g0188 a0001c0001t0004g0190 others(2): Show |
5 | NA18954.hp2 NA18969.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-17751C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28193311 | |||||||
| chr11:28193438 | G | A | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.271-17624G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28193438 | |||||||
| chr11:28193547 | C | T | 1 | a0001c0001t0005g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.271-17515C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28193547 | |||||||
| chr11:28193581 | G | A | 2 | a0001c0001t0012g0073 a0001c0001t0012g0075 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.271-17481G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28193581 | |||||||
| chr11:28193863 | C | T | 1 | a0004c0003t0002g0113 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.271-17199C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28193863 | |||||||
| chr11:28193969 | A | G | 1 | a0002c0002t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.271-17093A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28193969 | |||||||
| chr11:28194122 | A | ATCTATCT others(13): Show |
1 | a0001c0001t0002g0125 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.271-16937_271-1693 others(24): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTT | 18 | a0001c0001t0002g0146 a0001c0001t0003g0018 a0001c0001t0004g0173 others(15): Show |
18 | HG00609.hp2 HG01123.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-16890_271-1688 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTTCTT others(16): Show |
1 | a0001c0001t0004g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.271-16936_271-1693 others(27): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTTTCT others(17): Show |
2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.271-16933_271-1693 others(28): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTTTCT others(1): Show |
31 | a0001c0001t0002g0104 a0001c0001t0002g0116 a0001c0001t0003g0038 others(28): Show |
32 | HG00408.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.271-16894_271-1688 others(12): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTTTCT others(5): Show |
42 | a0001c0001t0003g0002 a0001c0001t0003g0017 a0001c0001t0003g0030 others(39): Show |
44 | HG01074.hp2 HG01081.hp1 HG01943.hp1 others(41): Show |
intron_variant | MODIFIER | c.271-16898_271-1688 others(16): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTTTCT others(9): Show |
64 | a0001c0001t0002g0005 a0001c0001t0002g0084 a0001c0001t0002g0094 others(61): Show |
64 | HG00423.hp1 HG00609.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.271-16902_271-1688 others(20): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTTTCT others(13): Show |
73 | a0001c0001t0002g0085 a0001c0001t0002g0088 a0001c0001t0002g0089 others(70): Show |
74 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.271-16906_271-1688 others(24): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTTTCT others(17): Show |
50 | a0001c0001t0002g0006 a0001c0001t0002g0092 a0001c0001t0002g0095 others(47): Show |
50 | HG00544.hp1 HG00544.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.271-16910_271-1688 others(28): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTTTCT others(21): Show |
21 | a0001c0001t0001g0214 a0001c0001t0002g0098 a0001c0001t0002g0102 others(18): Show |
21 | HG01099.hp1 HG01496.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.271-16914_271-1688 others(32): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTTTCT others(25): Show |
3 | a0001c0001t0003g0019 a0001c0001t0003g0025 a0001c0001t0003g0027 |
3 | HG02080.hp1 NA18747.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.271-16918_271-1688 others(36): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATCTTTCT others(29): Show |
2 | a0001c0001t0002g0126 a0001c0001t0003g0066 |
2 | HG01069.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.271-16922_271-1688 others(40): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194122 | A | ATTCTTTC others(6): Show |
1 | a0002c0002t0001g0310 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.271-16939_271-1693 others(17): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194122 | ||||||
| chr11:28194162 | TTCTTTCT others(3): Show |
T | 2 | a0002c0002t0001g0263 a0002c0002t0001g0270 |
2 | HG02602.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.271-16898_271-1688 others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194162 | ||||||
| chr11:28194174 | T | TTCTTTCT others(6): Show |
1 | a0001c0001t0011g0210 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.271-16887_271-1688 others(17): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194174 | ||||||
| chr11:28194174 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0003g0058 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.271-16887_271-1688 others(26): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194174 | ||||||
| chr11:28194174 | T | TTCTTTCT others(19): Show |
1 | a0001c0001t0006g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.271-16887_271-1688 others(30): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194174 | ||||||
| chr11:28194175 | T | TCTTTCTT others(10): Show |
1 | a0001c0001t0002g0141 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.271-16887_271-1688 others(21): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194175 | |||||||
| chr11:28194175 | T | TCTTTCTT others(14): Show |
2 | a0001c0001t0004g0178 a0001c0001t0004g0200 |
2 | HG00733.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.271-16887_271-1688 others(25): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194175 | |||||||
| chr11:28194175 | T | TCTTTCTT others(17): Show |
1 | a0003c0004t0001g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.271-16887_271-1688 others(28): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194175 | |||||||
| chr11:28194175 | T | TCTTTCTT others(18): Show |
1 | a0001c0001t0006g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.271-16887_271-1688 others(29): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194175 | |||||||
| chr11:28194175 | T | TCTTTCTT others(22): Show |
1 | a0001c0001t0010g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.271-16887_271-1688 others(33): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194175 | |||||||
| chr11:28194175 | T | TCTTTCTT others(26): Show |
1 | a0001c0001t0002g0091 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.271-16887_271-1688 others(37): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194175 | |||||||
| chr11:28194176 | T | C | 4 | a0002c0002t0001g0254 a0002c0002t0001g0263 a0002c0002t0001g0270 others(1): Show |
4 | HG01496.hp2 HG02602.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-16886T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194176 | |||||||
| chr11:28194191 | T | C | 4 | a0002c0002t0001g0254 a0002c0002t0001g0263 a0002c0002t0001g0270 others(1): Show |
4 | HG01496.hp2 HG02602.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-16871T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194191 | |||||||
| chr11:28194192 | C | CCTCT | 8 | a0001c0001t0003g0017 a0001c0001t0003g0026 a0001c0001t0003g0027 others(5): Show |
8 | HG00544.hp2 NA18747.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-16853_271-1685 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194192 | ||||||
| chr11:28194192 | C | T | 4 | a0002c0002t0001g0254 a0002c0002t0001g0263 a0002c0002t0001g0270 others(1): Show |
4 | HG01496.hp2 HG02602.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-16870C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194192 | |||||||
| chr11:28194518 | G | A | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.271-16544G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194518 | |||||||
| chr11:28194841 | C | G | 1 | a0002c0002t0001g0303 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.271-16221C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194841 | |||||||
| chr11:28194848 | G | A | 1 | a0009c0010t0002g0101 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.271-16214G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194848 | |||||||
| chr11:28195410 | G | A | 1 | a0002c0002t0001g0243 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.271-15652G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28195410 | |||||||
| chr11:28195556 | G | A | 1 | a0001c0001t0004g0228 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.271-15506G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28195556 | |||||||
| chr11:28195590 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-15472G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28195590 | |||||||
| chr11:28195596 | A | G | 2 | a0001c0001t0003g0041 a0001c0001t0003g0042 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.271-15466A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28195596 | |||||||
| chr11:28195676 | G | T | 1 | a0002c0002t0001g0294 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.271-15386G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28195676 | |||||||
| chr11:28195711 | T | C | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG00609.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.271-15351T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28195711 | |||||||
| chr11:28195840 | C | G | 6 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-15222C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28195840 | |||||||
| chr11:28195936 | T | G | 68 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(65): Show |
68 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.271-15126T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28195936 | |||||||
| chr11:28196367 | A | G | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.271-14695A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28196367 | |||||||
| chr11:28196451 | G | GT | 5 | a0001c0001t0002g0132 a0001c0001t0003g0032 a0001c0001t0004g0206 others(2): Show |
6 | HG01346.hp1 HG02647.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-14603dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28196451 | ||||||
| chr11:28196594 | T | G | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.271-14468T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28196594 | |||||||
| chr11:28196700 | C | T | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.271-14362C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28196700 | |||||||
| chr11:28196993 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-14069C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28196993 | |||||||
| chr11:28197190 | T | C | 1 | a0001c0001t0004g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271-13872T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28197190 | |||||||
| chr11:28197365 | C | T | 1 | a0003c0004t0001g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.271-13697C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28197365 | |||||||
| chr11:28197790 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.271-13272G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28197790 | |||||||
| chr11:28197816 | A | C | 1 | a0001c0001t0007g0231 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.271-13246A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28197816 | |||||||
| chr11:28197870 | G | T | 1 | a0001c0001t0003g0065 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.271-13192G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28197870 | |||||||
| chr11:28198132 | A | T | 10 | a0001c0001t0004g0212 a0001c0001t0008g0083 a0001c0001t0008g0177 others(7): Show |
10 | HG00735.hp1 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-12930A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28198132 | |||||||
| chr11:28198154 | A | G | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.271-12908A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28198154 | |||||||
| chr11:28198433 | GATTTATT others(6): Show |
G | 5 | a0001c0001t0003g0002 a0001c0001t0003g0047 a0001c0001t0003g0049 others(2): Show |
6 | NA18964.hp2 NA18983.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-12626_271-1261 others(17): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28198433 | ||||||
| chr11:28198497 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-12565A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28198497 | |||||||
| chr11:28198708 | C | G | 1 | a0002c0002t0001g0324 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.271-12354C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28198708 | |||||||
| chr11:28198949 | A | G | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.271-12113A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28198949 | |||||||
| chr11:28198959 | G | T | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.271-12103G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28198959 | |||||||
| chr11:28198982 | A | AT | 160 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(157): Show |
162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.271-12066dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28198982 | ||||||
| chr11:28199051 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-12011C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28199051 | |||||||
| chr11:28199200 | A | G | 5 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0143 others(2): Show |
5 | HG00609.hp1 HG02523.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-11862A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28199200 | |||||||
| chr11:28199389 | A | T | 3 | a0002c0002t0001g0278 a0002c0002t0001g0292 a0002c0002t0001g0293 |
3 | NA18612.hp1 NA18955.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.271-11673A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28199389 | |||||||
| chr11:28199887 | C | T | 1 | a0002c0002t0001g0250 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.271-11175C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28199887 | |||||||
| chr11:28199932 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.271-11130C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28199932 | |||||||
| chr11:28199964 | G | A | 1 | a0011c0012t0003g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.271-11098G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28199964 | |||||||
| chr11:28200071 | T | A | 3 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0005g0072 |
3 | HG00621.hp2 NA18943.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.271-10991T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28200071 | |||||||
| chr11:28200130 | T | C | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.271-10932T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28200130 | |||||||
| chr11:28200225 | C | A | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.271-10837C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28200225 | |||||||
| chr11:28200351 | T | A | 9 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(6): Show |
9 | HG00544.hp1 HG02040.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-10711T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28200351 | |||||||
| chr11:28200533 | C | T | 2 | a0002c0002t0001g0320 a0002c0002t0001g0321 |
2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.271-10529C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28200533 | |||||||
| chr11:28200683 | A | T | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.271-10379A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28200683 | |||||||
| chr11:28200982 | T | C | 1 | a0002c0002t0001g0263 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.271-10080T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28200982 | |||||||
| chr11:28200989 | G | C | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.271-10073G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28200989 | |||||||
| chr11:28201121 | G | A | 2 | a0001c0001t0006g0225 a0009c0010t0002g0101 |
2 | NA18522.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.271-9941G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28201121 | |||||||
| chr11:28201223 | A | G | 1 | a0002c0002t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.271-9839A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28201223 | |||||||
| chr11:28201247 | G | A | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.271-9815G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28201247 | |||||||
| chr11:28201298 | T | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-9764T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28201298 | |||||||
| chr11:28201384 | T | C | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.271-9678T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28201384 | |||||||
| chr11:28201610 | G | GGGGTGTG others(17): Show |
1 | a0001c0001t0004g0232 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.271-9451_271-9450i others(26): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28201610 | ||||||
| chr11:28201610 | G | GGGGTGTG others(21): Show |
3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.271-9451_271-9450i others(30): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28201610 | ||||||
| chr11:28201610 | G | GGGTGTGT others(18): Show |
1 | a0001c0001t0018g0010 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.271-9451_271-9450i others(27): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28201610 | ||||||
| chr11:28201610 | G | GGTGTGTG others(11): Show |
1 | a0001c0001t0002g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.271-9438_271-9437i others(20): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28201610 | ||||||
| chr11:28201610 | G | GGTGTGTG others(13): Show |
7 | a0001c0001t0001g0214 a0001c0001t0003g0065 a0001c0001t0009g0167 others(4): Show |
7 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-9438_271-9437i others(22): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28201610 | ||||||
| chr11:28201610 | G | GGTGTGTG others(15): Show |
77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(74): Show |
77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.271-9438_271-9437i others(24): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28201610 | ||||||
| chr11:28201610 | G | GGTGTGTG others(19): Show |
13 | a0001c0001t0003g0029 a0001c0001t0004g0196 a0001c0001t0004g0197 others(10): Show |
14 | HG00621.hp2 HG01515.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.271-9438_271-9437i others(28): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28201610 | ||||||
| chr11:28201610 | G | GGTGTGTG others(21): Show |
5 | a0001c0001t0003g0008 a0001c0001t0012g0075 a0002c0002t0001g0244 others(2): Show |
5 | HG02602.hp2 HG03098.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-9438_271-9437i others(30): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28201610 | ||||||
| chr11:28201610 | G | GGTGTGTG others(23): Show |
1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-9438_271-9437i others(32): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28201610 | ||||||
| chr11:28201610 | G | GTGTGTGT others(16): Show |
1 | a0001c0001t0002g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.271-9452_271-9451i others(25): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28201610 | |||||||
| chr11:28201881 | C | T | 1 | a0001c0001t0016g0020 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.271-9181C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28201881 | |||||||
| chr11:28201932 | T | A | 1 | a0001c0001t0002g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.271-9130T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28201932 | |||||||
| chr11:28202058 | T | G | 1 | a0001c0001t0006g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.271-9004T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28202058 | |||||||
| chr11:28202522 | A | G | 1 | a0001c0001t0005g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.271-8540A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28202522 | |||||||
| chr11:28202792 | A | G | 3 | a0002c0002t0001g0004 a0002c0002t0001g0322 a0002c0002t0001g0323 |
4 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-8270A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28202792 | |||||||
| chr11:28202978 | T | TA | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.271-8075dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28202978 | ||||||
| chr11:28203113 | A | G | 14 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0026 others(11): Show |
14 | HG01361.hp2 HG02602.hp2 HG02683.hp1 others(11): Show |
intron_variant | MODIFIER | c.271-7949A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28203113 | |||||||
| chr11:28203387 | A | C | 1 | a0002c0002t0001g0243 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.271-7675A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28203387 | |||||||
| chr11:28203506 | A | T | 86 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(83): Show |
88 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.271-7556A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28203506 | |||||||
| chr11:28203733 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.271-7329T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28203733 | |||||||
| chr11:28203863 | A | G | 1 | a0001c0001t0005g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.271-7199A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28203863 | |||||||
| chr11:28204197 | T | C | 1 | a0002c0002t0001g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.271-6865T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28204197 | |||||||
| chr11:28204234 | C | A | 6 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-6828C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28204234 | |||||||
| chr11:28204337 | T | G | 1 | a0002c0002t0001g0254 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.271-6725T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28204337 | |||||||
| chr11:28204393 | G | A | 1 | a0002c0002t0001g0310 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.271-6669G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28204393 | |||||||
| chr11:28204398 | T | C | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.271-6664T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28204398 | |||||||
| chr11:28204435 | C | CT | 80 | a0001c0001t0003g0038 a0001c0001t0004g0175 a0001c0001t0004g0178 others(77): Show |
81 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.271-6601dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28204435 | ||||||
| chr11:28204435 | C | CTT | 8 | a0001c0001t0010g0216 a0002c0002t0001g0268 a0002c0002t0001g0271 others(5): Show |
8 | HG02056.hp1 HG02257.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-6602_271-6601d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28204435 | ||||||
| chr11:28204435 | CT | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(174): Show |
179 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.271-6601delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28204435 | ||||||
| chr11:28204435 | CTTTTTTT others(5): Show |
C | 3 | a0002c0002t0001g0266 a0002c0002t0001g0267 a0002c0002t0001g0274 |
3 | NA18965.hp2 NA18966.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.271-6612_271-6601d others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28204435 | ||||||
| chr11:28204435 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG00544.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.271-6613_271-6601d others(15): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28204435 | ||||||
| chr11:28204472 | A | T | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-6590A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28204472 | |||||||
| chr11:28204532 | C | T | 1 | a0002c0002t0001g0251 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.271-6530C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28204532 | |||||||
| chr11:28204891 | A | G | 2 | a0002c0002t0001g0279 a0002c0002t0001g0281 |
2 | HG00733.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.271-6171A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28204891 | |||||||
| chr11:28204947 | C | A | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.271-6115C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28204947 | |||||||
| chr11:28205195 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.271-5867T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205195 | |||||||
| chr11:28205202 | C | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.271-5860C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205202 | |||||||
| chr11:28205392 | T | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-5670T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205392 | |||||||
| chr11:28205411 | C | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.271-5651C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205411 | |||||||
| chr11:28205506 | T | C | 1 | a0001c0001t0012g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.271-5556T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205506 | |||||||
| chr11:28205508 | G | A | 1 | a0002c0002t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.271-5554G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205508 | |||||||
| chr11:28205568 | C | T | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.271-5494C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205568 | |||||||
| chr11:28205602 | C | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-5460C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205602 | |||||||
| chr11:28205695 | A | G | 1 | a0001c0001t0003g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.271-5367A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205695 | |||||||
| chr11:28205703 | A | G | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.271-5359A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205703 | |||||||
| chr11:28205710 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-5352T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205710 | |||||||
| chr11:28205863 | G | A | 1 | a0009c0010t0002g0101 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.271-5199G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205863 | |||||||
| chr11:28205933 | C | T | 25 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0088 others(22): Show |
25 | HG00544.hp1 HG01952.hp2 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.271-5129C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205933 | |||||||
| chr11:28205942 | T | A | 1 | a0001c0001t0019g0208 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.271-5120T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205942 | |||||||
| chr11:28205980 | T | G | 157 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(154): Show |
159 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(156): Show |
intron_variant | MODIFIER | c.271-5082T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205980 | |||||||
| chr11:28205983 | G | A | 1 | a0002c0002t0001g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.271-5079G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28205983 | |||||||
| chr11:28206027 | G | A | 1 | a0001c0001t0004g0190 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.271-5035G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206027 | |||||||
| chr11:28206043 | G | C | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.271-5019G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206043 | |||||||
| chr11:28206104 | T | C | 1 | a0002c0002t0001g0293 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.271-4958T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206104 | |||||||
| chr11:28206144 | G | C | 42 | a0001c0001t0002g0085 a0001c0001t0002g0115 a0001c0001t0002g0116 others(39): Show |
42 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.271-4918G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206144 | |||||||
| chr11:28206180 | G | C | 238 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(235): Show |
240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.271-4882G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206180 | |||||||
| chr11:28206196 | A | G | 2 | a0001c0001t0003g0066 a0001c0001t0003g0067 |
2 | NA18988.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.271-4866A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206196 | |||||||
| chr11:28206201 | G | A | 1 | a0001c0001t0004g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.271-4861G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206201 | |||||||
| chr11:28206209 | T | G | 3 | a0002c0002t0001g0260 a0002c0002t0001g0261 a0002c0002t0001g0262 |
3 | HG01952.hp1 NA19062.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.271-4853T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206209 | |||||||
| chr11:28206241 | G | C | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.271-4821G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206241 | |||||||
| chr11:28206248 | G | A | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.271-4814G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206248 | |||||||
| chr11:28206254 | A | G | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.271-4808A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206254 | |||||||
| chr11:28206289 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-4773A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206289 | |||||||
| chr11:28206314 | C | G | 1 | a0003c0004t0027g0284 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.271-4748C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206314 | |||||||
| chr11:28206392 | A | T | 3 | a0001c0001t0002g0085 a0001c0001t0002g0115 a0001c0001t0002g0150 |
3 | HG03688.hp1 HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.271-4670A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206392 | |||||||
| chr11:28206398 | G | A | 1 | a0001c0001t0003g0051 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.271-4664G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206398 | |||||||
| chr11:28206571 | G | A | 40 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(37): Show |
40 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-4491G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206571 | |||||||
| chr11:28206706 | A | C | 229 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(226): Show |
231 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(228): Show |
intron_variant | MODIFIER | c.271-4356A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206706 | |||||||
| chr11:28206761 | G | T | 1 | a0001c0001t0003g0045 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.271-4301G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206761 | |||||||
| chr11:28206767 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.271-4295G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206767 | |||||||
| chr11:28206984 | C | T | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.271-4078C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206984 | |||||||
| chr11:28207175 | G | C | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-3887G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207175 | |||||||
| chr11:28207195 | A | G | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.271-3867A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207195 | |||||||
| chr11:28207208 | C | T | 1 | a0001c0001t0009g0185 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.271-3854C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207208 | |||||||
| chr11:28207218 | A | C | 1 | a0001c0001t0008g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.271-3844A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207218 | |||||||
| chr11:28207278 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-3784G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207278 | |||||||
| chr11:28207354 | G | C | 1 | a0002c0002t0001g0276 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.271-3708G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207354 | |||||||
| chr11:28207389 | C | G | 1 | a0002c0002t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.271-3673C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207389 | |||||||
| chr11:28207393 | T | G | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-3669T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207393 | |||||||
| chr11:28207506 | C | T | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.271-3556C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207506 | |||||||
| chr11:28207516 | T | TTTTATTG others(987): Show |
1 | a0002c0002t0001g0324 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.271-3530_271-3529i others(996): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28207516 | ||||||
| chr11:28207845 | T | C | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.271-3217T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207845 | |||||||
| chr11:28207957 | C | A | 2 | a0001c0001t0007g0231 a0001c0001t0007g0236 |
2 | NA18963.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.271-3105C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28207957 | |||||||
| chr11:28208024 | C | A | 1 | a0002c0002t0001g0300 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.271-3038C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208024 | |||||||
| chr11:28208045 | C | T | 8 | a0001c0001t0004g0232 a0001c0001t0006g0230 a0001c0001t0007g0231 others(5): Show |
8 | HG00621.hp1 HG00673.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-3017C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208045 | |||||||
| chr11:28208095 | A | G | 1 | a0004c0003t0002g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.271-2967A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208095 | |||||||
| chr11:28208321 | G | A | 3 | a0001c0001t0001g0214 a0001c0001t0003g0027 a0001c0001t0005g0036 |
3 | HG00544.hp2 HG01496.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.271-2741G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208321 | |||||||
| chr11:28208389 | G | C | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.271-2673G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208389 | |||||||
| chr11:28208446 | C | G | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.271-2616C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208446 | |||||||
| chr11:28208584 | C | A | 1 | a0002c0002t0001g0246 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.271-2478C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208584 | |||||||
| chr11:28208586 | A | G | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.271-2476A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208586 | |||||||
| chr11:28208628 | G | T | 2 | a0001c0001t0012g0074 a0001c0001t0023g0037 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.271-2434G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208628 | |||||||
| chr11:28208734 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.271-2328A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208734 | |||||||
| chr11:28208905 | A | C | 1 | a0002c0002t0001g0278 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.271-2157A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208905 | |||||||
| chr11:28208951 | T | C | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.271-2111T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208951 | |||||||
| chr11:28209007 | G | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.271-2055G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28209007 | |||||||
| chr11:28209076 | C | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-1986C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28209076 | |||||||
| chr11:28209080 | G | T | 6 | a0002c0002t0001g0279 a0002c0002t0001g0280 a0002c0002t0001g0282 others(3): Show |
6 | HG00733.hp2 HG01081.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-1982G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28209080 | |||||||
| chr11:28209096 | A | G | 1 | a0001c0001t0003g0008 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.271-1966A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28209096 | |||||||
| chr11:28209309 | C | T | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.271-1753C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28209309 | |||||||
| chr11:28209643 | C | T | 4 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
4 | NA18956.hp1 NA18970.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1419C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28209643 | |||||||
| chr11:28209912 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-1150A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28209912 | |||||||
| chr11:28209920 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-1142A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28209920 | |||||||
| chr11:28210015 | G | T | 1 | a0001c0001t0002g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.271-1047G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28210015 | |||||||
| chr11:28210239 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-823C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28210239 | |||||||
| chr11:28210271 | C | A | 1 | a0002c0002t0001g0254 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.271-791C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28210271 | |||||||
| chr11:28210278 | T | C | 1 | a0002c0002t0026g0326 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.271-784T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28210278 | |||||||
| chr11:28210474 | A | C | 1 | a0002c0002t0001g0290 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.271-588A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28210474 | |||||||
| chr11:28210535 | A | G | 4 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 others(1): Show |
4 | NA18949.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-527A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28210535 | |||||||
| chr11:28210738 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-324G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28210738 | |||||||
| chr11:28210886 | C | T | 1 | a0011c0012t0003g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.271-176C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28210886 | |||||||
| chr11:28211322 | T | C | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.407+124T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28211322 | |||||||
| chr11:28211442 | T | C | 1 | a0002c0002t0001g0265 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.407+244T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28211442 | |||||||
| chr11:28211492 | C | T | 1 | a0001c0001t0003g0078 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.407+294C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28211492 | |||||||
| chr11:28211610 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+412A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28211610 | |||||||
| chr11:28211612 | T | C | 2 | a0001c0001t0004g0178 a0001c0001t0006g0203 |
2 | NA18966.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.407+414T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28211612 | |||||||
| chr11:28211785 | A | T | 2 | a0001c0001t0003g0027 a0001c0001t0005g0036 |
2 | HG00544.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.407+587A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28211785 | |||||||
| chr11:28211918 | G | T | 1 | a0001c0001t0002g0099 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.407+720G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28211918 | |||||||
| chr11:28212221 | A | G | 40 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(37): Show |
40 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.407+1023A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28212221 | |||||||
| chr11:28212470 | A | G | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.407+1272A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28212470 | |||||||
| chr11:28212651 | G | T | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.407+1453G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28212651 | |||||||
| chr11:28212667 | T | C | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG00544.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.407+1469T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28212667 | |||||||
| chr11:28213059 | A | G | 1 | a0001c0001t0002g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.407+1861A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28213059 | |||||||
| chr11:28213411 | C | A | 7 | a0001c0001t0012g0073 a0001c0001t0012g0074 a0001c0001t0012g0075 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+2213C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28213411 | |||||||
| chr11:28213616 | T | TA | 9 | a0001c0001t0002g0085 a0001c0001t0003g0044 a0001c0001t0003g0065 others(6): Show |
9 | HG01943.hp2 HG02132.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.407+2435dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28213616 | ||||||
| chr11:28213658 | C | CT | 7 | a0001c0001t0002g0147 a0001c0001t0004g0161 a0001c0001t0004g0162 others(4): Show |
7 | HG01952.hp1 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+2475dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28213658 | ||||||
| chr11:28213717 | G | T | 1 | a0001c0001t0005g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.407+2519G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28213717 | |||||||
| chr11:28213838 | G | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(74): Show |
77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.407+2640G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28213838 | |||||||
| chr11:28213946 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.407+2748C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28213946 | |||||||
| chr11:28214239 | G | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+3041G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28214239 | |||||||
| chr11:28214260 | C | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+3062C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28214260 | |||||||
| chr11:28214496 | A | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.407+3298A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28214496 | |||||||
| chr11:28214506 | C | G | 1 | a0001c0001t0008g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.407+3308C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28214506 | |||||||
| chr11:28214582 | T | C | 1 | a0002c0002t0001g0271 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.407+3384T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28214582 | |||||||
| chr11:28215098 | A | G | 4 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0258 others(1): Show |
4 | NA18971.hp2 NA18983.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.407+3900A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28215098 | |||||||
| chr11:28215146 | G | C | 2 | a0001c0001t0011g0210 a0001c0001t0011g0241 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.407+3948G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28215146 | |||||||
| chr11:28215406 | C | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+4208C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28215406 | |||||||
| chr11:28215551 | C | T | 1 | a0011c0012t0003g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.407+4353C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28215551 | |||||||
| chr11:28215703 | G | A | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.407+4505G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28215703 | |||||||
| chr11:28215902 | A | AGGTACTC others(13): Show |
1 | a0002c0002t0001g0325 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.407+4718_407+4737d others(22): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28215902 | ||||||
| chr11:28215926 | A | G | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.407+4728A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28215926 | |||||||
| chr11:28215969 | C | T | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.407+4771C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28215969 | |||||||
| chr11:28215991 | C | T | 1 | a0002c0002t0001g0310 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.407+4793C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28215991 | |||||||
| chr11:28216015 | G | A | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.407+4817G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216015 | |||||||
| chr11:28216051 | A | G | 1 | a0002c0002t0015g0318 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.407+4853A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216051 | |||||||
| chr11:28216062 | AAATGAAA others(6): Show |
A | 2 | a0002c0002t0001g0320 a0002c0002t0001g0321 |
2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.407+4869_407+4881d others(15): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28216062 | ||||||
| chr11:28216323 | C | A | 19 | a0002c0002t0001g0243 a0002c0002t0001g0246 a0002c0002t0001g0248 others(16): Show |
19 | HG00597.hp1 HG02027.hp2 HG02602.hp1 others(16): Show |
intron_variant | MODIFIER | c.407+5125C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216323 | |||||||
| chr11:28216402 | T | G | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.407+5204T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216402 | |||||||
| chr11:28216566 | C | CT | 11 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0026 others(8): Show |
11 | HG01361.hp2 HG02602.hp2 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.407+5376dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28216566 | ||||||
| chr11:28216808 | G | A | 2 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
2 | HG00738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.407+5610G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216808 | |||||||
| chr11:28216895 | CT | C | 90 | a0001c0001t0003g0067 a0001c0001t0004g0171 a0002c0002t0001g0003 others(87): Show |
92 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.407+5704delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28216895 | ||||||
| chr11:28216950 | C | T | 7 | a0001c0001t0002g0239 a0004c0003t0002g0086 a0004c0003t0002g0109 others(4): Show |
7 | HG00642.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.407+5752C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216950 | |||||||
| chr11:28216953 | G | C | 1 | a0001c0001t0003g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.407+5755G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216953 | |||||||
| chr11:28216983 | C | A | 1 | a0002c0002t0001g0271 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.407+5785C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216983 | |||||||
| chr11:28217011 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+5813A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28217011 | |||||||
| chr11:28217024 | G | A | 1 | a0001c0001t0024g0184 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.407+5826G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28217024 | |||||||
| chr11:28217226 | G | A | 1 | a0001c0001t0003g0008 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.407+6028G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28217226 | |||||||
| chr11:28217380 | G | A | 1 | a0002c0002t0001g0270 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.407+6182G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28217380 | |||||||
| chr11:28217566 | G | T | 1 | a0001c0001t0002g0093 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.407+6368G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28217566 | |||||||
| chr11:28217619 | A | T | 1 | a0002c0002t0026g0326 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.407+6421A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28217619 | |||||||
| chr11:28217753 | A | T | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.407+6555A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28217753 | |||||||
| chr11:28217859 | A | C | 1 | a0001c0001t0005g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.407+6661A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28217859 | |||||||
| chr11:28217941 | A | G | 1 | a0002c0002t0001g0262 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.407+6743A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28217941 | |||||||
| chr11:28218147 | A | G | 1 | a0001c0001t0003g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.407+6949A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218147 | |||||||
| chr11:28218148 | T | C | 1 | a0001c0001t0003g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.407+6950T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218148 | |||||||
| chr11:28218166 | T | G | 1 | a0001c0001t0003g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.407+6968T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218166 | |||||||
| chr11:28218240 | G | A | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.407+7042G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218240 | |||||||
| chr11:28218258 | G | A | 4 | a0001c0001t0004g0176 a0001c0001t0004g0180 a0001c0001t0004g0207 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.407+7060G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218258 | |||||||
| chr11:28218285 | G | C | 3 | a0003c0004t0001g0285 a0003c0004t0001g0296 a0003c0004t0001g0305 |
3 | HG01891.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.407+7087G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218285 | |||||||
| chr11:28218465 | C | T | 5 | a0002c0002t0001g0247 a0002c0002t0001g0286 a0002c0002t0001g0287 others(2): Show |
5 | HG00609.hp2 NA18950.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.407+7267C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218465 | |||||||
| chr11:28218479 | A | T | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.407+7281A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218479 | |||||||
| chr11:28218565 | G | C | 2 | a0001c0014t0021g0229 a0002c0002t0001g0300 |
2 | HG03453.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.407+7367G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218565 | |||||||
| chr11:28218646 | A | T | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.407+7448A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218646 | |||||||
| chr11:28218703 | A | G | 1 | a0001c0001t0007g0234 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.407+7505A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218703 | |||||||
| chr11:28218873 | G | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+7675G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218873 | |||||||
| chr11:28218901 | G | A | 3 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0155 |
3 | NA18956.hp1 NA18979.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.407+7703G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218901 | |||||||
| chr11:28218921 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.407+7723G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28218921 | |||||||
| chr11:28219106 | A | G | 1 | a0002c0002t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.407+7908A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28219106 | |||||||
| chr11:28219278 | T | G | 1 | a0003c0004t0001g0313 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.407+8080T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28219278 | |||||||
| chr11:28219829 | A | G | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.407+8631A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28219829 | |||||||
| chr11:28219897 | C | G | 1 | a0001c0001t0003g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.407+8699C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28219897 | |||||||
| chr11:28219932 | G | A | 1 | a0002c0002t0001g0290 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.407+8734G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28219932 | |||||||
| chr11:28220063 | G | T | 2 | a0001c0001t0012g0074 a0001c0001t0023g0037 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.407+8865G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220063 | |||||||
| chr11:28220128 | G | T | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.407+8930G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220128 | |||||||
| chr11:28220195 | G | A | 42 | a0001c0001t0002g0085 a0001c0001t0002g0115 a0001c0001t0002g0116 others(39): Show |
42 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.407+8997G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220195 | |||||||
| chr11:28220354 | G | T | 3 | a0002c0002t0001g0254 a0002c0002t0001g0263 a0002c0002t0001g0270 |
3 | HG02602.hp1 HG03654.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.407+9156G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220354 | |||||||
| chr11:28220380 | C | T | 1 | a0001c0001t0009g0235 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.407+9182C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220380 | |||||||
| chr11:28220530 | G | A | 3 | a0002c0002t0001g0278 a0002c0002t0001g0292 a0002c0002t0001g0293 |
3 | NA18612.hp1 NA18955.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.407+9332G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220530 | |||||||
| chr11:28220628 | C | T | 1 | a0001c0001t0003g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.407+9430C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220628 | |||||||
| chr11:28220653 | G | A | 1 | a0001c0001t0009g0185 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.407+9455G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220653 | |||||||
| chr11:28220752 | G | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+9554G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220752 | |||||||
| chr11:28220819 | G | A | 2 | a0001c0001t0012g0073 a0001c0001t0012g0075 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.407+9621G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220819 | |||||||
| chr11:28220988 | T | C | 3 | a0001c0001t0006g0222 a0001c0001t0006g0223 a0001c0001t0006g0227 |
3 | HG06807.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407+9790T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28220988 | |||||||
| chr11:28221035 | T | A | 1 | a0001c0001t0002g0239 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.407+9837T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28221035 | |||||||
| chr11:28221152 | C | G | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.407+9954C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28221152 | |||||||
| chr11:28221206 | T | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+10008T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28221206 | |||||||
| chr11:28221237 | T | G | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.407+10039T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28221237 | |||||||
| chr11:28221330 | C | A | 3 | a0001c0001t0006g0222 a0001c0001t0006g0223 a0001c0001t0006g0227 |
3 | HG06807.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407+10132C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28221330 | |||||||
| chr11:28221376 | G | A | 83 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(80): Show |
85 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.407+10178G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28221376 | |||||||
| chr11:28221392 | G | A | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.407+10194G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28221392 | |||||||
| chr11:28221408 | C | G | 2 | a0001c0001t0003g0026 a0001c0001t0005g0031 |
2 | NA18992.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.407+10210C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28221408 | |||||||
| chr11:28221497 | T | C | 1 | a0003c0004t0001g0313 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.407+10299T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28221497 | |||||||
| chr11:28221901 | C | T | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.407+10703C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28221901 | |||||||
| chr11:28222143 | C | T | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.407+10945C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28222143 | |||||||
| chr11:28222147 | A | G | 1 | a0002c0002t0001g0298 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.407+10949A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28222147 | |||||||
| chr11:28222149 | A | T | 2 | a0001c0001t0002g0152 a0001c0001t0002g0155 |
2 | NA18979.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.407+10951A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28222149 | |||||||
| chr11:28222160 | A | G | 5 | a0002c0002t0001g0279 a0002c0002t0001g0280 a0002c0002t0001g0281 others(2): Show |
5 | HG00733.hp2 HG01081.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.407+10962A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28222160 | |||||||
| chr11:28222243 | T | A | 22 | a0001c0001t0003g0002 a0001c0001t0003g0044 a0001c0001t0003g0045 others(19): Show |
23 | HG00621.hp2 HG02132.hp1 NA18943.hp1 others(20): Show |
intron_variant | MODIFIER | c.407+11045T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28222243 | |||||||
| chr11:28222254 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.407+11056G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28222254 | |||||||
| chr11:28222316 | A | G | 1 | a0002c0002t0001g0311 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.407+11118A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28222316 | |||||||
| chr11:28222400 | A | G | 42 | a0002c0002t0001g0004 a0002c0002t0001g0243 a0002c0002t0001g0246 others(39): Show |
43 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.407+11202A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28222400 | |||||||
| chr11:28222702 | T | A | 1 | a0001c0001t0002g0100 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.407+11504T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28222702 | |||||||
| chr11:28222998 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+11800A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28222998 | |||||||
| chr11:28223172 | G | A | 1 | a0001c0001t0003g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.407+11974G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28223172 | |||||||
| chr11:28223442 | G | C | 1 | a0001c0001t0003g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.407+12244G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28223442 | |||||||
| chr11:28223461 | A | C | 1 | a0001c0001t0023g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.407+12263A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28223461 | |||||||
| chr11:28223607 | G | C | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.407+12409G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28223607 | |||||||
| chr11:28223763 | G | C | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.407+12565G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28223763 | |||||||
| chr11:28223886 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.407+12688A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28223886 | |||||||
| chr11:28224037 | A | G | 1 | a0001c0001t0003g0082 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.407+12839A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28224037 | |||||||
| chr11:28224142 | G | A | 3 | a0004c0003t0002g0109 a0004c0003t0002g0111 a0004c0003t0002g0112 |
3 | HG02572.hp1 HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.407+12944G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28224142 | |||||||
| chr11:28224268 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.407+13070T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28224268 | |||||||
| chr11:28224295 | G | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+13097G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28224295 | |||||||
| chr11:28224601 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.407+13403C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28224601 | |||||||
| chr11:28225088 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+13890A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28225088 | |||||||
| chr11:28225272 | A | C | 5 | a0001c0001t0003g0002 a0001c0001t0003g0047 a0001c0001t0003g0049 others(2): Show |
6 | NA18964.hp2 NA18983.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.407+14074A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28225272 | |||||||
| chr11:28225277 | C | G | 1 | a0001c0001t0006g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.407+14079C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28225277 | |||||||
| chr11:28225354 | G | A | 1 | a0002c0002t0001g0279 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.407+14156G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28225354 | |||||||
| chr11:28225471 | C | T | 1 | a0001c0001t0016g0020 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.407+14273C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28225471 | |||||||
| chr11:28225810 | T | A | 1 | a0001c0001t0003g0027 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.407+14612T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28225810 | |||||||
| chr11:28226067 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.407+14869C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28226067 | |||||||
| chr11:28226222 | T | C | 1 | a0002c0002t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.407+15024T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28226222 | |||||||
| chr11:28226502 | A | C | 2 | a0001c0001t0003g0026 a0001c0001t0005g0031 |
2 | NA18992.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.407+15304A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28226502 | |||||||
| chr11:28226574 | A | G | 11 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0004g0183 others(8): Show |
11 | HG00733.hp1 HG01106.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.407+15376A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28226574 | |||||||
| chr11:28226806 | A | C | 1 | a0001c0001t0002g0239 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.407+15608A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28226806 | |||||||
| chr11:28226869 | T | A | 1 | a0001c0001t0008g0195 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.407+15671T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28226869 | |||||||
| chr11:28227065 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.407+15867C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28227065 | |||||||
| chr11:28227839 | C | A | 1 | a0001c0001t0004g0171 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.407+16641C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28227839 | |||||||
| chr11:28227900 | A | G | 3 | a0001c0001t0003g0032 a0001c0001t0003g0046 a0001c0001t0005g0043 |
3 | HG02683.hp1 HG02735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.407+16702A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28227900 | |||||||
| chr11:28227942 | C | A | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.407+16744C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28227942 | |||||||
| chr11:28227945 | A | G | 1 | a0002c0002t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.407+16747A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28227945 | |||||||
| chr11:28228180 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.407+16982C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28228180 | |||||||
| chr11:28228343 | AAT | A | 79 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(76): Show |
81 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.407+17147_407+1714 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28228343 | ||||||
| chr11:28228430 | A | G | 3 | a0001c0001t0003g0051 a0001c0001t0003g0065 a0001c0001t0003g0068 |
3 | NA18952.hp2 NA19070.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.407+17232A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28228430 | |||||||
| chr11:28228486 | T | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+17288T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28228486 | |||||||
| chr11:28228713 | C | G | 3 | a0005c0005t0014g0079 a0005c0005t0014g0080 a0005c0005t0025g0081 |
3 | HG02559.hp2 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.407+17515C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28228713 | |||||||
| chr11:28228735 | A | G | 1 | a0001c0001t0005g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.407+17537A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28228735 | |||||||
| chr11:28228919 | T | C | 1 | a0001c0007t0003g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.407+17721T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28228919 | |||||||
| chr11:28229038 | G | A | 1 | a0002c0002t0001g0253 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.407+17840G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28229038 | |||||||
| chr11:28229071 | G | A | 159 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(156): Show |
161 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.407+17873G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28229071 | |||||||
| chr11:28229429 | T | C | 1 | a0001c0001t0002g0102 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.407+18231T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28229429 | |||||||
| chr11:28229773 | C | A | 11 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0212 others(8): Show |
11 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.407+18575C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28229773 | |||||||
| chr11:28229785 | G | C | 2 | a0001c0001t0004g0196 a0001c0001t0004g0197 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.407+18587G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28229785 | |||||||
| chr11:28229822 | A | G | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.407+18624A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28229822 | |||||||
| chr11:28229857 | C | A | 1 | a0001c0001t0004g0238 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.407+18659C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28229857 | |||||||
| chr11:28230541 | A | G | 1 | a0002c0002t0001g0324 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.407+19343A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28230541 | |||||||
| chr11:28230562 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+19364A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28230562 | |||||||
| chr11:28230605 | T | C | 3 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0005g0072 |
3 | HG00621.hp2 NA18943.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.407+19407T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28230605 | |||||||
| chr11:28230610 | G | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+19412G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28230610 | |||||||
| chr11:28230719 | G | A | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.407+19521G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28230719 | |||||||
| chr11:28230892 | A | C | 1 | a0001c0001t0002g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.407+19694A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28230892 | |||||||
| chr11:28231218 | A | G | 1 | a0002c0002t0001g0275 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.407+20020A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28231218 | |||||||
| chr11:28231399 | T | G | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.407+20201T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28231399 | |||||||
| chr11:28231446 | A | G | 2 | a0001c0001t0003g0032 a0001c0001t0005g0043 |
2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.407+20248A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28231446 | |||||||
| chr11:28232114 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.407+20916T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28232114 | |||||||
| chr11:28232194 | A | G | 1 | a0001c0001t0007g0237 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.407+20996A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28232194 | |||||||
| chr11:28232312 | G | C | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+21114G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28232312 | |||||||
| chr11:28232582 | A | G | 1 | a0005c0005t0014g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.407+21384A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28232582 | |||||||
| chr11:28232586 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.407+21388C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28232586 | |||||||
| chr11:28232667 | C | T | 2 | a0001c0001t0004g0196 a0001c0001t0004g0197 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.407+21469C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28232667 | |||||||
| chr11:28232668 | C | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+21470C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28232668 | |||||||
| chr11:28232698 | C | G | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.407+21500C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28232698 | |||||||
| chr11:28232757 | G | C | 1 | a0001c0001t0002g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.407+21559G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28232757 | |||||||
| chr11:28232960 | G | A | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.407+21762G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28232960 | |||||||
| chr11:28233085 | A | G | 1 | a0002c0002t0001g0247 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.407+21887A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28233085 | |||||||
| chr11:28233099 | ATTTCATG others(1694): Show |
A | 1 | a0001c0001t0006g0230 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.407+21904_407+2360 others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28233099 | ||||||
| chr11:28233184 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.407+21986G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28233184 | |||||||
| chr11:28233329 | A | G | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.407+22131A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28233329 | |||||||
| chr11:28233506 | A | C | 79 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(76): Show |
79 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.407+22308A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28233506 | |||||||
| chr11:28233585 | G | A | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.407+22387G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28233585 | |||||||
| chr11:28233646 | A | G | 1 | a0002c0002t0001g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.407+22448A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28233646 | |||||||
| chr11:28233693 | G | C | 1 | a0001c0001t0003g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.407+22495G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28233693 | |||||||
| chr11:28233911 | G | A | 1 | a0001c0001t0003g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.407+22713G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28233911 | |||||||
| chr11:28233926 | G | T | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.407+22728G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28233926 | |||||||
| chr11:28233956 | C | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.407+22758C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28233956 | |||||||
| chr11:28234072 | G | C | 1 | a0001c0001t0004g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.407+22874G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234072 | |||||||
| chr11:28234074 | G | T | 1 | a0002c0002t0001g0246 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.407+22876G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234074 | |||||||
| chr11:28234082 | A | G | 1 | a0002c0002t0001g0246 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.407+22884A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234082 | |||||||
| chr11:28234094 | A | G | 1 | a0002c0002t0001g0246 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.407+22896A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234094 | |||||||
| chr11:28234137 | T | A | 1 | a0002c0002t0001g0254 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.407+22939T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234137 | |||||||
| chr11:28234153 | C | G | 1 | a0001c0001t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.407+22955C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234153 | |||||||
| chr11:28234224 | T | A | 1 | a0002c0002t0001g0300 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.407+23026T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234224 | |||||||
| chr11:28234337 | C | G | 159 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(156): Show |
161 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.407+23139C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234337 | |||||||
| chr11:28234391 | A | C | 1 | a0001c0001t0002g0126 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.407+23193A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234391 | |||||||
| chr11:28234543 | T | C | 1 | a0002c0002t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.407+23345T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234543 | |||||||
| chr11:28234741 | C | G | 1 | a0003c0004t0001g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.407+23543C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234741 | |||||||
| chr11:28234747 | T | C | 1 | a0003c0004t0001g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.407+23549T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234747 | |||||||
| chr11:28234935 | T | G | 1 | a0001c0001t0003g0078 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.407+23737T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234935 | |||||||
| chr11:28234987 | A | G | 238 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(235): Show |
240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.407+23789A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28234987 | |||||||
| chr11:28235018 | A | G | 11 | a0001c0001t0006g0160 a0001c0001t0006g0218 a0001c0001t0006g0220 others(8): Show |
11 | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.407+23820A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235018 | |||||||
| chr11:28235037 | T | C | 1 | a0002c0002t0001g0255 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.407+23839T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235037 | |||||||
| chr11:28235063 | C | A | 1 | a0011c0012t0003g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.407+23865C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235063 | |||||||
| chr11:28235141 | G | C | 7 | a0001c0001t0012g0073 a0001c0001t0012g0074 a0001c0001t0012g0075 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+23943G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235141 | |||||||
| chr11:28235220 | A | G | 1 | a0002c0002t0001g0252 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.407+24022A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235220 | |||||||
| chr11:28235238 | G | A | 2 | a0001c0001t0012g0074 a0001c0001t0023g0037 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.407+24040G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235238 | |||||||
| chr11:28235261 | G | T | 40 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(37): Show |
40 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.407+24063G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235261 | |||||||
| chr11:28235286 | C | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG00609.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.407+24088C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235286 | |||||||
| chr11:28235390 | C | T | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.407+24192C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235390 | |||||||
| chr11:28235406 | A | G | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.407+24208A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235406 | |||||||
| chr11:28235447 | G | C | 9 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(6): Show |
9 | HG00544.hp1 HG02040.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.407+24249G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235447 | |||||||
| chr11:28235448 | C | T | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.407+24250C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235448 | |||||||
| chr11:28235714 | A | G | 42 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(39): Show |
42 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.407+24516A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235714 | |||||||
| chr11:28235763 | T | C | 1 | a0002c0002t0026g0326 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.407+24565T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235763 | |||||||
| chr11:28235813 | C | G | 1 | a0002c0002t0001g0275 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.407+24615C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235813 | |||||||
| chr11:28235899 | A | G | 1 | a0002c0002t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.407+24701A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235899 | |||||||
| chr11:28235975 | C | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+24777C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235975 | |||||||
| chr11:28236018 | G | C | 1 | a0001c0001t0004g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.407+24820G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236018 | |||||||
| chr11:28236020 | T | C | 74 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(71): Show |
74 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.407+24822T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236020 | |||||||
| chr11:28236032 | G | T | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.407+24834G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236032 | |||||||
| chr11:28236139 | G | T | 1 | a0001c0001t0006g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.407+24941G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236139 | |||||||
| chr11:28236192 | T | C | 56 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(53): Show |
56 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.407+24994T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236192 | |||||||
| chr11:28236246 | A | G | 1 | a0001c0001t0011g0242 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.407+25048A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236246 | |||||||
| chr11:28236275 | G | T | 1 | a0001c0001t0012g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.407+25077G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236275 | |||||||
| chr11:28236323 | A | C | 1 | a0002c0002t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.407+25125A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236323 | |||||||
| chr11:28236359 | T | C | 1 | a0002c0002t0001g0314 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.407+25161T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236359 | |||||||
| chr11:28236639 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.407+25441C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236639 | |||||||
| chr11:28236672 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+25474A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236672 | |||||||
| chr11:28236730 | T | C | 238 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(235): Show |
240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.407+25532T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236730 | |||||||
| chr11:28236866 | C | A | 5 | a0001c0001t0003g0002 a0001c0001t0003g0047 a0001c0001t0003g0049 others(2): Show |
6 | NA18964.hp2 NA18983.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.407+25668C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236866 | |||||||
| chr11:28236880 | T | C | 1 | a0001c0001t0004g0206 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.407+25682T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236880 | |||||||
| chr11:28236969 | C | T | 13 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0026 others(10): Show |
13 | HG01361.hp2 HG02602.hp2 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.407+25771C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28236969 | |||||||
| chr11:28237208 | G | T | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.407+26010G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237208 | |||||||
| chr11:28237335 | G | A | 79 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(76): Show |
79 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.407+26137G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237335 | |||||||
| chr11:28237415 | T | G | 7 | a0001c0001t0012g0073 a0001c0001t0012g0074 a0001c0001t0012g0075 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+26217T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237415 | |||||||
| chr11:28237440 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.407+26242C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237440 | |||||||
| chr11:28237555 | T | C | 238 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(235): Show |
240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.407+26357T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237555 | |||||||
| chr11:28237578 | G | A | 1 | a0002c0002t0001g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.407+26380G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237578 | |||||||
| chr11:28237599 | A | G | 2 | a0002c0002t0001g0320 a0002c0002t0001g0321 |
2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.407+26401A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237599 | |||||||
| chr11:28237633 | C | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+26435C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237633 | |||||||
| chr11:28237674 | C | T | 1 | a0002c0002t0001g0277 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.407+26476C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237674 | |||||||
| chr11:28237747 | G | A | 1 | a0001c0001t0003g0078 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.407+26549G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237747 | |||||||
| chr11:28237747 | G | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+26549G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237747 | |||||||
| chr11:28237914 | C | T | 3 | a0005c0005t0014g0079 a0005c0005t0014g0080 a0005c0005t0025g0081 |
3 | HG02559.hp2 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.407+26716C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237914 | |||||||
| chr11:28237917 | G | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+26719G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237917 | |||||||
| chr11:28237925 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.407+26727G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237925 | |||||||
| chr11:28238027 | C | G | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
6 | HG00544.hp1 HG02040.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.407+26829C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238027 | |||||||
| chr11:28238274 | C | T | 3 | a0001c0001t0004g0206 a0001c0001t0005g0034 a0001c0001t0013g0035 |
3 | HG01346.hp1 NA18947.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.407+27076C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238274 | |||||||
| chr11:28238367 | G | A | 2 | a0002c0002t0001g0299 a0002c0002t0001g0309 |
2 | HG00423.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.407+27169G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238367 | |||||||
| chr11:28238405 | T | C | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.407+27207T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238405 | |||||||
| chr11:28238455 | C | T | 1 | a0002c0002t0001g0314 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.407+27257C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238455 | |||||||
| chr11:28238464 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.407+27266G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238464 | |||||||
| chr11:28238621 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.407+27423C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238621 | |||||||
| chr11:28238637 | C | T | 2 | a0001c0001t0004g0180 a0001c0001t0007g0179 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.407+27439C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238637 | |||||||
| chr11:28238817 | A | T | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.407+27619A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238817 | |||||||
| chr11:28238835 | C | T | 2 | a0001c0001t0007g0231 a0001c0001t0007g0236 |
2 | NA18963.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.407+27637C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238835 | |||||||
| chr11:28238872 | T | A | 3 | a0002c0002t0001g0266 a0002c0002t0001g0267 a0002c0002t0001g0274 |
3 | NA18965.hp2 NA18966.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.407+27674T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238872 | |||||||
| chr11:28238897 | T | C | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.407+27699T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238897 | |||||||
| chr11:28238959 | G | C | 1 | a0002c0002t0001g0251 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.407+27761G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238959 | |||||||
| chr11:28238983 | G | T | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.407+27785G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28238983 | |||||||
| chr11:28239117 | C | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+27919C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239117 | |||||||
| chr11:28239131 | A | T | 2 | a0001c0001t0004g0200 a0001c0001t0004g0201 |
2 | HG00733.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.407+27933A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239131 | |||||||
| chr11:28239134 | A | C | 1 | a0001c0001t0007g0234 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.407+27936A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239134 | |||||||
| chr11:28239317 | G | A | 1 | a0002c0002t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.407+28119G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239317 | |||||||
| chr11:28239481 | C | G | 1 | a0001c0001t0004g0232 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.407+28283C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239481 | |||||||
| chr11:28239533 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.407+28335C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239533 | |||||||
| chr11:28239610 | T | C | 2 | a0001c0001t0003g0026 a0001c0001t0005g0031 |
2 | NA18992.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.407+28412T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239610 | |||||||
| chr11:28239802 | A | G | 1 | a0002c0002t0001g0310 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.407+28604A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239802 | |||||||
| chr11:28239884 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+28686A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239884 | |||||||
| chr11:28239951 | T | A | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.407+28753T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239951 | |||||||
| chr11:28239958 | A | C | 1 | a0002c0002t0001g0302 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.407+28760A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239958 | |||||||
| chr11:28239973 | T | A | 1 | a0002c0002t0001g0254 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.407+28775T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28239973 | |||||||
| chr11:28240111 | C | T | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.407+28913C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28240111 | |||||||
| chr11:28240115 | A | C | 1 | a0001c0001t0003g0027 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.407+28917A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28240115 | |||||||
| chr11:28240279 | A | G | 1 | a0002c0002t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.407+29081A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28240279 | |||||||
| chr11:28240581 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.407+29383T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28240581 | |||||||
| chr11:28240593 | C | T | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.407+29395C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28240593 | |||||||
| chr11:28240618 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.407+29420C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28240618 | |||||||
| chr11:28240781 | A | T | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.407+29583A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28240781 | |||||||
| chr11:28241000 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.407+29802A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28241000 | |||||||
| chr11:28241212 | A | G | 1 | a0001c0001t0002g0119 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.407+30014A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28241212 | |||||||
| chr11:28241595 | A | T | 12 | a0002c0002t0001g0003 a0002c0002t0001g0245 a0002c0002t0001g0247 others(9): Show |
13 | HG00423.hp2 HG00609.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.407+30397A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28241595 | |||||||
| chr11:28241680 | C | T | 1 | a0001c0001t0008g0195 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.407+30482C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28241680 | |||||||
| chr11:28241711 | A | G | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.407+30513A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28241711 | |||||||
| chr11:28241768 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+30570G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28241768 | |||||||
| chr11:28241933 | A | G | 1 | a0002c0002t0001g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.407+30735A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28241933 | |||||||
| chr11:28242087 | A | C | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.407+30889A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28242087 | |||||||
| chr11:28242155 | G | A | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.407+30957G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28242155 | |||||||
| chr11:28242274 | T | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+31076T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28242274 | |||||||
| chr11:28242294 | C | G | 1 | a0001c0001t0004g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.407+31096C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28242294 | |||||||
| chr11:28242393 | C | T | 1 | a0001c0001t0005g0053 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.407+31195C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28242393 | |||||||
| chr11:28242402 | T | G | 77 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(74): Show |
79 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.407+31204T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28242402 | |||||||
| chr11:28242503 | C | T | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.407+31305C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28242503 | |||||||
| chr11:28242794 | A | G | 238 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(235): Show |
240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.407+31596A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28242794 | |||||||
| chr11:28242947 | C | T | 3 | a0001c0001t0004g0180 a0001c0001t0007g0179 a0002c0002t0001g0309 |
3 | HG03225.hp2 HG03516.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.407+31749C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28242947 | |||||||
| chr11:28242980 | A | G | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.407+31782A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28242980 | |||||||
| chr11:28243081 | T | TA | 6 | a0001c0001t0001g0214 a0001c0001t0002g0084 a0001c0001t0002g0088 others(3): Show |
6 | HG01496.hp1 HG03098.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.407+31896dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28243081 | ||||||
| chr11:28243435 | G | C | 1 | a0002c0002t0001g0308 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.407+32237G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243435 | |||||||
| chr11:28243492 | G | T | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.407+32294G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243492 | |||||||
| chr11:28243493 | T | C | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.407+32295T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243493 | |||||||
| chr11:28243688 | T | A | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.407+32490T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243688 | |||||||
| chr11:28243689 | C | T | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.407+32491C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243689 | |||||||
| chr11:28243692 | T | A | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.407+32494T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243692 | |||||||
| chr11:28243702 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.407+32504C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243702 | |||||||
| chr11:28243703 | G | A | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.407+32505G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243703 | |||||||
| chr11:28243710 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+32512A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243710 | |||||||
| chr11:28243785 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+32587C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243785 | |||||||
| chr11:28243994 | G | T | 1 | a0002c0002t0001g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.407+32796G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28243994 | |||||||
| chr11:28244051 | C | A | 84 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(81): Show |
86 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.407+32853C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28244051 | |||||||
| chr11:28244249 | A | G | 1 | a0002c0002t0001g0250 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.407+33051A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28244249 | |||||||
| chr11:28244357 | T | C | 1 | a0002c0002t0001g0312 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.407+33159T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28244357 | |||||||
| chr11:28244443 | GT | G | 7 | a0001c0001t0012g0073 a0001c0001t0012g0074 a0001c0001t0012g0075 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+33252delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28244443 | ||||||
| chr11:28244701 | A | G | 2 | a0002c0002t0001g0256 a0002c0002t0001g0258 |
2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.407+33503A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28244701 | |||||||
| chr11:28244710 | A | C | 1 | a0002c0002t0001g0243 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.407+33512A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28244710 | |||||||
| chr11:28244995 | A | G | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.407+33797A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28244995 | |||||||
| chr11:28245139 | A | T | 5 | a0001c0001t0003g0002 a0001c0001t0003g0047 a0001c0001t0003g0049 others(2): Show |
6 | NA18964.hp2 NA18983.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.407+33941A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28245139 | |||||||
| chr11:28245153 | A | G | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.407+33955A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28245153 | |||||||
| chr11:28245464 | A | G | 7 | a0001c0001t0012g0073 a0001c0001t0012g0074 a0001c0001t0012g0075 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+34266A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28245464 | |||||||
| chr11:28245490 | T | A | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.407+34292T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28245490 | |||||||
| chr11:28245497 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+34299A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28245497 | |||||||
| chr11:28245918 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+34720C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28245918 | |||||||
| chr11:28246052 | G | A | 1 | a0001c0001t0010g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.407+34854G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28246052 | |||||||
| chr11:28246058 | G | A | 4 | a0001c0001t0003g0026 a0001c0001t0005g0031 a0001c0001t0005g0034 others(1): Show |
4 | NA18947.hp2 NA18978.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.407+34860G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28246058 | |||||||
| chr11:28246234 | A | C | 1 | a0002c0002t0001g0325 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.407+35036A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28246234 | |||||||
| chr11:28246286 | G | A | 1 | a0001c0001t0019g0208 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.407+35088G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28246286 | |||||||
| chr11:28246487 | G | A | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.407+35289G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28246487 | |||||||
| chr11:28246532 | C | T | 2 | a0001c0001t0004g0162 a0001c0001t0004g0163 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.407+35334C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28246532 | |||||||
| chr11:28246806 | C | T | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.407+35608C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28246806 | |||||||
| chr11:28246977 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+35779G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28246977 | |||||||
| chr11:28247591 | A | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407+36393A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28247591 | |||||||
| chr11:28248043 | G | T | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.407+36845G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28248043 | |||||||
| chr11:28248337 | G | A | 39 | a0002c0002t0001g0003 a0002c0002t0001g0245 a0002c0002t0001g0247 others(36): Show |
40 | HG00423.hp2 HG00609.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.407+37139G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28248337 | |||||||
| chr11:28248393 | C | T | 2 | a0001c0001t0003g0014 a0001c0001t0003g0019 |
2 | NA18954.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.407+37195C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28248393 | |||||||
| chr11:28248470 | C | T | 12 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0011 others(9): Show |
13 | HG02074.hp2 HG02080.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.407+37272C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28248470 | |||||||
| chr11:28248972 | T | G | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.407+37774T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28248972 | |||||||
| chr11:28249143 | T | G | 1 | a0001c0001t0002g0097 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.407+37945T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28249143 | |||||||
| chr11:28249453 | A | G | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.407+38255A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28249453 | |||||||
| chr11:28249575 | A | G | 32 | a0001c0001t0004g0158 a0001c0001t0004g0175 a0001c0001t0004g0178 others(29): Show |
32 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.407+38377A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28249575 | |||||||
| chr11:28249638 | T | C | 5 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0258 others(2): Show |
5 | HG02056.hp1 NA18971.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.407+38440T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28249638 | |||||||
| chr11:28249859 | T | G | 1 | a0001c0001t0002g0239 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.407+38661T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28249859 | |||||||
| chr11:28249946 | C | T | 86 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(83): Show |
88 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.407+38748C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28249946 | |||||||
| chr11:28250099 | T | C | 324 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(321): Show |
328 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(325): Show |
intron_variant | MODIFIER | c.407+38901T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28250099 | |||||||
| chr11:28250566 | TA | T | 162 | a0001c0001t0002g0142 a0001c0001t0003g0058 a0001c0001t0004g0158 others(159): Show |
164 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.407+39379delA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28250566 | ||||||
| chr11:28250567 | A | T | 164 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(161): Show |
166 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.407+39369A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28250567 | |||||||
| chr11:28250568 | A | T | 163 | a0001c0001t0002g0095 a0001c0001t0002g0142 a0001c0001t0003g0011 others(160): Show |
165 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(162): Show |
intron_variant | MODIFIER | c.407+39370A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28250568 | |||||||
| chr11:28250569 | A | T | 84 | a0001c0001t0006g0230 a0001c0014t0021g0229 a0002c0002t0001g0003 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.407+39371A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28250569 | |||||||
| chr11:28250570 | A | T | 1 | a0002c0002t0001g0299 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.407+39372A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28250570 | |||||||
| chr11:28250605 | T | C | 1 | a0009c0010t0002g0101 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.407+39407T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28250605 | |||||||
| chr11:28250981 | C | A | 1 | a0001c0001t0003g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.408-39225C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28250981 | |||||||
| chr11:28251328 | A | G | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.408-38878A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28251328 | |||||||
| chr11:28251628 | C | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-38578C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28251628 | |||||||
| chr11:28251825 | C | T | 1 | a0001c0001t0003g0060 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.408-38381C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28251825 | |||||||
| chr11:28251827 | C | A | 11 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0212 others(8): Show |
11 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.408-38379C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28251827 | |||||||
| chr11:28252135 | A | G | 2 | a0002c0002t0001g0297 a0002c0002t0001g0304 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.408-38071A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28252135 | |||||||
| chr11:28252271 | G | A | 1 | a0001c0001t0003g0049 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.408-37935G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28252271 | |||||||
| chr11:28252347 | G | C | 74 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(71): Show |
74 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.408-37859G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28252347 | |||||||
| chr11:28252366 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-37840C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28252366 | |||||||
| chr11:28252755 | C | T | 2 | a0001c0001t0002g0104 a0001c0001t0002g0114 |
2 | NA18965.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.408-37451C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28252755 | |||||||
| chr11:28253176 | G | T | 1 | a0001c0001t0008g0209 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.408-37030G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28253176 | |||||||
| chr11:28253256 | G | A | 40 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(37): Show |
40 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.408-36950G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28253256 | |||||||
| chr11:28253329 | A | T | 13 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0026 others(10): Show |
13 | HG01361.hp2 HG02602.hp2 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.408-36877A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28253329 | |||||||
| chr11:28253476 | A | C | 68 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(65): Show |
68 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.408-36730A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28253476 | |||||||
| chr11:28253485 | A | G | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.408-36721A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28253485 | |||||||
| chr11:28253525 | T | G | 1 | a0004c0003t0002g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.408-36681T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28253525 | |||||||
| chr11:28253562 | T | G | 1 | a0001c0001t0006g0230 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.408-36644T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28253562 | |||||||
| chr11:28253665 | C | A | 10 | a0002c0002t0001g0250 a0002c0002t0001g0253 a0002c0002t0001g0256 others(7): Show |
10 | HG00408.hp1 HG02056.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.408-36541C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28253665 | |||||||
| chr11:28253700 | G | A | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.408-36506G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28253700 | |||||||
| chr11:28254051 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.408-36155C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28254051 | |||||||
| chr11:28254087 | C | T | 1 | a0001c0001t0012g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.408-36119C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28254087 | |||||||
| chr11:28254220 | C | T | 1 | a0001c0001t0004g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.408-35986C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28254220 | |||||||
| chr11:28254248 | T | TTA | 4 | a0001c0001t0004g0176 a0001c0001t0004g0180 a0001c0001t0004g0207 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.408-35953_408-3595 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28254248 | ||||||
| chr11:28254691 | C | T | 5 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0143 others(2): Show |
5 | HG00609.hp1 HG02523.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.408-35515C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28254691 | |||||||
| chr11:28255132 | A | G | 25 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0088 others(22): Show |
25 | HG00544.hp1 HG01952.hp2 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.408-35074A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28255132 | |||||||
| chr11:28255183 | T | A | 1 | a0002c0002t0001g0312 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.408-35023T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28255183 | |||||||
| chr11:28255272 | A | G | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.408-34934A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28255272 | |||||||
| chr11:28255386 | T | C | 1 | a0001c0001t0005g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.408-34820T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28255386 | |||||||
| chr11:28255488 | A | T | 1 | a0002c0002t0001g0253 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.408-34718A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28255488 | |||||||
| chr11:28255535 | G | T | 1 | a0001c0001t0008g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.408-34671G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28255535 | |||||||
| chr11:28255954 | C | T | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408-34252C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28255954 | |||||||
| chr11:28256000 | G | C | 74 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(71): Show |
74 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.408-34206G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28256000 | |||||||
| chr11:28256115 | A | G | 1 | a0002c0002t0001g0270 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.408-34091A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28256115 | |||||||
| chr11:28256146 | C | T | 161 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(158): Show |
163 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(160): Show |
intron_variant | MODIFIER | c.408-34060C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28256146 | |||||||
| chr11:28256196 | T | C | 1 | a0004c0003t0002g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.408-34010T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28256196 | |||||||
| chr11:28256295 | T | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-33911T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28256295 | |||||||
| chr11:28256419 | G | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.408-33787G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28256419 | |||||||
| chr11:28256478 | A | C | 1 | a0001c0001t0003g0015 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.408-33728A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28256478 | |||||||
| chr11:28256580 | T | C | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.408-33626T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28256580 | |||||||
| chr11:28257039 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.408-33167C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28257039 | |||||||
| chr11:28257183 | C | T | 1 | a0001c0001t0008g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.408-33023C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28257183 | |||||||
| chr11:28257310 | A | C | 1 | a0002c0002t0001g0261 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.408-32896A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28257310 | |||||||
| chr11:28257477 | C | A | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.408-32729C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28257477 | |||||||
| chr11:28257548 | A | T | 237 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(234): Show |
239 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(236): Show |
intron_variant | MODIFIER | c.408-32658A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28257548 | |||||||
| chr11:28257635 | C | G | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408-32571C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28257635 | |||||||
| chr11:28257665 | C | T | 1 | a0001c0001t0008g0195 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.408-32541C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28257665 | |||||||
| chr11:28257695 | A | G | 1 | a0001c0001t0004g0238 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.408-32511A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28257695 | |||||||
| chr11:28258793 | G | C | 1 | a0001c0001t0004g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.408-31413G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28258793 | |||||||
| chr11:28259134 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0005g0036 |
2 | HG00544.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.408-31072G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28259134 | |||||||
| chr11:28259255 | A | G | 53 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0009 others(50): Show |
55 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.408-30951A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28259255 | |||||||
| chr11:28259280 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.408-30926G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28259280 | |||||||
| chr11:28259292 | A | G | 2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
2 | NA18612.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.408-30914A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28259292 | |||||||
| chr11:28259644 | A | G | 1 | a0001c0001t0003g0077 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.408-30562A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28259644 | |||||||
| chr11:28259779 | T | C | 1 | a0001c0001t0003g0065 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.408-30427T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28259779 | |||||||
| chr11:28260030 | A | G | 1 | a0002c0002t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.408-30176A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28260030 | |||||||
| chr11:28260060 | G | A | 8 | a0001c0001t0004g0232 a0001c0001t0006g0230 a0001c0001t0007g0231 others(5): Show |
8 | HG00621.hp1 HG00673.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.408-30146G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28260060 | |||||||
| chr11:28260105 | A | C | 1 | a0001c0001t0003g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.408-30101A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28260105 | |||||||
| chr11:28260284 | G | A | 1 | a0002c0002t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.408-29922G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28260284 | |||||||
| chr11:28260351 | T | G | 1 | a0001c0001t0008g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.408-29855T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28260351 | |||||||
| chr11:28260361 | C | T | 40 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(37): Show |
40 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.408-29845C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28260361 | |||||||
| chr11:28260616 | C | T | 1 | a0001c0001t0009g0235 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.408-29590C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28260616 | |||||||
| chr11:28260896 | A | G | 3 | a0001c0001t0004g0158 a0001c0001t0004g0199 a0001c0001t0007g0198 |
3 | HG02074.hp1 HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.408-29310A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28260896 | |||||||
| chr11:28261141 | C | T | 1 | a0001c0001t0003g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.408-29065C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28261141 | |||||||
| chr11:28261323 | T | C | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.408-28883T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28261323 | |||||||
| chr11:28261364 | A | T | 1 | a0002c0002t0001g0324 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.408-28842A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28261364 | |||||||
| chr11:28261480 | A | G | 3 | a0002c0002t0001g0294 a0002c0002t0001g0303 a0002c0002t0001g0311 |
3 | HG01361.hp1 HG01993.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.408-28726A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28261480 | |||||||
| chr11:28261743 | A | G | 1 | a0002c0002t0001g0309 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.408-28463A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28261743 | |||||||
| chr11:28261906 | A | G | 1 | a0002c0002t0001g0250 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.408-28300A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28261906 | |||||||
| chr11:28261915 | G | C | 1 | a0001c0001t0004g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.408-28291G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28261915 | |||||||
| chr11:28262303 | A | T | 1 | a0001c0001t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.408-27903A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28262303 | |||||||
| chr11:28262436 | A | G | 1 | a0002c0002t0001g0324 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.408-27770A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28262436 | |||||||
| chr11:28262468 | T | G | 3 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0148 |
3 | NA18973.hp1 NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.408-27738T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28262468 | |||||||
| chr11:28262544 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.408-27662T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28262544 | |||||||
| chr11:28262574 | C | A | 1 | a0001c0001t0003g0008 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.408-27632C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28262574 | |||||||
| chr11:28262590 | T | C | 1 | a0001c0001t0022g0157 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.408-27616T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28262590 | |||||||
| chr11:28262613 | C | A | 1 | a0001c0001t0002g0103 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.408-27593C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28262613 | |||||||
| chr11:28262897 | ACTACATC others(3): Show |
A | 1 | a0001c0001t0003g0067 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.408-27308_408-2729 others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28262897 | |||||||
| chr11:28263056 | A | G | 1 | a0001c0001t0003g0051 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.408-27150A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28263056 | |||||||
| chr11:28263183 | G | C | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-27023G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28263183 | |||||||
| chr11:28263667 | A | G | 1 | a0002c0002t0001g0254 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.408-26539A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28263667 | |||||||
| chr11:28263913 | T | C | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.408-26293T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28263913 | |||||||
| chr11:28264065 | A | ACACAGTT others(4): Show |
1 | a0001c0001t0003g0067 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.408-26140_408-2613 others(15): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28264065 | ||||||
| chr11:28264119 | G | A | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.408-26087G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28264119 | |||||||
| chr11:28264141 | T | C | 2 | a0001c0001t0004g0174 a0001c0001t0022g0157 |
2 | HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.408-26065T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28264141 | |||||||
| chr11:28264418 | C | T | 11 | a0001c0001t0006g0160 a0001c0001t0006g0218 a0001c0001t0006g0220 others(8): Show |
11 | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.408-25788C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28264418 | |||||||
| chr11:28264448 | T | G | 1 | a0002c0002t0001g0308 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.408-25758T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28264448 | |||||||
| chr11:28264455 | ATGTT | A | 3 | a0001c0001t0002g0131 a0001c0001t0010g0215 a0001c0001t0010g0216 |
3 | HG02257.hp2 HG02683.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.408-25733_408-2573 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28264455 | ||||||
| chr11:28264561 | T | C | 1 | a0001c0001t0004g0228 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.408-25645T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28264561 | |||||||
| chr11:28264697 | T | C | 1 | a0001c0001t0002g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.408-25509T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28264697 | |||||||
| chr11:28264985 | T | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-25221T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28264985 | |||||||
| chr11:28265027 | G | A | 1 | a0001c0001t0002g0121 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.408-25179G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28265027 | |||||||
| chr11:28265257 | G | A | 1 | a0001c0001t0003g0033 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.408-24949G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28265257 | |||||||
| chr11:28265374 | C | A | 1 | a0002c0002t0001g0288 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.408-24832C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28265374 | |||||||
| chr11:28265492 | C | T | 1 | a0002c0002t0001g0298 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.408-24714C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28265492 | |||||||
| chr11:28265795 | G | C | 62 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(59): Show |
62 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.408-24411G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28265795 | |||||||
| chr11:28265829 | C | T | 2 | a0001c0001t0004g0176 a0001c0001t0004g0207 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.408-24377C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28265829 | |||||||
| chr11:28266089 | G | A | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.408-24117G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266089 | |||||||
| chr11:28266132 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.408-24074G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266132 | |||||||
| chr11:28266262 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.408-23944A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266262 | |||||||
| chr11:28266272 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.408-23934C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266272 | |||||||
| chr11:28266276 | G | A | 2 | a0001c0001t0005g0034 a0001c0001t0013g0035 |
2 | NA18947.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.408-23930G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266276 | |||||||
| chr11:28266322 | A | G | 1 | a0003c0004t0001g0313 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.408-23884A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266322 | |||||||
| chr11:28266742 | T | C | 1 | a0001c0001t0010g0118 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.408-23464T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266742 | |||||||
| chr11:28266779 | A | G | 1 | a0001c0001t0010g0216 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.408-23427A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266779 | |||||||
| chr11:28266869 | G | A | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.408-23337G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266869 | |||||||
| chr11:28266961 | A | G | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.408-23245A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266961 | |||||||
| chr11:28266975 | C | T | 1 | a0002c0002t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.408-23231C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28266975 | |||||||
| chr11:28267160 | C | CA | 11 | a0001c0001t0001g0214 a0001c0001t0006g0203 a0001c0001t0007g0198 others(8): Show |
11 | HG01433.hp2 HG01496.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.408-23023dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28267160 | ||||||
| chr11:28267160 | CA | C | 85 | a0001c0001t0002g0121 a0001c0001t0002g0145 a0001c0001t0003g0001 others(82): Show |
87 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.408-23023delA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28267160 | ||||||
| chr11:28267160 | CAA | C | 6 | a0001c0001t0003g0015 a0001c0001t0003g0042 a0001c0001t0003g0067 others(3): Show |
6 | HG00673.hp2 HG03041.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.408-23024_408-2302 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28267160 | ||||||
| chr11:28267160 | CAAAAAAA others(6): Show |
C | 1 | a0002c0002t0001g0314 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.408-23035_408-2302 others(17): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28267160 | ||||||
| chr11:28267183 | A | G | 1 | a0001c0001t0005g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.408-23023A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28267183 | |||||||
| chr11:28267195 | G | T | 2 | a0001c0001t0002g0005 a0001c0001t0002g0006 |
2 | HG01952.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.408-23011G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28267195 | |||||||
| chr11:28267408 | A | G | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.408-22798A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28267408 | |||||||
| chr11:28267614 | A | G | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.408-22592A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28267614 | |||||||
| chr11:28267705 | A | G | 1 | a0001c0001t0004g0228 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.408-22501A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28267705 | |||||||
| chr11:28267884 | A | C | 1 | a0001c0001t0002g0005 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.408-22322A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28267884 | |||||||
| chr11:28267917 | G | C | 1 | a0001c0001t0003g0068 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.408-22289G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28267917 | |||||||
| chr11:28267919 | C | T | 14 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(11): Show |
14 | HG02559.hp1 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.408-22287C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28267919 | |||||||
| chr11:28267923 | C | T | 42 | a0001c0001t0002g0085 a0001c0001t0002g0115 a0001c0001t0002g0116 others(39): Show |
42 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.408-22283C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28267923 | |||||||
| chr11:28268025 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-22181G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268025 | |||||||
| chr11:28268069 | C | T | 1 | a0002c0002t0001g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.408-22137C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268069 | |||||||
| chr11:28268155 | C | T | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.408-22051C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268155 | |||||||
| chr11:28268175 | C | T | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 |
3 | NA18981.hp1 NA18994.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.408-22031C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268175 | |||||||
| chr11:28268183 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0004g0164 |
2 | HG01496.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.408-22023C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268183 | |||||||
| chr11:28268196 | C | CA | 84 | a0001c0001t0001g0214 a0001c0001t0002g0121 a0001c0001t0002g0239 others(81): Show |
86 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.408-21986dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28268196 | ||||||
| chr11:28268196 | C | CAA | 150 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(147): Show |
152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.408-21987_408-2198 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28268196 | ||||||
| chr11:28268196 | C | CAAA | 20 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0093 others(17): Show |
20 | HG01515.hp2 HG02027.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.408-21988_408-2198 others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28268196 | ||||||
| chr11:28268279 | A | G | 1 | a0003c0004t0001g0313 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.408-21927A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268279 | |||||||
| chr11:28268566 | C | T | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.408-21640C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268566 | |||||||
| chr11:28268668 | A | G | 10 | a0001c0001t0002g0116 a0001c0001t0002g0124 a0001c0001t0002g0125 others(7): Show |
10 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.408-21538A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268668 | |||||||
| chr11:28268689 | C | G | 1 | a0002c0002t0001g0255 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.408-21517C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268689 | |||||||
| chr11:28268780 | T | G | 1 | a0001c0001t0005g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.408-21426T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268780 | |||||||
| chr11:28268919 | A | G | 25 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0088 others(22): Show |
25 | HG00544.hp1 HG01952.hp2 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.408-21287A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28268919 | |||||||
| chr11:28269031 | T | C | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.408-21175T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28269031 | |||||||
| chr11:28269319 | A | T | 74 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(71): Show |
74 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.408-20887A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28269319 | |||||||
| chr11:28269343 | G | A | 56 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(53): Show |
56 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.408-20863G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28269343 | |||||||
| chr11:28269361 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-20845C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28269361 | |||||||
| chr11:28269659 | C | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.408-20547C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28269659 | |||||||
| chr11:28269873 | A | C | 13 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0011 others(10): Show |
14 | HG02074.hp2 HG02080.hp1 NA18949.hp2 others(11): Show |
intron_variant | MODIFIER | c.408-20333A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28269873 | |||||||
| chr11:28270008 | G | A | 86 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(83): Show |
88 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.408-20198G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28270008 | |||||||
| chr11:28270014 | T | A | 3 | a0002c0002t0001g0278 a0002c0002t0001g0292 a0002c0002t0001g0293 |
3 | NA18612.hp1 NA18955.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.408-20192T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28270014 | |||||||
| chr11:28270029 | G | A | 1 | a0001c0001t0003g0027 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.408-20177G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28270029 | |||||||
| chr11:28270522 | A | G | 1 | a0001c0001t0003g0032 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.408-19684A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28270522 | |||||||
| chr11:28270531 | A | G | 238 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(235): Show |
240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.408-19675A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28270531 | |||||||
| chr11:28270658 | G | T | 1 | a0002c0002t0001g0258 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.408-19548G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28270658 | |||||||
| chr11:28270881 | C | A | 1 | a0002c0002t0001g0286 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.408-19325C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28270881 | |||||||
| chr11:28271283 | G | C | 1 | a0001c0001t0003g0027 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.408-18923G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28271283 | |||||||
| chr11:28271387 | T | C | 1 | a0001c0001t0003g0078 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.408-18819T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28271387 | |||||||
| chr11:28271570 | C | A | 71 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(68): Show |
73 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.408-18636C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28271570 | |||||||
| chr11:28271722 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-18484G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28271722 | |||||||
| chr11:28271753 | C | T | 2 | a0001c0001t0004g0180 a0001c0001t0007g0179 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.408-18453C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28271753 | |||||||
| chr11:28272043 | G | C | 3 | a0001c0001t0004g0200 a0001c0001t0004g0201 a0001c0001t0004g0206 |
3 | HG00733.hp1 HG01346.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.408-18163G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28272043 | |||||||
| chr11:28272069 | C | G | 6 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.408-18137C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28272069 | |||||||
| chr11:28272416 | C | T | 1 | a0002c0002t0001g0302 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.408-17790C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28272416 | |||||||
| chr11:28272779 | A | T | 1 | a0001c0001t0028g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.408-17427A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28272779 | |||||||
| chr11:28272870 | A | C | 23 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0026 others(20): Show |
23 | HG00738.hp1 HG01243.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.408-17336A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28272870 | |||||||
| chr11:28273050 | A | G | 4 | a0001c0001t0004g0176 a0001c0001t0004g0180 a0001c0001t0004g0207 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.408-17156A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28273050 | |||||||
| chr11:28273300 | A | G | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.408-16906A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28273300 | |||||||
| chr11:28273323 | T | C | 1 | a0001c0001t0004g0202 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.408-16883T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28273323 | |||||||
| chr11:28273581 | C | T | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.408-16625C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28273581 | |||||||
| chr11:28273981 | G | C | 1 | a0001c0001t0017g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.408-16225G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28273981 | |||||||
| chr11:28274136 | T | C | 4 | a0002c0002t0001g0003 a0002c0002t0001g0245 a0002c0002t0001g0306 others(1): Show |
5 | HG02132.hp2 NA18979.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.408-16070T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28274136 | |||||||
| chr11:28274168 | T | G | 1 | a0002c0002t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.408-16038T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28274168 | |||||||
| chr11:28274561 | A | G | 1 | a0001c0001t0003g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.408-15645A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28274561 | |||||||
| chr11:28274621 | A | T | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.408-15585A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28274621 | |||||||
| chr11:28274745 | A | T | 1 | a0001c0001t0003g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.408-15461A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28274745 | |||||||
| chr11:28274867 | AT | A | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.408-15338delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28274867 | |||||||
| chr11:28274900 | C | T | 1 | a0001c0001t0003g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.408-15306C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28274900 | |||||||
| chr11:28274940 | AATAT | A | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408-15256_408-1525 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28274940 | ||||||
| chr11:28274982 | A | G | 158 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.408-15224A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28274982 | |||||||
| chr11:28275045 | A | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-15161A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28275045 | |||||||
| chr11:28275170 | A | G | 1 | a0007c0009t0003g0023 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.408-15036A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28275170 | |||||||
| chr11:28275322 | A | G | 5 | a0004c0003t0002g0109 a0004c0003t0002g0110 a0004c0003t0002g0111 others(2): Show |
5 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.408-14884A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28275322 | |||||||
| chr11:28275477 | A | G | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.408-14729A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28275477 | |||||||
| chr11:28275519 | C | T | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408-14687C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28275519 | |||||||
| chr11:28275574 | G | C | 25 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0088 others(22): Show |
25 | HG00544.hp1 HG01952.hp2 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.408-14632G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28275574 | |||||||
| chr11:28275642 | C | CA | 163 | a0001c0001t0002g0104 a0001c0001t0002g0114 a0001c0001t0002g0132 others(160): Show |
165 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(162): Show |
intron_variant | MODIFIER | c.408-14550dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28275642 | ||||||
| chr11:28275642 | C | CAA | 63 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(60): Show |
63 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.408-14551_408-1455 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28275642 | ||||||
| chr11:28275642 | C | CAAA | 9 | a0001c0001t0002g0116 a0001c0001t0002g0124 a0001c0001t0002g0126 others(6): Show |
9 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.408-14552_408-1455 others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28275642 | ||||||
| chr11:28275673 | C | T | 77 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(74): Show |
79 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.408-14533C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28275673 | |||||||
| chr11:28275998 | T | TAAAGAGA others(337): Show |
1 | a0003c0004t0001g0296 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.408-14195_408-1419 others(348): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28275998 | ||||||
| chr11:28276112 | G | A | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.408-14094G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28276112 | |||||||
| chr11:28276240 | A | T | 1 | a0001c0001t0003g0068 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.408-13966A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28276240 | |||||||
| chr11:28276336 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-13870C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28276336 | |||||||
| chr11:28276392 | G | A | 5 | a0001c0001t0003g0002 a0001c0001t0003g0047 a0001c0001t0003g0049 others(2): Show |
6 | NA18964.hp2 NA18983.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.408-13814G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28276392 | |||||||
| chr11:28276545 | G | A | 1 | a0002c0002t0001g0308 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.408-13661G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28276545 | |||||||
| chr11:28277463 | C | T | 1 | a0001c0001t0005g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.408-12743C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28277463 | |||||||
| chr11:28277468 | C | T | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.408-12738C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28277468 | |||||||
| chr11:28277511 | A | G | 1 | a0001c0001t0006g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.408-12695A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28277511 | |||||||
| chr11:28277527 | G | A | 1 | a0002c0002t0001g0250 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.408-12679G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28277527 | |||||||
| chr11:28277543 | C | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-12663C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28277543 | |||||||
| chr11:28277679 | G | T | 1 | a0001c0001t0005g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.408-12527G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28277679 | |||||||
| chr11:28277751 | A | G | 4 | a0001c0001t0004g0175 a0001c0001t0004g0188 a0001c0001t0004g0190 others(1): Show |
4 | NA18954.hp2 NA18969.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-12455A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28277751 | |||||||
| chr11:28277866 | G | C | 1 | a0001c0001t0003g0068 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.408-12340G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28277866 | |||||||
| chr11:28278173 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408-12033G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28278173 | |||||||
| chr11:28278515 | T | C | 1 | a0001c0001t0004g0178 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.408-11691T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28278515 | |||||||
| chr11:28278539 | G | T | 1 | a0001c0001t0002g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.408-11667G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28278539 | |||||||
| chr11:28278591 | A | G | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.408-11615A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28278591 | |||||||
| chr11:28278836 | T | C | 4 | a0001c0001t0004g0176 a0001c0001t0004g0180 a0001c0001t0004g0207 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.408-11370T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28278836 | |||||||
| chr11:28279079 | G | A | 1 | a0002c0002t0001g0263 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.408-11127G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28279079 | |||||||
| chr11:28279114 | G | A | 2 | a0001c0001t0009g0165 a0001c0001t0009g0166 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.408-11092G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28279114 | |||||||
| chr11:28279268 | T | A | 1 | a0001c0001t0008g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.408-10938T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28279268 | |||||||
| chr11:28279498 | C | G | 6 | a0003c0004t0001g0285 a0003c0004t0001g0295 a0003c0004t0001g0296 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.408-10708C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28279498 | |||||||
| chr11:28279622 | C | T | 2 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.408-10584C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28279622 | |||||||
| chr11:28279666 | C | T | 2 | a0001c0001t0009g0165 a0001c0001t0009g0166 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.408-10540C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28279666 | |||||||
| chr11:28279667 | G | T | 1 | a0001c0001t0004g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.408-10539G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28279667 | |||||||
| chr11:28279792 | C | T | 86 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(83): Show |
88 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.408-10414C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28279792 | |||||||
| chr11:28279914 | CA | C | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.408-10275delA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28279914 | ||||||
| chr11:28280220 | AC | A | 78 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.408-9985delC | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28280220 | |||||||
| chr11:28280457 | A | G | 5 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0143 others(2): Show |
5 | HG00609.hp1 HG02523.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.408-9749A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28280457 | |||||||
| chr11:28280667 | CT | C | 229 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(226): Show |
231 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.408-9524delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28280667 | ||||||
| chr11:28280687 | C | A | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.408-9519C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28280687 | |||||||
| chr11:28280703 | A | T | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.408-9503A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28280703 | |||||||
| chr11:28280863 | A | G | 159 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(156): Show |
161 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.408-9343A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28280863 | |||||||
| chr11:28280919 | T | C | 238 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(235): Show |
240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.408-9287T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28280919 | |||||||
| chr11:28281240 | G | A | 3 | a0001c0001t0004g0158 a0001c0001t0004g0199 a0001c0001t0007g0198 |
3 | HG02074.hp1 HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.408-8966G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28281240 | |||||||
| chr11:28281245 | C | T | 4 | a0002c0002t0001g0291 a0002c0002t0001g0294 a0002c0002t0001g0303 others(1): Show |
4 | HG01361.hp1 HG01993.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-8961C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28281245 | |||||||
| chr11:28281266 | A | G | 1 | a0002c0002t0001g0302 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.408-8940A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28281266 | |||||||
| chr11:28281503 | G | A | 2 | a0002c0002t0001g0294 a0002c0002t0001g0303 |
2 | HG01361.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.408-8703G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28281503 | |||||||
| chr11:28281878 | A | G | 4 | a0001c0001t0004g0200 a0001c0001t0004g0201 a0001c0001t0004g0202 others(1): Show |
4 | HG00733.hp1 HG01106.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-8328A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28281878 | |||||||
| chr11:28282217 | C | G | 1 | a0001c0001t0004g0181 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.408-7989C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28282217 | |||||||
| chr11:28282313 | G | A | 2 | a0002c0002t0001g0261 a0002c0002t0001g0262 |
2 | HG01952.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.408-7893G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28282313 | |||||||
| chr11:28282746 | T | C | 40 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(37): Show |
40 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.408-7460T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28282746 | |||||||
| chr11:28283131 | C | G | 1 | a0001c0001t0002g0139 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.408-7075C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28283131 | |||||||
| chr11:28283161 | T | C | 1 | a0001c0001t0016g0020 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.408-7045T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28283161 | |||||||
| chr11:28283168 | G | A | 1 | a0001c0001t0003g0078 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.408-7038G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28283168 | |||||||
| chr11:28283383 | G | T | 12 | a0001c0001t0003g0002 a0001c0001t0003g0047 a0001c0001t0003g0049 others(9): Show |
13 | NA18964.hp2 NA18968.hp2 NA18980.hp2 others(10): Show |
intron_variant | MODIFIER | c.408-6823G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28283383 | |||||||
| chr11:28283625 | G | A | 1 | a0001c0001t0008g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.408-6581G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28283625 | |||||||
| chr11:28283788 | A | T | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.408-6418A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28283788 | |||||||
| chr11:28284684 | C | T | 25 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0088 others(22): Show |
25 | HG00544.hp1 HG01952.hp2 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.408-5522C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28284684 | |||||||
| chr11:28284750 | T | C | 1 | a0001c0001t0005g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.408-5456T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28284750 | |||||||
| chr11:28285024 | T | C | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.408-5182T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28285024 | |||||||
| chr11:28285082 | C | T | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.408-5124C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28285082 | |||||||
| chr11:28285115 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.408-5091G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28285115 | |||||||
| chr11:28285198 | A | G | 1 | a0002c0002t0001g0294 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.408-5008A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28285198 | |||||||
| chr11:28285362 | A | AT | 90 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(87): Show |
92 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.408-4829dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28285362 | ||||||
| chr11:28285362 | AT | A | 80 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(77): Show |
80 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.408-4829delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28285362 | ||||||
| chr11:28285624 | T | G | 4 | a0001c0001t0003g0058 a0001c0001t0003g0060 a0001c0001t0003g0061 others(1): Show |
4 | HG00673.hp2 HG02040.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-4582T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28285624 | |||||||
| chr11:28285627 | A | G | 1 | a0002c0002t0001g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.408-4579A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28285627 | |||||||
| chr11:28285857 | C | T | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.408-4349C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28285857 | |||||||
| chr11:28285914 | G | T | 53 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0009 others(50): Show |
55 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.408-4292G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28285914 | |||||||
| chr11:28285926 | G | A | 68 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(65): Show |
68 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.408-4280G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28285926 | |||||||
| chr11:28286047 | T | C | 9 | a0001c0001t0008g0083 a0001c0001t0008g0177 a0001c0001t0008g0192 others(6): Show |
9 | HG00735.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.408-4159T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286047 | |||||||
| chr11:28286304 | C | T | 2 | a0001c0001t0002g0133 a0001c0001t0002g0140 |
2 | NA18993.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.408-3902C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286304 | |||||||
| chr11:28286346 | G | T | 10 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(7): Show |
10 | HG02559.hp1 HG02818.hp1 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.408-3860G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286346 | |||||||
| chr11:28286486 | C | T | 4 | a0002c0002t0001g0291 a0002c0002t0001g0294 a0002c0002t0001g0303 others(1): Show |
4 | HG01361.hp1 HG01993.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-3720C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286486 | |||||||
| chr11:28286490 | T | C | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.408-3716T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286490 | |||||||
| chr11:28286504 | G | A | 76 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.408-3702G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286504 | |||||||
| chr11:28286652 | C | T | 13 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0026 others(10): Show |
13 | HG01361.hp2 HG02602.hp2 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.408-3554C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286652 | |||||||
| chr11:28286674 | G | A | 6 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.408-3532G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286674 | |||||||
| chr11:28286723 | T | C | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408-3483T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286723 | |||||||
| chr11:28286784 | G | C | 1 | a0002c0002t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.408-3422G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286784 | |||||||
| chr11:28286934 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.408-3272G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28286934 | |||||||
| chr11:28287009 | CTA | C | 81 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(78): Show |
81 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.408-3183_408-3182d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287009 | ||||||
| chr11:28287038 | TATATATA others(19): Show |
T | 1 | a0001c0001t0003g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.408-3153_408-3128d others(28): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287038 | ||||||
| chr11:28287142 | G | T | 10 | a0001c0001t0002g0097 a0001c0001t0003g0063 a0001c0001t0004g0176 others(7): Show |
10 | HG00733.hp1 HG01106.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.408-3064G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287142 | |||||||
| chr11:28287150 | G | C | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.408-3056G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287150 | |||||||
| chr11:28287152 | G | A | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.408-3054G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287152 | |||||||
| chr11:28287153 | A | T | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.408-3053A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287153 | |||||||
| chr11:28287154 | C | G | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.408-3052C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287154 | |||||||
| chr11:28287155 | A | T | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.408-3051A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287155 | |||||||
| chr11:28287156 | A | ATG | 13 | a0001c0001t0003g0068 a0001c0001t0004g0170 a0001c0001t0004g0186 others(10): Show |
13 | HG01891.hp1 HG01943.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.408-3010_408-3009d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | A | ATGTG | 16 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0258 others(13): Show |
16 | HG00423.hp2 HG01074.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.408-3012_408-3009d others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | A | ATGTGTG | 49 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(46): Show |
51 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.408-3014_408-3009d others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | A | ATGTGTGT others(1): Show |
7 | a0002c0002t0001g0248 a0002c0002t0001g0249 a0002c0002t0001g0262 others(4): Show |
7 | HG00642.hp1 HG01952.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.408-3016_408-3009d others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | A | ATGTGTGT others(3): Show |
1 | a0002c0002t0001g0307 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.408-3018_408-3009d others(12): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | A | ATGTGTGT others(15): Show |
1 | a0002c0002t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.408-3030_408-3009d others(24): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | A | G | 4 | a0002c0002t0001g0271 a0002c0002t0001g0273 a0002c0002t0001g0327 others(1): Show |
4 | HG01433.hp2 HG02258.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-3050A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287156 | |||||||
| chr11:28287156 | ATG | A | 79 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0088 others(76): Show |
79 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.408-3010_408-3009d others(4): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | ATGTG | A | 93 | a0001c0001t0001g0214 a0001c0001t0002g0084 a0001c0001t0002g0085 others(90): Show |
94 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.408-3012_408-3009d others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | ATGTGTG | A | 16 | a0001c0001t0002g0104 a0001c0001t0003g0024 a0001c0001t0004g0212 others(13): Show |
16 | HG02559.hp1 HG02738.hp2 HG02818.hp1 others(13): Show |
intron_variant | MODIFIER | c.408-3014_408-3009d others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | ATGTGTGT others(1): Show |
A | 13 | a0001c0001t0002g0142 a0001c0001t0002g0239 a0001c0001t0004g0158 others(10): Show |
13 | HG00642.hp2 HG02074.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.408-3016_408-3009d others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0002g0143 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.408-3018_408-3009d others(12): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287156 | ATGTGTGT others(7): Show |
A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.408-3022_408-3009d others(16): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287156 | ||||||
| chr11:28287190 | G | A | 1 | a0008c0013t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.408-3016G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287190 | |||||||
| chr11:28287198 | T | G | 3 | a0005c0005t0014g0079 a0005c0005t0014g0080 a0005c0005t0025g0081 |
3 | HG02559.hp2 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.408-3008T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287198 | |||||||
| chr11:28287206 | CATTTT | C | 6 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.408-2995_408-2991d others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287206 | ||||||
| chr11:28287293 | C | T | 1 | a0002c0002t0001g0260 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.408-2913C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287293 | |||||||
| chr11:28287392 | A | G | 1 | a0001c0001t0007g0234 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.408-2814A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287392 | |||||||
| chr11:28287455 | G | T | 1 | a0001c0001t0004g0204 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.408-2751G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287455 | |||||||
| chr11:28287620 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.408-2586C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287620 | |||||||
| chr11:28287634 | C | T | 1 | a0002c0002t0015g0318 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.408-2572C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28287634 | |||||||
| chr11:28287947 | C | CT | 80 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(77): Show |
80 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.408-2258dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 28287947 | ||||||
| chr11:28288183 | C | T | 1 | a0003c0004t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.408-2023C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28288183 | |||||||
| chr11:28288619 | A | G | 53 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0009 others(50): Show |
55 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.408-1587A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28288619 | |||||||
| chr11:28288655 | C | T | 5 | a0001c0001t0004g0200 a0001c0001t0004g0201 a0001c0001t0004g0202 others(2): Show |
5 | HG00733.hp1 HG01106.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.408-1551C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28288655 | |||||||
| chr11:28288857 | T | A | 9 | a0002c0002t0001g0243 a0002c0002t0001g0264 a0002c0002t0001g0266 others(6): Show |
9 | HG00597.hp1 NA18965.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.408-1349T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28288857 | |||||||
| chr11:28288922 | T | C | 85 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(82): Show |
87 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.408-1284T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28288922 | |||||||
| chr11:28288978 | C | T | 1 | a0002c0002t0001g0299 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.408-1228C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28288978 | |||||||
| chr11:28289969 | A | T | 1 | a0001c0001t0002g0093 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.408-237A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28289969 | |||||||
| chr11:28290576 | G | A | 13 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0026 others(10): Show |
13 | HG01361.hp2 HG02602.hp2 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.599+179G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28290576 | |||||||
| chr11:28290936 | A | G | 1 | a0001c0001t0003g0045 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.599+539A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28290936 | |||||||
| chr11:28291050 | C | CT | 152 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(149): Show |
154 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(151): Show |
intron_variant | MODIFIER | c.599+670dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 28291050 | ||||||
| chr11:28291050 | CT | C | 6 | a0001c0001t0002g0088 a0001c0001t0002g0123 a0001c0001t0002g0147 others(3): Show |
6 | HG06807.hp2 NA18957.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.599+670delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 28291050 | ||||||
| chr11:28291106 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.599+709G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28291106 | |||||||
| chr11:28291191 | C | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.599+794C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28291191 | |||||||
| chr11:28291324 | G | A | 1 | a0002c0002t0001g0264 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.599+927G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28291324 | |||||||
| chr11:28291485 | C | T | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.599+1088C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28291485 | |||||||
| chr11:28291550 | C | T | 67 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(64): Show |
67 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.599+1153C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28291550 | |||||||
| chr11:28291565 | G | T | 1 | a0002c0002t0001g0298 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.599+1168G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28291565 | |||||||
| chr11:28291570 | TGACCTGT others(9): Show |
T | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.599+1177_599+1192d others(18): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 28291570 | ||||||
| chr11:28291657 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.599+1260A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28291657 | |||||||
| chr11:28291732 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.599+1335G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28291732 | |||||||
| chr11:28291803 | A | G | 1 | a0001c0001t0008g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.599+1406A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28291803 | |||||||
| chr11:28291828 | G | A | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.599+1431G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28291828 | |||||||
| chr11:28292284 | C | T | 2 | a0002c0002t0001g0282 a0002c0002t0001g0283 |
2 | HG02698.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.599+1887C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292284 | |||||||
| chr11:28292323 | C | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.599+1926C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292323 | |||||||
| chr11:28292496 | G | A | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.599+2099G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292496 | |||||||
| chr11:28292520 | C | T | 11 | a0001c0001t0006g0160 a0001c0001t0006g0218 a0001c0001t0006g0220 others(8): Show |
11 | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.599+2123C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292520 | |||||||
| chr11:28292527 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.599+2130G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292527 | |||||||
| chr11:28292624 | G | A | 1 | a0002c0002t0001g0310 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.599+2227G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292624 | |||||||
| chr11:28292688 | G | T | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.599+2291G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292688 | |||||||
| chr11:28292744 | T | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.599+2347T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292744 | |||||||
| chr11:28292781 | G | A | 77 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(74): Show |
77 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.599+2384G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292781 | |||||||
| chr11:28292803 | T | C | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.599+2406T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292803 | |||||||
| chr11:28292846 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.599+2449A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292846 | |||||||
| chr11:28292928 | G | T | 2 | a0001c0001t0002g0150 a0002c0002t0001g0290 |
2 | HG01943.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.599+2531G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292928 | |||||||
| chr11:28293255 | G | A | 1 | a0002c0002t0026g0326 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.599+2858G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28293255 | |||||||
| chr11:28293307 | C | T | 1 | a0001c0001t0004g0232 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.599+2910C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28293307 | |||||||
| chr11:28293598 | C | T | 2 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
2 | HG00738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.600-3155C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28293598 | |||||||
| chr11:28293631 | A | G | 5 | a0001c0001t0003g0058 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
5 | HG00673.hp2 HG02040.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.600-3122A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28293631 | |||||||
| chr11:28293869 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.600-2884G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28293869 | |||||||
| chr11:28293964 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.600-2789G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28293964 | |||||||
| chr11:28294044 | T | A | 56 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(53): Show |
56 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.600-2709T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28294044 | |||||||
| chr11:28294084 | A | C | 1 | a0001c0001t0002g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.600-2669A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28294084 | |||||||
| chr11:28294390 | T | G | 1 | a0002c0002t0001g0265 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.600-2363T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28294390 | |||||||
| chr11:28294851 | A | G | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.600-1902A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28294851 | |||||||
| chr11:28295494 | G | A | 1 | a0002c0002t0001g0243 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.600-1259G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28295494 | |||||||
| chr11:28295545 | G | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0140 |
2 | NA18993.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.600-1208G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28295545 | |||||||
| chr11:28295588 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.600-1165G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28295588 | |||||||
| chr11:28295611 | A | T | 74 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(71): Show |
74 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.600-1142A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28295611 | |||||||
| chr11:28295978 | C | T | 85 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(82): Show |
87 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.600-775C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28295978 | |||||||
| chr11:28296070 | A | T | 1 | a0001c0001t0004g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.600-683A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28296070 | |||||||
| chr11:28296161 | G | T | 74 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(71): Show |
74 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.600-592G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28296161 | |||||||
| chr11:28296196 | G | A | 1 | a0004c0003t0002g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.600-557G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28296196 | |||||||
| chr11:28296230 | G | C | 2 | a0002c0002t0001g0294 a0002c0002t0001g0303 |
2 | HG01361.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.600-523G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28296230 | |||||||
| chr11:28296262 | G | C | 11 | a0001c0001t0006g0160 a0001c0001t0006g0218 a0001c0001t0006g0220 others(8): Show |
11 | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.600-491G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28296262 | |||||||
| chr11:28296598 | A | G | 1 | a0001c0001t0003g0021 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.600-155A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28296598 | |||||||
| chr11:28296647 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.600-106C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28296647 | |||||||
| chr11:28296649 | A | G | 6 | a0001c0001t0007g0168 a0001c0001t0007g0240 a0001c0001t0009g0165 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.600-104A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28296649 | |||||||
| chr11:28296698 | C | T | 1 | a0002c0002t0001g0306 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.600-55C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28296698 | |||||||
| chr11:28296749 | G | A | 1 | a0001c0001t0002g0107 | 1 | NA19010.hp2 | splice_region_variant&intron_variant | LOW | c.600-4G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28296749 | |||||||
| chr11:28297013 | G | A | 1 | a0002c0002t0001g0286 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.778+82G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28297013 | |||||||
| chr11:28297118 | T | C | 1 | a0001c0001t0005g0053 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.778+187T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28297118 | |||||||
| chr11:28297135 | C | A | 1 | a0001c0001t0003g0068 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.778+204C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28297135 | |||||||
| chr11:28297298 | G | A | 2 | a0002c0002t0001g0320 a0002c0002t0001g0321 |
2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.778+367G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28297298 | |||||||
| chr11:28297444 | A | G | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.778+513A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28297444 | |||||||
| chr11:28297730 | A | C | 3 | a0002c0002t0001g0299 a0002c0002t0001g0309 a0002c0002t0001g0312 |
3 | HG00423.hp2 HG01123.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.778+799A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28297730 | |||||||
| chr11:28297825 | T | C | 1 | a0002c0002t0001g0302 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.778+894T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28297825 | |||||||
| chr11:28297974 | A | G | 1 | a0002c0002t0001g0276 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.778+1043A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28297974 | |||||||
| chr11:28298184 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0009c0010t0002g0101 |
3 | HG01952.hp2 HG01993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.778+1253G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28298184 | |||||||
| chr11:28298226 | C | T | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.778+1295C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28298226 | |||||||
| chr11:28298739 | A | G | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.778+1808A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28298739 | |||||||
| chr11:28298755 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.778+1824A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28298755 | |||||||
| chr11:28298917 | A | G | 2 | a0002c0002t0001g0261 a0002c0002t0001g0262 |
2 | HG01952.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.778+1986A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28298917 | |||||||
| chr11:28299183 | A | G | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.778+2252A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28299183 | |||||||
| chr11:28299468 | A | C | 13 | a0001c0001t0002g0239 a0003c0004t0001g0285 a0003c0004t0001g0295 others(10): Show |
13 | HG00642.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.778+2537A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28299468 | |||||||
| chr11:28299496 | A | G | 8 | a0001c0001t0008g0083 a0001c0001t0008g0177 a0001c0001t0008g0192 others(5): Show |
8 | HG00735.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.778+2565A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28299496 | |||||||
| chr11:28299649 | G | T | 56 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(53): Show |
56 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.778+2718G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28299649 | |||||||
| chr11:28299715 | G | A | 1 | a0002c0002t0001g0263 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.778+2784G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28299715 | |||||||
| chr11:28299777 | C | T | 1 | a0001c0001t0004g0178 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.778+2846C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28299777 | |||||||
| chr11:28300021 | A | T | 1 | a0001c0001t0002g0099 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.778+3090A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28300021 | |||||||
| chr11:28300494 | A | G | 2 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.778+3563A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28300494 | |||||||
| chr11:28300556 | G | A | 1 | a0011c0012t0003g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.778+3625G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28300556 | |||||||
| chr11:28301019 | C | G | 77 | a0001c0001t0004g0158 a0001c0001t0004g0161 a0001c0001t0004g0162 others(74): Show |
77 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.778+4088C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301019 | |||||||
| chr11:28301038 | G | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778+4107G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301038 | |||||||
| chr11:28301097 | T | C | 68 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(65): Show |
68 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.778+4166T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301097 | |||||||
| chr11:28301198 | A | G | 32 | a0001c0001t0004g0158 a0001c0001t0004g0175 a0001c0001t0004g0178 others(29): Show |
32 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.778+4267A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301198 | |||||||
| chr11:28301296 | T | C | 1 | a0001c0001t0004g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.778+4365T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301296 | |||||||
| chr11:28301421 | C | T | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.778+4490C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301421 | |||||||
| chr11:28301826 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.778+4895G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301826 | |||||||
| chr11:28301846 | G | A | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.778+4915G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301846 | |||||||
| chr11:28301865 | A | T | 1 | a0005c0005t0014g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.778+4934A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301865 | |||||||
| chr11:28302125 | C | T | 1 | a0002c0002t0026g0326 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.778+5194C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28302125 | |||||||
| chr11:28302293 | T | G | 1 | a0001c0001t0028g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.778+5362T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28302293 | |||||||
| chr11:28302326 | A | T | 1 | a0001c0001t0002g0103 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.778+5395A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28302326 | |||||||
| chr11:28302691 | A | G | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.778+5760A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28302691 | |||||||
| chr11:28302977 | G | C | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.778+6046G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28302977 | |||||||
| chr11:28303000 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.778+6069G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28303000 | |||||||
| chr11:28303145 | T | A | 1 | a0002c0002t0001g0307 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.778+6214T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28303145 | |||||||
| chr11:28303153 | C | T | 1 | a0002c0002t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.778+6222C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28303153 | |||||||
| chr11:28303336 | A | G | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.778+6405A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28303336 | |||||||
| chr11:28303739 | A | T | 2 | a0002c0002t0001g0320 a0002c0002t0001g0321 |
2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.778+6808A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28303739 | |||||||
| chr11:28303865 | A | G | 161 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(158): Show |
163 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(160): Show |
intron_variant | MODIFIER | c.778+6934A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28303865 | |||||||
| chr11:28304149 | G | A | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.778+7218G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28304149 | |||||||
| chr11:28304296 | A | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778+7365A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28304296 | |||||||
| chr11:28304310 | A | T | 1 | a0002c0002t0001g0243 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.778+7379A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28304310 | |||||||
| chr11:28304697 | C | G | 40 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(37): Show |
40 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.778+7766C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28304697 | |||||||
| chr11:28304715 | C | A | 5 | a0003c0004t0001g0285 a0003c0004t0001g0295 a0003c0004t0001g0296 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.778+7784C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28304715 | |||||||
| chr11:28304891 | A | C | 2 | a0001c0001t0012g0073 a0001c0001t0012g0075 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.778+7960A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28304891 | |||||||
| chr11:28305228 | C | A | 1 | a0002c0002t0001g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.778+8297C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28305228 | |||||||
| chr11:28305413 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.778+8482C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28305413 | |||||||
| chr11:28305477 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.778+8546T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28305477 | |||||||
| chr11:28305591 | T | C | 1 | a0001c0001t0005g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.778+8660T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28305591 | |||||||
| chr11:28305772 | A | G | 1 | a0002c0002t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.778+8841A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28305772 | |||||||
| chr11:28305847 | T | TAAA | 3 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0258 |
3 | NA18971.hp2 NA19056.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.778+8917_778+8918i others(5): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28305847 | ||||||
| chr11:28305849 | G | A | 3 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0258 |
3 | NA18971.hp2 NA19056.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.778+8918G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28305849 | |||||||
| chr11:28306024 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.778+9093C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28306024 | |||||||
| chr11:28306218 | G | A | 1 | a0001c0001t0004g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.778+9287G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28306218 | |||||||
| chr11:28306248 | T | A | 1 | a0001c0001t0002g0102 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.778+9317T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28306248 | |||||||
| chr11:28306373 | A | G | 89 | a0001c0001t0007g0179 a0002c0002t0001g0003 a0002c0002t0001g0004 others(86): Show |
91 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.778+9442A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28306373 | |||||||
| chr11:28306865 | A | G | 1 | a0001c0001t0003g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.778+9934A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28306865 | |||||||
| chr11:28307614 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.778+10683A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28307614 | |||||||
| chr11:28308205 | T | C | 3 | a0001c0001t0002g0119 a0001c0001t0010g0117 a0001c0001t0010g0118 |
3 | NA18948.hp2 NA18961.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.778+11274T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28308205 | |||||||
| chr11:28308393 | C | T | 1 | a0001c0001t0002g0108 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.778+11462C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28308393 | |||||||
| chr11:28308421 | G | C | 6 | a0002c0002t0001g0250 a0002c0002t0001g0256 a0002c0002t0001g0257 others(3): Show |
6 | HG02056.hp1 NA18971.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778+11490G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28308421 | |||||||
| chr11:28308442 | A | C | 1 | a0011c0012t0003g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.778+11511A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28308442 | |||||||
| chr11:28308665 | T | C | 1 | a0001c0001t0007g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.778+11734T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28308665 | |||||||
| chr11:28308738 | G | A | 1 | a0002c0002t0001g0302 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.778+11807G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28308738 | |||||||
| chr11:28308827 | A | G | 1 | a0001c0001t0005g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.778+11896A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28308827 | |||||||
| chr11:28308892 | G | GTAGA | 95 | a0001c0001t0002g0084 a0001c0001t0002g0088 a0001c0001t0002g0089 others(92): Show |
95 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.778+12001_778+1200 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28308892 | ||||||
| chr11:28308892 | G | GTAGATAG others(1): Show |
57 | a0001c0001t0002g0005 a0001c0001t0002g0085 a0001c0001t0002g0091 others(54): Show |
57 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.778+11997_778+1200 others(12): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28308892 | ||||||
| chr11:28308892 | G | GTAGATAG others(5): Show |
36 | a0001c0001t0002g0006 a0001c0001t0002g0092 a0001c0001t0002g0099 others(33): Show |
36 | HG00621.hp1 HG01081.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.778+11993_778+1200 others(16): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28308892 | ||||||
| chr11:28308892 | G | GTAGATAG others(9): Show |
6 | a0001c0001t0002g0108 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG00733.hp1 HG01943.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+11989_778+1200 others(20): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28308892 | ||||||
| chr11:28308892 | G | GTAGATAG others(13): Show |
1 | a0001c0001t0004g0178 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.778+11985_778+1200 others(24): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28308892 | ||||||
| chr11:28308892 | G | GTAGGTAG others(9): Show |
2 | a0001c0001t0006g0230 a0001c0014t0021g0229 |
2 | HG03453.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.778+11964_778+1196 others(20): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28308892 | ||||||
| chr11:28308892 | GTAGA | G | 8 | a0001c0001t0002g0125 a0001c0001t0003g0018 a0001c0001t0003g0076 others(5): Show |
8 | HG01433.hp1 HG02027.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.778+12001_778+1200 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28308892 | ||||||
| chr11:28308896 | A | G | 2 | a0001c0001t0003g0024 a0007c0009t0003g0023 |
2 | HG00423.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.778+11965A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28308896 | |||||||
| chr11:28308977 | A | G | 1 | a0001c0001t0013g0035 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.778+12046A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28308977 | |||||||
| chr11:28309080 | G | T | 1 | a0002c0002t0001g0308 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.778+12149G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28309080 | |||||||
| chr11:28309132 | G | A | 2 | a0001c0001t0003g0008 a0001c0001t0003g0022 |
2 | HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.778+12201G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28309132 | |||||||
| chr11:28309552 | G | A | 1 | a0001c0001t0005g0036 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.778+12621G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28309552 | |||||||
| chr11:28309704 | G | A | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.778+12773G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28309704 | |||||||
| chr11:28309878 | T | G | 1 | a0002c0002t0015g0319 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.778+12947T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28309878 | |||||||
| chr11:28310185 | T | A | 1 | a0002c0002t0001g0262 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.778+13254T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310185 | |||||||
| chr11:28310351 | T | TAC | 78 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 others(75): Show |
79 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.778+13445_778+1344 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310351 | ||||||
| chr11:28310351 | T | TACAC | 20 | a0001c0001t0002g0085 a0001c0001t0002g0150 a0001c0001t0002g0239 others(17): Show |
21 | HG00642.hp2 HG02572.hp1 HG02647.hp1 others(18): Show |
intron_variant | MODIFIER | c.778+13443_778+1344 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310351 | ||||||
| chr11:28310351 | T | TACACAC | 53 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(50): Show |
53 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.778+13441_778+1344 others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310351 | ||||||
| chr11:28310351 | T | TACACACA others(1): Show |
10 | a0001c0001t0002g0084 a0001c0001t0002g0089 a0001c0001t0002g0136 others(7): Show |
10 | HG00597.hp2 NA18522.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.778+13439_778+1344 others(12): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310351 | ||||||
| chr11:28310559 | A | G | 3 | a0002c0002t0001g0004 a0002c0002t0001g0322 a0002c0002t0001g0323 |
4 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.778+13628A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310559 | |||||||
| chr11:28310803 | A | G | 2 | a0002c0002t0001g0276 a0002c0002t0001g0277 |
2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.778+13872A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310803 | |||||||
| chr11:28310824 | A | G | 1 | a0002c0002t0001g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.778+13893A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310824 | |||||||
| chr11:28310878 | A | ATGC | 32 | a0001c0001t0003g0026 a0001c0001t0004g0158 a0001c0001t0004g0170 others(29): Show |
32 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.778+13983_778+1398 others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310878 | ||||||
| chr11:28310878 | A | ATGCTGC | 11 | a0001c0001t0003g0021 a0001c0001t0003g0025 a0001c0001t0003g0065 others(8): Show |
11 | HG00423.hp1 HG02080.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.778+13980_778+1398 others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310878 | ||||||
| chr11:28310878 | A | ATGCTGCT others(5): Show |
7 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.778+13974_778+1398 others(16): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310878 | ||||||
| chr11:28310878 | A | ATGCTGCT others(8): Show |
1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778+13971_778+1398 others(19): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310878 | ||||||
| chr11:28310878 | ATGCTGC | A | 24 | a0001c0001t0002g0084 a0001c0001t0002g0096 a0001c0001t0002g0097 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.778+13980_778+1398 others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310878 | ||||||
| chr11:28310878 | ATGCTGCT others(2): Show |
A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0091 others(32): Show |
35 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.778+13977_778+1398 others(13): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310878 | ||||||
| chr11:28310878 | ATGCTGCT others(5): Show |
A | 2 | a0001c0001t0010g0117 a0001c0001t0010g0118 |
2 | NA18948.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.778+13974_778+1398 others(16): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310878 | ||||||
| chr11:28310893 | CTGCTGCT others(23): Show |
C | 1 | a0001c0001t0006g0191 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.778+13965_778+1399 others(34): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310893 | ||||||
| chr11:28310899 | CTGCTGCT others(14): Show |
C | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.778+13971_778+1399 others(25): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310899 | ||||||
| chr11:28310902 | CTGCTGCT others(11): Show |
C | 1 | a0001c0001t0002g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.778+13974_778+1399 others(22): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310902 | ||||||
| chr11:28310902 | CTGCTGCT others(23): Show |
C | 1 | a0001c0001t0002g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.778+13974_778+1400 others(34): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310902 | ||||||
| chr11:28310905 | C | G | 9 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(6): Show |
9 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.778+13974C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310905 | |||||||
| chr11:28310905 | CTGCTGCT others(8): Show |
C | 3 | a0001c0001t0004g0180 a0001c0001t0007g0179 a0001c0001t0019g0208 |
3 | HG02258.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.778+13977_778+1399 others(19): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310905 | ||||||
| chr11:28310905 | CTGCTGCT others(11): Show |
C | 13 | a0001c0001t0004g0176 a0001c0001t0004g0196 a0001c0001t0004g0197 others(10): Show |
13 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.778+13977_778+1399 others(22): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310905 | ||||||
| chr11:28310905 | CTGCTGCT others(14): Show |
C | 1 | a0001c0001t0004g0174 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.778+13977_778+1399 others(25): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310905 | ||||||
| chr11:28310908 | C | G | 10 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(7): Show |
10 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.778+13977C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310908 | |||||||
| chr11:28310911 | C | G | 36 | a0001c0001t0002g0084 a0001c0001t0002g0088 a0001c0001t0002g0089 others(33): Show |
36 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.778+13980C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310911 | |||||||
| chr11:28310914 | C | CTGCTGCT others(29): Show |
1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778+13985_778+1398 others(40): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310914 | ||||||
| chr11:28310914 | C | G | 71 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(68): Show |
71 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.778+13983C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310914 | |||||||
| chr11:28310914 | CTGG | C | 9 | a0002c0002t0001g0003 a0002c0002t0001g0245 a0002c0002t0001g0286 others(6): Show |
10 | HG00609.hp2 HG03831.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.778+14032_778+1403 others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310914 | ||||||
| chr11:28310917 | G | C | 200 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(197): Show |
203 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(200): Show |
intron_variant | MODIFIER | c.778+13986G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310917 | |||||||
| chr11:28310920 | G | C | 201 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(198): Show |
205 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.778+13989G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310920 | |||||||
| chr11:28310923 | G | C | 68 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0028 others(65): Show |
69 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.778+13992G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310923 | |||||||
| chr11:28310926 | G | C | 19 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(16): Show |
19 | HG00609.hp2 HG00733.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.778+13995G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310926 | |||||||
| chr11:28310929 | G | C | 5 | a0001c0001t0004g0171 a0001c0001t0004g0181 a0001c0001t0004g0201 others(2): Show |
5 | HG01943.hp2 HG02896.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.778+13998G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310929 | |||||||
| chr11:28310954 | T | G | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0145 |
3 | HG00738.hp2 NA18981.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.778+14023T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310954 | |||||||
| chr11:28310955 | G | T | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0145 |
3 | HG00738.hp2 NA18981.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.778+14024G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310955 | |||||||
| chr11:28310955 | GGTGGT | G | 4 | a0001c0001t0002g0130 a0004c0003t0002g0086 a0004c0003t0002g0111 others(1): Show |
4 | HG00735.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.778+14026_778+1403 others(9): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310955 | ||||||
| chr11:28310956 | GTGGTGGT others(4): Show |
G | 2 | a0001c0001t0011g0210 a0001c0001t0011g0241 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.778+14026_778+1403 others(15): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310956 | |||||||
| chr11:28310957 | TGGTG | T | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0145 |
3 | HG00738.hp2 NA18981.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.778+14028_778+1403 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310957 | ||||||
| chr11:28310958 | GGT | G | 18 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0096 others(15): Show |
18 | HG00544.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.778+14029_778+1403 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310958 | ||||||
| chr11:28310959 | G | T | 1 | a0001c0001t0002g0090 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.778+14028G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310959 | |||||||
| chr11:28310960 | T | G | 6 | a0001c0001t0002g0090 a0001c0001t0002g0125 a0001c0001t0003g0030 others(3): Show |
6 | HG01433.hp1 HG02647.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.778+14029T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310960 | |||||||
| chr11:28310960 | T | TG | 5 | a0001c0001t0002g0239 a0001c0001t0007g0189 a0005c0005t0014g0079 others(2): Show |
5 | HG00642.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.778+14031dupG | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310960 | ||||||
| chr11:28310961 | G | GGTGT | 3 | a0001c0001t0007g0168 a0001c0001t0009g0165 a0001c0001t0009g0169 |
3 | HG01243.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.778+14033_778+1403 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310961 | ||||||
| chr11:28310961 | G | T | 6 | a0001c0001t0002g0090 a0001c0001t0002g0125 a0001c0001t0003g0030 others(3): Show |
6 | HG01433.hp1 HG02647.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.778+14030G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310961 | |||||||
| chr11:28310962 | GT | G | 40 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0091 others(37): Show |
40 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.778+14032delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310962 | |||||||
| chr11:28310962 | GTGGGT | G | 3 | a0001c0001t0001g0214 a0002c0002t0001g0247 a0002c0002t0001g0272 |
3 | HG01496.hp1 HG02056.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.778+14032_778+1403 others(9): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310962 | |||||||
| chr11:28310963 | TG | T | 8 | a0001c0001t0004g0205 a0001c0001t0006g0220 a0001c0001t0006g0221 others(5): Show |
8 | HG01123.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.778+14035delG | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310963 | ||||||
| chr11:28310963 | TGG | T | 3 | a0002c0002t0001g0252 a0002c0002t0001g0302 a0002c0002t0001g0306 |
3 | HG02027.hp2 HG02132.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.778+14034_778+1403 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310963 | ||||||
| chr11:28310965 | G | GGT | 14 | a0002c0002t0001g0004 a0002c0002t0001g0243 a0002c0002t0001g0246 others(11): Show |
15 | HG00597.hp1 HG00642.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.778+14072_778+1407 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310965 | ||||||
| chr11:28310965 | G | GGTGGGTG others(3): Show |
1 | a0001c0001t0005g0012 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.778+14037_778+1403 others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310965 | ||||||
| chr11:28310965 | G | GGTGT | 7 | a0001c0001t0003g0025 a0001c0001t0003g0032 a0001c0001t0005g0043 others(4): Show |
7 | HG01069.hp2 HG01361.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.778+14070_778+1407 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310965 | ||||||
| chr11:28310965 | G | GGTGTGT | 11 | a0001c0001t0003g0021 a0001c0001t0003g0027 a0001c0001t0003g0028 others(8): Show |
11 | HG00621.hp2 HG00738.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.778+14068_778+1407 others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310965 | ||||||
| chr11:28310965 | G | GGTGTGTG others(1): Show |
3 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0042 |
3 | HG03491.hp2 HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.778+14066_778+1407 others(12): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310965 | ||||||
| chr11:28310965 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0005g0036 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.778+14064_778+1407 others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310965 | ||||||
| chr11:28310965 | G | GT | 6 | a0001c0001t0003g0008 a0001c0001t0004g0171 a0001c0001t0004g0228 others(3): Show |
6 | HG01496.hp2 HG02602.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.778+14034_778+1403 others(5): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310965 | |||||||
| chr11:28310965 | G | GTGGGT | 3 | a0001c0001t0003g0024 a0001c0001t0004g0201 a0001c0001t0007g0198 |
3 | HG01943.hp2 HG02738.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.778+14034_778+1403 others(9): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310965 | |||||||
| chr11:28310965 | G | GTGGGTGG others(6): Show |
1 | a0001c0001t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.778+14034_778+1403 others(17): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310965 | |||||||
| chr11:28310965 | G | GTGGGTGT | 7 | a0001c0001t0003g0002 a0001c0001t0003g0047 a0001c0001t0003g0049 others(4): Show |
8 | HG02809.hp2 NA18964.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.778+14034_778+1403 others(11): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310965 | |||||||
| chr11:28310965 | G | GTGGGTGT others(2): Show |
28 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0011 others(25): Show |
28 | HG00673.hp2 HG02040.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.778+14034_778+1403 others(13): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310965 | |||||||
| chr11:28310965 | G | GTGGGTGT others(4): Show |
4 | a0001c0001t0003g0039 a0001c0001t0003g0067 a0001c0001t0005g0056 others(1): Show |
4 | HG03927.hp2 NA18946.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.778+14034_778+1403 others(15): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310965 | |||||||
| chr11:28310965 | G | GTGGGTGT others(6): Show |
2 | a0001c0001t0003g0045 a0001c0001t0005g0007 |
2 | NA18955.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.778+14034_778+1403 others(17): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310965 | |||||||
| chr11:28310965 | G | GTGGTGTG others(3): Show |
4 | a0001c0001t0003g0001 a0001c0001t0003g0014 a0001c0001t0003g0078 others(1): Show |
4 | NA18963.hp2 NA18980.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.778+14034_778+1403 others(14): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310965 | |||||||
| chr11:28310965 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0009g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.778+14034_778+1403 others(15): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310965 | |||||||
| chr11:28310965 | G | T | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(88): Show |
91 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.778+14034G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310965 | |||||||
| chr11:28310965 | GGT | G | 12 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0212 others(9): Show |
12 | HG00735.hp1 HG01361.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.778+14072_778+1407 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310965 | ||||||
| chr11:28310965 | GGTGT | G | 4 | a0002c0002t0001g0277 a0002c0002t0001g0293 a0002c0002t0001g0300 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+14070_778+1407 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310965 | ||||||
| chr11:28310966 | G | T | 7 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(4): Show |
7 | HG02615.hp2 HG02965.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.778+14035G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310966 | |||||||
| chr11:28310967 | T | G | 9 | a0001c0001t0004g0164 a0001c0001t0004g0171 a0001c0001t0004g0228 others(6): Show |
9 | HG02615.hp2 HG02698.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.778+14036T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310967 | |||||||
| chr11:28310967 | T | TGG | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.778+14037_778+1403 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28310967 | ||||||
| chr11:28310969 | T | G | 8 | a0001c0001t0004g0205 a0001c0001t0006g0220 a0001c0001t0006g0221 others(5): Show |
8 | HG01123.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.778+14038T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310969 | |||||||
| chr11:28310971 | T | G | 5 | a0001c0001t0006g0160 a0001c0001t0006g0218 a0001c0001t0006g0222 others(2): Show |
5 | HG02976.hp2 HG03471.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.778+14040T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310971 | |||||||
| chr11:28310973 | T | G | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778+14042T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310973 | |||||||
| chr11:28310977 | T | G | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.778+14046T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310977 | |||||||
| chr11:28311003 | T | A | 12 | a0001c0001t0001g0214 a0001c0001t0004g0212 a0001c0001t0004g0232 others(9): Show |
12 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.778+14072T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311003 | |||||||
| chr11:28311003 | TGA | T | 6 | a0001c0001t0006g0160 a0001c0001t0006g0218 a0001c0001t0006g0222 others(3): Show |
6 | HG02976.hp2 HG03471.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.778+14092_778+1409 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28311003 | ||||||
| chr11:28311003 | TGAGA | T | 6 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0224 others(3): Show |
6 | HG02559.hp1 HG02818.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+14090_778+1409 others(8): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28311003 | ||||||
| chr11:28311005 | A | T | 14 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(11): Show |
14 | HG01952.hp2 HG01993.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.778+14074A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311005 | |||||||
| chr11:28311007 | A | T | 6 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(3): Show |
6 | HG02615.hp2 HG02976.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+14076A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311007 | |||||||
| chr11:28311036 | C | A | 1 | a0001c0001t0003g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.778+14105C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311036 | |||||||
| chr11:28311190 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.778+14259T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311190 | |||||||
| chr11:28311238 | A | T | 56 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(53): Show |
56 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.778+14307A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311238 | |||||||
| chr11:28311392 | C | T | 74 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(71): Show |
74 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.778+14461C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311392 | |||||||
| chr11:28311453 | A | C | 56 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(53): Show |
56 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.778+14522A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311453 | |||||||
| chr11:28311561 | T | C | 1 | a0001c0001t0022g0157 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.778+14630T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311561 | |||||||
| chr11:28311854 | T | G | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.778+14923T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311854 | |||||||
| chr11:28311919 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.778+14988A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28311919 | |||||||
| chr11:28312431 | G | A | 1 | a0001c0001t0003g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.778+15500G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28312431 | |||||||
| chr11:28312565 | CT | C | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.778+15641delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28312565 | ||||||
| chr11:28312602 | A | G | 1 | a0001c0001t0012g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.778+15671A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28312602 | |||||||
| chr11:28312977 | T | C | 1 | a0001c0001t0003g0016 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.778+16046T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28312977 | |||||||
| chr11:28312986 | T | C | 88 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(85): Show |
90 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.778+16055T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28312986 | |||||||
| chr11:28312993 | G | C | 1 | a0001c0001t0008g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.778+16062G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28312993 | |||||||
| chr11:28313000 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.778+16069C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28313000 | |||||||
| chr11:28313007 | G | A | 2 | a0001c0001t0004g0164 a0002c0002t0001g0263 |
2 | HG02602.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.778+16076G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28313007 | |||||||
| chr11:28313041 | A | G | 84 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0243 others(81): Show |
86 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.778+16110A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28313041 | |||||||
| chr11:28313058 | T | C | 1 | a0001c0001t0003g0045 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.778+16127T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28313058 | |||||||
| chr11:28313315 | T | TA | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.778+16388dupA | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28313315 | ||||||
| chr11:28313749 | T | C | 1 | a0004c0003t0002g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.779-16647T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28313749 | |||||||
| chr11:28313887 | T | A | 1 | a0002c0002t0001g0314 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.779-16509T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28313887 | |||||||
| chr11:28313905 | T | C | 62 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(59): Show |
62 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.779-16491T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28313905 | |||||||
| chr11:28314031 | G | A | 1 | a0001c0001t0019g0208 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.779-16365G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314031 | |||||||
| chr11:28314077 | A | G | 89 | a0001c0001t0002g0115 a0002c0002t0001g0003 a0002c0002t0001g0004 others(86): Show |
91 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.779-16319A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314077 | |||||||
| chr11:28314195 | A | T | 1 | a0001c0001t0004g0238 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.779-16201A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314195 | |||||||
| chr11:28314268 | T | G | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.779-16128T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314268 | |||||||
| chr11:28314278 | G | A | 1 | a0001c0001t0005g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.779-16118G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314278 | |||||||
| chr11:28314304 | G | C | 75 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(72): Show |
75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.779-16092G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314304 | |||||||
| chr11:28314325 | A | C | 62 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(59): Show |
62 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.779-16071A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314325 | |||||||
| chr11:28314498 | G | A | 1 | a0001c0001t0004g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.779-15898G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314498 | |||||||
| chr11:28314558 | A | G | 1 | a0001c0001t0003g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.779-15838A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314558 | |||||||
| chr11:28314618 | A | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.779-15778A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314618 | |||||||
| chr11:28314640 | A | G | 1 | a0001c0001t0003g0045 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.779-15756A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314640 | |||||||
| chr11:28314727 | G | T | 1 | a0001c0001t0003g0068 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.779-15669G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314727 | |||||||
| chr11:28314954 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.779-15442C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28314954 | |||||||
| chr11:28315427 | T | C | 2 | a0001c0001t0003g0032 a0001c0001t0005g0043 |
2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.779-14969T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28315427 | |||||||
| chr11:28315498 | A | C | 1 | a0002c0002t0001g0262 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.779-14898A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28315498 | |||||||
| chr11:28315666 | C | G | 12 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0212 others(9): Show |
12 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.779-14730C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28315666 | |||||||
| chr11:28315867 | G | A | 1 | a0002c0002t0001g0243 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.779-14529G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28315867 | |||||||
| chr11:28315925 | A | C | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.779-14471A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28315925 | |||||||
| chr11:28315950 | G | T | 1 | a0001c0001t0004g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.779-14446G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28315950 | |||||||
| chr11:28316397 | T | G | 11 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(8): Show |
11 | HG00544.hp2 HG00738.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.779-13999T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28316397 | |||||||
| chr11:28316403 | T | C | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.779-13993T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28316403 | |||||||
| chr11:28316507 | T | C | 1 | a0001c0001t0003g0069 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.779-13889T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28316507 | |||||||
| chr11:28316521 | T | C | 16 | a0001c0001t0004g0176 a0001c0001t0004g0180 a0001c0001t0004g0196 others(13): Show |
16 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.779-13875T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28316521 | |||||||
| chr11:28316727 | G | C | 1 | a0002c0002t0001g0310 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.779-13669G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28316727 | |||||||
| chr11:28316760 | G | A | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.779-13636G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28316760 | |||||||
| chr11:28316813 | C | T | 88 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(85): Show |
90 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.779-13583C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28316813 | |||||||
| chr11:28316985 | A | C | 1 | a0001c0001t0002g0239 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.779-13411A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28316985 | |||||||
| chr11:28317024 | T | C | 1 | a0001c0008t0020g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.779-13372T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28317024 | |||||||
| chr11:28317179 | C | T | 4 | a0001c0001t0003g0026 a0001c0001t0005g0031 a0001c0001t0005g0034 others(1): Show |
4 | NA18947.hp2 NA18978.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.779-13217C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28317179 | |||||||
| chr11:28317275 | C | T | 1 | a0002c0002t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.779-13121C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28317275 | |||||||
| chr11:28317881 | A | G | 6 | a0001c0001t0007g0168 a0001c0001t0007g0240 a0001c0001t0009g0165 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.779-12515A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28317881 | |||||||
| chr11:28317954 | T | G | 2 | a0001c0001t0009g0185 a0001c0001t0024g0184 |
2 | HG02080.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.779-12442T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28317954 | |||||||
| chr11:28318178 | G | A | 1 | a0002c0002t0001g0288 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.779-12218G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28318178 | |||||||
| chr11:28318179 | T | A | 1 | a0001c0001t0003g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.779-12217T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28318179 | |||||||
| chr11:28318365 | T | A | 1 | a0001c0001t0004g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.779-12031T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28318365 | |||||||
| chr11:28318365 | T | TTA | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.779-12016_779-1201 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28318365 | ||||||
| chr11:28318473 | C | T | 1 | a0002c0002t0001g0268 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.779-11923C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28318473 | |||||||
| chr11:28318705 | T | A | 1 | a0002c0002t0001g0290 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.779-11691T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28318705 | |||||||
| chr11:28318784 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.779-11612C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28318784 | |||||||
| chr11:28318802 | A | T | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.779-11594A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28318802 | |||||||
| chr11:28318913 | G | T | 1 | a0001c0001t0003g0027 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.779-11483G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28318913 | |||||||
| chr11:28318961 | CAAT | C | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.779-11432_779-1143 others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28318961 | ||||||
| chr11:28319455 | G | GT | 7 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(4): Show |
7 | HG00738.hp1 HG03516.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.779-10939dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28319455 | ||||||
| chr11:28319457 | TG | T | 11 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(8): Show |
11 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.779-10938delG | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28319457 | |||||||
| chr11:28319458 | G | T | 315 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(312): Show |
319 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.779-10938G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28319458 | |||||||
| chr11:28320071 | C | A | 3 | a0001c0001t0011g0210 a0001c0001t0011g0241 a0001c0001t0011g0242 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.779-10325C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320071 | |||||||
| chr11:28320072 | A | G | 3 | a0001c0001t0002g0119 a0001c0001t0010g0117 a0001c0001t0010g0118 |
3 | NA18948.hp2 NA18961.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.779-10324A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320072 | |||||||
| chr11:28320126 | T | A | 1 | a0001c0001t0003g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.779-10270T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320126 | |||||||
| chr11:28320176 | AAATAGT | A | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.779-10219_779-1021 others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320176 | |||||||
| chr11:28320181 | GT | G | 101 | a0001c0001t0002g0115 a0001c0001t0003g0001 a0001c0001t0003g0009 others(98): Show |
104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.779-10195delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28320181 | ||||||
| chr11:28320181 | GTT | G | 147 | a0001c0001t0001g0214 a0001c0001t0002g0005 a0001c0001t0002g0006 others(144): Show |
148 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.779-10196_779-1019 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28320181 | ||||||
| chr11:28320181 | GTTT | G | 55 | a0001c0001t0002g0120 a0001c0001t0002g0136 a0001c0001t0002g0146 others(52): Show |
55 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.779-10197_779-1019 others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28320181 | ||||||
| chr11:28320183 | T | G | 12 | a0001c0001t0004g0164 a0001c0001t0006g0160 a0001c0001t0006g0218 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.779-10213T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320183 | |||||||
| chr11:28320190 | T | G | 1 | a0001c0001t0002g0096 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.779-10206T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320190 | |||||||
| chr11:28320339 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.779-10057G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320339 | |||||||
| chr11:28320481 | T | C | 6 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.779-9915T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320481 | |||||||
| chr11:28320587 | G | C | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.779-9809G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320587 | |||||||
| chr11:28320672 | A | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.779-9724A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320672 | |||||||
| chr11:28320730 | C | A | 1 | a0001c0001t0003g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.779-9666C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320730 | |||||||
| chr11:28320841 | G | T | 1 | a0003c0004t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.779-9555G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320841 | |||||||
| chr11:28320940 | G | A | 1 | a0002c0002t0001g0270 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.779-9456G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320940 | |||||||
| chr11:28320961 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.779-9435C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28320961 | |||||||
| chr11:28321033 | A | G | 85 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(82): Show |
87 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.779-9363A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28321033 | |||||||
| chr11:28321113 | A | G | 67 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0084 others(64): Show |
67 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.779-9283A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28321113 | |||||||
| chr11:28321163 | T | G | 2 | a0002c0002t0001g0003 a0002c0002t0001g0245 |
3 | NA18979.hp1 NA18981.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.779-9233T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28321163 | |||||||
| chr11:28321314 | A | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.779-9082A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28321314 | |||||||
| chr11:28321318 | G | A | 2 | a0001c0001t0004g0178 a0001c0001t0006g0203 |
2 | NA18966.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.779-9078G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28321318 | |||||||
| chr11:28321400 | T | C | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.779-8996T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28321400 | |||||||
| chr11:28321862 | G | A | 3 | a0002c0002t0001g0278 a0002c0002t0001g0292 a0002c0002t0001g0293 |
3 | NA18612.hp1 NA18955.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.779-8534G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28321862 | |||||||
| chr11:28321865 | TCAATGGA others(1): Show |
T | 79 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(76): Show |
81 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.779-8528_779-8521d others(10): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28321865 | ||||||
| chr11:28321874 | C | T | 79 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(76): Show |
81 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.779-8522C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28321874 | |||||||
| chr11:28321875 | A | C | 79 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(76): Show |
81 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.779-8521A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28321875 | |||||||
| chr11:28321936 | G | T | 1 | a0001c0001t0008g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.779-8460G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28321936 | |||||||
| chr11:28322107 | T | G | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.779-8289T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28322107 | |||||||
| chr11:28322394 | G | A | 1 | a0002c0002t0001g0256 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.779-8002G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28322394 | |||||||
| chr11:28322406 | G | A | 56 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(53): Show |
56 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.779-7990G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28322406 | |||||||
| chr11:28322558 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.779-7838A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28322558 | |||||||
| chr11:28322749 | A | C | 160 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(157): Show |
162 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.779-7647A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28322749 | |||||||
| chr11:28322827 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.779-7569G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28322827 | |||||||
| chr11:28322872 | T | G | 1 | a0002c0002t0001g0254 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.779-7524T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28322872 | |||||||
| chr11:28322962 | A | G | 91 | a0001c0001t0002g0115 a0002c0002t0001g0003 a0002c0002t0001g0004 others(88): Show |
93 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.779-7434A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28322962 | |||||||
| chr11:28323192 | T | A | 1 | a0001c0001t0002g0130 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.779-7204T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28323192 | |||||||
| chr11:28323294 | T | C | 1 | a0001c0001t0002g0130 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.779-7102T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28323294 | |||||||
| chr11:28323575 | A | G | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 |
3 | HG02622.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.779-6821A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28323575 | |||||||
| chr11:28324102 | G | A | 2 | a0001c0001t0004g0176 a0001c0001t0004g0207 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.779-6294G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324102 | |||||||
| chr11:28324241 | T | C | 3 | a0001c0001t0002g0119 a0001c0001t0010g0117 a0001c0001t0010g0118 |
3 | NA18948.hp2 NA18961.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.779-6155T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324241 | |||||||
| chr11:28324710 | T | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0009c0010t0002g0101 |
3 | HG01952.hp2 HG01993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.779-5686T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324710 | |||||||
| chr11:28324725 | C | T | 1 | a0001c0001t0004g0171 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.779-5671C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324725 | |||||||
| chr11:28324818 | T | C | 2 | a0002c0002t0001g0244 a0002c0002t0001g0315 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.779-5578T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324818 | |||||||
| chr11:28324842 | T | C | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.779-5554T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324842 | |||||||
| chr11:28324848 | C | A | 1 | a0001c0001t0002g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.779-5548C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324848 | |||||||
| chr11:28324856 | A | C | 1 | a0001c0001t0004g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.779-5540A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324856 | |||||||
| chr11:28324882 | C | T | 1 | a0001c0001t0012g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.779-5514C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324882 | |||||||
| chr11:28324893 | G | C | 1 | a0001c0001t0002g0134 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.779-5503G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324893 | |||||||
| chr11:28324921 | C | T | 1 | a0002c0002t0001g0321 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.779-5475C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324921 | |||||||
| chr11:28324982 | C | G | 1 | a0001c0001t0002g0130 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.779-5414C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28324982 | |||||||
| chr11:28325047 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.779-5349C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28325047 | |||||||
| chr11:28325155 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.779-5241A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28325155 | |||||||
| chr11:28325259 | A | G | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.779-5137A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28325259 | |||||||
| chr11:28325405 | A | G | 4 | a0001c0001t0002g0141 a0001c0001t0002g0143 a0001c0001t0002g0144 others(1): Show |
4 | HG00609.hp1 HG02523.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.779-4991A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28325405 | |||||||
| chr11:28325435 | A | G | 1 | a0001c0014t0021g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.779-4961A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28325435 | |||||||
| chr11:28325492 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.779-4904C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28325492 | |||||||
| chr11:28326244 | C | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.779-4152C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28326244 | |||||||
| chr11:28326287 | GT | G | 13 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0026 others(10): Show |
13 | HG01361.hp2 HG02602.hp2 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.779-4097delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28326287 | ||||||
| chr11:28326397 | A | G | 1 | a0001c0001t0009g0185 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.779-3999A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28326397 | |||||||
| chr11:28326535 | G | C | 1 | a0011c0012t0003g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.779-3861G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28326535 | |||||||
| chr11:28326630 | G | A | 2 | a0001c0001t0004g0196 a0001c0001t0004g0197 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.779-3766G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28326630 | |||||||
| chr11:28326780 | T | G | 79 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(76): Show |
81 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.779-3616T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28326780 | |||||||
| chr11:28326960 | CTTTT | C | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(75): Show |
80 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.779-3435_779-3432d others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28326960 | |||||||
| chr11:28327166 | A | G | 8 | a0001c0001t0004g0232 a0001c0001t0006g0230 a0001c0001t0007g0231 others(5): Show |
8 | HG00621.hp1 HG00673.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.779-3230A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28327166 | |||||||
| chr11:28327872 | G | C | 1 | a0001c0001t0003g0028 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.779-2524G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28327872 | |||||||
| chr11:28327928 | AGTTAT | A | 56 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(53): Show |
56 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.779-2464_779-2460d others(7): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28327928 | ||||||
| chr11:28328134 | A | T | 1 | a0001c0001t0002g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.779-2262A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28328134 | |||||||
| chr11:28328169 | A | T | 1 | a0010c0011t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.779-2227A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28328169 | |||||||
| chr11:28328572 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.779-1824A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28328572 | |||||||
| chr11:28328666 | A | G | 1 | a0002c0002t0001g0251 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.779-1730A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28328666 | |||||||
| chr11:28328802 | A | C | 1 | a0001c0001t0007g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.779-1594A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28328802 | |||||||
| chr11:28329203 | C | T | 1 | a0001c0001t0003g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.779-1193C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28329203 | |||||||
| chr11:28329391 | A | G | 2 | a0004c0003t0002g0111 a0004c0003t0002g0112 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.779-1005A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28329391 | |||||||
| chr11:28329573 | G | T | 89 | a0001c0001t0002g0115 a0002c0002t0001g0003 a0002c0002t0001g0004 others(86): Show |
91 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.779-823G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28329573 | |||||||
| chr11:28329708 | C | T | 1 | a0001c0001t0008g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.779-688C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28329708 | |||||||
| chr11:28330239 | G | A | 40 | a0001c0001t0004g0158 a0001c0001t0004g0170 a0001c0001t0004g0171 others(37): Show |
40 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.779-157G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28330239 | |||||||
| chr11:28330256 | T | G | 8 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0007g0168 others(5): Show |
8 | HG01243.hp2 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.779-140T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28330256 |