Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23041 |
|---|---|
| ensemblid | ENSG00000061987.16 |
| hgncid | 29177 |
| symbol | MON2 |
| name | MON2 homolog, regulator of endosome-to-Golgi trafficking |
| refseq_nuc | NM_015026.3 |
| refseq_prot | NP_055841.2 |
| ensembl_nuc | ENST00000393630.8 |
| ensembl_prot | ENSP00000377250.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 62466826 |
| end | 62600476 |
| strand | + |
| ver | v1.2 |
| region | chr12:62466826-62600476 |
| region5000 | chr12:62461826-62605476 |
| regionname0 | MON2_chr12_62466826_62600476 |
| regionname5000 | MON2_chr12_62461826_62605476 |
| 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 | 1/1 | 1717 | 201 | 59 | 44 | 72 | 5 | 19 | 57 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002 | 0/0 | 1717 | 118 | 28 | 13 | 57 | 6 | 14 | 45 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0003 | 0/0 | 1717 | 33 | 2 | 8 | 18 | 3 | 2 | 16 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0004 | 0/0 | 1717 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0005 | 0/0 | 1717 | 4 | 1 | 0 | 3 | 0 | 0 | 3 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0006 | 0/0 | 1717 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0007 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0008 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0009 | 0/0 | 1717 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0010 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0011 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0012 | 0/0 | 1717 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| 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 | 0/0 | 5154 | 117 | 28 | 13 | 57 | 6 | 13 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0002 | 1/0 | 5154 | 78 | 19 | 19 | 28 | 3 | 8 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0003 | 0/1 | 5154 | 69 | 11 | 9 | 41 | 1 | 6 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0004 | 0/0 | 5154 | 33 | 2 | 8 | 18 | 3 | 2 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0005 | 0/0 | 5154 | 24 | 2 | 13 | 3 | 1 | 5 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0006 | 0/0 | 5154 | 24 | 23 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0007 | 0/0 | 5154 | 4 | 0 | 0 | 4 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0008 | 0/0 | 5154 | 4 | 1 | 0 | 3 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0009 | 0/0 | 5154 | 2 | 2 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0010 | 0/0 | 5154 | 2 | 0 | 0 | 0 | 2 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0011 | 0/0 | 5154 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0012 | 0/0 | 5154 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0013 | 0/0 | 5154 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0014 | 0/0 | 5154 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0015 | 0/0 | 5154 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0016 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0017 | 0/0 | 5154 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0018 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0019 | 0/0 | 5154 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0020 | 0/0 | 5154 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| c0021 | 0/0 | 5154 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| 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 | 8109 | 84 | 25 | 9 | 41 | 4 | 5 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0002 | 0/0 | 8110 | 65 | 5 | 15 | 37 | 3 | 5 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0003 | 0/0 | 8110 | 38 | 15 | 11 | 7 | 0 | 5 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0004 | 0/0 | 8110 | 31 | 1 | 8 | 17 | 3 | 2 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0005 | 0/1 | 8110 | 30 | 8 | 3 | 12 | 1 | 5 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0006 | 0/0 | 8109 | 21 | 0 | 2 | 17 | 0 | 2 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0007 | 0/0 | 8109 | 12 | 11 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0008 | 0/0 | 8110 | 11 | 0 | 0 | 11 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0009 | 0/0 | 8109 | 5 | 0 | 2 | 0 | 0 | 3 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0010 | 0/0 | 8110 | 5 | 5 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0011 | 1/0 | 8110 | 5 | 0 | 0 | 3 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0012 | 0/0 | 8110 | 4 | 2 | 0 | 1 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0013 | 0/0 | 8110 | 4 | 1 | 3 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0014 | 0/0 | 8110 | 4 | 1 | 1 | 0 | 2 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0015 | 0/0 | 8111 | 4 | 0 | 0 | 3 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0016 | 0/0 | 8110 | 3 | 0 | 3 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0017 | 0/0 | 8110 | 3 | 2 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0018 | 0/0 | 8109 | 2 | 0 | 1 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0019 | 0/0 | 8110 | 2 | 2 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0020 | 0/0 | 8110 | 2 | 0 | 2 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0021 | 0/0 | 8110 | 2 | 0 | 2 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0022 | 0/0 | 8110 | 2 | 2 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0023 | 0/0 | 8111 | 2 | 0 | 0 | 2 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0024 | 0/0 | 8109 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0025 | 0/0 | 8110 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0026 | 0/0 | 8110 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0027 | 0/0 | 8109 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0028 | 0/0 | 8109 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0029 | 0/0 | 8109 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0030 | 0/0 | 8109 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0031 | 0/0 | 8110 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0032 | 0/0 | 8109 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0033 | 0/0 | 8109 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0034 | 0/0 | 8109 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0035 | 0/0 | 8110 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0036 | 0/0 | 8110 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0037 | 0/0 | 8110 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0038 | 0/0 | 8110 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0039 | 0/0 | 8110 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0040 | 0/0 | 8110 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0041 | 0/0 | 8110 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0042 | 0/0 | 8110 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0043 | 0/0 | 8110 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0044 | 0/0 | 8110 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0045 | 0/0 | 8110 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0046 | 0/0 | 8110 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0047 | 0/0 | 8110 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0048 | 0/0 | 8110 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0049 | 0/0 | 8111 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| t0050 | 0/0 | 8110 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| 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 | 2 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0313 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 5154 | 78 | 19 | 19 | 28 | 3 | 8 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003 | 0/1 | 5154 | 69 | 11 | 9 | 41 | 1 | 6 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0005 | 0/0 | 5154 | 24 | 2 | 13 | 3 | 1 | 5 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0006 | 0/0 | 5154 | 24 | 23 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0009 | 0/0 | 5154 | 2 | 2 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0016 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0017 | 0/0 | 5154 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0018 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0020 | 0/0 | 5154 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001 | 0/0 | 5154 | 117 | 28 | 13 | 57 | 6 | 13 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0015 | 0/0 | 5154 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0003c0004 | 0/0 | 5154 | 33 | 2 | 8 | 18 | 3 | 2 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0004c0007 | 0/0 | 5154 | 4 | 0 | 0 | 4 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0005c0008 | 0/0 | 5154 | 4 | 1 | 0 | 3 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0006c0010 | 0/0 | 5154 | 2 | 0 | 0 | 0 | 2 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0007c0021 | 0/0 | 5154 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0008c0011 | 0/0 | 5154 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0009c0019 | 0/0 | 5154 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0010c0012 | 0/0 | 5154 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0011c0013 | 0/0 | 5154 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0012c0014 | 0/0 | 5154 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 0/0 | 13263 | 40 | 3 | 11 | 20 | 1 | 5 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0003 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0005 | 0/0 | 13263 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0010 | 0/0 | 13263 | 5 | 5 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0011 | 1/0 | 13263 | 5 | 0 | 0 | 3 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0013 | 0/0 | 13263 | 4 | 1 | 3 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0014 | 0/0 | 13263 | 4 | 1 | 1 | 0 | 2 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0015 | 0/0 | 13264 | 4 | 0 | 0 | 3 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0017 | 0/0 | 13263 | 3 | 2 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0020 | 0/0 | 13263 | 2 | 0 | 2 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0022 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0026 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0031 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0035 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0037 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0039 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0045 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0047 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0002t0048 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003t0002 | 0/0 | 13263 | 15 | 0 | 3 | 12 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003t0003 | 0/0 | 13263 | 8 | 3 | 1 | 4 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003t0005 | 0/1 | 13263 | 28 | 8 | 2 | 11 | 1 | 5 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003t0008 | 0/0 | 13263 | 11 | 0 | 0 | 11 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003t0021 | 0/0 | 13263 | 2 | 0 | 2 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003t0023 | 0/0 | 13264 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003t0036 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003t0041 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003t0049 | 0/0 | 13264 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0003t0050 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0005t0003 | 0/0 | 13263 | 19 | 2 | 10 | 3 | 0 | 4 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0005t0016 | 0/0 | 13263 | 3 | 0 | 3 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0005t0040 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0005t0043 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0006t0003 | 0/0 | 13263 | 9 | 9 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0006t0007 | 0/0 | 13262 | 12 | 11 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0006t0033 | 0/0 | 13262 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0006t0034 | 0/0 | 13262 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0006t0042 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0009t0019 | 0/0 | 13263 | 2 | 2 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0016t0032 | 0/0 | 13262 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0017t0002 | 0/0 | 13263 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0018t0002 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0001c0020t0038 | 0/0 | 13263 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001t0001 | 0/0 | 13262 | 82 | 25 | 9 | 39 | 4 | 5 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001t0006 | 0/0 | 13262 | 20 | 0 | 2 | 16 | 0 | 2 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001t0009 | 0/0 | 13262 | 4 | 0 | 1 | 0 | 0 | 3 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001t0012 | 0/0 | 13263 | 4 | 2 | 0 | 1 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001t0018 | 0/0 | 13262 | 2 | 0 | 1 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001t0025 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001t0027 | 0/0 | 13262 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001t0028 | 0/0 | 13262 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001t0029 | 0/0 | 13262 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0001t0030 | 0/0 | 13262 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0002c0015t0024 | 0/0 | 13262 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0003c0004t0004 | 0/0 | 13263 | 31 | 1 | 8 | 17 | 3 | 2 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0003c0004t0022 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0003c0004t0044 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0004c0007t0002 | 0/0 | 13263 | 3 | 0 | 0 | 3 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0004c0007t0046 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0005c0008t0002 | 0/0 | 13263 | 3 | 1 | 0 | 2 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0005c0008t0023 | 0/0 | 13264 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0006c0010t0002 | 0/0 | 13263 | 2 | 0 | 0 | 0 | 2 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0007c0021t0001 | 0/0 | 13262 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0008c0011t0005 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0009c0019t0003 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0010c0012t0001 | 0/0 | 13262 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0011c0013t0006 | 0/0 | 13262 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| a0012c0014t0009 | 0/0 | 13262 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | copy fasta | chr12 | 62461826 | 62605476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0005g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0011g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0011g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0011g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0011g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0011g0313 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0013g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0013g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0013g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0013g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0014g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0014g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0014g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0014g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0015g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0015g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0015g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0015g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0017g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0017g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0017g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0020g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0020g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0022g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0026g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0031g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0035g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0037g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0039g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0045g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0047g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0048g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0021g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0023g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0036g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0041g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0049g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0050g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0016g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0016g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0016g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0040g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0043g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0033g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0034g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0042g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0009t0019g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0009t0019g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0016t0032g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0017t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0018t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0020t0038g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0009g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0009g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0009g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0009g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0012g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0012g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0012g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0018g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0018g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0025g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0027g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0028g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0029g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0030g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0015t0024g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0022g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0044g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0004c0007t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0004c0007t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0004c0007t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0004c0007t0046g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0005c0008t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0005c0008t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0005c0008t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0005c0008t0023g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0006c0010t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0006c0010t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0007c0021t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0008c0011t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0009c0019t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0010c0012t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0011c0013t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0012c0014t0009g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0153 | EUR | GBR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00099 | hp2 | a0001 | c0002 | t0014 | g0286 | EUR | GBR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00140 | hp1 | a0001 | c0003 | t0005 | g0064 | EUR | GBR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00140 | hp2 | a0002 | c0001 | t0018 | g0174 | EUR | GBR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00280 | hp1 | a0003 | c0004 | t0004 | g0292 | EUR | FIN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00280 | hp2 | a0002 | c0001 | t0001 | g0155 | EUR | FIN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0177 | EUR | FIN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00323 | hp2 | a0003 | c0004 | t0004 | g0281 | EUR | FIN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0233 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0323 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00438 | hp1 | a0001 | c0002 | t0048 | g0320 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00438 | hp2 | a0002 | c0001 | t0006 | g0214 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0088 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0250 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0249 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00597 | hp2 | a0001 | c0003 | t0005 | g0101 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00621 | hp1 | a0001 | c0003 | t0005 | g0087 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00639 | hp1 | a0003 | c0004 | t0004 | g0365 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00639 | hp2 | a0001 | c0003 | t0005 | g0080 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00642 | hp1 | a0012 | c0014 | t0009 | g0218 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0347 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0167 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00673 | hp2 | a0003 | c0004 | t0004 | g0260 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00733 | hp1 | a0002 | c0001 | t0009 | g0194 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00733 | hp2 | a0003 | c0004 | t0004 | g0290 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00735 | hp1 | a0001 | c0017 | t0002 | g0344 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00735 | hp2 | a0001 | c0005 | t0016 | g0117 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0166 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00738 | hp2 | a0001 | c0005 | t0003 | g0124 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0207 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00741 | hp2 | a0001 | c0003 | t0005 | g0098 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01069 | hp1 | a0001 | c0003 | t0021 | g0001 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01069 | hp2 | a0003 | c0004 | t0004 | g0282 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01070 | hp1 | a0001 | c0002 | t0020 | g0285 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01070 | hp2 | a0003 | c0004 | t0004 | g0291 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01071 | hp1 | a0001 | c0003 | t0021 | g0001 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01071 | hp2 | a0001 | c0002 | t0020 | g0289 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01074 | hp1 | a0001 | c0002 | t0013 | g0298 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01074 | hp2 | a0003 | c0004 | t0004 | g0283 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01081 | hp1 | a0001 | c0005 | t0003 | g0113 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01081 | hp2 | a0002 | c0001 | t0001 | g0144 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01099 | hp1 | a0001 | c0006 | t0007 | g0015 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0310 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01106 | hp1 | a0001 | c0005 | t0016 | g0116 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0179 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01109 | hp1 | a0001 | c0005 | t0003 | g0134 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01109 | hp2 | a0001 | c0002 | t0017 | g0033 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01167 | hp1 | a0003 | c0004 | t0004 | g0258 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01167 | hp2 | a0001 | c0020 | t0038 | g0312 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0159 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01168 | hp2 | a0001 | c0005 | t0003 | g0111 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01169 | hp1 | a0001 | c0005 | t0003 | g0112 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01169 | hp2 | a0003 | c0004 | t0004 | g0259 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01192 | hp1 | a0001 | c0005 | t0003 | g0126 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0084 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01255 | hp1 | a0001 | c0005 | t0003 | g0122 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0363 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01256 | hp1 | a0001 | c0002 | t0013 | g0303 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01256 | hp2 | a0001 | c0005 | t0003 | g0129 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0171 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0346 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01258 | hp1 | a0001 | c0005 | t0003 | g0128 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0349 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01261 | hp1 | a0001 | c0005 | t0016 | g0118 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01261 | hp2 | a0002 | c0001 | t0006 | g0198 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01346 | hp1 | a0001 | c0005 | t0003 | g0125 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01346 | hp2 | a0002 | c0001 | t0018 | g0248 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0348 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01361 | hp2 | a0001 | c0003 | t0003 | g0035 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0071 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0343 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01516 | hp1 | a0002 | c0001 | t0028 | g0181 | EUR | IBS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01516 | hp2 | a0006 | c0010 | t0002 | g0350 | EUR | IBS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01517 | hp1 | a0006 | c0010 | t0002 | g0336 | EUR | IBS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0209 | EUR | IBS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01884 | hp1 | a0003 | c0004 | t0022 | g0296 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01884 | hp2 | a0002 | c0001 | t0001 | g0234 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01891 | hp1 | a0002 | c0001 | t0001 | g0247 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01891 | hp2 | a0001 | c0006 | t0007 | g0011 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01928 | hp1 | a0002 | c0001 | t0006 | g0189 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0345 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0222 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0358 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0221 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01975 | hp2 | a0001 | c0003 | t0002 | g0056 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02004 | hp1 | a0001 | c0002 | t0013 | g0299 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0223 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02015 | hp1 | a0002 | c0001 | t0006 | g0185 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0317 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0318 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0162 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0141 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02055 | hp2 | a0001 | c0006 | t0003 | g0109 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02071 | hp1 | a0002 | c0001 | t0006 | g0201 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0356 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02074 | hp1 | a0001 | c0003 | t0005 | g0097 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02074 | hp2 | a0002 | c0001 | t0006 | g0206 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02083 | hp1 | a0002 | c0001 | t0006 | g0188 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02083 | hp2 | a0001 | c0003 | t0005 | g0086 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02135 | hp1 | a0002 | c0001 | t0001 | g0176 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0352 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02145 | hp1 | a0002 | c0001 | t0012 | g0140 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02145 | hp2 | a0001 | c0002 | t0010 | g0031 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02148 | hp1 | a0001 | c0002 | t0005 | g0362 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02148 | hp2 | a0001 | c0003 | t0049 | g0096 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02165 | hp1 | a0001 | c0003 | t0050 | g0077 | EAS | CDX | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02165 | hp2 | a0004 | c0007 | t0002 | g0327 | EAS | CDX | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0036 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02257 | hp2 | a0001 | c0006 | t0003 | g0105 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02258 | hp1 | a0003 | c0004 | t0004 | g0284 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02258 | hp2 | a0001 | c0003 | t0005 | g0039 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02280 | hp1 | a0001 | c0002 | t0047 | g0308 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02280 | hp2 | a0001 | c0002 | t0035 | g0025 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0354 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02293 | hp2 | a0003 | c0004 | t0004 | g0297 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02300 | hp1 | a0001 | c0002 | t0014 | g0280 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0357 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02523 | hp1 | a0003 | c0004 | t0004 | g0263 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02523 | hp2 | a0001 | c0003 | t0036 | g0048 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02572 | hp1 | a0001 | c0006 | t0007 | g0010 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02572 | hp2 | a0001 | c0018 | t0002 | g0306 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02602 | hp1 | a0002 | c0001 | t0001 | g0225 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02602 | hp2 | a0009 | c0019 | t0003 | g0133 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02615 | hp1 | a0002 | c0001 | t0001 | g0230 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0100 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0211 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02622 | hp2 | a0001 | c0005 | t0003 | g0119 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02630 | hp1 | a0002 | c0001 | t0001 | g0138 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02630 | hp2 | a0001 | c0002 | t0010 | g0027 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02647 | hp1 | a0001 | c0006 | t0007 | g0019 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02647 | hp2 | a0002 | c0001 | t0012 | g0244 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02717 | hp1 | a0001 | c0002 | t0039 | g0302 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02717 | hp2 | a0001 | c0006 | t0007 | g0021 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02723 | hp1 | a0001 | c0002 | t0022 | g0295 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02723 | hp2 | a0001 | c0003 | t0003 | g0099 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02735 | hp1 | a0001 | c0005 | t0003 | g0127 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02735 | hp2 | a0001 | c0002 | t0011 | g0255 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02809 | hp1 | a0001 | c0006 | t0007 | g0016 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02809 | hp2 | a0001 | c0009 | t0019 | g0104 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02886 | hp1 | a0002 | c0001 | t0001 | g0237 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02886 | hp2 | a0001 | c0003 | t0005 | g0046 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02895 | hp1 | a0002 | c0001 | t0001 | g0202 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02896 | hp1 | a0002 | c0001 | t0001 | g0003 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02896 | hp2 | a0001 | c0006 | t0007 | g0009 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02897 | hp1 | a0002 | c0001 | t0001 | g0003 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02922 | hp1 | a0002 | c0001 | t0001 | g0242 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02922 | hp2 | a0001 | c0006 | t0007 | g0018 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02970 | hp1 | a0001 | c0002 | t0017 | g0032 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02970 | hp2 | a0002 | c0001 | t0001 | g0243 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02976 | hp1 | a0001 | c0006 | t0003 | g0007 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02976 | hp2 | a0001 | c0006 | t0007 | g0014 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03017 | hp1 | a0001 | c0005 | t0003 | g0123 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03017 | hp2 | a0001 | c0003 | t0041 | g0053 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03098 | hp1 | a0001 | c0009 | t0019 | g0103 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03098 | hp2 | a0002 | c0001 | t0030 | g0139 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03130 | hp1 | a0001 | c0002 | t0017 | g0024 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03130 | hp2 | a0001 | c0006 | t0003 | g0108 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03139 | hp1 | a0002 | c0001 | t0001 | g0137 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03139 | hp2 | a0001 | c0006 | t0034 | g0020 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03195 | hp1 | a0001 | c0006 | t0042 | g0004 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03195 | hp2 | a0001 | c0006 | t0003 | g0107 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03209 | hp1 | a0001 | c0006 | t0003 | g0005 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03209 | hp2 | a0002 | c0001 | t0001 | g0146 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03225 | hp1 | a0001 | c0002 | t0031 | g0136 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03225 | hp2 | a0001 | c0016 | t0032 | g0252 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03239 | hp1 | a0003 | c0004 | t0004 | g0268 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03239 | hp2 | a0002 | c0001 | t0009 | g0193 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03453 | hp1 | a0001 | c0006 | t0033 | g0022 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03453 | hp2 | a0002 | c0001 | t0001 | g0228 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03486 | hp1 | a0001 | c0002 | t0026 | g0301 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03486 | hp2 | a0002 | c0001 | t0001 | g0236 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03490 | hp1 | a0001 | c0002 | t0037 | g0304 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03490 | hp2 | a0002 | c0001 | t0006 | g0191 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0325 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03491 | hp2 | a0002 | c0001 | t0001 | g0235 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0102 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03516 | hp2 | a0001 | c0002 | t0010 | g0028 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03579 | hp1 | a0001 | c0006 | t0007 | g0017 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0204 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03654 | hp1 | a0001 | c0003 | t0005 | g0066 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03654 | hp2 | a0002 | c0001 | t0029 | g0149 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03669 | hp1 | a0001 | c0005 | t0003 | g0120 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03669 | hp2 | a0002 | c0001 | t0001 | g0240 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03688 | hp1 | a0001 | c0003 | t0005 | g0081 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0165 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03704 | hp1 | a0001 | c0003 | t0005 | g0057 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0330 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03834 | hp1 | a0002 | c0015 | t0024 | g0184 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03834 | hp2 | a0001 | c0003 | t0005 | g0072 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03927 | hp1 | a0002 | c0001 | t0012 | g0232 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03927 | hp2 | a0001 | c0002 | t0015 | g0319 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03942 | hp1 | a0002 | c0001 | t0009 | g0210 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0254 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04115 | hp1 | a0002 | c0001 | t0006 | g0200 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0342 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0335 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04184 | hp2 | a0001 | c0005 | t0040 | g0135 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04199 | hp1 | a0001 | c0003 | t0005 | g0089 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04199 | hp2 | a0002 | c0001 | t0009 | g0192 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04228 | hp1 | a0002 | c0001 | t0025 | g0186 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04228 | hp2 | a0003 | c0004 | t0004 | g0293 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18522 | hp1 | a0002 | c0001 | t0001 | g0238 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18522 | hp2 | a0001 | c0006 | t0007 | g0012 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18612 | hp1 | a0001 | c0002 | t0045 | g0360 | EAS | CHB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0150 | EAS | CHB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18906 | hp1 | a0001 | c0006 | t0003 | g0006 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18906 | hp2 | a0001 | c0002 | t0010 | g0029 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18939 | hp1 | a0001 | c0002 | t0011 | g0307 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0160 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0359 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18940 | hp2 | a0002 | c0001 | t0001 | g0147 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18941 | hp1 | a0001 | c0003 | t0005 | g0051 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18941 | hp2 | a0002 | c0001 | t0006 | g0215 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0226 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0054 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18943 | hp1 | a0002 | c0001 | t0027 | g0164 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18943 | hp2 | a0004 | c0007 | t0046 | g0326 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0338 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18944 | hp2 | a0003 | c0004 | t0004 | g0272 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18945 | hp1 | a0001 | c0003 | t0008 | g0059 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0322 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0180 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18946 | hp2 | a0001 | c0003 | t0005 | g0092 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18949 | hp1 | a0004 | c0007 | t0002 | g0361 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18949 | hp2 | a0011 | c0013 | t0006 | g0196 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0333 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0157 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18954 | hp1 | a0001 | c0003 | t0005 | g0070 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0142 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18956 | hp1 | a0001 | c0003 | t0023 | g0065 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18956 | hp2 | a0002 | c0001 | t0001 | g0154 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18957 | hp1 | a0001 | c0003 | t0002 | g0076 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0169 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18962 | hp1 | a0001 | c0003 | t0002 | g0067 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0110 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18963 | hp2 | a0001 | c0003 | t0008 | g0060 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18966 | hp1 | a0005 | c0008 | t0002 | g0340 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18966 | hp2 | a0002 | c0001 | t0006 | g0251 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18967 | hp1 | a0003 | c0004 | t0004 | g0279 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18967 | hp2 | a0001 | c0003 | t0005 | g0091 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0145 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0182 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18969 | hp2 | a0001 | c0005 | t0003 | g0131 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18971 | hp1 | a0002 | c0001 | t0006 | g0197 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0055 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18972 | hp2 | a0002 | c0001 | t0001 | g0163 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18973 | hp1 | a0001 | c0003 | t0005 | g0049 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18973 | hp2 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18975 | hp1 | a0003 | c0004 | t0004 | g0278 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18975 | hp2 | a0004 | c0007 | t0002 | g0328 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18977 | hp1 | a0002 | c0001 | t0001 | g0253 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18977 | hp2 | a0001 | c0005 | t0003 | g0115 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0227 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18983 | hp2 | a0003 | c0004 | t0004 | g0265 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18986 | hp1 | a0001 | c0003 | t0008 | g0090 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18986 | hp2 | a0003 | c0004 | t0004 | g0264 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18987 | hp1 | a0003 | c0004 | t0004 | g0277 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18987 | hp2 | a0001 | c0003 | t0002 | g0075 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0331 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18988 | hp2 | a0001 | c0003 | t0002 | g0095 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18990 | hp1 | a0001 | c0002 | t0015 | g0315 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18994 | hp1 | a0001 | c0002 | t0011 | g0257 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18994 | hp2 | a0001 | c0003 | t0008 | g0058 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18995 | hp1 | a0003 | c0004 | t0004 | g0273 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18995 | hp2 | a0001 | c0003 | t0008 | g0083 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18998 | hp1 | a0001 | c0003 | t0008 | g0073 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18998 | hp2 | a0002 | c0001 | t0006 | g0190 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19001 | hp1 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19001 | hp2 | a0001 | c0002 | t0015 | g0316 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19003 | hp1 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0161 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19004 | hp2 | a0001 | c0003 | t0003 | g0041 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0341 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0175 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0148 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19009 | hp1 | a0003 | c0004 | t0004 | g0274 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0246 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19010 | hp1 | a0001 | c0003 | t0002 | g0082 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19010 | hp2 | a0003 | c0004 | t0004 | g0270 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19011 | hp1 | a0001 | c0005 | t0003 | g0130 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19030 | hp1 | a0001 | c0006 | t0003 | g0008 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0208 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19043 | hp1 | a0002 | c0001 | t0001 | g0219 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19043 | hp2 | a0001 | c0002 | t0013 | g0300 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19054 | hp1 | a0001 | c0003 | t0003 | g0047 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0172 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19055 | hp1 | a0002 | c0001 | t0006 | g0199 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19056 | hp1 | a0002 | c0001 | t0001 | g0220 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19056 | hp2 | a0001 | c0003 | t0008 | g0061 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19057 | hp1 | a0002 | c0001 | t0006 | g0143 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19060 | hp1 | a0005 | c0008 | t0002 | g0334 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19060 | hp2 | a0002 | c0001 | t0006 | g0195 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19062 | hp1 | a0003 | c0004 | t0004 | g0267 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19064 | hp1 | a0008 | c0011 | t0005 | g0093 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19064 | hp2 | a0001 | c0002 | t0011 | g0309 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19065 | hp1 | a0001 | c0003 | t0005 | g0052 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19065 | hp2 | a0007 | c0021 | t0001 | g0337 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19066 | hp2 | a0001 | c0003 | t0005 | g0050 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19068 | hp1 | a0010 | c0012 | t0001 | g0152 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19068 | hp2 | a0003 | c0004 | t0004 | g0266 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0178 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19070 | hp2 | a0001 | c0003 | t0003 | g0042 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0168 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19074 | hp2 | a0001 | c0002 | t0015 | g0314 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19075 | hp1 | a0003 | c0004 | t0004 | g0271 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19075 | hp2 | a0002 | c0001 | t0006 | g0183 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19077 | hp1 | a0003 | c0004 | t0004 | g0276 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19077 | hp2 | a0001 | c0003 | t0008 | g0074 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19080 | hp1 | a0002 | c0001 | t0006 | g0213 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19080 | hp2 | a0001 | c0003 | t0008 | g0063 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19081 | hp1 | a0001 | c0003 | t0003 | g0043 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19082 | hp1 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19082 | hp2 | a0003 | c0004 | t0004 | g0261 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19083 | hp1 | a0003 | c0004 | t0004 | g0275 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0170 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19085 | hp1 | a0001 | c0003 | t0002 | g0068 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19085 | hp2 | a0002 | c0001 | t0006 | g0187 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19086 | hp1 | a0001 | c0003 | t0008 | g0062 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19086 | hp2 | a0002 | c0001 | t0006 | g0216 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19087 | hp1 | a0005 | c0008 | t0023 | g0294 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19087 | hp2 | a0003 | c0004 | t0044 | g0262 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19088 | hp1 | a0001 | c0003 | t0002 | g0069 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19088 | hp2 | a0002 | c0001 | t0001 | g0231 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19090 | hp1 | a0001 | c0003 | t0002 | g0094 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0173 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0311 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19240 | hp2 | a0001 | c0003 | t0005 | g0040 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0224 | AFR | ASW | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20129 | hp2 | a0001 | c0003 | t0005 | g0037 | AFR | ASW | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0321 | EUR | TSI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20752 | hp2 | a0001 | c0005 | t0043 | g0132 | EUR | TSI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20805 | hp1 | a0003 | c0004 | t0004 | g0269 | EUR | TSI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20805 | hp2 | a0001 | c0002 | t0014 | g0288 | EUR | TSI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0241 | SAS | GIH | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20905 | hp2 | a0001 | c0005 | t0003 | g0121 | SAS | GIH | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02109 | hp1 | a0001 | c0003 | t0005 | g0045 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0203 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02486 | hp1 | a0002 | c0001 | t0001 | g0229 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02486 | hp2 | a0001 | c0006 | t0003 | g0106 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02559 | hp1 | a0001 | c0006 | t0007 | g0013 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02559 | hp2 | a0002 | c0001 | t0001 | g0212 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03471 | hp1 | a0002 | c0001 | t0001 | g0217 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03471 | hp2 | a0001 | c0003 | t0005 | g0038 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG06807 | hp1 | a0001 | c0003 | t0005 | g0034 | AFR | USA | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG06807 | hp2 | a0001 | c0002 | t0014 | g0287 | AFR | USA | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18955 | hp1 | a0002 | c0001 | t0012 | g0239 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18955 | hp2 | a0001 | c0003 | t0008 | g0085 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20300 | hp1 | a0001 | c0005 | t0003 | g0114 | AFR | USA | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20300 | hp2 | a0005 | c0008 | t0002 | g0364 | AFR | USA | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA21309 | hp1 | a0001 | c0003 | t0005 | g0044 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA21309 | hp2 | a0001 | c0002 | t0010 | g0023 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0005 | g0078 | REF | REF | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0011 | g0313 | REF | REF | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:62467263
|
G | A | 1 | a0004 | 4 | HG02165.hp2 NA18943.hp2 NA18949.hp1 others(1): Show |
missense_variant | MODERATE | c.56G>A | p.Ser19Asn | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/35 | 438/13263 | 56/5154 | 19/1717 | chr12 | 62467263 | ||
| chr12:62534853
|
G | A | 4 | a0002a0010a0011others(1): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
missense_variant | MODERATE | c.1642G>A | p.Ala548Thr | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/35 | 2024/13263 | 1642/5154 | 548/1717 | chr12 | 62534853 | ||
| chr12:62535626
|
C | T | 1 | a0007 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.1817C>T | p.Thr606Ile | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/35 | 2199/13263 | 1817/5154 | 606/1717 | chr12 | 62535626 | ||
| chr12:62535709
|
T | C | 1 | a0010 | 1 | NA19068.hp1 | missense_variant&splice_region_variant | MODERATE | c.1900T>C | p.Ser634Pro | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/35 | 2282/13263 | 1900/5154 | 634/1717 | chr12 | 62535709 | ||
| chr12:62543155
|
G | C | 1 | a0011 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.2423G>C | p.Arg808Pro | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/35 | 2805/13263 | 2423/5154 | 808/1717 | chr12 | 62543155 | ||
| chr12:62547024
|
G | T | 1 | a0009 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2705G>T | p.Gly902Val | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/35 | 3087/13263 | 2705/5154 | 902/1717 | chr12 | 62547024 | ||
| chr12:62552959
|
A | C | 1 | a0005 | 4 | NA18966.hp1 NA19060.hp1 NA19087.hp1 others(1): Show |
missense_variant | MODERATE | c.2995A>C | p.Lys999Gln | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/35 | 3377/13263 | 2995/5154 | 999/1717 | chr12 | 62552959 | ||
| chr12:62556022
|
G | A | 1 | a0006 | 2 | HG01516.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.3239G>A | p.Arg1080Gln | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/35 | 3621/13263 | 3239/5154 | 1080/1717 | chr12 | 62556022 | ||
| chr12:62565357
|
A | G | 1 | a0003 | 33 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(30): Show |
missense_variant | MODERATE | c.4153A>G | p.Ile1385Val | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/35 | 4535/13263 | 4153/5154 | 1385/1717 | chr12 | 62565357 | ||
| chr12:62571501
|
G | A | 1 | a0008 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.4433G>A | p.Arg1478Gln | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/35 | 4815/13263 | 4433/5154 | 1478/1717 | chr12 | 62571501 | ||
| chr12:62585472
|
A | C | 1 | a0012 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.4878A>C | p.Glu1626Asp | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/35 | 5260/13263 | 4878/5154 | 1626/1717 | chr12 | 62585472 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:62500856
|
T | A | 2 | a0001c0003a0008c0011 | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
synonymous_variant | LOW | c.639T>A | p.Ala213Ala | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 6/35 | 1021/13263 | 639/5154 | 213/1717 | chr12 | 62500856 | ||
| chr12:62532618
|
G | A | 7 | a0001c0009a0001c0016a0002c0001others(4): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
synonymous_variant | LOW | c.1581G>A | p.Ser527Ser | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/35 | 1963/13263 | 1581/5154 | 527/1717 | chr12 | 62532618 | ||
| chr12:62537158
|
C | T | 1 | a0001c0006 | 24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
synonymous_variant | LOW | c.1908C>T | p.Ser636Ser | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/35 | 2290/13263 | 1908/5154 | 636/1717 | chr12 | 62537158 | ||
| chr12:62537616
|
T | C | 1 | a0001c0017 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.2028T>C | p.Asn676Asn | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/35 | 2410/13263 | 2028/5154 | 676/1717 | chr12 | 62537616 | ||
| chr12:62537637
|
A | G | 1 | a0008c0011 | 1 | NA19064.hp1 | synonymous_variant | LOW | c.2049A>G | p.Leu683Leu | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/35 | 2431/13263 | 2049/5154 | 683/1717 | chr12 | 62537637 | ||
| chr12:62537661
|
G | T | 1 | a0001c0020 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.2073G>T | p.Gly691Gly | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/35 | 2455/13263 | 2073/5154 | 691/1717 | chr12 | 62537661 | ||
| chr12:62556101
|
C | T | 1 | a0001c0016 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.3318C>T | p.Thr1106Thr | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/35 | 3700/13263 | 3318/5154 | 1106/1717 | chr12 | 62556101 | ||
| chr12:62561035
|
T | C | 1 | a0001c0018 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.3954T>C | p.Phe1318Phe | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/35 | 4336/13263 | 3954/5154 | 1318/1717 | chr12 | 62561035 | ||
| chr12:62561053
|
C | T | 1 | a0002c0015 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.3972C>T | p.Thr1324Thr | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/35 | 4354/13263 | 3972/5154 | 1324/1717 | chr12 | 62561053 | ||
| chr12:62585436
|
G | A | 2 | a0001c0005a0009c0019 | 25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
synonymous_variant | LOW | c.4842G>A | p.Arg1614Arg | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/35 | 5224/13263 | 4842/5154 | 1614/1717 | chr12 | 62585436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:62466937
|
G | A | 6 | a0002c0001t0006a0002c0001t0009a0002c0001t0025others(3): Show | 28 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-271G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/35 | 271 | chr12 | 62466937 | |||||
| chr12:62466990
|
G | A | 1 | a0001c0002t0026 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-218G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/35 | 218 | chr12 | 62466990 | |||||
| chr12:62467014
|
G | A | 1 | a0002c0001t0018 | 2 | HG00140.hp2 HG01346.hp2 |
5_prime_UTR_variant | MODIFIER | c.-194G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/35 | 194 | chr12 | 62467014 | |||||
| chr12:62592840
|
G | A | 20 | a0001c0002t0031a0001c0006t0007a0001c0006t0033others(17): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*91G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 91 | chr12 | 62592840 | |||||
| chr12:62592981
|
G | A | 1 | a0001c0002t0035 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*232G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 232 | chr12 | 62592981 | |||||
| chr12:62593218
|
T | C | 1 | a0001c0003t0008 | 11 | NA18945.hp1 NA18955.hp2 NA18963.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*469T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 469 | chr12 | 62593218 | |||||
| chr12:62593509
|
T | G | 1 | a0001c0003t0036 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 760 | chr12 | 62593509 | |||||
| chr12:62594045
|
A | T | 1 | a0001c0003t0050 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1296A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 1296 | chr12 | 62594045 | |||||
| chr12:62594079
|
G | A | 1 | a0001c0002t0037 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 1330 | chr12 | 62594079 | |||||
| chr12:62594305
|
T | C | 1 | a0001c0020t0038 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1556T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 1556 | chr12 | 62594305 | |||||
| chr12:62594508
|
G | A | 15 | a0002c0001t0001a0002c0001t0006a0002c0001t0009others(12): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1759G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 1759 | chr12 | 62594508 | |||||
| chr12:62594645
|
G | A | 48 | a0001c0002t0003a0001c0002t0005a0001c0002t0013others(45): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1896G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 1896 | chr12 | 62594645 | |||||
| chr12:62595141
|
G | GT | 5 | a0001c0003t0023a0001c0003t0049a0002c0001t0012others(2): Show | 8 | HG02145.hp1 HG02148.hp2 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2408dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2409 | INFO_REALIGN_3_PRIME | chr12 | 62595141 | ||||
| chr12:62595146
|
T | G | 4 | a0001c0002t0013a0001c0002t0026a0001c0002t0037others(1): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2397T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2397 | chr12 | 62595146 | |||||
| chr12:62595315
|
T | A | 1 | a0002c0001t0027 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2566T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2566 | chr12 | 62595315 | |||||
| chr12:62595330
|
A | C | 24 | a0001c0002t0022a0001c0002t0031a0001c0006t0007others(21): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*2581A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2581 | chr12 | 62595330 | |||||
| chr12:62595348
|
T | G | 1 | a0003c0004t0044 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2599T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2599 | chr12 | 62595348 | |||||
| chr12:62595361
|
T | A | 1 | a0001c0005t0040 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2612T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2612 | chr12 | 62595361 | |||||
| chr12:62595488
|
G | A | 1 | a0001c0006t0007 | 12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2739G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2739 | chr12 | 62595488 | |||||
| chr12:62595578
|
T | G | 1 | a0001c0002t0017 | 3 | HG01109.hp2 HG02970.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2829T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2829 | chr12 | 62595578 | |||||
| chr12:62595633
|
T | C | 1 | a0001c0003t0036 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2884T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2884 | chr12 | 62595633 | |||||
| chr12:62595662
|
A | T | 1 | a0001c0002t0048 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2913A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2913 | chr12 | 62595662 | |||||
| chr12:62595902
|
C | G | 1 | a0001c0002t0047 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3153C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 3153 | chr12 | 62595902 | |||||
| chr12:62596142
|
G | A | 2 | a0002c0001t0009a0012c0014t0009 | 5 | HG00642.hp1 HG00733.hp1 HG03239.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3393G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 3393 | chr12 | 62596142 | |||||
| chr12:62596623
|
A | G | 24 | a0001c0002t0022a0001c0002t0031a0001c0006t0007others(21): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*3874A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 3874 | chr12 | 62596623 | |||||
| chr12:62596635
|
T | C | 24 | a0001c0002t0022a0001c0002t0031a0001c0006t0007others(21): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*3886T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 3886 | chr12 | 62596635 | |||||
| chr12:62597091
|
C | A | 20 | a0001c0002t0031a0001c0006t0007a0001c0006t0033others(17): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*4342C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4342 | chr12 | 62597091 | |||||
| chr12:62597166
|
G | A | 1 | a0001c0009t0019 | 2 | HG02809.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4417G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4417 | chr12 | 62597166 | |||||
| chr12:62597208
|
C | T | 1 | a0001c0006t0034 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4459C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4459 | chr12 | 62597208 | |||||
| chr12:62597265
|
C | T | 3 | a0001c0006t0007a0001c0006t0033a0001c0006t0034 | 14 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4516C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4516 | chr12 | 62597265 | |||||
| chr12:62597266
|
G | A | 3 | a0001c0002t0010a0001c0002t0017a0001c0002t0035 | 9 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4517G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4517 | chr12 | 62597266 | |||||
| chr12:62597468
|
G | A | 1 | a0002c0001t0028 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4719G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4719 | chr12 | 62597468 | |||||
| chr12:62597838
|
A | G | 1 | a0001c0003t0049 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5089A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5089 | chr12 | 62597838 | |||||
| chr12:62597891
|
T | G | 1 | a0001c0003t0041 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5142T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5142 | chr12 | 62597891 | |||||
| chr12:62598221
|
G | A | 65 | a0001c0002t0002a0001c0002t0003a0001c0002t0005others(62): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*5472G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5472 | chr12 | 62598221 | |||||
| chr12:62598248
|
A | C | 1 | a0001c0005t0016 | 3 | HG00735.hp2 HG01106.hp1 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5499A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5499 | chr12 | 62598248 | |||||
| chr12:62598467
|
T | C | 1 | a0001c0002t0020 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5718T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5718 | chr12 | 62598467 | |||||
| chr12:62598582
|
G | A | 1 | a0001c0002t0014 | 4 | HG00099.hp2 HG02300.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5833G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5833 | chr12 | 62598582 | |||||
| chr12:62598706
|
C | T | 1 | a0002c0001t0030 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5957C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5957 | chr12 | 62598706 | |||||
| chr12:62598762
|
G | A | 1 | a0001c0006t0042 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6013G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6013 | chr12 | 62598762 | |||||
| chr12:62598847
|
T | C | 1 | a0001c0002t0045 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6098T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6098 | chr12 | 62598847 | |||||
| chr12:62598879
|
T | A | 1 | a0002c0015t0024 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6130T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6130 | chr12 | 62598879 | |||||
| chr12:62598984
|
T | TA | 1 | a0001c0002t0015 | 4 | HG03927.hp2 NA18990.hp1 NA19001.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6235_*6236insA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6236 | chr12 | 62598984 | |||||
| chr12:62599077
|
T | C | 1 | a0001c0003t0021 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6328T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6328 | chr12 | 62599077 | |||||
| chr12:62599116
|
GA | G | 19 | a0001c0006t0007a0001c0006t0033a0001c0006t0034others(16): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*6377delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6377 | INFO_REALIGN_3_PRIME | chr12 | 62599116 | ||||
| chr12:62599151
|
T | C | 1 | a0004c0007t0046 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6402T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6402 | chr12 | 62599151 | |||||
| chr12:62599244
|
G | A | 1 | a0001c0002t0047 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6495G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6495 | chr12 | 62599244 | |||||
| chr12:62599290
|
A | G | 1 | a0001c0005t0043 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6541A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6541 | chr12 | 62599290 | |||||
| chr12:62599434
|
A | G | 1 | a0002c0001t0029 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6685A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6685 | chr12 | 62599434 | |||||
| chr12:62599493
|
A | T | 1 | a0001c0002t0031 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6744A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6744 | chr12 | 62599493 | |||||
| chr12:62600013
|
G | A | 15 | a0002c0001t0001a0002c0001t0006a0002c0001t0009others(12): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*7264G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 7264 | chr12 | 62600013 | |||||
| chr12:62600156
|
C | T | 39 | a0001c0002t0003a0001c0002t0013a0001c0002t0014others(36): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*7407C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 7407 | chr12 | 62600156 | |||||
| chr12:62600162
|
G | A | 2 | a0003c0004t0004a0003c0004t0044 | 32 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*7413G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 7413 | chr12 | 62600162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:62467331
|
T | C | 253 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(250): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.111+13T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467331 | ||||||
| chr12:62467531
|
T | C | 1 | a0001c0002t0002g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.111+213T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467531 | ||||||
| chr12:62467538
|
G | A | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.111+220G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467538 | ||||||
| chr12:62467741
|
T | C | 1 | a0001c0002t0011g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.111+423T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467741 | ||||||
| chr12:62467891
|
G | C | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+573G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467891 | ||||||
| chr12:62467964
|
TC | T | 80 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(77): Show | 81 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.111+648delC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62467964 | |||||
| chr12:62467965
|
C | T | 172 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(169): Show | 174 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.111+647C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467965 | ||||||
| chr12:62468155
|
T | TA | 9 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+849dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62468155 | |||||
| chr12:62468155
|
TA | T | 119 | a0001c0016t0032g0252a0002c0001t0001g0002a0002c0001t0001g0003others(116): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.111+849delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62468155 | |||||
| chr12:62468180
|
C | A | 98 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(95): Show | 99 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.111+862C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468180 | ||||||
| chr12:62468585
|
A | G | 7 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0027others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+1267A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468585 | ||||||
| chr12:62468656
|
C | G | 1 | a0003c0004t0004g0365 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111+1338C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468656 | ||||||
| chr12:62468666
|
A | G | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+1348A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468666 | ||||||
| chr12:62468800
|
C | T | 1 | a0002c0001t0001g0253 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.111+1482C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468800 | ||||||
| chr12:62468932
|
G | A | 1 | a0001c0003t0005g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.111+1614G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468932 | ||||||
| chr12:62468959
|
T | G | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.111+1641T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468959 | ||||||
| chr12:62469075
|
G | A | 1 | a0001c0002t0002g0256 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.111+1757G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469075 | ||||||
| chr12:62469100
|
A | G | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.111+1782A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469100 | ||||||
| chr12:62469113
|
G | A | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.111+1795G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469113 | ||||||
| chr12:62469115
|
C | CT | 6 | a0001c0002t0002g0256a0001c0002t0002g0363a0001c0002t0005g0362others(3): Show | 6 | HG00621.hp2 HG01255.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+1815dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469115 | |||||
| chr12:62469115
|
CT | C | 65 | a0001c0002t0003g0102a0001c0002t0022g0295a0001c0003t0002g0054others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.111+1815delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469115 | |||||
| chr12:62469115
|
CTT | C | 221 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.111+1814_111+1815d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469115 | |||||
| chr12:62469428
|
G | C | 2 | a0003c0004t0004g0258a0003c0004t0004g0259 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.111+2110G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469428 | ||||||
| chr12:62469576
|
T | C | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.111+2258T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469576 | ||||||
| chr12:62469735
|
G | A | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.111+2417G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469735 | ||||||
| chr12:62469881
|
A | ATTTT | 36 | a0001c0002t0002g0254a0001c0002t0002g0256a0001c0002t0002g0329others(33): Show | 36 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.111+2564_111+2567d others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469881 | |||||
| chr12:62469882
|
T | TTTTA | 6 | a0001c0002t0002g0310a0001c0002t0011g0255a0001c0002t0011g0257others(3): Show | 6 | HG01099.hp2 HG02280.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+2604_111+2607d others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469882 | |||||
| chr12:62469882
|
T | TTTTATTT others(1): Show |
3 | a0001c0002t0002g0305a0001c0002t0045g0360a0001c0018t0002g0306 | 3 | HG02572.hp2 NA18612.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.111+2600_111+2607d others(10): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469882 | |||||
| chr12:62469882
|
T | TTTTTTTT others(1): Show |
13 | a0001c0002t0002g0317a0001c0002t0002g0318a0001c0002t0002g0321others(10): Show | 13 | HG00423.hp2 HG00438.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.111+2567_111+2568i others(10): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469882 | |||||
| chr12:62469882
|
T | TTTTTTTT others(5): Show |
3 | a0001c0002t0015g0314a0001c0002t0015g0315a0001c0002t0015g0316 | 3 | NA18990.hp1 NA19001.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.111+2567_111+2568i others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469882 | |||||
| chr12:62469886
|
A | T | 1 | a0001c0005t0040g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.111+2568A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469886 | ||||||
| chr12:62469910
|
ATTTATTT others(6): Show |
A | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.111+2595_111+2607d others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469910 | |||||
| chr12:62469914
|
ATTTATTT others(2): Show |
A | 84 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(81): Show | 85 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.111+2599_111+2607d others(11): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469914 | |||||
| chr12:62469918
|
ATTTAT | A | 127 | a0001c0002t0003g0102a0001c0002t0014g0280a0001c0006t0003g0105others(124): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.111+2603_111+2607d others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469918 | |||||
| chr12:62469922
|
AT | A | 32 | a0001c0002t0014g0286a0001c0002t0014g0287a0001c0002t0014g0288others(29): Show | 33 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.111+2607delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469922 | |||||
| chr12:62469923
|
T | TTTA | 7 | a0002c0001t0001g0241a0002c0001t0001g0242a0002c0001t0001g0243others(4): Show | 7 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+2607_111+2608i others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469923 | |||||
| chr12:62469923
|
T | TTTATTTA | 10 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(7): Show | 10 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.111+2607_111+2608i others(9): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469923 | |||||
| chr12:62469923
|
T | TTTATTTA others(4): Show |
18 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0005t0003g0119others(15): Show | 18 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.111+2607_111+2608i others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469923 | |||||
| chr12:62469923
|
T | TTTATTTA others(8): Show |
3 | a0001c0005t0040g0135a0001c0005t0043g0132a0009c0019t0003g0133 | 3 | HG02602.hp2 HG04184.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.111+2607_111+2608i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469923 | |||||
| chr12:62469923
|
T | TTTATTTA others(12): Show |
1 | a0001c0005t0003g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.111+2607_111+2608i others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469923 | |||||
| chr12:62470040
|
G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.111+2722G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470040 | ||||||
| chr12:62470153
|
C | T | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.111+2835C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470153 | ||||||
| chr12:62470363
|
A | G | 4 | a0002c0001t0001g0221a0002c0001t0001g0222a0002c0001t0001g0223others(1): Show | 4 | HG01934.hp1 HG01975.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+3045A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470363 | ||||||
| chr12:62470421
|
T | G | 1 | a0001c0002t0002g0311 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.111+3103T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470421 | ||||||
| chr12:62470468
|
T | C | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.111+3150T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470468 | ||||||
| chr12:62470469
|
G | A | 1 | a0001c0003t0021g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.111+3151G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470469 | ||||||
| chr12:62470476
|
A | G | 2 | a0002c0001t0001g0110a0002c0001t0001g0220 | 2 | NA18963.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.111+3158A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470476 | ||||||
| chr12:62470526
|
G | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111+3208G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470526 | ||||||
| chr12:62470637
|
A | C | 99 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(96): Show | 100 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.111+3319A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470637 | ||||||
| chr12:62470748
|
G | A | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.111+3430G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470748 | ||||||
| chr12:62471004
|
A | G | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+3686A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471004 | ||||||
| chr12:62471031
|
G | C | 5 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(2): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.111+3713G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471031 | ||||||
| chr12:62471097
|
A | T | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+3779A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471097 | ||||||
| chr12:62471105
|
C | T | 1 | a0001c0002t0002g0359 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.111+3787C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471105 | ||||||
| chr12:62471151
|
A | G | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+3833A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471151 | ||||||
| chr12:62471312
|
A | G | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+3994A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471312 | ||||||
| chr12:62471328
|
G | A | 27 | a0001c0002t0031g0136a0001c0003t0021g0001a0001c0005t0003g0111others(24): Show | 28 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.111+4010G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471328 | ||||||
| chr12:62471329
|
C | T | 1 | a0002c0001t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.111+4011C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471329 | ||||||
| chr12:62471372
|
C | T | 127 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.111+4054C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471372 | ||||||
| chr12:62471430
|
C | T | 1 | a0001c0002t0002g0358 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.111+4112C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471430 | ||||||
| chr12:62471464
|
G | C | 1 | a0001c0003t0005g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111+4146G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471464 | ||||||
| chr12:62471508
|
T | C | 1 | a0002c0001t0001g0225 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.111+4190T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471508 | ||||||
| chr12:62471511
|
G | A | 124 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(121): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.111+4193G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471511 | ||||||
| chr12:62471565
|
T | C | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+4247T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471565 | ||||||
| chr12:62471648
|
A | G | 1 | a0012c0014t0009g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.111+4330A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471648 | ||||||
| chr12:62471680
|
G | A | 1 | a0001c0005t0043g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.111+4362G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471680 | ||||||
| chr12:62471955
|
T | A | 1 | a0003c0004t0004g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.111+4637T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471955 | ||||||
| chr12:62472178
|
C | T | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.111+4860C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472178 | ||||||
| chr12:62472224
|
A | C | 1 | a0002c0001t0001g0217 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.111+4906A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472224 | ||||||
| chr12:62472279
|
G | A | 2 | a0001c0005t0003g0111a0001c0005t0003g0112 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.111+4961G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472279 | ||||||
| chr12:62472339
|
G | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111+5021G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472339 | ||||||
| chr12:62472601
|
T | G | 2 | a0001c0003t0005g0045a0001c0003t0005g0046 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.111+5283T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472601 | ||||||
| chr12:62472761
|
A | G | 1 | a0003c0004t0004g0284 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.111+5443A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472761 | ||||||
| chr12:62472987
|
A | AT | 53 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(50): Show | 53 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.111+5672dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62472987 | |||||
| chr12:62473022
|
A | G | 1 | a0001c0002t0002g0357 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.111+5704A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62473022 | ||||||
| chr12:62473203
|
G | A | 3 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107 | 3 | HG02257.hp2 HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.111+5885G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62473203 | ||||||
| chr12:62473208
|
T | G | 1 | a0001c0002t0002g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.111+5890T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62473208 | ||||||
| chr12:62473241
|
A | G | 2 | a0001c0005t0003g0130a0001c0005t0003g0131 | 2 | NA18969.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.111+5923A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62473241 | ||||||
| chr12:62473316
|
AAAATGGT others(2): Show |
A | 253 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(250): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.111+6015_111+6023d others(11): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62473316 | |||||
| chr12:62473427
|
T | C | 1 | a0001c0002t0010g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111+6109T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62473427 | ||||||
| chr12:62474318
|
A | T | 153 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(150): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.111+7000A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474318 | ||||||
| chr12:62474494
|
G | A | 1 | a0001c0020t0038g0312 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.111+7176G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474494 | ||||||
| chr12:62474518
|
G | A | 99 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(96): Show | 100 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.111+7200G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474518 | ||||||
| chr12:62474557
|
T | G | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+7239T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474557 | ||||||
| chr12:62474610
|
G | A | 2 | a0003c0004t0004g0261a0003c0004t0004g0293 | 2 | HG04228.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.111+7292G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474610 | ||||||
| chr12:62474613
|
G | A | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.111+7295G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474613 | ||||||
| chr12:62474675
|
C | T | 127 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.111+7357C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474675 | ||||||
| chr12:62474719
|
C | T | 127 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.111+7401C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474719 | ||||||
| chr12:62474720
|
A | C | 127 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.111+7402A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474720 | ||||||
| chr12:62475105
|
T | G | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.111+7787T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475105 | ||||||
| chr12:62475107
|
C | T | 1 | a0002c0001t0001g0240 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.111+7789C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475107 | ||||||
| chr12:62475449
|
C | T | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+8131C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475449 | ||||||
| chr12:62475470
|
CTATCTT | C | 52 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(49): Show | 52 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.111+8155_111+8160d others(8): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62475470 | |||||
| chr12:62475572
|
G | A | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+8254G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475572 | ||||||
| chr12:62475749
|
C | A | 5 | a0002c0001t0001g0137a0002c0001t0001g0138a0002c0001t0001g0141others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-8421C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475749 | ||||||
| chr12:62475883
|
C | T | 4 | a0004c0007t0002g0327a0004c0007t0002g0328a0004c0007t0002g0361others(1): Show | 4 | HG02165.hp2 NA18943.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-8287C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475883 | ||||||
| chr12:62475959
|
C | T | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-8211C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475959 | ||||||
| chr12:62476012
|
AAAAAG | A | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-8147_112-8143d others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62476012 | |||||
| chr12:62476024
|
AAAGG | A | 34 | a0001c0002t0022g0295a0003c0004t0004g0258a0003c0004t0004g0259others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.112-8139_112-8136d others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62476024 | |||||
| chr12:62476218
|
A | C | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.112-7952A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476218 | ||||||
| chr12:62476268
|
G | C | 2 | a0001c0002t0002g0363a0001c0002t0005g0362 | 2 | HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.112-7902G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476268 | ||||||
| chr12:62476333
|
A | T | 80 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(77): Show | 81 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.112-7837A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476333 | ||||||
| chr12:62476594
|
A | C | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.112-7576A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476594 | ||||||
| chr12:62476625
|
C | T | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.112-7545C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476625 | ||||||
| chr12:62476639
|
G | A | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.112-7531G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476639 | ||||||
| chr12:62476703
|
G | A | 1 | a0002c0001t0001g0225 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.112-7467G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476703 | ||||||
| chr12:62476730
|
C | G | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-7440C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476730 | ||||||
| chr12:62476756
|
C | G | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-7414C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476756 | ||||||
| chr12:62476794
|
C | G | 129 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.112-7376C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476794 | ||||||
| chr12:62476951
|
T | A | 1 | a0001c0002t0002g0329 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.112-7219T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476951 | ||||||
| chr12:62476992
|
A | C | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.112-7178A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476992 | ||||||
| chr12:62477034
|
C | T | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.112-7136C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477034 | ||||||
| chr12:62477044
|
G | A | 2 | a0001c0005t0003g0111a0001c0005t0003g0112 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.112-7126G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477044 | ||||||
| chr12:62477511
|
G | A | 4 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-6659G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477511 | ||||||
| chr12:62477581
|
A | AT | 6 | a0001c0002t0003g0102a0001c0003t0005g0091a0001c0003t0021g0001others(3): Show | 7 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-6571dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62477581 | |||||
| chr12:62477581
|
AT | A | 10 | a0001c0002t0002g0330a0001c0002t0013g0298a0001c0002t0020g0285others(7): Show | 10 | HG01070.hp1 HG01074.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.112-6571delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62477581 | |||||
| chr12:62477588
|
T | TC | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-6582_112-6581i others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477588 | ||||||
| chr12:62477629
|
C | CT | 301 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(298): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.112-6541_112-6540i others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477629 | ||||||
| chr12:62477636
|
G | A | 1 | a0001c0002t0014g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.112-6534G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477636 | ||||||
| chr12:62477676
|
A | G | 1 | a0001c0003t0008g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.112-6494A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477676 | ||||||
| chr12:62477695
|
C | T | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.112-6475C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477695 | ||||||
| chr12:62477772
|
G | A | 3 | a0002c0001t0001g0145a0002c0001t0001g0245a0002c0001t0001g0246 | 3 | NA18968.hp2 NA19009.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.112-6398G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477772 | ||||||
| chr12:62478041
|
T | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112-6129T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478041 | ||||||
| chr12:62478047
|
T | A | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-6123T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478047 | ||||||
| chr12:62478082
|
C | A | 4 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(1): Show | 4 | HG00099.hp2 HG02300.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-6088C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478082 | ||||||
| chr12:62478092
|
G | A | 4 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-6078G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478092 | ||||||
| chr12:62478121
|
T | TTG | 74 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.112-6025_112-6024d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62478121 | |||||
| chr12:62478121
|
T | TTGTG | 7 | a0001c0002t0002g0356a0001c0006t0003g0005a0001c0006t0003g0006others(4): Show | 7 | HG01081.hp2 HG02071.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-6027_112-6024d others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62478121 | |||||
| chr12:62478121
|
T | TTGTGTG | 22 | a0001c0005t0003g0113a0001c0005t0003g0114a0001c0005t0003g0115others(19): Show | 22 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.112-6029_112-6024d others(8): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62478121 | |||||
| chr12:62478228
|
T | C | 1 | a0001c0002t0002g0359 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.112-5942T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478228 | ||||||
| chr12:62478291
|
A | C | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-5879A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478291 | ||||||
| chr12:62478431
|
C | T | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-5739C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478431 | ||||||
| chr12:62478482
|
A | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112-5688A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478482 | ||||||
| chr12:62478554
|
T | A | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-5616T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478554 | ||||||
| chr12:62479093
|
G | T | 1 | a0003c0004t0004g0283 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.112-5077G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479093 | ||||||
| chr12:62479176
|
A | C | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.112-4994A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479176 | ||||||
| chr12:62479265
|
C | A | 4 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-4905C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479265 | ||||||
| chr12:62479286
|
A | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.112-4884A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479286 | ||||||
| chr12:62479289
|
T | G | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-4881T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479289 | ||||||
| chr12:62479335
|
T | A | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-4835T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479335 | ||||||
| chr12:62479397
|
G | A | 294 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0331others(291): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.112-4773G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479397 | ||||||
| chr12:62479428
|
A | G | 27 | a0001c0002t0002g0355a0001c0002t0031g0136a0001c0005t0003g0111others(24): Show | 27 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.112-4742A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479428 | ||||||
| chr12:62479431
|
T | TC | 15 | a0001c0002t0002g0317a0001c0002t0002g0325a0001c0002t0002g0351others(12): Show | 15 | HG00544.hp1 HG00621.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.112-4725dupC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62479431 | |||||
| chr12:62479431
|
TC | T | 81 | a0001c0002t0002g0318a0001c0002t0010g0031a0001c0002t0013g0300others(78): Show | 81 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.112-4725delC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62479431 | |||||
| chr12:62479431
|
TCC | T | 157 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(154): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.112-4726_112-4725d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62479431 | |||||
| chr12:62479431
|
TCCC | T | 15 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(12): Show | 15 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-4727_112-4725d others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62479431 | |||||
| chr12:62479433
|
C | A | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-4737C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479433 | ||||||
| chr12:62479434
|
C | T | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-4736C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479434 | ||||||
| chr12:62479566
|
C | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112-4604C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479566 | ||||||
| chr12:62479639
|
G | A | 59 | a0002c0001t0001g0002a0002c0001t0001g0110a0002c0001t0001g0142others(56): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.112-4531G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479639 | ||||||
| chr12:62479863
|
G | A | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.112-4307G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479863 | ||||||
| chr12:62480093
|
G | A | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-4077G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480093 | ||||||
| chr12:62480231
|
T | A | 1 | a0001c0018t0002g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112-3939T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480231 | ||||||
| chr12:62480374
|
C | G | 3 | a0001c0005t0003g0115a0001c0005t0003g0130a0001c0005t0003g0131 | 3 | NA18969.hp2 NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.112-3796C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480374 | ||||||
| chr12:62480460
|
G | C | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.112-3710G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480460 | ||||||
| chr12:62480649
|
G | A | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.112-3521G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480649 | ||||||
| chr12:62480680
|
A | G | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-3490A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480680 | ||||||
| chr12:62480707
|
G | C | 30 | a0001c0005t0003g0111a0001c0005t0003g0112a0002c0001t0006g0143others(27): Show | 30 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.112-3463G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480707 | ||||||
| chr12:62480708
|
A | T | 30 | a0001c0005t0003g0111a0001c0005t0003g0112a0002c0001t0006g0143others(27): Show | 30 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.112-3462A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480708 | ||||||
| chr12:62481169
|
T | G | 1 | a0001c0002t0048g0320 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.112-3001T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481169 | ||||||
| chr12:62481198
|
A | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.112-2972A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481198 | ||||||
| chr12:62481302
|
G | A | 34 | a0001c0002t0022g0295a0003c0004t0004g0258a0003c0004t0004g0259others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.112-2868G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481302 | ||||||
| chr12:62481333
|
T | A | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.112-2837T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481333 | ||||||
| chr12:62481487
|
G | A | 5 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-2683G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481487 | ||||||
| chr12:62481510
|
C | T | 53 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(50): Show | 53 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.112-2660C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481510 | ||||||
| chr12:62481515
|
C | CA | 137 | a0001c0002t0002g0030a0001c0002t0002g0305a0001c0002t0002g0318others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.112-2635dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62481515 | |||||
| chr12:62481515
|
C | CAA | 93 | a0001c0002t0002g0026a0001c0002t0003g0102a0001c0002t0010g0023others(90): Show | 94 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.112-2636_112-2635d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62481515 | |||||
| chr12:62481515
|
C | CAAA | 10 | a0001c0002t0017g0033a0001c0003t0002g0054a0001c0003t0002g0055others(7): Show | 10 | HG01106.hp1 HG01109.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.112-2637_112-2635d others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62481515 | |||||
| chr12:62481515
|
CA | C | 12 | a0001c0002t0037g0304a0001c0006t0007g0009a0001c0006t0007g0012others(9): Show | 12 | HG01099.hp1 HG01516.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.112-2635delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62481515 | |||||
| chr12:62481636
|
C | T | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-2534C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481636 | ||||||
| chr12:62481704
|
A | G | 2 | a0003c0004t0004g0258a0003c0004t0004g0259 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.112-2466A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481704 | ||||||
| chr12:62481907
|
A | G | 4 | a0001c0005t0003g0128a0001c0005t0003g0129a0001c0005t0003g0134others(1): Show | 4 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-2263A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481907 | ||||||
| chr12:62482059
|
C | T | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.112-2111C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482059 | ||||||
| chr12:62482130
|
T | A | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.112-2040T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482130 | ||||||
| chr12:62482323
|
C | G | 80 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(77): Show | 81 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.112-1847C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482323 | ||||||
| chr12:62482425
|
C | T | 11 | a0001c0002t0002g0310a0001c0002t0002g0343a0001c0002t0002g0345others(8): Show | 11 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.112-1745C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482425 | ||||||
| chr12:62482478
|
G | C | 1 | a0002c0001t0001g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.112-1692G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482478 | ||||||
| chr12:62482488
|
A | C | 1 | a0001c0002t0002g0342 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.112-1682A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482488 | ||||||
| chr12:62482658
|
A | G | 1 | a0003c0004t0004g0365 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.112-1512A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482658 | ||||||
| chr12:62482717
|
C | T | 300 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(297): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.112-1453C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482717 | ||||||
| chr12:62482811
|
C | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112-1359C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482811 | ||||||
| chr12:62482907
|
AC | A | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-1261delC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62482907 | |||||
| chr12:62482933
|
C | T | 34 | a0001c0002t0022g0295a0003c0004t0004g0258a0003c0004t0004g0259others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.112-1237C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482933 | ||||||
| chr12:62483207
|
G | C | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-963G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483207 | ||||||
| chr12:62483256
|
A | G | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-914A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483256 | ||||||
| chr12:62483391
|
A | G | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.112-779A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483391 | ||||||
| chr12:62483429
|
G | A | 2 | a0001c0003t0005g0045a0001c0003t0005g0046 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.112-741G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483429 | ||||||
| chr12:62483485
|
G | T | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-685G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483485 | ||||||
| chr12:62483651
|
G | A | 2 | a0001c0002t0013g0300a0001c0002t0026g0301 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.112-519G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483651 | ||||||
| chr12:62483774
|
A | AT | 8 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(5): Show | 8 | HG01891.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-389dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62483774 | |||||
| chr12:62484370
|
A | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.175+137A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62484370 | ||||||
| chr12:62484502
|
C | T | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175+269C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62484502 | ||||||
| chr12:62484590
|
T | G | 1 | a0001c0005t0003g0115 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.175+357T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62484590 | ||||||
| chr12:62484631
|
A | G | 1 | a0002c0001t0028g0181 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.175+398A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62484631 | ||||||
| chr12:62484915
|
CT | C | 17 | a0001c0002t0002g0305a0001c0002t0002g0310a0001c0002t0002g0321others(14): Show | 17 | HG01074.hp1 HG01099.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.175+702delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62484915 | |||||
| chr12:62484915
|
CTT | C | 51 | a0001c0002t0013g0300a0001c0002t0014g0280a0001c0002t0014g0286others(48): Show | 52 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.175+701_175+702del others(2): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62484915 | |||||
| chr12:62484915
|
CTTT | C | 228 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(225): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.175+700_175+702del others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62484915 | |||||
| chr12:62484915
|
CTTTT | C | 12 | a0001c0003t0002g0056a0001c0003t0005g0057a0001c0003t0036g0048others(9): Show | 12 | HG01081.hp2 HG01168.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+699_175+702del others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62484915 | |||||
| chr12:62484938
|
G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.175+705G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62484938 | ||||||
| chr12:62485083
|
A | G | 1 | a0002c0001t0001g0250 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.175+850A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485083 | ||||||
| chr12:62485131
|
T | C | 1 | a0001c0003t0008g0085 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.175+898T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485131 | ||||||
| chr12:62485132
|
G | C | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.175+899G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485132 | ||||||
| chr12:62485190
|
T | C | 293 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.175+957T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485190 | ||||||
| chr12:62485435
|
C | T | 1 | a0001c0003t0005g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175+1202C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485435 | ||||||
| chr12:62485437
|
G | T | 3 | a0001c0005t0003g0115a0001c0005t0003g0130a0001c0005t0003g0131 | 3 | NA18969.hp2 NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.175+1204G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485437 | ||||||
| chr12:62485485
|
G | A | 1 | a0005c0008t0002g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.175+1252G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485485 | ||||||
| chr12:62485579
|
CAT | C | 23 | a0001c0005t0003g0113a0001c0005t0003g0114a0001c0005t0003g0115others(20): Show | 23 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.175+1347_175+1348d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485579 | ||||||
| chr12:62485710
|
T | C | 3 | a0001c0003t0005g0086a0001c0003t0005g0087a0001c0003t0005g0101 | 3 | HG00597.hp2 HG00621.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.175+1477T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485710 | ||||||
| chr12:62485860
|
C | T | 1 | a0001c0002t0002g0349 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.175+1627C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485860 | ||||||
| chr12:62486009
|
G | A | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.175+1776G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486009 | ||||||
| chr12:62486121
|
C | T | 5 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(2): Show | 5 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+1888C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486121 | ||||||
| chr12:62486183
|
C | A | 1 | a0001c0018t0002g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.175+1950C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486183 | ||||||
| chr12:62486184
|
G | A | 1 | a0001c0002t0002g0332 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.175+1951G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486184 | ||||||
| chr12:62486244
|
A | T | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.175+2011A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486244 | ||||||
| chr12:62486255
|
T | TAAAAAAA others(317): Show |
1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175+2039_175+2040i others(326): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | |||||
| chr12:62486255
|
T | TAAAAAAA others(323): Show |
3 | a0001c0005t0016g0116a0001c0005t0016g0117a0001c0005t0016g0118 | 3 | HG00735.hp2 HG01106.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.175+2039_175+2040i others(332): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | |||||
| chr12:62486255
|
T | TAAAAAAA others(319): Show |
4 | a0001c0005t0003g0114a0001c0005t0003g0125a0001c0005t0003g0126others(1): Show | 4 | HG01192.hp1 HG01346.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+2039_175+2040i others(328): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | |||||
| chr12:62486255
|
T | TAAAAAAA others(320): Show |
7 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0005t0003g0113others(4): Show | 7 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+2039_175+2040i others(329): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | |||||
| chr12:62486255
|
T | TAAAAAAA others(321): Show |
4 | a0001c0005t0003g0122a0001c0005t0003g0128a0001c0005t0003g0129others(1): Show | 4 | HG01255.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+2039_175+2040i others(330): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | |||||
| chr12:62486255
|
T | TAAAAAAA others(322): Show |
6 | a0001c0005t0003g0115a0001c0005t0003g0120a0001c0005t0003g0121others(3): Show | 6 | HG03669.hp1 NA18969.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+2039_175+2040i others(331): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | |||||
| chr12:62486255
|
T | TAAAAAAA others(323): Show |
1 | a0001c0005t0003g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.175+2039_175+2040i others(332): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | |||||
| chr12:62486482
|
G | A | 12 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+2249G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486482 | ||||||
| chr12:62486496
|
C | G | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.175+2263C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486496 | ||||||
| chr12:62486651
|
A | G | 3 | a0001c0003t0005g0086a0001c0003t0005g0087a0001c0003t0005g0101 | 3 | HG00597.hp2 HG00621.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.175+2418A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486651 | ||||||
| chr12:62487306
|
G | A | 1 | a0001c0006t0003g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.175+3073G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487306 | ||||||
| chr12:62487439
|
C | T | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175+3206C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487439 | ||||||
| chr12:62487440
|
G | A | 2 | a0003c0004t0004g0264a0003c0004t0004g0265 | 2 | NA18983.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.175+3207G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487440 | ||||||
| chr12:62487547
|
G | A | 1 | a0001c0003t0003g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.175+3314G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487547 | ||||||
| chr12:62487955
|
T | A | 301 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(298): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.175+3722T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487955 | ||||||
| chr12:62487996
|
G | T | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.175+3763G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487996 | ||||||
| chr12:62488202
|
C | A | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.175+3969C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488202 | ||||||
| chr12:62488202
|
C | G | 18 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(15): Show | 18 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.175+3969C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488202 | ||||||
| chr12:62488293
|
A | G | 1 | a0001c0005t0003g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175+4060A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488293 | ||||||
| chr12:62488485
|
T | C | 1 | a0001c0002t0002g0305 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.175+4252T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488485 | ||||||
| chr12:62488516
|
T | C | 3 | a0001c0002t0002g0305a0001c0002t0002g0322a0001c0002t0002g0331 | 3 | NA18945.hp2 NA18988.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.175+4283T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488516 | ||||||
| chr12:62488645
|
A | G | 80 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(77): Show | 81 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.175+4412A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488645 | ||||||
| chr12:62488741
|
A | T | 123 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(120): Show | 124 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.175+4508A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488741 | ||||||
| chr12:62489009
|
G | T | 1 | a0001c0006t0007g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.175+4776G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489009 | ||||||
| chr12:62489287
|
T | C | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.176-4628T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489287 | ||||||
| chr12:62489336
|
A | G | 1 | a0001c0002t0002g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.176-4579A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489336 | ||||||
| chr12:62489689
|
A | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.176-4226A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489689 | ||||||
| chr12:62489690
|
A | G | 123 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(120): Show | 124 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.176-4225A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489690 | ||||||
| chr12:62489829
|
C | T | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-4086C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489829 | ||||||
| chr12:62489864
|
G | T | 1 | a0002c0001t0001g0179 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.176-4051G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489864 | ||||||
| chr12:62489882
|
T | C | 80 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(77): Show | 81 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.176-4033T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489882 | ||||||
| chr12:62490145
|
C | T | 4 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-3770C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490145 | ||||||
| chr12:62490210
|
C | CT | 253 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(250): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.176-3704dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62490210 | |||||
| chr12:62490328
|
G | GT | 7 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(4): Show | 7 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-3578dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62490328 | |||||
| chr12:62490329
|
T | G | 1 | a0002c0001t0001g0148 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.176-3586T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490329 | ||||||
| chr12:62490343
|
G | T | 3 | a0001c0003t0005g0037a0001c0003t0005g0038a0001c0003t0005g0039 | 3 | HG02258.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.176-3572G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490343 | ||||||
| chr12:62490370
|
A | C | 1 | a0002c0001t0001g0178 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.176-3545A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490370 | ||||||
| chr12:62490406
|
G | A | 80 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(77): Show | 81 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.176-3509G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490406 | ||||||
| chr12:62490589
|
G | A | 4 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-3326G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490589 | ||||||
| chr12:62490694
|
A | G | 1 | a0001c0002t0002g0330 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.176-3221A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490694 | ||||||
| chr12:62490731
|
A | G | 1 | a0001c0018t0002g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.176-3184A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490731 | ||||||
| chr12:62490762
|
T | C | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.176-3153T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490762 | ||||||
| chr12:62490772
|
A | G | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.176-3143A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490772 | ||||||
| chr12:62490821
|
A | C | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.176-3094A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490821 | ||||||
| chr12:62490852
|
T | C | 253 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(250): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.176-3063T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490852 | ||||||
| chr12:62490934
|
ATTT | A | 129 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.176-2979_176-2977d others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62490934 | |||||
| chr12:62491153
|
G | A | 1 | a0002c0001t0029g0149 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.176-2762G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491153 | ||||||
| chr12:62491192
|
G | A | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.176-2723G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491192 | ||||||
| chr12:62491436
|
A | C | 2 | a0002c0001t0001g0150a0002c0001t0001g0180 | 2 | NA18612.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.176-2479A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491436 | ||||||
| chr12:62491436
|
A | T | 250 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(247): Show | 253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.176-2479A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491436 | ||||||
| chr12:62491537
|
A | G | 1 | a0001c0018t0002g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.176-2378A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491537 | ||||||
| chr12:62491566
|
C | A | 2 | a0002c0001t0001g0242a0002c0001t0001g0243 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.176-2349C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491566 | ||||||
| chr12:62491672
|
G | A | 1 | a0002c0001t0001g0205 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.176-2243G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491672 | ||||||
| chr12:62491709
|
C | T | 123 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(120): Show | 124 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.176-2206C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491709 | ||||||
| chr12:62492012
|
A | G | 1 | a0002c0001t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.176-1903A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492012 | ||||||
| chr12:62492101
|
A | C | 1 | a0002c0001t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.176-1814A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492101 | ||||||
| chr12:62492174
|
C | T | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-1741C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492174 | ||||||
| chr12:62492221
|
T | A | 129 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.176-1694T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492221 | ||||||
| chr12:62492334
|
C | T | 1 | a0002c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.176-1581C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492334 | ||||||
| chr12:62492343
|
A | G | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.176-1572A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492343 | ||||||
| chr12:62492348
|
T | G | 1 | a0001c0002t0013g0298 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.176-1567T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492348 | ||||||
| chr12:62492362
|
C | CT | 198 | a0001c0002t0002g0026a0001c0002t0014g0280a0001c0002t0014g0286others(195): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.176-1533dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62492362 | |||||
| chr12:62492362
|
C | CTA | 6 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(3): Show | 6 | NA18945.hp1 NA18955.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-1552_176-1551i others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62492362 | |||||
| chr12:62492362
|
C | CTT | 22 | a0001c0002t0002g0030a0001c0002t0003g0102a0001c0002t0010g0027others(19): Show | 22 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.176-1534_176-1533d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62492362 | |||||
| chr12:62492399
|
C | G | 1 | a0002c0001t0001g0238 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.176-1516C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492399 | ||||||
| chr12:62492404
|
G | A | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.176-1511G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492404 | ||||||
| chr12:62492404
|
GC | G | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.176-1508delC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62492404 | |||||
| chr12:62492413
|
G | A | 2 | a0001c0002t0002g0322a0001c0002t0002g0331 | 2 | NA18945.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.176-1502G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492413 | ||||||
| chr12:62492547
|
A | G | 1 | a0002c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.176-1368A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492547 | ||||||
| chr12:62492592
|
C | G | 129 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.176-1323C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492592 | ||||||
| chr12:62492618
|
G | T | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.176-1297G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492618 | ||||||
| chr12:62492632
|
A | G | 1 | a0001c0003t0005g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.176-1283A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492632 | ||||||
| chr12:62492685
|
T | C | 1 | a0001c0005t0003g0131 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.176-1230T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492685 | ||||||
| chr12:62492701
|
C | T | 1 | a0001c0005t0003g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.176-1214C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492701 | ||||||
| chr12:62492836
|
G | A | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.176-1079G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492836 | ||||||
| chr12:62492861
|
C | T | 5 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-1054C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492861 | ||||||
| chr12:62492869
|
C | T | 129 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.176-1046C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492869 | ||||||
| chr12:62492979
|
G | A | 241 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(238): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.176-936G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492979 | ||||||
| chr12:62492999
|
C | A | 1 | a0002c0001t0029g0149 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.176-916C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492999 | ||||||
| chr12:62493038
|
TACAC | T | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.176-869_176-866del others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62493038 | |||||
| chr12:62493043
|
A | C | 1 | a0002c0001t0001g0235 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.176-872A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493043 | ||||||
| chr12:62493047
|
A | T | 1 | a0001c0003t0003g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.176-868A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493047 | ||||||
| chr12:62493149
|
T | C | 1 | a0001c0002t0002g0357 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.176-766T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493149 | ||||||
| chr12:62493227
|
TGTGCATT others(10): Show |
T | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.176-670_176-654del others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62493227 | |||||
| chr12:62493489
|
A | C | 2 | a0001c0003t0005g0057a0001c0003t0005g0080 | 2 | HG00639.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.176-426A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493489 | ||||||
| chr12:62493698
|
A | C | 16 | a0003c0004t0004g0260a0003c0004t0004g0263a0003c0004t0004g0264others(13): Show | 16 | HG00673.hp2 HG02523.hp1 NA18944.hp2 others(13): Show |
intron_variant | MODIFIER | c.176-217A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493698 | ||||||
| chr12:62493828
|
C | T | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(62): Show | 66 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.176-87C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493828 | ||||||
| chr12:62493865
|
T | G | 12 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.176-50T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493865 | ||||||
| chr12:62493905
|
C | T | 1 | a0003c0004t0004g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.176-10C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493905 | ||||||
| chr12:62494158
|
C | T | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+116C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494158 | ||||||
| chr12:62494282
|
T | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.303+240T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494282 | ||||||
| chr12:62494353
|
G | A | 293 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.303+311G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494353 | ||||||
| chr12:62494371
|
TTATATGG others(4): Show |
T | 1 | a0002c0015t0024g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.303+330_303+340del others(11): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494371 | ||||||
| chr12:62494439
|
A | C | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.303+397A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494439 | ||||||
| chr12:62494531
|
G | A | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.304-485G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494531 | ||||||
| chr12:62494617
|
G | T | 1 | a0001c0003t0041g0053 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.304-399G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494617 | ||||||
| chr12:62494669
|
A | T | 1 | a0005c0008t0002g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.304-347A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494669 | ||||||
| chr12:62494718
|
A | G | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-298A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494718 | ||||||
| chr12:62494862
|
A | G | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.304-154A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494862 | ||||||
| chr12:62494867
|
T | C | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.304-149T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494867 | ||||||
| chr12:62494878
|
A | G | 1 | a0002c0001t0001g0237 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.304-138A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494878 | ||||||
| chr12:62494949
|
C | T | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.304-67C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494949 | ||||||
| chr12:62494961
|
G | A | 1 | a0001c0002t0002g0321 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.304-55G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494961 | ||||||
| chr12:62495260
|
A | G | 1 | a0001c0002t0011g0309 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.435+113A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495260 | ||||||
| chr12:62495290
|
C | T | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.435+143C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495290 | ||||||
| chr12:62495439
|
G | A | 1 | a0002c0001t0001g0217 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.435+292G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495439 | ||||||
| chr12:62495607
|
G | A | 1 | a0003c0004t0004g0269 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.435+460G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495607 | ||||||
| chr12:62495622
|
A | G | 126 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(123): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.435+475A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495622 | ||||||
| chr12:62495629
|
G | A | 126 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(123): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.435+482G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495629 | ||||||
| chr12:62495689
|
C | CA | 8 | a0001c0002t0002g0317a0001c0002t0002g0318a0001c0002t0002g0335others(5): Show | 8 | HG00735.hp1 HG02015.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.435+568dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62495689 | |||||
| chr12:62495689
|
CA | C | 63 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0329others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.435+568delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62495689 | |||||
| chr12:62495689
|
CAA | C | 92 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(89): Show | 92 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.435+567_435+568del others(2): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62495689 | |||||
| chr12:62495689
|
CAAA | C | 10 | a0001c0003t0003g0035a0001c0003t0003g0041a0001c0003t0003g0042others(7): Show | 11 | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.435+566_435+568del others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62495689 | |||||
| chr12:62495689
|
CAAAAAAA others(6): Show |
C | 129 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.435+556_435+568del others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62495689 | |||||
| chr12:62495754
|
C | T | 2 | a0002c0001t0001g0208a0002c0001t0001g0211 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.435+607C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495754 | ||||||
| chr12:62495854
|
A | G | 5 | a0001c0002t0002g0317a0005c0008t0002g0334a0005c0008t0002g0340others(2): Show | 5 | HG02015.hp2 NA18966.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+707A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495854 | ||||||
| chr12:62495961
|
T | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.435+814T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495961 | ||||||
| chr12:62495975
|
T | G | 1 | a0001c0002t0002g0329 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.435+828T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495975 | ||||||
| chr12:62496015
|
A | G | 1 | a0001c0003t0002g0079 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.435+868A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496015 | ||||||
| chr12:62496096
|
T | C | 1 | a0002c0001t0001g0151 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.435+949T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496096 | ||||||
| chr12:62496380
|
T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.435+1233T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496380 | ||||||
| chr12:62496436
|
G | C | 34 | a0001c0002t0022g0295a0003c0004t0004g0258a0003c0004t0004g0259others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.435+1289G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496436 | ||||||
| chr12:62496495
|
G | A | 1 | a0003c0004t0004g0282 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.435+1348G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496495 | ||||||
| chr12:62496577
|
T | C | 2 | a0001c0003t0002g0054a0001c0003t0002g0088 | 2 | HG00544.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.435+1430T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496577 | ||||||
| chr12:62496620
|
A | G | 1 | a0001c0002t0017g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.435+1473A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496620 | ||||||
| chr12:62496711
|
C | A | 126 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(123): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.435+1564C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496711 | ||||||
| chr12:62496743
|
G | C | 53 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(50): Show | 53 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.435+1596G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496743 | ||||||
| chr12:62496823
|
C | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.435+1676C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496823 | ||||||
| chr12:62496959
|
A | G | 1 | a0002c0001t0001g0211 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.435+1812A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496959 | ||||||
| chr12:62497067
|
A | G | 123 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(120): Show | 124 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.436-1852A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497067 | ||||||
| chr12:62497073
|
C | T | 253 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(250): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.436-1846C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497073 | ||||||
| chr12:62497169
|
A | AG | 14 | a0001c0002t0002g0310a0001c0002t0002g0339a0001c0002t0002g0353others(11): Show | 14 | HG00423.hp1 HG01099.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.436-1744dupG | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62497169 | |||||
| chr12:62497176
|
A | G | 1 | a0002c0001t0001g0249 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.436-1743A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497176 | ||||||
| chr12:62497281
|
T | A | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.436-1638T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497281 | ||||||
| chr12:62497365
|
G | A | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.436-1554G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497365 | ||||||
| chr12:62497413
|
C | T | 5 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(2): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-1506C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497413 | ||||||
| chr12:62497549
|
A | G | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.436-1370A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497549 | ||||||
| chr12:62497558
|
A | T | 1 | a0001c0003t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.436-1361A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497558 | ||||||
| chr12:62497626
|
T | C | 80 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(77): Show | 81 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.436-1293T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497626 | ||||||
| chr12:62497632
|
T | G | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.436-1287T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497632 | ||||||
| chr12:62497638
|
A | G | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-1281A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497638 | ||||||
| chr12:62497819
|
T | C | 1 | a0010c0012t0001g0152 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.436-1100T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497819 | ||||||
| chr12:62498004
|
C | G | 2 | a0001c0005t0003g0113a0001c0005t0003g0114 | 2 | HG01081.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.436-915C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498004 | ||||||
| chr12:62498048
|
CT | C | 132 | a0001c0002t0045g0360a0001c0005t0003g0111a0001c0005t0003g0112others(129): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.436-857delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62498048 | |||||
| chr12:62498325
|
G | C | 60 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(57): Show | 60 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.436-594G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498325 | ||||||
| chr12:62498330
|
G | C | 1 | a0002c0001t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.436-589G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498330 | ||||||
| chr12:62498332
|
G | A | 12 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.436-587G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498332 | ||||||
| chr12:62498377
|
G | A | 2 | a0001c0005t0003g0111a0001c0005t0003g0112 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.436-542G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498377 | ||||||
| chr12:62498393
|
T | C | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.436-526T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498393 | ||||||
| chr12:62498498
|
C | G | 1 | a0005c0008t0002g0340 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.436-421C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498498 | ||||||
| chr12:62498697
|
C | G | 1 | a0001c0003t0005g0078 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.436-222C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498697 | ||||||
| chr12:62498822
|
T | C | 7 | a0001c0003t0005g0049a0001c0003t0005g0050a0001c0003t0005g0051others(4): Show | 7 | NA18941.hp1 NA18946.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-97T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498822 | ||||||
| chr12:62499079
|
G | T | 1 | a0001c0003t0003g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.565+31G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499079 | ||||||
| chr12:62499125
|
C | G | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.565+77C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499125 | ||||||
| chr12:62499190
|
C | A | 3 | a0001c0002t0002g0305a0001c0002t0002g0322a0001c0002t0002g0331 | 3 | NA18945.hp2 NA18988.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.565+142C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499190 | ||||||
| chr12:62499344
|
G | A | 3 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0003t0005g0078 | 3 | HG02615.hp2 HG02723.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.565+296G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499344 | ||||||
| chr12:62499387
|
C | A | 5 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+339C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499387 | ||||||
| chr12:62499419
|
T | C | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.565+371T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499419 | ||||||
| chr12:62499472
|
C | T | 3 | a0001c0002t0003g0102a0001c0003t0003g0099a0001c0003t0003g0100 | 3 | HG02615.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.565+424C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499472 | ||||||
| chr12:62499525
|
C | T | 1 | a0002c0001t0001g0220 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.565+477C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499525 | ||||||
| chr12:62499749
|
T | A | 2 | a0001c0002t0013g0300a0001c0002t0026g0301 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.565+701T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499749 | ||||||
| chr12:62499884
|
A | T | 5 | a0001c0002t0003g0102a0001c0003t0005g0037a0001c0003t0005g0038others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+836A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499884 | ||||||
| chr12:62499885
|
T | A | 6 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(3): Show | 6 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+837T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499885 | ||||||
| chr12:62499893
|
A | T | 301 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0333others(298): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.565+845A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499893 | ||||||
| chr12:62500075
|
C | T | 1 | a0001c0003t0050g0077 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.566-708C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500075 | ||||||
| chr12:62500101
|
T | A | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.566-682T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500101 | ||||||
| chr12:62500278
|
A | G | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.566-505A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500278 | ||||||
| chr12:62500634
|
C | T | 1 | a0001c0002t0035g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.566-149C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500634 | ||||||
| chr12:62500671
|
A | C | 2 | a0001c0006t0003g0006a0001c0006t0003g0007 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.566-112A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500671 | ||||||
| chr12:62500778
|
T | C | 1 | a0001c0003t0008g0063 | 1 | NA19080.hp2 | splice_region_variant&intron_variant | LOW | c.566-5T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500778 | ||||||
| chr12:62500917
|
T | C | 2 | a0001c0003t0005g0045a0001c0003t0005g0046 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.663+37T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 6/34 | chr12 | 62500917 | ||||||
| chr12:62501000
|
GTAT | G | 34 | a0001c0002t0022g0295a0003c0004t0004g0258a0003c0004t0004g0259others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.663+123_663+125del others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chr12 | 62501000 | |||||
| chr12:62501145
|
A | G | 1 | a0001c0003t0021g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.663+265A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 6/34 | chr12 | 62501145 | ||||||
| chr12:62501294
|
G | C | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.664-279G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 6/34 | chr12 | 62501294 | ||||||
| chr12:62502189
|
C | T | 32 | a0003c0004t0004g0258a0003c0004t0004g0259a0003c0004t0004g0260others(29): Show | 32 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.789+491C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62502189 | ||||||
| chr12:62502240
|
A | C | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.789+542A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62502240 | ||||||
| chr12:62502248
|
T | A | 1 | a0002c0001t0001g0110 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.789+550T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62502248 | ||||||
| chr12:62502343
|
C | T | 1 | a0002c0001t0006g0183 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.789+645C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62502343 | ||||||
| chr12:62502407
|
T | TA | 32 | a0001c0002t0022g0295a0003c0004t0004g0258a0003c0004t0004g0259others(29): Show | 32 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.789+723dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62502407 | |||||
| chr12:62502538
|
A | C | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.789+840A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62502538 | ||||||
| chr12:62503186
|
G | A | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+1488G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503186 | ||||||
| chr12:62503294
|
A | C | 1 | a0001c0002t0013g0303 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.789+1596A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503294 | ||||||
| chr12:62503470
|
G | A | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.789+1772G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503470 | ||||||
| chr12:62503488
|
T | C | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.789+1790T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503488 | ||||||
| chr12:62503741
|
G | C | 364 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0254others(361): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.789+2043G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503741 | ||||||
| chr12:62503800
|
G | A | 1 | a0001c0002t0002g0342 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.789+2102G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503800 | ||||||
| chr12:62503957
|
G | GAC | 35 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(32): Show | 35 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.789+2272_789+2273d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62503957 | |||||
| chr12:62504150
|
G | A | 126 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(123): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.789+2452G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504150 | ||||||
| chr12:62504216
|
C | T | 251 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(248): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.789+2518C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504216 | ||||||
| chr12:62504245
|
C | CT | 101 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0359others(98): Show | 102 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.789+2564dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62504245 | |||||
| chr12:62504245
|
CT | C | 119 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(116): Show | 121 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.789+2564delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62504245 | |||||
| chr12:62504303
|
C | T | 2 | a0001c0002t0047g0308a0001c0020t0038g0312 | 2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.789+2605C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504303 | ||||||
| chr12:62504331
|
G | A | 129 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.789+2633G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504331 | ||||||
| chr12:62504537
|
G | A | 1 | a0001c0002t0010g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.789+2839G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504537 | ||||||
| chr12:62504683
|
C | CT | 126 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(123): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.789+2992dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62504683 | |||||
| chr12:62504710
|
C | T | 126 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(123): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.789+3012C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504710 | ||||||
| chr12:62505328
|
T | C | 1 | a0004c0007t0046g0326 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.790-2958T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62505328 | ||||||
| chr12:62505433
|
G | A | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.790-2853G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62505433 | ||||||
| chr12:62505725
|
T | TA | 52 | a0001c0002t0022g0295a0001c0006t0003g0005a0001c0006t0003g0006others(49): Show | 52 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.790-2547dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62505725 | |||||
| chr12:62505726
|
A | T | 1 | a0001c0005t0003g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.790-2560A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62505726 | ||||||
| chr12:62505769
|
G | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.790-2517G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62505769 | ||||||
| chr12:62505977
|
G | A | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.790-2309G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62505977 | ||||||
| chr12:62506003
|
G | C | 1 | a0001c0003t0005g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.790-2283G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62506003 | ||||||
| chr12:62506515
|
A | T | 1 | a0001c0002t0011g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.790-1771A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62506515 | ||||||
| chr12:62506725
|
C | CA | 245 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0353others(242): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.790-1548dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62506725 | |||||
| chr12:62506748
|
A | T | 1 | a0002c0001t0001g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.790-1538A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62506748 | ||||||
| chr12:62506823
|
T | C | 5 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(2): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-1463T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62506823 | ||||||
| chr12:62506968
|
A | C | 1 | a0005c0008t0002g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.790-1318A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62506968 | ||||||
| chr12:62507016
|
A | G | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.790-1270A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507016 | ||||||
| chr12:62507069
|
T | C | 1 | a0002c0001t0006g0201 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.790-1217T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507069 | ||||||
| chr12:62507157
|
CT | C | 364 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0254others(361): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.790-1127delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62507157 | |||||
| chr12:62507259
|
A | G | 1 | a0001c0003t0041g0053 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.790-1027A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507259 | ||||||
| chr12:62507315
|
C | CT | 26 | a0001c0002t0002g0353a0001c0002t0031g0136a0001c0003t0002g0094others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.790-959dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62507315 | |||||
| chr12:62507372
|
G | A | 241 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(238): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.790-914G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507372 | ||||||
| chr12:62507754
|
T | C | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.790-532T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507754 | ||||||
| chr12:62507901
|
T | G | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.790-385T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507901 | ||||||
| chr12:62508055
|
G | A | 1 | a0001c0020t0038g0312 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.790-231G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62508055 | ||||||
| chr12:62508117
|
C | A | 1 | a0001c0003t0005g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.790-169C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62508117 | ||||||
| chr12:62508640
|
C | T | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.984+160C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62508640 | ||||||
| chr12:62508643
|
T | C | 1 | a0001c0003t0005g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.984+163T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62508643 | ||||||
| chr12:62508770
|
T | C | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.984+290T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62508770 | ||||||
| chr12:62508858
|
C | T | 1 | a0001c0005t0003g0126 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.984+378C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62508858 | ||||||
| chr12:62509053
|
A | G | 241 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(238): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.984+573A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509053 | ||||||
| chr12:62509095
|
C | T | 45 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(42): Show | 45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.984+615C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509095 | ||||||
| chr12:62509116
|
C | CT | 13 | a0001c0002t0002g0359a0001c0002t0014g0280a0001c0002t0014g0286others(10): Show | 13 | HG00099.hp2 HG00642.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.984+652dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62509116 | |||||
| chr12:62509116
|
CT | C | 7 | a0001c0002t0039g0302a0001c0003t0023g0065a0002c0001t0001g0177others(4): Show | 7 | HG00323.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+652delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62509116 | |||||
| chr12:62509184
|
G | A | 1 | a0001c0002t0022g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.984+704G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509184 | ||||||
| chr12:62509368
|
A | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.984+888A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509368 | ||||||
| chr12:62509515
|
A | T | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.984+1035A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509515 | ||||||
| chr12:62509638
|
T | C | 60 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(57): Show | 60 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.984+1158T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509638 | ||||||
| chr12:62509736
|
G | T | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.984+1256G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509736 | ||||||
| chr12:62509859
|
A | G | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.984+1379A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509859 | ||||||
| chr12:62509875
|
G | GT | 129 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0005t0043g0132others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.984+1405dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62509875 | |||||
| chr12:62510013
|
A | G | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.984+1533A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510013 | ||||||
| chr12:62510207
|
C | T | 4 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.984+1727C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510207 | ||||||
| chr12:62510472
|
C | T | 129 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.984+1992C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510472 | ||||||
| chr12:62510492
|
A | G | 2 | a0001c0002t0002g0363a0001c0002t0005g0362 | 2 | HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.984+2012A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510492 | ||||||
| chr12:62510499
|
A | G | 5 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.984+2019A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510499 | ||||||
| chr12:62510524
|
A | G | 45 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(42): Show | 45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.984+2044A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510524 | ||||||
| chr12:62510635
|
T | C | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.984+2155T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510635 | ||||||
| chr12:62510640
|
C | G | 1 | a0001c0002t0002g0305 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.984+2160C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510640 | ||||||
| chr12:62510737
|
C | T | 2 | a0001c0003t0005g0034a0001c0003t0005g0040 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.984+2257C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510737 | ||||||
| chr12:62510852
|
T | C | 5 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(2): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.984+2372T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510852 | ||||||
| chr12:62510926
|
T | G | 1 | a0001c0002t0002g0330 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.984+2446T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510926 | ||||||
| chr12:62511116
|
A | G | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.984+2636A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511116 | ||||||
| chr12:62511192
|
C | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.984+2712C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511192 | ||||||
| chr12:62511287
|
C | T | 1 | a0001c0003t0021g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.984+2807C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511287 | ||||||
| chr12:62511545
|
A | G | 60 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(57): Show | 60 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.984+3065A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511545 | ||||||
| chr12:62511600
|
CA | C | 126 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(123): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.984+3126delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62511600 | |||||
| chr12:62511719
|
G | A | 241 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(238): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.984+3239G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511719 | ||||||
| chr12:62511727
|
A | G | 1 | a0001c0003t0002g0054 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.984+3247A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511727 | ||||||
| chr12:62511909
|
T | C | 3 | a0002c0001t0001g0150a0002c0001t0001g0176a0002c0001t0001g0180 | 3 | HG02135.hp1 NA18612.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.984+3429T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511909 | ||||||
| chr12:62511943
|
G | A | 34 | a0001c0002t0022g0295a0003c0004t0004g0258a0003c0004t0004g0259others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.984+3463G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511943 | ||||||
| chr12:62511992
|
A | AC | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.984+3518dupC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62511992 | |||||
| chr12:62512048
|
G | A | 7 | a0002c0001t0001g0146a0002c0001t0001g0153a0002c0001t0001g0177others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+3568G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512048 | ||||||
| chr12:62512102
|
C | T | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.984+3622C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512102 | ||||||
| chr12:62512139
|
C | T | 1 | a0002c0001t0001g0225 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.984+3659C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512139 | ||||||
| chr12:62512538
|
T | C | 7 | a0001c0003t0005g0049a0001c0003t0005g0050a0001c0003t0005g0051others(4): Show | 7 | NA18941.hp1 NA18946.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.984+4058T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512538 | ||||||
| chr12:62512677
|
C | T | 2 | a0002c0001t0001g0208a0002c0001t0001g0211 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.984+4197C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512677 | ||||||
| chr12:62512708
|
G | A | 128 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.984+4228G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512708 | ||||||
| chr12:62512782
|
C | T | 3 | a0002c0001t0001g0208a0002c0001t0001g0211a0002c0001t0001g0212 | 3 | HG02559.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.984+4302C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512782 | ||||||
| chr12:62512851
|
T | A | 1 | a0003c0004t0004g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.984+4371T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512851 | ||||||
| chr12:62513071
|
G | A | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.984+4591G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513071 | ||||||
| chr12:62513185
|
C | G | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.984+4705C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513185 | ||||||
| chr12:62513267
|
C | T | 1 | a0002c0001t0001g0172 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.984+4787C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513267 | ||||||
| chr12:62513312
|
G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.984+4832G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513312 | ||||||
| chr12:62513328
|
T | C | 4 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.984+4848T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513328 | ||||||
| chr12:62513371
|
G | A | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.984+4891G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513371 | ||||||
| chr12:62513386
|
C | T | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.984+4906C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513386 | ||||||
| chr12:62513422
|
C | T | 152 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(149): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.984+4942C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513422 | ||||||
| chr12:62513518
|
G | A | 34 | a0001c0002t0022g0295a0003c0004t0004g0258a0003c0004t0004g0259others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.984+5038G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513518 | ||||||
| chr12:62513692
|
ATCCCAGC others(388): Show |
A | 54 | a0002c0001t0001g0002a0002c0001t0001g0110a0002c0001t0001g0142others(51): Show | 55 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.984+5215_984+5609d others(2): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62513692 | |||||
| chr12:62513752
|
G | A | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.984+5272G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513752 | ||||||
| chr12:62513842
|
G | C | 187 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(184): Show | 189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.984+5362G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513842 | ||||||
| chr12:62513888
|
T | C | 24 | a0001c0002t0031g0136a0001c0005t0003g0113a0001c0005t0003g0114others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.984+5408T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513888 | ||||||
| chr12:62513892
|
A | G | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.984+5412A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513892 | ||||||
| chr12:62513898
|
C | T | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.984+5418C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513898 | ||||||
| chr12:62513936
|
C | T | 2 | a0001c0005t0003g0111a0001c0005t0003g0112 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.984+5456C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513936 | ||||||
| chr12:62513937
|
G | A | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.984+5457G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513937 | ||||||
| chr12:62513945
|
A | G | 2 | a0001c0003t0002g0076a0001c0003t0002g0079 | 2 | NA18957.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.984+5465A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513945 | ||||||
| chr12:62513957
|
A | G | 1 | a0003c0004t0004g0274 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.984+5477A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513957 | ||||||
| chr12:62514012
|
C | T | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.984+5532C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514012 | ||||||
| chr12:62514131
|
A | G | 76 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(73): Show | 77 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.984+5651A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514131 | ||||||
| chr12:62514284
|
G | A | 1 | a0001c0005t0003g0130 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.984+5804G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514284 | ||||||
| chr12:62514540
|
C | T | 1 | a0001c0002t0002g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.984+6060C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514540 | ||||||
| chr12:62514543
|
T | C | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.984+6063T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514543 | ||||||
| chr12:62514609
|
A | G | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.984+6129A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514609 | ||||||
| chr12:62514643
|
G | A | 1 | a0002c0001t0001g0175 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.984+6163G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514643 | ||||||
| chr12:62514702
|
G | T | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.984+6222G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514702 | ||||||
| chr12:62514927
|
A | G | 1 | a0001c0002t0010g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.984+6447A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514927 | ||||||
| chr12:62515003
|
G | A | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.984+6523G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515003 | ||||||
| chr12:62515016
|
G | T | 1 | a0001c0018t0002g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.984+6536G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515016 | ||||||
| chr12:62515314
|
G | A | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.984+6834G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515314 | ||||||
| chr12:62515399
|
T | C | 45 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(42): Show | 45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.984+6919T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515399 | ||||||
| chr12:62515684
|
G | A | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.984+7204G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515684 | ||||||
| chr12:62515750
|
C | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.984+7270C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515750 | ||||||
| chr12:62515810
|
C | T | 112 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(109): Show | 113 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.984+7330C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515810 | ||||||
| chr12:62515977
|
T | A | 5 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0303others(2): Show | 5 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.984+7497T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515977 | ||||||
| chr12:62516066
|
A | G | 293 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.984+7586A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62516066 | ||||||
| chr12:62516635
|
C | T | 1 | a0001c0002t0002g0335 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.985-7880C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62516635 | ||||||
| chr12:62516934
|
A | T | 126 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0006t0003g0105others(123): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.985-7581A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62516934 | ||||||
| chr12:62517052
|
C | A | 5 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(2): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-7463C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62517052 | ||||||
| chr12:62517069
|
G | A | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-7446G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62517069 | ||||||
| chr12:62517385
|
T | C | 1 | a0001c0003t0005g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.985-7130T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62517385 | ||||||
| chr12:62517717
|
G | A | 11 | a0001c0002t0002g0318a0001c0002t0002g0323a0001c0002t0015g0314others(8): Show | 11 | HG00423.hp2 HG02027.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.985-6798G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62517717 | ||||||
| chr12:62518050
|
A | T | 2 | a0001c0003t0005g0034a0001c0003t0005g0040 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.985-6465A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518050 | ||||||
| chr12:62518204
|
A | G | 1 | a0001c0003t0002g0075 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.985-6311A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518204 | ||||||
| chr12:62518279
|
G | A | 242 | a0001c0002t0003g0102a0001c0002t0031g0136a0001c0003t0002g0054others(239): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.985-6236G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518279 | ||||||
| chr12:62518346
|
T | A | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.985-6169T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518346 | ||||||
| chr12:62518471
|
C | T | 4 | a0001c0005t0003g0128a0001c0005t0003g0129a0001c0005t0003g0134others(1): Show | 4 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-6044C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518471 | ||||||
| chr12:62518485
|
T | C | 19 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(16): Show | 19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.985-6030T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518485 | ||||||
| chr12:62518514
|
T | C | 1 | a0001c0005t0043g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.985-6001T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518514 | ||||||
| chr12:62518586
|
A | G | 3 | a0002c0001t0001g0240a0002c0001t0001g0241a0002c0001t0012g0232 | 3 | HG03669.hp2 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.985-5929A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518586 | ||||||
| chr12:62518775
|
C | T | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-5740C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518775 | ||||||
| chr12:62518951
|
A | C | 2 | a0001c0002t0013g0300a0001c0002t0026g0301 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.985-5564A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518951 | ||||||
| chr12:62519009
|
C | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.985-5506C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519009 | ||||||
| chr12:62519293
|
C | T | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.985-5222C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519293 | ||||||
| chr12:62519295
|
C | A | 1 | a0001c0002t0002g0311 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.985-5220C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519295 | ||||||
| chr12:62519308
|
A | C | 2 | a0001c0002t0002g0338a0001c0002t0002g0353 | 2 | NA18944.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.985-5207A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519308 | ||||||
| chr12:62519680
|
T | C | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.985-4835T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519680 | ||||||
| chr12:62519871
|
C | T | 1 | a0001c0002t0011g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.985-4644C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519871 | ||||||
| chr12:62519917
|
G | A | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.985-4598G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519917 | ||||||
| chr12:62519960
|
C | T | 2 | a0001c0002t0031g0136a0002c0001t0006g0197 | 2 | HG03225.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.985-4555C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519960 | ||||||
| chr12:62519981
|
A | G | 1 | a0001c0005t0043g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.985-4534A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519981 | ||||||
| chr12:62520106
|
A | G | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.985-4409A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520106 | ||||||
| chr12:62520138
|
C | G | 1 | a0003c0004t0004g0365 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.985-4377C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520138 | ||||||
| chr12:62520285
|
A | G | 4 | a0002c0001t0001g0208a0002c0001t0001g0211a0002c0001t0001g0212others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-4230A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520285 | ||||||
| chr12:62520420
|
A | G | 1 | a0002c0001t0001g0171 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.985-4095A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520420 | ||||||
| chr12:62520429
|
C | A | 20 | a0003c0004t0004g0260a0003c0004t0004g0261a0003c0004t0004g0263others(17): Show | 20 | HG00673.hp2 HG02523.hp1 HG04228.hp2 others(17): Show |
intron_variant | MODIFIER | c.985-4086C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520429 | ||||||
| chr12:62520430
|
G | A | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.985-4085G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520430 | ||||||
| chr12:62520433
|
C | CTTTG | 252 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.985-4079_985-4078i others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62520433 | |||||
| chr12:62520507
|
G | T | 241 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(238): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.985-4008G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520507 | ||||||
| chr12:62520552
|
T | A | 1 | a0002c0001t0001g0154 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.985-3963T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520552 | ||||||
| chr12:62520593
|
A | G | 56 | a0001c0002t0002g0254a0001c0002t0002g0256a0001c0002t0002g0305others(53): Show | 56 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.985-3922A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520593 | ||||||
| chr12:62520905
|
CA | C | 83 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0353others(80): Show | 84 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.985-3599delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62520905 | |||||
| chr12:62520968
|
T | C | 53 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(50): Show | 53 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-3547T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520968 | ||||||
| chr12:62520996
|
TA | T | 121 | a0001c0009t0019g0103a0001c0009t0019g0104a0002c0001t0001g0002others(118): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.985-3509delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62520996 | |||||
| chr12:62520997
|
A | T | 5 | a0001c0002t0002g0333a0001c0002t0013g0300a0001c0002t0026g0301others(2): Show | 5 | HG03486.hp1 NA18951.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-3518A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520997 | ||||||
| chr12:62521056
|
A | G | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.985-3459A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521056 | ||||||
| chr12:62521069
|
G | T | 1 | a0001c0003t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.985-3446G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521069 | ||||||
| chr12:62521177
|
A | T | 1 | a0001c0003t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.985-3338A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521177 | ||||||
| chr12:62521239
|
C | T | 42 | a0002c0001t0001g0225a0002c0001t0001g0228a0002c0001t0001g0229others(39): Show | 42 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.985-3276C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521239 | ||||||
| chr12:62521309
|
C | T | 1 | a0001c0003t0003g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.985-3206C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521309 | ||||||
| chr12:62521501
|
C | T | 1 | a0002c0001t0006g0214 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.985-3014C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521501 | ||||||
| chr12:62521971
|
T | A | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.985-2544T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521971 | ||||||
| chr12:62522091
|
G | A | 1 | a0001c0003t0003g0041 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.985-2424G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522091 | ||||||
| chr12:62522093
|
ACAAGAAT others(9): Show |
A | 24 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(21): Show | 24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.985-2420_985-2405d others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62522093 | |||||
| chr12:62522274
|
G | A | 1 | a0002c0001t0025g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.985-2241G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522274 | ||||||
| chr12:62522279
|
A | T | 1 | a0001c0002t0002g0352 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.985-2236A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522279 | ||||||
| chr12:62522364
|
G | T | 241 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(238): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.985-2151G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522364 | ||||||
| chr12:62522386
|
C | T | 3 | a0001c0003t0005g0086a0001c0003t0005g0087a0001c0003t0005g0101 | 3 | HG00597.hp2 HG00621.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.985-2129C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522386 | ||||||
| chr12:62522521
|
A | T | 1 | a0001c0003t0008g0060 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.985-1994A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522521 | ||||||
| chr12:62522650
|
T | C | 300 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(297): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.985-1865T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522650 | ||||||
| chr12:62522750
|
G | A | 1 | a0001c0002t0002g0311 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.985-1765G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522750 | ||||||
| chr12:62522770
|
A | G | 45 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(42): Show | 45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.985-1745A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522770 | ||||||
| chr12:62522774
|
C | G | 1 | a0002c0001t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.985-1741C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522774 | ||||||
| chr12:62522966
|
G | A | 8 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(5): Show | 8 | HG01891.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.985-1549G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522966 | ||||||
| chr12:62522999
|
C | T | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.985-1516C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522999 | ||||||
| chr12:62523035
|
A | G | 12 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.985-1480A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523035 | ||||||
| chr12:62523051
|
C | A | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.985-1464C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523051 | ||||||
| chr12:62523086
|
A | G | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-1429A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523086 | ||||||
| chr12:62523260
|
C | A | 4 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(1): Show | 4 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-1255C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523260 | ||||||
| chr12:62523563
|
T | A | 1 | a0001c0002t0010g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.985-952T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523563 | ||||||
| chr12:62523851
|
T | A | 119 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(116): Show | 120 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.985-664T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523851 | ||||||
| chr12:62523924
|
A | G | 119 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0110others(116): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.985-591A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523924 | ||||||
| chr12:62524058
|
A | G | 45 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(42): Show | 45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.985-457A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62524058 | ||||||
| chr12:62524390
|
G | C | 45 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(42): Show | 45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.985-125G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62524390 | ||||||
| chr12:62524725
|
C | T | 1 | a0002c0001t0012g0239 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1109+86C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 9/34 | chr12 | 62524725 | ||||||
| chr12:62524768
|
A | G | 1 | a0001c0002t0002g0310 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1109+129A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 9/34 | chr12 | 62524768 | ||||||
| chr12:62525000
|
A | G | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1110-84A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 9/34 | chr12 | 62525000 | ||||||
| chr12:62525260
|
G | A | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1246+40G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525260 | ||||||
| chr12:62525504
|
A | C | 1 | a0002c0001t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1246+284A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525504 | ||||||
| chr12:62525575
|
GTCA | G | 300 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(297): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1246+357_1246+359d others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | INFO_REALIGN_3_PRIME | chr12 | 62525575 | |||||
| chr12:62525579
|
T | C | 1 | a0001c0002t0002g0341 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1246+359T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525579 | ||||||
| chr12:62525663
|
T | C | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1247-286T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525663 | ||||||
| chr12:62525673
|
C | T | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1247-276C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525673 | ||||||
| chr12:62525717
|
C | T | 242 | a0001c0002t0003g0102a0001c0002t0031g0136a0001c0003t0002g0054others(239): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1247-232C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525717 | ||||||
| chr12:62526154
|
T | C | 1 | a0003c0004t0004g0282 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1400+52T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62526154 | ||||||
| chr12:62526328
|
C | A | 24 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(21): Show | 24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1400+226C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62526328 | ||||||
| chr12:62526853
|
A | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1400+751A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62526853 | ||||||
| chr12:62526987
|
A | T | 253 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(250): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1400+885A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62526987 | ||||||
| chr12:62527018
|
C | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1400+916C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527018 | ||||||
| chr12:62527080
|
C | G | 119 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0110others(116): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1400+978C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527080 | ||||||
| chr12:62527088
|
T | C | 24 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(21): Show | 24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1400+986T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527088 | ||||||
| chr12:62527170
|
A | G | 80 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(77): Show | 81 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1400+1068A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527170 | ||||||
| chr12:62527248
|
C | T | 1 | a0001c0002t0017g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1400+1146C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527248 | ||||||
| chr12:62527282
|
G | A | 293 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1400+1180G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527282 | ||||||
| chr12:62527477
|
C | T | 119 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0110others(116): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1400+1375C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527477 | ||||||
| chr12:62527643
|
A | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1400+1541A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527643 | ||||||
| chr12:62527676
|
C | T | 53 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(50): Show | 53 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1400+1574C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527676 | ||||||
| chr12:62527727
|
G | A | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1400+1625G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527727 | ||||||
| chr12:62527901
|
A | T | 80 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(77): Show | 81 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1400+1799A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527901 | ||||||
| chr12:62528085
|
T | C | 1 | a0002c0001t0006g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1400+1983T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528085 | ||||||
| chr12:62528198
|
A | G | 25 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0005t0003g0113others(22): Show | 25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1400+2096A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528198 | ||||||
| chr12:62528363
|
G | A | 121 | a0001c0009t0019g0103a0001c0009t0019g0104a0002c0001t0001g0002others(118): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1400+2261G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528363 | ||||||
| chr12:62528406
|
A | C | 106 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(103): Show | 107 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.1400+2304A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528406 | ||||||
| chr12:62528649
|
A | G | 24 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(21): Show | 24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1400+2547A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528649 | ||||||
| chr12:62528810
|
G | A | 1 | a0002c0001t0001g0171 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1400+2708G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528810 | ||||||
| chr12:62528975
|
A | G | 2 | a0001c0003t0005g0045a0001c0003t0005g0046 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1400+2873A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528975 | ||||||
| chr12:62528999
|
T | C | 1 | a0001c0002t0002g0330 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1400+2897T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528999 | ||||||
| chr12:62529123
|
G | A | 1 | a0001c0003t0005g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1400+3021G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62529123 | ||||||
| chr12:62529126
|
G | A | 1 | a0003c0004t0022g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1400+3024G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62529126 | ||||||
| chr12:62529560
|
T | C | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1401-2878T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62529560 | ||||||
| chr12:62529891
|
G | A | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1401-2547G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62529891 | ||||||
| chr12:62530049
|
T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1401-2389T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530049 | ||||||
| chr12:62530057
|
C | T | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1401-2381C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530057 | ||||||
| chr12:62530175
|
A | G | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1401-2263A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530175 | ||||||
| chr12:62530227
|
A | AT | 23 | a0001c0002t0002g0332a0001c0002t0002g0341a0001c0002t0002g0358others(20): Show | 23 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1401-2190dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr12 | 62530227 | |||||
| chr12:62530227
|
AT | A | 45 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0027others(42): Show | 45 | HG01074.hp1 HG01099.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.1401-2190delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr12 | 62530227 | |||||
| chr12:62530262
|
G | A | 1 | a0001c0005t0003g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1401-2176G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530262 | ||||||
| chr12:62530316
|
T | C | 14 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(11): Show | 14 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1401-2122T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530316 | ||||||
| chr12:62530520
|
C | T | 2 | a0001c0002t0013g0300a0001c0002t0026g0301 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1401-1918C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530520 | ||||||
| chr12:62530784
|
C | G | 1 | a0003c0004t0004g0281 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1401-1654C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530784 | ||||||
| chr12:62530850
|
A | G | 2 | a0002c0001t0001g0242a0002c0001t0001g0243 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1401-1588A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530850 | ||||||
| chr12:62530970
|
TC | T | 4 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401-1465delC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr12 | 62530970 | |||||
| chr12:62531285
|
C | T | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1401-1153C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62531285 | ||||||
| chr12:62531292
|
C | G | 1 | a0002c0001t0001g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1401-1146C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62531292 | ||||||
| chr12:62531490
|
C | T | 293 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1401-948C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62531490 | ||||||
| chr12:62531962
|
G | A | 1 | a0001c0002t0017g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1401-476G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62531962 | ||||||
| chr12:62532004
|
C | T | 34 | a0001c0002t0022g0295a0003c0004t0004g0258a0003c0004t0004g0259others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1401-434C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62532004 | ||||||
| chr12:62532167
|
A | G | 2 | a0001c0003t0005g0045a0001c0003t0005g0046 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1401-271A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62532167 | ||||||
| chr12:62532169
|
G | A | 1 | a0001c0003t0005g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1401-269G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62532169 | ||||||
| chr12:62532229
|
G | T | 1 | a0001c0005t0003g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1401-209G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62532229 | ||||||
| chr12:62532337
|
G | A | 4 | a0001c0006t0007g0012a0001c0006t0007g0013a0001c0006t0007g0014others(1): Show | 4 | HG01099.hp1 HG02559.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401-101G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62532337 | ||||||
| chr12:62532993
|
G | C | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(66): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1633+323G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62532993 | ||||||
| chr12:62533243
|
A | G | 1 | a0001c0005t0003g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1633+573A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533243 | ||||||
| chr12:62533292
|
T | G | 11 | a0003c0004t0004g0258a0003c0004t0004g0259a0003c0004t0004g0281others(8): Show | 11 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.1633+622T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533292 | ||||||
| chr12:62533378
|
A | G | 1 | a0002c0015t0024g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1633+708A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533378 | ||||||
| chr12:62533765
|
G | C | 241 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(238): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1634-1080G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533765 | ||||||
| chr12:62533783
|
C | T | 4 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0028others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634-1062C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533783 | ||||||
| chr12:62533822
|
T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1634-1023T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533822 | ||||||
| chr12:62533915
|
A | G | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1634-930A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533915 | ||||||
| chr12:62534218
|
C | T | 1 | a0001c0003t0050g0077 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1634-627C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534218 | ||||||
| chr12:62534226
|
T | TA | 148 | a0001c0003t0005g0037a0001c0003t0005g0038a0001c0003t0005g0039others(145): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1634-608dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534226 | |||||
| chr12:62534404
|
A | G | 1 | a0007c0021t0001g0337 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1634-441A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534404 | ||||||
| chr12:62534465
|
G | A | 4 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(1): Show | 4 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-380G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534465 | ||||||
| chr12:62534517
|
G | T | 241 | a0001c0002t0031g0136a0001c0003t0002g0054a0001c0003t0002g0055others(238): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1634-328G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534517 | ||||||
| chr12:62534518
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0002t0011g0255a0001c0002t0011g0257a0001c0002t0011g0307others(3): Show | 6 | HG01167.hp2 HG02004.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-310_1634-302d others(11): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534518 | |||||
| chr12:62534518
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0001t0001g0227 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1634-311_1634-302d others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534518 | |||||
| chr12:62534531
|
A | T | 6 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(3): Show | 6 | HG02055.hp2 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-314A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534531 | ||||||
| chr12:62534532
|
A | T | 15 | a0001c0003t0005g0051a0001c0003t0005g0052a0001c0003t0005g0064others(12): Show | 15 | HG00140.hp1 NA18941.hp1 NA18945.hp1 others(12): Show |
intron_variant | MODIFIER | c.1634-313A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534532 | ||||||
| chr12:62534532
|
AAAAAAAA others(5): Show |
A | 6 | a0002c0001t0001g0171a0002c0001t0001g0229a0002c0001t0001g0236others(3): Show | 6 | HG00733.hp1 HG01257.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1634-311_1634-300d others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534532 | |||||
| chr12:62534533
|
A | AATATATA others(3): Show |
7 | a0001c0006t0007g0011a0001c0006t0007g0015a0001c0006t0007g0016others(4): Show | 7 | HG01099.hp1 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-311_1634-310i others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534533 | |||||
| chr12:62534533
|
A | ATATATAT others(8): Show |
1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1634-312_1634-311i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534533 | ||||||
| chr12:62534533
|
A | T | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1634-312A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534533 | ||||||
| chr12:62534533
|
AAAAAAAA others(4): Show |
A | 9 | a0001c0003t0003g0036a0002c0001t0001g0153a0002c0001t0001g0169others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1634-310_1634-300d others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534533 | |||||
| chr12:62534533
|
AAAAAAAA others(6): Show |
A | 3 | a0001c0009t0019g0103a0001c0009t0019g0104a0002c0001t0001g0144 | 3 | HG01081.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1634-310_1634-298d others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534533 | |||||
| chr12:62534534
|
A | AT | 3 | a0001c0003t0005g0057a0001c0003t0005g0078a0001c0003t0005g0080 | 3 | HG00639.hp2 HG03704.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1634-311_1634-310i others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534534 | ||||||
| chr12:62534534
|
A | ATATATAT others(4): Show |
1 | a0002c0001t0012g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1634-311_1634-310i others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534534 | ||||||
| chr12:62534534
|
A | T | 35 | a0001c0002t0003g0102a0001c0003t0002g0084a0001c0003t0005g0034others(32): Show | 35 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1634-311A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534534 | ||||||
| chr12:62534534
|
AAAAAAAA others(3): Show |
A | 32 | a0002c0001t0001g0002a0002c0001t0001g0147a0002c0001t0001g0148others(29): Show | 33 | HG00544.hp2 HG00597.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.1634-309_1634-300d others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534534 | |||||
| chr12:62534534
|
AAAAAAAA others(5): Show |
A | 58 | a0002c0001t0001g0003a0002c0001t0001g0110a0002c0001t0001g0142others(55): Show | 59 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1634-309_1634-298d others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534534 | |||||
| chr12:62534534
|
AAAAAAAA others(7): Show |
A | 1 | a0002c0001t0012g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1634-309_1634-296d others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534534 | |||||
| chr12:62534535
|
A | AATATATA others(3): Show |
3 | a0001c0006t0007g0012a0001c0006t0007g0013a0001c0006t0007g0014 | 3 | HG02559.hp1 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1634-309_1634-308i others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534535 | |||||
| chr12:62534535
|
A | T | 20 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(17): Show | 20 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1634-310A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534535 | ||||||
| chr12:62534535
|
AAAAAAAA others(4): Show |
A | 4 | a0001c0003t0003g0035a0001c0005t0003g0128a0001c0005t0003g0129others(1): Show | 4 | HG00323.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-308_1634-298d others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534535 | |||||
| chr12:62534536
|
A | T | 65 | a0001c0002t0003g0102a0001c0003t0002g0054a0001c0003t0002g0055others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1634-309A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534536 | ||||||
| chr12:62534536
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0005t0003g0131 | 3 | HG02615.hp2 HG02723.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1634-307_1634-298d others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534536 | |||||
| chr12:62534536
|
AAAAAAAA others(5): Show |
A | 3 | a0002c0001t0001g0155a0002c0001t0001g0203a0002c0001t0006g0201 | 3 | HG00280.hp2 HG02071.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1634-307_1634-296d others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534536 | |||||
| chr12:62534537
|
A | T | 23 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(20): Show | 23 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1634-308A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534537 | ||||||
| chr12:62534537
|
AAAAAAAT others(4): Show |
A | 20 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0005t0003g0115others(17): Show | 20 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1634-306_1634-296d others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534537 | |||||
| chr12:62534538
|
A | T | 71 | a0001c0002t0003g0102a0001c0003t0002g0054a0001c0003t0002g0055others(68): Show | 71 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1634-307A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534538 | ||||||
| chr12:62534538
|
AAAAAATA others(3): Show |
A | 2 | a0001c0005t0003g0113a0001c0005t0003g0114 | 2 | HG01081.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1634-305_1634-296d others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534538 | |||||
| chr12:62534539
|
A | T | 23 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(20): Show | 23 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1634-306A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534539 | ||||||
| chr12:62534540
|
A | AT | 16 | a0001c0002t0002g0324a0001c0002t0002g0331a0001c0002t0002g0332others(13): Show | 16 | HG00642.hp2 HG01255.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1634-305_1634-304i others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534540 | ||||||
| chr12:62534540
|
A | ATATATAT others(6): Show |
2 | a0003c0004t0004g0284a0003c0004t0004g0365 | 2 | HG00639.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1634-305_1634-304i others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534540 | ||||||
| chr12:62534540
|
A | ATATATAT others(11): Show |
1 | a0003c0004t0004g0274 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1634-305_1634-304i others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534540 | ||||||
| chr12:62534540
|
A | ATATATAT others(7): Show |
4 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634-305_1634-304i others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534540 | ||||||
| chr12:62534540
|
A | T | 77 | a0001c0002t0002g0318a0001c0002t0002g0322a0001c0002t0002g0325others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1634-305A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534540 | ||||||
| chr12:62534541
|
A | T | 20 | a0001c0002t0002g0310a0001c0006t0003g0005a0001c0006t0003g0006others(17): Show | 20 | HG01099.hp1 HG01099.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1634-304A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534541 | ||||||
| chr12:62534542
|
A | AAAAAAAA others(98): Show |
1 | a0001c0002t0035g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(107): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAAAA others(22): Show |
1 | a0001c0002t0037g0304 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(31): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAAAA others(62): Show |
1 | a0001c0002t0017g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(71): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAAAA others(64): Show |
1 | a0001c0002t0017g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(73): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAAAA others(37): Show |
1 | a0001c0002t0010g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(46): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAAAA others(62): Show |
1 | a0001c0002t0010g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(71): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAAAA others(13): Show |
1 | a0001c0002t0026g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAAAA others(59): Show |
1 | a0001c0002t0017g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(68): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAAAT others(8): Show |
1 | a0001c0002t0014g0280 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAAAT others(54): Show |
1 | a0001c0002t0010g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(63): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAAAT others(56): Show |
1 | a0001c0002t0002g0030 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(65): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAATA others(7): Show |
1 | a0001c0002t0014g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAATA others(15): Show |
2 | a0001c0002t0013g0299a0001c0002t0013g0300 | 2 | HG02004.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1634-302_1634-301i others(24): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAATA others(17): Show |
1 | a0001c0002t0039g0302 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(26): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAATA others(23): Show |
1 | a0001c0002t0013g0298 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(32): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAATA others(57): Show |
1 | a0001c0002t0010g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(66): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAAAATA others(55): Show |
1 | a0001c0002t0002g0026 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(64): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAATATA others(3): Show |
2 | a0001c0002t0020g0285a0001c0002t0020g0289 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1634-302_1634-301i others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAAATATA others(7): Show |
2 | a0001c0002t0014g0288a0003c0004t0004g0276 | 2 | NA19077.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1634-302_1634-301i others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAATATAT others(6): Show |
5 | a0001c0002t0014g0286a0003c0004t0004g0258a0003c0004t0004g0259others(2): Show | 5 | HG00099.hp2 HG01074.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634-302_1634-301i others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAATATAT others(8): Show |
4 | a0003c0004t0004g0263a0003c0004t0004g0275a0003c0004t0004g0279others(1): Show | 4 | HG02523.hp1 NA18967.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-302_1634-301i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AAATATAT others(24): Show |
1 | a0003c0004t0004g0282 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(33): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AATATATA others(7): Show |
1 | a0003c0004t0004g0267 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1634-290_1634-277d others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AATATATA others(9): Show |
1 | a0003c0004t0004g0273 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1634-292_1634-277d others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | AATATATA others(13): Show |
1 | a0003c0004t0022g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1634-296_1634-277d others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | |||||
| chr12:62534542
|
A | ATATATAT others(6): Show |
1 | a0003c0004t0004g0281 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1634-303_1634-302i others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | ||||||
| chr12:62534542
|
A | ATATATAT others(8): Show |
5 | a0003c0004t0004g0261a0003c0004t0004g0265a0003c0004t0004g0270others(2): Show | 5 | NA18975.hp1 NA18983.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634-303_1634-302i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | ||||||
| chr12:62534542
|
A | ATATATAT others(10): Show |
6 | a0003c0004t0004g0264a0003c0004t0004g0266a0003c0004t0004g0290others(3): Show | 6 | HG00280.hp1 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-303_1634-302i others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | ||||||
| chr12:62534542
|
A | ATATATAT others(12): Show |
3 | a0003c0004t0004g0268a0003c0004t0004g0269a0003c0004t0004g0272 | 3 | HG03239.hp1 NA18944.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1634-303_1634-302i others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | ||||||
| chr12:62534542
|
A | ATATATAT others(16): Show |
1 | a0003c0004t0004g0271 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1634-303_1634-302i others(25): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | ||||||
| chr12:62534542
|
A | ATATATAT others(44): Show |
1 | a0001c0002t0002g0310 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1634-303_1634-302i others(53): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | ||||||
| chr12:62534542
|
A | ATATATAT others(7): Show |
1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1634-303_1634-302i others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | ||||||
| chr12:62534542
|
A | ATATATAT others(5): Show |
6 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(3): Show | 6 | HG02572.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-303_1634-302i others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | ||||||
| chr12:62534542
|
A | T | 128 | a0001c0002t0002g0256a0001c0002t0002g0305a0001c0002t0002g0317others(125): Show | 128 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1634-303A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | ||||||
| chr12:62534543
|
A | AATATATA others(21): Show |
1 | a0001c0002t0002g0335 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(30): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534543 | ||||||
| chr12:62534543
|
A | ATATATAT others(8): Show |
1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1634-289_1634-288i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534543 | |||||
| chr12:62534543
|
A | ATATATAT others(35): Show |
1 | a0002c0001t0001g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1634-289_1634-288i others(44): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534543 | |||||
| chr12:62534543
|
A | T | 13 | a0001c0002t0002g0310a0001c0006t0007g0009a0001c0006t0007g0011others(10): Show | 13 | HG01099.hp1 HG01099.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1634-302A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534543 | ||||||
| chr12:62534544
|
T | A | 3 | a0001c0002t0013g0303a0006c0010t0002g0336a0006c0010t0002g0350 | 3 | HG01256.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1634-301T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534544 | ||||||
| chr12:62534545
|
A | ATATATAT others(50): Show |
1 | a0001c0003t0005g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1634-285_1634-284i others(59): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534545 | |||||
| chr12:62534545
|
A | ATATATAT others(33): Show |
1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1634-287_1634-286i others(42): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534545 | |||||
| chr12:62534545
|
A | ATATATAT others(6): Show |
3 | a0002c0001t0001g0137a0002c0001t0001g0238a0002c0001t0030g0139 | 3 | HG03098.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1634-289_1634-288i others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534545 | |||||
| chr12:62534545
|
A | ATATATAT others(31): Show |
1 | a0002c0001t0001g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1634-289_1634-288i others(40): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534545 | |||||
| chr12:62534546
|
T | A | 1 | a0001c0002t0013g0303 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1634-299T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534546 | ||||||
| chr12:62534547
|
A | ATATATAT others(43): Show |
2 | a0006c0010t0002g0336a0006c0010t0002g0350 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1634-261_1634-260i others(52): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(12): Show |
1 | a0001c0003t0003g0042 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1634-281_1634-280i others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(52): Show |
2 | a0001c0003t0002g0069a0001c0003t0002g0075 | 2 | NA18987.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1634-281_1634-280i others(61): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(69): Show |
1 | a0001c0003t0005g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1634-283_1634-282i others(78): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(58): Show |
1 | a0001c0003t0008g0062 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1634-285_1634-284i others(67): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(56): Show |
1 | a0001c0003t0008g0060 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1634-285_1634-284i others(65): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(54): Show |
6 | a0001c0003t0008g0059a0001c0003t0008g0061a0001c0003t0008g0073others(3): Show | 6 | NA18945.hp1 NA18955.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1634-285_1634-284i others(63): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(50): Show |
1 | a0001c0003t0008g0083 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1634-285_1634-284i others(59): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(48): Show |
14 | a0001c0003t0002g0054a0001c0003t0002g0067a0001c0003t0002g0068others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1634-285_1634-284i others(57): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(46): Show |
3 | a0001c0003t0005g0066a0001c0003t0005g0097a0001c0003t0050g0077 | 3 | HG02074.hp1 HG02165.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1634-285_1634-284i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(48): Show |
1 | a0001c0003t0005g0086 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1634-285_1634-284i others(57): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(46): Show |
2 | a0001c0003t0002g0076a0001c0003t0002g0079 | 2 | NA18957.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1634-285_1634-284i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534547
|
A | ATATATAT others(46): Show |
1 | a0001c0003t0005g0057 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1634-287_1634-286i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | |||||
| chr12:62534548
|
T | A | 1 | a0001c0002t0013g0303 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1634-297T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534548 | ||||||
| chr12:62534549
|
A | ATATATAT others(50): Show |
2 | a0001c0003t0005g0045a0001c0003t0005g0046 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1634-281_1634-280i others(59): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | |||||
| chr12:62534549
|
A | ATATATAT others(143): Show |
3 | a0001c0003t0005g0037a0001c0003t0005g0038a0001c0003t0005g0039 | 3 | HG02258.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1634-283_1634-282i others(152): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | |||||
| chr12:62534549
|
A | ATATATAT others(48): Show |
4 | a0001c0003t0005g0049a0001c0003t0005g0050a0001c0003t0005g0092others(1): Show | 4 | NA18946.hp2 NA18973.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-283_1634-282i others(57): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | |||||
| chr12:62534549
|
A | ATATATAT others(46): Show |
1 | a0001c0003t0005g0052 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1634-283_1634-282i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | |||||
| chr12:62534549
|
A | ATATATAT others(46): Show |
2 | a0001c0003t0005g0034a0001c0003t0005g0040 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1634-283_1634-282i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | |||||
| chr12:62534549
|
A | ATATATAT others(52): Show |
2 | a0001c0003t0008g0058a0001c0003t0008g0063 | 2 | NA18994.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1634-285_1634-284i others(61): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | |||||
| chr12:62534549
|
A | ATATATAT others(46): Show |
2 | a0001c0003t0005g0087a0001c0003t0005g0091 | 2 | HG00621.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1634-285_1634-284i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | |||||
| chr12:62534549
|
A | ATATATAT others(44): Show |
1 | a0001c0003t0005g0072 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1634-285_1634-284i others(53): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | |||||
| chr12:62534549
|
A | ATATATAT others(44): Show |
2 | a0001c0003t0005g0078a0001c0003t0005g0080 | 2 | HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1634-287_1634-286i others(53): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | |||||
| chr12:62534551
|
A | ATATATAT others(74): Show |
1 | a0001c0002t0010g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1634-277_1634-276i others(83): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534551 | |||||
| chr12:62534551
|
A | ATATATAT others(46): Show |
1 | a0001c0003t0005g0051 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1634-283_1634-282i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534551 | |||||
| chr12:62534551
|
A | ATATATAT others(44): Show |
5 | a0001c0003t0002g0055a0001c0003t0002g0071a0001c0003t0002g0082others(2): Show | 5 | HG01192.hp2 HG01496.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1634-285_1634-284i others(53): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534551 | |||||
| chr12:62534551
|
A | ATATATAT others(42): Show |
1 | a0001c0003t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1634-287_1634-286i others(51): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534551 | |||||
| chr12:62534551
|
A | ATTT | 6 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0029others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-293_1634-292i others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534551 | |||||
| chr12:62534552
|
T | TATATTTT others(15): Show |
1 | a0002c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1634-289_1634-288i others(24): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534552 | |||||
| chr12:62534553
|
A | ATTT | 4 | a0001c0002t0010g0027a0001c0002t0010g0028a0001c0002t0017g0032others(1): Show | 4 | HG01109.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-291_1634-290i others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534553 | |||||
| chr12:62534553
|
A | T | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1634-292A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534553 | ||||||
| chr12:62534569
|
T | A | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1634-276T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534569 | ||||||
| chr12:62534672
|
G | A | 11 | a0001c0002t0002g0318a0001c0002t0002g0323a0001c0002t0015g0314others(8): Show | 11 | HG00423.hp2 HG02027.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1634-173G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534672 | ||||||
| chr12:62534959
|
G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1715+33G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/34 | chr12 | 62534959 | ||||||
| chr12:62534967
|
TA | T | 364 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0254others(361): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1715+49delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr12 | 62534967 | |||||
| chr12:62535038
|
T | C | 2 | a0001c0003t0002g0069a0001c0003t0002g0075 | 2 | NA18987.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1715+112T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/34 | chr12 | 62535038 | ||||||
| chr12:62535242
|
T | C | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1716-283T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/34 | chr12 | 62535242 | ||||||
| chr12:62535248
|
G | A | 1 | a0002c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1716-277G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/34 | chr12 | 62535248 | ||||||
| chr12:62535884
|
G | T | 4 | a0001c0005t0003g0120a0001c0005t0003g0122a0001c0005t0003g0123others(1): Show | 4 | HG01255.hp1 HG02602.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1900+175G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62535884 | ||||||
| chr12:62535947
|
A | G | 1 | a0001c0003t0005g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1900+238A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62535947 | ||||||
| chr12:62536008
|
A | G | 1 | a0001c0006t0003g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1900+299A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536008 | ||||||
| chr12:62536047
|
G | C | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1900+338G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536047 | ||||||
| chr12:62536051
|
A | G | 1 | a0001c0003t0003g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1900+342A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536051 | ||||||
| chr12:62536053
|
A | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1900+344A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536053 | ||||||
| chr12:62536109
|
G | A | 1 | a0004c0007t0002g0327 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1900+400G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536109 | ||||||
| chr12:62536203
|
A | T | 1 | a0009c0019t0003g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1900+494A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536203 | ||||||
| chr12:62536224
|
A | AT | 173 | a0001c0002t0002g0030a0001c0002t0003g0102a0001c0002t0031g0136others(170): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1900+524dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr12 | 62536224 | |||||
| chr12:62536269
|
T | C | 1 | a0001c0002t0047g0308 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1900+560T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536269 | ||||||
| chr12:62536309
|
A | T | 7 | a0001c0003t0005g0049a0001c0003t0005g0050a0001c0003t0005g0051others(4): Show | 7 | NA18941.hp1 NA18946.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.1900+600A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536309 | ||||||
| chr12:62536484
|
T | C | 1 | a0001c0002t0002g0311 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1901-667T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536484 | ||||||
| chr12:62536506
|
T | C | 1 | a0001c0002t0035g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1901-645T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536506 | ||||||
| chr12:62536550
|
A | C | 2 | a0001c0005t0003g0128a0001c0005t0003g0129 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1901-601A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536550 | ||||||
| chr12:62536694
|
G | GTT | 24 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(21): Show | 24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1901-445_1901-444d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr12 | 62536694 | |||||
| chr12:62536775
|
G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1901-376G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536775 | ||||||
| chr12:62536780
|
C | G | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1901-371C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536780 | ||||||
| chr12:62536800
|
TG | T | 3 | a0002c0001t0006g0143a0002c0001t0006g0187a0002c0001t0006g0195 | 3 | NA19057.hp1 NA19060.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1901-350delG | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536800 | ||||||
| chr12:62536823
|
A | G | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1901-328A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536823 | ||||||
| chr12:62536841
|
G | A | 122 | a0001c0002t0003g0102a0001c0009t0019g0103a0001c0009t0019g0104others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1901-310G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536841 | ||||||
| chr12:62537018
|
C | T | 122 | a0001c0002t0003g0102a0001c0009t0019g0103a0001c0009t0019g0104others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1901-133C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62537018 | ||||||
| chr12:62537303
|
C | G | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.2013+40C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/34 | chr12 | 62537303 | ||||||
| chr12:62537376
|
A | C | 3 | a0002c0001t0001g0142a0002c0001t0001g0167a0002c0001t0001g0168 | 3 | HG00673.hp1 NA18954.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2013+113A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/34 | chr12 | 62537376 | ||||||
| chr12:62537418
|
A | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2013+155A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/34 | chr12 | 62537418 | ||||||
| chr12:62537515
|
C | A | 1 | a0001c0002t0015g0314 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2014-87C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/34 | chr12 | 62537515 | ||||||
| chr12:62537531
|
G | T | 4 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(1): Show | 4 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2014-71G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/34 | chr12 | 62537531 | ||||||
| chr12:62537870
|
G | A | 1 | a0001c0003t0005g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2118+164G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/34 | chr12 | 62537870 | ||||||
| chr12:62537910
|
T | G | 26 | a0001c0002t0031g0136a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.2119-186T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/34 | chr12 | 62537910 | ||||||
| chr12:62537951
|
A | T | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2119-145A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/34 | chr12 | 62537951 | ||||||
| chr12:62538003
|
G | C | 24 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(21): Show | 24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2119-93G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/34 | chr12 | 62538003 | ||||||
| chr12:62538066
|
ATTTGT | A | 122 | a0001c0002t0003g0102a0001c0009t0019g0103a0001c0009t0019g0104others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2119-25_2119-21del others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr12 | 62538066 | |||||
| chr12:62538249
|
C | A | 24 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(21): Show | 24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.2200-3C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 17/34 | chr12 | 62538249 | ||||||
| chr12:62538598
|
A | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2364+93A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62538598 | ||||||
| chr12:62538646
|
T | C | 80 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(77): Show | 81 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2364+141T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62538646 | ||||||
| chr12:62538828
|
AT | A | 25 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0005t0003g0113others(22): Show | 25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2364+326delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr12 | 62538828 | |||||
| chr12:62538997
|
G | A | 173 | a0001c0002t0003g0102a0001c0002t0031g0136a0001c0005t0003g0111others(170): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2364+492G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62538997 | ||||||
| chr12:62539006
|
G | T | 1 | a0002c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2364+501G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539006 | ||||||
| chr12:62539036
|
A | G | 119 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0110others(116): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2364+531A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539036 | ||||||
| chr12:62539090
|
A | G | 300 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(297): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2364+585A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539090 | ||||||
| chr12:62539246
|
A | G | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2364+741A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539246 | ||||||
| chr12:62539298
|
C | T | 1 | a0001c0006t0003g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2364+793C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539298 | ||||||
| chr12:62539337
|
G | A | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2364+832G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539337 | ||||||
| chr12:62539420
|
C | T | 1 | a0001c0006t0007g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2364+915C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539420 | ||||||
| chr12:62539513
|
C | T | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2364+1008C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539513 | ||||||
| chr12:62539537
|
G | GATTACAG others(18): Show |
1 | a0002c0001t0001g0150 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2364+1033_2364+105 others(29): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr12 | 62539537 | |||||
| chr12:62539557
|
G | A | 1 | a0001c0005t0003g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2364+1052G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539557 | ||||||
| chr12:62539558
|
C | T | 1 | a0005c0008t0002g0340 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2364+1053C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539558 | ||||||
| chr12:62539754
|
C | T | 1 | a0001c0003t0005g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2364+1249C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539754 | ||||||
| chr12:62539901
|
G | A | 1 | a0002c0001t0001g0247 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2364+1396G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539901 | ||||||
| chr12:62539984
|
T | A | 1 | a0001c0006t0003g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2364+1479T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539984 | ||||||
| chr12:62540037
|
T | C | 1 | a0002c0001t0012g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2364+1532T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62540037 | ||||||
| chr12:62540259
|
G | A | 21 | a0001c0002t0002g0310a0001c0002t0002g0329a0001c0002t0002g0332others(18): Show | 21 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.2364+1754G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62540259 | ||||||
| chr12:62540662
|
G | A | 173 | a0001c0002t0003g0102a0001c0002t0031g0136a0001c0005t0003g0111others(170): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2364+2157G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62540662 | ||||||
| chr12:62540805
|
A | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2365-2292A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62540805 | ||||||
| chr12:62541046
|
G | A | 1 | a0003c0004t0004g0297 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2365-2051G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541046 | ||||||
| chr12:62541066
|
T | C | 1 | a0001c0006t0007g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2365-2031T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541066 | ||||||
| chr12:62541170
|
C | T | 1 | a0001c0002t0002g0311 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2365-1927C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541170 | ||||||
| chr12:62541374
|
C | CA | 9 | a0001c0002t0002g0358a0001c0003t0003g0041a0001c0003t0003g0042others(6): Show | 10 | HG01069.hp1 HG01071.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.2365-1705dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr12 | 62541374 | |||||
| chr12:62541374
|
CA | C | 120 | a0001c0002t0002g0305a0001c0002t0003g0102a0001c0002t0014g0286others(117): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.2365-1705delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr12 | 62541374 | |||||
| chr12:62541464
|
A | C | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.2365-1633A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541464 | ||||||
| chr12:62541542
|
A | G | 1 | a0001c0005t0003g0122 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2365-1555A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541542 | ||||||
| chr12:62541557
|
G | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2365-1540G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541557 | ||||||
| chr12:62541645
|
G | A | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.2365-1452G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541645 | ||||||
| chr12:62541863
|
G | A | 30 | a0001c0002t0022g0295a0003c0004t0004g0258a0003c0004t0004g0259others(27): Show | 30 | HG00639.hp1 HG00673.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2365-1234G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541863 | ||||||
| chr12:62541908
|
A | G | 11 | a0001c0002t0002g0318a0001c0002t0002g0323a0001c0002t0015g0314others(8): Show | 11 | HG00423.hp2 HG02027.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.2365-1189A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541908 | ||||||
| chr12:62541925
|
C | T | 119 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0110others(116): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2365-1172C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541925 | ||||||
| chr12:62541931
|
A | G | 1 | a0003c0004t0004g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2365-1166A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541931 | ||||||
| chr12:62542087
|
A | G | 2 | a0002c0001t0001g0003a0002c0001t0001g0237 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2365-1010A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542087 | ||||||
| chr12:62542151
|
T | C | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2365-946T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542151 | ||||||
| chr12:62542222
|
C | T | 15 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(12): Show | 15 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2365-875C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542222 | ||||||
| chr12:62542254
|
A | G | 1 | a0002c0001t0012g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2365-843A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542254 | ||||||
| chr12:62542387
|
A | G | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2365-710A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542387 | ||||||
| chr12:62542486
|
A | G | 292 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(289): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2365-611A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542486 | ||||||
| chr12:62542633
|
G | A | 1 | a0001c0002t0013g0298 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2365-464G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542633 | ||||||
| chr12:62542974
|
C | T | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2365-123C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542974 | ||||||
| chr12:62543204
|
TTC | T | 10 | a0001c0006t0007g0010a0001c0006t0007g0011a0001c0006t0007g0012others(7): Show | 10 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2466+10_2466+11del others(2): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr12 | 62543204 | |||||
| chr12:62543220
|
T | C | 1 | a0002c0001t0006g0198 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2466+22T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543220 | ||||||
| chr12:62543318
|
G | A | 1 | a0002c0001t0009g0193 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2466+120G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543318 | ||||||
| chr12:62543364
|
G | T | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2466+166G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543364 | ||||||
| chr12:62543408
|
A | G | 1 | a0001c0002t0014g0288 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2466+210A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543408 | ||||||
| chr12:62543479
|
A | G | 139 | a0001c0002t0011g0255a0001c0002t0011g0257a0001c0002t0011g0307others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2466+281A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543479 | ||||||
| chr12:62543568
|
T | G | 129 | a0001c0002t0002g0329a0001c0002t0003g0102a0001c0002t0013g0298others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2466+370T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543568 | ||||||
| chr12:62543609
|
C | T | 213 | a0001c0002t0002g0321a0001c0002t0010g0023a0001c0002t0010g0027others(210): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2466+411C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543609 | ||||||
| chr12:62543677
|
G | A | 3 | a0001c0003t0005g0037a0001c0003t0005g0038a0001c0003t0005g0039 | 3 | HG02258.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2466+479G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543677 | ||||||
| chr12:62543691
|
G | A | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2466+493G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543691 | ||||||
| chr12:62543752
|
C | T | 147 | a0001c0002t0002g0256a0001c0002t0010g0027a0001c0002t0031g0136others(144): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.2466+554C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543752 | ||||||
| chr12:62543992
|
T | C | 1 | a0002c0001t0006g0206 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2466+794T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543992 | ||||||
| chr12:62544114
|
T | C | 1 | a0001c0003t0003g0042 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2467-784T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544114 | ||||||
| chr12:62544250
|
G | T | 2 | a0003c0004t0004g0277a0003c0004t0004g0278 | 2 | NA18975.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.2467-648G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544250 | ||||||
| chr12:62544258
|
A | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2467-640A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544258 | ||||||
| chr12:62544291
|
A | G | 1 | a0009c0019t0003g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2467-607A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544291 | ||||||
| chr12:62544498
|
C | G | 1 | a0002c0001t0001g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2467-400C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544498 | ||||||
| chr12:62544846
|
T | G | 1 | a0001c0020t0038g0312 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2467-52T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544846 | ||||||
| chr12:62544847
|
G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2467-51G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544847 | ||||||
| chr12:62545249
|
C | A | 2 | a0002c0001t0001g0242a0002c0001t0001g0243 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2577+241C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545249 | ||||||
| chr12:62545275
|
T | C | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2577+267T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545275 | ||||||
| chr12:62545611
|
T | C | 364 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0254others(361): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.2577+603T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545611 | ||||||
| chr12:62545612
|
G | A | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2577+604G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545612 | ||||||
| chr12:62545630
|
C | G | 1 | a0001c0002t0014g0288 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2577+622C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545630 | ||||||
| chr12:62545693
|
T | TAATAACC others(310): Show |
2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2577+698_2577+699i others(319): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr12 | 62545693 | |||||
| chr12:62545777
|
C | A | 225 | a0001c0002t0003g0102a0001c0002t0013g0298a0001c0002t0013g0299others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2577+769C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545777 | ||||||
| chr12:62545853
|
A | G | 1 | a0003c0004t0004g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2577+845A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545853 | ||||||
| chr12:62545893
|
A | G | 1 | a0001c0005t0003g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2577+885A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545893 | ||||||
| chr12:62546087
|
G | T | 2 | a0002c0001t0009g0193a0002c0001t0009g0194 | 2 | HG00733.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2578-810G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62546087 | ||||||
| chr12:62546149
|
C | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2578-748C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62546149 | ||||||
| chr12:62546329
|
C | T | 1 | a0001c0003t0005g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2578-568C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62546329 | ||||||
| chr12:62546476
|
G | A | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2578-421G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62546476 | ||||||
| chr12:62546568
|
A | G | 1 | a0002c0001t0001g0154 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2578-329A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62546568 | ||||||
| chr12:62547141
|
A | G | 1 | a0001c0003t0050g0077 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2753+69A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547141 | ||||||
| chr12:62547289
|
G | A | 2 | a0002c0001t0001g0154a0002c0001t0001g0205 | 2 | NA18956.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2753+217G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547289 | ||||||
| chr12:62547646
|
T | C | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2753+574T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547646 | ||||||
| chr12:62547664
|
A | G | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2753+592A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547664 | ||||||
| chr12:62547718
|
A | G | 3 | a0001c0003t0002g0055a0001c0003t0002g0082a0001c0003t0002g0095 | 3 | NA18971.hp2 NA18988.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2753+646A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547718 | ||||||
| chr12:62547863
|
C | T | 25 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0005t0003g0113others(22): Show | 25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2753+791C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547863 | ||||||
| chr12:62548057
|
A | G | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2753+985A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548057 | ||||||
| chr12:62548072
|
A | C | 7 | a0001c0003t0005g0049a0001c0003t0005g0050a0001c0003t0005g0051others(4): Show | 7 | NA18941.hp1 NA18946.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.2753+1000A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548072 | ||||||
| chr12:62548149
|
A | T | 120 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0110others(117): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2753+1077A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548149 | ||||||
| chr12:62548223
|
C | T | 12 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2753+1151C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548223 | ||||||
| chr12:62548292
|
T | C | 48 | a0001c0002t0003g0102a0001c0002t0013g0298a0001c0002t0013g0299others(45): Show | 49 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2753+1220T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548292 | ||||||
| chr12:62548296
|
G | C | 1 | a0001c0002t0002g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2753+1224G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548296 | ||||||
| chr12:62548418
|
G | A | 12 | a0002c0001t0006g0143a0002c0001t0006g0183a0002c0001t0006g0187others(9): Show | 12 | HG01928.hp1 HG02071.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.2754-1250G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548418 | ||||||
| chr12:62548478
|
C | T | 120 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0110others(117): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2754-1190C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548478 | ||||||
| chr12:62548628
|
C | T | 1 | a0002c0001t0006g0183 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2754-1040C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548628 | ||||||
| chr12:62548883
|
A | G | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2754-785A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548883 | ||||||
| chr12:62548962
|
A | C | 1 | a0002c0001t0001g0168 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2754-706A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548962 | ||||||
| chr12:62548995
|
C | T | 1 | a0002c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2754-673C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548995 | ||||||
| chr12:62549095
|
A | C | 4 | a0001c0003t0008g0063a0001c0003t0008g0073a0001c0003t0008g0074others(1): Show | 4 | NA18986.hp1 NA18998.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.2754-573A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62549095 | ||||||
| chr12:62549219
|
A | T | 1 | a0003c0004t0004g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2754-449A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62549219 | ||||||
| chr12:62549401
|
C | T | 1 | a0001c0002t0035g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2754-267C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62549401 | ||||||
| chr12:62549456
|
C | CA | 10 | a0001c0002t0002g0348a0001c0003t0002g0055a0001c0003t0002g0056others(7): Show | 10 | HG01192.hp2 HG01361.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.2754-195dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | INFO_REALIGN_3_PRIME | chr12 | 62549456 | |||||
| chr12:62549456
|
CA | C | 134 | a0001c0002t0031g0136a0001c0005t0040g0135a0001c0006t0007g0009others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.2754-195delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | INFO_REALIGN_3_PRIME | chr12 | 62549456 | |||||
| chr12:62549591
|
G | A | 77 | a0001c0002t0003g0102a0001c0002t0013g0298a0001c0002t0013g0299others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.2754-77G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62549591 | ||||||
| chr12:62550045
|
G | A | 2 | a0002c0001t0001g0003a0002c0001t0001g0237 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2916+215G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550045 | ||||||
| chr12:62550142
|
T | C | 1 | a0001c0002t0022g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2916+312T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550142 | ||||||
| chr12:62550258
|
G | A | 1 | a0002c0001t0001g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2916+428G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550258 | ||||||
| chr12:62550315
|
G | A | 1 | a0002c0001t0001g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2916+485G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550315 | ||||||
| chr12:62550320
|
G | A | 1 | a0003c0004t0004g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2916+490G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550320 | ||||||
| chr12:62550376
|
G | A | 1 | a0002c0001t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2916+546G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550376 | ||||||
| chr12:62550475
|
T | A | 12 | a0002c0001t0001g0002a0002c0001t0001g0148a0002c0001t0001g0151others(9): Show | 13 | HG00544.hp2 HG00597.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2916+645T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550475 | ||||||
| chr12:62550562
|
A | G | 44 | a0002c0001t0001g0225a0002c0001t0001g0228a0002c0001t0001g0229others(41): Show | 44 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2916+732A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550562 | ||||||
| chr12:62550654
|
T | C | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2916+824T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550654 | ||||||
| chr12:62550813
|
G | C | 12 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(9): Show | 12 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2916+983G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550813 | ||||||
| chr12:62550905
|
CTTTCTTT others(3): Show |
C | 136 | a0001c0002t0031g0136a0001c0003t0003g0035a0001c0003t0003g0036others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2916+1079_2916+108 others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550905 | |||||
| chr12:62550905
|
CTTTCTTT others(6): Show |
C | 1 | a0001c0003t0008g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2916+1079_2916+109 others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550905 | |||||
| chr12:62550905
|
CTTTCTTT others(10): Show |
C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2916+1079_2916+109 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550905 | |||||
| chr12:62550909
|
C | CT | 16 | a0001c0002t0002g0256a0001c0002t0002g0329a0001c0002t0002g0342others(13): Show | 16 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2916+1104dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550909 | |||||
| chr12:62550909
|
CT | C | 24 | a0001c0002t0002g0318a0001c0002t0003g0102a0001c0002t0013g0298others(21): Show | 24 | HG01074.hp1 HG01074.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.2916+1104delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550909 | |||||
| chr12:62550909
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0005t0043g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2916+1094_2916+110 others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550909 | |||||
| chr12:62550939
|
G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2916+1109G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550939 | ||||||
| chr12:62550952
|
G | A | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2916+1122G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550952 | ||||||
| chr12:62551022
|
T | C | 241 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2916+1192T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551022 | ||||||
| chr12:62551077
|
G | A | 1 | a0001c0002t0022g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2916+1247G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551077 | ||||||
| chr12:62551158
|
G | T | 6 | a0001c0005t0003g0113a0001c0005t0003g0114a0001c0005t0003g0124others(3): Show | 6 | HG00738.hp2 HG01081.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2916+1328G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551158 | ||||||
| chr12:62551312
|
T | A | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.2916+1482T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551312 | ||||||
| chr12:62551378
|
GGAAACAA others(9): Show |
G | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2917-1496_2917-148 others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62551378 | |||||
| chr12:62551465
|
G | A | 148 | a0001c0002t0031g0136a0001c0006t0003g0005a0001c0006t0003g0006others(145): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2917-1416G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551465 | ||||||
| chr12:62551569
|
A | G | 5 | a0002c0001t0001g0145a0002c0001t0001g0155a0002c0001t0001g0171others(2): Show | 5 | HG00280.hp2 HG01257.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.2917-1312A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551569 | ||||||
| chr12:62551925
|
G | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2917-956G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551925 | ||||||
| chr12:62552049
|
T | C | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2917-832T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552049 | ||||||
| chr12:62552190
|
C | G | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2917-691C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552190 | ||||||
| chr12:62552191
|
A | G | 285 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(282): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.2917-690A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552191 | ||||||
| chr12:62552347
|
C | A | 1 | a0001c0002t0013g0299 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2917-534C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552347 | ||||||
| chr12:62552430
|
TATAAG | T | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2917-447_2917-443d others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62552430 | |||||
| chr12:62552436
|
A | G | 4 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.2917-445A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552436 | ||||||
| chr12:62552667
|
A | G | 37 | a0001c0003t0005g0044a0001c0003t0005g0049a0001c0003t0005g0050others(34): Show | 37 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.2917-214A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552667 | ||||||
| chr12:62552752
|
T | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2917-129T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552752 | ||||||
| chr12:62553434
|
T | G | 1 | a0001c0002t0011g0309 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3210+260T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62553434 | ||||||
| chr12:62553606
|
G | A | 1 | a0002c0001t0001g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3210+432G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62553606 | ||||||
| chr12:62553935
|
G | C | 2 | a0002c0001t0001g0241a0002c0001t0012g0232 | 2 | HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3210+761G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62553935 | ||||||
| chr12:62554171
|
T | C | 1 | a0001c0003t0005g0092 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3210+997T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554171 | ||||||
| chr12:62554497
|
CT | C | 39 | a0001c0003t0005g0044a0001c0003t0005g0045a0001c0003t0005g0046others(36): Show | 39 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.3210+1330delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr12 | 62554497 | |||||
| chr12:62554510
|
T | G | 1 | a0001c0002t0002g0359 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3210+1336T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554510 | ||||||
| chr12:62554667
|
A | T | 3 | a0001c0002t0002g0335a0006c0010t0002g0336a0006c0010t0002g0350 | 3 | HG01516.hp2 HG01517.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3211-1327A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554667 | ||||||
| chr12:62554688
|
G | A | 1 | a0001c0002t0013g0299 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3211-1306G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554688 | ||||||
| chr12:62554752
|
G | A | 1 | a0003c0004t0004g0273 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3211-1242G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554752 | ||||||
| chr12:62554956
|
G | A | 120 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0110others(117): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.3211-1038G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554956 | ||||||
| chr12:62555042
|
C | T | 7 | a0002c0001t0006g0189a0002c0001t0006g0190a0002c0001t0006g0201others(4): Show | 7 | HG01928.hp1 HG02071.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.3211-952C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555042 | ||||||
| chr12:62555330
|
A | C | 148 | a0001c0002t0031g0136a0001c0006t0003g0005a0001c0006t0003g0006others(145): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.3211-664A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555330 | ||||||
| chr12:62555338
|
T | G | 1 | a0001c0003t0005g0070 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3211-656T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555338 | ||||||
| chr12:62555353
|
G | GT | 12 | a0001c0002t0002g0254a0001c0002t0013g0298a0001c0002t0013g0299others(9): Show | 12 | HG01074.hp1 HG01256.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.3211-631dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr12 | 62555353 | |||||
| chr12:62555572
|
G | A | 1 | a0002c0001t0001g0168 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3211-422G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555572 | ||||||
| chr12:62555657
|
A | G | 1 | a0001c0003t0005g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3211-337A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555657 | ||||||
| chr12:62555807
|
T | TA | 59 | a0001c0002t0002g0305a0001c0002t0002g0317a0001c0002t0002g0322others(56): Show | 59 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.3211-168dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr12 | 62555807 | |||||
| chr12:62555807
|
TA | T | 118 | a0001c0002t0002g0351a0001c0002t0011g0307a0001c0002t0031g0136others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.3211-168delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr12 | 62555807 | |||||
| chr12:62555808
|
A | C | 1 | a0002c0001t0006g0187 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3211-186A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555808 | ||||||
| chr12:62555825
|
A | T | 1 | a0002c0001t0006g0187 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3211-169A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555825 | ||||||
| chr12:62555953
|
A | G | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3211-41A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555953 | ||||||
| chr12:62556328
|
C | T | 3 | a0001c0005t0003g0115a0001c0005t0003g0130a0001c0005t0003g0131 | 3 | NA18969.hp2 NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3409+136C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556328 | ||||||
| chr12:62556455
|
T | C | 241 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.3409+263T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556455 | ||||||
| chr12:62556487
|
G | A | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3409+295G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556487 | ||||||
| chr12:62556593
|
A | G | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3409+401A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556593 | ||||||
| chr12:62556776
|
G | C | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.3409+584G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556776 | ||||||
| chr12:62556989
|
T | A | 59 | a0002c0001t0001g0002a0002c0001t0001g0110a0002c0001t0001g0142others(56): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.3409+797T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556989 | ||||||
| chr12:62557029
|
A | T | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3409+837A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557029 | ||||||
| chr12:62557093
|
A | G | 1 | a0002c0001t0006g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3409+901A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557093 | ||||||
| chr12:62557331
|
G | A | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3409+1139G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557331 | ||||||
| chr12:62557447
|
A | G | 1 | a0002c0001t0001g0205 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3409+1255A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557447 | ||||||
| chr12:62557475
|
A | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3409+1283A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557475 | ||||||
| chr12:62557498
|
G | A | 1 | a0002c0001t0009g0193 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3409+1306G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557498 | ||||||
| chr12:62557874
|
C | T | 1 | a0001c0005t0003g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3409+1682C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557874 | ||||||
| chr12:62557928
|
T | TTA | 7 | a0001c0002t0002g0331a0001c0003t0002g0056a0001c0003t0002g0067others(4): Show | 7 | HG00639.hp2 HG01975.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.3409+1770_3409+177 others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557928
|
T | TTATATA | 4 | a0001c0002t0002g0026a0001c0003t0005g0051a0001c0003t0005g0087others(1): Show | 4 | HG00621.hp1 HG02895.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.3409+1766_3409+177 others(10): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557928
|
T | TTATATAT others(3): Show |
1 | a0001c0003t0002g0094 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3409+1762_3409+177 others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557928
|
T | TTATATAT others(7): Show |
2 | a0001c0002t0022g0295a0001c0003t0005g0101 | 2 | HG00597.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3409+1758_3409+177 others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557928
|
T | TTATATAT others(9): Show |
1 | a0001c0002t0014g0280 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3409+1756_3409+177 others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557928
|
TTA | T | 3 | a0001c0003t0005g0037a0001c0003t0005g0038a0001c0003t0005g0039 | 3 | HG02258.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3409+1770_3409+177 others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557928
|
TTATATAT others(5): Show |
T | 1 | a0001c0003t0021g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3409+1760_3409+177 others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557928
|
TTATATAT others(7): Show |
T | 4 | a0002c0001t0001g0211a0002c0001t0001g0212a0002c0001t0001g0245others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.3409+1758_3409+177 others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557928
|
TTATATAT others(9): Show |
T | 24 | a0002c0001t0001g0147a0002c0001t0001g0148a0002c0001t0001g0151others(21): Show | 24 | HG00673.hp1 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.3409+1756_3409+177 others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557928
|
TTATATAT others(11): Show |
T | 10 | a0002c0001t0001g0003a0002c0001t0001g0146a0002c0001t0001g0173others(7): Show | 11 | HG00423.hp1 HG02015.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.3409+1754_3409+177 others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557928
|
TTATATAT others(15): Show |
T | 1 | a0001c0003t0005g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3409+1750_3409+177 others(26): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | |||||
| chr12:62557930
|
A | T | 2 | a0001c0016t0032g0252a0003c0004t0004g0284 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3409+1738A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557930 | ||||||
| chr12:62557941
|
TATATATA others(6): Show |
T | 1 | a0002c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3409+1750_3409+176 others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557941 | ||||||
| chr12:62557941
|
TATATATA others(8): Show |
T | 1 | a0002c0001t0001g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3409+1750_3409+176 others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557941 | ||||||
| chr12:62557941
|
TATATATA others(10): Show |
T | 3 | a0002c0001t0001g0137a0002c0001t0001g0138a0002c0001t0001g0238 | 3 | HG02630.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3409+1750_3409+176 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557941 | ||||||
| chr12:62557942
|
ATATATAT others(21): Show |
A | 1 | a0002c0001t0001g0169 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3409+1752_3409+177 others(32): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557942 | |||||
| chr12:62557942
|
ATATATAT others(25): Show |
A | 1 | a0002c0001t0001g0225 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3409+1752_3409+178 others(36): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557942 | |||||
| chr12:62557943
|
TATATATA others(8): Show |
T | 2 | a0002c0001t0001g0224a0002c0001t0001g0241 | 2 | NA20129.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3409+1752_3409+176 others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557943 | ||||||
| chr12:62557943
|
TATATATA others(10): Show |
T | 59 | a0002c0001t0001g0002a0002c0001t0001g0110a0002c0001t0001g0142others(56): Show | 60 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.3409+1752_3409+176 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557943 | ||||||
| chr12:62557945
|
TATATATA others(8): Show |
T | 2 | a0002c0001t0001g0204a0002c0001t0006g0215 | 2 | HG03579.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3409+1754_3409+176 others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557945 | ||||||
| chr12:62557945
|
TATATATA others(10): Show |
T | 12 | a0002c0001t0001g0144a0002c0001t0001g0153a0002c0001t0001g0161others(9): Show | 12 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.3409+1754_3409+177 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557945 | ||||||
| chr12:62557946
|
ATATATAT others(14): Show |
A | 1 | a0003c0004t0004g0274 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3409+1756_3409+177 others(25): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557946 | |||||
| chr12:62557948
|
ATATATAT others(10): Show |
A | 1 | a0001c0009t0019g0104 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3409+1758_3409+177 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557948 | |||||
| chr12:62557948
|
ATATATAT others(14): Show |
A | 5 | a0003c0004t0004g0263a0003c0004t0004g0275a0003c0004t0004g0276others(2): Show | 5 | HG02523.hp1 NA18967.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.3409+1758_3409+177 others(25): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557948 | |||||
| chr12:62557956
|
A | T | 1 | a0002c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3409+1764A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557956 | ||||||
| chr12:62557958
|
A | T | 8 | a0001c0018t0002g0306a0002c0001t0001g0141a0002c0001t0001g0147others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3409+1766A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557958 | ||||||
| chr12:62557959
|
TA | T | 4 | a0001c0002t0002g0325a0001c0002t0002g0330a0001c0002t0011g0255others(1): Show | 4 | HG02280.hp1 HG02735.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.3409+1768delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557959 | ||||||
| chr12:62557960
|
A | AT | 9 | a0001c0002t0002g0318a0001c0002t0002g0353a0001c0002t0002g0363others(6): Show | 9 | HG01255.hp2 HG02027.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3409+1769dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557960 | |||||
| chr12:62557960
|
A | ATT | 3 | a0001c0002t0011g0309a0005c0008t0002g0334a0005c0008t0002g0364 | 3 | NA19060.hp1 NA19064.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3409+1769_3409+177 others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557960 | |||||
| chr12:62557960
|
A | T | 41 | a0001c0002t0002g0254a0001c0002t0002g0321a0001c0002t0002g0351others(38): Show | 42 | HG00673.hp1 HG00741.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.3409+1768A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557960 | ||||||
| chr12:62557960
|
ATATTTT | A | 11 | a0001c0005t0003g0113a0001c0005t0003g0114a0001c0005t0003g0115others(8): Show | 11 | HG00738.hp2 HG01081.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.3409+1770_3409+177 others(10): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557960 | |||||
| chr12:62557961
|
TA | T | 4 | a0001c0002t0002g0339a0001c0002t0015g0314a0004c0007t0002g0327others(1): Show | 4 | HG01517.hp1 HG02165.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.3409+1770delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557961 | ||||||
| chr12:62557962
|
A | AT | 8 | a0001c0002t0002g0256a0001c0002t0002g0305a0001c0002t0002g0324others(5): Show | 8 | HG00621.hp2 HG01928.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.3409+1799dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATAT | 11 | a0001c0003t0002g0068a0001c0003t0002g0069a0001c0003t0002g0075others(8): Show | 11 | HG00140.hp1 HG02165.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(4): Show |
1 | a0001c0003t0003g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(16): Show |
1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(27): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(11): Show |
1 | a0001c0006t0003g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(17): Show |
1 | a0001c0006t0003g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(28): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(14): Show |
1 | a0001c0006t0007g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(25): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(15): Show |
1 | a0001c0006t0003g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(26): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(8): Show |
1 | a0001c0006t0003g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(11): Show |
1 | a0001c0006t0042g0004 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(9): Show |
1 | a0001c0006t0007g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(11): Show |
2 | a0001c0006t0007g0009a0001c0006t0007g0015 | 2 | HG01099.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(14): Show |
1 | a0001c0006t0003g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(25): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(6): Show |
1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(7): Show |
3 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107 | 3 | HG02257.hp2 HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(9): Show |
2 | a0001c0006t0007g0017a0001c0006t0007g0019 | 2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(10): Show |
1 | a0001c0006t0007g0016 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(5): Show |
1 | a0001c0003t0003g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATAT others(6): Show |
1 | a0001c0006t0007g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATTT others(3): Show |
1 | a0001c0003t0003g0042 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATTT others(5): Show |
2 | a0001c0006t0007g0014a0001c0006t0007g0018 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATATATTT others(6): Show |
1 | a0001c0006t0007g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | ATTT | 17 | a0001c0002t0002g0317a0001c0002t0010g0023a0001c0002t0010g0031others(14): Show | 17 | HG02015.hp2 HG02145.hp2 HG02886.hp2 others(14): Show |
intron_variant | MODIFIER | c.3409+1797_3409+179 others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557962
|
A | T | 150 | a0001c0002t0002g0254a0001c0002t0002g0318a0001c0002t0002g0321others(147): Show | 153 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.3409+1770A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557962 | ||||||
| chr12:62557962
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0002t0048g0320 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3409+1790_3409+179 others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | |||||
| chr12:62557963
|
T | TA | 3 | a0001c0002t0002g0343a0001c0002t0014g0288a0001c0003t0005g0066 | 3 | HG01496.hp2 HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | ||||||
| chr12:62557963
|
T | TATA | 7 | a0001c0003t0002g0055a0001c0003t0002g0082a0001c0003t0002g0084others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | ||||||
| chr12:62557963
|
T | TATATA | 10 | a0001c0002t0002g0311a0003c0004t0004g0258a0003c0004t0004g0259others(7): Show | 10 | HG01069.hp2 HG01074.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(9): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | ||||||
| chr12:62557963
|
T | TATATATA | 10 | a0001c0002t0013g0298a0001c0002t0014g0287a0001c0002t0037g0304others(7): Show | 10 | HG00673.hp2 HG01074.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(11): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | ||||||
| chr12:62557963
|
T | TATATATA others(4): Show |
7 | a0001c0002t0013g0299a0001c0002t0026g0301a0003c0004t0004g0264others(4): Show | 7 | HG00323.hp2 HG00733.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | ||||||
| chr12:62557963
|
T | TATATATA others(10): Show |
1 | a0001c0006t0007g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | ||||||
| chr12:62557964
|
T | A | 9 | a0001c0002t0013g0303a0001c0002t0014g0280a0001c0003t0002g0056others(6): Show | 9 | HG00735.hp2 HG01070.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3409+1772T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557964 | ||||||
| chr12:62557965
|
T | A | 31 | a0001c0002t0002g0343a0001c0002t0014g0287a0001c0002t0014g0288others(28): Show | 31 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.3409+1773T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557965 | ||||||
| chr12:62557966
|
T | A | 8 | a0001c0002t0014g0280a0001c0002t0020g0285a0001c0002t0020g0289others(5): Show | 8 | HG00735.hp2 HG01070.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.3409+1774T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557966 | ||||||
| chr12:62557967
|
T | A | 21 | a0001c0002t0014g0287a0001c0002t0014g0288a0003c0004t0004g0258others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.3409+1775T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557967 | ||||||
| chr12:62557968
|
T | A | 3 | a0001c0002t0014g0280a0003c0004t0004g0269a0003c0004t0004g0291 | 3 | HG01070.hp2 HG02300.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3409+1776T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557968 | ||||||
| chr12:62557969
|
T | A | 10 | a0001c0002t0014g0287a0003c0004t0004g0258a0003c0004t0004g0259others(7): Show | 10 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.3409+1777T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557969 | ||||||
| chr12:62557970
|
T | A | 2 | a0001c0002t0002g0325a0003c0004t0004g0291 | 2 | HG01070.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.3409+1778T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557970 | ||||||
| chr12:62557971
|
T | A | 5 | a0003c0004t0004g0258a0003c0004t0004g0259a0003c0004t0004g0268others(2): Show | 5 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.3409+1779T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557971 | ||||||
| chr12:62557974
|
T | A | 1 | a0001c0002t0048g0320 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3409+1782T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557974 | ||||||
| chr12:62557997
|
G | C | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3409+1805G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557997 | ||||||
| chr12:62558059
|
C | G | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3409+1867C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558059 | ||||||
| chr12:62558106
|
C | T | 1 | a0002c0001t0001g0175 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.3409+1914C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558106 | ||||||
| chr12:62558184
|
G | A | 1 | a0005c0008t0002g0340 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3409+1992G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558184 | ||||||
| chr12:62558497
|
C | T | 12 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3410-1994C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558497 | ||||||
| chr12:62558500
|
G | A | 1 | a0001c0002t0002g0359 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3410-1991G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558500 | ||||||
| chr12:62558689
|
A | AT | 22 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(19): Show | 22 | HG00099.hp2 HG01071.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.3410-1785dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62558689 | |||||
| chr12:62558689
|
AT | A | 12 | a0001c0002t0002g0346a0001c0002t0013g0298a0001c0002t0013g0299others(9): Show | 12 | HG01074.hp1 HG01256.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3410-1785delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62558689 | |||||
| chr12:62558814
|
C | T | 1 | a0002c0001t0025g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3410-1677C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558814 | ||||||
| chr12:62558881
|
C | T | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3410-1610C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558881 | ||||||
| chr12:62558916
|
C | T | 148 | a0001c0002t0031g0136a0001c0006t0003g0005a0001c0006t0003g0006others(145): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.3410-1575C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558916 | ||||||
| chr12:62558917
|
C | T | 5 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3410-1574C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558917 | ||||||
| chr12:62559080
|
A | T | 4 | a0001c0005t0003g0128a0001c0005t0003g0129a0001c0005t0003g0134others(1): Show | 4 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3410-1411A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559080 | ||||||
| chr12:62559121
|
A | G | 28 | a0002c0001t0006g0143a0002c0001t0006g0183a0002c0001t0006g0187others(25): Show | 28 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.3410-1370A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559121 | ||||||
| chr12:62559130
|
C | T | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.3410-1361C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559130 | ||||||
| chr12:62559201
|
A | G | 2 | a0001c0002t0002g0322a0001c0002t0002g0331 | 2 | NA18945.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.3410-1290A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559201 | ||||||
| chr12:62559417
|
A | G | 1 | a0002c0001t0001g0148 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3410-1074A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559417 | ||||||
| chr12:62559577
|
A | G | 1 | a0002c0001t0012g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3410-914A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559577 | ||||||
| chr12:62559742
|
T | C | 1 | a0003c0004t0044g0262 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3410-749T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559742 | ||||||
| chr12:62559774
|
TA | T | 228 | a0001c0002t0003g0102a0001c0002t0013g0298a0001c0002t0013g0299others(225): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.3410-704delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62559774 | |||||
| chr12:62559873
|
T | C | 60 | a0002c0001t0001g0002a0002c0001t0001g0110a0002c0001t0001g0142others(57): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.3410-618T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559873 | ||||||
| chr12:62559909
|
T | C | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3410-582T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559909 | ||||||
| chr12:62559932
|
A | G | 2 | a0001c0002t0013g0300a0001c0002t0026g0301 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3410-559A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559932 | ||||||
| chr12:62559993
|
A | C | 38 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(35): Show | 38 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.3410-498A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559993 | ||||||
| chr12:62560065
|
G | A | 1 | a0001c0003t0041g0053 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3410-426G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62560065 | ||||||
| chr12:62560092
|
A | G | 33 | a0003c0004t0004g0258a0003c0004t0004g0259a0003c0004t0004g0260others(30): Show | 33 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.3410-399A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62560092 | ||||||
| chr12:62560113
|
A | AT | 241 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.3410-370dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62560113 | |||||
| chr12:62560436
|
A | G | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3410-55A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62560436 | ||||||
| chr12:62561210
|
A | C | 5 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0303others(2): Show | 5 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.4032+97A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62561210 | ||||||
| chr12:62561664
|
G | A | 1 | a0001c0003t0005g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4032+551G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62561664 | ||||||
| chr12:62561860
|
G | A | 1 | a0003c0004t0004g0274 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4032+747G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62561860 | ||||||
| chr12:62562233
|
C | T | 56 | a0001c0002t0002g0254a0001c0002t0002g0256a0001c0002t0002g0305others(53): Show | 56 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.4032+1120C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562233 | ||||||
| chr12:62562656
|
G | A | 3 | a0002c0001t0001g0137a0002c0001t0001g0238a0002c0001t0030g0139 | 3 | HG03098.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4032+1543G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562656 | ||||||
| chr12:62562711
|
G | A | 3 | a0001c0003t0002g0055a0001c0003t0002g0082a0001c0003t0002g0095 | 3 | NA18971.hp2 NA18988.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.4032+1598G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562711 | ||||||
| chr12:62562772
|
T | A | 1 | a0002c0001t0001g0240 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4032+1659T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562772 | ||||||
| chr12:62562787
|
A | G | 1 | a0001c0006t0007g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4032+1674A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562787 | ||||||
| chr12:62562829
|
T | C | 12 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.4032+1716T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562829 | ||||||
| chr12:62562973
|
A | G | 1 | a0001c0003t0050g0077 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4032+1860A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562973 | ||||||
| chr12:62563041
|
T | C | 5 | a0002c0001t0009g0192a0002c0001t0009g0193a0002c0001t0009g0194others(2): Show | 5 | HG00642.hp1 HG00733.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.4032+1928T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563041 | ||||||
| chr12:62563046
|
T | A | 5 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4032+1933T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563046 | ||||||
| chr12:62563047
|
T | A | 5 | a0001c0006t0003g0105a0001c0006t0003g0106a0001c0006t0003g0107others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4032+1934T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563047 | ||||||
| chr12:62563255
|
T | G | 45 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(42): Show | 45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.4033-1982T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563255 | ||||||
| chr12:62563371
|
C | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4033-1866C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563371 | ||||||
| chr12:62563505
|
T | C | 1 | a0001c0006t0007g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4033-1732T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563505 | ||||||
| chr12:62563512
|
C | T | 5 | a0002c0001t0009g0192a0002c0001t0009g0193a0002c0001t0009g0194others(2): Show | 5 | HG00642.hp1 HG00733.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.4033-1725C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563512 | ||||||
| chr12:62563650
|
G | A | 1 | a0002c0001t0001g0144 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4033-1587G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563650 | ||||||
| chr12:62563775
|
T | A | 1 | a0001c0003t0023g0065 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4033-1462T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563775 | ||||||
| chr12:62563829
|
A | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4033-1408A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563829 | ||||||
| chr12:62563858
|
A | G | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4033-1379A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563858 | ||||||
| chr12:62564108
|
A | G | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.4033-1129A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564108 | ||||||
| chr12:62564126
|
G | C | 137 | a0001c0002t0031g0136a0001c0003t0005g0081a0001c0006t0007g0009others(134): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.4033-1111G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564126 | ||||||
| chr12:62564394
|
A | T | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4033-843A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564394 | ||||||
| chr12:62564471
|
A | G | 1 | a0002c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4033-766A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564471 | ||||||
| chr12:62564577
|
T | C | 16 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0056others(13): Show | 16 | HG00544.hp1 HG01192.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.4033-660T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564577 | ||||||
| chr12:62564627
|
A | G | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4033-610A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564627 | ||||||
| chr12:62564789
|
C | T | 1 | a0001c0002t0002g0348 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4033-448C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564789 | ||||||
| chr12:62564857
|
G | C | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4033-380G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564857 | ||||||
| chr12:62564945
|
T | C | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4033-292T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564945 | ||||||
| chr12:62565386
|
T | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.4176+6T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565386 | ||||||
| chr12:62565387
|
T | A | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.4176+7T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565387 | ||||||
| chr12:62565404
|
A | T | 1 | a0003c0004t0004g0365 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4176+24A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565404 | ||||||
| chr12:62565476
|
G | T | 1 | a0002c0001t0029g0149 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4176+96G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565476 | ||||||
| chr12:62565641
|
C | T | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4176+261C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565641 | ||||||
| chr12:62565664
|
T | G | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4176+284T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565664 | ||||||
| chr12:62565665
|
C | T | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.4176+285C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565665 | ||||||
| chr12:62565684
|
G | A | 2 | a0001c0002t0020g0285a0001c0002t0020g0289 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.4176+304G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565684 | ||||||
| chr12:62565733
|
T | A | 2 | a0001c0005t0003g0111a0001c0005t0003g0112 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4177-281T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565733 | ||||||
| chr12:62566180
|
T | G | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4195-142T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 28/34 | chr12 | 62566180 | ||||||
| chr12:62566237
|
G | A | 5 | a0002c0001t0009g0192a0002c0001t0009g0193a0002c0001t0009g0194others(2): Show | 5 | HG00642.hp1 HG00733.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.4195-85G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 28/34 | chr12 | 62566237 | ||||||
| chr12:62566725
|
C | T | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4323+275C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62566725 | ||||||
| chr12:62566742
|
T | TG | 41 | a0001c0002t0002g0254a0001c0002t0002g0310a0001c0002t0002g0324others(38): Show | 41 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.4323+298dupG | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62566742 | |||||
| chr12:62566832
|
A | G | 1 | a0002c0001t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4323+382A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62566832 | ||||||
| chr12:62566866
|
C | G | 1 | a0003c0004t0004g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4323+416C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62566866 | ||||||
| chr12:62566971
|
T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4323+521T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62566971 | ||||||
| chr12:62567097
|
T | C | 1 | a0002c0001t0001g0238 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4323+647T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567097 | ||||||
| chr12:62567100
|
A | G | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4323+650A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567100 | ||||||
| chr12:62567104
|
C | T | 1 | a0001c0003t0005g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4323+654C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567104 | ||||||
| chr12:62567204
|
A | G | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4323+754A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567204 | ||||||
| chr12:62567491
|
C | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4323+1041C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567491 | ||||||
| chr12:62567519
|
C | T | 120 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0110others(117): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.4323+1069C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567519 | ||||||
| chr12:62567619
|
G | A | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4323+1169G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567619 | ||||||
| chr12:62567714
|
C | T | 1 | a0001c0002t0014g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4323+1264C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567714 | ||||||
| chr12:62567844
|
A | T | 3 | a0001c0003t0002g0056a0001c0003t0002g0071a0001c0003t0002g0084 | 3 | HG01192.hp2 HG01496.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.4323+1394A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567844 | ||||||
| chr12:62568021
|
G | A | 120 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0110others(117): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.4323+1571G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568021 | ||||||
| chr12:62568064
|
C | T | 4 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(1): Show | 4 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4323+1614C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568064 | ||||||
| chr12:62568113
|
T | A | 7 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0027others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.4323+1663T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568113 | ||||||
| chr12:62568297
|
A | G | 1 | a0002c0001t0006g0197 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4323+1847A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568297 | ||||||
| chr12:62568332
|
A | T | 1 | a0001c0003t0005g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4323+1882A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568332 | ||||||
| chr12:62568417
|
C | T | 1 | a0001c0003t0002g0076 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4323+1967C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568417 | ||||||
| chr12:62568469
|
G | A | 1 | a0001c0002t0002g0321 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4323+2019G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568469 | ||||||
| chr12:62568598
|
C | T | 1 | a0001c0002t0014g0288 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4323+2148C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568598 | ||||||
| chr12:62568608
|
G | A | 1 | a0001c0003t0003g0041 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4323+2158G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568608 | ||||||
| chr12:62568659
|
C | T | 1 | a0002c0001t0001g0159 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4323+2209C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568659 | ||||||
| chr12:62569290
|
T | C | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4324-2102T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62569290 | ||||||
| chr12:62569590
|
A | G | 1 | a0001c0002t0022g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4324-1802A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62569590 | ||||||
| chr12:62569596
|
ATTC | A | 4 | a0002c0001t0001g0208a0002c0001t0001g0211a0002c0001t0001g0212others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4324-1787_4324-178 others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62569596 | |||||
| chr12:62569775
|
G | A | 1 | a0001c0003t0005g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4324-1617G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62569775 | ||||||
| chr12:62570115
|
G | A | 1 | a0001c0002t0002g0311 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4324-1277G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570115 | ||||||
| chr12:62570231
|
A | C | 3 | a0002c0001t0001g0228a0002c0001t0001g0229a0002c0001t0001g0234 | 3 | HG01884.hp2 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4324-1161A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570231 | ||||||
| chr12:62570365
|
T | C | 11 | a0003c0004t0004g0258a0003c0004t0004g0259a0003c0004t0004g0281others(8): Show | 11 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.4324-1027T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570365 | ||||||
| chr12:62570372
|
G | A | 3 | a0001c0002t0017g0024a0001c0002t0017g0032a0001c0002t0017g0033 | 3 | HG01109.hp2 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4324-1020G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570372 | ||||||
| chr12:62570416
|
A | G | 1 | a0001c0018t0002g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4324-976A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570416 | ||||||
| chr12:62570568
|
C | G | 1 | a0003c0004t0004g0270 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4324-824C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570568 | ||||||
| chr12:62570600
|
A | G | 1 | a0001c0002t0022g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4324-792A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570600 | ||||||
| chr12:62570642
|
A | G | 1 | a0002c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4324-750A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570642 | ||||||
| chr12:62570663
|
G | A | 15 | a0002c0001t0001g0225a0002c0001t0001g0228a0002c0001t0001g0229others(12): Show | 15 | HG00423.hp1 HG01884.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.4324-729G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570663 | ||||||
| chr12:62570722
|
C | CT | 52 | a0001c0002t0002g0318a0001c0002t0002g0324a0001c0002t0002g0342others(49): Show | 52 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.4324-641dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62570722 | |||||
| chr12:62570722
|
C | CTT | 9 | a0001c0002t0002g0335a0001c0002t0002g0359a0001c0002t0013g0298others(6): Show | 9 | HG01074.hp1 HG01256.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.4324-642_4324-641d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62570722 | |||||
| chr12:62570722
|
CT | C | 92 | a0001c0002t0002g0325a0001c0002t0002g0332a0001c0002t0011g0255others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.4324-641delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62570722 | |||||
| chr12:62570722
|
CTT | C | 6 | a0001c0003t0003g0099a0001c0003t0003g0100a0001c0005t0003g0111others(3): Show | 6 | HG01168.hp2 HG01255.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4324-642_4324-641d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62570722 | |||||
| chr12:62570772
|
T | C | 148 | a0001c0002t0031g0136a0001c0006t0003g0005a0001c0006t0003g0006others(145): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.4324-620T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570772 | ||||||
| chr12:62570827
|
G | A | 16 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(13): Show | 16 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.4324-565G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570827 | ||||||
| chr12:62570869
|
C | G | 1 | a0001c0003t0005g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4324-523C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570869 | ||||||
| chr12:62570880
|
T | A | 1 | a0002c0001t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4324-512T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570880 | ||||||
| chr12:62570916
|
G | C | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.4324-476G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570916 | ||||||
| chr12:62571025
|
T | C | 242 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0325others(239): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.4324-367T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62571025 | ||||||
| chr12:62571195
|
A | T | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4324-197A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62571195 | ||||||
| chr12:62571224
|
C | T | 2 | a0001c0003t0005g0034a0001c0003t0005g0040 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4324-168C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62571224 | ||||||
| chr12:62571369
|
T | C | 41 | a0001c0002t0003g0102a0001c0002t0014g0280a0001c0002t0014g0286others(38): Show | 42 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.4324-23T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62571369 | ||||||
| chr12:62571804
|
A | G | 3 | a0002c0001t0001g0240a0002c0001t0001g0241a0002c0001t0012g0232 | 3 | HG03669.hp2 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.4514+222A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62571804 | ||||||
| chr12:62572215
|
A | T | 1 | a0001c0006t0003g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4514+633A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62572215 | ||||||
| chr12:62572415
|
T | C | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.4514+833T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62572415 | ||||||
| chr12:62572804
|
C | T | 25 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0005t0003g0113others(22): Show | 25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.4514+1222C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62572804 | ||||||
| chr12:62572815
|
A | T | 2 | a0001c0003t0003g0099a0001c0003t0003g0100 | 2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.4514+1233A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62572815 | ||||||
| chr12:62572886
|
A | G | 1 | a0001c0006t0007g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4514+1304A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62572886 | ||||||
| chr12:62573171
|
G | C | 5 | a0003c0004t0004g0263a0003c0004t0004g0275a0003c0004t0004g0276others(2): Show | 5 | HG02523.hp1 NA18967.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.4514+1589G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573171 | ||||||
| chr12:62573189
|
G | A | 1 | a0002c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4514+1607G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573189 | ||||||
| chr12:62573315
|
T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4514+1733T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573315 | ||||||
| chr12:62573394
|
C | CT | 8 | a0001c0003t0005g0101a0001c0003t0008g0074a0001c0005t0003g0122others(5): Show | 8 | HG00597.hp2 HG01255.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.4514+1827dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr12 | 62573394 | |||||
| chr12:62573517
|
A | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4514+1935A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573517 | ||||||
| chr12:62573526
|
A | G | 4 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0099others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.4514+1944A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573526 | ||||||
| chr12:62573650
|
C | T | 25 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0005t0003g0113others(22): Show | 25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.4514+2068C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573650 | ||||||
| chr12:62573665
|
T | G | 3 | a0001c0003t0002g0067a0001c0006t0003g0008a0002c0001t0001g0247 | 3 | HG01891.hp1 NA18962.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4514+2083T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573665 | ||||||
| chr12:62573668
|
T | C | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4514+2086T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573668 | ||||||
| chr12:62574225
|
A | G | 1 | a0001c0003t0005g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4514+2643A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574225 | ||||||
| chr12:62574343
|
CTTGGAAA others(13): Show |
C | 3 | a0003c0004t0004g0258a0003c0004t0004g0259a0003c0004t0004g0297 | 3 | HG01167.hp1 HG01169.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.4514+2767_4514+278 others(24): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr12 | 62574343 | |||||
| chr12:62574407
|
C | T | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4514+2825C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574407 | ||||||
| chr12:62574436
|
G | A | 9 | a0002c0001t0001g0161a0002c0001t0001g0162a0002c0001t0001g0173others(6): Show | 9 | HG02027.hp2 HG02135.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.4514+2854G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574436 | ||||||
| chr12:62574500
|
T | C | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4514+2918T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574500 | ||||||
| chr12:62574596
|
A | T | 1 | a0001c0002t0048g0320 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4514+3014A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574596 | ||||||
| chr12:62574677
|
T | C | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4514+3095T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574677 | ||||||
| chr12:62574825
|
T | C | 1 | a0002c0001t0001g0202 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4514+3243T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574825 | ||||||
| chr12:62574960
|
CA | C | 148 | a0001c0002t0031g0136a0001c0006t0003g0005a0001c0006t0003g0006others(145): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.4514+3386delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr12 | 62574960 | |||||
| chr12:62575225
|
G | T | 1 | a0001c0003t0005g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4515-3220G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62575225 | ||||||
| chr12:62575291
|
G | A | 1 | a0002c0001t0012g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4515-3154G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62575291 | ||||||
| chr12:62575888
|
T | C | 45 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(42): Show | 45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.4515-2557T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62575888 | ||||||
| chr12:62575924
|
C | T | 60 | a0002c0001t0001g0003a0002c0001t0001g0137a0002c0001t0001g0138others(57): Show | 61 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4515-2521C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62575924 | ||||||
| chr12:62576006
|
G | A | 2 | a0002c0001t0001g0003a0002c0001t0001g0237 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4515-2439G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576006 | ||||||
| chr12:62576073
|
T | C | 1 | a0003c0004t0004g0284 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4515-2372T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576073 | ||||||
| chr12:62576172
|
G | A | 54 | a0002c0001t0001g0002a0002c0001t0001g0110a0002c0001t0001g0142others(51): Show | 55 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4515-2273G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576172 | ||||||
| chr12:62576358
|
G | T | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4515-2087G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576358 | ||||||
| chr12:62576526
|
C | T | 3 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043 | 3 | NA19004.hp2 NA19070.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.4515-1919C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576526 | ||||||
| chr12:62576657
|
C | T | 25 | a0001c0005t0003g0111a0001c0005t0003g0112a0001c0005t0003g0113others(22): Show | 25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.4515-1788C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576657 | ||||||
| chr12:62576678
|
A | G | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4515-1767A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576678 | ||||||
| chr12:62576702
|
A | G | 135 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.4515-1743A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576702 | ||||||
| chr12:62576728
|
T | C | 1 | a0002c0001t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4515-1717T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576728 | ||||||
| chr12:62576864
|
A | G | 364 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0254others(361): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.4515-1581A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576864 | ||||||
| chr12:62577045
|
A | T | 2 | a0001c0005t0003g0124a0001c0005t0003g0125 | 2 | HG00738.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4515-1400A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62577045 | ||||||
| chr12:62577052
|
C | T | 1 | a0001c0002t0002g0321 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4515-1393C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62577052 | ||||||
| chr12:62577154
|
G | A | 1 | a0002c0001t0001g0205 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4515-1291G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62577154 | ||||||
| chr12:62577598
|
T | C | 2 | a0001c0002t0035g0025a0002c0001t0001g0227 | 2 | HG02280.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.4515-847T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62577598 | ||||||
| chr12:62577672
|
T | C | 4 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(1): Show | 4 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4515-773T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62577672 | ||||||
| chr12:62578082
|
A | T | 1 | a0002c0001t0001g0147 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4515-363A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62578082 | ||||||
| chr12:62578114
|
C | T | 1 | a0001c0002t0002g0324 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4515-331C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62578114 | ||||||
| chr12:62578123
|
T | C | 2 | a0003c0004t0004g0258a0003c0004t0004g0259 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4515-322T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62578123 | ||||||
| chr12:62578162
|
C | T | 1 | a0002c0001t0001g0162 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4515-283C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62578162 | ||||||
| chr12:62578430
|
G | GT | 146 | a0001c0002t0031g0136a0001c0006t0003g0005a0001c0006t0003g0006others(143): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
splice_acceptor_variant&intron_variant | HIGH | c.4515-3dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr12 | 62578430 | |||||
| chr12:62578646
|
C | T | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4575+141C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62578646 | ||||||
| chr12:62578765
|
T | G | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.4575+260T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62578765 | ||||||
| chr12:62578810
|
A | G | 1 | a0001c0002t0002g0311 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4575+305A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62578810 | ||||||
| chr12:62579072
|
C | CA | 11 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.4575+579dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr12 | 62579072 | |||||
| chr12:62579446
|
G | A | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4576-851G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62579446 | ||||||
| chr12:62579450
|
G | A | 2 | a0003c0004t0004g0266a0003c0004t0004g0267 | 2 | NA19062.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.4576-847G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62579450 | ||||||
| chr12:62579550
|
C | T | 1 | a0003c0004t0004g0267 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.4576-747C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62579550 | ||||||
| chr12:62579559
|
T | TA | 134 | a0001c0002t0031g0136a0001c0003t0005g0091a0001c0003t0008g0073others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.4576-721dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr12 | 62579559 | |||||
| chr12:62580469
|
A | C | 1 | a0001c0003t0005g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4699+49A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62580469 | ||||||
| chr12:62580601
|
A | G | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4699+181A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62580601 | ||||||
| chr12:62580688
|
A | G | 1 | a0003c0004t0004g0273 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4699+268A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62580688 | ||||||
| chr12:62580958
|
G | A | 2 | a0001c0002t0002g0322a0001c0002t0002g0331 | 2 | NA18945.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.4699+538G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62580958 | ||||||
| chr12:62581189
|
A | G | 1 | a0001c0006t0007g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4699+769A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581189 | ||||||
| chr12:62581256
|
C | T | 2 | a0001c0002t0013g0300a0001c0002t0026g0301 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4699+836C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581256 | ||||||
| chr12:62581385
|
G | A | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4699+965G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581385 | ||||||
| chr12:62581459
|
A | G | 1 | a0001c0003t0005g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4699+1039A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581459 | ||||||
| chr12:62581485
|
C | G | 1 | a0001c0002t0013g0299 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4699+1065C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581485 | ||||||
| chr12:62581527
|
C | T | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4699+1107C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581527 | ||||||
| chr12:62581606
|
C | G | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4699+1186C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581606 | ||||||
| chr12:62581625
|
C | T | 2 | a0001c0002t0011g0307a0001c0002t0011g0309 | 2 | NA18939.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.4699+1205C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581625 | ||||||
| chr12:62581852
|
T | G | 12 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.4699+1432T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581852 | ||||||
| chr12:62581855
|
A | C | 1 | a0001c0003t0005g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4699+1435A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581855 | ||||||
| chr12:62581905
|
C | G | 6 | a0001c0002t0014g0280a0001c0002t0014g0286a0001c0002t0014g0287others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.4699+1485C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581905 | ||||||
| chr12:62582180
|
C | G | 1 | a0002c0001t0001g0159 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4699+1760C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62582180 | ||||||
| chr12:62582509
|
CTCTTTTT others(4): Show |
C | 2 | a0002c0001t0001g0138a0002c0001t0012g0140 | 2 | HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.4699+2101_4699+211 others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62582509 | |||||
| chr12:62582658
|
C | T | 1 | a0001c0003t0005g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4699+2238C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62582658 | ||||||
| chr12:62582722
|
T | TA | 93 | a0002c0001t0001g0002a0002c0001t0001g0110a0002c0001t0001g0142others(90): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.4699+2314dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62582722 | |||||
| chr12:62583361
|
A | G | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4700-1933A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583361 | ||||||
| chr12:62583374
|
A | G | 3 | a0003c0004t0004g0290a0003c0004t0004g0291a0003c0004t0004g0292 | 3 | HG00280.hp1 HG00733.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.4700-1920A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583374 | ||||||
| chr12:62583382
|
A | G | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4700-1912A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583382 | ||||||
| chr12:62583383
|
G | A | 148 | a0001c0002t0031g0136a0001c0006t0003g0005a0001c0006t0003g0006others(145): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.4700-1911G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583383 | ||||||
| chr12:62583395
|
AG | A | 136 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4700-1897delG | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62583395 | |||||
| chr12:62583447
|
A | G | 285 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(282): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.4700-1847A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583447 | ||||||
| chr12:62583675
|
A | G | 1 | a0001c0003t0005g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4700-1619A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583675 | ||||||
| chr12:62583786
|
T | TA | 11 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.4700-1492dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62583786 | |||||
| chr12:62583911
|
G | A | 20 | a0001c0002t0002g0310a0001c0002t0002g0329a0001c0002t0002g0332others(17): Show | 20 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.4700-1383G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583911 | ||||||
| chr12:62583960
|
C | CA | 10 | a0001c0002t0002g0347a0001c0002t0003g0102a0001c0003t0003g0041others(7): Show | 11 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.4700-1320dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62583960 | |||||
| chr12:62583968
|
A | C | 1 | a0001c0003t0008g0060 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4700-1326A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583968 | ||||||
| chr12:62583975
|
C | A | 2 | a0002c0001t0001g0208a0002c0001t0001g0211 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4700-1319C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583975 | ||||||
| chr12:62583975
|
C | CA | 21 | a0001c0002t0014g0280a0001c0006t0003g0005a0001c0006t0003g0006others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.4700-1307dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62583975 | |||||
| chr12:62583980
|
A | C | 1 | a0002c0001t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4700-1314A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583980 | ||||||
| chr12:62583987
|
A | C | 2 | a0002c0001t0009g0192a0012c0014t0009g0218 | 2 | HG00642.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4700-1307A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583987 | ||||||
| chr12:62584009
|
G | A | 16 | a0003c0004t0004g0260a0003c0004t0004g0263a0003c0004t0004g0264others(13): Show | 16 | HG00673.hp2 HG02523.hp1 NA18944.hp2 others(13): Show |
intron_variant | MODIFIER | c.4700-1285G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584009 | ||||||
| chr12:62584112
|
A | T | 1 | a0001c0002t0013g0303 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4700-1182A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584112 | ||||||
| chr12:62584221
|
G | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4700-1073G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584221 | ||||||
| chr12:62584479
|
G | A | 1 | a0001c0002t0010g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4700-815G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584479 | ||||||
| chr12:62584485
|
C | T | 1 | a0002c0001t0001g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4700-809C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584485 | ||||||
| chr12:62584705
|
C | CA | 100 | a0001c0002t0002g0254a0001c0002t0002g0311a0001c0002t0002g0331others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.4700-566dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62584705 | |||||
| chr12:62584705
|
C | CAA | 22 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(19): Show | 22 | HG00741.hp2 HG01074.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.4700-567_4700-566d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62584705 | |||||
| chr12:62584705
|
CA | C | 23 | a0001c0003t0003g0043a0001c0005t0003g0113a0001c0005t0003g0115others(20): Show | 23 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.4700-566delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62584705 | |||||
| chr12:62584775
|
C | T | 1 | a0005c0008t0002g0340 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.4700-519C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584775 | ||||||
| chr12:62584839
|
G | A | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4700-455G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584839 | ||||||
| chr12:62585065
|
GCA | G | 14 | a0001c0002t0002g0254a0001c0002t0002g0256a0001c0002t0002g0338others(11): Show | 14 | HG00099.hp2 HG00621.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.4700-184_4700-183d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | |||||
| chr12:62585065
|
GCACA | G | 94 | a0001c0002t0002g0305a0001c0002t0002g0311a0001c0002t0002g0317others(91): Show | 94 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.4700-186_4700-183d others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | |||||
| chr12:62585065
|
GCACACA | G | 28 | a0001c0002t0002g0322a0001c0002t0002g0331a0001c0002t0002g0335others(25): Show | 28 | HG00597.hp2 HG01074.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.4700-188_4700-183d others(8): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | |||||
| chr12:62585065
|
GCACACAC others(1): Show |
G | 54 | a0001c0002t0002g0321a0001c0002t0002g0352a0001c0002t0005g0362others(51): Show | 55 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.4700-190_4700-183d others(10): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | |||||
| chr12:62585065
|
GCACACAC others(3): Show |
G | 9 | a0001c0002t0002g0324a0001c0003t0003g0047a0001c0003t0005g0034others(6): Show | 9 | HG02258.hp2 HG03471.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.4700-192_4700-183d others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | |||||
| chr12:62585065
|
GCACACAC others(5): Show |
G | 18 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0010g0023others(15): Show | 18 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4700-194_4700-183d others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | |||||
| chr12:62585065
|
GCACACAC others(7): Show |
G | 11 | a0001c0006t0003g0006a0001c0006t0003g0007a0001c0006t0003g0106others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.4700-196_4700-183d others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | |||||
| chr12:62585065
|
GCACACAC others(11): Show |
G | 1 | a0001c0002t0003g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4700-200_4700-183d others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | |||||
| chr12:62585093
|
ACACACAC others(10): Show |
A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4700-200_4700-184d others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585093 | ||||||
| chr12:62585094
|
CACACACA others(12): Show |
C | 34 | a0001c0006t0033g0022a0002c0001t0001g0145a0002c0001t0001g0146others(31): Show | 34 | HG00733.hp1 HG01257.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.4700-196_4700-178d others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585094 | |||||
| chr12:62585096
|
CACACACA others(8): Show |
C | 7 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0012others(4): Show | 7 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.4700-196_4700-182d others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585096 | |||||
| chr12:62585096
|
CACACACA others(10): Show |
C | 9 | a0002c0001t0001g0204a0002c0001t0006g0143a0002c0001t0006g0199others(6): Show | 9 | HG00438.hp2 HG02647.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.4700-194_4700-178d others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585096 | |||||
| chr12:62585096
|
CACACACA others(13): Show |
C | 2 | a0002c0001t0001g0169a0002c0001t0001g0179 | 2 | HG01106.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.4700-196_4700-177d others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585096 | |||||
| chr12:62585097
|
ACACACAC others(6): Show |
A | 1 | a0001c0006t0007g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4700-196_4700-184d others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585097 | ||||||
| chr12:62585097
|
ACACACAC others(11): Show |
A | 11 | a0002c0001t0001g0147a0002c0001t0001g0173a0002c0001t0001g0175others(8): Show | 11 | HG00642.hp1 HG02895.hp1 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.4700-196_4700-179d others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585097 | ||||||
| chr12:62585098
|
CACACACA others(8): Show |
C | 3 | a0002c0001t0001g0138a0002c0001t0006g0198a0002c0001t0006g0206 | 3 | HG01261.hp2 HG02074.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.4700-192_4700-178d others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585098 | |||||
| chr12:62585098
|
CACACACA others(11): Show |
C | 9 | a0002c0001t0001g0003a0002c0001t0001g0158a0002c0001t0001g0166others(6): Show | 10 | HG00673.hp1 HG00738.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.4700-194_4700-177d others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585098 | |||||
| chr12:62585098
|
CACACACA others(12): Show |
C | 42 | a0002c0001t0001g0002a0002c0001t0001g0110a0002c0001t0001g0142others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.4700-194_4700-176d others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585098 | |||||
| chr12:62585098
|
CACACACA others(13): Show |
C | 1 | a0002c0001t0001g0172 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4700-194_4700-175d others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585098 | |||||
| chr12:62585100
|
CACACACA others(10): Show |
C | 6 | a0002c0001t0001g0137a0002c0001t0001g0151a0002c0001t0001g0238others(3): Show | 6 | HG03098.hp2 HG03139.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.4700-192_4700-176d others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585100 | |||||
| chr12:62585100
|
CACACACA others(11): Show |
C | 1 | a0002c0001t0001g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4700-192_4700-175d others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585100 | |||||
| chr12:62585101
|
ACACACAC others(7): Show |
A | 1 | a0002c0001t0012g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4700-192_4700-179d others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585101 | ||||||
| chr12:62585102
|
CACACACA others(10): Show |
C | 1 | a0002c0001t0001g0165 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4700-190_4700-174d others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585102 | |||||
| chr12:62585102
|
CACACACA others(12): Show |
C | 1 | a0002c0001t0001g0247 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4700-190_4700-172d others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585102 | |||||
| chr12:62585104
|
CACACACA others(5): Show |
C | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4700-188_4700-177d others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585104 | |||||
| chr12:62585114
|
A | C | 1 | a0001c0002t0002g0353 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.4700-180A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585114 | ||||||
| chr12:62585115
|
C | A | 25 | a0001c0002t0002g0353a0001c0006t0007g0009a0001c0006t0007g0010others(22): Show | 25 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.4700-179C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585115 | ||||||
| chr12:62585125
|
C | A | 140 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0303others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.4700-169C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585125 | ||||||
| chr12:62585131
|
A | C | 1 | a0002c0001t0001g0159 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4700-163A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585131 | ||||||
| chr12:62585154
|
A | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4700-140A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585154 | ||||||
| chr12:62585183
|
C | T | 1 | a0002c0001t0001g0222 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4700-111C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585183 | ||||||
| chr12:62585566
|
ACT | A | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4907+68_4907+69del others(2): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr12 | 62585566 | |||||
| chr12:62586037
|
G | A | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4907+536G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586037 | ||||||
| chr12:62586089
|
C | G | 1 | a0001c0003t0005g0078 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4907+588C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586089 | ||||||
| chr12:62586149
|
T | G | 1 | a0001c0018t0002g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4907+648T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586149 | ||||||
| chr12:62586232
|
C | T | 3 | a0001c0003t0005g0037a0001c0003t0005g0038a0001c0003t0005g0039 | 3 | HG02258.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4907+731C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586232 | ||||||
| chr12:62586333
|
G | A | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4907+832G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586333 | ||||||
| chr12:62586390
|
C | T | 1 | a0002c0001t0001g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4907+889C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586390 | ||||||
| chr12:62586597
|
A | T | 1 | a0001c0002t0002g0339 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4907+1096A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586597 | ||||||
| chr12:62586800
|
T | A | 148 | a0001c0002t0002g0305a0001c0006t0003g0005a0001c0006t0003g0006others(145): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.4908-1274T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586800 | ||||||
| chr12:62587069
|
C | T | 1 | a0001c0002t0002g0329 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.4908-1005C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587069 | ||||||
| chr12:62587175
|
A | G | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.4908-899A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587175 | ||||||
| chr12:62587259
|
A | G | 1 | a0001c0006t0007g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4908-815A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587259 | ||||||
| chr12:62587379
|
T | TA | 26 | a0001c0003t0005g0049a0001c0005t0003g0111a0001c0005t0003g0112others(23): Show | 26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.4908-682dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr12 | 62587379 | |||||
| chr12:62587379
|
TA | T | 53 | a0001c0002t0022g0295a0001c0002t0031g0136a0001c0003t0003g0099others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.4908-682delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr12 | 62587379 | |||||
| chr12:62587486
|
AGGCAGGA others(9): Show |
A | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4908-581_4908-566d others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr12 | 62587486 | |||||
| chr12:62587647
|
T | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4908-427T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587647 | ||||||
| chr12:62587664
|
C | T | 7 | a0002c0001t0006g0189a0002c0001t0006g0190a0002c0001t0006g0201others(4): Show | 7 | HG01928.hp1 HG02071.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.4908-410C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587664 | ||||||
| chr12:62587779
|
T | C | 1 | a0002c0001t0001g0247 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4908-295T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587779 | ||||||
| chr12:62587848
|
TGATAA | T | 3 | a0002c0001t0001g0145a0002c0001t0001g0245a0002c0001t0001g0246 | 3 | NA18968.hp2 NA19009.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4908-224_4908-220d others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr12 | 62587848 | |||||
| chr12:62587956
|
T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4908-118T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587956 | ||||||
| chr12:62588213
|
G | A | 2 | a0001c0002t0014g0280a0001c0002t0014g0287 | 2 | HG02300.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4990+57G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588213 | ||||||
| chr12:62588242
|
A | G | 2 | a0001c0003t0005g0051a0008c0011t0005g0093 | 2 | NA18941.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.4990+86A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588242 | ||||||
| chr12:62588258
|
C | A | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4990+102C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588258 | ||||||
| chr12:62588372
|
C | CT | 134 | a0001c0002t0031g0136a0001c0006t0007g0009a0001c0006t0007g0010others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.4990+228dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr12 | 62588372 | |||||
| chr12:62588482
|
A | G | 1 | a0002c0001t0001g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4990+326A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588482 | ||||||
| chr12:62588508
|
T | A | 5 | a0001c0003t0003g0041a0001c0003t0003g0042a0001c0003t0003g0043others(2): Show | 6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.4990+352T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588508 | ||||||
| chr12:62588821
|
A | C | 1 | a0001c0002t0002g0331 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4990+665A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588821 | ||||||
| chr12:62588861
|
A | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4990+705A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588861 | ||||||
| chr12:62589089
|
T | C | 1 | a0001c0002t0002g0318 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4990+933T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62589089 | ||||||
| chr12:62589255
|
A | G | 2 | a0001c0009t0019g0103a0001c0009t0019g0104 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4990+1099A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62589255 | ||||||
| chr12:62589363
|
C | T | 93 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(90): Show | 94 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.4990+1207C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62589363 | ||||||
| chr12:62589629
|
G | A | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4990+1473G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62589629 | ||||||
| chr12:62589744
|
T | TA | 18 | a0001c0003t0005g0045a0001c0003t0005g0046a0001c0003t0005g0086others(15): Show | 18 | HG01884.hp1 HG02055.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.4990+1609dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr12 | 62589744 | |||||
| chr12:62589744
|
TA | T | 132 | a0001c0002t0002g0030a0001c0002t0002g0331a0001c0002t0002g0351others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.4990+1609delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr12 | 62589744 | |||||
| chr12:62589744
|
TAA | T | 12 | a0001c0016t0032g0252a0002c0001t0001g0137a0002c0001t0001g0157others(9): Show | 12 | HG02083.hp1 HG02895.hp1 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.4990+1608_4990+160 others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr12 | 62589744 | |||||
| chr12:62589844
|
A | G | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4990+1688A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62589844 | ||||||
| chr12:62590121
|
T | C | 241 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.4990+1965T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590121 | ||||||
| chr12:62590226
|
G | A | 1 | a0002c0001t0001g0250 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4990+2070G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590226 | ||||||
| chr12:62590238
|
G | A | 9 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(6): Show | 9 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.4990+2082G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590238 | ||||||
| chr12:62590312
|
G | C | 241 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.4990+2156G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590312 | ||||||
| chr12:62590318
|
T | C | 241 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0003g0102others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.4990+2162T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590318 | ||||||
| chr12:62590352
|
G | A | 10 | a0001c0006t0003g0005a0001c0006t0003g0006a0001c0006t0003g0007others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4990+2196G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590352 | ||||||
| chr12:62590706
|
A | G | 13 | a0002c0001t0001g0003a0002c0001t0001g0137a0002c0001t0001g0138others(10): Show | 14 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.4991-1880A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590706 | ||||||
| chr12:62591035
|
G | A | 3 | a0002c0001t0001g0231a0002c0001t0001g0233a0002c0001t0012g0239 | 3 | HG00423.hp1 NA18955.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.4991-1551G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62591035 | ||||||
| chr12:62591147
|
CAACTG | C | 7 | a0001c0002t0013g0298a0001c0002t0013g0299a0001c0002t0013g0300others(4): Show | 7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4991-1436_4991-143 others(9): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr12 | 62591147 | |||||
| chr12:62591343
|
T | C | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4991-1243T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62591343 | ||||||
| chr12:62591554
|
A | C | 1 | a0001c0002t0002g0323 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4991-1032A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62591554 | ||||||
| chr12:62591788
|
A | G | 3 | a0002c0001t0001g0145a0002c0001t0001g0245a0002c0001t0001g0246 | 3 | NA18968.hp2 NA19009.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4991-798A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62591788 | ||||||
| chr12:62591826
|
A | G | 1 | a0001c0003t0005g0050 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4991-760A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62591826 | ||||||
| chr12:62592064
|
A | G | 4 | a0001c0005t0003g0120a0001c0005t0003g0122a0001c0005t0003g0123others(1): Show | 4 | HG01255.hp1 HG02602.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.4991-522A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62592064 | ||||||
| chr12:62592091
|
C | A | 135 | a0001c0006t0007g0009a0001c0006t0007g0010a0001c0006t0007g0011others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.4991-495C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62592091 | ||||||
| chr12:62592301
|
T | C | 4 | a0002c0001t0001g0221a0002c0001t0001g0222a0002c0001t0001g0223others(1): Show | 4 | HG01934.hp1 HG01975.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.4991-285T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62592301 | ||||||
| chr12:62592381
|
A | G | 1 | a0002c0001t0001g0249 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4991-205A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62592381 |