Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57134 |
|---|---|
| ensemblid | ENSG00000117643.16 |
| hgncid | 19080 |
| symbol | MAN1C1 |
| name | mannosidase alpha class 1C member 1 |
| refseq_nuc | NM_020379.4 |
| refseq_prot | NP_065112.1 |
| ensembl_nuc | ENST00000374332.9 |
| ensembl_prot | ENSP00000363452.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 25616791 |
| end | 25784450 |
| strand | + |
| ver | v1.2 |
| region | chr1:25616791-25784450 |
| region5000 | chr1:25611791-25789450 |
| regionname0 | MAN1C1_chr1_25616791_25784450 |
| regionname5000 | MAN1C1_chr1_25611791_25789450 |
| 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 | 630 | 246 | 77 | 51 | 94 | 4 | 18 | 60 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0002 | 0/0 | 630 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0003 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0004 | 0/0 | 630 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| 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 | 1893 | 143 | 28 | 31 | 63 | 4 | 15 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| c0002 | 0/0 | 1893 | 79 | 30 | 15 | 31 | 0 | 3 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| c0003 | 0/0 | 1893 | 14 | 10 | 4 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| c0004 | 0/0 | 1893 | 7 | 7 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| c0005 | 0/0 | 1893 | 3 | 2 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| c0006 | 0/0 | 1893 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| c0007 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| c0008 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| c0009 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| 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 | 1/1 | 1669 | 230 | 73 | 49 | 85 | 4 | 17 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0002 | 0/0 | 1669 | 5 | 0 | 0 | 5 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0003 | 0/0 | 1669 | 2 | 2 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0004 | 0/0 | 1669 | 2 | 0 | 2 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0005 | 0/0 | 1669 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0006 | 0/0 | 1669 | 2 | 2 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0007 | 0/0 | 1669 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0008 | 0/0 | 1669 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0009 | 0/0 | 1669 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0010 | 0/0 | 1669 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0011 | 0/0 | 1669 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0012 | 0/0 | 1669 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| t0013 | 0/0 | 1669 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| 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 | 1893 | 143 | 28 | 31 | 63 | 4 | 15 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0002 | 0/0 | 1893 | 79 | 30 | 15 | 31 | 0 | 3 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0003 | 0/0 | 1893 | 14 | 10 | 4 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0004 | 0/0 | 1893 | 7 | 7 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0005 | 0/0 | 1893 | 3 | 2 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0002c0008 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0002c0009 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0003c0007 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0004c0006 | 0/0 | 1893 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3561 | 134 | 26 | 28 | 59 | 4 | 15 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0001t0004 | 0/0 | 3561 | 2 | 0 | 2 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0001t0005 | 0/0 | 3561 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0001t0007 | 0/0 | 3561 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0001t0009 | 0/0 | 3561 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0001t0010 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0001t0011 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0001t0012 | 0/0 | 3561 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0002t0001 | 0/0 | 3561 | 69 | 26 | 15 | 26 | 0 | 2 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0002t0002 | 0/0 | 3561 | 5 | 0 | 0 | 5 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0002t0003 | 0/0 | 3561 | 2 | 2 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0002t0006 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0002t0008 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0002t0013 | 0/0 | 3561 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0003t0001 | 0/0 | 3561 | 13 | 9 | 4 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0003t0006 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0004t0001 | 0/0 | 3561 | 7 | 7 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0001c0005t0001 | 0/0 | 3561 | 3 | 2 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0002c0008t0001 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0002c0009t0001 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0003c0007t0001 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| a0004c0006t0001 | 0/0 | 3561 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | copy fasta | chr1 | 25611791 | 25789450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0009g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0012g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0013g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0003t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0004t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0005t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0005t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0005t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0002c0008t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0002c0009t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0003c0007t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0004c0006t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0240 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00639 | hp2 | a0001 | c0005 | t0001 | g0193 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00735 | hp2 | a0004 | c0006 | t0001 | g0138 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0237 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0231 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0239 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0184 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0111 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01978 | hp2 | a0001 | c0001 | t0012 | g0135 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0249 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CDX | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | CDX | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0071 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02280 | hp1 | a0001 | c0003 | t0006 | g0216 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02280 | hp2 | a0003 | c0007 | t0001 | g0148 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0246 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0142 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02615 | hp1 | a0001 | c0002 | t0008 | g0227 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0241 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02647 | hp2 | a0002 | c0008 | t0001 | g0019 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0016 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0242 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0234 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0062 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0201 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0155 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02976 | hp1 | a0001 | c0002 | t0003 | g0154 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0233 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0033 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | MSL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | MSL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0075 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0187 | SAS | STU | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | BEB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG04184 | hp2 | a0001 | c0002 | t0013 | g0202 | SAS | BEB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | YRI | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | CHB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18906 | hp1 | a0001 | c0005 | t0001 | g0229 | AFR | YRI | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | YRI | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18983 | hp2 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18990 | hp2 | a0001 | c0001 | t0009 | g0036 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18999 | hp2 | a0001 | c0001 | t0005 | g0139 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | LWK | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | LWK | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19064 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | GIH | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0218 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0243 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0244 | AFR | MSL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG06807 | hp1 | a0001 | c0002 | t0006 | g0217 | AFR | USA | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG06807 | hp2 | a0002 | c0009 | t0001 | g0021 | AFR | USA | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0224 | AFR | USA | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | USA | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | LWK | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | LWK | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0116 | REF | REF | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0118 | REF | REF | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:25617963
|
C | G | 1 | a0002 | 2 | HG02647.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.166C>G | p.Pro56Ala | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/12 | 1173/3561 | 166/1893 | 56/630 | chr1 | 25617963 | ||
| chr1:25618039
|
C | T | 1 | a0003 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.242C>T | p.Pro81Leu | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/12 | 1249/3561 | 242/1893 | 81/630 | chr1 | 25618039 | ||
| chr1:25783745
|
G | A | 1 | a0004 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1849G>A | p.Val617Met | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 12/12 | 2856/3561 | 1849/1893 | 617/630 | chr1 | 25783745 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:25618250
|
T | C | 3 | a0001c0002a0001c0003a0001c0005 | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
synonymous_variant | LOW | c.453T>C | p.Arg151Arg | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/12 | 1460/3561 | 453/1893 | 151/630 | chr1 | 25618250 | ||
| chr1:25749257
|
C | T | 1 | a0001c0005 | 3 | HG00639.hp2 HG02055.hp2 NA18906.hp1 |
splice_region_variant&synonymous_variant | LOW | c.756C>T | p.Ser252Ser | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/12 | 1763/3561 | 756/1893 | 252/630 | chr1 | 25749257 | ||
| chr1:25753561
|
C | T | 3 | a0001c0003a0001c0004a0002c0009 | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
synonymous_variant | LOW | c.912C>T | p.Gly304Gly | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/12 | 1919/3561 | 912/1893 | 304/630 | chr1 | 25753561 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:25616802
|
G | A | 1 | a0001c0001t0007 | 1 | NA18983.hp2 | 5_prime_UTR_variant | MODIFIER | c.-996G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/12 | 996 | chr1 | 25616802 | |||||
| chr1:25616814
|
C | T | 1 | a0001c0002t0013 | 1 | HG04184.hp2 | 5_prime_UTR_variant | MODIFIER | c.-984C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/12 | 984 | chr1 | 25616814 | |||||
| chr1:25616992
|
A | G | 2 | a0001c0002t0006a0001c0003t0006 | 2 | HG02280.hp1 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-806A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/12 | 806 | chr1 | 25616992 | |||||
| chr1:25617187
|
G | C | 1 | a0001c0002t0003 | 2 | HG02922.hp2 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-611G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/12 | 611 | chr1 | 25617187 | |||||
| chr1:25617453
|
C | G | 1 | a0001c0001t0012 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-345C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/12 | 345 | chr1 | 25617453 | |||||
| chr1:25617678
|
T | C | 1 | a0001c0002t0002 | 5 | NA18964.hp2 NA19011.hp2 NA19060.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-120T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/12 | chr1 | 25617678 | ||||||
| chr1:25783807
|
G | A | 1 | a0001c0001t0004 | 2 | HG01070.hp1 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*18G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 12/12 | 18 | chr1 | 25783807 | |||||
| chr1:25783830
|
C | G | 1 | a0001c0001t0011 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 12/12 | 41 | chr1 | 25783830 | |||||
| chr1:25784079
|
C | T | 1 | a0001c0001t0010 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 12/12 | 290 | chr1 | 25784079 | |||||
| chr1:25784139
|
G | A | 1 | a0001c0002t0008 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*350G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 12/12 | 350 | chr1 | 25784139 | |||||
| chr1:25784328
|
C | T | 1 | a0001c0001t0009 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*539C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 12/12 | 539 | chr1 | 25784328 | |||||
| chr1:25784358
|
G | A | 1 | a0001c0001t0005 | 2 | NA18999.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*569G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 12/12 | 569 | chr1 | 25784358 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:25618358
|
C | T | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+21C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25618358 | ||||||
| chr1:25618484
|
C | T | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.540+147C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25618484 | ||||||
| chr1:25618833
|
C | G | 1 | a0001c0002t0001g0248 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.540+496C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25618833 | ||||||
| chr1:25619223
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.540+886G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25619223 | ||||||
| chr1:25619337
|
A | G | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.540+1000A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25619337 | ||||||
| chr1:25619349
|
C | T | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.540+1012C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25619349 | ||||||
| chr1:25619415
|
G | A | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+1078G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25619415 | ||||||
| chr1:25619504
|
T | G | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | NA18985.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.540+1167T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25619504 | ||||||
| chr1:25619603
|
G | A | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+1266G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25619603 | ||||||
| chr1:25619710
|
G | A | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.540+1373G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25619710 | ||||||
| chr1:25620098
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.540+1761C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25620098 | ||||||
| chr1:25620100
|
C | T | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.540+1763C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25620100 | ||||||
| chr1:25620184
|
T | G | 1 | a0001c0003t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.540+1847T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25620184 | ||||||
| chr1:25620268
|
T | C | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+1931T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25620268 | ||||||
| chr1:25620308
|
A | G | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+1971A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25620308 | ||||||
| chr1:25620394
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.540+2057T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25620394 | ||||||
| chr1:25620444
|
T | TGTAGA | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+2110_540+2114d others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25620444 | |||||
| chr1:25620511
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.540+2174A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25620511 | ||||||
| chr1:25620565
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.540+2228C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25620565 | ||||||
| chr1:25620761
|
G | A | 62 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0159others(59): Show | 62 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.540+2424G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25620761 | ||||||
| chr1:25621612
|
G | T | 2 | a0001c0002t0006g0217a0001c0003t0006g0216 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.540+3275G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25621612 | ||||||
| chr1:25621615
|
T | G | 6 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+3278T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25621615 | ||||||
| chr1:25621734
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.540+3397G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25621734 | ||||||
| chr1:25622057
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.540+3720G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25622057 | ||||||
| chr1:25622385
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.540+4048C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25622385 | ||||||
| chr1:25622456
|
C | T | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+4119C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25622456 | ||||||
| chr1:25622707
|
G | T | 1 | a0001c0002t0001g0215 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.540+4370G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25622707 | ||||||
| chr1:25622864
|
T | C | 2 | a0001c0002t0006g0217a0001c0003t0006g0216 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.540+4527T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25622864 | ||||||
| chr1:25622973
|
A | T | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+4636A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25622973 | ||||||
| chr1:25623085
|
G | A | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+4748G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623085 | ||||||
| chr1:25623109
|
A | G | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+4772A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623109 | ||||||
| chr1:25623178
|
C | T | 62 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0159others(59): Show | 62 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.540+4841C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623178 | ||||||
| chr1:25623189
|
T | C | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+4852T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623189 | ||||||
| chr1:25623259
|
C | A | 1 | a0001c0001t0001g0006 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.540+4922C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623259 | ||||||
| chr1:25623276
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.540+4939G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623276 | ||||||
| chr1:25623284
|
T | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 176 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(173): Show |
intron_variant | MODIFIER | c.540+4947T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623284 | ||||||
| chr1:25623303
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.540+4966A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623303 | ||||||
| chr1:25623350
|
T | C | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+5013T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623350 | ||||||
| chr1:25623358
|
A | G | 96 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+5021A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623358 | ||||||
| chr1:25623454
|
TGG | T | 94 | a0001c0002t0001g0156a0001c0002t0001g0157a0001c0002t0001g0158others(91): Show | 94 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.540+5125_540+5126d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25623454 | |||||
| chr1:25623457
|
G | T | 8 | a0001c0001t0001g0076a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG01255.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+5120G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623457 | ||||||
| chr1:25623501
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.540+5164G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623501 | ||||||
| chr1:25623714
|
C | T | 9 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.540+5377C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623714 | ||||||
| chr1:25623863
|
G | A | 98 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0156others(95): Show | 98 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.540+5526G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25623863 | ||||||
| chr1:25624007
|
A | G | 2 | a0001c0002t0001g0213a0001c0002t0001g0214 | 2 | HG02165.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.540+5670A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624007 | ||||||
| chr1:25624029
|
G | A | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.540+5692G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624029 | ||||||
| chr1:25624158
|
C | T | 99 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0156others(96): Show | 99 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.540+5821C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624158 | ||||||
| chr1:25624182
|
A | G | 98 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0156others(95): Show | 98 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.540+5845A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624182 | ||||||
| chr1:25624357
|
C | G | 70 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0156others(67): Show | 70 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.540+6020C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624357 | ||||||
| chr1:25624409
|
CT | C | 70 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0156others(67): Show | 70 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.540+6073delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624409 | ||||||
| chr1:25624675
|
T | C | 70 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0156others(67): Show | 70 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.540+6338T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624675 | ||||||
| chr1:25624683
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.540+6346C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624683 | ||||||
| chr1:25624897
|
A | G | 3 | a0001c0001t0010g0075a0001c0002t0001g0247a0001c0003t0006g0216 | 3 | HG01167.hp1 HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.540+6560A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624897 | ||||||
| chr1:25624897
|
ATGTT | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG00735.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+6565_540+6568d others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25624897 | |||||
| chr1:25624983
|
T | A | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.540+6646T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624983 | ||||||
| chr1:25624983
|
T | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+6646T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25624983 | ||||||
| chr1:25624998
|
A | AT | 37 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0064others(34): Show | 37 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.540+6686dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25624998 | |||||
| chr1:25624998
|
A | ATT | 25 | a0001c0002t0001g0156a0001c0002t0001g0219a0001c0002t0001g0221others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.540+6685_540+6686d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25624998 | |||||
| chr1:25624998
|
A | ATTT | 10 | a0001c0001t0010g0075a0001c0002t0001g0211a0001c0002t0001g0222others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.540+6684_540+6686d others(5): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25624998 | |||||
| chr1:25624998
|
AT | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0076others(7): Show | 10 | HG00738.hp2 HG01069.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+6686delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25624998 | |||||
| chr1:25625046
|
T | C | 99 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0001t0010g0075others(96): Show | 99 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.540+6709T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25625046 | ||||||
| chr1:25625249
|
T | C | 64 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+6912T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25625249 | ||||||
| chr1:25625428
|
C | T | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.540+7091C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25625428 | ||||||
| chr1:25625429
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.540+7092G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25625429 | ||||||
| chr1:25625574
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.540+7237G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25625574 | ||||||
| chr1:25625663
|
A | C | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.540+7326A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25625663 | ||||||
| chr1:25625731
|
G | A | 8 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+7394G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25625731 | ||||||
| chr1:25625853
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.540+7516G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25625853 | ||||||
| chr1:25625877
|
G | A | 1 | a0001c0002t0001g0164 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.540+7540G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25625877 | ||||||
| chr1:25626003
|
G | C | 1 | a0001c0001t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.540+7666G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25626003 | ||||||
| chr1:25626212
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.540+7875G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25626212 | ||||||
| chr1:25626223
|
G | A | 63 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.540+7886G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25626223 | ||||||
| chr1:25626368
|
T | C | 1 | a0001c0002t0006g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.540+8031T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25626368 | ||||||
| chr1:25626460
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0002t0001g0212 | 3 | NA18945.hp1 NA19065.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.540+8123G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25626460 | ||||||
| chr1:25626688
|
A | C | 1 | a0001c0003t0001g0201 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.540+8351A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25626688 | ||||||
| chr1:25626765
|
G | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+8428G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25626765 | ||||||
| chr1:25626769
|
C | T | 63 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.540+8432C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25626769 | ||||||
| chr1:25627045
|
A | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(52): Show | 56 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.540+8708A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25627045 | ||||||
| chr1:25627211
|
T | C | 63 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.540+8874T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25627211 | ||||||
| chr1:25627251
|
T | TTTCTC | 55 | a0001c0001t0001g0008a0001c0001t0001g0076a0001c0001t0001g0153others(52): Show | 55 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.540+8937_540+8941d others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25627251 | |||||
| chr1:25627251
|
TTTCTC | T | 30 | a0001c0001t0001g0022a0001c0001t0001g0125a0001c0002t0001g0219others(27): Show | 30 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.540+8937_540+8941d others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25627251 | |||||
| chr1:25627274
|
C | G | 1 | a0001c0002t0001g0200 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.540+8937C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25627274 | ||||||
| chr1:25627279
|
G | C | 6 | a0001c0002t0001g0165a0001c0002t0001g0166a0001c0002t0001g0167others(3): Show | 6 | HG01243.hp2 HG01978.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+8942G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25627279 | ||||||
| chr1:25627286
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.540+8949C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25627286 | ||||||
| chr1:25627287
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.540+8950T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25627287 | ||||||
| chr1:25627287
|
T | TTCTTC | 57 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(54): Show | 57 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.540+8965_540+8969d others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25627287 | |||||
| chr1:25627287
|
T | TTGTCTTC others(8): Show |
5 | a0001c0002t0001g0165a0001c0002t0001g0166a0001c0002t0001g0167others(2): Show | 5 | HG01978.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+8951_540+8952i others(17): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25627287 | |||||
| chr1:25627463
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.540+9126C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25627463 | ||||||
| chr1:25627702
|
A | G | 2 | a0001c0002t0001g0199a0001c0003t0001g0201 | 2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.540+9365A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25627702 | ||||||
| chr1:25627867
|
TA | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0143a0001c0001t0001g0144others(40): Show | 43 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.540+9548delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25627867 | |||||
| chr1:25628181
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.540+9844T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628181 | ||||||
| chr1:25628190
|
T | C | 1 | a0001c0002t0001g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.540+9853T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628190 | ||||||
| chr1:25628257
|
G | A | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01255.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+9920G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628257 | ||||||
| chr1:25628372
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.540+10035A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628372 | ||||||
| chr1:25628455
|
A | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+10118A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628455 | ||||||
| chr1:25628464
|
T | C | 1 | a0001c0002t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.540+10127T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628464 | ||||||
| chr1:25628474
|
A | T | 1 | a0001c0002t0001g0197 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.540+10137A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628474 | ||||||
| chr1:25628522
|
G | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+10185G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628522 | ||||||
| chr1:25628533
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.540+10196C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628533 | ||||||
| chr1:25628638
|
C | T | 1 | a0001c0002t0001g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.540+10301C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628638 | ||||||
| chr1:25628650
|
G | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.540+10313G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628650 | ||||||
| chr1:25628944
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00280.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.540+10607C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628944 | ||||||
| chr1:25628986
|
A | T | 1 | a0001c0002t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540+10649A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25628986 | ||||||
| chr1:25629401
|
T | C | 1 | a0001c0002t0001g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.540+11064T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25629401 | ||||||
| chr1:25629552
|
C | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0120a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+11215C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25629552 | ||||||
| chr1:25629646
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.540+11309C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25629646 | ||||||
| chr1:25629675
|
C | T | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+11338C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25629675 | ||||||
| chr1:25629682
|
A | T | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.540+11345A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25629682 | ||||||
| chr1:25629741
|
AT | A | 66 | a0001c0001t0001g0008a0001c0001t0001g0120a0001c0001t0001g0153others(63): Show | 66 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.540+11416delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25629741 | |||||
| chr1:25629995
|
T | C | 64 | a0001c0001t0001g0008a0001c0001t0001g0120a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+11658T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25629995 | ||||||
| chr1:25630017
|
G | A | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.540+11680G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25630017 | ||||||
| chr1:25630066
|
A | G | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.540+11729A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25630066 | ||||||
| chr1:25630173
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 82 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.540+11836T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25630173 | ||||||
| chr1:25630383
|
C | G | 2 | a0001c0002t0001g0209a0001c0002t0001g0210 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.540+12046C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25630383 | ||||||
| chr1:25630464
|
T | C | 65 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0120others(62): Show | 65 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.540+12127T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25630464 | ||||||
| chr1:25630635
|
T | A | 36 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(33): Show | 36 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.540+12298T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25630635 | ||||||
| chr1:25630641
|
G | A | 1 | a0001c0002t0008g0227 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.540+12304G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25630641 | ||||||
| chr1:25630721
|
G | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(70): Show | 74 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.540+12384G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25630721 | ||||||
| chr1:25630947
|
T | TTTTG | 60 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(57): Show | 61 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.540+12634_540+1263 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25630947 | |||||
| chr1:25630947
|
TTTTGTTT others(1): Show |
T | 3 | a0001c0002t0001g0209a0001c0002t0001g0210a0001c0002t0001g0211 | 3 | HG01069.hp1 HG01071.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.540+12630_540+1263 others(12): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25630947 | |||||
| chr1:25630995
|
C | T | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+12658C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25630995 | ||||||
| chr1:25631063
|
T | C | 64 | a0001c0001t0001g0008a0001c0001t0001g0120a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+12726T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25631063 | ||||||
| chr1:25631247
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.540+12910C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25631247 | ||||||
| chr1:25631248
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 189 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(186): Show |
intron_variant | MODIFIER | c.540+12911A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25631248 | ||||||
| chr1:25631256
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(2): Show | 5 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+12919C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25631256 | ||||||
| chr1:25631388
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.540+13051T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25631388 | ||||||
| chr1:25631407
|
A | G | 8 | a0001c0002t0001g0225a0001c0002t0001g0238a0001c0002t0001g0245others(5): Show | 8 | HG00639.hp1 HG01099.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.540+13070A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25631407 | ||||||
| chr1:25631592
|
A | T | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+13255A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25631592 | ||||||
| chr1:25631741
|
T | C | 1 | a0001c0002t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.540+13404T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25631741 | ||||||
| chr1:25631832
|
G | A | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.540+13495G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25631832 | ||||||
| chr1:25631986
|
G | T | 6 | a0001c0002t0001g0238a0001c0002t0001g0245a0001c0003t0001g0239others(3): Show | 6 | HG00639.hp1 HG01099.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+13649G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25631986 | ||||||
| chr1:25632038
|
A | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+13701A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25632038 | ||||||
| chr1:25632259
|
G | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00609.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.540+13922G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25632259 | ||||||
| chr1:25632373
|
G | A | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01255.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+14036G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25632373 | ||||||
| chr1:25632571
|
C | T | 1 | a0001c0002t0001g0195 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.540+14234C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25632571 | ||||||
| chr1:25632683
|
G | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG00642.hp1 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+14346G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25632683 | ||||||
| chr1:25632865
|
AT | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(74): Show | 78 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.540+14549delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25632865 | |||||
| chr1:25632865
|
ATT | A | 98 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(95): Show | 98 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.540+14548_540+1454 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25632865 | |||||
| chr1:25632987
|
C | G | 1 | a0001c0001t0001g0006 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.540+14650C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25632987 | ||||||
| chr1:25633128
|
G | C | 1 | a0001c0002t0001g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.540+14791G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633128 | ||||||
| chr1:25633172
|
C | T | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.540+14835C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633172 | ||||||
| chr1:25633205
|
T | C | 1 | a0001c0002t0001g0248 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.540+14868T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633205 | ||||||
| chr1:25633518
|
G | A | 10 | a0001c0002t0001g0165a0001c0002t0001g0166a0001c0002t0001g0169others(7): Show | 10 | HG02027.hp1 HG02083.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+15181G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633518 | ||||||
| chr1:25633549
|
TC | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 119 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.540+15213delC | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633549 | ||||||
| chr1:25633550
|
C | T | 63 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.540+15213C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633550 | ||||||
| chr1:25633631
|
A | G | 1 | a0001c0001t0001g0001 | 2 | NA18945.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.540+15294A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633631 | ||||||
| chr1:25633714
|
G | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 73 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.540+15377G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633714 | ||||||
| chr1:25633787
|
A | G | 1 | a0001c0002t0001g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.540+15450A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633787 | ||||||
| chr1:25633848
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.540+15511A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633848 | ||||||
| chr1:25633880
|
G | C | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.540+15543G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25633880 | ||||||
| chr1:25634339
|
T | G | 2 | a0001c0002t0001g0199a0001c0003t0001g0201 | 2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.540+16002T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25634339 | ||||||
| chr1:25634828
|
AT | A | 3 | a0001c0001t0001g0029a0001c0002t0001g0157a0001c0002t0001g0210 | 3 | HG00741.hp2 HG01069.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.540+16492delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25634828 | ||||||
| chr1:25634829
|
T | A | 62 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(59): Show | 62 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.540+16492T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25634829 | ||||||
| chr1:25634882
|
A | G | 1 | a0001c0002t0001g0215 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.540+16545A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25634882 | ||||||
| chr1:25635053
|
A | G | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.540+16716A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635053 | ||||||
| chr1:25635097
|
G | C | 63 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.540+16760G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635097 | ||||||
| chr1:25635268
|
G | A | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+16931G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635268 | ||||||
| chr1:25635275
|
T | G | 7 | a0001c0002t0001g0228a0001c0002t0001g0230a0001c0002t0001g0232others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+16938T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635275 | ||||||
| chr1:25635278
|
G | T | 8 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+16941G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635278 | ||||||
| chr1:25635354
|
C | G | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.540+17017C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635354 | ||||||
| chr1:25635389
|
T | G | 1 | a0001c0002t0001g0205 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.540+17052T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635389 | ||||||
| chr1:25635438
|
CTT | C | 36 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(33): Show | 36 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.540+17117_540+1711 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25635438 | |||||
| chr1:25635442
|
T | C | 2 | a0001c0002t0001g0209a0001c0002t0001g0210 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.540+17105T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635442 | ||||||
| chr1:25635594
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.540+17257C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635594 | ||||||
| chr1:25635607
|
G | A | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+17270G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635607 | ||||||
| chr1:25635778
|
C | G | 104 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(101): Show | 104 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.540+17441C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635778 | ||||||
| chr1:25635897
|
C | T | 63 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.540+17560C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635897 | ||||||
| chr1:25635905
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.540+17568G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635905 | ||||||
| chr1:25635981
|
A | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG00597.hp2 HG02129.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.540+17644A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25635981 | ||||||
| chr1:25636355
|
A | G | 2 | a0001c0002t0001g0163a0001c0005t0001g0193 | 2 | HG00639.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.540+18018A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25636355 | ||||||
| chr1:25636373
|
G | T | 63 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.540+18036G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25636373 | ||||||
| chr1:25636379
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.540+18042G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25636379 | ||||||
| chr1:25636522
|
T | C | 1 | a0002c0008t0001g0019 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.540+18185T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25636522 | ||||||
| chr1:25636720
|
G | A | 104 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(101): Show | 104 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.540+18383G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25636720 | ||||||
| chr1:25636926
|
A | G | 100 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(97): Show | 100 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.540+18589A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25636926 | ||||||
| chr1:25637109
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.540+18772C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25637109 | ||||||
| chr1:25637111
|
C | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0150a0001c0004t0001g0015others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+18774C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25637111 | ||||||
| chr1:25637155
|
AAAAAAAA others(9): Show |
A | 17 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(14): Show | 17 | HG00423.hp2 HG00642.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.540+18825_540+1884 others(20): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25637155 | |||||
| chr1:25637394
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.540+19057T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25637394 | ||||||
| chr1:25637712
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 74 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.540+19375G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25637712 | ||||||
| chr1:25637908
|
T | TA | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 243 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(240): Show |
intron_variant | MODIFIER | c.540+19571_540+1957 others(5): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25637908 | ||||||
| chr1:25637987
|
T | C | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+19650T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25637987 | ||||||
| chr1:25638186
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+19849A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638186 | ||||||
| chr1:25638254
|
A | C | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+19917A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638254 | ||||||
| chr1:25638366
|
G | A | 1 | a0001c0002t0001g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.540+20029G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638366 | ||||||
| chr1:25638385
|
A | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+20048A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638385 | ||||||
| chr1:25638436
|
C | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0150others(4): Show | 7 | HG01109.hp2 HG01891.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+20099C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638436 | ||||||
| chr1:25638615
|
A | C | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+20278A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638615 | ||||||
| chr1:25638687
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 179 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(176): Show |
intron_variant | MODIFIER | c.540+20350G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638687 | ||||||
| chr1:25638705
|
T | C | 1 | a0001c0002t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.540+20368T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638705 | ||||||
| chr1:25638789
|
A | G | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.540+20452A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638789 | ||||||
| chr1:25638853
|
T | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+20516T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638853 | ||||||
| chr1:25638910
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 188 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(185): Show |
intron_variant | MODIFIER | c.540+20573A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25638910 | ||||||
| chr1:25639215
|
T | G | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+20878T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25639215 | ||||||
| chr1:25639341
|
T | C | 1 | a0001c0002t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.540+21004T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25639341 | ||||||
| chr1:25639345
|
T | G | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.540+21008T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25639345 | ||||||
| chr1:25639625
|
C | A | 1 | a0001c0003t0001g0244 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.540+21288C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25639625 | ||||||
| chr1:25639894
|
C | G | 1 | a0001c0002t0001g0198 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.540+21557C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25639894 | ||||||
| chr1:25640053
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(70): Show | 74 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.540+21716A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25640053 | ||||||
| chr1:25640144
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.540+21807C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25640144 | ||||||
| chr1:25640332
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.540+21995C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25640332 | ||||||
| chr1:25641020
|
C | T | 63 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.540+22683C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25641020 | ||||||
| chr1:25641071
|
T | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(57): Show | 61 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.540+22734T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25641071 | ||||||
| chr1:25641096
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 249 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.540+22759T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25641096 | ||||||
| chr1:25641135
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.540+22798G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25641135 | ||||||
| chr1:25641180
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.540+22843G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25641180 | ||||||
| chr1:25641283
|
A | G | 63 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.540+22946A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25641283 | ||||||
| chr1:25641660
|
T | C | 1 | a0001c0002t0001g0174 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.540+23323T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25641660 | ||||||
| chr1:25641852
|
A | G | 8 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0113others(5): Show | 8 | HG01070.hp1 HG01167.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+23515A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25641852 | ||||||
| chr1:25641861
|
G | A | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+23524G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25641861 | ||||||
| chr1:25642013
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.540+23676T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25642013 | ||||||
| chr1:25642159
|
C | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0084 | 2 | HG02074.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.540+23822C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25642159 | ||||||
| chr1:25642171
|
C | T | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+23834C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25642171 | ||||||
| chr1:25642199
|
A | G | 105 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(102): Show | 105 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.540+23862A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25642199 | ||||||
| chr1:25642423
|
A | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.540+24086A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25642423 | ||||||
| chr1:25642517
|
T | C | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.540+24180T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25642517 | ||||||
| chr1:25642582
|
A | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0065 | 3 | NA18946.hp1 NA19077.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.540+24245A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25642582 | ||||||
| chr1:25642818
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.540+24481G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25642818 | ||||||
| chr1:25643230
|
T | TTTAA | 10 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0069others(7): Show | 10 | HG01433.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.540+24916_540+2491 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643230 | |||||
| chr1:25643230
|
TTTAA | T | 63 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.540+24916_540+2491 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643230 | |||||
| chr1:25643241
|
A | T | 12 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0224others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.540+24904A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643241 | ||||||
| chr1:25643245
|
A | AATTT | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG00735.hp1 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+24911_540+2491 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643245 | |||||
| chr1:25643245
|
A | T | 25 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.540+24908A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643245 | ||||||
| chr1:25643249
|
A | AATTT | 8 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0045others(5): Show | 8 | HG01952.hp2 HG01993.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+24915_540+2491 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643249 | |||||
| chr1:25643249
|
A | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(101): Show | 104 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.540+24912A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643249 | ||||||
| chr1:25643253
|
A | AATTT | 57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(54): Show | 58 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.540+24922_540+2492 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643253 | |||||
| chr1:25643253
|
A | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(124): Show | 127 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.540+24916A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643253 | ||||||
| chr1:25643257
|
T | A | 2 | a0001c0001t0001g0081a0001c0002t0001g0212 | 2 | NA18945.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.540+24920T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643257 | ||||||
| chr1:25643336
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.540+24999C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643336 | ||||||
| chr1:25643357
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG00642.hp2 HG00741.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+25020C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643357 | ||||||
| chr1:25643403
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0004t0001g0016others(1): Show | 4 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+25066C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643403 | ||||||
| chr1:25643412
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.540+25075G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643412 | ||||||
| chr1:25643421
|
A | AT | 7 | a0001c0001t0001g0048a0001c0001t0001g0074a0001c0001t0001g0112others(4): Show | 7 | HG00735.hp2 HG01175.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+25105dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643421 | |||||
| chr1:25643421
|
AT | A | 37 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0086others(34): Show | 37 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.540+25105delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643421 | |||||
| chr1:25643421
|
ATT | A | 62 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(59): Show | 62 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.540+25104_540+2510 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643421 | |||||
| chr1:25643462
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.540+25125G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643462 | ||||||
| chr1:25643471
|
G | C | 3 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155 | 3 | HG02559.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.540+25134G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643471 | ||||||
| chr1:25643523
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.540+25186G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643523 | ||||||
| chr1:25643586
|
T | TTTA | 18 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 18 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.540+25276_540+2527 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643586 | |||||
| chr1:25643586
|
T | TTTATTA | 27 | a0001c0002t0001g0219a0001c0002t0001g0222a0001c0002t0001g0223others(24): Show | 27 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.540+25273_540+2527 others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643586 | |||||
| chr1:25643589
|
A | ATTATTAT others(6): Show |
1 | a0001c0002t0001g0161 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.540+25254_540+2526 others(17): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643589 | |||||
| chr1:25643589
|
A | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0125 | 3 | HG00609.hp2 HG02165.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.540+25252A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643589 | ||||||
| chr1:25643592
|
A | ATTATTAT others(3): Show |
62 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(59): Show | 62 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.540+25257_540+2526 others(14): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25643592 | |||||
| chr1:25643696
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02027.hp2 NA19011.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.540+25359G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643696 | ||||||
| chr1:25643756
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.540+25419C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643756 | ||||||
| chr1:25643863
|
C | G | 2 | a0001c0002t0001g0234a0001c0002t0001g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.540+25526C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25643863 | ||||||
| chr1:25644050
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.540+25713C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644050 | ||||||
| chr1:25644160
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.540+25823A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644160 | ||||||
| chr1:25644213
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(2): Show | 5 | HG02258.hp2 HG02717.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+25876C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644213 | ||||||
| chr1:25644457
|
A | T | 1 | a0004c0006t0001g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.540+26120A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644457 | ||||||
| chr1:25644497
|
C | CATAT | 6 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+26179_540+2618 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644497 | |||||
| chr1:25644497
|
C | CATATAT | 4 | a0001c0001t0001g0051a0001c0001t0001g0151a0001c0002t0001g0170others(1): Show | 4 | NA18612.hp1 NA18943.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+26177_540+2618 others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644497 | |||||
| chr1:25644497
|
C | CATATATA others(27): Show |
1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.540+26182_540+2618 others(38): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644497 | |||||
| chr1:25644500
|
A | G | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01255.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+26163A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644500 | ||||||
| chr1:25644514
|
A | ATTTT | 6 | a0001c0002t0001g0238a0001c0002t0001g0245a0001c0003t0001g0233others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+26178_540+2617 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644514 | |||||
| chr1:25644514
|
A | T | 3 | a0001c0002t0001g0225a0001c0002t0001g0236a0001c0003t0001g0218 | 3 | HG02109.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.540+26177A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644514 | ||||||
| chr1:25644516
|
A | ATTTT | 4 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG01934.hp1 HG01952.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+26180_540+2618 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644516 | |||||
| chr1:25644516
|
A | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0002t0001g0225others(10): Show | 13 | HG00639.hp1 HG01099.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+26179A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644516 | ||||||
| chr1:25644518
|
A | AT | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG00735.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+26206dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(4): Show |
1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(15): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(40): Show |
1 | a0001c0002t0003g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(51): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(39): Show |
1 | a0001c0002t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(50): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(29): Show |
1 | a0001c0002t0001g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(40): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(31): Show |
1 | a0001c0003t0001g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(42): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(32): Show |
1 | a0001c0002t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.540+26182_540+2618 others(43): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(28): Show |
1 | a0001c0002t0003g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.540+26182_540+2618 others(39): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(30): Show |
1 | a0001c0002t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.540+26182_540+2618 others(41): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(30): Show |
1 | a0001c0002t0001g0223 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.540+26182_540+2618 others(41): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(25): Show |
3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0004t0001g0142 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.540+26182_540+2618 others(36): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.540+26182_540+2618 others(37): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(31): Show |
1 | a0001c0002t0001g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.540+26182_540+2618 others(42): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(22): Show |
1 | a0001c0003t0001g0237 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(33): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(23): Show |
1 | a0001c0003t0001g0231 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.540+26182_540+2618 others(34): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(25): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0003t0001g0243 | 3 | HG02486.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.540+26182_540+2618 others(36): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(22): Show |
1 | a0001c0002t0008g0227 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.540+26182_540+2618 others(33): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(23): Show |
1 | a0001c0002t0001g0232 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(34): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(14): Show |
1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(25): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(10): Show |
1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(21): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0001a0001c0002t0001g0159a0001c0002t0001g0174 | 4 | HG02145.hp2 HG02258.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+26182_540+2618 others(14): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(5): Show |
4 | a0001c0002t0001g0196a0001c0002t0001g0209a0001c0002t0001g0210others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+26182_540+2618 others(16): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(12): Show |
1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(23): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(3): Show |
3 | a0001c0002t0001g0175a0001c0002t0001g0206a0001c0002t0001g0208 | 3 | HG02886.hp1 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.540+26182_540+2618 others(14): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0006g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.540+26182_540+2618 others(15): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATAT others(5): Show |
2 | a0001c0002t0001g0176a0001c0002t0001g0247 | 2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.540+26182_540+2618 others(16): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATATTT | 24 | a0001c0002t0001g0157a0001c0002t0001g0160a0001c0002t0001g0161others(21): Show | 24 | HG00544.hp2 HG00621.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.540+26182_540+2618 others(11): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATTTTT | 11 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0077others(8): Show | 11 | HG00597.hp1 HG01358.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.540+26182_540+2618 others(11): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATATTTTT others(6): Show |
2 | a0001c0002t0001g0234a0001c0002t0001g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.540+26182_540+2618 others(17): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATTTT | 23 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(20): Show | 23 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.540+26203_540+2620 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | ATTTTT | 6 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0057others(3): Show | 6 | HG02015.hp1 HG02027.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+26202_540+2620 others(9): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644518
|
A | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0030others(32): Show | 35 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.540+26181A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644518 | ||||||
| chr1:25644518
|
AT | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0081others(12): Show | 15 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+26206delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25644518 | |||||
| chr1:25644519
|
T | TATATA | 3 | a0001c0001t0001g0022a0001c0004t0001g0016a0001c0004t0001g0062 | 3 | HG02818.hp2 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.540+26182_540+2618 others(9): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644519 | ||||||
| chr1:25644519
|
T | TATATATA others(2): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0005t0001g0193 | 3 | HG00639.hp2 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.540+26182_540+2618 others(13): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644519 | ||||||
| chr1:25644519
|
T | TATATATA others(8): Show |
1 | a0001c0002t0001g0163 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.540+26182_540+2618 others(19): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644519 | ||||||
| chr1:25644519
|
T | TATATATA others(22): Show |
2 | a0001c0002t0001g0228a0001c0005t0001g0229 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.540+26182_540+2618 others(33): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644519 | ||||||
| chr1:25644520
|
T | A | 8 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(5): Show | 8 | HG01109.hp1 HG01255.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+26183T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644520 | ||||||
| chr1:25644521
|
T | A | 2 | a0001c0003t0006g0216a0001c0005t0001g0229 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.540+26184T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644521 | ||||||
| chr1:25644522
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.540+26185T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644522 | ||||||
| chr1:25644523
|
T | A | 2 | a0001c0003t0006g0216a0001c0005t0001g0229 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.540+26186T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644523 | ||||||
| chr1:25644525
|
T | A | 1 | a0001c0005t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.540+26188T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644525 | ||||||
| chr1:25644818
|
G | A | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+26481G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644818 | ||||||
| chr1:25644927
|
C | T | 36 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(33): Show | 36 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.540+26590C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644927 | ||||||
| chr1:25644967
|
G | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0137a0004c0006t0001g0138 | 3 | HG00735.hp2 HG00738.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.540+26630G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25644967 | ||||||
| chr1:25645110
|
C | G | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+26773C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25645110 | ||||||
| chr1:25645155
|
T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(56): Show | 60 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.540+26818T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25645155 | ||||||
| chr1:25645163
|
G | C | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.540+26826G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25645163 | ||||||
| chr1:25645186
|
C | T | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+26849C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25645186 | ||||||
| chr1:25645570
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.540+27233T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25645570 | ||||||
| chr1:25645681
|
G | A | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+27344G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25645681 | ||||||
| chr1:25645715
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.540+27378T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25645715 | ||||||
| chr1:25645844
|
A | C | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.540+27507A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25645844 | ||||||
| chr1:25645892
|
C | CGAT | 46 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(43): Show | 46 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.540+27557_540+2755 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25645892 | |||||
| chr1:25646229
|
C | G | 4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0137others(1): Show | 4 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+27892C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646229 | ||||||
| chr1:25646255
|
C | T | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+27918C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646255 | ||||||
| chr1:25646259
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.540+27922A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646259 | ||||||
| chr1:25646349
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.540+28012C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646349 | ||||||
| chr1:25646376
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.540+28039C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646376 | ||||||
| chr1:25646444
|
A | G | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.540+28107A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646444 | ||||||
| chr1:25646558
|
G | A | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+28221G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646558 | ||||||
| chr1:25646591
|
A | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG00642.hp1 HG01099.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+28254A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646591 | ||||||
| chr1:25646602
|
A | G | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+28265A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646602 | ||||||
| chr1:25646768
|
G | A | 4 | a0001c0002t0001g0226a0001c0002t0001g0236a0001c0003t0001g0233others(1): Show | 4 | HG03041.hp2 HG03471.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+28431G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646768 | ||||||
| chr1:25646967
|
T | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+28630T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25646967 | ||||||
| chr1:25647029
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+28692A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25647029 | ||||||
| chr1:25647249
|
T | C | 1 | a0001c0002t0008g0227 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.540+28912T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25647249 | ||||||
| chr1:25647294
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.540+28957G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25647294 | ||||||
| chr1:25647380
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.540+29043G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25647380 | ||||||
| chr1:25647558
|
CTG | C | 64 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+29224_540+2922 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25647558 | |||||
| chr1:25647809
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.540+29472G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25647809 | ||||||
| chr1:25647884
|
G | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+29547G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25647884 | ||||||
| chr1:25647885
|
A | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+29548A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25647885 | ||||||
| chr1:25647889
|
G | A | 1 | a0004c0006t0001g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.540+29552G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25647889 | ||||||
| chr1:25648023
|
A | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0069a0001c0001t0001g0070others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.540+29686A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25648023 | ||||||
| chr1:25648239
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.540+29902T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25648239 | ||||||
| chr1:25648290
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+29953A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25648290 | ||||||
| chr1:25648365
|
C | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+30028C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25648365 | ||||||
| chr1:25648410
|
G | C | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+30073G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25648410 | ||||||
| chr1:25648938
|
A | T | 106 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0143others(103): Show | 106 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.540+30601A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25648938 | ||||||
| chr1:25649093
|
CAA | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+30757_540+3075 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25649093 | ||||||
| chr1:25649355
|
C | T | 2 | a0001c0002t0001g0234a0001c0002t0001g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.540+31018C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25649355 | ||||||
| chr1:25649525
|
T | A | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+31188T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25649525 | ||||||
| chr1:25649794
|
T | A | 49 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(46): Show | 49 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.540+31457T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25649794 | ||||||
| chr1:25649886
|
T | G | 1 | a0001c0002t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.540+31549T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25649886 | ||||||
| chr1:25649927
|
C | T | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.540+31590C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25649927 | ||||||
| chr1:25649981
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.540+31644C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25649981 | ||||||
| chr1:25650042
|
A | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0150a0001c0004t0001g0015others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+31705A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650042 | ||||||
| chr1:25650088
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+31751A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650088 | ||||||
| chr1:25650144
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.540+31807G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650144 | ||||||
| chr1:25650241
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.540+31904T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650241 | ||||||
| chr1:25650286
|
C | CAA | 65 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(62): Show | 65 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.540+31949_540+3195 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650286 | ||||||
| chr1:25650339
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.540+32002G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650339 | ||||||
| chr1:25650359
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.540+32022G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650359 | ||||||
| chr1:25650427
|
G | A | 1 | a0001c0005t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.540+32090G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650427 | ||||||
| chr1:25650513
|
T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(56): Show | 60 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.540+32176T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650513 | ||||||
| chr1:25650681
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.540+32344A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650681 | ||||||
| chr1:25650850
|
A | G | 1 | a0001c0003t0006g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.540+32513A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25650850 | ||||||
| chr1:25651099
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.540+32762G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25651099 | ||||||
| chr1:25651235
|
G | T | 1 | a0001c0001t0001g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.540+32898G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25651235 | ||||||
| chr1:25651498
|
G | T | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.540+33161G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25651498 | ||||||
| chr1:25651679
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.540+33342A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25651679 | ||||||
| chr1:25651948
|
G | GCTGC | 12 | a0001c0002t0001g0225a0001c0002t0001g0226a0001c0002t0001g0236others(9): Show | 12 | HG00639.hp1 HG01099.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.540+33625_540+3362 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25651948 | |||||
| chr1:25652155
|
T | C | 65 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(62): Show | 65 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.540+33818T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25652155 | ||||||
| chr1:25652391
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.541-34049C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25652391 | ||||||
| chr1:25652392
|
G | A | 2 | a0001c0003t0001g0231a0001c0003t0001g0237 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.541-34048G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25652392 | ||||||
| chr1:25652436
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(63): Show | 67 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.541-34004G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25652436 | ||||||
| chr1:25652489
|
C | T | 3 | a0001c0002t0001g0209a0001c0002t0001g0210a0001c0002t0001g0211 | 3 | HG01069.hp1 HG01071.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.541-33951C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25652489 | ||||||
| chr1:25652684
|
G | A | 64 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.541-33756G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25652684 | ||||||
| chr1:25652956
|
C | G | 1 | a0002c0009t0001g0021 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.541-33484C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25652956 | ||||||
| chr1:25653157
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0115 | 2 | HG02071.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.541-33283G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25653157 | ||||||
| chr1:25653169
|
C | T | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.541-33271C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25653169 | ||||||
| chr1:25653439
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0105a0001c0001t0001g0136 | 3 | HG00423.hp1 HG02135.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.541-33001C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25653439 | ||||||
| chr1:25653469
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 188 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(185): Show |
intron_variant | MODIFIER | c.541-32971T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25653469 | ||||||
| chr1:25653640
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(64): Show | 68 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.541-32800G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25653640 | ||||||
| chr1:25653658
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.541-32782T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25653658 | ||||||
| chr1:25653901
|
C | T | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.541-32539C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25653901 | ||||||
| chr1:25653935
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.541-32505A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25653935 | ||||||
| chr1:25653964
|
T | G | 65 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(62): Show | 65 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.541-32476T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25653964 | ||||||
| chr1:25654543
|
A | G | 65 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(62): Show | 65 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.541-31897A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25654543 | ||||||
| chr1:25654636
|
T | C | 10 | a0001c0002t0001g0228a0001c0002t0001g0230a0001c0002t0001g0232others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.541-31804T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25654636 | ||||||
| chr1:25654732
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.541-31708C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25654732 | ||||||
| chr1:25654772
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA19011.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.541-31668G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25654772 | ||||||
| chr1:25655267
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.541-31173G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25655267 | ||||||
| chr1:25655298
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 67 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.541-31142G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25655298 | ||||||
| chr1:25655343
|
G | A | 1 | a0001c0003t0006g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.541-31097G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25655343 | ||||||
| chr1:25655380
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.541-31060A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25655380 | ||||||
| chr1:25655675
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.541-30765T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25655675 | ||||||
| chr1:25655913
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.541-30527C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25655913 | ||||||
| chr1:25655948
|
G | C | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.541-30492G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25655948 | ||||||
| chr1:25656095
|
C | CT | 5 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0123others(2): Show | 5 | HG01175.hp1 HG01891.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-30323dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTT | 5 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0074others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-30324_541-3032 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTT | 56 | a0001c0001t0001g0008a0001c0002t0001g0158a0001c0002t0001g0159others(53): Show | 56 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.541-30328_541-3032 others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT | 7 | a0001c0001t0001g0153a0001c0002t0001g0157a0001c0002t0001g0160others(4): Show | 7 | HG00639.hp2 HG01069.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-30329_541-3032 others(11): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541-30334_541-3032 others(16): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0077others(1): Show | 4 | HG02155.hp2 NA18612.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-30335_541-3032 others(17): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(7): Show |
24 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0023others(21): Show | 24 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.541-30336_541-3032 others(18): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(8): Show |
24 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(21): Show | 25 | HG00621.hp1 HG00642.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.541-30337_541-3032 others(19): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(9): Show |
17 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(14): Show | 17 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.541-30338_541-3032 others(20): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(10): Show |
9 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-30339_541-3032 others(21): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(11): Show |
7 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(4): Show | 7 | HG02280.hp1 HG02886.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-30340_541-3032 others(22): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0150a0001c0002t0001g0245 | 3 | HG01109.hp2 HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.541-30341_541-3032 others(23): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0001g0046a0001c0003t0001g0237 | 2 | HG01070.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.541-30343_541-3032 others(25): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(15): Show |
2 | a0001c0002t0001g0232a0001c0003t0001g0231 | 2 | HG01071.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.541-30344_541-3032 others(26): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(16): Show |
2 | a0001c0002t0001g0228a0001c0003t0001g0243 | 2 | HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.541-30323_541-3032 others(27): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0072a0001c0004t0001g0071 | 2 | HG02257.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.541-30323_541-3032 others(29): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(23): Show |
1 | a0001c0005t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.541-30323_541-3032 others(34): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
C | CTTTTTTT others(30): Show |
1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-30323_541-3032 others(41): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
CT | C | 7 | a0001c0001t0001g0085a0001c0001t0001g0093a0001c0001t0001g0136others(4): Show | 7 | HG00423.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-30323delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656095
|
CTTTTT | C | 5 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0146others(2): Show | 5 | HG01255.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-30327_541-3032 others(9): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656095 | |||||
| chr1:25656136
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.541-30304C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25656136 | ||||||
| chr1:25656137
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541-30303G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25656137 | ||||||
| chr1:25656156
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.541-30284G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25656156 | ||||||
| chr1:25656218
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.541-30222C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25656218 | ||||||
| chr1:25656421
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG02258.hp2 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-30019G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25656421 | ||||||
| chr1:25656524
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.541-29916A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25656524 | ||||||
| chr1:25656545
|
G | A | 1 | a0001c0002t0001g0197 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.541-29895G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25656545 | ||||||
| chr1:25656565
|
G | A | 1 | a0001c0003t0006g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.541-29875G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25656565 | ||||||
| chr1:25656768
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.541-29672G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25656768 | ||||||
| chr1:25656828
|
CT | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(55): Show | 59 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.541-29597delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25656828 | |||||
| chr1:25657027
|
G | T | 24 | a0001c0001t0001g0153a0001c0002t0001g0157a0001c0002t0001g0158others(21): Show | 24 | HG00738.hp2 HG01081.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.541-29413G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25657027 | ||||||
| chr1:25657114
|
C | G | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.541-29326C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25657114 | ||||||
| chr1:25657299
|
G | A | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.541-29141G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25657299 | ||||||
| chr1:25657302
|
T | C | 3 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0164 | 3 | NA18985.hp2 NA19002.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.541-29138T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25657302 | ||||||
| chr1:25657519
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.541-28921A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25657519 | ||||||
| chr1:25657668
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.541-28772C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25657668 | ||||||
| chr1:25657750
|
G | A | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.541-28690G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25657750 | ||||||
| chr1:25657773
|
C | T | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.541-28667C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25657773 | ||||||
| chr1:25657774
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.541-28666A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25657774 | ||||||
| chr1:25658020
|
T | G | 76 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(73): Show | 76 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.541-28420T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25658020 | ||||||
| chr1:25658074
|
G | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(5): Show | 8 | HG01167.hp1 HG01255.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-28366G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25658074 | ||||||
| chr1:25658427
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.541-28013A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25658427 | ||||||
| chr1:25658459
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.541-27981T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25658459 | ||||||
| chr1:25658730
|
T | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-27710T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25658730 | ||||||
| chr1:25658747
|
G | A | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.541-27693G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25658747 | ||||||
| chr1:25658853
|
G | A | 5 | a0001c0002t0001g0156a0001c0002t0002g0192a0001c0002t0003g0154others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-27587G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25658853 | ||||||
| chr1:25658924
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.541-27516A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25658924 | ||||||
| chr1:25658960
|
A | G | 104 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(101): Show | 104 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.541-27480A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25658960 | ||||||
| chr1:25658990
|
G | A | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.541-27450G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25658990 | ||||||
| chr1:25659133
|
T | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-27307T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25659133 | ||||||
| chr1:25659346
|
C | G | 104 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(101): Show | 104 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.541-27094C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25659346 | ||||||
| chr1:25659540
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.541-26900A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25659540 | ||||||
| chr1:25659749
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.541-26691A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25659749 | ||||||
| chr1:25660031
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 187 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(184): Show |
intron_variant | MODIFIER | c.541-26409T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660031 | ||||||
| chr1:25660057
|
T | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0064 | 3 | HG00642.hp2 HG04199.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.541-26383T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660057 | ||||||
| chr1:25660070
|
G | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0064 | 3 | HG00642.hp2 HG04199.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.541-26370G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660070 | ||||||
| chr1:25660176
|
C | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.541-26264C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660176 | ||||||
| chr1:25660294
|
G | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(16): Show | 19 | HG00423.hp2 HG00642.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.541-26146G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660294 | ||||||
| chr1:25660308
|
G | A | 28 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0222others(25): Show | 28 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.541-26132G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660308 | ||||||
| chr1:25660316
|
A | G | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-26124A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660316 | ||||||
| chr1:25660396
|
C | CT | 51 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(48): Show | 51 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.541-26016dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25660396 | |||||
| chr1:25660396
|
C | CTT | 10 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0010g0075others(7): Show | 10 | HG00735.hp1 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.541-26017_541-2601 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25660396 | |||||
| chr1:25660396
|
CT | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0052others(4): Show | 7 | HG01261.hp2 HG01993.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-26016delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25660396 | |||||
| chr1:25660396
|
CTTTTTT | C | 7 | a0001c0001t0001g0061a0001c0001t0001g0150a0001c0002t0001g0198others(4): Show | 7 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-26021_541-2601 others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25660396 | |||||
| chr1:25660396
|
CTTTTTTT | C | 71 | a0001c0001t0001g0086a0001c0001t0001g0143a0001c0001t0001g0144others(68): Show | 71 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.541-26022_541-2601 others(11): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25660396 | |||||
| chr1:25660396
|
CTTTTTTT others(1): Show |
C | 5 | a0001c0001t0001g0008a0001c0001t0001g0096a0001c0001t0001g0145others(2): Show | 5 | HG02071.hp2 HG02451.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-26023_541-2601 others(12): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25660396 | |||||
| chr1:25660396
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.541-26027_541-2601 others(16): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25660396 | |||||
| chr1:25660461
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.541-25979C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660461 | ||||||
| chr1:25660582
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.541-25858C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660582 | ||||||
| chr1:25660594
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.541-25846G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660594 | ||||||
| chr1:25660757
|
C | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 82 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.541-25683C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660757 | ||||||
| chr1:25660885
|
T | A | 64 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0157others(61): Show | 64 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.541-25555T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660885 | ||||||
| chr1:25660928
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.541-25512T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660928 | ||||||
| chr1:25660967
|
A | G | 96 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0156others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.541-25473A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25660967 | ||||||
| chr1:25661083
|
G | GT | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(69): Show | 73 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.541-25346dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25661083 | |||||
| chr1:25661083
|
GT | G | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-25346delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25661083 | |||||
| chr1:25661144
|
T | C | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01255.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-25296T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25661144 | ||||||
| chr1:25661247
|
G | T | 4 | a0001c0001t0001g0087a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | NA18960.hp2 NA18970.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-25193G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25661247 | ||||||
| chr1:25661271
|
C | T | 10 | a0001c0002t0001g0228a0001c0002t0001g0230a0001c0002t0001g0232others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.541-25169C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25661271 | ||||||
| chr1:25661392
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.541-25048G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25661392 | ||||||
| chr1:25661487
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.541-24953C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25661487 | ||||||
| chr1:25661683
|
T | C | 68 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0002t0001g0156others(65): Show | 68 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.541-24757T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25661683 | ||||||
| chr1:25661767
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.541-24673A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25661767 | ||||||
| chr1:25661825
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.541-24615A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25661825 | ||||||
| chr1:25661950
|
AT | A | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-24483delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25661950 | |||||
| chr1:25662348
|
A | G | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541-24092A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25662348 | ||||||
| chr1:25662525
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.541-23915A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25662525 | ||||||
| chr1:25662553
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.541-23887A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25662553 | ||||||
| chr1:25662570
|
G | GCA | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 190 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(187): Show |
intron_variant | MODIFIER | c.541-23859_541-2385 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25662570 | |||||
| chr1:25662847
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.541-23593G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25662847 | ||||||
| chr1:25662915
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 249 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.541-23525T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25662915 | ||||||
| chr1:25662919
|
T | C | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-23521T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25662919 | ||||||
| chr1:25662952
|
A | G | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-23488A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25662952 | ||||||
| chr1:25662953
|
G | A | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-23487G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25662953 | ||||||
| chr1:25663030
|
G | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(5): Show | 8 | HG01167.hp1 HG01255.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-23410G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25663030 | ||||||
| chr1:25663052
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.541-23388C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25663052 | ||||||
| chr1:25663072
|
T | C | 1 | a0001c0003t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.541-23368T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25663072 | ||||||
| chr1:25663106
|
C | T | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-23334C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25663106 | ||||||
| chr1:25663115
|
A | T | 65 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0153others(62): Show | 65 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.541-23325A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25663115 | ||||||
| chr1:25663116
|
T | A | 1 | a0001c0002t0001g0183 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.541-23324T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25663116 | ||||||
| chr1:25663195
|
A | C | 1 | a0001c0001t0001g0003 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.541-23245A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25663195 | ||||||
| chr1:25663208
|
A | AAAAT | 4 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-23217_541-2321 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25663208 | |||||
| chr1:25663641
|
C | T | 5 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 5 | HG01255.hp1 HG02280.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-22799C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25663641 | ||||||
| chr1:25663658
|
A | G | 104 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(101): Show | 104 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.541-22782A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25663658 | ||||||
| chr1:25663746
|
T | C | 1 | a0001c0002t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.541-22694T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25663746 | ||||||
| chr1:25664094
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.541-22346G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25664094 | ||||||
| chr1:25664150
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.541-22290G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25664150 | ||||||
| chr1:25664168
|
T | C | 1 | a0001c0002t0001g0160 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.541-22272T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25664168 | ||||||
| chr1:25664260
|
G | GT | 41 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0069others(38): Show | 41 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.541-22167dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25664260 | |||||
| chr1:25664260
|
G | GTTT | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01255.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-22169_541-2216 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25664260 | |||||
| chr1:25664260
|
GT | G | 43 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0102others(40): Show | 43 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.541-22167delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25664260 | |||||
| chr1:25664333
|
A | G | 3 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155 | 3 | HG02559.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.541-22107A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25664333 | ||||||
| chr1:25664336
|
G | A | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-22104G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25664336 | ||||||
| chr1:25664354
|
G | A | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-22086G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25664354 | ||||||
| chr1:25664583
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.541-21857G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25664583 | ||||||
| chr1:25664628
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.541-21812C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25664628 | ||||||
| chr1:25664865
|
T | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 187 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(184): Show |
intron_variant | MODIFIER | c.541-21575T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25664865 | ||||||
| chr1:25665263
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.541-21177G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25665263 | ||||||
| chr1:25665407
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(71): Show | 75 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.541-21033A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25665407 | ||||||
| chr1:25665669
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.541-20771G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25665669 | ||||||
| chr1:25665855
|
C | CT | 96 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(93): Show | 96 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.541-20563dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25665855 | |||||
| chr1:25665855
|
C | CTT | 53 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(50): Show | 54 | HG00423.hp2 HG00597.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.541-20564_541-2056 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25665855 | |||||
| chr1:25665855
|
C | CTTT | 36 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0029others(33): Show | 36 | HG00621.hp1 HG00741.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.541-20565_541-2056 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25665855 | |||||
| chr1:25665855
|
C | CTTTT | 6 | a0001c0001t0001g0018a0001c0001t0001g0048a0001c0001t0001g0059others(3): Show | 6 | HG00609.hp1 HG01109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-20566_541-2056 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25665855 | |||||
| chr1:25665855
|
C | CTTTTTTT others(6): Show |
1 | a0001c0002t0001g0191 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.541-20575_541-2056 others(17): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25665855 | |||||
| chr1:25666082
|
G | GA | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-20349dupA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25666082 | |||||
| chr1:25666230
|
T | C | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-20210T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666230 | ||||||
| chr1:25666235
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(56): Show | 60 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.541-20205A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666235 | ||||||
| chr1:25666287
|
G | A | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-20153G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666287 | ||||||
| chr1:25666332
|
C | T | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-20108C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666332 | ||||||
| chr1:25666444
|
T | C | 37 | a0001c0001t0001g0022a0001c0001t0001g0069a0001c0001t0001g0070others(34): Show | 37 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.541-19996T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666444 | ||||||
| chr1:25666453
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(69): Show | 73 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.541-19987C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666453 | ||||||
| chr1:25666537
|
G | T | 1 | a0001c0002t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.541-19903G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666537 | ||||||
| chr1:25666571
|
A | T | 1 | a0001c0002t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.541-19869A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666571 | ||||||
| chr1:25666586
|
T | G | 1 | a0001c0002t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.541-19854T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666586 | ||||||
| chr1:25666591
|
T | G | 1 | a0001c0002t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.541-19849T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666591 | ||||||
| chr1:25666603
|
G | T | 1 | a0001c0002t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.541-19837G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666603 | ||||||
| chr1:25666615
|
A | T | 1 | a0001c0002t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.541-19825A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666615 | ||||||
| chr1:25666626
|
C | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 186 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(183): Show |
intron_variant | MODIFIER | c.541-19814C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666626 | ||||||
| chr1:25666704
|
G | A | 1 | a0001c0003t0006g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.541-19736G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666704 | ||||||
| chr1:25666753
|
C | T | 1 | a0001c0002t0008g0227 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.541-19687C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666753 | ||||||
| chr1:25666953
|
G | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 74 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.541-19487G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25666953 | ||||||
| chr1:25666958
|
AG | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 249 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.541-19480delG | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25666958 | |||||
| chr1:25667101
|
A | G | 3 | a0001c0002t0001g0209a0001c0002t0001g0210a0001c0002t0001g0211 | 3 | HG01069.hp1 HG01071.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.541-19339A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25667101 | ||||||
| chr1:25667196
|
C | G | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541-19244C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25667196 | ||||||
| chr1:25667484
|
C | CA | 52 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0038others(49): Show | 52 | HG00621.hp1 HG00639.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.541-18936dupA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25667484 | |||||
| chr1:25667484
|
C | CAA | 66 | a0001c0001t0001g0083a0001c0001t0001g0151a0001c0001t0001g0152others(63): Show | 66 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.541-18937_541-1893 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25667484 | |||||
| chr1:25667484
|
C | CAAA | 12 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(9): Show | 12 | HG01255.hp1 HG02071.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.541-18938_541-1893 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25667484 | |||||
| chr1:25667511
|
C | A | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-18929C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25667511 | ||||||
| chr1:25668156
|
C | T | 1 | a0001c0002t0001g0191 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.541-18284C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25668156 | ||||||
| chr1:25668547
|
T | TTTTC | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 108 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.541-17881_541-1787 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25668547 | |||||
| chr1:25668549
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.541-17891T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25668549 | ||||||
| chr1:25668559
|
C | CTTTCT | 69 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(66): Show | 69 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.541-17878_541-1787 others(9): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25668559 | |||||
| chr1:25668560
|
T | TTTC | 12 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(9): Show | 12 | HG01167.hp1 HG01255.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.541-17878_541-1787 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25668560 | |||||
| chr1:25668563
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.541-17877T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25668563 | ||||||
| chr1:25668564
|
T | C | 3 | a0001c0002t0001g0156a0001c0002t0003g0154a0001c0002t0003g0155 | 3 | HG02559.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.541-17876T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25668564 | ||||||
| chr1:25668584
|
C | G | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-17856C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25668584 | ||||||
| chr1:25668618
|
C | T | 1 | a0001c0002t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.541-17822C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25668618 | ||||||
| chr1:25668802
|
C | G | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-17638C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25668802 | ||||||
| chr1:25668908
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(69): Show | 73 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.541-17532G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25668908 | ||||||
| chr1:25669262
|
C | G | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-17178C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25669262 | ||||||
| chr1:25669445
|
A | G | 114 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0069others(111): Show | 114 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.541-16995A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25669445 | ||||||
| chr1:25669452
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.541-16988T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25669452 | ||||||
| chr1:25669500
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.541-16940C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25669500 | ||||||
| chr1:25669532
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0009g0036 | 3 | NA18942.hp1 NA18990.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.541-16908C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25669532 | ||||||
| chr1:25669604
|
T | A | 19 | a0001c0001t0001g0032a0001c0002t0001g0219a0001c0002t0001g0221others(16): Show | 19 | HG00639.hp1 HG01099.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.541-16836T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25669604 | ||||||
| chr1:25669743
|
G | C | 1 | a0001c0002t0001g0248 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.541-16697G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25669743 | ||||||
| chr1:25669770
|
G | A | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-16670G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25669770 | ||||||
| chr1:25669993
|
A | G | 12 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(9): Show | 12 | HG01167.hp1 HG01255.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.541-16447A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25669993 | ||||||
| chr1:25670012
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.541-16428A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25670012 | ||||||
| chr1:25670499
|
G | A | 12 | a0001c0002t0001g0225a0001c0002t0001g0226a0001c0002t0001g0236others(9): Show | 12 | HG00639.hp1 HG01099.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.541-15941G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25670499 | ||||||
| chr1:25670651
|
T | C | 66 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0125others(63): Show | 66 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.541-15789T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25670651 | ||||||
| chr1:25670728
|
C | G | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-15712C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25670728 | ||||||
| chr1:25671116
|
C | T | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.541-15324C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25671116 | ||||||
| chr1:25671377
|
T | C | 77 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0125others(74): Show | 77 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.541-15063T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25671377 | ||||||
| chr1:25671478
|
A | C | 1 | a0001c0001t0001g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.541-14962A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25671478 | ||||||
| chr1:25671505
|
G | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA19011.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.541-14935G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25671505 | ||||||
| chr1:25671850
|
T | G | 6 | a0001c0001t0001g0083a0001c0002t0001g0248a0001c0002t0002g0179others(3): Show | 6 | NA18964.hp2 NA19011.hp2 NA19060.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-14590T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25671850 | ||||||
| chr1:25671873
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.541-14567G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25671873 | ||||||
| chr1:25671885
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.541-14555G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25671885 | ||||||
| chr1:25672124
|
G | T | 1 | a0001c0002t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.541-14316G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25672124 | ||||||
| chr1:25672217
|
G | A | 1 | a0001c0002t0001g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.541-14223G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25672217 | ||||||
| chr1:25672281
|
A | T | 66 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0125others(63): Show | 66 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.541-14159A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25672281 | ||||||
| chr1:25672412
|
T | A | 40 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(37): Show | 40 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.541-14028T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25672412 | ||||||
| chr1:25672543
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.541-13897G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25672543 | ||||||
| chr1:25672566
|
G | T | 106 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0125others(103): Show | 106 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.541-13874G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25672566 | ||||||
| chr1:25672875
|
C | G | 1 | a0001c0002t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.541-13565C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25672875 | ||||||
| chr1:25673002
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541-13438G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25673002 | ||||||
| chr1:25673026
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(184): Show |
intron_variant | MODIFIER | c.541-13414G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25673026 | ||||||
| chr1:25673201
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.541-13239G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25673201 | ||||||
| chr1:25673249
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0067 | 3 | HG00423.hp2 HG01993.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.541-13191G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25673249 | ||||||
| chr1:25673484
|
TA | T | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-12952delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25673484 | |||||
| chr1:25673684
|
C | T | 1 | a0001c0001t0001g0001 | 2 | NA18945.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.541-12756C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25673684 | ||||||
| chr1:25674216
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.541-12224T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25674216 | ||||||
| chr1:25674355
|
C | T | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-12085C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25674355 | ||||||
| chr1:25674358
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.541-12082A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25674358 | ||||||
| chr1:25674461
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 191 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(188): Show |
intron_variant | MODIFIER | c.541-11979A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25674461 | ||||||
| chr1:25674773
|
T | TG | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 249 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.541-11664dupG | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25674773 | |||||
| chr1:25675446
|
A | G | 67 | a0001c0001t0001g0008a0001c0001t0001g0125a0001c0001t0001g0153others(64): Show | 67 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.541-10994A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25675446 | ||||||
| chr1:25675459
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 249 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.541-10981G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25675459 | ||||||
| chr1:25675554
|
A | T | 71 | a0001c0001t0001g0008a0001c0001t0001g0070a0001c0001t0001g0072others(68): Show | 71 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.541-10886A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25675554 | ||||||
| chr1:25675584
|
C | CG | 18 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(15): Show | 18 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.541-10844dupG | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25675584 | |||||
| chr1:25675584
|
CG | C | 88 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0024others(85): Show | 88 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.541-10844delG | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25675584 | |||||
| chr1:25675589
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.541-10851G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25675589 | ||||||
| chr1:25675590
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.541-10850G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25675590 | ||||||
| chr1:25675590
|
G | C | 1 | a0001c0002t0001g0213 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.541-10850G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25675590 | ||||||
| chr1:25675592
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.541-10848G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25675592 | ||||||
| chr1:25675592
|
G | C | 14 | a0001c0001t0001g0058a0001c0001t0001g0087a0001c0001t0001g0100others(11): Show | 14 | HG01255.hp1 HG02055.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.541-10848G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25675592 | ||||||
| chr1:25675676
|
C | T | 2 | a0001c0001t0001g0081a0001c0002t0001g0212 | 2 | NA18945.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.541-10764C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25675676 | ||||||
| chr1:25675690
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG00642.hp1 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-10750C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25675690 | ||||||
| chr1:25676044
|
C | T | 4 | a0001c0002t0001g0199a0001c0003t0001g0201a0002c0008t0001g0019others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-10396C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25676044 | ||||||
| chr1:25676052
|
C | G | 1 | a0001c0002t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.541-10388C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25676052 | ||||||
| chr1:25676094
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 136 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.541-10346G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25676094 | ||||||
| chr1:25676284
|
G | A | 1 | a0001c0001t0004g0109 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.541-10156G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25676284 | ||||||
| chr1:25676350
|
C | T | 5 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 5 | HG01255.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-10090C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25676350 | ||||||
| chr1:25676351
|
G | A | 2 | a0001c0002t0001g0219a0001c0002t0001g0224 | 2 | NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.541-10089G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25676351 | ||||||
| chr1:25676559
|
T | C | 11 | a0001c0001t0001g0058a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG01255.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.541-9881T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25676559 | ||||||
| chr1:25676610
|
C | T | 44 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0153others(41): Show | 44 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.541-9830C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25676610 | ||||||
| chr1:25676682
|
A | G | 3 | a0001c0001t0001g0018a0001c0004t0001g0016a0001c0004t0001g0062 | 3 | HG02145.hp1 HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.541-9758A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25676682 | ||||||
| chr1:25677087
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02027.hp2 NA19011.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.541-9353G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25677087 | ||||||
| chr1:25677233
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.541-9207C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25677233 | ||||||
| chr1:25677265
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(67): Show | 71 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.541-9175A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25677265 | ||||||
| chr1:25677318
|
A | G | 1 | a0001c0002t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.541-9122A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25677318 | ||||||
| chr1:25677411
|
G | GAC | 41 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0017others(38): Show | 41 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.541-9010_541-9009d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25677411 | |||||
| chr1:25677411
|
G | GACAC | 21 | a0001c0001t0001g0069a0001c0001t0001g0077a0001c0001t0001g0137others(18): Show | 21 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.541-9012_541-9009d others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25677411 | |||||
| chr1:25677411
|
G | GACACAC | 5 | a0001c0001t0001g0152a0001c0002t0001g0234a0001c0002t0001g0235others(2): Show | 5 | HG02280.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-9014_541-9009d others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25677411 | |||||
| chr1:25677531
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0152a0001c0001t0011g0033others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-8909G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25677531 | ||||||
| chr1:25677562
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.541-8878T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25677562 | ||||||
| chr1:25677608
|
C | A | 9 | a0001c0001t0001g0153a0001c0002t0001g0161a0001c0002t0001g0167others(6): Show | 9 | HG01081.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-8832C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25677608 | ||||||
| chr1:25677608
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.541-8832C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25677608 | ||||||
| chr1:25677846
|
C | CT | 17 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0054others(14): Show | 17 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.541-8567dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25677846 | |||||
| chr1:25677846
|
C | CTT | 41 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0032others(38): Show | 42 | HG00597.hp1 HG00609.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.541-8568_541-8567d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25677846 | |||||
| chr1:25677846
|
CT | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0052others(25): Show | 28 | HG01167.hp2 HG01255.hp1 HG01993.hp1 others(25): Show |
intron_variant | MODIFIER | c.541-8567delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25677846 | |||||
| chr1:25677846
|
CTT | C | 19 | a0001c0001t0001g0022a0001c0001t0001g0069a0001c0001t0001g0151others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.541-8568_541-8567d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25677846 | |||||
| chr1:25677990
|
A | G | 36 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0058others(33): Show | 36 | HG01069.hp2 HG01243.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.541-8450A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25677990 | ||||||
| chr1:25678153
|
T | C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.541-8287T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25678153 | ||||||
| chr1:25678155
|
G | C | 2 | a0001c0002t0001g0221a0001c0005t0001g0249 | 2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.541-8285G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25678155 | ||||||
| chr1:25678326
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.541-8114A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25678326 | ||||||
| chr1:25678772
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.541-7668A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25678772 | ||||||
| chr1:25678869
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0010g0075others(1): Show | 4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-7571C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25678869 | ||||||
| chr1:25678937
|
C | T | 1 | a0001c0002t0013g0202 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.541-7503C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25678937 | ||||||
| chr1:25679048
|
CAA | C | 7 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG01167.hp1 HG01255.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-7391_541-7390d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679048 | ||||||
| chr1:25679233
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.541-7207G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679233 | ||||||
| chr1:25679291
|
T | C | 1 | a0001c0001t0001g0006 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.541-7149T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679291 | ||||||
| chr1:25679558
|
TA | T | 68 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0018others(65): Show | 68 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.541-6867delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679558 | |||||
| chr1:25679599
|
A | G | 1 | a0001c0002t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.541-6841A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679599 | ||||||
| chr1:25679644
|
G | A | 3 | a0001c0004t0001g0015a0001c0004t0001g0020a0001c0005t0001g0249 | 3 | HG02055.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.541-6796G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679644 | ||||||
| chr1:25679745
|
T | G | 24 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(21): Show | 24 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.541-6695T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679745 | ||||||
| chr1:25679865
|
C | CT | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(107): Show | 111 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.541-6567dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679865 | |||||
| chr1:25679937
|
C | CA | 19 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0029others(16): Show | 20 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.541-6489dupA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679937 | |||||
| chr1:25679937
|
C | CAA | 39 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0032others(36): Show | 39 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.541-6490_541-6489d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679937 | |||||
| chr1:25679937
|
C | CAAA | 6 | a0001c0001t0001g0078a0001c0002t0002g0180a0001c0003t0001g0239others(3): Show | 6 | HG00639.hp1 HG01099.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-6491_541-6489d others(5): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679937 | |||||
| chr1:25679937
|
C | CAAAA | 5 | a0001c0001t0001g0119a0001c0002t0001g0205a0001c0002t0001g0207others(2): Show | 5 | HG01433.hp1 NA18943.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-6492_541-6489d others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679937 | |||||
| chr1:25679950
|
A | AAAAT | 16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.541-6489_541-6488i others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679950 | |||||
| chr1:25679950
|
AAT | A | 10 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(7): Show | 10 | HG01071.hp1 HG01167.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.541-6462_541-6461d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679950 | |||||
| chr1:25679950
|
AATATAT | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(28): Show | 31 | HG00423.hp1 HG01168.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.541-6466_541-6461d others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679950 | |||||
| chr1:25679950
|
AATATATA others(1): Show |
A | 25 | a0001c0001t0001g0018a0001c0001t0001g0058a0001c0001t0001g0070others(22): Show | 25 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.541-6468_541-6461d others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679950 | |||||
| chr1:25679951
|
A | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0152a0001c0002t0001g0221others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-6489A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679951 | ||||||
| chr1:25679951
|
AT | A | 12 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0061others(9): Show | 12 | HG01070.hp1 HG01109.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.541-6488delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679951 | ||||||
| chr1:25679951
|
ATAT | A | 3 | a0001c0003t0001g0237a0001c0004t0001g0015a0001c0004t0001g0020 | 3 | HG01070.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.541-6488_541-6486d others(5): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679951 | ||||||
| chr1:25679951
|
ATATAT | A | 3 | a0001c0001t0001g0060a0001c0001t0010g0075a0001c0005t0001g0249 | 3 | HG02055.hp2 HG02083.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.541-6488_541-6484d others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679951 | ||||||
| chr1:25679951
|
ATATATAT | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0038others(5): Show | 8 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.541-6488_541-6482d others(9): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679951 | ||||||
| chr1:25679952
|
T | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(112): Show | 116 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.541-6488T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679952 | ||||||
| chr1:25679954
|
T | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(75): Show | 79 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.541-6486T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679954 | ||||||
| chr1:25679955
|
A | T | 1 | a0001c0002t0001g0232 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.541-6485A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679955 | ||||||
| chr1:25679956
|
T | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0029others(26): Show | 30 | HG00609.hp1 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.541-6484T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679956 | ||||||
| chr1:25679957
|
A | T | 1 | a0001c0002t0003g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.541-6483A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679957 | ||||||
| chr1:25679958
|
T | A | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(35): Show | 38 | HG00423.hp1 HG01167.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.541-6482T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679958 | ||||||
| chr1:25679959
|
A | T | 26 | a0001c0001t0001g0018a0001c0001t0001g0058a0001c0001t0001g0070others(23): Show | 26 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.541-6481A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679959 | ||||||
| chr1:25679960
|
T | A | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG00597.hp2 HG01168.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-6480T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679960 | ||||||
| chr1:25679970
|
TATATATA others(3): Show |
T | 6 | a0001c0001t0001g0004a0001c0001t0001g0152a0001c0002t0001g0221others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-6468_541-6459d others(12): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25679970 | |||||
| chr1:25679974
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.541-6466T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679974 | ||||||
| chr1:25679976
|
T | C | 2 | a0001c0001t0001g0022a0003c0007t0001g0148 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.541-6464T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679976 | ||||||
| chr1:25679978
|
T | C | 17 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0029others(14): Show | 17 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.541-6462T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679978 | ||||||
| chr1:25679996
|
T | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0152a0001c0002t0001g0221others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-6444T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679996 | ||||||
| chr1:25680102
|
G | T | 1 | a0001c0001t0005g0108 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.541-6338G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25680102 | ||||||
| chr1:25680205
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0010g0075others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-6235G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25680205 | ||||||
| chr1:25680384
|
C | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(3): Show | 6 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-6056C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25680384 | ||||||
| chr1:25680602
|
G | A | 3 | a0001c0003t0001g0231a0001c0003t0001g0237a0001c0003t0001g0243 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.541-5838G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25680602 | ||||||
| chr1:25680635
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(105): Show | 109 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.541-5805G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25680635 | ||||||
| chr1:25680918
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.541-5522T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25680918 | ||||||
| chr1:25680950
|
G | A | 7 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG01167.hp1 HG01255.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-5490G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25680950 | ||||||
| chr1:25680986
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0152a0001c0002t0001g0221others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-5454C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25680986 | ||||||
| chr1:25681077
|
T | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0023others(61): Show | 64 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.541-5363T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681077 | ||||||
| chr1:25681099
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(105): Show | 109 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.541-5341A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681099 | ||||||
| chr1:25681226
|
CA | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(103): Show | 107 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.541-5200delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25681226 | |||||
| chr1:25681236
|
A | G | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-5204A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681236 | ||||||
| chr1:25681302
|
G | A | 2 | a0001c0002t0001g0156a0001c0002t0001g0196 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.541-5138G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681302 | ||||||
| chr1:25681411
|
A | G | 1 | a0001c0002t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.541-5029A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681411 | ||||||
| chr1:25681673
|
T | C | 41 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(38): Show | 41 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.541-4767T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681673 | ||||||
| chr1:25681681
|
T | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(18): Show | 21 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.541-4759T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681681 | ||||||
| chr1:25681737
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.541-4703C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681737 | ||||||
| chr1:25681738
|
G | A | 1 | a0001c0002t0001g0195 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.541-4702G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681738 | ||||||
| chr1:25681772
|
G | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0065others(2): Show | 5 | HG02135.hp1 NA18946.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-4668G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681772 | ||||||
| chr1:25681954
|
TA | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0029others(50): Show | 53 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.541-4475delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25681954 | |||||
| chr1:25682126
|
A | G | 2 | a0001c0001t0001g0069a0001c0002t0001g0174 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.541-4314A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682126 | ||||||
| chr1:25682168
|
T | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0023others(61): Show | 64 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.541-4272T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682168 | ||||||
| chr1:25682735
|
C | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0058others(32): Show | 35 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.541-3705C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682735 | ||||||
| chr1:25682759
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 246 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.541-3681T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682759 | ||||||
| chr1:25682760
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0022 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.541-3680G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682760 | ||||||
| chr1:25682840
|
C | A | 1 | a0001c0003t0006g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.541-3600C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682840 | ||||||
| chr1:25682866
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.541-3574C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682866 | ||||||
| chr1:25682916
|
T | G | 1 | a0001c0002t0001g0203 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.541-3524T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682916 | ||||||
| chr1:25682942
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0145 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.541-3498G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682942 | ||||||
| chr1:25682968
|
G | A | 13 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-3472G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682968 | ||||||
| chr1:25682973
|
G | C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.541-3467G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25682973 | ||||||
| chr1:25683022
|
A | G | 20 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 20 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.541-3418A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683022 | ||||||
| chr1:25683037
|
C | CA | 7 | a0001c0001t0010g0075a0001c0002t0001g0197a0001c0002t0001g0203others(4): Show | 7 | HG02027.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-3387dupA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25683037 | |||||
| chr1:25683037
|
CA | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0050others(10): Show | 13 | HG00639.hp2 HG01070.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-3387delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 25683037 | |||||
| chr1:25683180
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.541-3260G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683180 | ||||||
| chr1:25683241
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.541-3199T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683241 | ||||||
| chr1:25683351
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0070others(31): Show | 34 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.541-3089G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683351 | ||||||
| chr1:25683359
|
T | A | 1 | a0001c0001t0001g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.541-3081T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683359 | ||||||
| chr1:25683367
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.541-3073G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683367 | ||||||
| chr1:25683395
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0145 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.541-3045C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683395 | ||||||
| chr1:25683416
|
T | C | 2 | a0001c0001t0001g0069a0001c0002t0001g0174 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.541-3024T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683416 | ||||||
| chr1:25683516
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.541-2924C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683516 | ||||||
| chr1:25683693
|
GC | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG00642.hp2 HG00741.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-2746delC | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683693 | ||||||
| chr1:25683720
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.541-2720C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683720 | ||||||
| chr1:25683847
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.541-2593G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25683847 | ||||||
| chr1:25684031
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0145 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.541-2409G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684031 | ||||||
| chr1:25684088
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.541-2352A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684088 | ||||||
| chr1:25684120
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.541-2320C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684120 | ||||||
| chr1:25684282
|
A | T | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541-2158A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684282 | ||||||
| chr1:25684439
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.541-2001G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684439 | ||||||
| chr1:25684612
|
T | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.541-1828T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684612 | ||||||
| chr1:25684633
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.541-1807G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684633 | ||||||
| chr1:25684747
|
C | T | 2 | a0001c0003t0001g0233a0001c0003t0001g0244 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.541-1693C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684747 | ||||||
| chr1:25684827
|
C | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.541-1613C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684827 | ||||||
| chr1:25684828
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.541-1612G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684828 | ||||||
| chr1:25684872
|
C | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.541-1568C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684872 | ||||||
| chr1:25684892
|
A | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0070others(34): Show | 37 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.541-1548A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684892 | ||||||
| chr1:25684965
|
G | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.541-1475G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684965 | ||||||
| chr1:25685099
|
G | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.541-1341G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25685099 | ||||||
| chr1:25685196
|
A | G | 1 | a0004c0006t0001g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.541-1244A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25685196 | ||||||
| chr1:25685199
|
G | A | 1 | a0001c0002t0001g0214 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.541-1241G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25685199 | ||||||
| chr1:25685367
|
C | G | 37 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0072others(34): Show | 37 | HG01069.hp2 HG01243.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.541-1073C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25685367 | ||||||
| chr1:25685400
|
C | T | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541-1040C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25685400 | ||||||
| chr1:25685629
|
G | C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.541-811G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25685629 | ||||||
| chr1:25685664
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0076a0001c0001t0001g0096 | 3 | HG02602.hp2 HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.541-776A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25685664 | ||||||
| chr1:25686026
|
A | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(18): Show | 21 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.541-414A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25686026 | ||||||
| chr1:25686236
|
G | A | 2 | a0001c0001t0001g0047a0003c0007t0001g0148 | 2 | HG02280.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.541-204G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25686236 | ||||||
| chr1:25686268
|
A | C | 1 | a0001c0002t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.541-172A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25686268 | ||||||
| chr1:25686295
|
G | A | 1 | a0001c0002t0001g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.541-145G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25686295 | ||||||
| chr1:25686578
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+42C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25686578 | ||||||
| chr1:25686761
|
T | C | 20 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 20 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.637+225T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25686761 | ||||||
| chr1:25686970
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.637+434A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25686970 | ||||||
| chr1:25686998
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.637+462G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25686998 | ||||||
| chr1:25687437
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0152 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637+901C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25687437 | ||||||
| chr1:25687504
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.637+968A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25687504 | ||||||
| chr1:25687533
|
A | G | 20 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 20 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.637+997A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25687533 | ||||||
| chr1:25687764
|
G | T | 1 | a0001c0002t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.637+1228G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25687764 | ||||||
| chr1:25687789
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.637+1253G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25687789 | ||||||
| chr1:25687795
|
A | G | 5 | a0001c0002t0001g0236a0001c0003t0001g0239a0001c0003t0001g0240others(2): Show | 5 | HG00639.hp1 HG01099.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1259A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25687795 | ||||||
| chr1:25687919
|
C | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0043others(55): Show | 58 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.637+1383C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25687919 | ||||||
| chr1:25688012
|
G | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+1476G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25688012 | ||||||
| chr1:25688062
|
A | T | 1 | a0001c0002t0001g0232 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.637+1526A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25688062 | ||||||
| chr1:25688321
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0022 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637+1785A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25688321 | ||||||
| chr1:25688876
|
T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 241 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.637+2340T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25688876 | ||||||
| chr1:25688887
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0152 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637+2351C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25688887 | ||||||
| chr1:25688945
|
G | A | 5 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0042others(2): Show | 5 | HG00735.hp1 HG01175.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+2409G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25688945 | ||||||
| chr1:25688963
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.637+2427C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25688963 | ||||||
| chr1:25689035
|
G | C | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.637+2499G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689035 | ||||||
| chr1:25689046
|
G | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+2510G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689046 | ||||||
| chr1:25689108
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.637+2572A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689108 | ||||||
| chr1:25689122
|
C | A | 1 | a0001c0002t0001g0162 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.637+2586C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689122 | ||||||
| chr1:25689289
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.637+2753G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689289 | ||||||
| chr1:25689314
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.637+2778G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689314 | ||||||
| chr1:25689346
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.637+2810G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689346 | ||||||
| chr1:25689371
|
G | A | 2 | a0001c0003t0001g0220a0001c0004t0001g0071 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.637+2835G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689371 | ||||||
| chr1:25689436
|
T | C | 27 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0072others(24): Show | 27 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.637+2900T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689436 | ||||||
| chr1:25689513
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.637+2977C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689513 | ||||||
| chr1:25689555
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.637+3019G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689555 | ||||||
| chr1:25689728
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0022 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637+3192T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689728 | ||||||
| chr1:25689729
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(107): Show | 111 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.637+3193C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689729 | ||||||
| chr1:25689775
|
C | T | 2 | a0001c0002t0001g0199a0001c0002t0001g0247 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.637+3239C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689775 | ||||||
| chr1:25689779
|
TG | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+3245delG | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25689779 | |||||
| chr1:25689881
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 8 | HG00597.hp2 HG00621.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+3345C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689881 | ||||||
| chr1:25689887
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.637+3351C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689887 | ||||||
| chr1:25689888
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.637+3352G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689888 | ||||||
| chr1:25690066
|
C | G | 1 | a0001c0001t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.637+3530C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25690066 | ||||||
| chr1:25690262
|
G | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+3726G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25690262 | ||||||
| chr1:25690288
|
C | CT | 43 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0024others(40): Show | 43 | HG00423.hp2 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.637+3774dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25690288 | |||||
| chr1:25690288
|
C | CTT | 5 | a0001c0001t0001g0074a0001c0001t0001g0151a0001c0002t0001g0228others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+3773_637+3774d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25690288 | |||||
| chr1:25690288
|
C | CTTT | 12 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0011g0033others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+3772_637+3774d others(5): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25690288 | |||||
| chr1:25690288
|
C | CTTTT | 9 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+3771_637+3774d others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25690288 | |||||
| chr1:25690718
|
G | A | 1 | a0001c0001t0004g0109 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.637+4182G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25690718 | ||||||
| chr1:25690825
|
G | T | 2 | a0001c0003t0001g0233a0001c0003t0001g0244 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.637+4289G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25690825 | ||||||
| chr1:25690953
|
C | T | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.637+4417C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25690953 | ||||||
| chr1:25691186
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.637+4650A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25691186 | ||||||
| chr1:25691403
|
G | A | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.637+4867G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25691403 | ||||||
| chr1:25691405
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0070others(25): Show | 28 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+4869C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25691405 | ||||||
| chr1:25691567
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637+5031C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25691567 | ||||||
| chr1:25691674
|
C | T | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.637+5138C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25691674 | ||||||
| chr1:25691752
|
T | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(35): Show | 38 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.637+5216T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25691752 | ||||||
| chr1:25691896
|
T | TTGAAAG | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+5362_637+5367d others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25691896 | |||||
| chr1:25692033
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+5497C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25692033 | ||||||
| chr1:25692163
|
C | T | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.637+5627C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25692163 | ||||||
| chr1:25692367
|
T | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+5831T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25692367 | ||||||
| chr1:25693081
|
C | T | 1 | a0001c0002t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.637+6545C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693081 | ||||||
| chr1:25693492
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(111): Show | 115 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.637+6956G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693492 | ||||||
| chr1:25693592
|
C | T | 3 | a0001c0003t0001g0218a0001c0004t0001g0015a0001c0004t0001g0020 | 3 | HG02109.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.637+7056C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693592 | ||||||
| chr1:25693632
|
G | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+7096G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693632 | ||||||
| chr1:25693667
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.637+7131C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693667 | ||||||
| chr1:25693668
|
G | A | 3 | a0001c0001t0001g0151a0001c0002t0001g0228a0001c0002t0001g0230 | 3 | HG02109.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.637+7132G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693668 | ||||||
| chr1:25693821
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.637+7285C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693821 | ||||||
| chr1:25693846
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.637+7310A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693846 | ||||||
| chr1:25693858
|
T | G | 4 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+7322T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693858 | ||||||
| chr1:25693870
|
A | T | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.637+7334A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693870 | ||||||
| chr1:25693918
|
G | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+7382G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693918 | ||||||
| chr1:25693937
|
A | G | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+7401A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693937 | ||||||
| chr1:25693984
|
T | C | 2 | a0001c0002t0001g0199a0001c0002t0001g0247 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.637+7448T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25693984 | ||||||
| chr1:25694017
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.637+7481A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694017 | ||||||
| chr1:25694045
|
T | C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+7509T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694045 | ||||||
| chr1:25694046
|
G | C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+7510G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694046 | ||||||
| chr1:25694122
|
A | G | 1 | a0001c0002t0001g0181 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.637+7586A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694122 | ||||||
| chr1:25694258
|
C | T | 8 | a0001c0003t0001g0231a0001c0003t0001g0233a0001c0003t0001g0237others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+7722C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694258 | ||||||
| chr1:25694293
|
C | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(111): Show | 115 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.637+7757C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694293 | ||||||
| chr1:25694393
|
G | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(37): Show | 40 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.637+7857G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694393 | ||||||
| chr1:25694499
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.637+7963G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694499 | ||||||
| chr1:25694625
|
G | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+8089G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694625 | ||||||
| chr1:25694715
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0093 | 2 | NA18941.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.637+8179G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694715 | ||||||
| chr1:25694809
|
C | T | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196 | 3 | HG02145.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.637+8273C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694809 | ||||||
| chr1:25694909
|
A | C | 2 | a0001c0002t0001g0199a0001c0002t0001g0247 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.637+8373A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694909 | ||||||
| chr1:25694958
|
A | G | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196 | 3 | HG02145.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.637+8422A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25694958 | ||||||
| chr1:25695064
|
T | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0145 | 3 | HG02451.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.637+8528T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25695064 | ||||||
| chr1:25695261
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.637+8725G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25695261 | ||||||
| chr1:25695325
|
G | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(48): Show | 52 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.637+8789G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25695325 | ||||||
| chr1:25695331
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+8795C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25695331 | ||||||
| chr1:25695443
|
G | A | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.637+8907G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25695443 | ||||||
| chr1:25695627
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+9091C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25695627 | ||||||
| chr1:25695825
|
C | T | 15 | a0001c0001t0001g0150a0001c0002t0001g0159a0001c0002t0001g0209others(12): Show | 15 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.637+9289C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25695825 | ||||||
| chr1:25695832
|
G | C | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.637+9296G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25695832 | ||||||
| chr1:25695869
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.637+9333A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25695869 | ||||||
| chr1:25695959
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.637+9423G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25695959 | ||||||
| chr1:25696169
|
G | A | 2 | a0001c0002t0001g0199a0001c0002t0001g0247 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.637+9633G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25696169 | ||||||
| chr1:25696364
|
G | GC | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(41): Show | 45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.637+9828_637+9829i others(3): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25696364 | ||||||
| chr1:25696369
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.637+9833A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25696369 | ||||||
| chr1:25696409
|
AT | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(108): Show | 112 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.637+9883delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25696409 | |||||
| chr1:25696476
|
T | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(111): Show | 115 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.637+9940T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25696476 | ||||||
| chr1:25696586
|
C | T | 23 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(20): Show | 23 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.637+10050C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25696586 | ||||||
| chr1:25696602
|
T | C | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.637+10066T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25696602 | ||||||
| chr1:25696858
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(108): Show | 112 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.637+10322G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25696858 | ||||||
| chr1:25696934
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.637+10398A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25696934 | ||||||
| chr1:25697053
|
T | C | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.637+10517T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25697053 | ||||||
| chr1:25697095
|
G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+10559G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25697095 | ||||||
| chr1:25697617
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637+11081A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25697617 | ||||||
| chr1:25697625
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0022 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637+11089C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25697625 | ||||||
| chr1:25697734
|
T | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(41): Show | 45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.637+11198T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25697734 | ||||||
| chr1:25697747
|
G | A | 4 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+11211G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25697747 | ||||||
| chr1:25698065
|
C | T | 4 | a0001c0002t0001g0221a0001c0003t0001g0220a0001c0003t0001g0246others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+11529C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25698065 | ||||||
| chr1:25698149
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+11613C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25698149 | ||||||
| chr1:25698442
|
A | G | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.637+11906A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25698442 | ||||||
| chr1:25698446
|
G | A | 7 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG01167.hp1 HG01255.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.637+11910G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25698446 | ||||||
| chr1:25698519
|
C | T | 1 | a0001c0002t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.637+11983C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25698519 | ||||||
| chr1:25698546
|
G | C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+12010G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25698546 | ||||||
| chr1:25698587
|
G | A | 3 | a0001c0001t0001g0107a0001c0002t0001g0157a0001c0002t0001g0164 | 3 | HG00609.hp2 NA18985.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.637+12051G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25698587 | ||||||
| chr1:25698949
|
G | GA | 45 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(42): Show | 46 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.637+12428dupA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25698949 | |||||
| chr1:25699071
|
C | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | HG02015.hp2 HG02056.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+12535C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25699071 | ||||||
| chr1:25699126
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(41): Show | 45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.637+12590G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25699126 | ||||||
| chr1:25699301
|
A | C | 1 | a0001c0002t0001g0181 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.637+12765A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25699301 | ||||||
| chr1:25699305
|
TA | T | 9 | a0001c0001t0001g0026a0001c0001t0001g0053a0001c0001t0001g0059others(6): Show | 9 | HG00609.hp1 HG01168.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+12785delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25699305 | |||||
| chr1:25699316
|
A | G | 15 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+12780A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25699316 | ||||||
| chr1:25699319
|
A | G | 27 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(24): Show | 27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.637+12783A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25699319 | ||||||
| chr1:25699325
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(41): Show | 45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.637+12789G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25699325 | ||||||
| chr1:25699753
|
G | C | 2 | a0001c0002t0001g0199a0001c0002t0001g0247 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.637+13217G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25699753 | ||||||
| chr1:25699788
|
C | A | 43 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(40): Show | 43 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.637+13252C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25699788 | ||||||
| chr1:25699815
|
A | C | 41 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(38): Show | 41 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.637+13279A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25699815 | ||||||
| chr1:25699972
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.637+13436A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25699972 | ||||||
| chr1:25700070
|
G | C | 9 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 9 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+13534G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25700070 | ||||||
| chr1:25700255
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0131 | 2 | HG01167.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.637+13719G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25700255 | ||||||
| chr1:25700433
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(111): Show | 115 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.637+13897A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25700433 | ||||||
| chr1:25700521
|
A | C | 1 | a0001c0002t0001g0205 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.637+13985A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25700521 | ||||||
| chr1:25700547
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+14011C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25700547 | ||||||
| chr1:25700573
|
T | G | 2 | a0001c0001t0004g0109a0001c0001t0004g0111 | 2 | HG01070.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.637+14037T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25700573 | ||||||
| chr1:25700689
|
A | G | 2 | a0001c0002t0001g0209a0001c0002t0001g0210 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.637+14153A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25700689 | ||||||
| chr1:25700856
|
A | C | 4 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+14320A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25700856 | ||||||
| chr1:25700869
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.637+14333G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25700869 | ||||||
| chr1:25700967
|
G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(111): Show | 115 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.637+14431G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25700967 | ||||||
| chr1:25701153
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0034 | 2 | HG02015.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.637+14617C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25701153 | ||||||
| chr1:25701275
|
A | G | 1 | a0001c0002t0001g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.637+14739A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25701275 | ||||||
| chr1:25701302
|
A | G | 2 | a0001c0003t0001g0220a0001c0004t0001g0071 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.637+14766A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25701302 | ||||||
| chr1:25701347
|
C | T | 4 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+14811C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25701347 | ||||||
| chr1:25701634
|
T | TG | 4 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+15102dupG | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25701634 | |||||
| chr1:25701805
|
A | G | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196 | 3 | HG02145.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.637+15269A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25701805 | ||||||
| chr1:25701830
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.637+15294C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25701830 | ||||||
| chr1:25701907
|
A | C | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.637+15371A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25701907 | ||||||
| chr1:25702022
|
G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(111): Show | 115 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.637+15486G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25702022 | ||||||
| chr1:25702121
|
A | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(88): Show | 92 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.637+15585A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25702121 | ||||||
| chr1:25702164
|
G | C | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196 | 3 | HG02145.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.637+15628G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25702164 | ||||||
| chr1:25702284
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG00642.hp2 HG00741.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+15748C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25702284 | ||||||
| chr1:25702422
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.637+15886G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25702422 | ||||||
| chr1:25703397
|
G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0047others(39): Show | 43 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.637+16861G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25703397 | ||||||
| chr1:25703439
|
T | G | 1 | a0001c0002t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.637+16903T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25703439 | ||||||
| chr1:25703515
|
C | T | 1 | a0001c0002t0001g0197 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.637+16979C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25703515 | ||||||
| chr1:25703551
|
C | T | 1 | a0001c0002t0001g0165 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.637+17015C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25703551 | ||||||
| chr1:25703744
|
C | T | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.637+17208C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25703744 | ||||||
| chr1:25703927
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 249 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.637+17391T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25703927 | ||||||
| chr1:25704025
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(45): Show | 49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.637+17489G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704025 | ||||||
| chr1:25704122
|
G | A | 8 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG00642.hp2 HG00741.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+17586G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704122 | ||||||
| chr1:25704329
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(41): Show | 45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.637+17793C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704329 | ||||||
| chr1:25704384
|
A | C | 2 | a0001c0004t0001g0016a0001c0004t0001g0062 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.637+17848A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704384 | ||||||
| chr1:25704452
|
AG | A | 5 | a0001c0002t0001g0160a0001c0002t0001g0188a0001c0002t0001g0204others(2): Show | 5 | HG00544.hp2 HG02135.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+17919delG | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25704452 | |||||
| chr1:25704470
|
T | C | 24 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0072others(21): Show | 24 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+17934T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704470 | ||||||
| chr1:25704523
|
G | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG00642.hp2 HG00741.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+17987G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704523 | ||||||
| chr1:25704673
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.637+18137C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704673 | ||||||
| chr1:25704702
|
A | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(112): Show | 116 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.637+18166A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704702 | ||||||
| chr1:25704712
|
G | C | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.637+18176G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704712 | ||||||
| chr1:25704726
|
A | G | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 11 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.637+18190A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704726 | ||||||
| chr1:25704847
|
G | A | 4 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+18311G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704847 | ||||||
| chr1:25704916
|
C | G | 1 | a0001c0002t0001g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.637+18380C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25704916 | ||||||
| chr1:25705388
|
A | G | 15 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+18852A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25705388 | ||||||
| chr1:25705543
|
G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(111): Show | 115 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.637+19007G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25705543 | ||||||
| chr1:25706188
|
C | G | 2 | a0001c0001t0001g0069a0001c0002t0001g0174 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.637+19652C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25706188 | ||||||
| chr1:25706239
|
T | G | 2 | a0001c0001t0005g0108a0001c0001t0005g0139 | 2 | NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.637+19703T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25706239 | ||||||
| chr1:25706764
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.637+20228C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25706764 | ||||||
| chr1:25707631
|
G | C | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.637+21095G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25707631 | ||||||
| chr1:25707683
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.637+21147G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25707683 | ||||||
| chr1:25707712
|
C | G | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.637+21176C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25707712 | ||||||
| chr1:25707894
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.637+21358G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25707894 | ||||||
| chr1:25708000
|
A | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(88): Show | 92 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.637+21464A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25708000 | ||||||
| chr1:25708181
|
T | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(45): Show | 49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.637+21645T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25708181 | ||||||
| chr1:25708651
|
G | A | 23 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(20): Show | 23 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.637+22115G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25708651 | ||||||
| chr1:25708973
|
T | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0145 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.637+22437T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25708973 | ||||||
| chr1:25708974
|
G | A | 4 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+22438G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25708974 | ||||||
| chr1:25708983
|
T | C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+22447T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25708983 | ||||||
| chr1:25709309
|
C | T | 1 | a0001c0002t0003g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.637+22773C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25709309 | ||||||
| chr1:25709662
|
C | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0070others(26): Show | 29 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+23126C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25709662 | ||||||
| chr1:25709675
|
C | A | 1 | a0001c0001t0001g0115 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.637+23139C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25709675 | ||||||
| chr1:25709716
|
C | CTCTA | 15 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 15 | HG00280.hp2 HG00642.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.637+23202_637+2320 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25709716 | |||||
| chr1:25710241
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.637+23705A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25710241 | ||||||
| chr1:25711482
|
C | G | 6 | a0001c0002t0001g0219a0001c0002t0001g0222a0001c0002t0001g0223others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+24946C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25711482 | ||||||
| chr1:25711589
|
G | A | 1 | a0001c0002t0001g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.637+25053G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25711589 | ||||||
| chr1:25711682
|
G | A | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.637+25146G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25711682 | ||||||
| chr1:25711809
|
G | A | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196 | 3 | HG02145.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.637+25273G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25711809 | ||||||
| chr1:25711917
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.637+25381G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25711917 | ||||||
| chr1:25712053
|
A | T | 1 | a0001c0002t0001g0181 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.637+25517A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25712053 | ||||||
| chr1:25712178
|
G | A | 1 | a0001c0002t0001g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.637+25642G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25712178 | ||||||
| chr1:25712191
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.637+25655G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25712191 | ||||||
| chr1:25712208
|
C | T | 44 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 44 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.637+25672C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25712208 | ||||||
| chr1:25712248
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0145 | 3 | HG02451.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.637+25712G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25712248 | ||||||
| chr1:25712299
|
G | A | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196 | 3 | HG02145.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.637+25763G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25712299 | ||||||
| chr1:25712632
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.637+26096A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25712632 | ||||||
| chr1:25712718
|
G | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(127): Show | 131 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.637+26182G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25712718 | ||||||
| chr1:25712943
|
A | C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+26407A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25712943 | ||||||
| chr1:25712946
|
T | C | 1 | a0001c0002t0001g0205 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.637+26410T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25712946 | ||||||
| chr1:25713538
|
A | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(101): Show | 105 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.637+27002A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25713538 | ||||||
| chr1:25713638
|
G | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.637+27102G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25713638 | ||||||
| chr1:25713648
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(98): Show | 102 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.637+27112C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25713648 | ||||||
| chr1:25713828
|
G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+27292G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25713828 | ||||||
| chr1:25713951
|
A | G | 4 | a0001c0002t0001g0221a0001c0003t0001g0220a0001c0003t0001g0246others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+27415A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25713951 | ||||||
| chr1:25714023
|
T | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(101): Show | 105 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.637+27487T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25714023 | ||||||
| chr1:25714146
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.637+27610C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25714146 | ||||||
| chr1:25714471
|
T | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(108): Show | 112 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.637+27935T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25714471 | ||||||
| chr1:25714586
|
TA | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(112): Show | 116 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.637+28059delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25714586 | |||||
| chr1:25714654
|
A | T | 8 | a0001c0003t0001g0231a0001c0003t0001g0233a0001c0003t0001g0237others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+28118A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25714654 | ||||||
| chr1:25714756
|
G | A | 2 | a0001c0004t0001g0016a0001c0004t0001g0062 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.637+28220G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25714756 | ||||||
| chr1:25715701
|
C | T | 10 | a0001c0001t0001g0150a0001c0002t0001g0159a0001c0002t0001g0209others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+29165C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25715701 | ||||||
| chr1:25716001
|
G | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0070others(26): Show | 29 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+29465G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25716001 | ||||||
| chr1:25716170
|
G | A | 5 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+29634G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25716170 | ||||||
| chr1:25716191
|
C | T | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.637+29655C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25716191 | ||||||
| chr1:25717016
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.638-29652C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25717016 | ||||||
| chr1:25717029
|
G | A | 1 | a0001c0002t0001g0173 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.638-29639G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25717029 | ||||||
| chr1:25717070
|
T | C | 1 | a0001c0002t0001g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.638-29598T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25717070 | ||||||
| chr1:25717575
|
C | CT | 12 | a0001c0001t0001g0081a0001c0001t0001g0099a0001c0001t0001g0144others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.638-29076dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25717575 | |||||
| chr1:25717615
|
G | C | 1 | a0001c0002t0001g0158 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.638-29053G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25717615 | ||||||
| chr1:25717639
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(107): Show | 111 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.638-29029A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25717639 | ||||||
| chr1:25717694
|
T | C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-28974T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25717694 | ||||||
| chr1:25717778
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(107): Show | 111 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.638-28890A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25717778 | ||||||
| chr1:25717860
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.638-28808G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25717860 | ||||||
| chr1:25717999
|
T | TACAC | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(88): Show | 92 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.638-28645_638-2864 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25717999 | |||||
| chr1:25717999
|
T | TACACAC | 20 | a0001c0001t0001g0069a0001c0001t0001g0119a0001c0001t0001g0144others(17): Show | 20 | HG01167.hp1 HG01255.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.638-28647_638-2864 others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25717999 | |||||
| chr1:25717999
|
T | TACACACA others(3): Show |
3 | a0001c0001t0001g0143a0001c0002t0001g0176a0001c0002t0001g0221 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.638-28651_638-2864 others(14): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25717999 | |||||
| chr1:25718025
|
CAT | C | 9 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0045others(6): Show | 9 | HG00621.hp2 HG02135.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.638-28641_638-2864 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25718025 | |||||
| chr1:25718174
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.638-28494G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25718174 | ||||||
| chr1:25718188
|
C | T | 25 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0072others(22): Show | 25 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.638-28480C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25718188 | ||||||
| chr1:25718302
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0084a0001c0001t0001g0091others(1): Show | 4 | HG00544.hp1 HG02074.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-28366C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25718302 | ||||||
| chr1:25718483
|
T | C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-28185T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25718483 | ||||||
| chr1:25718599
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-28069C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25718599 | ||||||
| chr1:25718760
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(68): Show | 72 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.638-27908G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25718760 | ||||||
| chr1:25719051
|
C | CTTA | 108 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(105): Show | 109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.638-27581_638-2757 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719051 | |||||
| chr1:25719051
|
C | CTTATTA | 2 | a0001c0001t0001g0125a0001c0002t0001g0181 | 2 | HG02572.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.638-27584_638-2757 others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719051 | |||||
| chr1:25719051
|
C | CTTATTAT others(2): Show |
2 | a0001c0001t0001g0041a0001c0002t0001g0188 | 2 | HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.638-27587_638-2757 others(13): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719051 | |||||
| chr1:25719051
|
CTTA | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0115others(4): Show | 7 | HG02074.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.638-27581_638-2757 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719051 | |||||
| chr1:25719051
|
CTTATTAT others(8): Show |
C | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-27593_638-2757 others(19): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719051 | |||||
| chr1:25719172
|
A | T | 24 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0072others(21): Show | 24 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.638-27496A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25719172 | ||||||
| chr1:25719316
|
G | A | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.638-27352G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25719316 | ||||||
| chr1:25719320
|
G | A | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.638-27348G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25719320 | ||||||
| chr1:25719365
|
G | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-27303G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25719365 | ||||||
| chr1:25719395
|
T | A | 1 | a0001c0003t0001g0201 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.638-27273T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25719395 | ||||||
| chr1:25719395
|
T | TTTTA | 4 | a0001c0001t0001g0050a0001c0001t0001g0079a0001c0001t0001g0137others(1): Show | 4 | HG02683.hp2 HG03486.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-27226_638-2722 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719395 | |||||
| chr1:25719395
|
TTTTA | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(80): Show | 84 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.638-27226_638-2722 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719395 | |||||
| chr1:25719395
|
TTTTATTT others(1): Show |
T | 25 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(22): Show | 25 | HG00642.hp2 HG00741.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.638-27230_638-2722 others(12): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719395 | |||||
| chr1:25719395
|
TTTTATTT others(5): Show |
T | 2 | a0001c0001t0010g0075a0001c0002t0003g0155 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.638-27234_638-2722 others(16): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719395 | |||||
| chr1:25719395
|
TTTTATTT others(9): Show |
T | 27 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0070others(24): Show | 27 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.638-27238_638-2722 others(20): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719395 | |||||
| chr1:25719395
|
TTTTATTT others(13): Show |
T | 4 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-27242_638-2722 others(24): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25719395 | |||||
| chr1:25719586
|
G | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-27082G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25719586 | ||||||
| chr1:25719664
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(71): Show | 75 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.638-27004G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25719664 | ||||||
| chr1:25719861
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.638-26807G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25719861 | ||||||
| chr1:25719876
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01255.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-26792C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25719876 | ||||||
| chr1:25720081
|
G | T | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.638-26587G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25720081 | ||||||
| chr1:25720205
|
C | CT | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(71): Show | 75 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.638-26452dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25720205 | |||||
| chr1:25720443
|
T | G | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-26225T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25720443 | ||||||
| chr1:25720463
|
G | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0070others(26): Show | 29 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.638-26205G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25720463 | ||||||
| chr1:25720727
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-25941C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25720727 | ||||||
| chr1:25720758
|
A | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG00642.hp1 HG01099.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-25910A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25720758 | ||||||
| chr1:25720935
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-25733C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25720935 | ||||||
| chr1:25720936
|
C | T | 15 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.638-25732C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25720936 | ||||||
| chr1:25721481
|
A | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(71): Show | 75 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.638-25187A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25721481 | ||||||
| chr1:25721562
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-25106C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25721562 | ||||||
| chr1:25721717
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01255.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-24951C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25721717 | ||||||
| chr1:25722122
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(71): Show | 75 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.638-24546C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25722122 | ||||||
| chr1:25722846
|
C | A | 5 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-23822C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25722846 | ||||||
| chr1:25723272
|
A | G | 1 | a0001c0002t0001g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638-23396A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25723272 | ||||||
| chr1:25723347
|
A | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(41): Show | 45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.638-23321A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25723347 | ||||||
| chr1:25723854
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.638-22814G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25723854 | ||||||
| chr1:25724026
|
C | CT | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(11): Show | 14 | HG02074.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.638-22623dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25724026 | |||||
| chr1:25724097
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(69): Show | 73 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.638-22571C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25724097 | ||||||
| chr1:25724098
|
G | A | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.638-22570G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25724098 | ||||||
| chr1:25724114
|
C | T | 1 | a0001c0002t0001g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.638-22554C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25724114 | ||||||
| chr1:25724178
|
G | A | 1 | a0001c0002t0001g0174 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.638-22490G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25724178 | ||||||
| chr1:25724522
|
T | C | 2 | a0001c0003t0001g0220a0001c0004t0001g0071 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.638-22146T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25724522 | ||||||
| chr1:25724587
|
C | T | 2 | a0001c0005t0001g0193a0001c0005t0001g0229 | 2 | HG00639.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.638-22081C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25724587 | ||||||
| chr1:25724933
|
C | T | 4 | a0001c0002t0001g0221a0001c0003t0001g0220a0001c0003t0001g0246others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-21735C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25724933 | ||||||
| chr1:25724960
|
C | G | 2 | a0001c0003t0001g0233a0001c0003t0001g0244 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.638-21708C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25724960 | ||||||
| chr1:25725032
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(102): Show | 106 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.638-21636A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25725032 | ||||||
| chr1:25725333
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.638-21335G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25725333 | ||||||
| chr1:25725785
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.638-20883C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25725785 | ||||||
| chr1:25725789
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.638-20879G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25725789 | ||||||
| chr1:25725905
|
C | T | 2 | a0001c0004t0001g0015a0001c0004t0001g0020 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.638-20763C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25725905 | ||||||
| chr1:25725950
|
G | C | 18 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0073others(15): Show | 18 | HG01069.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.638-20718G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25725950 | ||||||
| chr1:25726007
|
C | A | 1 | a0001c0002t0002g0194 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.638-20661C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25726007 | ||||||
| chr1:25726079
|
C | T | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.638-20589C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25726079 | ||||||
| chr1:25726271
|
G | A | 9 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0221others(6): Show | 9 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-20397G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25726271 | ||||||
| chr1:25726285
|
C | T | 42 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0043others(39): Show | 42 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.638-20383C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25726285 | ||||||
| chr1:25726691
|
C | A | 8 | a0001c0001t0001g0153a0001c0002t0001g0161a0001c0002t0001g0162others(5): Show | 8 | HG00738.hp2 HG01081.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-19977C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25726691 | ||||||
| chr1:25726893
|
T | TA | 9 | a0001c0001t0001g0050a0001c0001t0001g0120a0001c0002t0001g0206others(6): Show | 9 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-19758dupA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25726893 | |||||
| chr1:25726893
|
T | TAA | 9 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-19759_638-1975 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25726893 | |||||
| chr1:25726893
|
T | TAAAAAA | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02258.hp2 HG02717.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.638-19763_638-1975 others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25726893 | |||||
| chr1:25726893
|
TA | T | 16 | a0001c0001t0001g0150a0001c0002t0001g0159a0001c0002t0001g0209others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.638-19758delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25726893 | |||||
| chr1:25727012
|
G | A | 2 | a0001c0004t0001g0016a0001c0004t0001g0062 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.638-19656G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727012 | ||||||
| chr1:25727020
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.638-19648G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727020 | ||||||
| chr1:25727032
|
G | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-19636G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727032 | ||||||
| chr1:25727165
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.638-19503G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727165 | ||||||
| chr1:25727221
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(9): Show | 12 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.638-19447G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727221 | ||||||
| chr1:25727397
|
G | A | 1 | a0001c0004t0001g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.638-19271G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727397 | ||||||
| chr1:25727437
|
G | A | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.638-19231G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727437 | ||||||
| chr1:25727467
|
C | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 42 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.638-19201C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727467 | ||||||
| chr1:25727506
|
C | G | 41 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0043others(38): Show | 41 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.638-19162C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727506 | ||||||
| chr1:25727669
|
C | A | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-18999C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727669 | ||||||
| chr1:25727701
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.638-18967C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727701 | ||||||
| chr1:25727867
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.638-18801G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25727867 | ||||||
| chr1:25728149
|
C | G | 9 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0221others(6): Show | 9 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-18519C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25728149 | ||||||
| chr1:25728205
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.638-18463G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25728205 | ||||||
| chr1:25728231
|
G | T | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.638-18437G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25728231 | ||||||
| chr1:25728356
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.638-18312A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25728356 | ||||||
| chr1:25728363
|
T | C | 3 | a0001c0001t0001g0120a0001c0002t0001g0234a0001c0002t0001g0235 | 3 | HG02486.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.638-18305T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25728363 | ||||||
| chr1:25728565
|
G | A | 1 | a0001c0001t0011g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.638-18103G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25728565 | ||||||
| chr1:25728568
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-18100A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25728568 | ||||||
| chr1:25728863
|
C | G | 2 | a0001c0003t0001g0220a0001c0004t0001g0071 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.638-17805C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25728863 | ||||||
| chr1:25729010
|
C | G | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196 | 3 | HG02145.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.638-17658C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25729010 | ||||||
| chr1:25729140
|
G | A | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.638-17528G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25729140 | ||||||
| chr1:25729202
|
C | G | 3 | a0001c0002t0001g0170a0001c0002t0001g0197a0001c0002t0001g0203 | 3 | HG02027.hp1 NA18612.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.638-17466C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25729202 | ||||||
| chr1:25729215
|
C | G | 1 | a0001c0002t0001g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638-17453C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25729215 | ||||||
| chr1:25729308
|
A | T | 41 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0043others(38): Show | 41 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.638-17360A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25729308 | ||||||
| chr1:25729430
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.638-17238A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25729430 | ||||||
| chr1:25729477
|
C | CT | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 18 | HG01255.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.638-17177dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25729477 | |||||
| chr1:25729800
|
G | A | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-16868G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25729800 | ||||||
| chr1:25730023
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.638-16645T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25730023 | ||||||
| chr1:25730356
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.638-16312A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25730356 | ||||||
| chr1:25730402
|
AT | A | 43 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0043others(40): Show | 43 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.638-16251delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25730402 | |||||
| chr1:25730435
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.638-16233T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25730435 | ||||||
| chr1:25730519
|
C | T | 3 | a0001c0002t0001g0170a0001c0002t0001g0197a0001c0002t0001g0203 | 3 | HG02027.hp1 NA18612.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.638-16149C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25730519 | ||||||
| chr1:25730549
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0032others(42): Show | 46 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.638-16119C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25730549 | ||||||
| chr1:25730568
|
G | A | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.638-16100G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25730568 | ||||||
| chr1:25730818
|
T | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(113): Show | 117 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.638-15850T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25730818 | ||||||
| chr1:25730925
|
A | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0149 | 2 | HG00280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.638-15743A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25730925 | ||||||
| chr1:25730973
|
A | G | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG02258.hp2 HG02451.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.638-15695A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25730973 | ||||||
| chr1:25731275
|
A | C | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.638-15393A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25731275 | ||||||
| chr1:25731336
|
G | GTCA | 22 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(19): Show | 22 | HG01255.hp1 HG02145.hp1 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.638-15298_638-1529 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25731336 | |||||
| chr1:25731336
|
G | GTCATCA | 4 | a0001c0001t0001g0150a0001c0003t0001g0201a0002c0008t0001g0019others(1): Show | 4 | HG01891.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-15301_638-1529 others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25731336 | |||||
| chr1:25731336
|
GTCA | G | 40 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(37): Show | 40 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.638-15298_638-1529 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25731336 | |||||
| chr1:25731336
|
GTCATCAT others(2): Show |
G | 3 | a0001c0002t0001g0219a0001c0002t0001g0225a0001c0004t0001g0142 | 3 | HG02572.hp2 HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.638-15304_638-1529 others(13): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25731336 | |||||
| chr1:25731846
|
T | A | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.638-14822T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25731846 | ||||||
| chr1:25731860
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG01255.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-14808C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25731860 | ||||||
| chr1:25732122
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-14546G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25732122 | ||||||
| chr1:25732282
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-14386C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25732282 | ||||||
| chr1:25732429
|
C | T | 3 | a0001c0003t0001g0201a0002c0008t0001g0019a0002c0009t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638-14239C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25732429 | ||||||
| chr1:25732471
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.638-14197G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25732471 | ||||||
| chr1:25732477
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.638-14191T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25732477 | ||||||
| chr1:25732567
|
G | A | 5 | a0001c0003t0001g0231a0001c0003t0001g0233a0001c0003t0001g0237others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-14101G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25732567 | ||||||
| chr1:25732632
|
A | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-14036A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25732632 | ||||||
| chr1:25733158
|
G | C | 40 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0043others(37): Show | 40 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.638-13510G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733158 | ||||||
| chr1:25733159
|
C | T | 40 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0043others(37): Show | 40 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.638-13509C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733159 | ||||||
| chr1:25733188
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.638-13480C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733188 | ||||||
| chr1:25733206
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0145 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.638-13462G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733206 | ||||||
| chr1:25733539
|
C | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(7): Show | 10 | HG01255.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-13129C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733539 | ||||||
| chr1:25733610
|
T | C | 27 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(24): Show | 27 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.638-13058T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733610 | ||||||
| chr1:25733663
|
G | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 11 | HG02258.hp2 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.638-13005G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733663 | ||||||
| chr1:25733807
|
TA | T | 9 | a0001c0002t0001g0221a0001c0003t0001g0231a0001c0003t0001g0233others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-12860delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733807 | ||||||
| chr1:25733808
|
A | T | 2 | a0001c0003t0001g0220a0001c0004t0001g0071 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.638-12860A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733808 | ||||||
| chr1:25733991
|
G | A | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.638-12677G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733991 | ||||||
| chr1:25734001
|
G | A | 4 | a0001c0002t0001g0221a0001c0003t0001g0220a0001c0003t0001g0246others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-12667G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734001 | ||||||
| chr1:25734020
|
T | C | 1 | a0001c0002t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.638-12648T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734020 | ||||||
| chr1:25734153
|
G | C | 2 | a0001c0002t0001g0199a0001c0002t0001g0247 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.638-12515G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734153 | ||||||
| chr1:25734193
|
A | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-12475A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734193 | ||||||
| chr1:25734198
|
G | A | 21 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0221others(18): Show | 21 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.638-12470G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734198 | ||||||
| chr1:25734245
|
C | T | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196 | 3 | HG02145.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.638-12423C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734245 | ||||||
| chr1:25734294
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(127): Show | 131 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.638-12374G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734294 | ||||||
| chr1:25734436
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.638-12232A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734436 | ||||||
| chr1:25734629
|
A | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-12039A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734629 | ||||||
| chr1:25734775
|
C | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(23): Show | 26 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-11893C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734775 | ||||||
| chr1:25734832
|
A | G | 3 | a0001c0003t0001g0218a0001c0004t0001g0015a0001c0004t0001g0020 | 3 | HG02109.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.638-11836A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734832 | ||||||
| chr1:25734953
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.638-11715C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25734953 | ||||||
| chr1:25735130
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.638-11538C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25735130 | ||||||
| chr1:25735174
|
G | A | 16 | a0001c0002t0001g0221a0001c0002t0001g0236a0001c0003t0001g0220others(13): Show | 16 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.638-11494G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25735174 | ||||||
| chr1:25735235
|
T | C | 3 | a0001c0001t0001g0110a0001c0001t0001g0122a0001c0001t0001g0131 | 3 | HG01167.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.638-11433T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25735235 | ||||||
| chr1:25735238
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.638-11430C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25735238 | ||||||
| chr1:25735405
|
C | T | 2 | a0001c0001t0001g0119a0001c0002t0001g0198 | 2 | HG00597.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.638-11263C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25735405 | ||||||
| chr1:25735460
|
G | T | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.638-11208G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25735460 | ||||||
| chr1:25735516
|
A | G | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.638-11152A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25735516 | ||||||
| chr1:25735651
|
A | C | 1 | a0001c0002t0001g0200 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.638-11017A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25735651 | ||||||
| chr1:25735727
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0061others(2): Show | 5 | HG00735.hp1 HG01109.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-10941C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25735727 | ||||||
| chr1:25735958
|
G | A | 2 | a0001c0002t0001g0175a0001c0002t0001g0208 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.638-10710G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25735958 | ||||||
| chr1:25736122
|
G | A | 12 | a0001c0002t0001g0236a0001c0003t0001g0231a0001c0003t0001g0233others(9): Show | 12 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.638-10546G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736122 | ||||||
| chr1:25736145
|
C | G | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196 | 3 | HG02145.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.638-10523C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736145 | ||||||
| chr1:25736155
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0032others(42): Show | 46 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.638-10513T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736155 | ||||||
| chr1:25736165
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(119): Show | 123 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.638-10503G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736165 | ||||||
| chr1:25736548
|
G | A | 10 | a0001c0001t0001g0069a0001c0001t0001g0150a0001c0002t0001g0174others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-10120G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736548 | ||||||
| chr1:25736552
|
G | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(23): Show | 26 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-10116G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736552 | ||||||
| chr1:25736565
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(3): Show | 6 | HG00642.hp2 HG00741.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-10103C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736565 | ||||||
| chr1:25736676
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-9992G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736676 | ||||||
| chr1:25736792
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-9876G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736792 | ||||||
| chr1:25736823
|
C | T | 2 | a0001c0003t0001g0220a0001c0004t0001g0071 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.638-9845C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736823 | ||||||
| chr1:25736939
|
C | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0046others(3): Show | 6 | HG02135.hp1 NA18946.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-9729C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736939 | ||||||
| chr1:25737039
|
G | A | 30 | a0001c0001t0001g0004a0001c0001t0001g0120a0001c0001t0001g0143others(27): Show | 30 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.638-9629G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737039 | ||||||
| chr1:25737145
|
C | T | 1 | a0001c0002t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.638-9523C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737145 | ||||||
| chr1:25737291
|
A | G | 28 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.638-9377A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737291 | ||||||
| chr1:25737326
|
G | A | 2 | a0001c0002t0001g0158a0001c0002t0001g0178 | 2 | HG00621.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.638-9342G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737326 | ||||||
| chr1:25737360
|
T | G | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.638-9308T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737360 | ||||||
| chr1:25737400
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.638-9268G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737400 | ||||||
| chr1:25737405
|
C | T | 2 | a0001c0002t0001g0199a0001c0002t0001g0247 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.638-9263C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737405 | ||||||
| chr1:25737409
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG01255.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-9259A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737409 | ||||||
| chr1:25737505
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.638-9163C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737505 | ||||||
| chr1:25737506
|
T | C | 1 | a0001c0002t0001g0183 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.638-9162T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737506 | ||||||
| chr1:25737546
|
A | G | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.638-9122A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737546 | ||||||
| chr1:25737668
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG01255.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-9000G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737668 | ||||||
| chr1:25737789
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0032others(42): Show | 46 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.638-8879C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737789 | ||||||
| chr1:25737869
|
G | A | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0002t0001g0196 | 3 | HG02145.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.638-8799G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737869 | ||||||
| chr1:25737965
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.638-8703G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25737965 | ||||||
| chr1:25738108
|
T | TCTA | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-8559_638-8557d others(5): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25738108 | |||||
| chr1:25738453
|
C | T | 2 | a0001c0004t0001g0141a0001c0005t0001g0249 | 2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.638-8215C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25738453 | ||||||
| chr1:25738643
|
T | C | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.638-8025T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25738643 | ||||||
| chr1:25738659
|
A | G | 21 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0221others(18): Show | 21 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.638-8009A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25738659 | ||||||
| chr1:25738795
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(124): Show | 128 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.638-7873G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25738795 | ||||||
| chr1:25739228
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG01255.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-7440A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25739228 | ||||||
| chr1:25739563
|
A | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0120a0001c0001t0001g0143others(27): Show | 30 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.638-7105A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25739563 | ||||||
| chr1:25739644
|
T | C | 2 | a0001c0002t0001g0215a0001c0002t0001g0248 | 2 | NA19060.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.638-7024T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25739644 | ||||||
| chr1:25739932
|
G | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-6736G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25739932 | ||||||
| chr1:25740000
|
C | T | 26 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(23): Show | 26 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-6668C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740000 | ||||||
| chr1:25740023
|
G | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-6645G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740023 | ||||||
| chr1:25740419
|
TTTGTTGT others(2): Show |
T | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-6232_638-6224d others(11): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25740419 | |||||
| chr1:25740422
|
G | T | 2 | a0001c0002t0001g0199a0001c0002t0001g0247 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.638-6246G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740422 | ||||||
| chr1:25740442
|
T | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-6226T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740442 | ||||||
| chr1:25740522
|
C | T | 26 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(23): Show | 26 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-6146C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740522 | ||||||
| chr1:25740597
|
C | T | 1 | a0001c0002t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.638-6071C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740597 | ||||||
| chr1:25740598
|
G | A | 28 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.638-6070G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740598 | ||||||
| chr1:25740627
|
G | A | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.638-6041G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740627 | ||||||
| chr1:25740726
|
G | A | 30 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(27): Show | 30 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.638-5942G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740726 | ||||||
| chr1:25740772
|
G | T | 1 | a0001c0002t0001g0212 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.638-5896G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740772 | ||||||
| chr1:25740794
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.638-5874G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740794 | ||||||
| chr1:25740831
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0029 | 2 | HG00741.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.638-5837C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740831 | ||||||
| chr1:25740834
|
G | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0150others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.638-5834G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740834 | ||||||
| chr1:25740912
|
G | A | 4 | a0001c0001t0001g0151a0001c0002t0001g0163a0001c0002t0001g0228others(1): Show | 4 | HG01069.hp2 HG02109.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-5756G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740912 | ||||||
| chr1:25740937
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.638-5731C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740937 | ||||||
| chr1:25740970
|
G | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(23): Show | 26 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-5698G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25740970 | ||||||
| chr1:25741058
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.638-5610C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25741058 | ||||||
| chr1:25741139
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.638-5529G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25741139 | ||||||
| chr1:25741330
|
G | A | 30 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(27): Show | 30 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.638-5338G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25741330 | ||||||
| chr1:25741396
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0032others(44): Show | 48 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.638-5272A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25741396 | ||||||
| chr1:25741572
|
C | T | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.638-5096C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25741572 | ||||||
| chr1:25741583
|
T | G | 2 | a0001c0003t0001g0220a0001c0004t0001g0071 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.638-5085T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25741583 | ||||||
| chr1:25741620
|
A | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-5048A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25741620 | ||||||
| chr1:25741718
|
C | T | 1 | a0001c0002t0001g0172 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.638-4950C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25741718 | ||||||
| chr1:25742099
|
C | A | 1 | a0001c0002t0001g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638-4569C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25742099 | ||||||
| chr1:25742272
|
T | C | 2 | a0001c0003t0001g0201a0002c0008t0001g0019 | 2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.638-4396T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25742272 | ||||||
| chr1:25742372
|
C | A | 2 | a0001c0002t0001g0199a0001c0002t0001g0247 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.638-4296C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25742372 | ||||||
| chr1:25742424
|
G | A | 2 | a0001c0002t0001g0234a0001c0002t0001g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.638-4244G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25742424 | ||||||
| chr1:25742477
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.638-4191C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25742477 | ||||||
| chr1:25742505
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0047others(40): Show | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.638-4163C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25742505 | ||||||
| chr1:25742573
|
C | T | 1 | a0001c0002t0003g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.638-4095C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25742573 | ||||||
| chr1:25742582
|
C | A | 10 | a0001c0001t0001g0069a0001c0001t0001g0150a0001c0002t0001g0174others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-4086C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25742582 | ||||||
| chr1:25742731
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.638-3937G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25742731 | ||||||
| chr1:25742924
|
G | A | 49 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(46): Show | 49 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.638-3744G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25742924 | ||||||
| chr1:25743016
|
A | G | 40 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0043others(37): Show | 40 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.638-3652A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25743016 | ||||||
| chr1:25743417
|
C | T | 2 | a0001c0003t0001g0201a0002c0008t0001g0019 | 2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.638-3251C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25743417 | ||||||
| chr1:25743693
|
G | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(23): Show | 26 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-2975G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25743693 | ||||||
| chr1:25743709
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.638-2959C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25743709 | ||||||
| chr1:25744076
|
C | A | 2 | a0001c0001t0001g0001a0001c0001t0009g0036 | 3 | NA18945.hp2 NA18983.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.638-2592C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25744076 | ||||||
| chr1:25744163
|
G | A | 11 | a0001c0002t0001g0236a0001c0003t0001g0231a0001c0003t0001g0233others(8): Show | 11 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.638-2505G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25744163 | ||||||
| chr1:25744239
|
C | G | 40 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0043others(37): Show | 40 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.638-2429C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25744239 | ||||||
| chr1:25744320
|
C | T | 4 | a0001c0001t0001g0087a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | NA18960.hp2 NA18970.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-2348C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25744320 | ||||||
| chr1:25744418
|
C | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0023others(56): Show | 59 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.638-2250C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25744418 | ||||||
| chr1:25744766
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.638-1902G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25744766 | ||||||
| chr1:25744767
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.638-1901C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25744767 | ||||||
| chr1:25744806
|
A | G | 4 | a0001c0003t0001g0220a0001c0003t0001g0246a0001c0004t0001g0071others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-1862A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25744806 | ||||||
| chr1:25744812
|
C | T | 1 | a0001c0002t0001g0158 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.638-1856C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25744812 | ||||||
| chr1:25744925
|
G | A | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.638-1743G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25744925 | ||||||
| chr1:25745113
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.638-1555G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25745113 | ||||||
| chr1:25745249
|
C | T | 10 | a0001c0001t0001g0069a0001c0001t0001g0150a0001c0002t0001g0174others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-1419C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25745249 | ||||||
| chr1:25745283
|
G | A | 1 | a0001c0003t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.638-1385G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25745283 | ||||||
| chr1:25745335
|
CTT | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(144): Show | 148 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.638-1322_638-1321d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25745335 | |||||
| chr1:25745348
|
A | G | 1 | a0002c0009t0001g0021 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.638-1320A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25745348 | ||||||
| chr1:25745511
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.638-1157A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25745511 | ||||||
| chr1:25745565
|
G | A | 1 | a0001c0001t0007g0095 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.638-1103G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25745565 | ||||||
| chr1:25745612
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG02258.hp2 HG02486.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.638-1056C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25745612 | ||||||
| chr1:25746001
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.638-667A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25746001 | ||||||
| chr1:25746043
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG02258.hp2 HG02486.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.638-625C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25746043 | ||||||
| chr1:25746064
|
G | A | 2 | a0001c0002t0001g0175a0001c0002t0001g0208 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.638-604G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25746064 | ||||||
| chr1:25746166
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0122a0001c0001t0001g0131 | 3 | HG01167.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.638-502G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25746166 | ||||||
| chr1:25746306
|
A | AAAAC | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG02258.hp2 HG02486.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.638-350_638-347dup others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25746306 | |||||
| chr1:25746435
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.638-233G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25746435 | ||||||
| chr1:25746451
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG02258.hp2 HG02486.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.638-217G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25746451 | ||||||
| chr1:25746560
|
C | T | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-108C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25746560 | ||||||
| chr1:25746621
|
A | G | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.638-47A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25746621 | ||||||
| chr1:25746909
|
A | G | 1 | a0002c0009t0001g0021 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.753+126A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25746909 | ||||||
| chr1:25746911
|
T | A | 1 | a0001c0001t0001g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.753+128T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25746911 | ||||||
| chr1:25746952
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 238 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.753+169T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25746952 | ||||||
| chr1:25747023
|
C | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.753+240C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25747023 | ||||||
| chr1:25747033
|
T | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0032others(42): Show | 46 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.753+250T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25747033 | ||||||
| chr1:25747226
|
G | A | 28 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.753+443G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25747226 | ||||||
| chr1:25747238
|
C | T | 28 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.753+455C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25747238 | ||||||
| chr1:25747546
|
C | T | 28 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.753+763C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25747546 | ||||||
| chr1:25747593
|
A | C | 4 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG01255.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+810A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25747593 | ||||||
| chr1:25747889
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.753+1106T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25747889 | ||||||
| chr1:25747916
|
AT | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 7 | HG01255.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+1134delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25747916 | ||||||
| chr1:25748013
|
C | T | 1 | a0001c0002t0001g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.753+1230C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25748013 | ||||||
| chr1:25748075
|
G | C | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754-1180G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25748075 | ||||||
| chr1:25748093
|
G | GT | 7 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 7 | HG01255.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.754-1161dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 25748093 | |||||
| chr1:25748149
|
T | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA19011.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.754-1106T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25748149 | ||||||
| chr1:25748449
|
T | A | 2 | a0001c0003t0006g0216a0001c0004t0001g0141 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.754-806T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25748449 | ||||||
| chr1:25748450
|
G | A | 1 | a0001c0002t0001g0232 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.754-805G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25748450 | ||||||
| chr1:25748472
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(45): Show | 49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.754-783C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25748472 | ||||||
| chr1:25748886
|
A | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.754-369A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25748886 | ||||||
| chr1:25749571
|
C | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 117 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.834+236C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25749571 | ||||||
| chr1:25749990
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(45): Show | 49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.834+655G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25749990 | ||||||
| chr1:25749998
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.834+663A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25749998 | ||||||
| chr1:25750083
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(54): Show | 58 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.834+748C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750083 | ||||||
| chr1:25750146
|
T | G | 1 | a0001c0002t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.834+811T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750146 | ||||||
| chr1:25750223
|
TCTC | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 117 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.834+893_834+895del others(3): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 25750223 | |||||
| chr1:25750439
|
CAA | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.834+1106_834+1107d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 25750439 | |||||
| chr1:25750489
|
G | A | 17 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0231others(14): Show | 17 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.834+1154G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750489 | ||||||
| chr1:25750550
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.834+1215C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750550 | ||||||
| chr1:25750735
|
C | T | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.834+1400C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750735 | ||||||
| chr1:25750736
|
G | A | 1 | a0001c0003t0001g0201 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.834+1401G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750736 | ||||||
| chr1:25750839
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0122a0001c0001t0001g0131 | 3 | HG01167.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.834+1504C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750839 | ||||||
| chr1:25750862
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0059others(37): Show | 41 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.834+1527A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750862 | ||||||
| chr1:25750865
|
A | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.834+1530A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750865 | ||||||
| chr1:25750903
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.834+1568G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750903 | ||||||
| chr1:25750995
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0093 | 2 | NA18941.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.834+1660C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25750995 | ||||||
| chr1:25751079
|
G | A | 28 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.834+1744G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25751079 | ||||||
| chr1:25751125
|
ATCCT | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(7): Show | 10 | HG01167.hp1 HG01255.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.834+1798_834+1801d others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 25751125 | |||||
| chr1:25751203
|
T | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0042others(2): Show | 5 | HG00735.hp1 HG01175.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+1868T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25751203 | ||||||
| chr1:25751205
|
G | A | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+1870G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25751205 | ||||||
| chr1:25751258
|
C | CTTTTCTC others(51): Show |
105 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.834+1964_834+2021d others(60): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 25751258 | |||||
| chr1:25751694
|
A | G | 1 | a0001c0002t0001g0173 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.835-1790A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25751694 | ||||||
| chr1:25751749
|
G | A | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.835-1735G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25751749 | ||||||
| chr1:25751769
|
G | A | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.835-1715G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25751769 | ||||||
| chr1:25751781
|
G | C | 1 | a0001c0001t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.835-1703G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25751781 | ||||||
| chr1:25752106
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.835-1378C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25752106 | ||||||
| chr1:25752289
|
G | A | 3 | a0001c0003t0001g0246a0001c0003t0006g0216a0001c0004t0001g0141 | 3 | HG02280.hp1 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.835-1195G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25752289 | ||||||
| chr1:25752891
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.835-593G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25752891 | ||||||
| chr1:25752983
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0069a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.835-501G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25752983 | ||||||
| chr1:25753063
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.835-421C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25753063 | ||||||
| chr1:25753064
|
G | A | 2 | a0001c0001t0001g0057a0001c0002t0002g0182 | 2 | NA18985.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.835-420G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25753064 | ||||||
| chr1:25753115
|
C | T | 1 | a0001c0002t0002g0180 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.835-369C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25753115 | ||||||
| chr1:25753187
|
A | G | 2 | a0001c0002t0001g0159a0003c0007t0001g0148 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.835-297A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25753187 | ||||||
| chr1:25753320
|
G | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 7 | HG01255.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.835-164G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25753320 | ||||||
| chr1:25753325
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0106 | 2 | HG00544.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.835-159C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25753325 | ||||||
| chr1:25753359
|
C | A | 1 | a0001c0002t0001g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.835-125C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 4/11 | chr1 | 25753359 | ||||||
| chr1:25753693
|
A | T | 2 | a0001c0005t0001g0193a0001c0005t0001g0229 | 2 | HG00639.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.929+115A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25753693 | ||||||
| chr1:25753726
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(62): Show | 66 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.929+148C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25753726 | ||||||
| chr1:25754227
|
C | G | 3 | a0001c0003t0001g0246a0001c0003t0006g0216a0001c0004t0001g0141 | 3 | HG02280.hp1 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.929+649C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25754227 | ||||||
| chr1:25754279
|
G | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 102 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.929+701G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25754279 | ||||||
| chr1:25754449
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.929+871A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25754449 | ||||||
| chr1:25754454
|
C | G | 3 | a0001c0002t0001g0156a0001c0002t0001g0199a0001c0002t0001g0247 | 3 | HG01167.hp1 HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.929+876C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25754454 | ||||||
| chr1:25754464
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.929+886G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25754464 | ||||||
| chr1:25754514
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929+936T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25754514 | ||||||
| chr1:25754560
|
G | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.929+982G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25754560 | ||||||
| chr1:25754679
|
CA | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(45): Show | 49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.929+1102delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25754679 | ||||||
| chr1:25754718
|
G | C | 1 | a0001c0002t0001g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.929+1140G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25754718 | ||||||
| chr1:25754836
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.929+1258G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25754836 | ||||||
| chr1:25755146
|
G | C | 3 | a0001c0002t0001g0156a0001c0002t0001g0199a0001c0002t0001g0247 | 3 | HG01167.hp1 HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.929+1568G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25755146 | ||||||
| chr1:25755227
|
G | A | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.929+1649G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25755227 | ||||||
| chr1:25755450
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.929+1872T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25755450 | ||||||
| chr1:25755558
|
G | T | 4 | a0001c0003t0001g0239a0001c0003t0001g0240a0001c0003t0001g0241others(1): Show | 4 | HG00639.hp1 HG01099.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.929+1980G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25755558 | ||||||
| chr1:25755775
|
C | T | 39 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(36): Show | 39 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.929+2197C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25755775 | ||||||
| chr1:25755831
|
C | A | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.929+2253C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25755831 | ||||||
| chr1:25755839
|
G | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.929+2261G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25755839 | ||||||
| chr1:25755863
|
G | A | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.929+2285G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25755863 | ||||||
| chr1:25756055
|
A | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.929+2477A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25756055 | ||||||
| chr1:25756064
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.929+2486G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25756064 | ||||||
| chr1:25756217
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0100 | 2 | NA18960.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.930-2375G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25756217 | ||||||
| chr1:25756321
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(45): Show | 49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.930-2271C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25756321 | ||||||
| chr1:25756336
|
G | A | 1 | a0001c0005t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.930-2256G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25756336 | ||||||
| chr1:25756446
|
G | A | 3 | a0001c0002t0001g0156a0001c0002t0001g0199a0001c0002t0001g0247 | 3 | HG01167.hp1 HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.930-2146G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25756446 | ||||||
| chr1:25756464
|
G | GA | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.930-2124dupA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 25756464 | |||||
| chr1:25756475
|
C | G | 1 | a0001c0002t0001g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.930-2117C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25756475 | ||||||
| chr1:25756613
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.930-1979G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25756613 | ||||||
| chr1:25756706
|
T | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.930-1886T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25756706 | ||||||
| chr1:25756917
|
C | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(45): Show | 49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.930-1675C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25756917 | ||||||
| chr1:25757044
|
G | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.930-1548G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25757044 | ||||||
| chr1:25757323
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(3): Show | 6 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.930-1269C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25757323 | ||||||
| chr1:25757500
|
CGGG | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(83): Show | 87 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.930-1082_930-1080d others(5): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 25757500 | |||||
| chr1:25757500
|
CGGGG | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.930-1083_930-1080d others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 25757500 | |||||
| chr1:25757610
|
T | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 240 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.930-982T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25757610 | ||||||
| chr1:25757668
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(54): Show | 58 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.930-924T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25757668 | ||||||
| chr1:25757673
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.930-919G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25757673 | ||||||
| chr1:25757755
|
G | A | 1 | a0001c0002t0001g0197 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.930-837G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25757755 | ||||||
| chr1:25758231
|
C | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 240 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.930-361C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25758231 | ||||||
| chr1:25758306
|
C | G | 39 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(36): Show | 39 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.930-286C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25758306 | ||||||
| chr1:25758308
|
A | G | 17 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0231others(14): Show | 17 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.930-284A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25758308 | ||||||
| chr1:25758439
|
G | T | 2 | a0001c0002t0001g0234a0001c0002t0001g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.930-153G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25758439 | ||||||
| chr1:25758557
|
AG | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 240 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.930-29delG | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 25758557 | |||||
| chr1:25758756
|
G | A | 4 | a0001c0002t0001g0156a0001c0002t0001g0199a0001c0002t0001g0247others(1): Show | 4 | HG01167.hp1 HG02055.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047+47G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25758756 | ||||||
| chr1:25758760
|
G | C | 1 | a0001c0002t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1047+51G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25758760 | ||||||
| chr1:25758798
|
T | C | 9 | a0001c0001t0001g0069a0001c0001t0001g0150a0001c0002t0001g0174others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1047+89T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25758798 | ||||||
| chr1:25758907
|
G | T | 28 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1047+198G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25758907 | ||||||
| chr1:25759029
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1047+320A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25759029 | ||||||
| chr1:25759342
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1047+633G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25759342 | ||||||
| chr1:25759842
|
C | T | 1 | a0004c0006t0001g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1047+1133C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25759842 | ||||||
| chr1:25759858
|
TGCC | T | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1047+1153_1047+115 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25759858 | |||||
| chr1:25760164
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1047+1455C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25760164 | ||||||
| chr1:25760399
|
G | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 240 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.1047+1690G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25760399 | ||||||
| chr1:25760404
|
C | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(45): Show | 49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1047+1695C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25760404 | ||||||
| chr1:25760534
|
C | T | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1047+1825C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25760534 | ||||||
| chr1:25760765
|
T | C | 7 | a0001c0001t0001g0150a0001c0002t0001g0209a0001c0002t0001g0210others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1047+2056T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25760765 | ||||||
| chr1:25760878
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1047+2169C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25760878 | ||||||
| chr1:25761168
|
C | T | 1 | a0001c0003t0001g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1047+2459C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761168 | ||||||
| chr1:25761178
|
T | G | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1047+2469T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761178 | ||||||
| chr1:25761204
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1047+2495C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761204 | ||||||
| chr1:25761253
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 101 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1047+2544G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761253 | ||||||
| chr1:25761297
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1048-2577C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761297 | ||||||
| chr1:25761620
|
C | CT | 99 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1048-2233dupT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25761620 | |||||
| chr1:25761620
|
C | CTT | 10 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0024others(7): Show | 10 | HG00642.hp1 HG01081.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1048-2234_1048-223 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25761620 | |||||
| chr1:25761620
|
C | CTTTTTTT | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0029others(73): Show | 77 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1048-2239_1048-223 others(11): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25761620 | |||||
| chr1:25761620
|
C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0064others(15): Show | 18 | HG00621.hp2 HG01071.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1048-2240_1048-223 others(12): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25761620 | |||||
| chr1:25761620
|
CT | C | 5 | a0001c0001t0001g0086a0001c0002t0001g0159a0001c0004t0001g0015others(2): Show | 5 | HG01168.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048-2233delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25761620 | |||||
| chr1:25761662
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(44): Show | 48 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1048-2212C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761662 | ||||||
| chr1:25761687
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 240 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.1048-2187T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761687 | ||||||
| chr1:25761717
|
G | A | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1048-2157G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761717 | ||||||
| chr1:25761731
|
T | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(94): Show | 98 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1048-2143T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761731 | ||||||
| chr1:25761748
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(45): Show | 49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1048-2126G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761748 | ||||||
| chr1:25761856
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048-2018C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25761856 | ||||||
| chr1:25762108
|
CTTTCT | C | 108 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1048-1747_1048-174 others(9): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25762108 | |||||
| chr1:25762123
|
TTTTC | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0023others(86): Show | 90 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1048-1747_1048-174 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25762123 | |||||
| chr1:25762124
|
TTTC | T | 31 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0042others(28): Show | 31 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1048-1747_1048-174 others(7): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25762124 | |||||
| chr1:25762178
|
G | A | 1 | a0003c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1048-1696G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25762178 | ||||||
| chr1:25762190
|
G | A | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1048-1684G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25762190 | ||||||
| chr1:25762446
|
CT | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 232 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.1048-1416delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25762446 | |||||
| chr1:25762540
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 240 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.1048-1334T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25762540 | ||||||
| chr1:25762638
|
G | A | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1048-1236G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25762638 | ||||||
| chr1:25762760
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(102): Show | 106 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.1048-1114A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25762760 | ||||||
| chr1:25763164
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1048-710A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25763164 | ||||||
| chr1:25763241
|
C | T | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1048-633C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25763241 | ||||||
| chr1:25763315
|
C | T | 17 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0231others(14): Show | 17 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1048-559C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25763315 | ||||||
| chr1:25763486
|
C | CA | 72 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 72 | HG00280.hp1 HG00597.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1048-366dupA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25763486 | |||||
| chr1:25763486
|
C | CAA | 36 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(33): Show | 36 | HG00423.hp2 HG00621.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1048-367_1048-366d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25763486 | |||||
| chr1:25763486
|
CA | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0059others(33): Show | 37 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1048-366delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25763486 | |||||
| chr1:25763486
|
CAA | C | 8 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0116others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048-367_1048-366d others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25763486 | |||||
| chr1:25763486
|
CAAA | C | 39 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0043others(36): Show | 39 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.1048-368_1048-366d others(5): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25763486 | |||||
| chr1:25763486
|
CAAAA | C | 19 | a0001c0003t0001g0201a0001c0003t0001g0220a0001c0003t0001g0231others(16): Show | 19 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1048-369_1048-366d others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 25763486 | |||||
| chr1:25763581
|
A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 240 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.1048-293A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25763581 | ||||||
| chr1:25763794
|
T | G | 46 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0043others(43): Show | 46 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1048-80T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25763794 | ||||||
| chr1:25763868
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19084.hp2 | splice_region_variant&intron_variant | LOW | c.1048-6C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25763868 | ||||||
| chr1:25763982
|
G | A | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141+15G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25763982 | ||||||
| chr1:25764002
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 7 | HG01255.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1141+35G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764002 | ||||||
| chr1:25764098
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 7 | HG01255.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1141+131C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764098 | ||||||
| chr1:25764117
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1141+150C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764117 | ||||||
| chr1:25764275
|
G | A | 9 | a0001c0001t0001g0069a0001c0001t0001g0150a0001c0002t0001g0174others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1141+308G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764275 | ||||||
| chr1:25764318
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1141+351G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764318 | ||||||
| chr1:25764473
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 7 | HG01255.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1141+506C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764473 | ||||||
| chr1:25764512
|
A | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1141+545A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764512 | ||||||
| chr1:25764526
|
A | G | 46 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0043others(43): Show | 46 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1141+559A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764526 | ||||||
| chr1:25764537
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1141+570C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764537 | ||||||
| chr1:25764638
|
G | A | 28 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1141+671G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764638 | ||||||
| chr1:25764733
|
AAAAC | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG01255.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1141+790_1141+793d others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25764733 | |||||
| chr1:25764824
|
C | T | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1141+857C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764824 | ||||||
| chr1:25764832
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1141+865G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764832 | ||||||
| chr1:25764973
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1141+1006G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25764973 | ||||||
| chr1:25765004
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1141+1037C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25765004 | ||||||
| chr1:25765057
|
CAA | C | 3 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01255.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1141+1093_1141+109 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25765057 | |||||
| chr1:25765283
|
C | G | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1141+1316C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25765283 | ||||||
| chr1:25765346
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0030others(44): Show | 48 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1141+1379G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25765346 | ||||||
| chr1:25765432
|
A | G | 2 | a0001c0003t0001g0231a0001c0003t0001g0237 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1141+1465A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25765432 | ||||||
| chr1:25765757
|
A | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 107 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1141+1790A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25765757 | ||||||
| chr1:25765860
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1141+1893C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25765860 | ||||||
| chr1:25765913
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0078a0001c0001t0001g0105 | 3 | HG02135.hp1 NA18969.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1141+1946G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25765913 | ||||||
| chr1:25766161
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 240 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.1141+2194T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25766161 | ||||||
| chr1:25766273
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1141+2306G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25766273 | ||||||
| chr1:25766348
|
GT | G | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141+2391delT | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25766348 | |||||
| chr1:25766349
|
T | G | 2 | a0001c0004t0001g0015a0001c0004t0001g0020 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1141+2382T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25766349 | ||||||
| chr1:25766350
|
T | G | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141+2383T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25766350 | ||||||
| chr1:25766628
|
AC | A | 31 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(28): Show | 31 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1141+2664delC | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25766628 | |||||
| chr1:25766760
|
G | C | 1 | a0002c0008t0001g0019 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1141+2793G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25766760 | ||||||
| chr1:25766764
|
C | G | 5 | a0001c0003t0001g0220a0001c0003t0001g0246a0001c0003t0006g0216others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1141+2797C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25766764 | ||||||
| chr1:25766889
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1141+2922C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25766889 | ||||||
| chr1:25767042
|
C | T | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1141+3075C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767042 | ||||||
| chr1:25767149
|
C | G | 1 | a0001c0001t0001g0003 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1141+3182C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767149 | ||||||
| chr1:25767151
|
T | TACACAC | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1141+3195_1141+320 others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767151 | |||||
| chr1:25767223
|
A | ACACACAC others(1): Show |
22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1141+3262_1141+326 others(12): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767223 | |||||
| chr1:25767262
|
C | T | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1141+3295C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767262 | ||||||
| chr1:25767272
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA19011.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1141+3305T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767272 | ||||||
| chr1:25767317
|
C | A | 1 | a0001c0002t0001g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1141+3350C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767317 | ||||||
| chr1:25767358
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1141+3391A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767358 | ||||||
| chr1:25767379
|
C | CCA | 21 | a0001c0002t0003g0154a0001c0003t0001g0201a0001c0003t0001g0218others(18): Show | 21 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1141+3430_1141+343 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767379 | |||||
| chr1:25767379
|
CCA | C | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.1141+3430_1141+343 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767379 | |||||
| chr1:25767379
|
CCACA | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1141+3428_1141+343 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767379 | |||||
| chr1:25767562
|
TCA | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 11 | HG02145.hp1 HG02258.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1141+3603_1141+360 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767562 | |||||
| chr1:25767622
|
C | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1141+3655C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767622 | ||||||
| chr1:25767625
|
TCA | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1141+3669_1141+367 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767625 | |||||
| chr1:25767646
|
T | TC | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(192): Show | 196 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.1141+3685dupC | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767646 | |||||
| chr1:25767646
|
T | TCC | 30 | a0001c0001t0001g0008a0001c0001t0001g0041a0001c0001t0001g0057others(27): Show | 30 | HG00423.hp1 HG00544.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1141+3684_1141+368 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767646 | |||||
| chr1:25767653
|
A | C | 1 | a0001c0004t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1141+3686A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767653 | ||||||
| chr1:25767710
|
T | C | 23 | a0001c0002t0003g0154a0001c0003t0001g0201a0001c0003t0001g0218others(20): Show | 23 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1141+3743T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767710 | ||||||
| chr1:25767731
|
ACACACAG others(183): Show |
A | 6 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(3): Show | 6 | HG01255.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1141+3800_1142-370 others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767731 | |||||
| chr1:25767759
|
CTCACATA others(501): Show |
C | 1 | a0001c0002t0003g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1141+3800_1142-338 others(4): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767759 | |||||
| chr1:25767766
|
A | AC | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(229): Show | 233 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.1141+3799_1141+380 others(5): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767766 | ||||||
| chr1:25767862
|
C | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1142-3795C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767862 | ||||||
| chr1:25767880
|
T | C | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1142-3777T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767880 | ||||||
| chr1:25767885
|
T | C | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1142-3772T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767885 | ||||||
| chr1:25767885
|
T | TCACACTC others(42): Show |
96 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(93): Show | 97 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1142-3759_1142-375 others(53): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25767885 | |||||
| chr1:25767946
|
C | G | 1 | a0001c0003t0001g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1142-3711C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25767946 | ||||||
| chr1:25768007
|
A | C | 2 | a0001c0002t0001g0159a0003c0007t0001g0148 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1142-3650A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768007 | ||||||
| chr1:25768059
|
T | TCA | 55 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0032others(52): Show | 56 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1142-3584_1142-358 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768059 | |||||
| chr1:25768059
|
T | TCACA | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(9): Show | 12 | HG01952.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1142-3586_1142-358 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768059 | |||||
| chr1:25768059
|
T | TCACACA | 29 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0029others(26): Show | 29 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1142-3588_1142-358 others(10): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768059 | |||||
| chr1:25768059
|
TCA | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 107 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1142-3584_1142-358 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768059 | |||||
| chr1:25768059
|
TCACA | T | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1142-3586_1142-358 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768059 | |||||
| chr1:25768073
|
A | T | 2 | a0001c0002t0001g0159a0003c0007t0001g0148 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1142-3584A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768073 | ||||||
| chr1:25768075
|
T | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(61): Show | 65 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1142-3582T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768075 | ||||||
| chr1:25768075
|
T | TC | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1142-3575dupC | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768075 | |||||
| chr1:25768077
|
C | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(60): Show | 64 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1142-3580C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768077 | ||||||
| chr1:25768079
|
C | G | 2 | a0001c0002t0001g0159a0003c0007t0001g0148 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1142-3578C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768079 | ||||||
| chr1:25768081
|
C | A | 22 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0220others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1142-3576C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768081 | ||||||
| chr1:25768081
|
CCA | C | 28 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0042others(25): Show | 28 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1142-3569_1142-356 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768081 | |||||
| chr1:25768083
|
A | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(61): Show | 65 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1142-3574A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768083 | ||||||
| chr1:25768137
|
ACTACATA others(8): Show |
A | 5 | a0001c0003t0001g0220a0001c0003t0001g0246a0001c0003t0006g0216others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1142-3504_1142-349 others(19): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768137 | |||||
| chr1:25768267
|
A | ATCCACAC others(86): Show |
1 | a0001c0003t0001g0201 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1142-3388_1142-338 others(97): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768267 | |||||
| chr1:25768267
|
A | ATCCACAC others(88): Show |
232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 233 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.1142-3388_1142-338 others(99): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768267 | |||||
| chr1:25768267
|
A | ATCCACAC others(88): Show |
5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1142-3388_1142-338 others(99): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768267 | |||||
| chr1:25768267
|
A | ATCCACAC others(88): Show |
9 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0110others(6): Show | 9 | HG00280.hp2 HG01167.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1142-3388_1142-338 others(99): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768267 | |||||
| chr1:25768290
|
C | A | 1 | a0001c0002t0003g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1142-3367C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768290 | ||||||
| chr1:25768314
|
T | C | 1 | a0001c0002t0003g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1142-3343T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768314 | ||||||
| chr1:25768317
|
A | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1142-3340A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768317 | ||||||
| chr1:25768336
|
TCACA | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(3): Show | 6 | HG01255.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1142-3315_1142-331 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768336 | |||||
| chr1:25768375
|
A | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1142-3282A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768375 | ||||||
| chr1:25768469
|
C | T | 1 | a0001c0003t0001g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1142-3188C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768469 | ||||||
| chr1:25768517
|
CACAT | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(3): Show | 6 | HG01255.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1142-3135_1142-313 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768517 | |||||
| chr1:25768573
|
CA | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1142-3083delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768573 | ||||||
| chr1:25768589
|
C | A | 2 | a0001c0002t0001g0156a0001c0005t0001g0249 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1142-3068C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768589 | ||||||
| chr1:25768648
|
CCA | C | 29 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(26): Show | 29 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1142-3000_1142-299 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768648 | |||||
| chr1:25768650
|
A | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 116 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1142-3007A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768650 | ||||||
| chr1:25768744
|
CCCACAGT others(14): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1142-2907_1142-288 others(25): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768744 | |||||
| chr1:25768769
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(43): Show | 47 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1142-2888C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768769 | ||||||
| chr1:25768803
|
G | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(100): Show | 104 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.1142-2854G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25768803 | ||||||
| chr1:25768883
|
CACCACAC others(4): Show |
C | 10 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1142-2772_1142-276 others(15): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25768883 | |||||
| chr1:25769067
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1142-2590C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25769067 | ||||||
| chr1:25769253
|
G | GAC | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(99): Show | 103 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.1142-2393_1142-239 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25769253 | |||||
| chr1:25769253
|
GAC | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01255.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1142-2393_1142-239 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25769253 | |||||
| chr1:25769390
|
T | TAC | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(100): Show | 104 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.1142-2249_1142-224 others(6): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25769390 | |||||
| chr1:25769390
|
T | TACAC | 11 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0231others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1142-2251_1142-224 others(8): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 25769390 | |||||
| chr1:25769462
|
G | T | 17 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0231others(14): Show | 17 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1142-2195G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25769462 | ||||||
| chr1:25769485
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(59): Show | 63 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.1142-2172C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25769485 | ||||||
| chr1:25769641
|
C | T | 7 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1142-2016C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25769641 | ||||||
| chr1:25769743
|
C | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(61): Show | 65 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1142-1914C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25769743 | ||||||
| chr1:25769787
|
G | A | 2 | a0001c0002t0001g0159a0003c0007t0001g0148 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1142-1870G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25769787 | ||||||
| chr1:25769800
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1142-1857G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25769800 | ||||||
| chr1:25769994
|
G | A | 1 | a0001c0002t0003g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1142-1663G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25769994 | ||||||
| chr1:25770066
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1142-1591A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25770066 | ||||||
| chr1:25770265
|
C | T | 1 | a0001c0002t0001g0167 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1142-1392C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25770265 | ||||||
| chr1:25770273
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1142-1384A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25770273 | ||||||
| chr1:25770557
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1142-1100A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25770557 | ||||||
| chr1:25770811
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1142-846C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25770811 | ||||||
| chr1:25770851
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1142-806C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25770851 | ||||||
| chr1:25770867
|
T | A | 2 | a0001c0003t0001g0220a0001c0004t0001g0071 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1142-790T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25770867 | ||||||
| chr1:25770998
|
A | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1142-659A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25770998 | ||||||
| chr1:25771059
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1142-598G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25771059 | ||||||
| chr1:25771129
|
C | T | 3 | a0001c0003t0001g0239a0001c0003t0001g0241a0001c0003t0001g0242 | 3 | HG01099.hp1 HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1142-528C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25771129 | ||||||
| chr1:25771240
|
C | T | 86 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0022others(83): Show | 86 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.1142-417C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25771240 | ||||||
| chr1:25771417
|
C | T | 2 | a0001c0001t0001g0068a0001c0002t0001g0187 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1142-240C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25771417 | ||||||
| chr1:25771554
|
G | A | 1 | a0002c0008t0001g0019 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1142-103G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25771554 | ||||||
| chr1:25771612
|
C | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1142-45C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25771612 | ||||||
| chr1:25771612
|
C | T | 2 | a0001c0002t0001g0159a0003c0007t0001g0148 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1142-45C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25771612 | ||||||
| chr1:25771616
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1142-41G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 7/11 | chr1 | 25771616 | ||||||
| chr1:25771842
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.1257+70G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25771842 | ||||||
| chr1:25771859
|
G | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0029others(90): Show | 93 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1257+87G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25771859 | ||||||
| chr1:25771971
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1257+199C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25771971 | ||||||
| chr1:25772455
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0115a0001c0002t0001g0165others(5): Show | 8 | HG02083.hp2 HG04184.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.1257+683C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25772455 | ||||||
| chr1:25772753
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1257+981C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25772753 | ||||||
| chr1:25772837
|
C | T | 10 | a0001c0001t0001g0153a0001c0002t0001g0161a0001c0002t0001g0162others(7): Show | 10 | HG00738.hp2 HG01081.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1257+1065C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25772837 | ||||||
| chr1:25772906
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1257+1134G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25772906 | ||||||
| chr1:25773321
|
A | C | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0005t0001g0249 | 3 | HG02055.hp2 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1257+1549A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25773321 | ||||||
| chr1:25773369
|
G | T | 4 | a0001c0001t0010g0075a0001c0002t0001g0159a0001c0002t0001g0196others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257+1597G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25773369 | ||||||
| chr1:25773401
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1257+1629G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25773401 | ||||||
| chr1:25773411
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1257+1639A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25773411 | ||||||
| chr1:25773673
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(53): Show | 57 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1257+1901A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25773673 | ||||||
| chr1:25773694
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1257+1922A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25773694 | ||||||
| chr1:25773966
|
C | T | 1 | a0001c0002t0001g0177 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1257+2194C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25773966 | ||||||
| chr1:25774017
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1257+2245G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25774017 | ||||||
| chr1:25774391
|
A | C | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0005t0001g0249 | 3 | HG02055.hp2 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1257+2619A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25774391 | ||||||
| chr1:25774425
|
C | T | 1 | a0001c0002t0001g0188 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1257+2653C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25774425 | ||||||
| chr1:25774453
|
G | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1257+2681G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25774453 | ||||||
| chr1:25774576
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1257+2804G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25774576 | ||||||
| chr1:25774672
|
C | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1257+2900C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25774672 | ||||||
| chr1:25774823
|
TA | T | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1257+3063delA | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 25774823 | |||||
| chr1:25774863
|
T | C | 31 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(28): Show | 31 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1257+3091T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25774863 | ||||||
| chr1:25774917
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1257+3145A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25774917 | ||||||
| chr1:25775086
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1258-3019G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25775086 | ||||||
| chr1:25775405
|
C | T | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1258-2700C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25775405 | ||||||
| chr1:25775543
|
A | C | 1 | a0001c0001t0001g0007 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1258-2562A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25775543 | ||||||
| chr1:25775741
|
GC | G | 31 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(28): Show | 31 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1258-2363delC | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25775741 | ||||||
| chr1:25776273
|
A | G | 2 | a0001c0003t0001g0220a0001c0004t0001g0071 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1258-1832A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25776273 | ||||||
| chr1:25776318
|
A | G | 1 | a0001c0002t0001g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1258-1787A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25776318 | ||||||
| chr1:25776412
|
G | A | 2 | a0001c0001t0010g0075a0001c0002t0001g0196 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1258-1693G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25776412 | ||||||
| chr1:25776657
|
AC | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1258-1446delC | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 25776657 | |||||
| chr1:25776902
|
T | C | 15 | a0001c0003t0001g0201a0001c0003t0001g0218a0001c0003t0001g0231others(12): Show | 15 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1258-1203T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25776902 | ||||||
| chr1:25777027
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1258-1078T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25777027 | ||||||
| chr1:25777223
|
G | A | 5 | a0001c0001t0001g0120a0001c0002t0001g0206a0001c0002t0001g0234others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-882G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25777223 | ||||||
| chr1:25777381
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1258-724C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25777381 | ||||||
| chr1:25777407
|
A | G | 31 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(28): Show | 31 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1258-698A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25777407 | ||||||
| chr1:25777411
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1258-694C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25777411 | ||||||
| chr1:25777560
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1258-545A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25777560 | ||||||
| chr1:25777601
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1258-504G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25777601 | ||||||
| chr1:25777638
|
C | T | 1 | a0001c0002t0001g0172 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1258-467C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25777638 | ||||||
| chr1:25778482
|
G | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(33): Show | 36 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1477+158G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25778482 | ||||||
| chr1:25778849
|
T | G | 1 | a0002c0008t0001g0019 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1477+525T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25778849 | ||||||
| chr1:25779386
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1477+1062G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25779386 | ||||||
| chr1:25779458
|
T | C | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0005t0001g0249 | 3 | HG02055.hp2 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1477+1134T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25779458 | ||||||
| chr1:25779539
|
C | G | 17 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0070others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1477+1215C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25779539 | ||||||
| chr1:25779741
|
G | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1478-1199G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25779741 | ||||||
| chr1:25779949
|
G | A | 2 | a0001c0002t0001g0206a0001c0002t0008g0227 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1478-991G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25779949 | ||||||
| chr1:25780124
|
C | A | 1 | a0001c0001t0001g0065 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1478-816C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780124 | ||||||
| chr1:25780209
|
C | T | 7 | a0001c0001t0001g0120a0001c0002t0001g0234a0001c0002t0001g0235others(4): Show | 7 | HG00639.hp1 HG01099.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1478-731C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780209 | ||||||
| chr1:25780278
|
C | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(33): Show | 36 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1478-662C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780278 | ||||||
| chr1:25780482
|
A | C | 1 | a0001c0003t0006g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1478-458A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780482 | ||||||
| chr1:25780495
|
A | T | 2 | a0001c0002t0001g0206a0001c0002t0008g0227 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1478-445A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780495 | ||||||
| chr1:25780517
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1478-423C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780517 | ||||||
| chr1:25780567
|
G | A | 3 | a0001c0001t0001g0018a0001c0002t0001g0156a0001c0005t0001g0249 | 3 | HG02055.hp2 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1478-373G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780567 | ||||||
| chr1:25780585
|
G | A | 2 | a0001c0002t0001g0206a0001c0002t0008g0227 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1478-355G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780585 | ||||||
| chr1:25780728
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1478-212G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780728 | ||||||
| chr1:25780830
|
A | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(235): Show | 239 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(236): Show |
intron_variant | MODIFIER | c.1478-110A>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780830 | ||||||
| chr1:25780904
|
G | A | 2 | a0001c0002t0001g0206a0001c0002t0008g0227 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1478-36G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 9/11 | chr1 | 25780904 | ||||||
| chr1:25781191
|
T | A | 1 | a0001c0001t0010g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1650+79T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25781191 | ||||||
| chr1:25781197
|
C | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 230 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.1650+85C>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25781197 | ||||||
| chr1:25781236
|
G | T | 1 | a0001c0003t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1650+124G>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25781236 | ||||||
| chr1:25781455
|
C | T | 2 | a0001c0002t0001g0206a0001c0002t0008g0227 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1650+343C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25781455 | ||||||
| chr1:25781536
|
C | T | 1 | a0001c0002t0001g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1650+424C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25781536 | ||||||
| chr1:25781596
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1650+484A>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25781596 | ||||||
| chr1:25781864
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1651-721G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25781864 | ||||||
| chr1:25781903
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(215): Show | 219 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.1651-682A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25781903 | ||||||
| chr1:25781944
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1651-641A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25781944 | ||||||
| chr1:25782063
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 135 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1651-522C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25782063 | ||||||
| chr1:25782087
|
G | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 135 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1651-498G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25782087 | ||||||
| chr1:25782215
|
C | T | 115 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 115 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1651-370C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25782215 | ||||||
| chr1:25782254
|
T | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1651-331T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25782254 | ||||||
| chr1:25782365
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0143others(5): Show | 8 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1651-220G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 10/11 | chr1 | 25782365 | ||||||
| chr1:25782709
|
T | C | 1 | a0001c0002t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1766+9T>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25782709 | ||||||
| chr1:25782746
|
A | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 135 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1766+46A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25782746 | ||||||
| chr1:25782816
|
G | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 135 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1766+116G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25782816 | ||||||
| chr1:25782955
|
G | A | 2 | a0001c0002t0001g0159a0003c0007t0001g0148 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1766+255G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25782955 | ||||||
| chr1:25782998
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0011g0033a0001c0002t0001g0206others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1766+298G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25782998 | ||||||
| chr1:25783023
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1766+323G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25783023 | ||||||
| chr1:25783322
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1767-341C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25783322 | ||||||
| chr1:25783359
|
C | G | 5 | a0001c0001t0001g0144a0001c0001t0010g0075a0001c0002t0001g0159others(2): Show | 5 | HG01255.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1767-304C>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25783359 | ||||||
| chr1:25783574
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 120 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1767-89A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25783574 | ||||||
| chr1:25783652
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 140 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1767-11G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25783652 | ||||||
| chr1:25783660
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0143a0001c0001t0001g0145others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1767-3C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 11/11 | chr1 | 25783660 |