Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10198 |
|---|---|
| ensemblid | ENSG00000051825.15 |
| hgncid | 7215 |
| symbol | MPHOSPH9 |
| name | M-phase phosphoprotein 9 |
| refseq_nuc | NM_022782.4 |
| refseq_prot | NP_073619.3 |
| ensembl_nuc | ENST00000606320.6 |
| ensembl_prot | ENSP00000475489.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 123154215 |
| end | 123233141 |
| strand | - |
| ver | v1.2 |
| region | chr12:123154215-123233141 |
| region5000 | chr12:123149215-123238141 |
| regionname0 | MPHOSPH9_chr12_123154215_123233141 |
| regionname5000 | MPHOSPH9_chr12_123149215_123238141 |
| 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 | 1183 | 206 | 64 | 49 | 54 | 5 | 32 | 41 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002 | 0/0 | 1183 | 50 | 2 | 5 | 39 | 0 | 4 | 29 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0003 | 0/0 | 1183 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0004 | 0/0 | 1183 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0005 | 0/0 | 1183 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0006 | 0/0 | 1183 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0007 | 0/0 | 1183 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0008 | 0/0 | 1183 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0009 | 0/0 | 1183 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0010 | 0/0 | 1183 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0011 | 0/0 | 1183 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0012 | 0/0 | 1183 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| 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 | 1/1 | 3552 | 96 | 58 | 18 | 4 | 2 | 12 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0002 | 0/0 | 3552 | 83 | 1 | 23 | 42 | 0 | 17 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0003 | 0/0 | 3552 | 46 | 2 | 5 | 35 | 0 | 4 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0004 | 0/0 | 3552 | 19 | 2 | 7 | 4 | 3 | 3 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0005 | 0/0 | 3552 | 4 | 0 | 0 | 4 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0006 | 0/0 | 3552 | 3 | 0 | 0 | 3 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0007 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0008 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0009 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0010 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0011 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0012 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0013 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0014 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0015 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0016 | 0/0 | 3552 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0017 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0018 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0019 | 0/0 | 3552 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0020 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| c0021 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| 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 | 2814 | 89 | 2 | 28 | 44 | 3 | 12 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0002 | 0/0 | 2813 | 48 | 1 | 5 | 39 | 0 | 3 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0003 | 0/0 | 2817 | 35 | 32 | 3 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0004 | 1/1 | 2818 | 27 | 3 | 13 | 0 | 2 | 7 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0005 | 0/0 | 2816 | 17 | 17 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0006 | 0/0 | 2817 | 9 | 0 | 0 | 4 | 0 | 5 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0007 | 0/0 | 2813 | 8 | 0 | 1 | 5 | 0 | 2 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0008 | 0/0 | 2813 | 4 | 0 | 0 | 2 | 0 | 2 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0009 | 0/0 | 2818 | 3 | 3 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0010 | 0/0 | 2813 | 3 | 0 | 2 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0011 | 0/0 | 2813 | 2 | 1 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0012 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0013 | 0/0 | 2814 | 2 | 0 | 0 | 0 | 0 | 2 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0014 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0015 | 0/0 | 2818 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0016 | 0/0 | 2814 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0017 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0018 | 0/0 | 2814 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0019 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0020 | 0/0 | 2818 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0021 | 0/0 | 2818 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0022 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0023 | 0/0 | 2816 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0024 | 0/0 | 2813 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0025 | 0/0 | 2813 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0026 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0027 | 0/0 | 2814 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0028 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0029 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| t0030 | 0/0 | 2818 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| 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 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3552 | 96 | 58 | 18 | 4 | 2 | 12 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0002 | 0/0 | 3552 | 83 | 1 | 23 | 42 | 0 | 17 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0004 | 0/0 | 3552 | 19 | 2 | 7 | 4 | 3 | 3 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0005 | 0/0 | 3552 | 4 | 0 | 0 | 4 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0007 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0008 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0009 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0016 | 0/0 | 3552 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002c0003 | 0/0 | 3552 | 46 | 2 | 5 | 35 | 0 | 4 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002c0006 | 0/0 | 3552 | 3 | 0 | 0 | 3 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002c0012 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0003c0020 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0004c0019 | 0/0 | 3552 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0005c0018 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0006c0015 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0007c0017 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0008c0014 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0009c0013 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0010c0011 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0011c0010 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0012c0021 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003 | 0/0 | 6368 | 32 | 29 | 3 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0004 | 1/1 | 6369 | 26 | 3 | 13 | 0 | 1 | 7 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0005 | 0/0 | 6367 | 15 | 15 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0006 | 0/0 | 6368 | 9 | 0 | 0 | 4 | 0 | 5 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0009 | 0/0 | 6369 | 3 | 3 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0010 | 0/0 | 6364 | 3 | 0 | 2 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0012 | 0/0 | 6368 | 2 | 2 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0015 | 0/0 | 6369 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0020 | 0/0 | 6369 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0021 | 0/0 | 6369 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0023 | 0/0 | 6367 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0028 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0001t0030 | 0/0 | 6369 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0002t0001 | 0/0 | 6365 | 71 | 1 | 22 | 37 | 0 | 11 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0002t0007 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0002t0008 | 0/0 | 6364 | 4 | 0 | 0 | 2 | 0 | 2 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0002t0013 | 0/0 | 6365 | 2 | 0 | 0 | 0 | 0 | 2 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0002t0014 | 0/0 | 6365 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0002t0016 | 0/0 | 6365 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0002t0017 | 0/0 | 6363 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0002t0018 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0002t0019 | 0/0 | 6365 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0004t0001 | 0/0 | 6365 | 9 | 1 | 5 | 0 | 3 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0004t0007 | 0/0 | 6364 | 7 | 0 | 1 | 4 | 0 | 2 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0004t0011 | 0/0 | 6364 | 2 | 1 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0004t0024 | 0/0 | 6364 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0005t0001 | 0/0 | 6365 | 4 | 0 | 0 | 4 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0007t0029 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0008t0003 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0009t0022 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0001c0016t0001 | 0/0 | 6365 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002c0003t0001 | 0/0 | 6365 | 2 | 0 | 0 | 1 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002c0003t0002 | 0/0 | 6364 | 41 | 1 | 5 | 32 | 0 | 3 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002c0003t0025 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002c0003t0026 | 0/0 | 6363 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002c0003t0027 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002c0006t0002 | 0/0 | 6364 | 3 | 0 | 0 | 3 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0002c0012t0002 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0003c0020t0005 | 0/0 | 6367 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0004c0019t0004 | 0/0 | 6369 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0005c0018t0003 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0006c0015t0003 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0007c0017t0005 | 0/0 | 6367 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0008c0014t0002 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0009c0013t0002 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0010c0011t0002 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0011c0010t0001 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| a0012c0021t0001 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | copy fasta | chr12 | 123149215 | 123238141 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0010g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0010g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0010g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0012g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0015g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0020g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0021g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0023g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0028g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0001t0030g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0008g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0008g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0008g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0013g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0013g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0014g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0016g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0017g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0018g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0002t0019g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0007g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0007g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0007g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0007g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0011g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0004t0024g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0007t0029g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0008t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0009t0022g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0001c0016t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0025g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0026g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0003t0027g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0006t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0006t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0006t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0002c0012t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0003c0020t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0004c0019t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0005c0018t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0006c0015t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0007c0017t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0008c0014t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0009c0013t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0010c0011t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0011c0010t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| a0012c0021t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0010 | g0184 | EUR | GBR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0031 | EUR | GBR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00558 | hp1 | a0002 | c0003 | t0002 | g0264 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00558 | hp2 | a0001 | c0002 | t0007 | g0036 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00597 | hp1 | a0001 | c0005 | t0001 | g0095 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00609 | hp1 | a0001 | c0005 | t0001 | g0096 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00609 | hp2 | a0002 | c0003 | t0002 | g0260 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00621 | hp2 | a0002 | c0003 | t0002 | g0243 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0076 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00642 | hp2 | a0002 | c0003 | t0002 | g0223 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00673 | hp2 | a0002 | c0003 | t0002 | g0221 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0173 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01069 | hp2 | a0002 | c0003 | t0002 | g0226 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0192 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0224 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0191 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0077 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0074 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0176 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0185 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01175 | hp1 | a0001 | c0004 | t0011 | g0106 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0214 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01256 | hp2 | a0001 | c0001 | t0010 | g0175 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0189 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0075 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01361 | hp1 | a0001 | c0002 | t0016 | g0068 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01516 | hp1 | a0004 | c0019 | t0004 | g0197 | EUR | IBS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01516 | hp2 | a0001 | c0004 | t0001 | g0004 | EUR | IBS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0133 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0165 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01952 | hp1 | a0001 | c0016 | t0001 | g0098 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01952 | hp2 | a0001 | c0004 | t0007 | g0110 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0172 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0196 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0167 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02040 | hp1 | a0009 | c0013 | t0002 | g0249 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02071 | hp1 | a0012 | c0021 | t0001 | g0089 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02071 | hp2 | a0010 | c0011 | t0002 | g0220 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02080 | hp2 | a0002 | c0003 | t0002 | g0234 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02132 | hp1 | a0002 | c0006 | t0002 | g0252 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02132 | hp2 | a0001 | c0004 | t0007 | g0112 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02145 | hp1 | a0007 | c0017 | t0005 | g0204 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02155 | hp1 | a0002 | c0003 | t0002 | g0233 | EAS | CDX | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | CDX | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02293 | hp1 | a0002 | c0003 | t0002 | g0236 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0159 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02523 | hp2 | a0002 | c0003 | t0002 | g0229 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02602 | hp1 | a0001 | c0002 | t0014 | g0007 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02602 | hp2 | a0001 | c0001 | t0006 | g0266 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02622 | hp1 | a0001 | c0008 | t0003 | g0200 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02630 | hp2 | a0001 | c0001 | t0021 | g0206 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02683 | hp1 | a0001 | c0004 | t0024 | g0103 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02683 | hp2 | a0001 | c0002 | t0019 | g0038 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02735 | hp1 | a0002 | c0003 | t0002 | g0259 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02738 | hp1 | a0001 | c0004 | t0007 | g0104 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02738 | hp2 | a0001 | c0002 | t0008 | g0039 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02809 | hp2 | a0001 | c0009 | t0022 | g0163 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02886 | hp2 | a0006 | c0015 | t0003 | g0164 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02896 | hp1 | a0001 | c0001 | t0030 | g0212 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0152 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0145 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02970 | hp2 | a0003 | c0020 | t0005 | g0105 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02976 | hp1 | a0001 | c0001 | t0015 | g0108 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0179 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03139 | hp1 | a0001 | c0007 | t0029 | g0211 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03239 | hp2 | a0001 | c0004 | t0007 | g0114 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0201 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03491 | hp1 | a0001 | c0001 | t0006 | g0001 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03516 | hp1 | a0002 | c0003 | t0002 | g0213 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03516 | hp2 | a0001 | c0001 | t0020 | g0146 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0188 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0265 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03688 | hp2 | a0001 | c0002 | t0013 | g0091 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03831 | hp1 | a0002 | c0003 | t0002 | g0215 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03831 | hp2 | a0001 | c0002 | t0008 | g0030 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0230 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03834 | hp2 | a0001 | c0002 | t0013 | g0090 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0193 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0119 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0194 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG04228 | hp1 | a0002 | c0003 | t0002 | g0237 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18612 | hp1 | a0001 | c0002 | t0008 | g0061 | EAS | CHB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18612 | hp2 | a0002 | c0003 | t0002 | g0257 | EAS | CHB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | CHB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0232 | EAS | CHB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0151 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18941 | hp2 | a0002 | c0003 | t0002 | g0244 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18942 | hp2 | a0002 | c0003 | t0002 | g0256 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18948 | hp1 | a0011 | c0010 | t0001 | g0032 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18948 | hp2 | a0002 | c0003 | t0002 | g0262 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18949 | hp1 | a0002 | c0006 | t0002 | g0241 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0116 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18952 | hp2 | a0002 | c0006 | t0002 | g0261 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18953 | hp1 | a0001 | c0002 | t0008 | g0008 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18953 | hp2 | a0002 | c0003 | t0002 | g0235 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18957 | hp1 | a0002 | c0003 | t0002 | g0263 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18963 | hp1 | a0002 | c0003 | t0002 | g0218 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18972 | hp1 | a0001 | c0004 | t0007 | g0111 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18972 | hp2 | a0002 | c0003 | t0002 | g0242 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18974 | hp2 | a0002 | c0003 | t0002 | g0239 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18979 | hp1 | a0001 | c0005 | t0001 | g0094 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18979 | hp2 | a0001 | c0002 | t0018 | g0085 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18982 | hp1 | a0002 | c0003 | t0025 | g0081 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18987 | hp1 | a0002 | c0003 | t0002 | g0255 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18987 | hp2 | a0001 | c0005 | t0001 | g0093 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18989 | hp1 | a0002 | c0003 | t0027 | g0228 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18989 | hp2 | a0001 | c0004 | t0007 | g0113 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18990 | hp2 | a0002 | c0003 | t0002 | g0240 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18991 | hp2 | a0002 | c0003 | t0002 | g0250 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18992 | hp1 | a0002 | c0003 | t0002 | g0247 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18993 | hp2 | a0002 | c0003 | t0002 | g0251 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18995 | hp1 | a0002 | c0003 | t0002 | g0238 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18999 | hp1 | a0002 | c0003 | t0002 | g0246 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19003 | hp2 | a0002 | c0003 | t0002 | g0231 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19012 | hp1 | a0002 | c0003 | t0002 | g0245 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19054 | hp2 | a0002 | c0003 | t0002 | g0253 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19055 | hp1 | a0002 | c0003 | t0002 | g0248 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19055 | hp2 | a0001 | c0002 | t0017 | g0072 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19056 | hp1 | a0001 | c0004 | t0007 | g0109 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19057 | hp2 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19063 | hp1 | a0002 | c0012 | t0002 | g0225 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19064 | hp2 | a0002 | c0003 | t0002 | g0258 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19067 | hp1 | a0002 | c0003 | t0002 | g0216 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19082 | hp2 | a0002 | c0003 | t0002 | g0227 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19083 | hp1 | a0008 | c0014 | t0002 | g0222 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19084 | hp2 | a0002 | c0003 | t0002 | g0219 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19090 | hp1 | a0002 | c0003 | t0002 | g0217 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA19240 | hp2 | a0001 | c0001 | t0023 | g0210 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA20129 | hp1 | a0001 | c0004 | t0011 | g0107 | AFR | ASW | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | ASW | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0073 | EUR | TSI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0186 | EUR | TSI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02486 | hp2 | a0001 | c0001 | t0028 | g0166 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| HG03471 | hp2 | a0002 | c0003 | t0026 | g0254 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | USA | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA20300 | hp2 | a0005 | c0018 | t0003 | g0141 | AFR | USA | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0174 | REF | REF | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0178 | REF | REF | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123156874
|
C | T | 1 | a0007 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.3485G>A | p.Arg1162Gln | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 3710/6369 | 3485/3552 | 1162/1183 | chr12 | 123156874 | ||
| chr12:123163031
|
A | C | 1 | a0006 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.3012T>G | p.Asn1004Lys | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 20/24 | 3237/6369 | 3012/3552 | 1004/1183 | chr12 | 123163031 | ||
| chr12:123163083
|
C | T | 1 | a0010 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2960G>A | p.Arg987Gln | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 20/24 | 3185/6369 | 2960/3552 | 987/1183 | chr12 | 123163083 | ||
| chr12:123202775
|
T | C | 1 | a0009 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.1630A>G | p.Ser544Gly | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 10/24 | 1855/6369 | 1630/3552 | 544/1183 | chr12 | 123202775 | ||
| chr12:123218389
|
G | A | 1 | a0008 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.983C>T | p.Thr328Ile | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/24 | 1208/6369 | 983/3552 | 328/1183 | chr12 | 123218389 | ||
| chr12:123221415
|
C | T | 4 | a0002a0008a0009others(1): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
missense_variant | MODERATE | c.829G>A | p.Gly277Ser | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 1054/6369 | 829/3552 | 277/1183 | chr12 | 123221415 | ||
| chr12:123221417
|
A | G | 1 | a0011 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.827T>C | p.Leu276Pro | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 1052/6369 | 827/3552 | 276/1183 | chr12 | 123221417 | ||
| chr12:123221759
|
C | A | 1 | a0005 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.485G>T | p.Arg162Ile | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 710/6369 | 485/3552 | 162/1183 | chr12 | 123221759 | ||
| chr12:123221766
|
T | G | 1 | a0004 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.478A>C | p.Ser160Arg | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 703/6369 | 478/3552 | 160/1183 | chr12 | 123221766 | ||
| chr12:123221812
|
G | C | 1 | a0003 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.432C>G | p.Asn144Lys | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 657/6369 | 432/3552 | 144/1183 | chr12 | 123221812 | ||
| chr12:123230286
|
G | C | 1 | a0012 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.79C>G | p.Leu27Val | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/24 | 304/6369 | 79/3552 | 27/1183 | chr12 | 123230286 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123161256
|
G | A | 12 | a0001c0002a0001c0004a0001c0005others(9): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
synonymous_variant | LOW | c.3261C>T | p.Tyr1087Tyr | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 22/24 | 3486/6369 | 3261/3552 | 1087/1183 | chr12 | 123161256 | ||
| chr12:123166771
|
G | A | 1 | a0002c0012 | 1 | NA19063.hp1 | synonymous_variant | LOW | c.2475C>T | p.Asp825Asp | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/24 | 2700/6369 | 2475/3552 | 825/1183 | chr12 | 123166771 | ||
| chr12:123179967
|
G | A | 5 | a0001c0002a0001c0005a0001c0016others(2): Show | 90 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(87): Show |
synonymous_variant | LOW | c.2313C>T | p.Asn771Asn | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/24 | 2538/6369 | 2313/3552 | 771/1183 | chr12 | 123179967 | ||
| chr12:123198313
|
A | G | 1 | a0001c0016 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.1959T>C | p.Ala653Ala | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/24 | 2184/6369 | 1959/3552 | 653/1183 | chr12 | 123198313 | ||
| chr12:123202854
|
C | T | 1 | a0006c0015 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1551G>A | p.Pro517Pro | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 10/24 | 1776/6369 | 1551/3552 | 517/1183 | chr12 | 123202854 | ||
| chr12:123210125
|
G | A | 3 | a0002c0006a0002c0012a0009c0013 | 5 | HG02040.hp1 HG02132.hp1 NA18949.hp1 others(2): Show |
synonymous_variant | LOW | c.1125C>T | p.His375His | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/24 | 1350/6369 | 1125/3552 | 375/1183 | chr12 | 123210125 | ||
| chr12:123221473
|
A | G | 1 | a0001c0009 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.771T>C | p.His257His | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 996/6369 | 771/3552 | 257/1183 | chr12 | 123221473 | ||
| chr12:123221539
|
C | T | 1 | a0001c0008 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.705G>A | p.Pro235Pro | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 930/6369 | 705/3552 | 235/1183 | chr12 | 123221539 | ||
| chr12:123221560
|
C | T | 1 | a0001c0007 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.684G>A | p.Gln228Gln | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 909/6369 | 684/3552 | 228/1183 | chr12 | 123221560 | ||
| chr12:123221641
|
G | T | 1 | a0001c0005 | 4 | HG00597.hp1 HG00609.hp1 NA18979.hp1 others(1): Show |
synonymous_variant | LOW | c.603C>A | p.Thr201Thr | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 828/6369 | 603/3552 | 201/1183 | chr12 | 123221641 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123154322
|
A | G | 1 | a0001c0009t0022 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2485T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 2485 | chr12 | 123154322 | |||||
| chr12:123154383
|
G | A | 27 | a0001c0002t0001a0001c0002t0007a0001c0002t0008others(24): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*2424C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 2424 | chr12 | 123154383 | |||||
| chr12:123154527
|
C | T | 1 | a0002c0003t0025 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2280G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 2280 | chr12 | 123154527 | |||||
| chr12:123154636
|
C | T | 2 | a0001c0004t0011a0001c0004t0024 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2171G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 2171 | chr12 | 123154636 | |||||
| chr12:123154877
|
G | A | 1 | a0001c0002t0013 | 2 | HG03688.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1930C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1930 | chr12 | 123154877 | |||||
| chr12:123154992
|
T | TA | 27 | a0001c0001t0009a0001c0001t0020a0001c0002t0001others(24): Show | 161 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1814dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1814 | chr12 | 123154992 | |||||
| chr12:123155214
|
TAAATA | T | 28 | a0001c0001t0010a0001c0002t0001a0001c0002t0007others(25): Show | 165 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1588_*1592delTATT others(1): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1588 | chr12 | 123155214 | |||||
| chr12:123155322
|
G | C | 9 | a0002c0003t0002a0002c0003t0025a0002c0003t0026others(6): Show | 51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1485C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1485 | chr12 | 123155322 | |||||
| chr12:123155415
|
C | T | 1 | a0001c0004t0024 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1392G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1392 | chr12 | 123155415 | |||||
| chr12:123155461
|
G | C | 1 | a0001c0009t0022 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1346 | chr12 | 123155461 | |||||
| chr12:123155500
|
G | A | 1 | a0001c0001t0023 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1307C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1307 | chr12 | 123155500 | |||||
| chr12:123155627
|
T | C | 1 | a0001c0002t0018 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1180A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1180 | chr12 | 123155627 | |||||
| chr12:123155694
|
A | G | 1 | a0001c0002t0016 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1113T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1113 | chr12 | 123155694 | |||||
| chr12:123155715
|
G | C | 1 | a0001c0001t0006 | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1092C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1092 | chr12 | 123155715 | |||||
| chr12:123155814
|
C | T | 1 | a0001c0001t0020 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*993G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 993 | chr12 | 123155814 | |||||
| chr12:123156117
|
C | A | 27 | a0001c0002t0001a0001c0002t0007a0001c0002t0008others(24): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*690G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 690 | chr12 | 123156117 | |||||
| chr12:123156306
|
C | G | 41 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(38): Show | 223 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*501G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 501 | chr12 | 123156306 | |||||
| chr12:123156323
|
T | G | 1 | a0001c0002t0019 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 484 | chr12 | 123156323 | |||||
| chr12:123156653
|
C | T | 14 | a0001c0002t0001a0001c0002t0008a0001c0002t0013others(11): Show | 100 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*154G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 154 | chr12 | 123156653 | |||||
| chr12:123156771
|
A | T | 1 | a0001c0001t0015 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 36 | chr12 | 123156771 | |||||
| chr12:123230393
|
T | C | 1 | a0001c0002t0013 | 2 | HG03688.hp2 HG03834.hp2 |
5_prime_UTR_variant | MODIFIER | c.-29A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/24 | 29 | chr12 | 123230393 | |||||
| chr12:123230460
|
T | C | 1 | a0001c0001t0028 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/24 | 96 | chr12 | 123230460 | |||||
| chr12:123230466
|
G | C | 2 | a0001c0001t0030a0001c0007t0029 | 2 | HG02896.hp1 HG03139.hp1 |
5_prime_UTR_variant | MODIFIER | c.-102C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/24 | 102 | chr12 | 123230466 | |||||
| chr12:123230516
|
A | G | 1 | a0001c0002t0014 | 1 | HG02602.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-152T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/24 | chr12 | 123230516 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123157207
|
G | A | 1 | a0007c0017t0005g0204 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3451-299C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157207 | ||||||
| chr12:123157304
|
C | T | 1 | a0001c0002t0001g0010 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3451-396G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157304 | ||||||
| chr12:123157352
|
A | G | 3 | a0001c0002t0001g0005a0001c0002t0001g0023a0001c0002t0001g0065 | 3 | HG00733.hp1 HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.3451-444T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157352 | ||||||
| chr12:123157383
|
TA | T | 192 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(189): Show | 192 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(189): Show |
intron_variant | MODIFIER | c.3451-476delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157383 | ||||||
| chr12:123157512
|
C | G | 1 | a0005c0018t0003g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3451-604G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157512 | ||||||
| chr12:123157673
|
G | T | 100 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(97): Show | 100 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.3451-765C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157673 | ||||||
| chr12:123157835
|
A | T | 1 | a0001c0001t0003g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3451-927T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157835 | ||||||
| chr12:123157986
|
A | AT | 11 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(8): Show | 11 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3451-1079dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157986 | ||||||
| chr12:123157991
|
T | A | 163 | a0001c0001t0005g0205a0001c0002t0001g0005a0001c0002t0001g0009others(160): Show | 163 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.3451-1083A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157991 | ||||||
| chr12:123157992
|
T | A | 1 | a0004c0019t0004g0197 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3451-1084A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157992 | ||||||
| chr12:123158193
|
T | C | 9 | a0001c0001t0003g0158a0001c0002t0007g0036a0001c0004t0007g0104others(6): Show | 9 | HG00558.hp2 HG01952.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.3451-1285A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158193 | ||||||
| chr12:123158387
|
G | C | 1 | a0003c0020t0005g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3451-1479C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158387 | ||||||
| chr12:123158408
|
C | G | 162 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(159): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.3451-1500G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158408 | ||||||
| chr12:123158810
|
T | C | 15 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(12): Show | 15 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.3451-1902A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158810 | ||||||
| chr12:123158873
|
T | C | 162 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(159): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.3450+1908A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158873 | ||||||
| chr12:123158906
|
C | A | 8 | a0001c0002t0007g0036a0001c0004t0007g0104a0001c0004t0007g0109others(5): Show | 8 | HG00558.hp2 HG01952.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.3450+1875G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158906 | ||||||
| chr12:123158963
|
T | C | 1 | a0002c0003t0002g0260 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3450+1818A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158963 | ||||||
| chr12:123159142
|
T | C | 162 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(159): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.3450+1639A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159142 | ||||||
| chr12:123159182
|
A | G | 200 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(197): Show | 200 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.3450+1599T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159182 | ||||||
| chr12:123159448
|
C | T | 5 | a0001c0001t0003g0168a0001c0001t0003g0198a0001c0001t0003g0199others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3450+1333G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159448 | ||||||
| chr12:123159454
|
C | T | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3450+1327G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159454 | ||||||
| chr12:123159496
|
T | C | 51 | a0002c0003t0002g0213a0002c0003t0002g0214a0002c0003t0002g0215others(48): Show | 51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.3450+1285A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159496 | ||||||
| chr12:123159509
|
C | A | 162 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(159): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.3450+1272G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159509 | ||||||
| chr12:123159543
|
C | T | 1 | a0001c0009t0022g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3450+1238G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159543 | ||||||
| chr12:123159806
|
C | T | 1 | a0001c0001t0006g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3450+975G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159806 | ||||||
| chr12:123159872
|
T | TA | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3450+908_3450+909i others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159872 | ||||||
| chr12:123159873
|
T | A | 220 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(217): Show | 220 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.3450+908A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159873 | ||||||
| chr12:123159955
|
C | T | 2 | a0002c0003t0002g0213a0002c0003t0002g0214 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3450+826G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159955 | ||||||
| chr12:123160086
|
G | A | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3450+695C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160086 | ||||||
| chr12:123160167
|
A | G | 200 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(197): Show | 200 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.3450+614T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160167 | ||||||
| chr12:123160261
|
C | T | 8 | a0001c0002t0007g0036a0001c0004t0007g0104a0001c0004t0007g0109others(5): Show | 8 | HG00558.hp2 HG01952.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.3450+520G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160261 | ||||||
| chr12:123160446
|
C | G | 4 | a0002c0003t0002g0216a0002c0003t0002g0227a0002c0003t0002g0250others(1): Show | 4 | NA18989.hp1 NA18991.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.3450+335G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160446 | ||||||
| chr12:123160684
|
A | G | 1 | a0001c0004t0007g0114 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3450+97T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160684 | ||||||
| chr12:123160776
|
T | C | 38 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(35): Show | 38 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(35): Show |
splice_region_variant&intron_variant | LOW | c.3450+5A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160776 | ||||||
| chr12:123161025
|
T | C | 1 | a0002c0003t0002g0224 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3381+111A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 22/23 | chr12 | 123161025 | ||||||
| chr12:123161441
|
T | C | 16 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(13): Show | 16 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3134-58A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 21/23 | chr12 | 123161441 | ||||||
| chr12:123161549
|
T | C | 1 | a0001c0001t0006g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3134-166A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 21/23 | chr12 | 123161549 | ||||||
| chr12:123161642
|
G | A | 1 | a0001c0004t0007g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3134-259C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 21/23 | chr12 | 123161642 | ||||||
| chr12:123161663
|
C | CA | 29 | a0001c0001t0003g0137a0001c0001t0003g0160a0001c0001t0004g0189others(26): Show | 29 | HG00642.hp2 HG01175.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.3134-281dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 21/23 | chr12 | 123161663 | ||||||
| chr12:123162492
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3030-274G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 20/23 | chr12 | 123162492 | ||||||
| chr12:123162866
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3029+148C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 20/23 | chr12 | 123162866 | ||||||
| chr12:123163178
|
G | C | 162 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(159): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2909-44C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 19/23 | chr12 | 123163178 | ||||||
| chr12:123163393
|
G | A | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2909-259C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 19/23 | chr12 | 123163393 | ||||||
| chr12:123163430
|
A | G | 1 | a0001c0002t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2909-296T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 19/23 | chr12 | 123163430 | ||||||
| chr12:123163485
|
C | T | 100 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(97): Show | 100 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.2909-351G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 19/23 | chr12 | 123163485 | ||||||
| chr12:123163592
|
G | GC | 234 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(231): Show | 234 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(231): Show |
intron_variant | MODIFIER | c.2908+357_2908+358i others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 19/23 | chr12 | 123163592 | ||||||
| chr12:123164134
|
C | G | 1 | a0002c0003t0002g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2768-44G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123164134 | ||||||
| chr12:123164334
|
C | T | 162 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(159): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2768-244G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123164334 | ||||||
| chr12:123164612
|
T | A | 1 | a0002c0003t0002g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2768-522A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123164612 | ||||||
| chr12:123164723
|
G | A | 6 | a0001c0002t0001g0011a0001c0002t0001g0037a0001c0002t0001g0049others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2767+579C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123164723 | ||||||
| chr12:123164939
|
A | G | 200 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(197): Show | 200 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.2767+363T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123164939 | ||||||
| chr12:123165015
|
C | CA | 141 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(138): Show | 141 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.2767+286dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123165015 | ||||||
| chr12:123165015
|
C | CAA | 11 | a0001c0001t0020g0146a0001c0002t0001g0005a0001c0002t0001g0013others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2767+285_2767+286d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123165015 | ||||||
| chr12:123165015
|
CA | C | 51 | a0001c0001t0010g0184a0001c0002t0007g0036a0001c0004t0007g0104others(48): Show | 51 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.2767+286delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123165015 | ||||||
| chr12:123165757
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2592-280G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123165757 | ||||||
| chr12:123165788
|
C | T | 111 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(108): Show | 111 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.2592-311G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123165788 | ||||||
| chr12:123166062
|
C | T | 1 | a0001c0004t0007g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2592-585G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166062 | ||||||
| chr12:123166089
|
G | T | 1 | a0002c0003t0002g0239 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2591+566C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166089 | ||||||
| chr12:123166098
|
G | A | 2 | a0001c0002t0007g0036a0001c0004t0007g0110 | 2 | HG00558.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2591+557C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166098 | ||||||
| chr12:123166163
|
T | C | 1 | a0001c0001t0010g0175 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2591+492A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166163 | ||||||
| chr12:123166167
|
A | G | 162 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(159): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2591+488T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166167 | ||||||
| chr12:123166471
|
T | C | 162 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(159): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2591+184A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166471 | ||||||
| chr12:123166558
|
A | C | 1 | a0001c0001t0021g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2591+97T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166558 | ||||||
| chr12:123166615
|
A | G | 162 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(159): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2591+40T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166615 | ||||||
| chr12:123166908
|
T | C | 1 | a0001c0004t0024g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2457-119A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123166908 | ||||||
| chr12:123167191
|
G | A | 3 | a0001c0001t0010g0175a0001c0001t0010g0184a0001c0001t0010g0185 | 3 | HG00140.hp1 HG01109.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2457-402C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123167191 | ||||||
| chr12:123167419
|
G | C | 162 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(159): Show | 162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2457-630C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123167419 | ||||||
| chr12:123167514
|
C | G | 14 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0149others(11): Show | 14 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2457-725G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123167514 | ||||||
| chr12:123168182
|
C | A | 8 | a0001c0002t0007g0036a0001c0004t0007g0104a0001c0004t0007g0109others(5): Show | 8 | HG00558.hp2 HG01952.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.2457-1393G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168182 | ||||||
| chr12:123168223
|
G | A | 2 | a0001c0002t0001g0087a0001c0002t0016g0068 | 2 | HG01361.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2457-1434C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168223 | ||||||
| chr12:123168236
|
A | G | 21 | a0002c0003t0002g0217a0002c0003t0002g0218a0002c0003t0002g0221others(18): Show | 21 | HG00673.hp2 HG01070.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.2457-1447T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168236 | ||||||
| chr12:123168341
|
C | CT | 21 | a0001c0001t0004g0173a0001c0001t0004g0190a0001c0001t0005g0128others(18): Show | 21 | HG00741.hp1 HG01175.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2457-1553dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168341 | ||||||
| chr12:123168341
|
C | CTT | 8 | a0001c0002t0007g0036a0001c0004t0007g0104a0001c0004t0007g0109others(5): Show | 8 | HG00558.hp2 HG01952.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.2457-1554_2457-155 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168341 | ||||||
| chr12:123168341
|
CT | C | 45 | a0001c0001t0004g0189a0002c0003t0002g0215a0002c0003t0002g0216others(42): Show | 45 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2457-1553delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168341 | ||||||
| chr12:123168381
|
A | G | 11 | a0001c0002t0007g0036a0001c0004t0007g0104a0001c0004t0007g0109others(8): Show | 11 | HG00558.hp2 HG01175.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.2457-1592T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168381 | ||||||
| chr12:123168490
|
T | C | 3 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027 | 3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2457-1701A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168490 | ||||||
| chr12:123168499
|
G | C | 1 | a0001c0001t0028g0166 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2457-1710C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168499 | ||||||
| chr12:123168499
|
G | T | 220 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(217): Show | 220 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.2457-1710C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168499 | ||||||
| chr12:123168631
|
C | T | 1 | a0001c0002t0016g0068 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2457-1842G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168631 | ||||||
| chr12:123168709
|
CCCT | C | 92 | a0001c0001t0004g0188a0001c0002t0001g0005a0001c0002t0001g0009others(89): Show | 92 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2457-1923_2457-192 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168709 | ||||||
| chr12:123168923
|
C | T | 1 | a0001c0002t0008g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2457-2134G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168923 | ||||||
| chr12:123169009
|
C | T | 171 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(168): Show | 171 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.2457-2220G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169009 | ||||||
| chr12:123169034
|
A | G | 2 | a0001c0001t0009g0159a0001c0002t0016g0068 | 2 | HG01361.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2457-2245T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169034 | ||||||
| chr12:123169045
|
C | A | 163 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(160): Show | 163 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.2457-2256G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169045 | ||||||
| chr12:123169295
|
A | G | 1 | a0001c0001t0005g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2457-2506T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169295 | ||||||
| chr12:123169358
|
G | T | 1 | a0001c0001t0003g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2457-2569C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169358 | ||||||
| chr12:123169494
|
G | A | 1 | a0002c0003t0002g0238 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2457-2705C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169494 | ||||||
| chr12:123169498
|
TA | T | 9 | a0001c0001t0003g0156a0001c0001t0005g0133a0001c0001t0005g0205others(6): Show | 9 | HG01069.hp2 HG01884.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.2457-2710delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169498 | ||||||
| chr12:123169612
|
T | C | 1 | a0005c0018t0003g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2457-2823A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169612 | ||||||
| chr12:123169818
|
A | G | 1 | a0001c0002t0001g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3029T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169818 | ||||||
| chr12:123169823
|
T | C | 1 | a0001c0002t0001g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3034A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169823 | ||||||
| chr12:123169832
|
T | C | 1 | a0001c0002t0001g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3043A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169832 | ||||||
| chr12:123169833
|
G | A | 16 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(13): Show | 16 | HG01952.hp2 HG02132.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.2457-3044C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169833 | ||||||
| chr12:123169834
|
C | A | 16 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(13): Show | 16 | HG01952.hp2 HG02132.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.2457-3045G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169834 | ||||||
| chr12:123169837
|
A | G | 1 | a0001c0002t0001g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3048T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169837 | ||||||
| chr12:123169841
|
T | C | 1 | a0001c0002t0001g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3052A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169841 | ||||||
| chr12:123169842
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3053C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169842 | ||||||
| chr12:123169845
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3056G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169845 | ||||||
| chr12:123169951
|
G | A | 39 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2457-3162C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169951 | ||||||
| chr12:123169982
|
CT | C | 7 | a0001c0001t0006g0117a0001c0001t0009g0145a0001c0001t0009g0159others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2457-3194delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169982 | ||||||
| chr12:123170124
|
C | T | 19 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(16): Show | 19 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.2457-3335G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170124 | ||||||
| chr12:123170231
|
C | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2457-3442G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170231 | ||||||
| chr12:123170265
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2457-3476A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170265 | ||||||
| chr12:123170347
|
G | A | 1 | a0002c0003t0002g0217 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2457-3558C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170347 | ||||||
| chr12:123170502
|
A | G | 235 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(232): Show | 235 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(232): Show |
intron_variant | MODIFIER | c.2457-3713T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170502 | ||||||
| chr12:123170910
|
C | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2457-4121G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170910 | ||||||
| chr12:123170920
|
T | G | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2457-4131A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170920 | ||||||
| chr12:123170934
|
A | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2457-4145T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170934 | ||||||
| chr12:123170987
|
T | C | 1 | a0001c0016t0001g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2457-4198A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170987 | ||||||
| chr12:123171180
|
A | G | 1 | a0007c0017t0005g0204 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2457-4391T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123171180 | ||||||
| chr12:123171523
|
C | T | 1 | a0001c0002t0007g0036 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2457-4734G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123171523 | ||||||
| chr12:123171749
|
AAAACAAA others(1): Show |
A | 15 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(12): Show | 15 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2456+4931_2456+493 others(12): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123171749 | ||||||
| chr12:123171986
|
C | T | 164 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(161): Show | 164 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(161): Show |
intron_variant | MODIFIER | c.2456+4702G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123171986 | ||||||
| chr12:123171997
|
G | A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2456+4691C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123171997 | ||||||
| chr12:123172017
|
C | A | 7 | a0001c0004t0007g0104a0001c0004t0007g0109a0001c0004t0007g0110others(4): Show | 7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2456+4671G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172017 | ||||||
| chr12:123172021
|
T | C | 1 | a0001c0008t0003g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2456+4667A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172021 | ||||||
| chr12:123172136
|
G | A | 1 | a0001c0002t0007g0036 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2456+4552C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172136 | ||||||
| chr12:123172178
|
G | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2456+4510C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172178 | ||||||
| chr12:123172262
|
G | A | 90 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(87): Show | 90 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.2456+4426C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172262 | ||||||
| chr12:123172337
|
C | CT | 5 | a0001c0001t0004g0169a0001c0002t0001g0100a0001c0002t0008g0008others(2): Show | 5 | HG01978.hp1 HG02071.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.2456+4350dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172337 | ||||||
| chr12:123172337
|
CT | C | 11 | a0001c0001t0004g0182a0001c0001t0005g0133a0001c0001t0021g0206others(8): Show | 11 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.2456+4350delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172337 | ||||||
| chr12:123172467
|
G | C | 1 | a0001c0002t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2456+4221C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172467 | ||||||
| chr12:123172535
|
G | A | 1 | a0003c0020t0005g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2456+4153C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172535 | ||||||
| chr12:123172553
|
G | A | 9 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(6): Show | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.2456+4135C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172553 | ||||||
| chr12:123172558
|
C | G | 1 | a0001c0004t0001g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2456+4130G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172558 | ||||||
| chr12:123172680
|
T | C | 3 | a0001c0001t0004g0179a0001c0001t0004g0194a0001c0001t0004g0201 | 3 | HG03017.hp2 HG03490.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2456+4008A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172680 | ||||||
| chr12:123172791
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2456+3897A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172791 | ||||||
| chr12:123172861
|
T | C | 2 | a0002c0003t0002g0224a0002c0003t0002g0236 | 2 | HG01070.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2456+3827A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172861 | ||||||
| chr12:123172871
|
C | CT | 21 | a0001c0001t0003g0122a0001c0001t0003g0126a0001c0001t0003g0137others(18): Show | 21 | HG01106.hp2 HG01109.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2456+3816dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | ||||||
| chr12:123172871
|
C | CTT | 7 | a0001c0001t0003g0202a0001c0002t0001g0025a0001c0002t0001g0026others(4): Show | 7 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2456+3815_2456+381 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | ||||||
| chr12:123172871
|
C | CTTT | 63 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0015others(60): Show | 63 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2456+3814_2456+381 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | ||||||
| chr12:123172871
|
C | CTTTT | 64 | a0001c0001t0004g0182a0001c0001t0004g0183a0001c0002t0001g0005others(61): Show | 64 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2456+3813_2456+381 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | ||||||
| chr12:123172871
|
C | CTTTTT | 23 | a0001c0001t0004g0173a0001c0002t0001g0012a0001c0002t0001g0040others(20): Show | 23 | HG00621.hp1 HG00673.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.2456+3812_2456+381 others(9): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | ||||||
| chr12:123172871
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0003t0002g0229 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2456+3806_2456+381 others(15): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | ||||||
| chr12:123172871
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2456+3803_2456+381 others(18): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | ||||||
| chr12:123173169
|
C | A | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2456+3519G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173169 | ||||||
| chr12:123173194
|
C | G | 1 | a0001c0001t0005g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2456+3494G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173194 | ||||||
| chr12:123173206
|
T | A | 1 | a0001c0002t0001g0009 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2456+3482A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173206 | ||||||
| chr12:123173467
|
G | A | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2456+3221C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173467 | ||||||
| chr12:123173600
|
T | TC | 39 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2456+3087dupG | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173600 | ||||||
| chr12:123173711
|
A | G | 230 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(227): Show | 230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.2456+2977T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173711 | ||||||
| chr12:123173841
|
A | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2456+2847T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173841 | ||||||
| chr12:123174375
|
A | ATT | 163 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(160): Show | 163 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.2456+2311_2456+231 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123174375 | ||||||
| chr12:123174375
|
A | ATTT | 5 | a0001c0002t0001g0100a0001c0002t0008g0039a0001c0004t0007g0111others(2): Show | 5 | HG01978.hp1 HG02738.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.2456+2310_2456+231 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123174375 | ||||||
| chr12:123174635
|
GTGCTGGG others(774): Show |
G | 1 | a0001c0001t0005g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2456+1272_2456+205 others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123174635 | ||||||
| chr12:123174833
|
G | C | 18 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(15): Show | 18 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2456+1855C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123174833 | ||||||
| chr12:123174995
|
C | T | 211 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(208): Show | 211 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.2456+1693G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123174995 | ||||||
| chr12:123175458
|
C | A | 39 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2456+1230G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175458 | ||||||
| chr12:123175472
|
C | T | 1 | a0001c0001t0003g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2456+1216G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175472 | ||||||
| chr12:123175489
|
A | G | 1 | a0002c0003t0002g0234 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2456+1199T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175489 | ||||||
| chr12:123175553
|
T | C | 54 | a0001c0001t0021g0206a0002c0003t0001g0230a0002c0003t0001g0232others(51): Show | 54 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2456+1135A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175553 | ||||||
| chr12:123175629
|
A | G | 13 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0149others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2456+1059T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175629 | ||||||
| chr12:123175637
|
C | T | 3 | a0001c0001t0003g0148a0001c0001t0003g0150a0001c0001t0003g0158 | 3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2456+1051G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175637 | ||||||
| chr12:123175821
|
T | TA | 6 | a0001c0001t0003g0149a0001c0001t0003g0160a0001c0001t0003g0162others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2456+866dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175821 | ||||||
| chr12:123175821
|
TA | T | 113 | a0001c0001t0005g0130a0001c0001t0005g0133a0001c0001t0006g0002others(110): Show | 113 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.2456+866delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175821 | ||||||
| chr12:123175821
|
TAA | T | 10 | a0001c0001t0006g0001a0001c0002t0001g0045a0001c0002t0001g0084others(7): Show | 10 | HG00639.hp1 HG00639.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2456+865_2456+866d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175821 | ||||||
| chr12:123175963
|
A | G | 235 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(232): Show | 235 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(232): Show |
intron_variant | MODIFIER | c.2456+725T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175963 | ||||||
| chr12:123176011
|
A | G | 1 | a0003c0020t0005g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2456+677T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176011 | ||||||
| chr12:123176169
|
T | G | 230 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(227): Show | 230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.2456+519A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176169 | ||||||
| chr12:123176170
|
T | C | 230 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(227): Show | 230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.2456+518A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176170 | ||||||
| chr12:123176174
|
A | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2456+514T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176174 | ||||||
| chr12:123176228
|
T | A | 1 | a0001c0002t0018g0085 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2456+460A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176228 | ||||||
| chr12:123176295
|
T | C | 1 | a0001c0001t0003g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2456+393A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176295 | ||||||
| chr12:123176586
|
A | G | 1 | a0001c0004t0001g0006 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2456+102T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176586 | ||||||
| chr12:123177098
|
G | C | 1 | a0005c0018t0003g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2355-309C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177098 | ||||||
| chr12:123177217
|
T | C | 9 | a0001c0004t0007g0104a0001c0004t0007g0109a0001c0004t0007g0110others(6): Show | 9 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2355-428A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177217 | ||||||
| chr12:123177485
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2355-696C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177485 | ||||||
| chr12:123177508
|
C | G | 4 | a0001c0005t0001g0093a0001c0005t0001g0094a0001c0005t0001g0095others(1): Show | 4 | HG00597.hp1 HG00609.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2355-719G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177508 | ||||||
| chr12:123177557
|
CA | C | 11 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(8): Show | 11 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2355-769delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177557 | ||||||
| chr12:123177771
|
T | A | 1 | a0002c0003t0002g0255 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2355-982A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177771 | ||||||
| chr12:123177773
|
A | C | 1 | a0002c0003t0002g0255 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2355-984T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177773 | ||||||
| chr12:123177859
|
A | AAC | 14 | a0001c0001t0006g0117a0001c0001t0006g0265a0001c0002t0001g0009others(11): Show | 14 | HG00597.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.2355-1071_2355-107 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177859 | ||||||
| chr12:123177860
|
A | AC | 106 | a0001c0001t0005g0170a0001c0001t0006g0001a0001c0001t0006g0002others(103): Show | 106 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.2355-1072_2355-107 others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177860 | ||||||
| chr12:123178076
|
C | T | 2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2355-1287G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123178076 | ||||||
| chr12:123178127
|
A | G | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2355-1338T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123178127 | ||||||
| chr12:123178804
|
G | A | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2354+1122C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123178804 | ||||||
| chr12:123178975
|
T | C | 2 | a0001c0001t0003g0144a0001c0001t0003g0156 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2354+951A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123178975 | ||||||
| chr12:123179113
|
G | A | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2354+813C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179113 | ||||||
| chr12:123179161
|
C | T | 14 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0149others(11): Show | 14 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2354+765G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179161 | ||||||
| chr12:123179294
|
G | T | 1 | a0001c0004t0001g0006 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2354+632C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179294 | ||||||
| chr12:123179297
|
G | A | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2354+629C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179297 | ||||||
| chr12:123179541
|
C | T | 1 | a0001c0001t0004g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2354+385G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179541 | ||||||
| chr12:123179658
|
C | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2354+268G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179658 | ||||||
| chr12:123179716
|
T | TA | 92 | a0001c0001t0004g0179a0001c0001t0004g0180a0001c0001t0004g0201others(89): Show | 92 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2354+209dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179716 | ||||||
| chr12:123179716
|
TA | T | 12 | a0001c0001t0003g0125a0001c0001t0003g0138a0001c0001t0003g0158others(9): Show | 12 | HG00558.hp1 HG01070.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2354+209delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179716 | ||||||
| chr12:123179734
|
A | G | 2 | a0002c0003t0002g0240a0002c0003t0002g0263 | 2 | NA18957.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2354+192T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179734 | ||||||
| chr12:123179891
|
A | C | 50 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0215others(47): Show | 50 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.2354+35T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179891 | ||||||
| chr12:123180566
|
G | C | 121 | a0001c0001t0003g0202a0001c0001t0006g0001a0001c0001t0006g0002others(118): Show | 121 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.2290-576C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 14/23 | chr12 | 123180566 | ||||||
| chr12:123180709
|
C | T | 173 | a0001c0001t0003g0202a0001c0001t0006g0001a0001c0001t0006g0002others(170): Show | 173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.2289+454G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 14/23 | chr12 | 123180709 | ||||||
| chr12:123180742
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2289+421C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 14/23 | chr12 | 123180742 | ||||||
| chr12:123180813
|
T | C | 1 | a0002c0003t0002g0229 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2289+350A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 14/23 | chr12 | 123180813 | ||||||
| chr12:123181148
|
A | G | 173 | a0001c0001t0003g0202a0001c0001t0006g0001a0001c0001t0006g0002others(170): Show | 173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.2289+15T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 14/23 | chr12 | 123181148 | ||||||
| chr12:123181528
|
G | A | 21 | a0001c0001t0003g0202a0001c0001t0006g0001a0001c0001t0006g0002others(18): Show | 21 | HG01175.hp1 HG01952.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.2242-318C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123181528 | ||||||
| chr12:123181667
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2242-457C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123181667 | ||||||
| chr12:123181750
|
T | G | 19 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(16): Show | 19 | HG01175.hp1 HG01952.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.2242-540A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123181750 | ||||||
| chr12:123181808
|
A | C | 1 | a0001c0001t0005g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2242-598T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123181808 | ||||||
| chr12:123181991
|
C | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2242-781G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123181991 | ||||||
| chr12:123182011
|
G | A | 1 | a0001c0004t0007g0110 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2242-801C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182011 | ||||||
| chr12:123182102
|
G | A | 99 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(96): Show | 99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2242-892C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182102 | ||||||
| chr12:123182120
|
T | C | 1 | a0002c0003t0002g0255 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2242-910A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182120 | ||||||
| chr12:123182186
|
G | A | 6 | a0001c0001t0003g0144a0001c0001t0003g0154a0001c0001t0003g0155others(3): Show | 6 | HG02109.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2242-976C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182186 | ||||||
| chr12:123182249
|
G | GTT | 10 | a0001c0002t0001g0043a0001c0004t0001g0003a0001c0004t0001g0004others(7): Show | 10 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.2242-1041_2242-104 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182249 | ||||||
| chr12:123182260
|
T | TTG | 47 | a0002c0003t0001g0230a0002c0003t0002g0213a0002c0003t0002g0216others(44): Show | 47 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.2242-1051_2242-105 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182260 | ||||||
| chr12:123182260
|
T | TTTG | 18 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(15): Show | 18 | HG01175.hp1 HG01243.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.2242-1051_2242-105 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182260 | ||||||
| chr12:123182261
|
G | C | 1 | a0001c0002t0001g0086 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2242-1051C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182261 | ||||||
| chr12:123182261
|
G | T | 159 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(156): Show | 159 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.2242-1051C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182261 | ||||||
| chr12:123182261
|
GT | G | 14 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0149others(11): Show | 14 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2242-1052delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182261 | ||||||
| chr12:123182262
|
T | TGTTC | 86 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(83): Show | 86 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.2242-1053_2242-105 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182262 | ||||||
| chr12:123182263
|
T | TC | 10 | a0001c0002t0001g0043a0001c0004t0001g0003a0001c0004t0001g0004others(7): Show | 10 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.2242-1054_2242-105 others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182263 | ||||||
| chr12:123182375
|
T | A | 1 | a0001c0002t0001g0010 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2242-1165A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182375 | ||||||
| chr12:123182401
|
A | G | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-1191T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182401 | ||||||
| chr12:123182426
|
G | A | 1 | a0001c0004t0001g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2242-1216C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182426 | ||||||
| chr12:123182431
|
A | C | 1 | a0001c0004t0001g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2242-1221T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182431 | ||||||
| chr12:123182710
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2242-1500C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182710 | ||||||
| chr12:123182732
|
C | T | 1 | a0001c0002t0001g0020 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2242-1522G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182732 | ||||||
| chr12:123182807
|
G | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-1597C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182807 | ||||||
| chr12:123182940
|
G | A | 1 | a0001c0002t0008g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2242-1730C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182940 | ||||||
| chr12:123182951
|
C | T | 1 | a0001c0001t0030g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2242-1741G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182951 | ||||||
| chr12:123182982
|
G | A | 2 | a0001c0001t0015g0108a0007c0017t0005g0204 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2242-1772C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182982 | ||||||
| chr12:123183051
|
C | G | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-1841G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183051 | ||||||
| chr12:123183063
|
A | T | 1 | a0003c0020t0005g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2242-1853T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183063 | ||||||
| chr12:123183237
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2242-2027G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183237 | ||||||
| chr12:123183332
|
G | C | 15 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(12): Show | 15 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2242-2122C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183332 | ||||||
| chr12:123183403
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-2193A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183403 | ||||||
| chr12:123183405
|
A | G | 98 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(95): Show | 98 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.2242-2195T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183405 | ||||||
| chr12:123183475
|
A | G | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-2265T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183475 | ||||||
| chr12:123183496
|
C | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2242-2286G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183496 | ||||||
| chr12:123183515
|
C | T | 1 | a0001c0002t0001g0056 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2242-2305G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183515 | ||||||
| chr12:123183547
|
C | CA | 29 | a0001c0001t0003g0157a0001c0001t0003g0199a0001c0001t0004g0169others(26): Show | 29 | HG00738.hp2 HG01106.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.2242-2338dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183547 | ||||||
| chr12:123183547
|
C | CAA | 84 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0002t0001g0005others(81): Show | 84 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.2242-2339_2242-233 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183547 | ||||||
| chr12:123183547
|
C | CAAA | 8 | a0001c0002t0001g0018a0001c0002t0001g0037a0001c0002t0001g0048others(5): Show | 8 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.2242-2340_2242-233 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183547 | ||||||
| chr12:123183547
|
CA | C | 6 | a0001c0001t0003g0162a0001c0001t0010g0184a0002c0003t0002g0218others(3): Show | 6 | HG00140.hp1 HG02895.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2242-2338delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183547 | ||||||
| chr12:123183565
|
A | G | 1 | a0002c0003t0002g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2242-2355T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183565 | ||||||
| chr12:123183571
|
G | A | 8 | a0001c0002t0001g0009a0001c0002t0001g0053a0001c0002t0001g0056others(5): Show | 8 | HG02040.hp2 NA18953.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.2242-2361C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183571 | ||||||
| chr12:123183937
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2242-2727C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183937 | ||||||
| chr12:123183940
|
C | A | 1 | a0005c0018t0003g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2242-2730G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183940 | ||||||
| chr12:123183954
|
A | C | 7 | a0001c0001t0003g0126a0001c0001t0003g0147a0001c0001t0009g0145others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242-2744T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183954 | ||||||
| chr12:123184113
|
G | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0037a0001c0002t0001g0048others(4): Show | 7 | HG00597.hp2 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242-2903C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184113 | ||||||
| chr12:123184371
|
G | A | 1 | a0001c0004t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2242-3161C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184371 | ||||||
| chr12:123184374
|
C | T | 3 | a0001c0001t0003g0148a0001c0001t0003g0150a0001c0001t0003g0158 | 3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2242-3164G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184374 | ||||||
| chr12:123184498
|
AT | A | 210 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(207): Show | 210 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(207): Show |
intron_variant | MODIFIER | c.2242-3289delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184498 | ||||||
| chr12:123184672
|
G | C | 19 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(16): Show | 19 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.2242-3462C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184672 | ||||||
| chr12:123184688
|
C | T | 119 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(116): Show | 119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2242-3478G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184688 | ||||||
| chr12:123184750
|
G | A | 4 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0017g0072others(1): Show | 4 | HG01952.hp1 HG01978.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2242-3540C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184750 | ||||||
| chr12:123184793
|
C | T | 7 | a0001c0004t0007g0104a0001c0004t0007g0109a0001c0004t0007g0110others(4): Show | 7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2242-3583G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184793 | ||||||
| chr12:123184855
|
G | A | 1 | a0001c0002t0016g0068 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2242-3645C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184855 | ||||||
| chr12:123184921
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-3711A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184921 | ||||||
| chr12:123184961
|
A | G | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-3751T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184961 | ||||||
| chr12:123185057
|
G | A | 1 | a0001c0001t0004g0173 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2242-3847C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123185057 | ||||||
| chr12:123185328
|
TA | T | 6 | a0001c0001t0003g0162a0001c0001t0006g0116a0001c0002t0001g0060others(3): Show | 6 | HG00558.hp2 HG01099.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2242-4119delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123185328 | ||||||
| chr12:123185926
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-4716A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123185926 | ||||||
| chr12:123185947
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2242-4737G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123185947 | ||||||
| chr12:123185980
|
A | G | 1 | a0002c0003t0002g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2242-4770T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123185980 | ||||||
| chr12:123186225
|
C | A | 1 | a0001c0002t0017g0072 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2242-5015G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186225 | ||||||
| chr12:123186227
|
CA | C | 38 | a0001c0001t0003g0120a0001c0001t0003g0143a0001c0001t0003g0147others(35): Show | 38 | HG00738.hp2 HG01099.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2242-5018delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | ||||||
| chr12:123186227
|
CAA | C | 128 | a0001c0001t0003g0121a0001c0001t0003g0123a0001c0001t0003g0124others(125): Show | 128 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.2242-5019_2242-501 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | ||||||
| chr12:123186227
|
CAAA | C | 63 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(60): Show | 63 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2242-5020_2242-501 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | ||||||
| chr12:123186227
|
CAAAA | C | 8 | a0001c0001t0006g0116a0001c0001t0006g0117a0002c0003t0002g0218others(5): Show | 8 | HG02293.hp1 HG02970.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.2242-5021_2242-501 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | ||||||
| chr12:123186227
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2242-5029_2242-501 others(16): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | ||||||
| chr12:123186227
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0003g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2242-5031_2242-501 others(18): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | ||||||
| chr12:123186245
|
A | C | 99 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(96): Show | 99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2242-5035T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186245 | ||||||
| chr12:123186763
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-5553A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186763 | ||||||
| chr12:123186891
|
G | A | 4 | a0001c0004t0001g0003a0001c0004t0001g0004a0001c0004t0001g0074others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.2242-5681C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186891 | ||||||
| chr12:123186939
|
C | T | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2242-5729G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186939 | ||||||
| chr12:123187118
|
G | C | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2242-5908C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187118 | ||||||
| chr12:123187214
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-6004A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187214 | ||||||
| chr12:123187425
|
CAA | C | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2242-6217_2242-621 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187425 | ||||||
| chr12:123187534
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-6324G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187534 | ||||||
| chr12:123187535
|
C | A | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-6325G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187535 | ||||||
| chr12:123187539
|
A | T | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-6329T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187539 | ||||||
| chr12:123187542
|
T | A | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-6332A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187542 | ||||||
| chr12:123187546
|
C | A | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-6336G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187546 | ||||||
| chr12:123187628
|
T | G | 1 | a0001c0002t0001g0064 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2242-6418A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187628 | ||||||
| chr12:123187642
|
C | G | 1 | a0001c0002t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2242-6432G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187642 | ||||||
| chr12:123187971
|
A | C | 9 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(6): Show | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.2241+6415T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187971 | ||||||
| chr12:123187971
|
A | G | 163 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(160): Show | 163 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.2241+6415T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187971 | ||||||
| chr12:123188026
|
T | C | 1 | a0001c0001t0003g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2241+6360A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188026 | ||||||
| chr12:123188039
|
T | C | 1 | a0003c0020t0005g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2241+6347A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188039 | ||||||
| chr12:123188087
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2241+6299A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188087 | ||||||
| chr12:123188110
|
G | C | 3 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138 | 3 | HG01884.hp2 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2241+6276C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188110 | ||||||
| chr12:123188153
|
A | T | 1 | a0001c0002t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2241+6233T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188153 | ||||||
| chr12:123188155
|
A | T | 1 | a0001c0002t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2241+6231T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188155 | ||||||
| chr12:123188156
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2241+6230G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188156 | ||||||
| chr12:123188327
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2241+6059G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188327 | ||||||
| chr12:123188412
|
A | AT | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2241+5973dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188412 | ||||||
| chr12:123188414
|
A | G | 1 | a0001c0001t0005g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2241+5972T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188414 | ||||||
| chr12:123188711
|
G | A | 98 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(95): Show | 98 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.2241+5675C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188711 | ||||||
| chr12:123188796
|
C | T | 1 | a0002c0003t0002g0240 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2241+5590G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188796 | ||||||
| chr12:123188968
|
CA | C | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2241+5417delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188968 | ||||||
| chr12:123189058
|
G | A | 3 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084 | 3 | HG00639.hp2 HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2241+5328C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189058 | ||||||
| chr12:123189292
|
C | T | 11 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(8): Show | 11 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2241+5094G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189292 | ||||||
| chr12:123189336
|
C | T | 2 | a0001c0002t0008g0030a0001c0002t0008g0039 | 2 | HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2241+5050G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189336 | ||||||
| chr12:123189608
|
A | C | 1 | a0001c0002t0017g0072 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2241+4778T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189608 | ||||||
| chr12:123189701
|
G | A | 2 | a0002c0003t0002g0213a0002c0003t0002g0214 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2241+4685C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189701 | ||||||
| chr12:123189704
|
G | A | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2241+4682C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189704 | ||||||
| chr12:123189710
|
G | A | 1 | a0001c0001t0012g0152 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2241+4676C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189710 | ||||||
| chr12:123189921
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2241+4465C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189921 | ||||||
| chr12:123189975
|
T | C | 1 | a0007c0017t0005g0204 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2241+4411A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189975 | ||||||
| chr12:123190191
|
C | T | 1 | a0002c0003t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2241+4195G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123190191 | ||||||
| chr12:123190235
|
C | T | 1 | a0001c0001t0003g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2241+4151G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123190235 | ||||||
| chr12:123190634
|
C | CAGGATAT others(2): Show |
3 | a0001c0001t0005g0203a0001c0001t0005g0207a0001c0001t0005g0208 | 3 | HG02486.hp1 HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2241+3743_2241+375 others(13): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123190634 | ||||||
| chr12:123191010
|
T | C | 2 | a0001c0001t0004g0177a0001c0001t0004g0188 | 2 | HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2241+3376A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123191010 | ||||||
| chr12:123191112
|
G | C | 1 | a0001c0004t0007g0114 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2241+3274C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123191112 | ||||||
| chr12:123191509
|
T | G | 1 | a0001c0001t0005g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2241+2877A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123191509 | ||||||
| chr12:123191606
|
T | C | 1 | a0001c0001t0006g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2241+2780A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123191606 | ||||||
| chr12:123191680
|
A | C | 3 | a0001c0001t0005g0128a0001c0001t0005g0131a0001c0001t0005g0133 | 3 | HG01884.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2241+2706T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123191680 | ||||||
| chr12:123192216
|
G | A | 119 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(116): Show | 119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2241+2170C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192216 | ||||||
| chr12:123192294
|
T | C | 19 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(16): Show | 19 | HG01175.hp1 HG01952.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.2241+2092A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192294 | ||||||
| chr12:123192426
|
C | T | 1 | a0011c0010t0001g0032 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2241+1960G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192426 | ||||||
| chr12:123192475
|
A | G | 2 | a0002c0003t0002g0244a0002c0003t0002g0247 | 2 | NA18941.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2241+1911T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192475 | ||||||
| chr12:123192490
|
T | C | 2 | a0002c0003t0002g0213a0002c0003t0002g0214 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2241+1896A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192490 | ||||||
| chr12:123192560
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2241+1826A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192560 | ||||||
| chr12:123192618
|
G | A | 1 | a0001c0004t0007g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2241+1768C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192618 | ||||||
| chr12:123192624
|
G | A | 20 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(17): Show | 20 | HG01175.hp1 HG01952.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2241+1762C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192624 | ||||||
| chr12:123192628
|
C | CA | 10 | a0001c0001t0004g0171a0001c0001t0004g0174a0001c0001t0004g0180others(7): Show | 10 | HG00738.hp2 HG01070.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.2241+1757dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192628 | ||||||
| chr12:123192628
|
CA | C | 13 | a0001c0002t0001g0021a0001c0002t0001g0029a0001c0002t0001g0037others(10): Show | 13 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.2241+1757delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192628 | ||||||
| chr12:123192628
|
CAA | C | 98 | a0001c0001t0003g0120a0001c0001t0006g0266a0001c0002t0001g0005others(95): Show | 98 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.2241+1756_2241+175 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192628 | ||||||
| chr12:123192628
|
CAAA | C | 67 | a0001c0001t0003g0137a0001c0001t0003g0139a0001c0001t0003g0168others(64): Show | 67 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.2241+1755_2241+175 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192628 | ||||||
| chr12:123192628
|
CAAAA | C | 54 | a0001c0001t0003g0121a0001c0001t0003g0122a0001c0001t0003g0123others(51): Show | 54 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.2241+1754_2241+175 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192628 | ||||||
| chr12:123192630
|
A | C | 1 | a0001c0002t0001g0071 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2241+1756T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192630 | ||||||
| chr12:123192631
|
A | C | 2 | a0001c0002t0001g0055a0001c0002t0001g0060 | 2 | NA18974.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.2241+1755T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192631 | ||||||
| chr12:123192744
|
T | C | 1 | a0001c0002t0001g0064 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2241+1642A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192744 | ||||||
| chr12:123192954
|
C | T | 1 | a0001c0001t0004g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2241+1432G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192954 | ||||||
| chr12:123193071
|
CA | C | 17 | a0001c0001t0003g0120a0001c0001t0003g0126a0001c0001t0003g0136others(14): Show | 17 | HG00738.hp2 HG01074.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.2241+1314delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | ||||||
| chr12:123193071
|
CAAA | C | 14 | a0001c0001t0003g0160a0001c0001t0004g0176a0001c0001t0005g0208others(11): Show | 14 | HG00558.hp1 HG00609.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2241+1312_2241+131 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | ||||||
| chr12:123193071
|
CAAAAA | C | 18 | a0001c0001t0003g0144a0001c0001t0003g0153a0001c0001t0003g0154others(15): Show | 18 | HG00673.hp1 HG00735.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.2241+1310_2241+131 others(9): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | ||||||
| chr12:123193071
|
CAAAAAAA | C | 16 | a0001c0001t0003g0148a0001c0001t0003g0162a0001c0002t0001g0016others(13): Show | 16 | HG00733.hp2 HG00735.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.2241+1308_2241+131 others(11): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | ||||||
| chr12:123193071
|
CAAAAAAA others(2): Show |
C | 12 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0012others(9): Show | 12 | HG01258.hp1 HG01361.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.2241+1306_2241+131 others(13): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | ||||||
| chr12:123193071
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2241+1305_2241+131 others(14): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | ||||||
| chr12:123193087
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0006g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2241+1288_2241+129 others(15): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193087 | ||||||
| chr12:123193088
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0002t0001g0021a0001c0002t0001g0027a0001c0002t0001g0083 | 3 | HG01069.hp1 HG01099.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2241+1288_2241+129 others(14): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193088 | ||||||
| chr12:123193089
|
AAAAAAAA others(2): Show |
A | 59 | a0001c0002t0001g0005a0001c0002t0001g0011a0001c0002t0001g0013others(56): Show | 59 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.2241+1288_2241+129 others(13): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193089 | ||||||
| chr12:123193090
|
A | ATAT | 3 | a0001c0001t0003g0149a0001c0001t0005g0170a0001c0001t0028g0166 | 3 | HG02486.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2241+1295_2241+129 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193090 | ||||||
| chr12:123193090
|
A | T | 9 | a0001c0001t0003g0126a0001c0001t0006g0117a0001c0001t0006g0118others(6): Show | 9 | HG01175.hp1 HG02132.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.2241+1296T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193090 | ||||||
| chr12:123193092
|
A | T | 17 | a0001c0001t0003g0126a0001c0001t0003g0149a0001c0001t0003g0161others(14): Show | 17 | HG01175.hp1 HG01952.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2241+1294T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193092 | ||||||
| chr12:123193094
|
A | AT | 3 | a0001c0001t0012g0151a0001c0007t0029g0211a0004c0019t0004g0197 | 3 | HG01516.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2241+1291_2241+129 others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193094 | ||||||
| chr12:123193094
|
A | T | 60 | a0001c0001t0003g0126a0001c0001t0003g0139a0001c0001t0003g0140others(57): Show | 60 | HG00621.hp2 HG00642.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.2241+1292T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193094 | ||||||
| chr12:123193096
|
A | AT | 6 | a0001c0001t0003g0121a0001c0001t0003g0122a0001c0001t0003g0123others(3): Show | 6 | HG02258.hp1 HG02630.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2241+1289_2241+129 others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193096 | ||||||
| chr12:123193096
|
A | T | 132 | a0001c0001t0003g0126a0001c0001t0003g0136a0001c0001t0003g0137others(129): Show | 132 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(129): Show |
intron_variant | MODIFIER | c.2241+1290T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193096 | ||||||
| chr12:123193102
|
T | C | 1 | a0001c0001t0003g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2241+1284A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193102 | ||||||
| chr12:123193104
|
T | C | 3 | a0001c0001t0003g0124a0001c0001t0003g0142a0006c0015t0003g0164 | 3 | HG02572.hp2 HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2241+1282A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193104 | ||||||
| chr12:123193106
|
T | C | 16 | a0001c0001t0003g0121a0001c0001t0003g0122a0001c0001t0003g0123others(13): Show | 16 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.2241+1280A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193106 | ||||||
| chr12:123193106
|
TATACACA others(5): Show |
T | 1 | a0001c0004t0007g0110 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2241+1268_2241+127 others(16): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193106 | ||||||
| chr12:123193108
|
T | C | 24 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(21): Show | 24 | HG01081.hp1 HG01099.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.2241+1278A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | ||||||
| chr12:123193108
|
T | TAC | 7 | a0001c0001t0004g0186a0001c0001t0004g0191a0001c0001t0004g0192others(4): Show | 7 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2241+1276_2241+127 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | ||||||
| chr12:123193108
|
T | TACAC | 3 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0202 | 3 | HG02559.hp1 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2241+1274_2241+127 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | ||||||
| chr12:123193108
|
T | TACACACA others(3): Show |
1 | a0001c0001t0010g0185 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2241+1268_2241+127 others(14): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | ||||||
| chr12:123193108
|
TACAC | T | 7 | a0001c0002t0001g0022a0001c0002t0001g0024a0001c0002t0001g0041others(4): Show | 7 | HG00673.hp1 HG02040.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.2241+1274_2241+127 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | ||||||
| chr12:123193108
|
TACACAC | T | 5 | a0001c0004t0007g0109a0001c0004t0007g0111a0001c0004t0007g0113others(2): Show | 5 | HG03239.hp2 NA18972.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+1272_2241+127 others(10): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | ||||||
| chr12:123193108
|
TACACACA others(1): Show |
T | 16 | a0001c0001t0021g0206a0001c0004t0007g0104a0002c0003t0002g0229others(13): Show | 16 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2241+1270_2241+127 others(12): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | ||||||
| chr12:123193108
|
TACACACA others(3): Show |
T | 47 | a0001c0001t0003g0162a0001c0001t0006g0117a0001c0001t0006g0118others(44): Show | 47 | HG00642.hp2 HG00673.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.2241+1268_2241+127 others(14): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | ||||||
| chr12:123193108
|
TACACACA others(15): Show |
T | 1 | a0001c0004t0007g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2241+1256_2241+127 others(26): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | ||||||
| chr12:123193110
|
C | T | 130 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0149others(127): Show | 130 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.2241+1276G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193110 | ||||||
| chr12:123193112
|
C | T | 96 | a0001c0001t0003g0148a0001c0001t0003g0150a0001c0001t0004g0180others(93): Show | 96 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.2241+1274G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193112 | ||||||
| chr12:123193114
|
C | T | 81 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(78): Show | 81 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.2241+1272G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193114 | ||||||
| chr12:123193116
|
C | T | 14 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0266others(11): Show | 14 | HG01256.hp1 HG01258.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.2241+1270G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193116 | ||||||
| chr12:123193118
|
C | T | 23 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0266others(20): Show | 23 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.2241+1268G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193118 | ||||||
| chr12:123193120
|
C | T | 30 | a0001c0001t0003g0162a0001c0001t0006g0119a0001c0001t0021g0206others(27): Show | 30 | HG00558.hp1 HG00609.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2241+1266G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193120 | ||||||
| chr12:123193122
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2241+1264G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193122 | ||||||
| chr12:123193263
|
A | G | 119 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(116): Show | 119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2241+1123T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193263 | ||||||
| chr12:123193388
|
G | T | 1 | a0001c0001t0004g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2241+998C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193388 | ||||||
| chr12:123193621
|
A | T | 1 | a0001c0004t0001g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2241+765T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193621 | ||||||
| chr12:123193691
|
T | A | 1 | a0001c0002t0001g0024 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2241+695A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193691 | ||||||
| chr12:123193808
|
C | A | 1 | a0001c0002t0001g0043 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2241+578G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193808 | ||||||
| chr12:123193817
|
GAC | G | 53 | a0001c0002t0001g0060a0002c0003t0001g0230a0002c0003t0001g0232others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2241+567_2241+568d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193817 | ||||||
| chr12:123193820
|
AC | A | 117 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(114): Show | 117 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.2241+565delG | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193820 | ||||||
| chr12:123193821
|
C | G | 1 | a0001c0004t0001g0075 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2241+565G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193821 | ||||||
| chr12:123193822
|
A | G | 117 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(114): Show | 117 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.2241+564T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193822 | ||||||
| chr12:123193822
|
A | T | 1 | a0001c0004t0001g0075 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2241+564T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193822 | ||||||
| chr12:123193823
|
G | GT | 6 | a0001c0001t0003g0168a0001c0001t0003g0198a0001c0001t0003g0199others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2241+562dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193823 | ||||||
| chr12:123193823
|
G | T | 118 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(115): Show | 118 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.2241+563C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193823 | ||||||
| chr12:123193824
|
T | G | 1 | a0002c0003t0002g0262 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2241+562A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193824 | ||||||
| chr12:123193922
|
C | T | 7 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0067others(4): Show | 7 | HG01258.hp1 HG01361.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.2241+464G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193922 | ||||||
| chr12:123194067
|
G | A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2241+319C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123194067 | ||||||
| chr12:123194624
|
A | AT | 94 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(91): Show | 94 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.2026-24dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123194624 | ||||||
| chr12:123194624
|
A | ATT | 113 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(110): Show | 113 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.2026-25_2026-24dup others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123194624 | ||||||
| chr12:123195075
|
T | C | 1 | a0001c0004t0001g0006 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2026-474A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195075 | ||||||
| chr12:123195314
|
CAGT | C | 38 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(35): Show | 38 | HG01099.hp1 HG01243.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.2026-716_2026-714d others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195314 | ||||||
| chr12:123195391
|
C | A | 1 | a0001c0004t0001g0003 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2026-790G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195391 | ||||||
| chr12:123195398
|
A | G | 1 | a0001c0001t0003g0161 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2026-797T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195398 | ||||||
| chr12:123195737
|
A | T | 1 | a0001c0001t0021g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2026-1136T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195737 | ||||||
| chr12:123195845
|
G | A | 5 | a0001c0001t0003g0149a0001c0001t0003g0153a0001c0001t0003g0160others(2): Show | 5 | HG01243.hp1 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2026-1244C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195845 | ||||||
| chr12:123195852
|
C | T | 3 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0016t0001g0098 | 3 | HG01952.hp1 HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2026-1251G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195852 | ||||||
| chr12:123195910
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2026-1309G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195910 | ||||||
| chr12:123196016
|
T | C | 99 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(96): Show | 99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2026-1415A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196016 | ||||||
| chr12:123196050
|
A | T | 5 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0004g0182others(2): Show | 5 | HG00741.hp1 HG01074.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.2026-1449T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196050 | ||||||
| chr12:123196147
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2026-1546G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196147 | ||||||
| chr12:123196218
|
T | C | 4 | a0001c0004t0001g0003a0001c0004t0001g0004a0001c0004t0001g0074others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026-1617A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196218 | ||||||
| chr12:123196272
|
C | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2026-1671G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196272 | ||||||
| chr12:123196388
|
T | C | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2026-1787A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196388 | ||||||
| chr12:123196480
|
C | T | 9 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(6): Show | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.2025+1767G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196480 | ||||||
| chr12:123196576
|
G | A | 1 | a0003c0020t0005g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2025+1671C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196576 | ||||||
| chr12:123196675
|
G | A | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2025+1572C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196675 | ||||||
| chr12:123196736
|
T | C | 1 | a0005c0018t0003g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2025+1511A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196736 | ||||||
| chr12:123196755
|
T | C | 2 | a0001c0002t0001g0029a0001c0002t0001g0045 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2025+1492A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196755 | ||||||
| chr12:123197031
|
G | GT | 39 | a0001c0001t0004g0169a0001c0001t0004g0173a0001c0001t0004g0187others(36): Show | 39 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.2025+1215dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | ||||||
| chr12:123197031
|
G | GTT | 23 | a0002c0003t0001g0232a0002c0003t0002g0213a0002c0003t0002g0214others(20): Show | 23 | HG00642.hp2 HG00673.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2025+1214_2025+121 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | ||||||
| chr12:123197031
|
GT | G | 19 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0143others(16): Show | 19 | HG01099.hp1 HG02451.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.2025+1215delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | ||||||
| chr12:123197031
|
GTT | G | 40 | a0001c0001t0003g0144a0001c0001t0003g0158a0001c0001t0003g0161others(37): Show | 40 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.2025+1214_2025+121 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | ||||||
| chr12:123197031
|
GTTT | G | 76 | a0001c0001t0003g0160a0001c0001t0006g0001a0001c0001t0006g0002others(73): Show | 76 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.2025+1213_2025+121 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | ||||||
| chr12:123197031
|
GTTTT | G | 5 | a0001c0002t0001g0021a0001c0002t0001g0062a0001c0004t0007g0109others(2): Show | 5 | HG01256.hp1 HG02132.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.2025+1212_2025+121 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | ||||||
| chr12:123197069
|
G | A | 3 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027 | 3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2025+1178C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197069 | ||||||
| chr12:123197090
|
G | C | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2025+1157C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197090 | ||||||
| chr12:123197298
|
C | A | 1 | a0001c0001t0003g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2025+949G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197298 | ||||||
| chr12:123197365
|
T | G | 2 | a0001c0004t0007g0111a0001c0004t0007g0113 | 2 | NA18972.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2025+882A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197365 | ||||||
| chr12:123197534
|
G | A | 119 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(116): Show | 119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2025+713C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197534 | ||||||
| chr12:123197714
|
G | A | 1 | a0001c0001t0004g0186 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2025+533C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197714 | ||||||
| chr12:123197769
|
G | A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2025+478C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197769 | ||||||
| chr12:123197790
|
G | GA | 13 | a0001c0001t0004g0181a0001c0001t0006g0001a0001c0001t0006g0002others(10): Show | 13 | HG00642.hp1 HG01516.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2025+456dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197790 | ||||||
| chr12:123197790
|
GA | G | 60 | a0001c0001t0003g0168a0001c0001t0003g0198a0001c0001t0003g0199others(57): Show | 60 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2025+456delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197790 | ||||||
| chr12:123197849
|
C | T | 152 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(149): Show | 152 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.2025+398G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197849 | ||||||
| chr12:123198015
|
C | G | 1 | a0002c0003t0002g0262 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2025+232G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123198015 | ||||||
| chr12:123198047
|
G | A | 99 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(96): Show | 99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2025+200C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123198047 | ||||||
| chr12:123198083
|
C | CA | 24 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(21): Show | 24 | HG00621.hp1 HG01175.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.2025+163dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123198083 | ||||||
| chr12:123198196
|
G | A | 1 | a0001c0001t0003g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2025+51C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123198196 | ||||||
| chr12:123198608
|
A | G | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1938-274T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198608 | ||||||
| chr12:123198809
|
C | CA | 44 | a0001c0001t0003g0124a0001c0001t0003g0136a0001c0001t0003g0137others(41): Show | 44 | HG00558.hp1 HG00621.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1938-476dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198809 | ||||||
| chr12:123198809
|
CA | C | 87 | a0001c0001t0003g0140a0001c0001t0003g0153a0001c0001t0003g0160others(84): Show | 87 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1938-476delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198809 | ||||||
| chr12:123198839
|
A | AAAATAAT others(305): Show |
1 | a0002c0003t0002g0218 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1938-506_1938-505i others(314): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198839 | ||||||
| chr12:123198839
|
A | AAAATAAT others(323): Show |
1 | a0002c0003t0002g0231 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1938-506_1938-505i others(332): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198839 | ||||||
| chr12:123198839
|
A | AAAATAAT others(324): Show |
1 | a0002c0003t0002g0217 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1938-506_1938-505i others(333): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198839 | ||||||
| chr12:123198839
|
A | AAAATAAT others(330): Show |
1 | a0002c0003t0002g0235 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1938-506_1938-505i others(339): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198839 | ||||||
| chr12:123198927
|
A | G | 1 | a0001c0002t0008g0030 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1938-593T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198927 | ||||||
| chr12:123199016
|
C | T | 171 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(168): Show | 171 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.1938-682G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199016 | ||||||
| chr12:123199121
|
T | C | 2 | a0001c0002t0001g0023a0001c0002t0001g0065 | 2 | HG00733.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1938-787A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199121 | ||||||
| chr12:123199228
|
C | A | 5 | a0001c0001t0003g0168a0001c0001t0003g0198a0001c0001t0003g0199others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938-894G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199228 | ||||||
| chr12:123199429
|
T | C | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1938-1095A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199429 | ||||||
| chr12:123199478
|
A | G | 9 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(6): Show | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.1938-1144T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199478 | ||||||
| chr12:123199661
|
C | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1938-1327G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199661 | ||||||
| chr12:123199788
|
C | CA | 7 | a0001c0001t0021g0206a0001c0002t0001g0011a0001c0002t0001g0037others(4): Show | 7 | HG01256.hp1 HG01258.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1938-1455dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199788 | ||||||
| chr12:123199991
|
A | G | 1 | a0001c0002t0001g0035 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1938-1657T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199991 | ||||||
| chr12:123200147
|
G | C | 10 | a0001c0002t0001g0021a0001c0002t0001g0034a0001c0002t0001g0058others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.1938-1813C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200147 | ||||||
| chr12:123200235
|
GA | G | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1938-1902delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200235 | ||||||
| chr12:123200271
|
T | C | 1 | a0001c0001t0003g0153 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1937+1893A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200271 | ||||||
| chr12:123200300
|
CT | C | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1937+1863delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200300 | ||||||
| chr12:123200567
|
G | C | 1 | a0001c0001t0004g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1937+1597C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200567 | ||||||
| chr12:123200651
|
A | AT | 5 | a0001c0001t0004g0179a0001c0001t0004g0180a0001c0001t0004g0194others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1937+1512dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200651 | ||||||
| chr12:123200651
|
AT | A | 6 | a0001c0001t0004g0177a0001c0001t0005g0205a0001c0001t0030g0212others(3): Show | 6 | HG01891.hp2 HG02735.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1937+1512delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200651 | ||||||
| chr12:123200992
|
A | G | 1 | a0002c0003t0002g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1937+1172T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200992 | ||||||
| chr12:123201032
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1937+1132G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201032 | ||||||
| chr12:123201231
|
C | CTGTTT | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1937+928_1937+932d others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201231 | ||||||
| chr12:123201580
|
A | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1937+584T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201580 | ||||||
| chr12:123201601
|
A | T | 2 | a0001c0001t0015g0108a0007c0017t0005g0204 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1937+563T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201601 | ||||||
| chr12:123201603
|
C | T | 3 | a0001c0001t0004g0173a0001c0001t0004g0182a0001c0001t0004g0183 | 3 | HG00741.hp1 HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1937+561G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201603 | ||||||
| chr12:123201677
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1937+487A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201677 | ||||||
| chr12:123201809
|
A | C | 1 | a0002c0003t0002g0231 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1937+355T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201809 | ||||||
| chr12:123201900
|
T | A | 1 | a0001c0001t0003g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1937+264A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201900 | ||||||
| chr12:123202044
|
A | C | 1 | a0001c0002t0001g0034 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1937+120T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123202044 | ||||||
| chr12:123203125
|
G | A | 9 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(6): Show | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.1321-41C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 9/23 | chr12 | 123203125 | ||||||
| chr12:123203227
|
C | T | 52 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(49): Show | 52 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1320+23G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 9/23 | chr12 | 123203227 | ||||||
| chr12:123203681
|
C | A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1195-306G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123203681 | ||||||
| chr12:123203736
|
T | A | 1 | a0001c0001t0004g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1195-361A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123203736 | ||||||
| chr12:123203858
|
A | T | 1 | a0001c0001t0004g0177 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1195-483T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123203858 | ||||||
| chr12:123203937
|
T | G | 120 | a0001c0001t0004g0181a0001c0001t0006g0001a0001c0001t0006g0002others(117): Show | 120 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.1195-562A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123203937 | ||||||
| chr12:123204090
|
G | A | 1 | a0001c0001t0004g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1195-715C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204090 | ||||||
| chr12:123204233
|
C | T | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1195-858G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204233 | ||||||
| chr12:123204236
|
A | T | 2 | a0001c0002t0001g0101a0001c0002t0001g0102 | 2 | NA18990.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1195-861T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204236 | ||||||
| chr12:123204258
|
C | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1195-883G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204258 | ||||||
| chr12:123204302
|
CA | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1195-928delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204302 | ||||||
| chr12:123204628
|
G | C | 1 | a0001c0002t0001g0020 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1195-1253C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204628 | ||||||
| chr12:123204781
|
G | A | 51 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0215others(48): Show | 51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1195-1406C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204781 | ||||||
| chr12:123204839
|
T | C | 230 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(227): Show | 230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.1195-1464A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204839 | ||||||
| chr12:123204974
|
C | T | 235 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(232): Show | 235 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(232): Show |
intron_variant | MODIFIER | c.1195-1599G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204974 | ||||||
| chr12:123205127
|
C | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1195-1752G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205127 | ||||||
| chr12:123205238
|
T | C | 1 | a0001c0004t0001g0075 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1195-1863A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205238 | ||||||
| chr12:123205350
|
G | A | 103 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(100): Show | 103 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1195-1975C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205350 | ||||||
| chr12:123205383
|
T | A | 1 | a0001c0001t0021g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1195-2008A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205383 | ||||||
| chr12:123205383
|
T | C | 1 | a0001c0002t0019g0038 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1195-2008A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205383 | ||||||
| chr12:123205477
|
C | T | 1 | a0001c0004t0007g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1195-2102G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205477 | ||||||
| chr12:123205561
|
C | T | 1 | a0001c0009t0022g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1195-2186G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205561 | ||||||
| chr12:123206122
|
C | T | 1 | a0001c0001t0009g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1195-2747G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206122 | ||||||
| chr12:123206192
|
T | C | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1195-2817A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206192 | ||||||
| chr12:123206302
|
C | CA | 119 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(116): Show | 119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.1195-2928dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206302 | ||||||
| chr12:123206376
|
C | T | 1 | a0001c0001t0003g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1195-3001G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206376 | ||||||
| chr12:123206496
|
AGAGAG | A | 34 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0123others(31): Show | 34 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1195-3126_1195-312 others(9): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206496 | ||||||
| chr12:123206511
|
G | A | 5 | a0001c0001t0003g0122a0001c0001t0003g0124a0001c0001t0003g0139others(2): Show | 5 | HG01099.hp1 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-3136C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206511 | ||||||
| chr12:123206511
|
GGAGAAGA others(13): Show |
G | 5 | a0001c0001t0004g0167a0001c0001t0004g0169a0001c0001t0004g0191others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-3156_1195-313 others(24): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206511 | ||||||
| chr12:123206531
|
T | A | 12 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(9): Show | 12 | HG01099.hp1 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1195-3156A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206531 | ||||||
| chr12:123206531
|
TGAGAA | T | 118 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(115): Show | 118 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.1195-3161_1195-315 others(9): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206531 | ||||||
| chr12:123206536
|
A | T | 1 | a0001c0002t0001g0010 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1195-3161T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206536 | ||||||
| chr12:123206609
|
G | A | 1 | a0001c0001t0005g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1195-3234C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206609 | ||||||
| chr12:123206625
|
T | C | 1 | a0001c0001t0023g0210 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1195-3250A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206625 | ||||||
| chr12:123206709
|
C | T | 2 | a0001c0002t0001g0066a0011c0010t0001g0032 | 2 | NA18948.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1195-3334G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206709 | ||||||
| chr12:123206824
|
G | C | 3 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084 | 3 | HG00639.hp2 HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1194+3232C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206824 | ||||||
| chr12:123206940
|
C | T | 1 | a0001c0001t0004g0180 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1194+3116G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206940 | ||||||
| chr12:123206950
|
C | T | 1 | a0006c0015t0003g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1194+3106G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206950 | ||||||
| chr12:123207053
|
TA | T | 6 | a0001c0001t0012g0151a0001c0001t0012g0152a0001c0002t0001g0060others(3): Show | 6 | HG02922.hp1 NA18906.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1194+3002delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207053 | ||||||
| chr12:123207056
|
A | T | 1 | a0001c0004t0007g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1194+3000T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207056 | ||||||
| chr12:123207099
|
G | C | 1 | a0001c0001t0003g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1194+2957C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207099 | ||||||
| chr12:123207123
|
T | A | 1 | a0002c0003t0002g0263 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1194+2933A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207123 | ||||||
| chr12:123207146
|
T | TA | 103 | a0001c0001t0003g0137a0001c0002t0001g0005a0001c0002t0001g0009others(100): Show | 103 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1194+2909dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207146 | ||||||
| chr12:123207146
|
T | TAA | 45 | a0001c0002t0001g0028a0002c0003t0001g0230a0002c0003t0001g0232others(42): Show | 45 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1194+2908_1194+290 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207146 | ||||||
| chr12:123207146
|
TA | T | 20 | a0001c0001t0003g0125a0001c0001t0003g0162a0001c0001t0004g0182others(17): Show | 20 | HG01167.hp1 HG01256.hp2 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.1194+2909delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207146 | ||||||
| chr12:123207195
|
T | G | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+2861A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207195 | ||||||
| chr12:123207758
|
T | C | 171 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(168): Show | 171 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.1194+2298A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207758 | ||||||
| chr12:123207759
|
G | C | 1 | a0001c0002t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+2297C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207759 | ||||||
| chr12:123207800
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1194+2256G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207800 | ||||||
| chr12:123207831
|
C | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+2225G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207831 | ||||||
| chr12:123207869
|
G | A | 1 | a0002c0003t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1194+2187C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207869 | ||||||
| chr12:123207869
|
GA | G | 208 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(205): Show | 208 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(205): Show |
intron_variant | MODIFIER | c.1194+2186delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207869 | ||||||
| chr12:123207870
|
A | G | 1 | a0002c0003t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1194+2186T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207870 | ||||||
| chr12:123207880
|
A | T | 1 | a0001c0002t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+2176T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207880 | ||||||
| chr12:123207881
|
T | A | 1 | a0001c0002t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+2175A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207881 | ||||||
| chr12:123207957
|
G | A | 1 | a0001c0001t0005g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1194+2099C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207957 | ||||||
| chr12:123208074
|
C | T | 1 | a0001c0001t0003g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1194+1982G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208074 | ||||||
| chr12:123208119
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1194+1937C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208119 | ||||||
| chr12:123208125
|
G | A | 1 | a0001c0002t0001g0042 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1194+1931C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208125 | ||||||
| chr12:123208184
|
G | A | 7 | a0001c0004t0007g0104a0001c0004t0007g0109a0001c0004t0007g0110others(4): Show | 7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+1872C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208184 | ||||||
| chr12:123208188
|
CA | C | 187 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(184): Show | 187 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(184): Show |
intron_variant | MODIFIER | c.1194+1867delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208188 | ||||||
| chr12:123208188
|
CAA | C | 6 | a0001c0001t0003g0162a0001c0002t0001g0088a0001c0002t0017g0072others(3): Show | 6 | HG02895.hp2 NA18982.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194+1866_1194+186 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208188 | ||||||
| chr12:123208209
|
A | T | 1 | a0002c0003t0002g0263 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1194+1847T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208209 | ||||||
| chr12:123208211
|
T | A | 1 | a0002c0003t0002g0263 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1194+1845A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208211 | ||||||
| chr12:123208261
|
C | G | 1 | a0001c0002t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+1795G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208261 | ||||||
| chr12:123208261
|
C | T | 1 | a0001c0016t0001g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1194+1795G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208261 | ||||||
| chr12:123208262
|
G | C | 1 | a0001c0002t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+1794C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208262 | ||||||
| chr12:123208265
|
C | A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+1791G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208265 | ||||||
| chr12:123208335
|
G | A | 1 | a0001c0001t0015g0108 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1194+1721C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208335 | ||||||
| chr12:123208408
|
G | T | 1 | a0001c0004t0007g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1194+1648C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208408 | ||||||
| chr12:123208418
|
A | T | 211 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(208): Show | 211 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.1194+1638T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208418 | ||||||
| chr12:123208438
|
G | A | 7 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(4): Show | 7 | HG03491.hp1 HG03492.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+1618C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208438 | ||||||
| chr12:123208533
|
C | CA | 54 | a0001c0001t0005g0203a0001c0001t0005g0207a0001c0002t0001g0066others(51): Show | 54 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1194+1522dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208533 | ||||||
| chr12:123208533
|
C | CAA | 115 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(112): Show | 115 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1194+1521_1194+152 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208533 | ||||||
| chr12:123208705
|
G | A | 1 | a0001c0004t0007g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1194+1351C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208705 | ||||||
| chr12:123208755
|
T | C | 1 | a0001c0002t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+1301A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208755 | ||||||
| chr12:123208768
|
G | T | 1 | a0002c0003t0002g0219 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1194+1288C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208768 | ||||||
| chr12:123208816
|
C | A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+1240G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208816 | ||||||
| chr12:123208873
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1194+1183A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208873 | ||||||
| chr12:123209055
|
C | A | 1 | a0002c0003t0002g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1194+1001G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209055 | ||||||
| chr12:123209088
|
A | C | 1 | a0002c0003t0002g0263 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1194+968T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209088 | ||||||
| chr12:123209090
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1194+966C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209090 | ||||||
| chr12:123209262
|
A | T | 1 | a0001c0002t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+794T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209262 | ||||||
| chr12:123209409
|
GT | G | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+646delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209409 | ||||||
| chr12:123209411
|
T | A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+645A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209411 | ||||||
| chr12:123209659
|
T | C | 230 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(227): Show | 230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.1194+397A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209659 | ||||||
| chr12:123209668
|
C | T | 3 | a0001c0001t0003g0148a0001c0001t0003g0150a0001c0001t0003g0158 | 3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1194+388G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209668 | ||||||
| chr12:123209703
|
C | T | 119 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(116): Show | 119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.1194+353G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209703 | ||||||
| chr12:123209737
|
G | GT | 113 | a0001c0001t0003g0122a0001c0001t0004g0176a0001c0001t0004g0180others(110): Show | 113 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.1194+318dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209737 | ||||||
| chr12:123209737
|
G | GTT | 13 | a0001c0001t0006g0116a0001c0001t0006g0119a0001c0001t0006g0265others(10): Show | 13 | HG00621.hp1 HG01952.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1194+317_1194+318d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209737 | ||||||
| chr12:123209737
|
G | T | 1 | a0001c0002t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+319C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209737 | ||||||
| chr12:123209894
|
G | A | 2 | a0001c0001t0015g0108a0007c0017t0005g0204 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1194+162C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209894 | ||||||
| chr12:123209898
|
A | G | 2 | a0001c0001t0015g0108a0007c0017t0005g0204 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1194+158T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209898 | ||||||
| chr12:123209926
|
C | T | 1 | a0001c0002t0001g0043 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1194+130G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209926 | ||||||
| chr12:123210025
|
C | A | 1 | a0001c0001t0003g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1194+31G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123210025 | ||||||
| chr12:123210044
|
T | G | 1 | a0001c0002t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+12A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123210044 | ||||||
| chr12:123210177
|
C | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1088-15G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210177 | ||||||
| chr12:123210529
|
C | T | 1 | a0008c0014t0002g0222 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1088-367G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210529 | ||||||
| chr12:123210885
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1088-723G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210885 | ||||||
| chr12:123210977
|
C | CT | 27 | a0001c0001t0003g0202a0001c0001t0004g0169a0001c0001t0004g0171others(24): Show | 27 | HG00735.hp2 HG00741.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1088-816dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210977 | ||||||
| chr12:123210977
|
C | CTT | 8 | a0001c0001t0004g0194a0001c0001t0023g0210a0001c0004t0007g0104others(5): Show | 8 | HG02132.hp2 HG02738.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.1088-817_1088-816d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210977 | ||||||
| chr12:123210977
|
CT | C | 80 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(77): Show | 80 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.1088-816delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210977 | ||||||
| chr12:123210982
|
T | C | 1 | a0001c0009t0022g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1088-820A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210982 | ||||||
| chr12:123210987
|
T | C | 2 | a0002c0003t0002g0215a0002c0003t0002g0219 | 2 | HG03831.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1088-825A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210987 | ||||||
| chr12:123210988
|
T | C | 51 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(48): Show | 51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1088-826A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210988 | ||||||
| chr12:123211371
|
C | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1088-1209G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211371 | ||||||
| chr12:123211410
|
T | G | 1 | a0002c0003t0002g0263 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1088-1248A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211410 | ||||||
| chr12:123211610
|
C | G | 1 | a0002c0003t0002g0263 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1088-1448G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211610 | ||||||
| chr12:123211684
|
C | CT | 5 | a0001c0001t0004g0193a0001c0001t0004g0196a0001c0001t0005g0129others(2): Show | 5 | HG01978.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088-1523dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211684 | ||||||
| chr12:123211684
|
CT | C | 146 | a0001c0001t0003g0126a0001c0001t0003g0158a0001c0001t0003g0162others(143): Show | 146 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.1088-1523delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211684 | ||||||
| chr12:123211684
|
CTT | C | 14 | a0001c0002t0001g0009a0001c0002t0001g0014a0001c0002t0001g0021others(11): Show | 14 | HG01070.hp2 HG01081.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1088-1524_1088-152 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211684 | ||||||
| chr12:123211684
|
CTTTTTTT others(1): Show |
C | 5 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0014g0007others(2): Show | 5 | HG01952.hp1 HG01978.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1088-1530_1088-152 others(12): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211684 | ||||||
| chr12:123211709
|
T | C | 1 | a0002c0003t0002g0257 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1088-1547A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211709 | ||||||
| chr12:123212416
|
G | A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1088-2254C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212416 | ||||||
| chr12:123212417
|
C | T | 2 | a0002c0003t0002g0224a0002c0003t0002g0236 | 2 | HG01070.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1088-2255G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212417 | ||||||
| chr12:123212460
|
C | T | 119 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(116): Show | 119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.1087+2284G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212460 | ||||||
| chr12:123212494
|
G | A | 35 | a0001c0001t0003g0168a0001c0001t0003g0198a0001c0001t0003g0199others(32): Show | 35 | HG00140.hp1 HG00738.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1087+2250C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212494 | ||||||
| chr12:123212673
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1087+2071G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212673 | ||||||
| chr12:123212711
|
C | CA | 14 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0004g0193others(11): Show | 14 | HG02132.hp2 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1087+2032dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212711 | ||||||
| chr12:123212711
|
CA | C | 141 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(138): Show | 141 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1087+2032delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212711 | ||||||
| chr12:123212761
|
G | A | 1 | a0001c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1087+1983C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212761 | ||||||
| chr12:123212766
|
C | CT | 5 | a0001c0001t0004g0173a0001c0001t0004g0177a0002c0003t0002g0224others(2): Show | 5 | HG00741.hp1 HG01070.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1087+1977dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | ||||||
| chr12:123212766
|
C | CTT | 45 | a0001c0002t0001g0021a0001c0002t0001g0027a0002c0003t0001g0230others(42): Show | 45 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1087+1976_1087+197 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | ||||||
| chr12:123212766
|
C | CTTT | 110 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(107): Show | 110 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.1087+1975_1087+197 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | ||||||
| chr12:123212766
|
C | CTTTT | 13 | a0001c0001t0006g0119a0001c0001t0006g0265a0001c0002t0001g0010others(10): Show | 13 | HG00741.hp2 HG02071.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1087+1974_1087+197 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | ||||||
| chr12:123212766
|
C | T | 1 | a0002c0003t0002g0263 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1087+1978G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | ||||||
| chr12:123212766
|
CT | C | 28 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(25): Show | 28 | HG01099.hp1 HG01109.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.1087+1977delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | ||||||
| chr12:123212796
|
T | C | 15 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(12): Show | 15 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1087+1948A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212796 | ||||||
| chr12:123212810
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+1934A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212810 | ||||||
| chr12:123212976
|
C | T | 1 | a0001c0002t0001g0034 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1087+1768G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212976 | ||||||
| chr12:123212984
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+1760A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212984 | ||||||
| chr12:123213005
|
G | A | 1 | a0001c0001t0005g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1087+1739C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213005 | ||||||
| chr12:123213009
|
G | A | 1 | a0001c0002t0001g0029 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1087+1735C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213009 | ||||||
| chr12:123213054
|
T | C | 2 | a0001c0002t0001g0023a0001c0002t0001g0065 | 2 | HG00733.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1087+1690A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213054 | ||||||
| chr12:123213079
|
T | A | 1 | a0002c0003t0002g0263 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1087+1665A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213079 | ||||||
| chr12:123213345
|
A | AT | 9 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(6): Show | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.1087+1398dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213345 | ||||||
| chr12:123213351
|
T | C | 99 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(96): Show | 99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1087+1393A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213351 | ||||||
| chr12:123213425
|
G | C | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1087+1319C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213425 | ||||||
| chr12:123213785
|
G | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+959C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213785 | ||||||
| chr12:123213787
|
GAAC | G | 2 | a0001c0001t0003g0153a0001c0001t0003g0160 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1087+954_1087+956d others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213787 | ||||||
| chr12:123213971
|
T | G | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+773A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213971 | ||||||
| chr12:123213972
|
G | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+772C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213972 | ||||||
| chr12:123214056
|
A | T | 234 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(231): Show | 234 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(231): Show |
intron_variant | MODIFIER | c.1087+688T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123214056 | ||||||
| chr12:123214243
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+501A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123214243 | ||||||
| chr12:123214259
|
C | T | 2 | a0002c0003t0002g0213a0002c0003t0002g0214 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1087+485G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123214259 | ||||||
| chr12:123214653
|
GTTT | G | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+88_1087+90del others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123214653 | ||||||
| chr12:123214698
|
G | A | 7 | a0001c0004t0007g0104a0001c0004t0007g0109a0001c0004t0007g0110others(4): Show | 7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+46C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123214698 | ||||||
| chr12:123214973
|
A | G | 235 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(232): Show | 235 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(232): Show |
intron_variant | MODIFIER | c.997-139T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123214973 | ||||||
| chr12:123215025
|
C | T | 1 | a0001c0002t0007g0036 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.997-191G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215025 | ||||||
| chr12:123215058
|
A | G | 1 | a0001c0002t0001g0078 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.997-224T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215058 | ||||||
| chr12:123215075
|
C | T | 5 | a0001c0001t0003g0149a0001c0001t0003g0153a0001c0001t0003g0160others(2): Show | 5 | HG01243.hp1 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-241G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215075 | ||||||
| chr12:123215146
|
G | A | 4 | a0001c0001t0006g0115a0001c0001t0006g0116a0001c0001t0006g0117others(1): Show | 4 | NA18951.hp2 NA18977.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.997-312C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215146 | ||||||
| chr12:123215202
|
A | T | 2 | a0001c0005t0001g0093a0001c0005t0001g0094 | 2 | NA18979.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.997-368T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215202 | ||||||
| chr12:123215678
|
C | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.997-844G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215678 | ||||||
| chr12:123215687
|
T | C | 2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.997-853A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215687 | ||||||
| chr12:123215916
|
C | G | 1 | a0002c0003t0002g0253 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.997-1082G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215916 | ||||||
| chr12:123215929
|
T | A | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.997-1095A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215929 | ||||||
| chr12:123215959
|
C | T | 2 | a0002c0003t0002g0224a0002c0003t0002g0236 | 2 | HG01070.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.997-1125G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215959 | ||||||
| chr12:123216216
|
T | C | 1 | a0001c0002t0001g0067 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.997-1382A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216216 | ||||||
| chr12:123216320
|
A | G | 39 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.997-1486T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216320 | ||||||
| chr12:123216423
|
G | A | 1 | a0001c0001t0005g0135 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.997-1589C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216423 | ||||||
| chr12:123216463
|
G | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.997-1629C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216463 | ||||||
| chr12:123216723
|
A | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.996+1653T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216723 | ||||||
| chr12:123216806
|
T | C | 119 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(116): Show | 119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.996+1570A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216806 | ||||||
| chr12:123216859
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.996+1517G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216859 | ||||||
| chr12:123216992
|
A | AAAAT | 3 | a0001c0001t0003g0122a0001c0001t0021g0206a0006c0015t0003g0164 | 3 | HG02258.hp1 HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.996+1380_996+1383d others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216992 | ||||||
| chr12:123216992
|
AAAAT | A | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.996+1380_996+1383d others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216992 | ||||||
| chr12:123217322
|
C | T | 39 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.996+1054G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217322 | ||||||
| chr12:123217323
|
G | A | 1 | a0002c0003t0002g0250 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.996+1053C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217323 | ||||||
| chr12:123217419
|
G | A | 1 | a0001c0001t0003g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.996+957C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217419 | ||||||
| chr12:123217525
|
T | A | 3 | a0001c0001t0003g0148a0001c0001t0003g0150a0001c0001t0003g0158 | 3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.996+851A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217525 | ||||||
| chr12:123217828
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.996+548C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217828 | ||||||
| chr12:123217902
|
G | A | 7 | a0001c0004t0007g0104a0001c0004t0007g0109a0001c0004t0007g0110others(4): Show | 7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.996+474C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217902 | ||||||
| chr12:123217906
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.996+470C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217906 | ||||||
| chr12:123217952
|
G | C | 1 | a0001c0002t0001g0024 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.996+424C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217952 | ||||||
| chr12:123218044
|
C | CA | 17 | a0001c0001t0003g0160a0001c0001t0004g0195a0001c0002t0001g0071others(14): Show | 17 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.996+331dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123218044 | ||||||
| chr12:123218147
|
G | A | 1 | a0009c0013t0002g0249 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.996+229C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123218147 | ||||||
| chr12:123218220
|
G | T | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.996+156C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123218220 | ||||||
| chr12:123218246
|
C | CA | 11 | a0001c0001t0003g0144a0001c0001t0003g0149a0001c0001t0003g0153others(8): Show | 11 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.996+129dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123218246 | ||||||
| chr12:123218525
|
T | C | 1 | a0001c0001t0003g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.873-26A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218525 | ||||||
| chr12:123218556
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.873-57A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218556 | ||||||
| chr12:123218582
|
G | A | 19 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(16): Show | 19 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.873-83C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218582 | ||||||
| chr12:123218677
|
C | T | 7 | a0001c0004t0007g0104a0001c0004t0007g0109a0001c0004t0007g0110others(4): Show | 7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.873-178G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218677 | ||||||
| chr12:123218679
|
T | A | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.873-180A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218679 | ||||||
| chr12:123218834
|
A | T | 1 | a0003c0020t0005g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.873-335T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218834 | ||||||
| chr12:123218875
|
A | AGTT | 230 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(227): Show | 230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.873-379_873-377dup others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218875 | ||||||
| chr12:123218893
|
TTTTG | T | 119 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(116): Show | 119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.873-398_873-395del others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218893 | ||||||
| chr12:123218926
|
CCTCT | C | 11 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(8): Show | 11 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.873-431_873-428del others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218926 | ||||||
| chr12:123218954
|
C | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.873-455G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218954 | ||||||
| chr12:123219031
|
T | C | 7 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0069others(4): Show | 7 | HG01258.hp1 HG01361.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.873-532A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219031 | ||||||
| chr12:123219034
|
A | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.873-535T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219034 | ||||||
| chr12:123219337
|
G | A | 1 | a0001c0001t0003g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.873-838C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219337 | ||||||
| chr12:123219470
|
G | A | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00733.hp2 HG02698.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-971C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219470 | ||||||
| chr12:123219501
|
C | T | 3 | a0001c0001t0003g0148a0001c0001t0003g0150a0001c0001t0003g0158 | 3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.873-1002G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219501 | ||||||
| chr12:123219504
|
G | T | 1 | a0001c0001t0003g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.873-1005C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219504 | ||||||
| chr12:123219552
|
C | CA | 18 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0004g0196others(15): Show | 18 | HG00673.hp2 HG01070.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.873-1054dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219552 | ||||||
| chr12:123219552
|
CA | C | 9 | a0001c0001t0003g0126a0001c0001t0005g0128a0001c0001t0005g0205others(6): Show | 9 | HG00733.hp2 HG02258.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.873-1054delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219552 | ||||||
| chr12:123219603
|
T | C | 1 | a0001c0001t0003g0161 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.873-1104A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219603 | ||||||
| chr12:123219672
|
G | A | 1 | a0001c0002t0017g0072 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.873-1173C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219672 | ||||||
| chr12:123219814
|
A | C | 2 | a0002c0003t0002g0257a0002c0003t0002g0260 | 2 | HG00609.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.873-1315T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219814 | ||||||
| chr12:123220022
|
C | T | 229 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(226): Show | 229 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(226): Show |
intron_variant | MODIFIER | c.872+1350G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220022 | ||||||
| chr12:123220051
|
G | A | 99 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(96): Show | 99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.872+1321C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220051 | ||||||
| chr12:123220123
|
G | A | 1 | a0003c0020t0005g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.872+1249C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220123 | ||||||
| chr12:123220167
|
C | G | 1 | a0001c0002t0001g0033 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.872+1205G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220167 | ||||||
| chr12:123220295
|
G | A | 2 | a0002c0003t0002g0215a0002c0003t0002g0237 | 2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.872+1077C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220295 | ||||||
| chr12:123220297
|
T | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.872+1075A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220297 | ||||||
| chr12:123220343
|
G | A | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.872+1029C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220343 | ||||||
| chr12:123220695
|
A | G | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.872+677T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220695 | ||||||
| chr12:123220714
|
C | G | 19 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(16): Show | 19 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.872+658G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220714 | ||||||
| chr12:123220777
|
T | C | 1 | a0001c0001t0003g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.872+595A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220777 | ||||||
| chr12:123220783
|
A | C | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.872+589T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220783 | ||||||
| chr12:123221012
|
G | A | 38 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(35): Show | 38 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.872+360C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123221012 | ||||||
| chr12:123221055
|
A | C | 1 | a0001c0002t0001g0101 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.872+317T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123221055 | ||||||
| chr12:123221123
|
T | A | 1 | a0001c0001t0003g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.872+249A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123221123 | ||||||
| chr12:123222106
|
G | A | 1 | a0001c0004t0007g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.349-211C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222106 | ||||||
| chr12:123222324
|
CA | C | 166 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(163): Show | 166 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.349-430delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222324 | ||||||
| chr12:123222324
|
CAA | C | 18 | a0002c0003t0001g0230a0002c0003t0002g0216a0002c0003t0002g0219others(15): Show | 18 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.349-431_349-430del others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222324 | ||||||
| chr12:123222403
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.349-508G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222403 | ||||||
| chr12:123222608
|
C | T | 1 | a0001c0001t0004g0173 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.348+430G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222608 | ||||||
| chr12:123222609
|
G | A | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.348+429C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222609 | ||||||
| chr12:123222770
|
T | C | 1 | a0001c0002t0001g0011 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.348+268A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222770 | ||||||
| chr12:123222962
|
A | ATG | 32 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(29): Show | 32 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.348+74_348+75dupCA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222962 | ||||||
| chr12:123222962
|
A | ATGTG | 4 | a0001c0001t0003g0149a0001c0001t0009g0165a0001c0001t0020g0146others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+72_348+75dupCA others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222962 | ||||||
| chr12:123222980
|
GTA | G | 171 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(168): Show | 171 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.348+56_348+57delTA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222980 | ||||||
| chr12:123222982
|
A | G | 2 | a0001c0001t0004g0176a0001c0004t0007g0104 | 2 | HG01106.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.348+56T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222982 | ||||||
| chr12:123223005
|
TA | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.348+32delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123223005 | ||||||
| chr12:123223279
|
G | A | 1 | a0002c0003t0026g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.259-152C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123223279 | ||||||
| chr12:123223430
|
C | T | 1 | a0001c0002t0001g0029 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.259-303G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123223430 | ||||||
| chr12:123223516
|
A | G | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.259-389T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123223516 | ||||||
| chr12:123223939
|
A | T | 1 | a0007c0017t0005g0204 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.259-812T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123223939 | ||||||
| chr12:123223943
|
T | A | 177 | a0001c0001t0003g0168a0001c0001t0003g0198a0001c0001t0003g0199others(174): Show | 177 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(174): Show |
intron_variant | MODIFIER | c.259-816A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123223943 | ||||||
| chr12:123224105
|
C | T | 1 | a0002c0003t0002g0256 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.259-978G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224105 | ||||||
| chr12:123224110
|
T | TTA | 20 | a0001c0001t0004g0171a0001c0001t0005g0127a0001c0001t0005g0128others(17): Show | 20 | HG01081.hp1 HG01175.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.259-985_259-984dup others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTATATAT others(17): Show |
1 | a0002c0003t0002g0223 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.259-984_259-983ins others(24): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTATATAT others(21): Show |
2 | a0002c0003t0002g0226a0002c0003t0025g0081 | 2 | HG01069.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.259-984_259-983ins others(28): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTATATA others(24): Show |
1 | a0008c0014t0002g0222 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.259-984_259-983ins others(31): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTTATAT others(11): Show |
1 | a0002c0003t0002g0224 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.259-984_259-983ins others(18): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTTATAT others(17): Show |
6 | a0002c0003t0001g0232a0002c0003t0002g0217a0002c0003t0002g0218others(3): Show | 6 | HG02080.hp2 HG02155.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(24): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTTATAT others(19): Show |
4 | a0002c0003t0002g0215a0002c0003t0002g0235a0002c0003t0002g0236others(1): Show | 4 | HG02293.hp1 HG03831.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(26): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTTATAT others(21): Show |
7 | a0002c0003t0002g0219a0002c0003t0002g0238a0002c0003t0002g0239others(4): Show | 7 | HG02071.hp2 NA18949.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(28): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTTATAT others(23): Show |
13 | a0002c0003t0002g0221a0002c0003t0002g0227a0002c0003t0002g0242others(10): Show | 13 | HG00621.hp2 HG00673.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(30): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTTATAT others(25): Show |
7 | a0002c0003t0002g0229a0002c0003t0002g0250a0002c0003t0002g0251others(4): Show | 7 | HG00558.hp1 HG02132.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(32): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTTATAT others(27): Show |
3 | a0002c0003t0002g0216a0002c0003t0002g0255a0002c0003t0002g0263 | 3 | NA18957.hp1 NA18987.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.259-984_259-983ins others(34): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTTATAT others(29): Show |
4 | a0002c0003t0002g0256a0002c0003t0002g0257a0002c0003t0002g0258others(1): Show | 4 | HG02735.hp1 NA18612.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(36): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTTATAT others(31): Show |
1 | a0002c0003t0002g0213 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259-984_259-983ins others(38): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
T | TTTTATAT others(33): Show |
2 | a0002c0003t0002g0214a0002c0003t0002g0260 | 2 | HG00609.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.259-984_259-983ins others(40): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224110
|
TTA | T | 28 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(25): Show | 28 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.259-985_259-984del others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | ||||||
| chr12:123224125
|
T | C | 6 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0147others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-998A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224125 | ||||||
| chr12:123224127
|
C | T | 100 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(97): Show | 100 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.259-1000G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224127 | ||||||
| chr12:123224128
|
AC | A | 6 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0147others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-1002delG | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224128 | ||||||
| chr12:123224130
|
A | AC | 9 | a0001c0002t0001g0016a0001c0002t0001g0025a0001c0002t0001g0029others(6): Show | 9 | HG00140.hp2 HG00621.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.259-1004_259-1003i others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224130 | ||||||
| chr12:123224130
|
A | AT | 11 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0005g0170others(8): Show | 11 | HG00741.hp1 HG01256.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-1004dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224130 | ||||||
| chr12:123224130
|
A | T | 6 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0147others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-1003T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224130 | ||||||
| chr12:123224130
|
AT | A | 15 | a0001c0001t0003g0202a0001c0001t0004g0201a0001c0001t0006g0001others(12): Show | 15 | HG01975.hp1 HG02572.hp1 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-1004delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224130 | ||||||
| chr12:123224131
|
T | A | 9 | a0001c0002t0001g0016a0001c0002t0001g0025a0001c0002t0001g0029others(6): Show | 9 | HG00140.hp2 HG00621.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.259-1004A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224131 | ||||||
| chr12:123224131
|
T | C | 89 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(86): Show | 89 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.259-1004A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224131 | ||||||
| chr12:123224132
|
T | A | 88 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(85): Show | 88 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.259-1005A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224132 | ||||||
| chr12:123224132
|
T | C | 2 | a0001c0002t0001g0011a0001c0002t0001g0097 | 2 | HG01975.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.259-1005A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224132 | ||||||
| chr12:123224133
|
T | A | 2 | a0001c0002t0001g0011a0001c0002t0001g0097 | 2 | HG01975.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.259-1006A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224133 | ||||||
| chr12:123224377
|
G | A | 19 | a0001c0001t0005g0127a0001c0001t0005g0128a0001c0001t0005g0129others(16): Show | 19 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.259-1250C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224377 | ||||||
| chr12:123224732
|
T | C | 1 | a0001c0001t0009g0165 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259-1605A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224732 | ||||||
| chr12:123224799
|
C | T | 1 | a0001c0004t0007g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.259-1672G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224799 | ||||||
| chr12:123224859
|
A | C | 3 | a0001c0004t0011g0106a0001c0004t0011g0107a0001c0004t0024g0103 | 3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.259-1732T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224859 | ||||||
| chr12:123224862
|
C | T | 99 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(96): Show | 99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.259-1735G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224862 | ||||||
| chr12:123225065
|
A | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027 | 3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.259-1938T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225065 | ||||||
| chr12:123225237
|
AGT | A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2112_259-2111d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225237 | ||||||
| chr12:123225242
|
AAGACTAA others(12): Show |
A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2134_259-2116d others(21): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225242 | ||||||
| chr12:123225262
|
A | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2135T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225262 | ||||||
| chr12:123225269
|
C | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2142G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225269 | ||||||
| chr12:123225270
|
C | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2143G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225270 | ||||||
| chr12:123225274
|
T | C | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2147A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225274 | ||||||
| chr12:123225275
|
C | A | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2148G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225275 | ||||||
| chr12:123225277
|
C | G | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2150G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225277 | ||||||
| chr12:123225279
|
A | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2152T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225279 | ||||||
| chr12:123225281
|
A | AT | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2155_259-2154i others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225281 | ||||||
| chr12:123225284
|
A | T | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2157T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225284 | ||||||
| chr12:123225285
|
A | C | 53 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(50): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2158T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225285 | ||||||
| chr12:123225367
|
C | A | 1 | a0002c0006t0002g0261 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.258+2096G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225367 | ||||||
| chr12:123225380
|
G | A | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.258+2083C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225380 | ||||||
| chr12:123225443
|
CA | C | 9 | a0001c0001t0003g0125a0001c0001t0003g0144a0001c0001t0004g0172others(6): Show | 9 | HG01175.hp1 HG01975.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+2019delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225443 | ||||||
| chr12:123225443
|
CAA | C | 158 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(155): Show | 158 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.258+2018_258+2019d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225443 | ||||||
| chr12:123225443
|
CAAA | C | 11 | a0001c0002t0001g0014a0001c0002t0001g0021a0001c0002t0001g0022others(8): Show | 11 | HG00733.hp1 HG01069.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+2017_258+2019d others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225443 | ||||||
| chr12:123225457
|
A | G | 54 | a0001c0002t0001g0020a0002c0003t0001g0230a0002c0003t0001g0232others(51): Show | 54 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.258+2006T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225457 | ||||||
| chr12:123225739
|
T | C | 1 | a0001c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.258+1724A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225739 | ||||||
| chr12:123225817
|
C | T | 99 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(96): Show | 99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.258+1646G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225817 | ||||||
| chr12:123226231
|
TATA | T | 14 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(11): Show | 14 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+1229_258+1231d others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226231 | ||||||
| chr12:123226288
|
A | C | 102 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(99): Show | 102 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.258+1175T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226288 | ||||||
| chr12:123226294
|
C | A | 1 | a0001c0001t0005g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.258+1169G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226294 | ||||||
| chr12:123226521
|
C | CT | 20 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(17): Show | 20 | HG01175.hp1 HG01952.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.258+941dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226521 | ||||||
| chr12:123226521
|
CT | C | 51 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(48): Show | 51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.258+941delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226521 | ||||||
| chr12:123226629
|
T | C | 9 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(6): Show | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+834A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226629 | ||||||
| chr12:123226882
|
C | T | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00733.hp2 HG02698.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+581G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226882 | ||||||
| chr12:123227388
|
A | G | 2 | a0001c0002t0001g0014a0001c0002t0001g0015 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.258+75T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123227388 | ||||||
| chr12:123227869
|
G | A | 210 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(207): Show | 210 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(207): Show |
intron_variant | MODIFIER | c.105-253C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123227869 | ||||||
| chr12:123228165
|
G | T | 172 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(169): Show | 172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.105-549C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123228165 | ||||||
| chr12:123228300
|
G | T | 1 | a0001c0001t0004g0171 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.105-684C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123228300 | ||||||
| chr12:123228465
|
G | A | 1 | a0001c0001t0015g0108 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.105-849C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123228465 | ||||||
| chr12:123228575
|
C | A | 3 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084 | 3 | HG00639.hp2 HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.105-959G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123228575 | ||||||
| chr12:123229043
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.104+1218G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229043 | ||||||
| chr12:123229210
|
G | A | 9 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(6): Show | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.104+1051C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229210 | ||||||
| chr12:123229314
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+947G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229314 | ||||||
| chr12:123229317
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+944C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229317 | ||||||
| chr12:123229318
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+943G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229318 | ||||||
| chr12:123229319
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+942A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229319 | ||||||
| chr12:123229320
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+941A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229320 | ||||||
| chr12:123229321
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+940C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229321 | ||||||
| chr12:123229322
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+939A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229322 | ||||||
| chr12:123229323
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+938G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229323 | ||||||
| chr12:123229325
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+936C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229325 | ||||||
| chr12:123229327
|
C | T | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+934G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229327 | ||||||
| chr12:123229330
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+931A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229330 | ||||||
| chr12:123229331
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+930C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229331 | ||||||
| chr12:123229332
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+929A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229332 | ||||||
| chr12:123229333
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+928C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229333 | ||||||
| chr12:123229334
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+927G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229334 | ||||||
| chr12:123229338
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+923A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229338 | ||||||
| chr12:123229339
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+922A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229339 | ||||||
| chr12:123229340
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+921C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229340 | ||||||
| chr12:123229344
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+917C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229344 | ||||||
| chr12:123229345
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+916A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229345 | ||||||
| chr12:123229349
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+912G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229349 | ||||||
| chr12:123229351
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+910C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229351 | ||||||
| chr12:123229352
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+909C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229352 | ||||||
| chr12:123229353
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+908G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229353 | ||||||
| chr12:123229354
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+907A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229354 | ||||||
| chr12:123229355
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+906G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229355 | ||||||
| chr12:123229356
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+905A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229356 | ||||||
| chr12:123229357
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+904C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229357 | ||||||
| chr12:123229360
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+901C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229360 | ||||||
| chr12:123229366
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+895G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229366 | ||||||
| chr12:123229370
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+891G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229370 | ||||||
| chr12:123229371
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+890G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229371 | ||||||
| chr12:123229376
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+885A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229376 | ||||||
| chr12:123229377
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+884G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229377 | ||||||
| chr12:123229378
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+883A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229378 | ||||||
| chr12:123229379
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+882C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229379 | ||||||
| chr12:123229380
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+881A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229380 | ||||||
| chr12:123229381
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+880C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229381 | ||||||
| chr12:123229382
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+879A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229382 | ||||||
| chr12:123229383
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+878A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229383 | ||||||
| chr12:123229386
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+875C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229386 | ||||||
| chr12:123229388
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+873G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229388 | ||||||
| chr12:123229389
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+872G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229389 | ||||||
| chr12:123229391
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+870A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229391 | ||||||
| chr12:123229392
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+869A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229392 | ||||||
| chr12:123229406
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+855G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229406 | ||||||
| chr12:123229407
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+854G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229407 | ||||||
| chr12:123229410
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+851A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229410 | ||||||
| chr12:123229411
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+850G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229411 | ||||||
| chr12:123229413
|
C | T | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+848G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229413 | ||||||
| chr12:123229415
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+846C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229415 | ||||||
| chr12:123229416
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+845C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229416 | ||||||
| chr12:123229418
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+843A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229418 | ||||||
| chr12:123229420
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+841C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229420 | ||||||
| chr12:123229421
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+840G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229421 | ||||||
| chr12:123229422
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+839A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229422 | ||||||
| chr12:123229423
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+838A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229423 | ||||||
| chr12:123229424
|
A | T | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+837T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229424 | ||||||
| chr12:123229429
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+832A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229429 | ||||||
| chr12:123229434
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+827A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229434 | ||||||
| chr12:123229435
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+826C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229435 | ||||||
| chr12:123229436
|
C | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+825G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229436 | ||||||
| chr12:123229439
|
T | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+822A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229439 | ||||||
| chr12:123229496
|
A | G | 1 | a0001c0001t0005g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104+765T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229496 | ||||||
| chr12:123229689
|
A | G | 173 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(170): Show | 173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.104+572T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229689 | ||||||
| chr12:123229821
|
A | AT | 8 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0125others(5): Show | 8 | HG02622.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+439dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229821 | ||||||
| chr12:123229821
|
A | ATT | 98 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(95): Show | 98 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.104+438_104+439dup others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229821 | ||||||
| chr12:123229821
|
A | ATTT | 66 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(63): Show | 66 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.104+437_104+439dup others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229821 | ||||||
| chr12:123229821
|
A | ATTTT | 8 | a0002c0003t0002g0215a0002c0003t0002g0216a0002c0003t0002g0217others(5): Show | 8 | HG00673.hp2 HG02071.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+436_104+439dup others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229821 | ||||||
| chr12:123229866
|
G | A | 1 | a0001c0001t0006g0118 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.104+395C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229866 | ||||||
| chr12:123229911
|
T | C | 2 | a0001c0002t0001g0086a0001c0002t0001g0087 | 2 | NA18992.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.104+350A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229911 | ||||||
| chr12:123230069
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+192C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123230069 | ||||||
| chr12:123230142
|
T | C | 52 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(49): Show | 52 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.104+119A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123230142 | ||||||
| chr12:123230189
|
T | A | 52 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(49): Show | 52 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.104+72A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123230189 | ||||||
| chr12:123230558
|
A | G | 1 | a0001c0001t0003g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-158-36T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123230558 | ||||||
| chr12:123230566
|
C | T | 173 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(170): Show | 173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.-158-44G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123230566 | ||||||
| chr12:123230719
|
T | C | 173 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(170): Show | 173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.-158-197A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123230719 | ||||||
| chr12:123230921
|
A | T | 1 | a0001c0001t0004g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-158-399T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123230921 | ||||||
| chr12:123230982
|
C | A | 1 | a0001c0001t0006g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-158-460G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123230982 | ||||||
| chr12:123231145
|
T | C | 1 | a0002c0003t0002g0263 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-158-623A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231145 | ||||||
| chr12:123231226
|
C | A | 50 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0215others(47): Show | 50 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-158-704G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231226 | ||||||
| chr12:123231385
|
G | C | 1 | a0002c0003t0002g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-158-863C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231385 | ||||||
| chr12:123231576
|
T | C | 9 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(6): Show | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.-158-1054A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231576 | ||||||
| chr12:123231757
|
GCTGGATA others(4): Show |
G | 5 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-1246_-158-123 others(15): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231757 | ||||||
| chr12:123231769
|
C | T | 5 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-1247G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231769 | ||||||
| chr12:123231829
|
C | T | 173 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(170): Show | 173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.-159+1246G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231829 | ||||||
| chr12:123231919
|
G | A | 52 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(49): Show | 52 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.-159+1156C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231919 | ||||||
| chr12:123231966
|
C | T | 173 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0115others(170): Show | 173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.-159+1109G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231966 | ||||||
| chr12:123232238
|
G | C | 5 | a0001c0002t0001g0092a0001c0005t0001g0093a0001c0005t0001g0094others(2): Show | 5 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+837C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232238 | ||||||
| chr12:123232383
|
A | T | 220 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(217): Show | 220 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-159+692T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232383 | ||||||
| chr12:123232593
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-159+482C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232593 | ||||||
| chr12:123232669
|
G | A | 50 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0215others(47): Show | 50 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-159+406C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232669 | ||||||
| chr12:123232678
|
T | A | 3 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0016t0001g0098 | 3 | HG01952.hp1 HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-159+397A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232678 | ||||||
| chr12:123232686
|
G | A | 2 | a0001c0002t0001g0101a0001c0002t0001g0102 | 2 | NA18990.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-159+389C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232686 | ||||||
| chr12:123232793
|
A | G | 2 | a0001c0002t0001g0005a0001c0004t0001g0006 | 2 | HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-159+282T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232793 | ||||||
| chr12:123232807
|
C | A | 52 | a0002c0003t0001g0230a0002c0003t0001g0232a0002c0003t0002g0213others(49): Show | 52 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.-159+268G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232807 | ||||||
| chr12:123232815
|
A | G | 100 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(97): Show | 100 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.-159+260T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232815 | ||||||
| chr12:123232849
|
G | A | 2 | a0001c0001t0006g0265a0001c0001t0006g0266 | 2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-159+226C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232849 | ||||||
| chr12:123232897
|
C | T | 2 | a0001c0004t0001g0003a0001c0004t0001g0004 | 2 | HG00735.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-159+178G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232897 | ||||||
| chr12:123232903
|
C | G | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-159+172G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232903 |