Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MLMRK others(625): Show |
chr1 | 25611791 | 25789450 |
| a0002 | 0/0 | 630 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | MLMRK others(625): Show |
chr1 | 25611791 | 25789450 |
| a0003 | 0/0 | 630 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | MLMRK others(625): Show |
chr1 | 25611791 | 25789450 |
| a0004 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | MLMRK others(625): Show |
chr1 | 25611791 | 25789450 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1890 | 143 | 28 | 31 | 63 | 4 | 15 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | ATGCT others(1885): Show |
chr1 | 25611791 | 25789450 | ||
| a0001c0002 | 0/0 | 1890 | 79 | 30 | 15 | 31 | 0 | 3 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | ATGCT others(1885): Show |
chr1 | 25611791 | 25789450 | ||
| a0001c0003 | 0/0 | 1890 | 14 | 10 | 4 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | ATGCT others(1885): Show |
chr1 | 25611791 | 25789450 | ||
| a0001c0004 | 0/0 | 1890 | 7 | 7 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | ATGCT others(1885): Show |
chr1 | 25611791 | 25789450 | ||
| a0001c0005 | 0/0 | 1890 | 3 | 2 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | ATGCT others(1885): Show |
chr1 | 25611791 | 25789450 | ||
| a0002c0008 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | ATGCT others(1885): Show |
chr1 | 25611791 | 25789450 | ||
| a0002c0009 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | ATGCT others(1885): Show |
chr1 | 25611791 | 25789450 | ||
| a0003c0006 | 0/0 | 1890 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | ATGCT others(1885): Show |
chr1 | 25611791 | 25789450 | ||
| a0004c0007 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | ATGCT others(1885): Show |
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 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0001t0004 | 0/0 | 3561 | 2 | 0 | 2 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0001t0005 | 0/0 | 3561 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0001t0007 | 0/0 | 3561 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0001t0009 | 0/0 | 3561 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0001t0010 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0001t0011 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0001t0012 | 0/0 | 3561 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0002t0001 | 0/0 | 3561 | 69 | 26 | 15 | 26 | 0 | 2 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0002t0002 | 0/0 | 3561 | 5 | 0 | 0 | 5 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0002t0003 | 0/0 | 3561 | 2 | 2 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0002t0006 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0002t0008 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0002t0013 | 0/0 | 3561 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0003t0001 | 0/0 | 3561 | 13 | 9 | 4 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0003t0006 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0004t0001 | 0/0 | 3561 | 7 | 7 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0001c0005t0001 | 0/0 | 3561 | 3 | 2 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0002c0008t0001 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0002c0009t0001 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0003c0006t0001 | 0/0 | 3561 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| a0004c0007t0001 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | AGTGA others(3556): Show |
chr1 | 25611791 | 25789450 |
| actghapid | grch38/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 |
| a0001c0001t0001g0033 | 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 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0036 | 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 |
| 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 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 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 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0009g0037 | 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 |
| a0001c0001t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0001t0012g0136 | 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 | 0 | 0 | 0 | 0 | 1 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0002t0002g0181 | 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 |
| a0001c0002t0002g0183 | 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 |
| a0003c0006t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| a0004c0007t0001g0148 | 0/0 | 1 | 1 | 0 | 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 | g0122 | EUR | FIN | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0092 | 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 | g0056 | 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 | g0039 | 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 | a0003 | c0006 | t0001 | g0138 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0091 | 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 | g0103 | 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 | g0209 | 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 | g0210 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0105 | 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 | g0025 | 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 | g0222 | 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 | g0146 | 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 | g0118 | 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 | g0185 | AMR | CLM | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0206 | 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 | g0186 | 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 | g0097 | 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 | g0035 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0026 | 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 | g0136 | AMR | PEL | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0053 | 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 | g0184 | 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 | g0099 | 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 | g0134 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0093 | 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 | g0034 | 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 | g0057 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0179 | 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 | g0038 | 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 | a0004 | c0007 | t0001 | g0148 | AFR | ACB | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0147 | 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 | g0121 | 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 | g0012 | AFR | GWD | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0145 | 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 | g0207 | 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 | g0235 | 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 | g0234 | 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 | g0040 | 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 | g0189 | 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 | g0144 | 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 | g0133 | 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 | g0175 | 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 | g0096 | 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 | g0100 | 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 | g0095 | 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 | g0055 | 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 | g0028 | 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 | g0052 | 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 | g0101 | 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 | g0027 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0172 | 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 | g0098 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0054 | 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 | g0037 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0032 | 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 | g0177 | 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 | g0102 | 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 | g0181 | 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 | g0223 | 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 | g0036 | 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 | g0183 | 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 | g0173 | 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 | g0013 | 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 | g0190 | AFR | LWK | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0116 | REF | REF | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0117 | REF | REF | MAN1C1_chr1_25611791_25789450 | MAN1C1 | chr1 | 25611791 | 25789450 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0004 | 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 | a0003 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:25618250 | T | C | 3 | a0001c0002 a0001c0003 a0001c0005 |
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 | a0001c0003 a0001c0004 a0002c0009 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0002t0006 a0001c0003t0006 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:25618358 | C | T | 96 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
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 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 others(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 | a0001c0002t0006g0217 a0001c0003t0006g0216 |
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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0006g0217 a0001c0003t0006g0216 |
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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0156 others(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 | a0001c0002t0001g0213 a0001c0002t0001g0214 |
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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0156 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0156 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0156 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0156 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0156 others(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 | a0001c0001t0010g0075 a0001c0002t0001g0247 a0001c0003t0006g0216 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0219 a0001c0002t0001g0221 others(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 | a0001c0001t0010g0075 a0001c0002t0001g0211 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0076 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0001t0010g0075 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0002t0001g0212 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0125 a0001c0002t0001g0219 others(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 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0167 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0167 others(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 | a0001c0002t0001g0199 a0001c0003t0001g0201 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0120 a0001c0001t0001g0153 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0120 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0120 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0002t0001g0209 a0001c0002t0001g0210 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | a0001c0002t0001g0209 a0001c0002t0001g0210 a0001c0002t0001g0211 |
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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0120 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0022 others(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 | a0001c0002t0001g0225 a0001c0002t0001g0238 a0001c0002t0001g0245 others(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 | a0001c0002t0001g0238 a0001c0002t0001g0245 a0001c0003t0001g0239 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0169 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0199 a0001c0003t0001g0201 |
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 | a0001c0001t0001g0029 a0001c0002t0001g0157 a0001c0002t0001g0209 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0228 a0001c0002t0001g0230 a0001c0002t0001g0232 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0002t0001g0209 a0001c0002t0001g0210 |
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 | a0001c0001t0001g0057 | 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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
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 | a0001c0002t0001g0163 a0001c0005t0001g0193 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0150 a0001c0004t0001g0015 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | |||||||
| chr1:25641135 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0084 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0065 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0224 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0081 a0001c0002t0001g0212 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0004t0001g0016 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0074 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0222 a0001c0002t0001g0223 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0125 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
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 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0003c0006t0001g0138 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0151 a0001c0002t0001g0170 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0002t0001g0238 a0001c0002t0001g0245 a0001c0003t0001g0233 others(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 | a0001c0002t0001g0225 a0001c0002t0001g0236 a0001c0003t0001g0218 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0121 a0001c0002t0001g0225 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0001g0223 | 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 | a0001c0002t0001g0222 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0004t0001g0142 |
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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0003t0001g0243 |
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 | a0004c0007t0001g0148 | 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 | a0001c0001t0001g0001 a0001c0002t0001g0159 a0001c0002t0001g0174 |
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 | a0001c0002t0001g0196 a0001c0002t0001g0209 a0001c0002t0001g0210 others(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 | a0001c0002t0001g0190 a0001c0002t0001g0207 a0001c0002t0001g0208 |
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 | a0001c0002t0001g0189 a0001c0002t0001g0247 |
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 | a0001c0002t0001g0157 a0001c0002t0001g0160 a0001c0002t0001g0161 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0043 a0001c0001t0001g0077 others(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 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0054 others(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 | 34 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0030 others(31): Show |
34 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(31): 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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0022 a0001c0004t0001g0016 a0001c0004t0001g0062 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0005t0001g0193 |
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 | a0001c0002t0001g0228 a0001c0005t0001g0229 |
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 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0003t0006g0216 a0001c0005t0001g0229 |
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 | a0001c0003t0006g0216 a0001c0005t0001g0229 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0133 a0003c0006t0001g0138 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | a0004c0007t0001g0148 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0105 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0002t0001g0226 a0001c0002t0001g0236 a0001c0003t0001g0233 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0003c0006t0001g0138 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0143 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0150 a0001c0004t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0225 a0001c0002t0001g0226 a0001c0002t0001g0236 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0003t0001g0231 a0001c0003t0001g0237 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | a0001c0002t0001g0209 a0001c0002t0001g0210 a0001c0002t0001g0211 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0093 a0001c0001t0001g0115 |
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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0104 a0001c0001t0001g0137 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0002t0001g0228 a0001c0002t0001g0230 a0001c0002t0001g0232 others(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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0008 a0001c0002t0001g0158 a0001c0002t0001g0159 others(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 | a0001c0001t0001g0153 a0001c0002t0001g0157 a0001c0002t0001g0160 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0077 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0150 a0001c0002t0001g0245 |
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 | a0001c0001t0001g0046 a0001c0003t0001g0237 |
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 | a0001c0002t0001g0232 a0001c0003t0001g0231 |
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 | a0001c0002t0001g0228 a0001c0003t0001g0243 |
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 | a0001c0001t0001g0072 a0001c0004t0001g0071 |
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 | a0004c0007t0001g0148 | 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 | a0001c0001t0001g0085 a0001c0001t0001g0094 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0153 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0164 |
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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0002t0001g0156 a0001c0002t0002g0192 a0001c0002t0003g0154 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0010g0075 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0150 a0001c0002t0001g0198 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0156 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0087 a0001c0001t0001g0101 a0001c0001t0001g0102 others(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 | a0001c0002t0001g0228 a0001c0002t0001g0230 a0001c0002t0001g0232 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0002t0001g0156 others(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 | a0001c0001t0001g0027 | 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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | |||||||
| chr1:25662919 | T | C | 4 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0153 others(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 | a0001c0002t0001g0184 | 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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0105 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | 95 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(92): Show |
95 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(92): 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | |||||||
| chr1:25667101 | A | G | 3 | a0001c0002t0001g0209 a0001c0002t0001g0210 a0001c0002t0001g0211 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0002t0001g0156 a0001c0002t0003g0154 a0001c0002t0003g0155 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0009g0037 |
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 | a0001c0001t0001g0033 a0001c0002t0001g0219 a0001c0002t0001g0221 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0056 | 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 | a0001c0002t0001g0225 a0001c0002t0001g0226 a0001c0002t0001g0236 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
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 | a0001c0001t0001g0083 a0001c0002t0001g0248 a0001c0002t0002g0181 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0067 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | |||||||
| chr1:25675446 | A | G | 67 | a0001c0001t0001g0008 a0001c0001t0001g0125 a0001c0001t0001g0153 others(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 | |||||||
| chr1:25675554 | A | T | 71 | a0001c0001t0001g0008 a0001c0001t0001g0070 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0081 a0001c0002t0001g0212 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0002t0001g0199 a0001c0003t0001g0201 a0002c0008t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0224 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0018 a0001c0004t0001g0016 a0001c0004t0001g0062 |
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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(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 | 40 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0017 others(37): Show |
40 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(37): 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 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0152 a0001c0002t0001g0234 a0001c0002t0001g0235 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0152 a0001c0001t0011g0040 others(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 | a0001c0001t0001g0153 a0001c0002t0001g0161 a0001c0002t0001g0167 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0069 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0058 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0002t0001g0221 a0001c0005t0001g0249 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0010g0075 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0002t0001g0207 | 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 | 67 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(64): Show |
67 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(64): 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 | a0001c0004t0001g0015 a0001c0004t0001g0020 a0001c0005t0001g0249 |
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 | 23 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(20): Show |
23 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.541-6695T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679745 | |||||||
| chr1:25679865 | C | CT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(106): Show |
110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): 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 | 18 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0029 others(15): Show |
19 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(16): 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 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0078 a0001c0002t0002g0183 a0001c0003t0001g0239 others(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 | a0001c0001t0001g0119 a0001c0002t0001g0205 a0001c0002t0001g0206 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0152 a0001c0002t0001g0221 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0061 others(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 | a0001c0003t0001g0237 a0001c0004t0001g0015 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0060 a0001c0001t0010g0075 a0001c0005t0001g0249 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0039 others(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 | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
115 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.541-6488T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25679952 | |||||||
| chr1:25679954 | T | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
78 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(75): 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 | 28 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0029 others(25): Show |
29 | HG00609.hp1 HG00642.hp2 HG00738.hp1 others(26): 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 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0152 a0001c0002t0001g0221 others(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 | a0001c0001t0001g0022 a0004c0007t0001g0148 |
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 | 16 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0029 others(13): Show |
16 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(13): 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 | a0001c0001t0001g0004 a0001c0001t0001g0152 a0001c0002t0001g0221 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0010g0075 others(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 | 5 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(2): 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 | a0001c0003t0001g0231 a0001c0003t0001g0237 a0001c0003t0001g0243 |
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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(104): Show |
108 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(105): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0152 a0001c0002t0001g0221 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0023 others(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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(104): Show |
108 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.541-5341A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25681099 | |||||||
| chr1:25681226 | CA | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
106 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(103): 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 | a0004c0007t0001g0148 | 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 | a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | 20 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(17): Show |
20 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(17): 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0065 others(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 | 52 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0029 others(49): Show |
52 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(49): 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 | a0001c0001t0001g0069 a0001c0002t0001g0174 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0058 others(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 | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
245 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(242): 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 | a0001c0001t0001g0009 a0001c0001t0001g0022 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(16): 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 | a0001c0001t0010g0075 a0001c0002t0001g0197 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0069 a0001c0002t0001g0174 |
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 | a0001c0002t0001g0186 | 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 | 4 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
4 | HG00642.hp2 HG00741.hp2 HG04199.hp2 others(1): 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): 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 | a0001c0001t0001g0143 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0091 | 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.541-2001G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684439 | |||||||
| chr1:25684612 | T | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.541-1828T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | chr1 | 25684612 | |||||||
| chr1:25684633 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): 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 | a0001c0003t0001g0233 a0001c0003t0001g0244 |
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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): 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 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0070 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0003c0006t0001g0138 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0072 others(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 | a0004c0007t0001g0148 | 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0076 a0001c0001t0001g0095 |
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 | 20 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(17): Show |
20 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(17): 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 | a0001c0001t0001g0047 a0004c0007t0001g0148 |
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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(16): 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): 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 | a0001c0001t0001g0004 a0001c0001t0001g0152 |
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 | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(16): 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 | a0001c0002t0001g0236 a0001c0003t0001g0239 a0001c0003t0001g0240 others(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 | 57 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0043 others(54): Show |
57 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(54): 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0022 |
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 | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
240 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(237): 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 | a0001c0001t0001g0004 a0001c0001t0001g0152 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0042 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.637+2753G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689289 | |||||||
| chr1:25689314 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.637+2778G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25689314 | |||||||
| chr1:25689346 | G | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): 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 | a0001c0003t0001g0220 a0001c0004t0001g0071 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0097 | 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(106): 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 | a0001c0001t0001g0009 a0001c0001t0001g0022 |
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 | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(106): Show |
110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): 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 | a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0039 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0151 a0001c0002t0001g0228 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0011g0040 others(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 | 8 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG00642.hp2 HG00741.hp2 HG02486.hp1 others(5): 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 | a0001c0003t0001g0233 a0001c0003t0001g0244 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0004c0007t0001g0148 | 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
114 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(111): 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 | a0001c0003t0001g0218 a0001c0004t0001g0015 a0001c0004t0001g0020 |
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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0151 a0001c0002t0001g0228 a0001c0002t0001g0230 |
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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 others(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 | a0004c0007t0001g0148 | 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0001t0001g0028 | 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0002t0001g0177 | 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 | a0001c0003t0001g0231 a0001c0003t0001g0233 a0001c0003t0001g0237 others(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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
114 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(111): 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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0094 |
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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0004c0007t0001g0148 | 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0150 a0001c0002t0001g0159 a0001c0002t0001g0209 others(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 | a0004c0007t0001g0148 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0118 | 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 | a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0100 | 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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(107): Show |
111 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(108): 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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
114 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.637+9940T>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25696476 | |||||||
| chr1:25696586 | C | T | 22 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(19): Show |
22 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(19): 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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(107): Show |
111 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(108): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0022 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0221 a0001c0003t0001g0220 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0004c0007t0001g0148 | 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0002t0001g0223 | 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0107 a0001c0002t0001g0157 a0001c0002t0001g0164 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0094 a0001c0001t0001g0099 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(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 | a0001c0002t0001g0177 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0055 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | 26 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): 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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(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 | a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(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 | 8 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(5): 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 | a0001c0001t0001g0110 a0001c0001t0001g0131 |
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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
114 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(111): 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0004g0109 a0001c0001t0004g0111 |
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 | a0001c0002t0001g0209 a0001c0002t0001g0210 |
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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 others(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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
114 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(111): 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 | a0001c0001t0001g0005 a0001c0001t0001g0032 |
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 | a0001c0003t0001g0220 a0001c0004t0001g0071 |
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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
114 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(111): 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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | 7 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG00642.hp2 HG00741.hp2 HG02145.hp2 others(4): 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0047 others(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 | a0004c0007t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.637+17208C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25703744 | |||||||
| chr1:25704025 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(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 | 7 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG00642.hp2 HG00741.hp2 HG02145.hp2 others(4): 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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(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 | a0001c0004t0001g0016 a0001c0004t0001g0062 |
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 | a0001c0002t0001g0160 a0001c0002t0001g0179 a0001c0002t0001g0204 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0072 others(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 | 7 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG00642.hp2 HG00741.hp2 HG02145.hp2 others(4): 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 | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(111): Show |
115 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(112): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0207 | 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
114 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(111): 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 | a0001c0001t0001g0069 a0001c0002t0001g0174 |
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 | a0001c0001t0005g0108 a0001c0001t0005g0139 |
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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(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 | 22 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(19): Show |
22 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(19): 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 | a0001c0001t0001g0143 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0222 a0001c0002t0001g0223 others(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 | a0001c0002t0001g0180 | 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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | a0001c0002t0001g0177 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(126): Show |
130 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(127): 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(100): Show |
104 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(101): 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(97): Show |
101 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(98): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0002t0001g0221 a0001c0003t0001g0220 a0001c0003t0001g0246 others(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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(100): Show |
104 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(101): 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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(107): Show |
111 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.637+27935T>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25714471 | |||||||
| chr1:25714586 | TA | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(111): Show |
115 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(112): 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 | a0001c0003t0001g0231 a0001c0003t0001g0233 a0001c0003t0001g0237 others(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 | a0001c0004t0001g0016 a0001c0004t0001g0062 |
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 | a0001c0001t0001g0150 a0001c0002t0001g0159 a0001c0002t0001g0209 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0004c0007t0001g0148 | 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 | a0001c0002t0001g0172 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0100 a0001c0001t0001g0144 others(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 | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(106): Show |
110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(106): Show |
110 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(107): 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 | a0001c0001t0001g0095 | 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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(87): Show |
91 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(88): 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 | a0001c0001t0001g0069 a0001c0001t0001g0119 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0143 a0001c0002t0001g0189 a0001c0002t0001g0221 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0038 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0084 a0001c0001t0001g0092 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(67): Show |
71 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.638-27908G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25718760 | |||||||
| chr1:25719051 | C | CTTA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(104): Show |
108 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(105): 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 | a0001c0001t0001g0125 a0001c0002t0001g0177 |
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 | a0001c0001t0001g0041 a0001c0002t0001g0179 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0115 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0072 others(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 | a0004c0007t0001g0148 | 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 | a0004c0007t0001g0148 | 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0079 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(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 | 24 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(21): Show |
24 | HG00642.hp2 HG00741.hp2 HG01167.hp1 others(21): 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 | a0001c0001t0010g0075 a0001c0002t0003g0155 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(70): Show |
74 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(71): 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(70): Show |
74 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(71): 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0070 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(70): Show |
74 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(71): 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(70): Show |
74 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(71): 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 71 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(68): Show |
72 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(69): 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 | a0001c0002t0001g0175 | 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 | a0001c0003t0001g0220 a0001c0004t0001g0071 |
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 | a0001c0005t0001g0193 a0001c0005t0001g0229 |
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 | a0001c0002t0001g0221 a0001c0003t0001g0220 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0233 a0001c0003t0001g0244 |
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 | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(101): Show |
105 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(102): 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 | a0001c0004t0001g0015 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0221 others(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 | 41 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0043 others(38): Show |
41 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(38): 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 | a0001c0001t0001g0153 a0001c0002t0001g0161 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0120 a0001c0002t0001g0207 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0150 a0001c0002t0001g0159 a0001c0002t0001g0209 others(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 | a0001c0004t0001g0016 a0001c0004t0001g0062 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | 40 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0043 others(37): Show |
40 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(37): 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0002t0001g0179 | 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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0221 others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0120 a0001c0002t0001g0234 a0001c0002t0001g0235 |
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 | a0001c0001t0011g0040 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0003t0001g0220 a0001c0004t0001g0071 |
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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | a0001c0002t0001g0170 a0001c0002t0001g0197 a0001c0002t0001g0203 |
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 | 40 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0043 others(37): Show |
40 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(37): 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0001c0001t0001g0013 | 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 | 42 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0043 others(39): Show |
42 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(39): 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 | a0001c0002t0001g0170 a0001c0002t0001g0197 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0033 others(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 | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
116 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(113): 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 | a0001c0001t0001g0090 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0004c0007t0001g0148 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0150 a0001c0003t0001g0201 a0002c0008t0001g0019 others(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 | 39 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(36): Show |
39 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(36): 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 | a0001c0002t0001g0219 a0001c0002t0001g0225 a0001c0004t0001g0142 |
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 | a0004c0007t0001g0148 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0003t0001g0201 a0002c0008t0001g0019 a0002c0009t0001g0021 |
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 | a0001c0002t0001g0179 | 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 | a0001c0003t0001g0231 a0001c0003t0001g0233 a0001c0003t0001g0237 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 39 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0043 others(36): Show |
39 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.638-13510G>C | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25733158 | |||||||
| chr1:25733159 | C | T | 39 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0043 others(36): Show |
39 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(36): 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | 26 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(23): Show |
26 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(23): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0002t0001g0221 a0001c0003t0001g0231 a0001c0003t0001g0233 others(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 | a0001c0003t0001g0220 a0001c0004t0001g0071 |
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 | a0001c0002t0001g0221 a0001c0003t0001g0220 a0001c0003t0001g0246 others(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 | a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0221 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(126): Show |
130 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(127): 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | 25 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(22): Show |
25 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(22): 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 | a0001c0003t0001g0218 a0001c0004t0001g0015 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0028 | 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 | a0001c0002t0001g0221 a0001c0002t0001g0236 a0001c0003t0001g0220 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0121 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0119 a0001c0002t0001g0198 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0061 others(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 | a0001c0002t0001g0190 a0001c0002t0001g0208 |
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 | a0001c0002t0001g0236 a0001c0003t0001g0231 a0001c0003t0001g0233 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0033 others(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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(118): Show |
122 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(119): 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 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0002t0001g0174 others(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 | 25 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(22): Show |
25 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.638-10116G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | chr1 | 25736552 | |||||||
| chr1:25736565 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00642.hp2 HG00741.hp2 HG03688.hp2 others(2): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0003t0001g0220 a0001c0004t0001g0071 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0120 a0001c0001t0001g0143 others(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 | 27 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
27 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(24): 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 | a0001c0002t0001g0158 a0001c0002t0001g0178 |
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 | a0004c0007t0001g0148 | 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 | |||||||
| chr1:25737400 | G | GC | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG02258.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-9261dupC | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 25737400 | ||||||
| chr1:25737405 | C | T | 2 | a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0002t0001g0184 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0002t0001g0196 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0004t0001g0141 a0001c0005t0001g0249 |
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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0221 others(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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(123): Show |
127 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(124): 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0120 a0001c0001t0001g0143 others(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 | a0001c0002t0001g0215 a0001c0002t0001g0248 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | 25 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(22): Show |
25 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(22): 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | 25 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(22): Show |
25 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(22): 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 | 27 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
27 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(24): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0151 a0001c0002t0001g0163 a0001c0002t0001g0228 others(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 | a0001c0001t0001g0035 | 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 | 25 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(22): Show |
25 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(22): 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0033 others(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 | a0001c0003t0001g0220 a0001c0004t0001g0071 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0002t0001g0173 | 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 |
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 | a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0002t0001g0174 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | 39 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0043 others(36): Show |
39 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(36): 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 | a0001c0003t0001g0201 a0002c0008t0001g0019 |
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 | 25 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(22): Show |
25 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(22): 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0001 a0001c0001t0009g0037 |
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 | a0001c0002t0001g0236 a0001c0003t0001g0231 a0001c0003t0001g0233 others(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 | 39 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0043 others(36): Show |
39 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(36): 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 | a0001c0001t0001g0087 a0001c0001t0001g0101 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0023 others(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 | a0001c0003t0001g0220 a0001c0003t0001g0246 a0001c0004t0001g0071 others(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 | a0004c0007t0001g0148 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0002t0001g0174 others(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 | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
147 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(144): 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0007g0098 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0002t0001g0190 a0001c0002t0001g0208 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0121 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0004c0007t0001g0148 | 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 | a0001c0001t0001g0034 | 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 | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(234): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0033 others(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 | 27 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.753+443G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25747226 | |||||||
| chr1:25747238 | C | T | 27 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.753+455C>T | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 3/11 | chr1 | 25747238 | |||||||
| chr1:25747546 | C | T | 27 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0002t0001g0189 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
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 | a0001c0003t0006g0216 a0001c0004t0001g0141 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
158 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(155): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | a0001c0002t0001g0223 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0231 others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0121 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0094 |
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 | 27 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0002t0001g0172 | 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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0001c0003t0001g0246 a0001c0003t0006g0216 a0001c0004t0001g0141 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0069 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0054 a0001c0002t0002g0182 |
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 | a0001c0002t0002g0183 | 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 | a0001c0002t0001g0159 a0004c0007t0001g0148 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0106 |
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 | a0001c0005t0001g0193 a0001c0005t0001g0229 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | a0001c0003t0001g0246 a0001c0003t0006g0216 a0001c0004t0001g0141 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0104 | 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 | a0001c0002t0001g0156 a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0099 | 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 | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
139 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(136): 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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0001c0003t0001g0239 a0001c0003t0001g0240 a0001c0003t0001g0241 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
139 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(136): 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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
139 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(136): 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 | a0001c0001t0001g0087 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | a0001c0002t0001g0156 a0001c0002t0001g0199 a0001c0002t0001g0247 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0134 | 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 | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
139 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(136): 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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
139 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.930-1548G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 5/11 | chr1 | 25757044 | |||||||
| chr1:25757323 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(2): 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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
140 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(137): 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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
239 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(236): 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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | a0001c0002t0001g0207 | 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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
239 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(236): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0231 others(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 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
239 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(236): 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 | a0001c0002t0001g0156 a0001c0002t0001g0199 a0001c0002t0001g0247 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0002t0001g0174 others(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 | 27 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): 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 | a0003c0006t0001g0138 | 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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
239 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(236): 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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0001t0001g0150 a0001c0002t0001g0209 a0001c0002t0001g0210 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0029 others(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 |
17 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0064 others(14): Show |
17 | HG00621.hp2 HG01071.hp2 HG01081.hp1 others(14): 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 | a0001c0001t0001g0086 a0001c0002t0001g0159 a0001c0004t0001g0015 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
239 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(236): 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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(93): Show |
97 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(94): 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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0023 others(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 | 30 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0042 others(27): Show |
30 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(27): 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 | a0004c0007t0001g0148 | 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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
231 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(228): 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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
239 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(236): 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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(101): Show |
105 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(102): 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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0231 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0059 others(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 | 7 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0125 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(4): 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 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0043 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0220 a0001c0003t0001g0231 others(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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
239 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(236): Show |
intron_variant | MODIFIER | c.1048-293A>G | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 6/11 | chr1 | 25763581 | |||||||
| chr1:25763794 | T | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0043 others(42): Show |
45 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(42): 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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0002t0001g0174 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 45 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0043 others(42): Show |
45 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(42): 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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | 27 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): 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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0030 others(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 | a0001c0003t0001g0231 a0001c0003t0001g0237 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0078 a0001c0001t0001g0104 |
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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
239 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(236): 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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0001c0004t0001g0015 a0001c0004t0001g0020 |
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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0003t0001g0220 a0001c0003t0001g0246 a0001c0003t0006g0216 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
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 | a0001c0002t0003g0154 a0001c0003t0001g0201 a0001c0003t0001g0218 others(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 | 36 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
36 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(33): 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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
195 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(192): 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 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0054 others(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 | a0001c0002t0003g0154 a0001c0003t0001g0201 a0001c0003t0001g0218 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(228): Show |
232 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(229): 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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 |
95 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(92): Show |
96 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(93): 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 | a0001c0002t0001g0159 a0004c0007t0001g0148 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0030 others(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 | 28 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0029 others(25): Show |
28 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(25): 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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | a0001c0002t0001g0159 a0004c0007t0001g0148 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0159 a0004c0007t0001g0148 |
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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0220 others(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 | 27 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0042 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): 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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | a0001c0003t0001g0220 a0001c0003t0001g0246 a0001c0003t0006g0216 others(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 |
231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(228): Show |
232 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(229): 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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0086 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0002t0001g0156 a0001c0005t0001g0249 |
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 | 28 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0043 others(25): Show |
28 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(25): 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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0033 others(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 | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(99): Show |
103 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(100): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(98): Show |
102 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(99): 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(99): Show |
103 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(100): 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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0231 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0231 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | 6 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(3): 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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0159 a0004c0007t0001g0148 |
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 | a0001c0003t0001g0220 a0001c0004t0001g0071 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0105 | 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 | a0001c0003t0001g0239 a0001c0003t0001g0241 a0001c0003t0001g0242 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0068 a0001c0002t0001g0175 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0002t0001g0159 a0004c0007t0001g0148 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
228 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.1257+70G>A | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25771842 | |||||||
| chr1:25771859 | G | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0029 others(89): Show |
92 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(89): 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 | a0001c0001t0001g0033 a0001c0001t0001g0115 a0001c0002t0001g0165 others(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 | a0001c0001t0001g0153 a0001c0002t0001g0161 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0005t0001g0249 |
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 | a0001c0001t0010g0075 a0001c0002t0001g0159 a0001c0002t0001g0196 others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0033 others(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 | a0001c0002t0001g0176 | 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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0005t0001g0249 |
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 | a0001c0002t0001g0179 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | 30 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0043 others(27): Show |
30 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(27): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 30 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0043 others(27): Show |
30 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1258-2363delC | MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 8/11 | chr1 | 25775741 | |||||||
| chr1:25776273 | A | G | 2 | a0001c0003t0001g0220 a0001c0004t0001g0071 |
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 | a0001c0001t0010g0075 a0001c0002t0001g0196 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0003t0001g0201 a0001c0003t0001g0218 a0001c0003t0001g0231 others(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 | a0001c0001t0001g0120 a0001c0002t0001g0207 a0001c0002t0001g0234 others(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 | a0001c0002t0001g0186 | 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 | 30 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0043 others(27): Show |
30 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(27): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0002t0001g0173 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0005t0001g0249 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0002t0001g0207 a0001c0002t0008g0227 |
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 | a0001c0001t0001g0120 a0001c0002t0001g0234 a0001c0002t0001g0235 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0002t0001g0207 a0001c0002t0008g0227 |
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 | a0001c0001t0001g0018 a0001c0002t0001g0156 a0001c0005t0001g0249 |
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 | a0001c0002t0001g0207 a0001c0002t0008g0227 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(235): 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 | a0001c0002t0001g0207 a0001c0002t0008g0227 |
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 | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): 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 | a0001c0002t0001g0207 a0001c0002t0008g0227 |
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 | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(214): Show |
218 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(215): 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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0002t0001g0159 a0004c0007t0001g0148 |
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 | a0001c0001t0001g0022 a0001c0001t0011g0040 a0001c0002t0001g0207 others(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 | a0001c0001t0001g0146 a0001c0001t0010g0075 a0001c0002t0001g0159 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 |