Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr11 | 28103388 | 28338507 |
| a0002 | 1/0 | 407 | 85 | 10 | 17 | 40 | 1 | 16 | 31 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0003 | 0/0 | 407 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0004 | 0/0 | 407 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0005 | 0/0 | 407 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0006 | 0/0 | 407 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0007 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0008 | 0/0 | 407 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0009 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0010 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0011 | 0/0 | 407 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1224 | 222 | 53 | 21 | 124 | 3 | 20 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0002 | 1/0 | 1224 | 85 | 10 | 17 | 40 | 1 | 16 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0003 | 0/0 | 1224 | 6 | 6 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0004 | 0/0 | 1224 | 6 | 6 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0005 | 0/0 | 1224 | 3 | 3 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0006 | 0/0 | 1224 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0007 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0008 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0009 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0010 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0011 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0012 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0013 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| c0014 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2985 | 87 | 15 | 18 | 37 | 1 | 16 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0002 | 0/1 | 2986 | 72 | 7 | 11 | 46 | 2 | 5 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0003 | 0/0 | 2990 | 58 | 2 | 1 | 47 | 0 | 8 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0004 | 0/0 | 2993 | 36 | 16 | 5 | 10 | 1 | 4 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0005 | 0/0 | 2991 | 12 | 2 | 0 | 9 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0006 | 0/0 | 2992 | 12 | 9 | 0 | 3 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0007 | 0/0 | 2994 | 10 | 2 | 1 | 6 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0008 | 0/0 | 2993 | 7 | 6 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0009 | 0/0 | 2995 | 6 | 4 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0010 | 0/0 | 2985 | 5 | 2 | 0 | 3 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0011 | 0/0 | 2985 | 4 | 4 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0012 | 0/0 | 2990 | 3 | 3 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0013 | 0/0 | 2992 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0014 | 0/0 | 2991 | 2 | 2 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0015 | 0/0 | 2985 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0016 | 0/0 | 2991 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0017 | 0/0 | 2992 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0018 | 0/0 | 2989 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0019 | 0/0 | 2993 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0020 | 0/0 | 2994 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0021 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0022 | 0/0 | 2993 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0023 | 0/0 | 2991 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0024 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0025 | 0/0 | 2992 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0026 | 1/0 | 2985 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0027 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0028 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| t0029 | 0/0 | 2986 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1224 | 222 | 53 | 21 | 124 | 3 | 20 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0007 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0008 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0014 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0002c0002 | 1/0 | 1224 | 85 | 10 | 17 | 40 | 1 | 16 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0003c0003 | 0/0 | 1224 | 6 | 6 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0004c0004 | 0/0 | 1224 | 6 | 6 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0005c0005 | 0/0 | 1224 | 3 | 3 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0006c0006 | 0/0 | 1224 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0007c0012 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0008c0011 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0009c0010 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0010c0009 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0011c0013 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | 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 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0002 | 0/1 | 4209 | 65 | 1 | 11 | 45 | 2 | 5 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0003 | 0/0 | 4213 | 52 | 1 | 1 | 42 | 0 | 8 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0004 | 0/0 | 4216 | 35 | 15 | 5 | 10 | 1 | 4 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0005 | 0/0 | 4214 | 12 | 2 | 0 | 9 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0006 | 0/0 | 4215 | 12 | 9 | 0 | 3 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0007 | 0/0 | 4217 | 10 | 2 | 1 | 6 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0008 | 0/0 | 4216 | 7 | 6 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0009 | 0/0 | 4218 | 6 | 4 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0010 | 0/0 | 4208 | 5 | 2 | 0 | 3 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0011 | 0/0 | 4208 | 4 | 4 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0012 | 0/0 | 4213 | 3 | 3 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0013 | 0/0 | 4215 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0016 | 0/0 | 4214 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0017 | 0/0 | 4215 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0018 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0019 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0022 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0023 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0024 | 0/0 | 4216 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0001t0029 | 0/0 | 4209 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0007t0003 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0008t0020 | 0/0 | 4217 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0001c0014t0021 | 0/0 | 4208 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0002c0002t0001 | 0/0 | 4208 | 81 | 10 | 17 | 37 | 1 | 16 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0002c0002t0015 | 0/0 | 4208 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0002c0002t0026 | 1/0 | 4208 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0002c0002t0027 | 0/0 | 4208 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0003c0003t0002 | 0/0 | 4209 | 6 | 6 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0004c0004t0001 | 0/0 | 4208 | 5 | 5 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0004c0004t0028 | 0/0 | 4208 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0005c0005t0014 | 0/0 | 4214 | 2 | 2 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0005c0005t0025 | 0/0 | 4215 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0006c0006t0003 | 0/0 | 4213 | 2 | 0 | 0 | 2 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0007c0012t0003 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0008c0011t0003 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0009c0010t0002 | 0/0 | 4209 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0010c0009t0003 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| a0011c0013t0004 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | copy fasta | chr11 | 28103388 | 28338507 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0004 | 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 |
| a0001c0001t0002g0101 | 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 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0125 | 0/1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0156 | 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 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0057 | 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 |
| a0001c0001t0003g0062 | 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 |
| a0001c0001t0003g0064 | 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 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0003g0075 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0198 | 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 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0035 | 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 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0005g0073 | 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 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0006g0187 | 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 |
| 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 |
| a0001c0001t0006g0226 | 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 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0008g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0008g0213 | 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 |
| a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0009g0203 | 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 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0010g0123 | 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 |
| a0001c0001t0011g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0011g0221 | 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 |
| a0001c0001t0012g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0012g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0012g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0013g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0013g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0016g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0017g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0018g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0019g0192 | 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 |
| a0001c0001t0023g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0024g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0001t0029g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0007t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0001c0008t0020g0194 | 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 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 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 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0305 | 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 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0001g0330 | 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 |
| a0002c0002t0026g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0002c0002t0027g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0003t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0003c0003t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0004t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0004t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0004t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0004c0004t0028g0282 | 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 |
| a0006c0006t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0006c0006t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0007c0012t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0008c0011t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0009c0010t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0010c0009t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| a0011c0013t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0255 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00423 | hp1 | a0010 | c0009 | t0003 | g0012 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0297 | 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 | g0073 | 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 | g0141 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0287 | 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 | g0066 | 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 | g0026 | EAS | CHS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0278 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0172 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0324 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0296 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0323 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0295 | 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 | g0135 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0307 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0325 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0169 | AMR | PUR | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0311 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0300 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01361 | hp2 | a0001 | c0001 | t0016 | g0076 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0329 | 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 | g0275 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | IBS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0305 | 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 | g0134 | EUR | IBS | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01891 | hp2 | a0004 | c0004 | t0001 | g0294 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0288 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0212 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0264 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0292 | AMR | PEL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0271 | 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 | g0184 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0203 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0028 | 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 | g0179 | 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 | g0330 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02258 | hp2 | a0001 | c0001 | t0019 | g0192 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0077 | 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 | g0027 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02572 | hp1 | a0003 | c0003 | t0002 | g0111 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0265 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0213 | 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 | a0003 | c0003 | t0002 | g0086 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02647 | hp1 | a0003 | 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 | g0054 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0281 | 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 | a0003 | c0003 | t0002 | g0110 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0279 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0299 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0183 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0180 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0067 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0177 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02886 | hp1 | a0001 | c0001 | t0023 | g0078 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0193 | 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 | g0211 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0191 | 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 | g0178 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0313 | 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 | a0004 | c0004 | t0001 | g0310 | 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 | g0058 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0068 | 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 | g0276 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0221 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0314 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03209 | hp1 | a0004 | c0004 | t0001 | g0283 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0222 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0289 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0050 | 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 | a0004 | c0004 | t0028 | g0282 | 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 | a0003 | c0003 | t0002 | g0109 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0298 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0315 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0197 | AFR | ESN | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0326 | 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 | g0225 | AFR | GWD | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0168 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03579 | hp2 | a0004 | c0004 | t0001 | g0301 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0256 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0205 | SAS | PJL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0074 | 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 | g0274 | SAS | STU | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0303 | 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 | g0327 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0251 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03927 | hp2 | a0001 | c0001 | t0029 | g0120 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0254 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0253 | 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 | g0151 | SAS | BEB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0317 | 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 | g0226 | AFR | YRI | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | CHB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CHB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0048 | 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 | a0011 | c0013 | t0004 | g0209 | 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 | g0064 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18948 | hp2 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0032 | 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 | g0284 | 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 | g0059 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0040 | 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 | g0129 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18961 | hp2 | a0001 | c0001 | t0010 | g0122 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0038 | 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 | g0037 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0001 | 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 | g0267 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0196 | 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 | g0029 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18968 | hp2 | a0001 | c0001 | t0013 | g0020 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0119 | 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 | g0249 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18978 | hp2 | a0001 | c0001 | t0013 | g0072 | 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 | g0153 | 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 | g0071 | 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 | g0002 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18982 | hp1 | a0002 | c0002 | t0027 | g0328 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18982 | hp2 | a0001 | c0001 | t0024 | g0202 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0146 | 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 | g0001 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0060 | 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 | g0266 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0053 | 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 | g0200 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0139 | 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 | g0013 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18995 | hp2 | a0006 | c0006 | t0003 | g0017 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19000 | hp2 | a0001 | c0001 | t0018 | g0033 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19005 | hp1 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19012 | hp2 | a0009 | c0010 | t0002 | g0100 | 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 | a0008 | c0011 | t0003 | g0217 | AFR | LWK | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19043 | hp1 | a0003 | 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 | g0174 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0258 | 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 | g0144 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0070 | 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 | a0007 | c0012 | t0003 | g0065 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0259 | 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 | g0063 | 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 | g0285 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0016 | 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 | g0102 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19077 | hp2 | a0006 | c0006 | t0003 | g0019 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0062 | 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 | g0069 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0023 | 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 | g0206 | AFR | ASW | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0204 | SAS | GIH | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0250 | SAS | GIH | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0309 | AMR | CLM | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0189 | 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 | a0004 | c0004 | t0001 | g0293 | AFR | ACB | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0219 | 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 | g0220 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | MSL | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0224 | 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 | g0290 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA20300 | hp1 | a0001 | c0008 | t0020 | g0194 | AFR | USA | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0308 | AFR | USA | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0223 | AFR | LWK | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | LWK | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0125 | REF | REF | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0026 | g0159 | REF | REF | METTL15_chr11_28103388_28338507 | METTL15 | chr11 | 28103388 | 28338507 |
| 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 | a0001a0003a0005others(6): Show | 241 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(238): 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 | a0011 | 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 | a0007 | 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 | a0004 | 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 | a0003 | 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 | a0008 | 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 | a0010 | 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 | a0005a0008 | 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 |
| 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 |
| 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 | a0001c0001t0002a0001c0001t0010a0001c0001t0029others(2): Show | 78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): 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 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(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 | a0005c0005t0014a0005c0005t0025 | 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 | |||||
| chr11:28331056
|
A | G | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
3_prime_UTR_variant | MODIFIER | c.*215A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 215 | chr11 | 28331056 | |||||
| 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 | a0001c0001t0012a0001c0001t0023a0005c0005t0014others(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 | a0001c0001t0003a0001c0001t0005a0001c0001t0012others(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 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(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 | a0002c0002t0027 | 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 | a0001c0001t0006a0001c0001t0017 | 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 | a0001c0001t0004a0001c0001t0008a0001c0001t0018others(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 | a0001c0001t0003a0001c0001t0007a0001c0001t0012others(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 | a0001c0001t0005a0001c0001t0009a0001c0001t0016others(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 | a0001c0001t0013a0005c0005t0025 | 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 | a0001c0001t0002a0001c0001t0029a0003c0003t0002others(1): Show | 73 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(70): 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 | a0004c0004t0028 | 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 | a0001c0001t0008a0001c0001t0019a0001c0008t0020 | 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 |
| 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 | a0001c0001t0002g0003a0001c0001t0002g0004 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0001t0007g0240a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | a0001c0001t0004g0232a0001c0001t0006g0230a0001c0001t0007g0231others(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 | a0002c0002t0027g0328 | 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 | a0001c0001t0006g0218a0001c0001t0006g0220a0001c0001t0006g0222others(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 | a0008c0011t0003g0217 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0003c0003t0002g0086 | 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 | 43 | a0001c0001t0002g0085a0001c0001t0002g0115a0001c0001t0002g0116others(40): Show | 43 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(40): 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 | a0002c0002t0001g0327 | 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 | a0002c0002t0001g0326 | 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 | 4 | a0002c0002t0001g0322a0002c0002t0001g0323a0002c0002t0001g0324others(1): Show | 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 | a0005c0005t0014g0079a0005c0005t0014g0080a0005c0005t0025g0081 | 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 | a0002c0002t0001g0320a0002c0002t0001g0321 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0008c0011t0003g0217 | 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0001c0001t0002g0239a0003c0003t0002g0086a0003c0003t0002g0109others(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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0002c0002t0015g0318a0002c0002t0015g0319 | 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 | a0001c0001t0007g0169a0001c0001t0009g0165a0001c0001t0009g0166others(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 | 166 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0085others(163): Show | 167 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(164): 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 | a0001c0001t0002g0084a0001c0001t0002g0107a0001c0001t0002g0108others(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 | a0001c0001t0007g0240a0001c0001t0011g0241a0001c0001t0011g0242others(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 | a0001c0001t0001g0214a0001c0001t0003g0005a0002c0002t0001g0248others(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 | a0001c0001t0002g0105a0001c0001t0002g0106 | 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 | 91 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0210others(88): 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 | a0002c0002t0001g0250 | 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 | a0001c0001t0004g0206 | 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0003c0003t0002g0086 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090 | 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 | a0001c0001t0004g0158a0001c0001t0004g0184a0001c0001t0004g0185others(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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(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 | a0001c0001t0004g0164a0001c0001t0004g0173a0001c0001t0004g0175others(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 | 21 | a0001c0001t0003g0005a0001c0001t0003g0032a0001c0001t0003g0034others(18): 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 | a0001c0001t0003g0031 | 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 | 114 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(111): Show | 114 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(111): 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(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 | a0001c0001t0004g0164a0001c0001t0004g0173a0001c0001t0004g0175others(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 | a0001c0001t0004g0158a0001c0001t0004g0184a0001c0001t0004g0185others(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 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0015others(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 | a0001c0001t0003g0001a0001c0001t0003g0007a0001c0001t0003g0016others(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 | a0001c0001t0002g0085a0001c0001t0003g0008a0001c0001t0003g0009others(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 | 38 | a0001c0001t0002g0104a0001c0001t0004g0204a0001c0001t0004g0205others(35): 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0115others(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 | 47 | a0001c0001t0002g0084a0001c0001t0002g0090a0001c0001t0002g0098others(44): Show | 47 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(44): 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 | a0001c0001t0001g0214a0001c0001t0002g0088a0001c0001t0002g0089others(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 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(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 | 92 | a0001c0001t0003g0005a0001c0001t0003g0032a0001c0001t0003g0034others(89): 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 | 111 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0014others(108): 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 | 119 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(116): 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 | 138 | a0001c0001t0002g0085a0001c0001t0003g0001a0001c0001t0003g0005others(135): 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 | 146 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0003g0001others(143): 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 | 159 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0085others(156): 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 | 184 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(181): Show | 186 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.270+3669A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117273 | ||||||
| chr11:28117275
|
A | G | 122 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(119): Show | 122 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.270+3671A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117275 | ||||||
| chr11:28117277
|
A | G | 83 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(80): Show | 83 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.270+3673A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117277 | ||||||
| chr11:28117279
|
A | G | 81 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(78): Show | 81 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.270+3675A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117279 | ||||||
| chr11:28117281
|
A | G | 79 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0088others(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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0003g0074 | 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 | a0002c0002t0001g0277 | 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 | a0002c0002t0015g0318a0002c0002t0015g0319 | 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.270+4073C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28117677 | ||||||
| chr11:28117835
|
T | C | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0002c0002t0001g0250 | 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 | a0002c0002t0001g0308 | 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 | 240 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(237): Show | 241 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(238): Show |
intron_variant | MODIFIER | c.270+4468A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118072 | ||||||
| chr11:28118207
|
A | G | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.270+4603A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118207 | ||||||
| chr11:28118340
|
T | C | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.270+4736T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118340 | ||||||
| chr11:28118410
|
A | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.270+4806A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28118410 | ||||||
| chr11:28118494
|
T | C | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | 4 | a0002c0002t0001g0322a0002c0002t0001g0323a0002c0002t0001g0324others(1): Show | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(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 | a0001c0001t0002g0128 | 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 | a0002c0002t0001g0275a0002c0002t0001g0276 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0012g0068 | 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0001c0001t0002g0128a0001c0001t0002g0156a0001c0001t0003g0075others(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 | a0001c0001t0003g0048a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0002c0002t0001g0278a0002c0002t0001g0279a0002c0002t0001g0280others(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 | a0001c0001t0002g0129 | 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 | a0001c0001t0007g0240a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0002g0151 | 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 | a0002c0002t0001g0327 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(156): 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0195others(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 | a0002c0002t0001g0307 | 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(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 | a0001c0001t0002g0097a0001c0001t0002g0102a0001c0001t0002g0107others(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 | a0001c0001t0002g0127a0001c0001t0002g0147a0001c0001t0002g0148others(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 | 50 | a0002c0002t0001g0002a0002c0002t0001g0244a0002c0002t0001g0245others(47): 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 | a0001c0001t0002g0085a0002c0002t0001g0246a0002c0002t0001g0248others(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 | a0002c0002t0001g0271a0002c0002t0001g0272a0002c0002t0001g0273 | 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 | a0002c0002t0001g0243a0002c0002t0001g0274a0002c0002t0001g0308others(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 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0024others(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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | 173 | a0001c0001t0001g0214a0001c0001t0002g0095a0001c0001t0002g0115others(170): Show | 173 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(170): 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 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0024others(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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | 64 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0011others(61): 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 | a0001c0001t0004g0171a0001c0001t0004g0191a0001c0001t0004g0195others(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 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(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 | 12 | a0001c0001t0002g0121a0001c0001t0002g0125a0001c0001t0002g0131others(9): Show | 12 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(9): 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 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.270+8771A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28122375 | ||||||
| chr11:28122377
|
A | G | 21 | a0001c0001t0002g0121a0001c0001t0002g0125a0001c0001t0002g0129others(18): Show | 21 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(18): 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 | a0001c0001t0002g0129a0003c0003t0002g0111 | 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 | a0001c0001t0003g0046 | 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 | a0001c0001t0003g0069 | 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 | a0002c0002t0001g0312 | 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 | a0001c0001t0002g0104 | 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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0001c0001t0004g0195 | 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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0008others(156): 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 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0210others(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 | a0001c0001t0003g0030 | 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 | a0003c0003t0002g0110 | 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 | a0001c0001t0003g0049a0001c0001t0003g0050 | 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 | 160 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(157): 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 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029others(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 | a0001c0001t0008g0180 | 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 | a0001c0001t0002g0098 | 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 | a0002c0002t0001g0304 | 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 | a0001c0001t0003g0045 | 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 | a0001c0001t0004g0171a0001c0001t0004g0191 | 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 | 5 | a0002c0002t0001g0274a0002c0002t0001g0322a0002c0002t0001g0323others(2): 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 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(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 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0207others(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 | a0001c0008t0020g0194 | 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 | a0001c0001t0007g0240a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | a0008c0011t0003g0217 | 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 | a0001c0001t0023g0078 | 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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0320a0002c0002t0001g0321 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0303 | 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 | a0002c0002t0027g0328 | 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 | a0001c0001t0004g0171a0001c0001t0004g0191 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | 70 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(67): Show | 70 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(67): 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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0251 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0004c0004t0001g0283 | 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 | a0002c0002t0001g0002a0002c0002t0001g0245a0002c0002t0001g0302others(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 | a0001c0001t0007g0240a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0001c0001t0002g0127a0001c0001t0002g0156 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0003g0006 | 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 | a0002c0002t0001g0327 | 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 | a0001c0001t0002g0155 | 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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0001c0001t0003g0016 | 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 | a0001c0001t0005g0021 | 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 | a0003c0003t0002g0113 | 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 | a0005c0005t0014g0079a0005c0005t0014g0080a0005c0005t0025g0081 | 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 | a0001c0001t0004g0204 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0002c0002t0001g0264 | 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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | a0001c0001t0002g0004 | 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 | a0005c0005t0014g0079a0005c0005t0014g0080a0005c0005t0025g0081 | 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 | 148 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(145): Show | 149 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(146): 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 | a0001c0001t0002g0090a0001c0001t0002g0101a0001c0001t0002g0106others(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 | a0001c0001t0004g0158a0001c0001t0004g0164a0001c0001t0004g0170others(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 | a0002c0002t0001g0289 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0003g0044 | 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 | a0001c0007t0003g0026 | 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 | a0002c0002t0001g0252 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0005g0056 | 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0001c0008t0020g0194 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0004g0211 | 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0003g0049a0001c0001t0003g0050 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0311 | 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 | a0001c0001t0013g0020 | 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0004g0207 | 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 | a0002c0002t0001g0290 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.270+20378T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28133982 | ||||||
| chr11:28134074
|
T | C | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.270+20470T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28134074 | ||||||
| chr11:28134202
|
G | A | 1 | a0002c0002t0001g0252 | 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0001c0001t0004g0158a0001c0001t0004g0184a0001c0001t0007g0183 | 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 | a0002c0002t0001g0291 | 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 | a0001c0001t0003g0074 | 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 | a0004c0004t0001g0301 | 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0004g0204a0001c0001t0004g0205 | 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 | a0001c0001t0002g0239a0003c0003t0002g0086a0003c0003t0002g0109others(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 | 72 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(69): 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 | a0004c0004t0001g0301 | 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 | 72 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(69): 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 | a0001c0001t0002g0152 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0277 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.270+22953C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28136557 | ||||||
| chr11:28137049
|
AT | A | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.270+23450delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28137049 | |||||
| chr11:28137060
|
A | G | 3 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0002g0124a0001c0001t0010g0122a0001c0001t0010g0123 | 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 | 78 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(75): 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 | a0001c0001t0002g0145a0001c0001t0002g0152 | 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 | 77 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(74): 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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(156): 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 | a0001c0001t0004g0171a0001c0001t0004g0191 | 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 | a0001c0001t0003g0014 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0005g0010 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0210others(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 | a0001c0001t0003g0051 | 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 | a0001c0001t0002g0104 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.270+26161A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28139765 | ||||||
| chr11:28139967
|
GGA | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.270+26366_270+2636 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28139967 | |||||
| chr11:28140096
|
C | T | 1 | a0001c0001t0004g0190 | 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 | a0001c0001t0002g0139a0001c0001t0002g0144 | 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 | a0001c0001t0005g0010 | 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 | a0002c0002t0001g0292 | 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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | a0001c0001t0012g0077a0001c0001t0023g0078 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0004g0206a0002c0002t0001g0317 | 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 | a0001c0001t0003g0006a0001c0001t0003g0007 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0003g0057 | 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 | a0001c0001t0004g0184 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0003g0015 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0003g0051 | 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 | a0001c0001t0006g0220a0001c0001t0011g0221 | 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0002c0002t0001g0305 | 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 | a0001c0001t0003g0011a0001c0001t0003g0063a0001c0001t0003g0064others(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 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(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 | 87 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(84): 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 | a0002c0002t0001g0273 | 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 | a0001c0001t0003g0047 | 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 | a0001c0001t0002g0108a0001c0001t0002g0114 | 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 | a0001c0001t0005g0013 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0002c0002t0001g0279 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0002g0129 | 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 | a0001c0001t0003g0049a0001c0001t0003g0050 | 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 | a0002c0002t0001g0251 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0003g0045 | 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0005g0055a0001c0001t0013g0072 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0002g0097 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0010g0122a0001c0001t0010g0123 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0008g0172 | 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 | a0002c0002t0001g0299a0002c0002t0001g0307 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0312 | 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 | 59 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(56): 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 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0002c0002t0001g0327 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0002c0002t0001g0327 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | ||||||
| chr11:28149903
|
C | T | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.270+36299C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28149903 | ||||||
| chr11:28150020
|
C | T | 2 | a0002c0002t0001g0298a0002c0002t0001g0303 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0004g0198a0001c0001t0007g0197 | 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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | a0001c0001t0002g0108 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | 157 | a0001c0001t0002g0139a0001c0001t0003g0001a0001c0001t0003g0005others(154): 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 | a0001c0001t0003g0057 | 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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0024g0202 | 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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0001c0001t0003g0008a0001c0001t0003g0009 | 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 | a0002c0002t0001g0312 | 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0002c0002t0001g0002a0002c0002t0001g0245a0002c0002t0001g0247others(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 | a0001c0001t0004g0206 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0002c0002t0001g0284 | 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 | a0001c0001t0002g0126 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.270+40787G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28154391 | ||||||
| chr11:28154633
|
G | A | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.270+41029G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28154633 | ||||||
| chr11:28154735
|
T | C | 6 | a0001c0001t0007g0169a0001c0001t0007g0240a0001c0001t0009g0165others(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 | ||||||
| chr11:28155538
|
C | T | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.270+41934C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28155538 | ||||||
| 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0004g0195 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0006g0176 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0016g0076 | 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 | a0001c0001t0006g0160a0001c0001t0006g0218a0001c0001t0006g0220others(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 | a0001c0001t0008g0179 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0010c0009t0003g0012 | 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 | a0001c0001t0003g0071 | 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 | a0001c0001t0003g0014 | 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 | a0001c0001t0003g0051 | 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 | a0001c0001t0003g0029 | 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 | a0002c0002t0001g0247a0002c0002t0001g0284a0002c0002t0001g0285others(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 | a0001c0001t0005g0013 | 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 | 54 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(51): 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0002c0002t0001g0254 | 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 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0003g0047others(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 | a0008c0011t0003g0217 | 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 | a0001c0001t0007g0169a0001c0001t0007g0240a0001c0001t0009g0165others(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 | ||||||
| chr11:28159750
|
A | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.270+46146A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28159750 | ||||||
| chr11:28160156
|
T | A | 80 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0005g0013 | 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 | a0001c0001t0005g0013 | 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 | a0004c0004t0001g0310 | 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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0292 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0001g0214a0002c0002t0001g0244a0002c0002t0001g0257others(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 | 81 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(78): 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 | 67 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(64): Show | 67 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(64): 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 | 158 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(155): 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 | a0002c0002t0001g0312 | 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 | a0002c0002t0001g0250 | 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 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0195others(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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0008c0011t0003g0217 | 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 | a0001c0008t0020g0194 | 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 | a0001c0001t0010g0122 | 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 | a0008c0011t0003g0217 | 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 | 90 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(87): 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 | a0002c0002t0001g0320a0002c0002t0001g0321 | 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 | a0001c0001t0003g0069 | 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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0004g0198a0001c0001t0005g0010a0001c0001t0007g0197 | 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 | a0002c0002t0001g0261 | 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 | a0001c0001t0006g0160a0001c0001t0006g0218a0001c0001t0006g0220others(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 | 78 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(75): Show | 78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): 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 | a0001c0001t0002g0149 | 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 | a0001c0001t0003g0059 | 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 | a0001c0001t0003g0059 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(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 | a0002c0002t0001g0250 | 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 | a0001c0001t0005g0066 | 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 | a0001c0001t0002g0118a0001c0001t0002g0138a0001c0001t0002g0140others(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 | a0001c0001t0002g0126 | 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 | a0001c0001t0004g0181a0001c0001t0004g0182 | 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | a0002c0002t0001g0312 | 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 | a0001c0001t0004g0171a0001c0001t0004g0191 | 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 | a0001c0001t0002g0124a0001c0001t0010g0122a0001c0001t0010g0123 | 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 | 88 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(85): 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 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(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 | a0001c0001t0003g0014 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | ||||||
| chr11:28166219
|
T | C | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.271-44843T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28166219 | ||||||
| chr11:28166530
|
C | T | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.271-44532C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28166530 | ||||||
| chr11:28166565
|
C | T | 1 | a0001c0001t0008g0172 | 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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090 | 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 | a0002c0002t0001g0327 | 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 | a0001c0001t0002g0126 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0003g0008a0001c0001t0003g0009 | 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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(156): 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 | a0001c0001t0004g0189 | 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 | a0002c0002t0001g0278 | 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 | 166 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0102others(163): 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0287 | 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 | a0001c0001t0004g0185a0001c0001t0004g0186a0001c0001t0004g0190others(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 | a0001c0001t0008g0177 | 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0002c0002t0001g0290 | 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 | a0002c0002t0001g0252a0002c0002t0001g0258a0002c0002t0001g0259others(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 | a0001c0001t0029g0120 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0001c0001t0012g0067a0001c0001t0012g0068a0001c0001t0012g0077others(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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0004g0200 | 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 | a0006c0006t0003g0017a0006c0006t0003g0019 | 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 | a0002c0002t0001g0252 | 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 | a0004c0004t0001g0283a0004c0004t0001g0293a0004c0004t0001g0294others(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 | a0002c0002t0001g0266 | 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 | 240 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(237): Show | 241 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(238): 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 | a0001c0001t0002g0105a0001c0001t0002g0106 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0002c0002t0001g0326 | 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 | a0001c0001t0003g0048 | 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 | a0008c0011t0003g0217 | 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 | 160 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(157): 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 | a0001c0001t0003g0029 | 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 | a0001c0001t0012g0077a0001c0001t0023g0078 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0002c0002t0001g0248 | 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 | 2 | a0001c0001t0002g0125a0001c0001t0002g0137 | 2 | HG02683.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.271-36357C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28174705 | ||||||
| chr11:28174710
|
G | A | 1 | a0001c0001t0003g0047 | 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 | a0001c0001t0003g0075 | 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 | a0001c0001t0002g0126 | 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 | 140 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(137): Show | 140 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(137): 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 | a0002c0002t0001g0254 | 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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(156): 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 | a0001c0001t0004g0211 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0006g0160a0001c0001t0006g0218a0001c0001t0006g0220others(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 | 40 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0118others(37): Show | 40 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(37): 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 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(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 | a0001c0001t0007g0174 | 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 | a0001c0001t0003g0022 | 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 | a0001c0001t0004g0204 | 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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0289a0002c0002t0001g0292a0002c0002t0001g0300others(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 | a0001c0001t0003g0005 | 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 | a0001c0001t0005g0058 | 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 | a0002c0002t0001g0243a0002c0002t0001g0248a0002c0002t0001g0249others(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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0142 | 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 | a0001c0001t0002g0148 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | 72 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(69): Show | 72 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(69): 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 | 92 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(89): 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 | a0002c0002t0001g0272 | 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 | a0001c0001t0002g0151 | 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 | 168 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(165): Show | 169 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(166): 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | 170 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(167): Show | 171 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(168): 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | ||||||
| chr11:28182058
|
C | T | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.271-29004C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28182058 | ||||||
| chr11:28182073
|
T | C | 3 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0005g0066 | 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 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0005g0066 | 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 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0005g0066 | 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 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0005g0066 | 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 | a0001c0001t0004g0185a0001c0001t0004g0186a0001c0001t0004g0190others(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 | a0008c0011t0003g0217 | 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 | a0001c0001t0003g0075 | 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 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0007g0169others(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 | a0002c0002t0001g0275 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | ||||||
| chr11:28183312
|
C | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.271-27750C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28183312 | ||||||
| chr11:28183326
|
G | T | 1 | a0002c0002t0001g0277 | 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 | a0001c0001t0005g0058 | 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 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(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 | a0001c0001t0002g0127 | 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 | 43 | a0002c0002t0001g0243a0002c0002t0001g0246a0002c0002t0001g0248others(40): 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 | a0002c0002t0001g0309 | 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 | a0004c0004t0001g0294 | 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 | a0002c0002t0001g0312 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0195others(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 | a0001c0001t0003g0074 | 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 | a0002c0002t0001g0295 | 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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0001c0001t0003g0029 | 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 | a0008c0011t0003g0217 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0002g0152 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.271-25031A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186031 | ||||||
| chr11:28186070
|
T | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.271-24992T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28186070 | ||||||
| chr11:28186085
|
G | A | 2 | a0001c0001t0002g0153a0001c0001t0002g0154 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260others(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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0002c0002t0001g0272 | 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 | a0001c0001t0006g0220a0001c0001t0011g0221 | 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 | a0001c0001t0003g0075 | 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 | a0002c0002t0001g0290 | 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 | a0001c0001t0004g0158a0001c0001t0004g0184a0001c0001t0007g0183 | 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 | a0001c0001t0003g0029a0001c0001t0004g0158a0001c0001t0004g0161others(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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | a0001c0001t0008g0179 | 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 | a0001c0001t0003g0050 | 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 | a0001c0001t0005g0013 | 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 | a0008c0011t0003g0217 | 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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | a0001c0001t0004g0171a0001c0001t0004g0181a0001c0001t0004g0182others(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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0138a0001c0001t0002g0140a0001c0001t0002g0142others(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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(156): 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0006g0218a0001c0001t0006g0222a0001c0001t0006g0225others(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 | a0001c0001t0003g0075 | 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 | a0001c0001t0008g0177 | 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 | a0001c0001t0006g0176 | 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 | a0009c0010t0002g0100 | 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 | a0001c0001t0002g0107 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0002c0002t0001g0275a0002c0002t0001g0276 | 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 | a0001c0001t0004g0170a0001c0001t0004g0173a0001c0001t0004g0175others(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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0005g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.271-17515C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28193547 | ||||||
| chr11:28193549
|
A | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.271-17513A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28193549 | ||||||
| chr11:28193581
|
G | A | 2 | a0001c0001t0012g0067a0001c0001t0012g0068 | 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 | a0003c0003t0002g0113 | 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 | a0002c0002t0001g0279 | 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 | a0001c0001t0002g0131 | 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 | a0001c0001t0002g0118a0001c0001t0003g0031a0001c0001t0004g0210others(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 | a0001c0001t0004g0170 | 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 |
32 | a0001c0001t0002g0108a0001c0001t0002g0121a0001c0001t0003g0074others(29): 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 | a0001c0001t0003g0001a0001c0001t0003g0007a0001c0001t0003g0008others(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 |
65 | a0001c0001t0002g0003a0001c0001t0002g0084a0001c0001t0002g0094others(62): Show | 65 | HG00423.hp1 HG00609.hp1 HG00733.hp2 others(62): 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 |
74 | a0001c0001t0002g0085a0001c0001t0002g0088a0001c0001t0002g0089others(71): 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 | a0001c0001t0002g0004a0001c0001t0002g0092a0001c0001t0002g0095others(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 | a0001c0001t0001g0214a0001c0001t0002g0097a0001c0001t0002g0101others(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 | a0001c0001t0003g0043a0001c0001t0003g0046a0001c0001t0003g0048 | 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 | a0001c0001t0002g0132a0001c0001t0003g0060 | 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 | a0002c0002t0001g0307 | 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 | a0002c0002t0001g0265a0002c0002t0001g0317 | 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 | a0001c0001t0011g0193 | 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 | a0001c0001t0003g0027 | 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 | a0001c0001t0006g0225 | 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0004g0185a0001c0001t0004g0196 | 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 | a0004c0004t0001g0293 | 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 | a0001c0001t0006g0223 | 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 | a0002c0002t0001g0256a0002c0002t0001g0265a0002c0002t0001g0275others(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 | a0002c0002t0001g0256a0002c0002t0001g0265a0002c0002t0001g0275others(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 | CCT | 315 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(312): Show | 317 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(314): Show |
intron_variant | MODIFIER | c.271-16851_271-1685 others(6): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 28194192 | |||||
| chr11:28194192
|
C | CCTCT | 8 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0075others(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 | a0002c0002t0001g0256a0002c0002t0001g0265a0002c0002t0001g0275others(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 | ||||||
| chr11:28194544
|
G | A | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.271-16518G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28194544 | ||||||
| chr11:28194841
|
C | G | 1 | a0002c0002t0001g0300 | 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 | a0009c0010t0002g0100 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0001t0003g0008a0001c0001t0003g0009 | 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 | a0002c0002t0001g0292 | 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 | a0001c0001t0002g0147a0001c0001t0002g0148 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(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 | 69 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(66): Show | 69 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.271-15126T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28195936 | ||||||
| chr11:28196281
|
C | T | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.271-14781C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28196281 | ||||||
| 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 | a0001c0001t0002g0138a0001c0001t0003g0054a0001c0001t0004g0190others(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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.271-14468T>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28196594 | ||||||
| chr11:28196700
|
C | T | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0001c0001t0004g0191 | 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 | a0004c0004t0001g0293 | 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 | a0001c0001t0003g0047 | 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 | a0001c0001t0003g0059 | 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 | a0001c0001t0004g0195a0001c0001t0008g0083a0001c0001t0008g0172others(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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0024others(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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0326 | 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.271-12103G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28198959 | ||||||
| chr11:28198982
|
A | AT | 162 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(159): Show | 163 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(160): 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(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 | a0002c0002t0001g0277a0002c0002t0001g0290a0002c0002t0001g0291 | 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 | a0002c0002t0001g0252 | 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 | a0001c0001t0002g0142 | 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 | a0007c0012t0003g0065 | 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 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0005g0066 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0007g0174 | 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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(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 | a0002c0002t0001g0320a0002c0002t0001g0321 | 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 | a0001c0001t0007g0174 | 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 | a0002c0002t0001g0265 | 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 | a0001c0001t0006g0226a0009c0010t0002g0100 | 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 | a0002c0002t0001g0250 | 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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(156): 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0018g0033 | 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0001g0214a0001c0001t0003g0059a0001c0001t0009g0167others(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 |
78 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(75): Show | 78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): 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(17): Show |
218 | a0001c0001t0002g0145a0001c0001t0002g0147a0001c0001t0002g0148others(215): Show | 219 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.271-9438_271-9437i others(26): 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 | a0001c0001t0003g0050a0001c0001t0004g0181a0001c0001t0004g0182others(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 | a0001c0001t0003g0005a0001c0001t0012g0068a0002c0002t0001g0244others(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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0097 | 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 | a0001c0001t0016g0076 | 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 | a0001c0001t0006g0226 | 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 | a0001c0001t0005g0056 | 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 | 4 | a0002c0002t0001g0322a0002c0002t0001g0323a0002c0002t0001g0324others(1): Show | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(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 | 87 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(84): 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 | a0001c0001t0002g0121 | 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 | a0001c0001t0005g0010 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.271-7199A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28203863 | ||||||
| chr11:28203912
|
G | A | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.271-7150G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28203912 | ||||||
| chr11:28204197
|
T | C | 1 | a0002c0002t0001g0287 | 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 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0210others(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 | a0002c0002t0001g0256 | 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 | a0002c0002t0001g0307 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | 81 | a0001c0001t0003g0074a0001c0001t0004g0170a0001c0001t0004g0196others(78): 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 | a0001c0001t0010g0216a0002c0002t0001g0249a0002c0002t0001g0270others(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 | 179 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(176): Show | 180 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(177): 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 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0273 | 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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0002c0002t0001g0253 | 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 | a0002c0002t0001g0278a0002c0002t0001g0279 | 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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0012g0068 | 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 | a0002c0002t0001g0295 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0003g0011 | 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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | a0009c0010t0002g0100 | 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0088others(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 | a0001c0001t0019g0192 | 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 | 158 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(155): 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 | a0002c0002t0001g0251 | 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 | a0001c0001t0004g0175 | 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0002c0002t0001g0291 | 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 | 43 | a0001c0001t0002g0085a0001c0001t0002g0115a0001c0001t0002g0116others(40): Show | 43 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4918G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28206144 | ||||||
| chr11:28206180
|
G | C | 240 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(237): Show | 241 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(238): 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 | a0001c0001t0003g0060a0001c0001t0003g0061 | 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 | a0001c0001t0004g0195 | 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 | a0002c0002t0001g0262a0002c0002t0001g0263a0002c0002t0001g0264 | 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0004c0004t0028g0282 | 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 | a0001c0001t0002g0085a0001c0001t0002g0115a0001c0001t0002g0151 | 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 | a0001c0001t0003g0016 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | 231 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(228): Show | 232 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(229): 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 | a0001c0001t0003g0014 | 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 | a0001c0001t0003g0014 | 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0001c0001t0009g0203 | 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 | a0001c0001t0008g0178 | 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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0275 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0002c0002t0001g0326 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0007g0231a0001c0001t0007g0236 | 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 | a0002c0002t0001g0298 | 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 | a0001c0001t0004g0232a0001c0001t0006g0230a0001c0001t0007g0231others(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 | a0003c0003t0002g0086 | 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 | a0001c0001t0001g0214a0001c0001t0003g0048a0001c0001t0005g0073 | 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | a0001c0001t0012g0077a0001c0001t0023g0078 | 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 | a0002c0002t0001g0277 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | ||||||
| chr11:28208999
|
G | C | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.271-2063G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | chr11 | 28208999 | ||||||
| chr11:28209007
|
G | T | 2 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0002c0002t0001g0278a0002c0002t0001g0280a0002c0002t0001g0281others(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 | a0001c0001t0003g0005 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(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 | a0002c0002t0001g0256 | 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 | a0002c0002t0027g0328 | 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 | a0002c0002t0001g0288 | 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 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0007c0012t0003g0065 | 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0002c0002t0001g0266 | 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 | a0001c0001t0003g0071 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0004g0196a0001c0001t0006g0187 | 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 | a0001c0001t0003g0048a0001c0001t0005g0073 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | a0001c0001t0012g0067a0001c0001t0012g0068a0001c0001t0012g0077others(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 | a0001c0001t0002g0085a0001c0001t0003g0011a0001c0001t0003g0059others(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 | a0001c0001t0002g0150a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0005g0058 | 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 | 78 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(75): Show | 78 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(75): 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 | a0001c0001t0002g0126 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0002c0002t0001g0270 | 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 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260others(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 | a0001c0001t0011g0193a0001c0001t0011g0241 | 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 | a0007c0012t0003g0065 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0327 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | a0002c0002t0001g0307 | 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 | a0001c0001t0007g0174 | 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 | a0002c0002t0001g0320a0002c0002t0001g0321 | 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 | |||||
| chr11:28216148
|
C | A | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.407+4950C>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216148 | ||||||
| chr11:28216323
|
C | A | 19 | a0002c0002t0001g0243a0002c0002t0001g0246a0002c0002t0001g0248others(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 | ||||||
| chr11:28216383
|
C | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.407+5185C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216383 | ||||||
| chr11:28216402
|
T | G | 4 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0210others(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 | ||||||
| chr11:28216441
|
T | C | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.407+5243T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28216441 | ||||||
| chr11:28216566
|
C | CT | 11 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(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 | a0001c0001t0003g0049a0001c0001t0003g0050 | 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 | 91 | a0001c0001t0003g0061a0001c0001t0004g0208a0002c0002t0001g0002others(88): 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 | a0001c0001t0002g0239a0003c0003t0002g0086a0003c0003t0002g0109others(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 | a0001c0001t0003g0030 | 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 | a0002c0002t0001g0270 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0024g0202 | 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 | a0001c0001t0003g0005 | 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 | a0002c0002t0001g0317 | 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 | a0002c0002t0027g0328 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0005g0058 | 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 | a0002c0002t0001g0264 | 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 | a0001c0001t0003g0075 | 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 | a0001c0001t0003g0075 | 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 | a0001c0001t0003g0075 | 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 | a0001c0001t0007g0174 | 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 | a0001c0001t0004g0171a0001c0001t0004g0191a0001c0001t0004g0198others(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 | a0004c0004t0001g0283a0004c0004t0001g0294a0004c0004t0001g0301 | 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 | a0002c0002t0001g0247a0002c0002t0001g0284a0002c0002t0001g0285others(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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0014t0021g0229a0002c0002t0001g0298 | 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0156 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0004c0004t0001g0310 | 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0003g0057 | 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 | a0002c0002t0001g0288 | 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 | a0001c0001t0012g0077a0001c0001t0023g0078 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | 43 | a0001c0001t0002g0085a0001c0001t0002g0115a0001c0001t0002g0116others(40): Show | 43 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(40): 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 | a0002c0002t0001g0256a0002c0002t0001g0265a0002c0002t0001g0317 | 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 | a0002c0002t0001g0277a0002c0002t0001g0290a0002c0002t0001g0291 | 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 | a0001c0001t0003g0031 | 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 | a0001c0001t0009g0203 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0012g0067a0001c0001t0012g0068 | 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 | a0001c0001t0006g0223a0001c0001t0006g0224a0001c0001t0006g0227 | 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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(156): 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0006g0223a0001c0001t0006g0224a0001c0001t0006g0227 | 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 | 84 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(81): 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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | a0001c0001t0003g0075a0001c0001t0005g0053 | 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 | a0004c0004t0001g0310 | 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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | a0002c0002t0001g0296 | 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 | a0001c0001t0002g0153a0001c0001t0002g0156 | 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 | a0002c0002t0001g0278a0002c0002t0001g0279a0002c0002t0001g0280others(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 | a0001c0001t0003g0001a0001c0001t0003g0011a0001c0001t0003g0014others(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 | a0001c0001t0005g0058 | 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 | a0002c0002t0001g0308 | 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 | 43 | a0002c0002t0001g0243a0002c0002t0001g0246a0002c0002t0001g0248others(40): 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0003g0057 | 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 | a0001c0001t0003g0051 | 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 | a0001c0001t0023g0078 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0002g0132 | 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 | a0003c0003t0002g0109a0003c0003t0002g0111a0003c0003t0002g0112 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0024others(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 | a0001c0001t0006g0225 | 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 | a0002c0002t0001g0278 | 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 | a0001c0001t0016g0076 | 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 | a0001c0001t0003g0048 | 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 | a0001c0001t0002g0130 | 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 | a0002c0002t0001g0299 | 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 | a0001c0001t0003g0075a0001c0001t0005g0053 | 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 | a0001c0001t0004g0185a0001c0001t0004g0186a0001c0001t0004g0190others(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 | a0001c0001t0008g0180 | 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 | a0002c0002t0001g0271 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.407+15867C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28227065 | ||||||
| chr11:28227462
|
A | T | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.407+16264A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28227462 | ||||||
| chr11:28227839
|
C | A | 1 | a0001c0001t0004g0208 | 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 | a0001c0001t0003g0015a0001c0001t0003g0054a0001c0001t0005g0010 | 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | a0002c0002t0001g0312 | 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 | a0001c0001t0002g0099 | 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 | 80 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(77): 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 | a0001c0001t0003g0016a0001c0001t0003g0059a0001c0001t0003g0062 | 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 | a0005c0005t0014g0079a0005c0005t0014g0080a0005c0005t0025g0081 | 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 | a0001c0001t0005g0056 | 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 | a0001c0007t0003g0026 | 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 | a0002c0002t0001g0255 | 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 | 160 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(157): 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 | a0001c0001t0002g0101 | 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 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0195others(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 | a0001c0001t0004g0181a0001c0001t0004g0182 | 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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | a0002c0002t0001g0326 | 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 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0005g0066 | 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 | a0001c0008t0020g0194 | 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 | a0001c0001t0002g0129 | 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 | a0002c0002t0001g0274 | 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | a0001c0001t0003g0054a0001c0001t0005g0010 | 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 | a0001c0001t0003g0074 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0004g0181a0001c0001t0004g0182 | 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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0008t0020g0194 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0002c0002t0001g0251 | 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 | a0001c0001t0003g0015 | 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 | a0001c0001t0003g0051 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0004g0205 | 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 | a0002c0002t0001g0256 | 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 | a0001c0001t0013g0020 | 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 | a0002c0002t0001g0298 | 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 | 160 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(157): 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 | a0001c0001t0002g0132 | 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 | a0002c0002t0001g0250 | 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 | a0004c0004t0001g0293 | 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 | a0004c0004t0001g0293 | 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 | a0001c0001t0003g0071 | 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 | 240 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(237): Show | 241 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(238): 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 | a0001c0001t0006g0160a0001c0001t0006g0218a0001c0001t0006g0220others(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 | a0002c0002t0001g0257 | 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 | a0007c0012t0003g0065 | 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 | a0001c0001t0012g0067a0001c0001t0012g0068a0001c0001t0012g0077others(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 | a0002c0002t0001g0254 | 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 | a0001c0001t0012g0077a0001c0001t0023g0078 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | a0001c0001t0002g0147a0001c0001t0002g0148 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.407+24192C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235390 | ||||||
| chr11:28235400
|
A | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.407+24202A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28235400 | ||||||
| chr11:28235406
|
A | G | 1 | a0001c0008t0020g0194 | 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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | a0002c0002t0027g0328 | 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 | a0002c0002t0001g0274 | 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 | a0001c0001t0004g0204 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | a0001c0001t0006g0226 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0001c0001t0012g0077 | 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 | a0002c0002t0001g0295 | 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 | a0002c0002t0001g0311 | 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 | a0008c0011t0003g0217 | 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 | 240 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(237): Show | 241 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(238): 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 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0024others(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 | a0001c0001t0004g0190 | 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 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(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 | a0001c0001t0002g0142 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0012g0067a0001c0001t0012g0068a0001c0001t0012g0077others(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 | 240 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(237): Show | 241 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(238): 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 | a0002c0002t0001g0287 | 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 | a0002c0002t0001g0320a0002c0002t0001g0321 | 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 | a0002c0002t0001g0276 | 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 | a0001c0001t0003g0071 | 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 | a0008c0011t0003g0217 | 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 | a0005c0005t0014g0079a0005c0005t0014g0080a0005c0005t0025g0081 | 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 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.407+26727G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237925 | ||||||
| chr11:28237992
|
A | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.407+26794A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28237992 | ||||||
| chr11:28238027
|
C | G | 6 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(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 | a0001c0001t0004g0190a0001c0001t0005g0055a0001c0001t0013g0072 | 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 | a0002c0002t0001g0297a0002c0002t0001g0306 | 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0002c0002t0001g0311 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0001t0004g0198a0001c0001t0007g0197 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0007g0231a0001c0001t0007g0236 | 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 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0273 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0002c0002t0001g0253 | 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0001c0001t0004g0185a0001c0001t0004g0212 | 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 | a0002c0002t0001g0312 | 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 | a0001c0001t0004g0190 | 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 | a0001c0001t0003g0075a0001c0001t0005g0053 | 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 | a0002c0002t0001g0307 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0316 | 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 | a0002c0002t0001g0256 | 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0003g0048 | 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 | a0002c0002t0001g0279 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0002g0124 | 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 | a0002c0002t0001g0002a0002c0002t0001g0245a0002c0002t0001g0247others(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 | a0001c0001t0008g0180 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0001c0001t0004g0205 | 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 | a0001c0001t0005g0018 | 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 | 78 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(75): 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 | a0001c0001t0007g0174 | 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 | 240 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(237): Show | 241 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(238): 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 | a0001c0001t0004g0198a0001c0001t0007g0197a0002c0002t0001g0306 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0001g0214a0001c0001t0002g0084a0001c0001t0002g0088others(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 | a0002c0002t0001g0304 | 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 | a0002c0002t0001g0290 | 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 | a0002c0002t0001g0290 | 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 | a0002c0002t0001g0290 | 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 | a0002c0002t0001g0290 | 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 | a0002c0002t0001g0290 | 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 | a0001c0001t0002g0127 | 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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0287 | 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 | 85 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(82): 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 | a0002c0002t0001g0252 | 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 | a0002c0002t0001g0309 | 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 | a0001c0001t0012g0067a0001c0001t0012g0068a0001c0001t0012g0077others(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 | a0002c0002t0001g0258a0002c0002t0001g0260 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0024others(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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0012g0067a0001c0001t0012g0068a0001c0001t0012g0077others(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 | a0001c0001t0007g0174 | 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 | a0008c0011t0003g0217 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0003g0075a0001c0001t0005g0053a0001c0001t0005g0055others(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 | a0002c0002t0001g0327 | 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 | a0001c0001t0019g0192 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0008c0011t0003g0217 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0002c0002t0001g0002a0002c0002t0001g0245a0002c0002t0001g0247others(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 | a0001c0001t0003g0037a0001c0001t0003g0043 | 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 | 13 | a0001c0001t0003g0032a0001c0001t0003g0034a0001c0001t0003g0036others(10): 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0001t0002g0107 | 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260others(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 | 87 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(84): 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 | ||||||
| chr11:28250084
|
T | A | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.407+38886T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28250084 | ||||||
| chr11:28250099
|
T | C | 327 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(324): Show | 329 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(326): Show |
intron_variant | MODIFIER | c.407+38901T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28250099 | ||||||
| chr11:28250566
|
TA | T | 163 | a0001c0001t0002g0146a0001c0001t0003g0027a0001c0001t0004g0158others(160): 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 | 166 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(163): Show | 167 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.407+39369A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28250567 | ||||||
| chr11:28250568
|
A | T | 164 | a0001c0001t0002g0095a0001c0001t0002g0146a0001c0001t0003g0034others(161): 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 | 85 | a0001c0001t0006g0230a0001c0014t0021g0229a0002c0002t0001g0002others(82): 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 | a0002c0002t0001g0297 | 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 | a0009c0010t0002g0100 | 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 | a0001c0001t0003g0051 | 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 | a0001c0008t0020g0194 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0003g0029 | 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 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0195others(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 | a0002c0002t0001g0295a0002c0002t0001g0305 | 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 | a0001c0001t0003g0024 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0108a0001c0001t0002g0114 | 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 | a0001c0001t0008g0213 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(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 | 69 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(66): Show | 69 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(66): 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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | a0003c0003t0002g0109 | 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 | ||||||
| chr11:28253610
|
G | C | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.408-36596G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28253610 | ||||||
| chr11:28253665
|
C | A | 10 | a0002c0002t0001g0252a0002c0002t0001g0255a0002c0002t0001g0258others(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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0002g0108 | 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 | a0001c0001t0012g0077 | 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 | a0001c0001t0004g0189 | 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 | a0001c0001t0004g0171a0001c0001t0004g0191a0001c0001t0004g0198others(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 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0088others(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 | a0002c0002t0001g0309 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0005g0056 | 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 | a0002c0002t0001g0255 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | 75 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(72): Show | 75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): 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 | a0002c0002t0001g0317 | 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 | 162 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(159): 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 | a0003c0003t0002g0086 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0003g0040 | 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 | a0001c0001t0008g0179 | 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 | a0002c0002t0001g0263 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | 239 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(236): Show | 240 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(237): 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0001c0001t0008g0180 | 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 | a0001c0001t0004g0206 | 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 | a0001c0001t0003g0048a0001c0001t0005g0073 | 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 | 54 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(51): 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 | a0001c0001t0005g0013 | 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 | a0001c0001t0003g0006a0001c0001t0003g0007 | 2 | NA18612.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.408-30914A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28259292 | ||||||
| chr11:28259408
|
G | C | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.408-30798G>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28259408 | ||||||
| chr11:28259644
|
A | G | 1 | a0001c0001t0003g0070 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.408-30562A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28259644 | ||||||
| chr11:28259757
|
C | T | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.408-30449C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28259757 | ||||||
| chr11:28259779
|
T | C | 1 | a0001c0001t0003g0059 | 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 | a0002c0002t0001g0312 | 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 | a0001c0001t0004g0232a0001c0001t0006g0230a0001c0001t0007g0231others(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 | a0001c0001t0003g0045 | 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 | a0002c0002t0001g0295 | 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 | a0001c0001t0008g0179 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | a0001c0001t0004g0158a0001c0001t0004g0184a0001c0001t0007g0183 | 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 | a0001c0001t0003g0074 | 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 | a0001c0008t0020g0194 | 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 | a0002c0002t0001g0326 | 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 | a0002c0002t0001g0292a0002c0002t0001g0300a0002c0002t0001g0308 | 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 | a0002c0002t0001g0306 | 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 | a0002c0002t0001g0252 | 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 | a0001c0001t0004g0195 | 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 | a0001c0001t0013g0020 | 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 | a0002c0002t0001g0326 | 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 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119 | 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 | a0001c0001t0002g0137 | 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 | a0001c0001t0003g0005 | 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 | a0001c0001t0002g0102 | 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 | a0001c0001t0003g0061 | 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 | a0001c0001t0003g0016 | 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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0256 | 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 | a0001c0008t0020g0194 | 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 | a0001c0001t0003g0061 | 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 | a0001c0008t0020g0194 | 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 | a0001c0001t0004g0211a0001c0001t0022g0157 | 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 | a0001c0001t0006g0160a0001c0001t0006g0218a0001c0001t0006g0220others(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 | a0002c0002t0001g0304 | 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 | 4 | a0001c0001t0002g0125a0001c0001t0002g0137a0001c0001t0010g0215others(1): Show | 4 | HG02257.hp2 HG02683.hp2 HG03486.hp1 others(1): Show |
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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0003g0052 | 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 | a0002c0002t0001g0286 | 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 | a0002c0002t0001g0296 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0001c0001t0004g0171a0001c0001t0004g0191 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0002c0002t0001g0254 | 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 | a0001c0001t0005g0055a0001c0001t0013g0072 | 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 | a0004c0004t0001g0310 | 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 | a0001c0001t0010g0123 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0007g0174 | 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 | a0002c0002t0001g0312 | 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 | a0001c0001t0001g0214a0001c0001t0006g0187a0001c0001t0007g0183others(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 | 86 | a0001c0001t0002g0127a0001c0001t0002g0149a0001c0001t0003g0001others(83): 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 | a0001c0001t0003g0009a0001c0001t0003g0040a0001c0001t0003g0061others(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 | a0002c0002t0001g0311 | 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 | a0001c0001t0005g0056 | 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 | a0001c0001t0002g0003a0001c0001t0002g0004 | 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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(156): 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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0001c0001t0002g0003 | 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 | a0001c0001t0003g0062 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(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 | 43 | a0001c0001t0002g0085a0001c0001t0002g0115a0001c0001t0002g0116others(40): Show | 43 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(40): 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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0251 | 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 | a0001c0001t0007g0174 | 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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090 | 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 | a0001c0001t0001g0214a0001c0001t0004g0164 | 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 | 85 | a0001c0001t0001g0214a0001c0001t0002g0127a0001c0001t0002g0239others(82): 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 | 152 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(149): Show | 153 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(150): 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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0093others(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 | a0004c0004t0001g0310 | 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | 11 | a0001c0001t0002g0121a0001c0001t0002g0125a0001c0001t0002g0130others(8): Show | 11 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(8): 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 | a0002c0002t0001g0257 | 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 | a0001c0001t0005g0066 | 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0088others(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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0008c0011t0003g0217 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | 14 | a0001c0001t0003g0032a0001c0001t0003g0034a0001c0001t0003g0036others(11): 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 | 87 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(84): 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 | a0002c0002t0001g0277a0002c0002t0001g0290a0002c0002t0001g0291 | 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 | a0001c0001t0003g0048 | 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 | a0001c0001t0003g0054 | 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 | 240 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(237): Show | 241 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(238): 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 | a0002c0002t0001g0260 | 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 | a0002c0002t0001g0284 | 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 | a0001c0001t0003g0048 | 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 | a0001c0001t0003g0071 | 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 | 72 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(69): 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0004g0198a0001c0001t0007g0197 | 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 | a0001c0001t0004g0185a0001c0001t0004g0190a0001c0001t0004g0212 | 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 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0210others(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 | a0002c0002t0001g0316 | 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 | a0001c0001t0029g0120 | 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 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(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 | a0001c0001t0004g0171a0001c0001t0004g0191a0001c0001t0004g0198others(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 | ||||||
| chr11:28273224
|
T | C | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.408-16982T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28273224 | ||||||
| chr11:28273300
|
A | G | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | a0001c0001t0004g0186 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | ||||||
| chr11:28273635
|
T | A | 1 | a0001c0001t0002g0125 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.408-16571T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28273635 | ||||||
| chr11:28273981
|
G | C | 1 | a0001c0001t0017g0219 | 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 | a0002c0002t0001g0002a0002c0002t0001g0245a0002c0002t0001g0302others(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 | a0002c0002t0001g0250 | 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 | a0001c0001t0003g0045 | 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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(156): 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 | a0001c0001t0003g0015 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.408-15338delT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28274867 | ||||||
| chr11:28274900
|
C | T | 1 | a0001c0001t0003g0047 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | 159 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(156): 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 | a0008c0011t0003g0217 | 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 | a0010c0009t0003g0012 | 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 | a0003c0003t0002g0109a0003c0003t0002g0110a0003c0003t0002g0111others(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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0088others(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 | 164 | a0001c0001t0002g0108a0001c0001t0002g0114a0001c0001t0002g0138others(161): 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(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 | 10 | a0001c0001t0002g0121a0001c0001t0002g0125a0001c0001t0002g0130others(7): Show | 10 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(7): 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 | 78 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(75): 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 | a0004c0004t0001g0294 | 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 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0210others(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 | a0001c0001t0003g0062 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0024others(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 | a0002c0002t0001g0304 | 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 | a0001c0001t0005g0010 | 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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | a0002c0002t0001g0252 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0005g0058 | 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 | a0001c0001t0004g0170a0001c0001t0004g0173a0001c0001t0004g0175others(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 | a0001c0001t0003g0062 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0004g0196 | 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 | a0001c0001t0002g0126 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0004g0171a0001c0001t0004g0191a0001c0001t0004g0198others(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 | a0002c0002t0001g0265 | 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 | a0001c0001t0009g0165a0001c0001t0009g0166 | 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 | a0001c0001t0008g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.408-10938T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28279268 | ||||||
| chr11:28279410
|
A | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.408-10796A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28279410 | ||||||
| chr11:28279498
|
C | G | 6 | a0004c0004t0001g0283a0004c0004t0001g0293a0004c0004t0001g0294others(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 | a0001c0001t0002g0133a0001c0001t0002g0134 | 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 | a0001c0001t0009g0165a0001c0001t0009g0166 | 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 | a0001c0001t0004g0189 | 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 | 87 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(84): 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | 79 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 79 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.408-9985delC | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28280220 | ||||||
| chr11:28280457
|
A | G | 5 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(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 | 231 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(228): Show | 232 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(229): 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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | 160 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(157): 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 | 240 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(237): Show | 241 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(238): 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 | a0001c0001t0004g0158a0001c0001t0004g0184a0001c0001t0007g0183 | 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 | a0002c0002t0001g0289a0002c0002t0001g0292a0002c0002t0001g0300others(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 | a0002c0002t0001g0316 | 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 | a0002c0002t0001g0292a0002c0002t0001g0300 | 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 | a0001c0001t0004g0185a0001c0001t0004g0186a0001c0001t0004g0190others(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 | a0001c0001t0004g0199 | 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 | a0002c0002t0001g0263a0002c0002t0001g0264 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | a0001c0001t0002g0143 | 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 | a0001c0001t0016g0076 | 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 | a0001c0001t0003g0071 | 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 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0024others(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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0088others(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 | a0001c0001t0005g0056 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0292 | 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 | 91 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(88): 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 | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(78): Show | 81 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(78): 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 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(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 | a0002c0002t0001g0271 | 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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | 54 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(51): 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 | 69 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(66): Show | 69 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(66): 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 | a0001c0001t0008g0083a0001c0001t0008g0172a0001c0001t0008g0177others(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 | a0001c0001t0002g0139a0001c0001t0002g0144 | 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 | a0001c0001t0006g0218a0001c0001t0006g0220a0001c0001t0006g0222others(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 | a0002c0002t0001g0289a0002c0002t0001g0292a0002c0002t0001g0300others(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 | 77 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(74): 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 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(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 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0210others(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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0001c0001t0003g0074 | 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 | a0001c0001t0002g0107a0001c0001t0003g0057a0001c0001t0004g0171others(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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | a0001c0001t0003g0062a0001c0001t0004g0181a0001c0001t0004g0204others(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 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260others(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 | 50 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(47): 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 | a0002c0002t0001g0250a0002c0002t0001g0251a0002c0002t0001g0264others(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 | a0002c0002t0001g0303 | 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 | a0002c0002t0001g0279 | 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 | a0002c0002t0001g0270a0002c0002t0001g0272a0002c0002t0001g0329others(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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0088others(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 | 95 | a0001c0001t0001g0214a0001c0001t0002g0084a0001c0001t0002g0085others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(92): 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 | a0001c0001t0002g0108a0001c0001t0003g0045a0001c0001t0004g0195others(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 | a0001c0001t0002g0146a0001c0001t0002g0239a0001c0001t0004g0158others(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 | a0001c0001t0002g0147 | 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 | a0011c0013t0004g0209 | 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 | a0005c0005t0014g0079a0005c0005t0014g0080a0005c0005t0025g0081 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(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 | a0002c0002t0001g0262 | 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 | a0001c0001t0004g0188 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0004c0004t0001g0283 | 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 | 54 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(51): 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 | a0001c0001t0004g0185a0001c0001t0004g0186a0001c0001t0004g0190others(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 | a0002c0002t0001g0243a0002c0002t0001g0248a0002c0002t0001g0249others(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 | 86 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(83): 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 | a0002c0002t0001g0297 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.408-1228C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28288978 | ||||||
| chr11:28289018
|
G | A | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.408-1188G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 4/6 | chr11 | 28289018 | ||||||
| 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 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(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 | a0001c0001t0003g0014 | 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 | 153 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(150): 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 | a0001c0001t0002g0088a0001c0001t0002g0129a0001c0001t0002g0150others(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 | a0001c0001t0002g0149 | 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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0248 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | 68 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(65): 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 | a0002c0002t0001g0296 | 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0008g0179 | 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 | ||||||
| chr11:28292149
|
A | C | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.599+1752A>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28292149 | ||||||
| chr11:28292284
|
C | T | 2 | a0002c0002t0001g0281a0002c0002t0001g0315 | 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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | a0001c0001t0006g0160a0001c0001t0006g0218a0001c0001t0006g0220others(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 | a0008c0011t0003g0217 | 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 | a0002c0002t0001g0307 | 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 | a0002c0002t0001g0290 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0151a0002c0002t0001g0288 | 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 | a0002c0002t0027g0328 | 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 | a0001c0001t0003g0049a0001c0001t0003g0050 | 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 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029others(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 | a0008c0011t0003g0217 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0002c0002t0001g0266 | 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0001c0001t0002g0139a0001c0001t0002g0144 | 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 | a0001c0001t0003g0047 | 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 | 75 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(72): Show | 75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.600-1142A>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 5/6 | chr11 | 28295611 | ||||||
| chr11:28295978
|
C | T | 86 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(83): 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 | a0001c0001t0004g0189 | 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 | 75 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(72): Show | 75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): 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 | a0003c0003t0002g0109 | 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 | a0002c0002t0001g0292a0002c0002t0001g0300 | 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 | a0001c0001t0006g0160a0001c0001t0006g0218a0001c0001t0006g0220others(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 | a0001c0001t0003g0044 | 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 | a0002c0002t0001g0254 | 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 | a0001c0001t0007g0169a0001c0001t0007g0240a0001c0001t0009g0165others(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 | a0002c0002t0001g0302 | 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 | a0001c0001t0002g0105 | 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 | a0002c0002t0001g0284 | 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 | a0001c0001t0005g0018 | 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 | a0001c0001t0003g0062 | 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 | a0002c0002t0001g0320a0002c0002t0001g0321 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0297a0002c0002t0001g0306a0002c0002t0001g0309 | 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 | a0002c0002t0001g0316 | 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 | a0002c0002t0001g0275 | 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0009c0010t0002g0100 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0102 | 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 | a0002c0002t0001g0263a0002c0002t0001g0264 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | ||||||
| chr11:28299299
|
G | GT | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.778+2372dupT | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 28299299 | |||||
| chr11:28299468
|
A | C | 13 | a0001c0001t0002g0239a0003c0003t0002g0086a0003c0003t0002g0109others(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 | a0001c0001t0008g0083a0001c0001t0008g0172a0001c0001t0008g0177others(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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0002c0002t0001g0265 | 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 | a0001c0001t0004g0196 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0002g0133a0001c0001t0002g0134 | 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 | a0007c0012t0003g0065 | 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 | a0001c0001t0004g0158a0001c0001t0004g0161a0001c0001t0004g0162others(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 | 69 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(66): Show | 69 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(66): 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | a0001c0001t0004g0195 | 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | a0001c0001t0003g0074 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.778+4895G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301826 | ||||||
| chr11:28301840
|
A | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.778+4909A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28301840 | ||||||
| chr11:28301846
|
G | A | 4 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0210others(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 | a0002c0002t0027g0328 | 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 | a0001c0001t0029g0120 | 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 | a0001c0001t0002g0102 | 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0002c0002t0001g0303 | 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 | a0002c0002t0001g0295 | 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0002c0002t0001g0320a0002c0002t0001g0321 | 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 | 162 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(159): 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | a0004c0004t0001g0283a0004c0004t0001g0293a0004c0004t0001g0294others(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 | a0001c0001t0012g0067a0001c0001t0012g0068 | 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 | a0002c0002t0001g0271 | 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 | a0001c0001t0005g0056 | 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 | a0002c0002t0001g0295 | 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 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260 | 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 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260 | 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 | a0001c0001t0002g0136 | 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 | a0001c0001t0004g0206 | 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 | a0001c0001t0002g0101 | 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 | 90 | a0001c0001t0007g0197a0002c0002t0001g0002a0002c0002t0001g0243others(87): 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 | a0001c0001t0003g0047 | 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 | ||||||
| chr11:28308064
|
G | A | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.778+11133G>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28308064 | ||||||
| chr11:28308205
|
T | C | 3 | a0001c0001t0002g0124a0001c0001t0010g0122a0001c0001t0010g0123 | 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 | a0001c0001t0002g0106 | 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 | a0002c0002t0001g0252a0002c0002t0001g0258a0002c0002t0001g0259others(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 | a0007c0012t0003g0065 | 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 | a0002c0002t0001g0316 | 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 | a0001c0001t0005g0058 | 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 | 96 | a0001c0001t0002g0084a0001c0001t0002g0088a0001c0001t0002g0089others(93): Show | 96 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(93): 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 | a0001c0001t0002g0003a0001c0001t0002g0085a0001c0001t0002g0091others(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 | a0001c0001t0002g0004a0001c0001t0002g0092a0001c0001t0002g0098others(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 | a0001c0001t0002g0106a0001c0001t0004g0185a0001c0001t0004g0212others(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 | a0001c0001t0004g0196 | 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 | a0001c0001t0006g0230a0001c0014t0021g0229 | 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 | a0001c0001t0002g0131a0001c0001t0003g0031a0001c0001t0003g0069others(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 | a0001c0001t0003g0045a0010c0009t0003g0012 | 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 | a0001c0001t0013g0072 | 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 | a0002c0002t0001g0304 | 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 | a0001c0001t0003g0005a0001c0001t0003g0047 | 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 | a0001c0001t0005g0073 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0264 | 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 | 79 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(76): 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 | a0001c0001t0002g0085a0001c0001t0002g0151a0001c0001t0002g0239others(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 | 54 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(51): Show | 54 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(51): 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 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0117others(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 | 4 | a0002c0002t0001g0322a0002c0002t0001g0323a0002c0002t0001g0324others(1): Show | 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 | ||||||
| chr11:28310719
|
T | A | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.778+13788T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28310719 | ||||||
| chr11:28310803
|
A | G | 2 | a0002c0002t0001g0275a0002c0002t0001g0276 | 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 | a0002c0002t0001g0287 | 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 | a0001c0001t0003g0075a0001c0001t0004g0158a0001c0001t0004g0170others(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 | a0001c0001t0003g0044a0001c0001t0003g0046a0001c0001t0003g0059others(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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(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 | 25 | a0001c0001t0002g0084a0001c0001t0002g0096a0001c0001t0002g0099others(22): Show | 25 | HG00544.hp1 HG01069.hp1 HG01074.hp1 others(22): 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0091others(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 | a0001c0001t0010g0122a0001c0001t0010g0123 | 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 | a0001c0001t0006g0176 | 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 | a0008c0011t0003g0217 | 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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(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 | a0001c0001t0004g0198a0001c0001t0007g0197a0001c0001t0019g0192 | 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 | a0001c0001t0004g0171a0001c0001t0004g0181a0001c0001t0004g0182others(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 | a0001c0001t0004g0211 | 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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(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 | 37 | a0001c0001t0002g0084a0001c0001t0002g0088a0001c0001t0002g0089others(34): Show | 37 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(34): 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 | 72 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(69): Show | 72 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(69): 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 | a0002c0002t0001g0002a0002c0002t0001g0245a0002c0002t0001g0284others(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 | 202 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(199): 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 | 203 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(200): 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 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(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 | a0001c0001t0004g0185a0001c0001t0004g0189a0001c0001t0004g0199others(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 | a0001c0001t0004g0199a0001c0001t0004g0208a0001c0001t0004g0212others(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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0149 | 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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0149 | 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 | a0001c0001t0002g0136a0003c0003t0002g0086a0003c0003t0002g0111others(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 | a0001c0001t0011g0193a0001c0001t0011g0241 | 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 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0149 | 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 | 19 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0096others(16): Show | 19 | HG00544.hp1 HG01074.hp1 HG01081.hp2 others(16): 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 | a0001c0001t0002g0090a0001c0001t0002g0131a0001c0001t0003g0051others(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 | a0001c0001t0002g0239a0001c0001t0007g0174a0005c0005t0014g0079others(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 | a0001c0001t0007g0169a0001c0001t0009g0165a0001c0001t0009g0168 | 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 | a0001c0001t0002g0090a0001c0001t0002g0131a0001c0001t0003g0051others(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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0091others(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 | a0001c0001t0001g0214a0002c0002t0001g0247a0002c0002t0001g0271 | 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 | a0001c0001t0004g0189a0001c0001t0006g0218a0001c0001t0006g0222others(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 | a0002c0002t0001g0254a0002c0002t0001g0302a0002c0002t0001g0316 | 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 | 15 | a0002c0002t0001g0243a0002c0002t0001g0246a0002c0002t0001g0249others(12): 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 | a0001c0001t0005g0035 | 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 | a0001c0001t0003g0046a0001c0001t0003g0054a0001c0001t0005g0010others(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 | a0001c0001t0003g0044a0001c0001t0003g0048a0001c0001t0003g0049others(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 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0047 | 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 | a0001c0001t0005g0073 | 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 | a0001c0001t0003g0005a0001c0001t0004g0208a0001c0001t0004g0228others(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 | a0001c0001t0003g0045a0001c0001t0004g0212a0001c0001t0007g0183 | 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 | a0001c0001t0013g0020 | 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 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0024others(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 | a0001c0001t0003g0007a0001c0001t0003g0011a0001c0001t0003g0016others(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 | a0001c0001t0003g0006a0001c0001t0003g0061a0001c0001t0005g0021others(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 | a0001c0001t0003g0014a0001c0001t0005g0013 | 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 | a0001c0001t0003g0037a0001c0001t0003g0039a0001c0001t0003g0071others(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 | 92 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(89): Show | 92 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(89): 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 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0195others(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 | a0002c0002t0001g0276a0002c0002t0001g0291a0002c0002t0001g0298others(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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0220others(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 | a0001c0001t0004g0164a0001c0001t0004g0208a0001c0001t0004g0228others(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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0004g0189a0001c0001t0006g0218a0001c0001t0006g0222others(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 | a0001c0001t0006g0160a0001c0001t0006g0220a0001c0001t0006g0223others(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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | a0001c0001t0001g0214a0001c0001t0004g0195a0001c0001t0004g0232others(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 | a0001c0001t0006g0160a0001c0001t0006g0220a0001c0001t0006g0223others(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 | a0001c0001t0006g0218a0001c0001t0006g0222a0001c0001t0006g0225others(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 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0220others(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 | a0001c0001t0003g0057 | 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | 75 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(72): Show | 75 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(72): 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0003g0051 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0012g0077 | 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 | a0001c0001t0003g0041 | 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 | 89 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0244others(86): 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 | a0001c0001t0008g0178 | 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 | a0001c0001t0004g0164a0002c0002t0001g0265 | 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 | 85 | a0002c0002t0001g0002a0002c0002t0001g0243a0002c0002t0001g0245others(82): 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 | a0001c0001t0003g0014 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0003c0003t0002g0110 | 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 | a0002c0002t0001g0311 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0001c0001t0019g0192 | 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 | 90 | a0001c0001t0002g0115a0002c0002t0001g0002a0002c0002t0001g0243others(87): 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0001c0001t0005g0056 | 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 | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(73): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0001c0001t0004g0185 | 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 | a0001c0001t0003g0051 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0003g0014 | 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 | a0001c0001t0003g0062 | 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 | a0001c0001t0003g0054a0001c0001t0005g0010 | 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 | a0002c0002t0001g0264 | 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 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0195others(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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0004g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.779-14446G>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28315950 | ||||||
| chr11:28316147
|
C | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.779-14249C>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28316147 | ||||||
| chr11:28316397
|
T | G | 11 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050others(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 | a0001c0001t0003g0063 | 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 | a0001c0001t0004g0171a0001c0001t0004g0181a0001c0001t0004g0182others(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 | a0002c0002t0001g0307 | 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 | 89 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(86): 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 | a0001c0008t0020g0194 | 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 | a0001c0001t0003g0075a0001c0001t0005g0053a0001c0001t0005g0055others(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 | a0002c0002t0001g0295 | 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 | a0001c0001t0007g0169a0001c0001t0007g0240a0001c0001t0009g0165others(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 | a0001c0001t0009g0203a0001c0001t0024g0202 | 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 | a0002c0002t0001g0286 | 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 | a0001c0001t0003g0015 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.779-12217T>A | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28318179 | ||||||
| chr11:28318190
|
A | G | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.779-12206A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28318190 | ||||||
| chr11:28318365
|
T | A | 1 | a0001c0001t0004g0205 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0002c0002t0001g0249 | 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 | a0002c0002t0001g0288 | 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 | a0001c0001t0004g0207 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0003g0048 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | |||||
| chr11:28319014
|
T | C | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.779-11382T>C | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28319014 | ||||||
| chr11:28319455
|
G | GT | 7 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(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 | 318 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(315): Show | 320 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(317): 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 | a0001c0001t0011g0193a0001c0001t0011g0241a0001c0001t0011g0242 | 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 | a0001c0001t0002g0124a0001c0001t0010g0122a0001c0001t0010g0123 | 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 | a0001c0001t0003g0047 | 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | 103 | a0001c0001t0002g0115a0001c0001t0003g0006a0001c0001t0003g0007others(100): 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 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(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 | 56 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(53): Show | 56 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(53): 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 | a0001c0001t0004g0164a0001c0001t0006g0160a0001c0001t0006g0218others(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 | a0001c0001t0002g0124 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(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 | a0008c0011t0003g0217 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0003g0051 | 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 | a0004c0004t0001g0283 | 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 | a0002c0002t0001g0317 | 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 | 86 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(83): 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 | 68 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0084others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(65): 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 | a0002c0002t0001g0002a0002c0002t0001g0245 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0001c0001t0004g0196a0001c0001t0006g0187 | 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 | a0002c0002t0001g0329a0002c0002t0001g0330 | 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 | a0002c0002t0001g0277a0002c0002t0001g0290a0002c0002t0001g0291 | 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 | 80 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(77): 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 | 80 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(77): 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 | 80 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(77): 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 | a0001c0001t0008g0172 | 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 | a0001c0001t0010g0215a0001c0001t0010g0216 | 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 | a0002c0002t0001g0258 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | 161 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(158): 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 | ||||||
| chr11:28322765
|
C | T | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.779-7631C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28322765 | ||||||
| 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 | a0002c0002t0001g0256 | 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 | 92 | a0001c0001t0002g0115a0002c0002t0001g0002a0002c0002t0001g0243others(89): 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 | a0001c0001t0002g0136 | 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 | a0001c0001t0002g0136 | 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 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 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 | a0001c0001t0004g0171a0001c0001t0004g0191 | 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 | a0001c0001t0002g0124a0001c0001t0010g0122a0001c0001t0010g0123 | 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 | a0001c0001t0002g0003a0001c0001t0002g0004a0009c0010t0002g0100 | 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 | a0001c0001t0004g0208 | 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 | a0002c0002t0001g0244a0002c0002t0001g0312 | 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 | a0001c0001t0007g0174 | 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 | a0001c0001t0002g0126 | 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 | a0001c0001t0012g0077 | 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 | a0001c0001t0002g0140 | 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 | a0001c0001t0002g0136 | 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 | a0001c0001t0002g0149 | 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 | a0002c0002t0001g0313a0002c0002t0001g0314 | 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 | a0001c0001t0002g0145a0001c0001t0002g0147a0001c0001t0002g0148others(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 | a0001c0001t0003g0011 | 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(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 | a0001c0001t0009g0203 | 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 | a0007c0012t0003g0065 | 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 | a0001c0001t0004g0181a0001c0001t0004g0182 | 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 | 80 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(77): 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 | 79 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(76): 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 | a0001c0001t0004g0232a0001c0001t0006g0230a0001c0001t0007g0231others(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 | ||||||
| chr11:28327222
|
C | T | 329 | a0001c0001t0001g0214a0001c0001t0002g0003a0001c0001t0002g0004others(326): Show | 331 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.779-3174C>T | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28327222 | ||||||
| chr11:28327872
|
G | C | 1 | a0001c0001t0003g0049 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0171others(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 | a0001c0001t0002g0148 | 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 | a0008c0011t0003g0217 | 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 | 2 | a0001c0001t0002g0125a0001c0001t0002g0137 | 2 | HG02683.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.779-1824A>G | METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | 28328572 | ||||||
| chr11:28328666
|
A | G | 1 | a0002c0002t0001g0253 | 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 | a0001c0001t0007g0174 | 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 | a0001c0001t0003g0051 | 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 | a0003c0003t0002g0111a0003c0003t0002g0112 | 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 | 90 | a0001c0001t0002g0115a0002c0002t0001g0002a0002c0002t0001g0243others(87): 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 | a0001c0001t0008g0178 | 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 | a0001c0001t0004g0158a0001c0001t0004g0170a0001c0001t0004g0173others(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 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0007g0169others(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 |