Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 157777 |
| ensemblid | ENSG00000178460.18 |
| hgncid | 26368 |
| symbol | MCMDC2 |
| name | minichromosome maintenance domain containing 2 |
| refseq_nuc | NM_173518.5 |
| refseq_prot | NP_775789.3 |
| ensembl_nuc | ENST00000422365.7 |
| ensembl_prot | ENSP00000413632.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 66870771 |
| end | 66922048 |
| strand | + |
| ver | v1.2 |
| region | chr8:66870771-66922048 |
| region5000 | chr8:66865771-66927048 |
| regionname0 | MCMDC2_chr8_66870771_66922048 |
| regionname5000 | MCMDC2_chr8_66865771_66927048 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 681 | 148 | 44 | 30 | 46 | 7 | 19 | 35 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0002 | 0/0 | 681 | 12 | 2 | 5 | 1 | 0 | 4 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0003 | 0/0 | 681 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0004 | 0/0 | 681 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0005 | 0/0 | 681 | 7 | 0 | 4 | 0 | 3 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0006 | 0/0 | 681 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0007 | 0/0 | 681 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0008 | 0/0 | 681 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0009 | 0/0 | 681 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0010 | 0/0 | 681 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0011 | 0/0 | 681 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0012 | 0/0 | 681 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| a0013 | 0/0 | 681 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | MSNLK others(676): Show |
chr8 | 66865771 | 66927048 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2043 | 147 | 44 | 30 | 46 | 7 | 18 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0001c0015 | 0/0 | 2043 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0002c0002 | 0/0 | 2043 | 10 | 0 | 5 | 1 | 0 | 4 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0002c0009 | 0/0 | 2043 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0003c0003 | 0/0 | 2043 | 10 | 10 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0004c0004 | 0/0 | 2043 | 9 | 7 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0005c0006 | 0/0 | 2043 | 7 | 0 | 4 | 0 | 3 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0006c0005 | 0/0 | 2043 | 7 | 6 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0007c0008 | 0/0 | 2043 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0008c0007 | 0/0 | 2043 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0009c0010 | 0/0 | 2043 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0010c0014 | 0/0 | 2043 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0011c0011 | 0/0 | 2043 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0012c0013 | 0/0 | 2043 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 | ||
| a0013c0012 | 0/0 | 2043 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | ATGTC others(2038): Show |
chr8 | 66865771 | 66927048 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5074 | 99 | 16 | 30 | 33 | 7 | 11 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0002 | 0/0 | 5074 | 23 | 16 | 0 | 1 | 0 | 6 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0005 | 0/0 | 5074 | 8 | 0 | 0 | 8 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0006 | 0/0 | 5074 | 5 | 5 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0007 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0008 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0009 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0011 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0012 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0013 | 0/0 | 5074 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0014 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0015 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0016 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0001t0017 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0001c0015t0001 | 0/0 | 5074 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0002c0002t0002 | 0/0 | 5074 | 9 | 0 | 5 | 0 | 0 | 4 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0002c0002t0018 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0002c0009t0002 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0003c0003t0002 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0003c0003t0004 | 0/0 | 5074 | 8 | 8 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0004c0004t0003 | 0/0 | 5074 | 9 | 7 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0005c0006t0001 | 0/0 | 5074 | 7 | 0 | 4 | 0 | 3 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0006c0005t0001 | 0/0 | 5074 | 7 | 6 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0007c0008t0002 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0008c0007t0001 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0009c0010t0001 | 0/0 | 5074 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0010c0014t0001 | 0/0 | 5074 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0011c0011t0010 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0012c0013t0001 | 0/0 | 5074 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| a0013c0012t0001 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | AGGAC others(5069): Show |
chr8 | 66865771 | 66927048 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0005g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0006g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0008g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0011g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0014g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0015g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0001t0017g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0001c0015t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0002t0018g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0009t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0002c0009t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0003c0003t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0003c0003t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0003c0003t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0003c0003t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0003c0003t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0003c0003t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0003c0003t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0003c0003t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0004c0004t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0004c0004t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0004c0004t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0004c0004t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0004c0004t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0004c0004t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0004c0004t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0005c0006t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0005c0006t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0005c0006t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0005c0006t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0005c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0005c0006t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0006c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0006c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0006c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0006c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0006c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0006c0005t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0006c0005t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0007c0008t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0007c0008t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0008c0007t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0008c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0009c0010t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0010c0014t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0011c0011t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0012c0013t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| a0013c0012t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0006 | t0001 | g0018 | EUR | GBR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00733 | hp1 | a0005 | c0006 | t0001 | g0117 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0161 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01070 | hp1 | a0004 | c0004 | t0003 | g0011 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01071 | hp2 | a0004 | c0004 | t0003 | g0011 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01081 | hp2 | a0005 | c0006 | t0001 | g0116 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0162 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01192 | hp2 | a0005 | c0006 | t0001 | g0119 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01243 | hp1 | a0006 | c0005 | t0001 | g0152 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01255 | hp1 | a0005 | c0006 | t0001 | g0115 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01346 | hp1 | a0009 | c0010 | t0001 | g0082 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01346 | hp2 | a0010 | c0014 | t0001 | g0087 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01516 | hp2 | a0005 | c0006 | t0001 | g0018 | EUR | IBS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01891 | hp2 | a0006 | c0005 | t0001 | g0151 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0164 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0153 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02055 | hp2 | a0007 | c0008 | t0002 | g0146 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02056 | hp2 | a0002 | c0002 | t0018 | g0159 | EAS | KHV | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02145 | hp2 | a0006 | c0005 | t0001 | g0150 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0158 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02615 | hp1 | a0003 | c0003 | t0004 | g0017 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02622 | hp2 | a0003 | c0003 | t0004 | g0105 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02647 | hp1 | a0004 | c0004 | t0003 | g0039 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0156 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02717 | hp2 | a0004 | c0004 | t0003 | g0036 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0157 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02818 | hp1 | a0004 | c0004 | t0003 | g0038 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02896 | hp1 | a0003 | c0003 | t0004 | g0139 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02922 | hp2 | a0004 | c0004 | t0003 | g0010 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02965 | hp1 | a0006 | c0005 | t0001 | g0041 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02965 | hp2 | a0003 | c0003 | t0004 | g0133 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02976 | hp1 | a0011 | c0011 | t0010 | g0055 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0160 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03041 | hp1 | a0004 | c0004 | t0003 | g0040 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0149 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0169 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03130 | hp2 | a0007 | c0008 | t0002 | g0035 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03139 | hp1 | a0006 | c0005 | t0001 | g0042 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03195 | hp2 | a0003 | c0003 | t0004 | g0017 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03225 | hp2 | a0006 | c0005 | t0001 | g0059 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03453 | hp1 | a0001 | c0001 | t0017 | g0148 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03453 | hp2 | a0003 | c0003 | t0004 | g0102 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03490 | hp1 | a0001 | c0015 | t0001 | g0054 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03516 | hp1 | a0002 | c0009 | t0002 | g0155 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03516 | hp2 | a0003 | c0003 | t0002 | g0005 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03579 | hp1 | a0003 | c0003 | t0002 | g0005 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03654 | hp1 | a0012 | c0013 | t0001 | g0001 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03688 | hp1 | a0001 | c0001 | t0013 | g0003 | SAS | STU | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | STU | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0163 | SAS | BEB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | STU | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18522 | hp1 | a0004 | c0004 | t0003 | g0037 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18906 | hp2 | a0006 | c0005 | t0001 | g0060 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18946 | hp1 | a0013 | c0012 | t0001 | g0138 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18946 | hp2 | a0001 | c0001 | t0014 | g0006 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18994 | hp1 | a0001 | c0001 | t0016 | g0030 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18994 | hp2 | a0001 | c0001 | t0011 | g0063 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19012 | hp2 | a0001 | c0001 | t0012 | g0108 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA19240 | hp2 | a0008 | c0007 | t0001 | g0020 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA20129 | hp2 | a0008 | c0007 | t0001 | g0021 | AFR | ASW | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA20752 | hp1 | a0005 | c0006 | t0001 | g0118 | EUR | TSI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | GIH | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | GIH | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02109 | hp2 | a0003 | c0003 | t0004 | g0132 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02486 | hp2 | a0003 | c0003 | t0004 | g0101 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02559 | hp1 | a0002 | c0009 | t0002 | g0154 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG02559 | hp2 | a0004 | c0004 | t0003 | g0010 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0147 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | USA | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | USA | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0066 | AFR | USA | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0123 | REF | REF | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0121 | REF | REF | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66874350 | A | G | 1 | a0003 | 10 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(7): Show |
missense_variant | MODERATE | c.119A>G | p.Tyr40Cys | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 3/15 | 268/5074 | 119/2046 | 40/681 | chr8 | 66874350 | |||
| chr8:66874398 | C | T | 1 | a0005 | 7 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(4): Show |
missense_variant | MODERATE | c.167C>T | p.Ala56Val | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 3/15 | 316/5074 | 167/2046 | 56/681 | chr8 | 66874398 | |||
| chr8:66874582 | C | T | 1 | a0002 | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
missense_variant | MODERATE | c.281C>T | p.Thr94Met | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/15 | 430/5074 | 281/2046 | 94/681 | chr8 | 66874582 | |||
| chr8:66877355 | A | G | 1 | a0007 | 2 | HG02055.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.292A>G | p.Ile98Val | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/15 | 441/5074 | 292/2046 | 98/681 | chr8 | 66877355 | |||
| chr8:66877444 | T | G | 1 | a0009 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.381T>G | p.Phe127Leu | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/15 | 530/5074 | 381/2046 | 127/681 | chr8 | 66877444 | |||
| chr8:66877473 | T | A | 1 | a0006 | 7 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
missense_variant | MODERATE | c.410T>A | p.Met137Lys | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/15 | 559/5074 | 410/2046 | 137/681 | chr8 | 66877473 | |||
| chr8:66883885 | C | G | 1 | a0010 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.964C>G | p.Leu322Val | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/15 | 1113/5074 | 964/2046 | 322/681 | chr8 | 66883885 | |||
| chr8:66883928 | G | A | 1 | a0011 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1007G>A | p.Arg336His | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/15 | 1156/5074 | 1007/2046 | 336/681 | chr8 | 66883928 | |||
| chr8:66890906 | G | T | 1 | a0012 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.1115G>T | p.Arg372Leu | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/15 | 1264/5074 | 1115/2046 | 372/681 | chr8 | 66890906 | |||
| chr8:66896859 | C | T | 1 | a0013 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1526C>T | p.Pro509Leu | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/15 | 1675/5074 | 1526/2046 | 509/681 | chr8 | 66896859 | |||
| chr8:66896903 | C | T | 1 | a0004 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
missense_variant | MODERATE | c.1570C>T | p.Pro524Ser | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/15 | 1719/5074 | 1570/2046 | 524/681 | chr8 | 66896903 | |||
| chr8:66896925 | C | G | 1 | a0008 | 2 | NA19240.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.1592C>G | p.Ala531Gly | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/15 | 1741/5074 | 1592/2046 | 531/681 | chr8 | 66896925 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66877471 | A | C | 1 | a0001c0015 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.408A>C | p.Ala136Ala | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/15 | 557/5074 | 408/2046 | 136/681 | chr8 | 66877471 | |||
| chr8:66890892 | C | A | 1 | a0011c0011 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1101C>A | p.Val367Val | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/15 | 1250/5074 | 1101/2046 | 367/681 | chr8 | 66890892 | |||
| chr8:66901247 | G | A | 1 | a0002c0002 | 10 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(7): Show |
synonymous_variant | LOW | c.1668G>A | p.Leu556Leu | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/15 | 1817/5074 | 1668/2046 | 556/681 | chr8 | 66901247 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66870828 | C | T | 1 | a0001c0001t0008 | 2 | HG02486.hp1 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-92C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/15 | 3313 | chr8 | 66870828 | ||||||
| chr8:66874117 | A | G | 1 | a0002c0002t0018 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 2/15 | 24 | chr8 | 66874117 | ||||||
| chr8:66919368 | A | C | 2 | a0001c0001t0007 a0001c0001t0017 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*199A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 199 | chr8 | 66919368 | ||||||
| chr8:66919632 | T | A | 1 | a0001c0001t0009 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*463T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 463 | chr8 | 66919632 | ||||||
| chr8:66920152 | G | A | 1 | a0011c0011t0010 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*983G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 983 | chr8 | 66920152 | ||||||
| chr8:66920281 | T | C | 1 | a0004c0004t0003 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1112T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1112 | chr8 | 66920281 | ||||||
| chr8:66920386 | A | G | 1 | a0004c0004t0003 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1217A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1217 | chr8 | 66920386 | ||||||
| chr8:66920423 | G | A | 1 | a0004c0004t0003 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1254G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1254 | chr8 | 66920423 | ||||||
| chr8:66920473 | A | G | 15 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(12): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1304A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1304 | chr8 | 66920473 | ||||||
| chr8:66920518 | G | A | 1 | a0001c0001t0006 | 5 | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1349G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1349 | chr8 | 66920518 | ||||||
| chr8:66920572 | C | T | 1 | a0001c0001t0013 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1403C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1403 | chr8 | 66920572 | ||||||
| chr8:66921263 | C | G | 1 | a0001c0001t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2094C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2094 | chr8 | 66921263 | ||||||
| chr8:66921268 | C | T | 1 | a0001c0001t0016 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2099C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2099 | chr8 | 66921268 | ||||||
| chr8:66921346 | C | A | 3 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0016 |
10 | NA18946.hp2 NA18952.hp2 NA18957.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2177C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2177 | chr8 | 66921346 | ||||||
| chr8:66921515 | C | A | 1 | a0004c0004t0003 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2346C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2346 | chr8 | 66921515 | ||||||
| chr8:66921574 | T | C | 1 | a0003c0003t0004 | 8 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2405T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2405 | chr8 | 66921574 | ||||||
| chr8:66921696 | G | A | 1 | a0001c0001t0014 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2527G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2527 | chr8 | 66921696 | ||||||
| chr8:66921935 | T | A | 1 | a0004c0004t0003 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2766T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2766 | chr8 | 66921935 | ||||||
| chr8:66921936 | G | A | 1 | a0001c0001t0011 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2767G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2767 | chr8 | 66921936 | ||||||
| chr8:66921983 | A | G | 1 | a0001c0001t0012 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2814A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2814 | chr8 | 66921983 | ||||||
| chr8:66922038 | C | G | 10 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(7): Show |
50 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2869C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2869 | chr8 | 66922038 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66870864 | A | G | 9 | a0001c0001t0002g0019 a0001c0001t0002g0171 a0001c0001t0002g0172 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89+33A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66870864 | |||||||
| chr8:66871057 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-89+226G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871057 | |||||||
| chr8:66871108 | C | G | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-89+277C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871108 | |||||||
| chr8:66871120 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-89+289A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871120 | |||||||
| chr8:66871401 | A | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG00733.hp2 HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-89+570A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871401 | |||||||
| chr8:66871478 | C | T | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.-89+647C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871478 | |||||||
| chr8:66871519 | G | A | 2 | a0008c0007t0001g0020 a0008c0007t0001g0021 |
2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-89+688G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871519 | |||||||
| chr8:66871610 | A | G | 3 | a0006c0005t0001g0150 a0006c0005t0001g0151 a0006c0005t0001g0152 |
3 | HG01243.hp1 HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-89+779A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871610 | |||||||
| chr8:66871640 | G | T | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-89+809G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871640 | |||||||
| chr8:66871729 | A | G | 4 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89+898A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871729 | |||||||
| chr8:66871900 | C | CA | 46 | a0001c0001t0001g0043 a0001c0001t0001g0170 a0001c0001t0002g0007 others(43): Show |
52 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.-89+1083dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66871900 | ||||||
| chr8:66871900 | C | CAA | 15 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0023 others(12): Show |
16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-89+1082_-89+1083d others(4): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66871900 | ||||||
| chr8:66872587 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-88-1466C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872587 | |||||||
| chr8:66872590 | T | C | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.-88-1463T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872590 | |||||||
| chr8:66872606 | G | A | 1 | a0001c0001t0002g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-88-1447G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872606 | |||||||
| chr8:66872774 | A | G | 1 | a0001c0001t0008g0012 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-88-1279A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872774 | |||||||
| chr8:66872787 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-88-1266G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872787 | |||||||
| chr8:66872894 | C | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-88-1159C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872894 | |||||||
| chr8:66872957 | C | CA | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
11 | HG01261.hp2 HG01515.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.-88-1074dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66872957 | ||||||
| chr8:66872957 | C | CAA | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
5 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88-1075_-88-1074d others(4): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66872957 | ||||||
| chr8:66872957 | CA | C | 5 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0001t0001g0167 others(2): Show |
5 | HG01074.hp2 HG01515.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-88-1074delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66872957 | ||||||
| chr8:66872957 | CAAAAAAA others(6): Show |
C | 1 | a0004c0004t0003g0040 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-88-1086_-88-1074d others(15): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66872957 | ||||||
| chr8:66872977 | A | C | 2 | a0001c0001t0001g0141 a0001c0001t0007g0149 |
2 | HG00639.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-88-1076A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872977 | |||||||
| chr8:66872980 | C | A | 1 | a0002c0009t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-88-1073C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872980 | |||||||
| chr8:66873340 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-88-713G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66873340 | |||||||
| chr8:66873467 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-88-586A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66873467 | |||||||
| chr8:66873559 | C | T | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.-88-494C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66873559 | |||||||
| chr8:66873628 | C | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-88-425C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66873628 | |||||||
| chr8:66873722 | C | G | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-88-331C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66873722 | |||||||
| chr8:66874249 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.94+15G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 2/14 | chr8 | 66874249 | |||||||
| chr8:66874662 | A | C | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.285+76A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66874662 | |||||||
| chr8:66874851 | C | T | 21 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(18): Show |
24 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(21): Show |
intron_variant | MODIFIER | c.285+265C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66874851 | |||||||
| chr8:66875199 | T | C | 1 | a0001c0001t0008g0012 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.285+613T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875199 | |||||||
| chr8:66875277 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.285+691T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875277 | |||||||
| chr8:66875383 | A | G | 1 | a0001c0001t0002g0009 | 2 | HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.285+797A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875383 | |||||||
| chr8:66875617 | T | C | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.285+1031T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875617 | |||||||
| chr8:66875646 | T | C | 1 | a0001c0015t0001g0054 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.285+1060T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875646 | |||||||
| chr8:66875653 | A | G | 1 | a0001c0001t0007g0149 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285+1067A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875653 | |||||||
| chr8:66875798 | C | A | 1 | a0011c0011t0010g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.285+1212C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875798 | |||||||
| chr8:66875995 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG01243.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.286-1354G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875995 | |||||||
| chr8:66876002 | A | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.286-1347A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876002 | |||||||
| chr8:66876003 | T | C | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.286-1346T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876003 | |||||||
| chr8:66876124 | C | T | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.286-1225C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876124 | |||||||
| chr8:66876399 | G | A | 9 | a0001c0001t0002g0019 a0001c0001t0002g0171 a0001c0001t0002g0172 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-950G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876399 | |||||||
| chr8:66876512 | G | A | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.286-837G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876512 | |||||||
| chr8:66876518 | T | G | 16 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(13): Show |
19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.286-831T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876518 | |||||||
| chr8:66876523 | G | A | 1 | a0007c0008t0002g0035 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.286-826G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876523 | |||||||
| chr8:66876534 | T | C | 2 | a0006c0005t0001g0059 a0006c0005t0001g0060 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.286-815T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876534 | |||||||
| chr8:66876712 | A | G | 2 | a0004c0004t0003g0011 a0004c0004t0003g0039 |
3 | HG01070.hp1 HG01071.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.286-637A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876712 | |||||||
| chr8:66876757 | ATGGAGTC others(18): Show |
A | 10 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(7): Show |
10 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.286-575_286-551del others(25): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr8 | 66876757 | ||||||
| chr8:66876799 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.286-550T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876799 | |||||||
| chr8:66876828 | T | G | 13 | a0001c0001t0015g0169 a0002c0002t0002g0153 a0002c0002t0002g0156 others(10): Show |
13 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.286-521T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876828 | |||||||
| chr8:66876877 | T | C | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.286-472T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876877 | |||||||
| chr8:66876885 | C | T | 1 | a0011c0011t0010g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286-464C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876885 | |||||||
| chr8:66876981 | C | T | 5 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-368C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876981 | |||||||
| chr8:66877007 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.286-342G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66877007 | |||||||
| chr8:66877054 | C | T | 9 | a0002c0002t0002g0153 a0002c0002t0002g0157 a0002c0002t0002g0158 others(6): Show |
9 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-295C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66877054 | |||||||
| chr8:66877055 | G | A | 1 | a0004c0004t0003g0011 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.286-294G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66877055 | |||||||
| chr8:66877627 | A | C | 9 | a0001c0001t0002g0019 a0001c0001t0002g0171 a0001c0001t0002g0172 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+83A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66877627 | |||||||
| chr8:66877863 | T | TA | 5 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0003c0003t0002g0005 others(2): Show |
6 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.481+340dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 66877863 | ||||||
| chr8:66877863 | T | TAA | 7 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0171 others(4): Show |
7 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+339_481+340dup others(2): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 66877863 | ||||||
| chr8:66877863 | TA | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0134 a0001c0001t0001g0136 others(2): Show |
5 | HG01516.hp1 HG02897.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+340delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 66877863 | ||||||
| chr8:66877886 | T | C | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.481+342T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66877886 | |||||||
| chr8:66878012 | G | T | 4 | a0004c0004t0003g0010 a0004c0004t0003g0037 a0004c0004t0003g0038 others(1): Show |
5 | HG02559.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+468G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878012 | |||||||
| chr8:66878035 | C | T | 3 | a0003c0003t0004g0132 a0003c0003t0004g0133 a0007c0008t0002g0035 |
3 | HG02109.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.481+491C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878035 | |||||||
| chr8:66878102 | C | T | 1 | a0011c0011t0010g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.482-472C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878102 | |||||||
| chr8:66878392 | A | C | 9 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0158 others(6): Show |
9 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-182A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878392 | |||||||
| chr8:66878407 | G | A | 1 | a0001c0001t0008g0012 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.482-167G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878407 | |||||||
| chr8:66878415 | T | A | 1 | a0011c0011t0010g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.482-159T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878415 | |||||||
| chr8:66878928 | A | G | 2 | a0006c0005t0001g0059 a0006c0005t0001g0060 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.709+9A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66878928 | |||||||
| chr8:66879007 | A | G | 2 | a0001c0001t0002g0176 a0001c0001t0002g0177 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.709+88A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879007 | |||||||
| chr8:66879008 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.709+89C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879008 | |||||||
| chr8:66879284 | T | C | 34 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(31): Show |
37 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(34): Show |
intron_variant | MODIFIER | c.709+365T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879284 | |||||||
| chr8:66879486 | G | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.709+567G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879486 | |||||||
| chr8:66879543 | A | G | 1 | a0001c0001t0002g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.709+624A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879543 | |||||||
| chr8:66879619 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.709+700G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879619 | |||||||
| chr8:66879663 | T | G | 1 | a0001c0001t0011g0063 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.709+744T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879663 | |||||||
| chr8:66879762 | A | G | 21 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(18): Show |
24 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(21): Show |
intron_variant | MODIFIER | c.709+843A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879762 | |||||||
| chr8:66880318 | C | G | 1 | a0001c0001t0002g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.710-531C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66880318 | |||||||
| chr8:66880472 | T | C | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.710-377T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66880472 | |||||||
| chr8:66880684 | A | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.710-165A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66880684 | |||||||
| chr8:66880821 | T | C | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.710-28T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66880821 | |||||||
| chr8:66881006 | A | G | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+32A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881006 | |||||||
| chr8:66881243 | A | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+269A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881243 | |||||||
| chr8:66881516 | A | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+542A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881516 | |||||||
| chr8:66881636 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.835+662A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881636 | |||||||
| chr8:66881690 | G | T | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.835+716G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881690 | |||||||
| chr8:66881834 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.835+860A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881834 | |||||||
| chr8:66882431 | T | G | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.836-1326T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66882431 | |||||||
| chr8:66882547 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.836-1210A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66882547 | |||||||
| chr8:66882589 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.836-1168C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66882589 | |||||||
| chr8:66882865 | G | C | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
5 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.836-892G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66882865 | |||||||
| chr8:66882976 | C | A | 5 | a0001c0001t0001g0065 a0001c0001t0006g0013 a0001c0001t0006g0064 others(2): Show |
6 | HG01891.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.836-781C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66882976 | |||||||
| chr8:66883170 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.836-587A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66883170 | |||||||
| chr8:66883262 | T | G | 34 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(31): Show |
37 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(34): Show |
intron_variant | MODIFIER | c.836-495T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66883262 | |||||||
| chr8:66883309 | C | G | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.836-448C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66883309 | |||||||
| chr8:66883567 | G | A | 2 | a0001c0001t0006g0013 a0001c0001t0006g0064 |
3 | HG01891.hp1 HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.836-190G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66883567 | |||||||
| chr8:66884253 | CT | C | 8 | a0001c0001t0001g0065 a0004c0004t0003g0010 a0004c0004t0003g0011 others(5): Show |
10 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1073+260delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884253 | |||||||
| chr8:66884306 | C | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG00609.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1073+312C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884306 | |||||||
| chr8:66884324 | C | A | 1 | a0001c0001t0008g0012 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1073+330C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884324 | |||||||
| chr8:66884416 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0069 |
4 | HG01070.hp2 HG01255.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+422G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884416 | |||||||
| chr8:66884738 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1073+744A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884738 | |||||||
| chr8:66884743 | C | G | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1073+749C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884743 | |||||||
| chr8:66884884 | CTCCA | C | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1073+891_1073+894d others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884884 | |||||||
| chr8:66885027 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1073+1033T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885027 | |||||||
| chr8:66885161 | G | A | 14 | a0001c0001t0001g0071 a0001c0001t0002g0019 a0001c0001t0002g0022 others(11): Show |
15 | HG01081.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1073+1167G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885161 | |||||||
| chr8:66885167 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1073+1173A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885167 | |||||||
| chr8:66885195 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1073+1201T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885195 | |||||||
| chr8:66885204 | G | T | 4 | a0001c0001t0006g0013 a0001c0001t0006g0064 a0001c0001t0006g0066 others(1): Show |
5 | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+1210G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885204 | |||||||
| chr8:66885206 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1073+1212G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885206 | |||||||
| chr8:66885455 | A | G | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1073+1461A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885455 | |||||||
| chr8:66885479 | G | A | 2 | a0002c0002t0002g0158 a0002c0002t0018g0159 |
2 | HG02056.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1073+1485G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885479 | |||||||
| chr8:66885611 | TG | T | 5 | a0001c0001t0001g0065 a0001c0001t0006g0013 a0001c0001t0006g0064 others(2): Show |
6 | HG01891.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1073+1618delG | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885611 | |||||||
| chr8:66885824 | A | G | 1 | a0001c0001t0006g0064 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1073+1830A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885824 | |||||||
| chr8:66885955 | A | G | 1 | a0003c0003t0004g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1073+1961A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885955 | |||||||
| chr8:66886046 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+2052G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886046 | |||||||
| chr8:66886092 | T | C | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1073+2098T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886092 | |||||||
| chr8:66886121 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG01243.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1073+2127A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886121 | |||||||
| chr8:66886145 | G | A | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1073+2151G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886145 | |||||||
| chr8:66886158 | C | CT | 12 | a0001c0001t0001g0122 a0001c0001t0002g0027 a0001c0001t0002g0175 others(9): Show |
12 | HG01243.hp1 HG01891.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1073+2187dupT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66886158 | ||||||
| chr8:66886158 | CT | C | 15 | a0001c0001t0001g0045 a0001c0001t0001g0056 a0001c0001t0001g0075 others(12): Show |
15 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1073+2187delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66886158 | ||||||
| chr8:66886186 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1073+2192C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886186 | |||||||
| chr8:66886535 | G | T | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1073+2541G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886535 | |||||||
| chr8:66886570 | T | G | 1 | a0004c0004t0003g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1073+2576T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886570 | |||||||
| chr8:66886815 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
196 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.1073+2821G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886815 | |||||||
| chr8:66886849 | A | G | 6 | a0005c0006t0001g0018 a0005c0006t0001g0115 a0005c0006t0001g0116 others(3): Show |
7 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+2855A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886849 | |||||||
| chr8:66887265 | C | T | 9 | a0001c0001t0005g0006 a0001c0001t0005g0008 a0001c0001t0005g0026 others(6): Show |
10 | NA18946.hp2 NA18952.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.1073+3271C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887265 | |||||||
| chr8:66887310 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1073+3316T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887310 | |||||||
| chr8:66887315 | G | A | 9 | a0001c0001t0002g0019 a0001c0001t0002g0171 a0001c0001t0002g0172 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+3321G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887315 | |||||||
| chr8:66887384 | C | CA | 5 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0083 others(2): Show |
7 | HG00642.hp1 HG00642.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073+3408dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66887384 | ||||||
| chr8:66887384 | CA | C | 52 | a0001c0001t0001g0114 a0001c0001t0002g0007 a0001c0001t0002g0009 others(49): Show |
57 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(54): Show |
intron_variant | MODIFIER | c.1073+3408delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66887384 | ||||||
| chr8:66887384 | CAA | C | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1073+3407_1073+340 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66887384 | ||||||
| chr8:66887399 | A | G | 1 | a0011c0011t0010g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1073+3405A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887399 | |||||||
| chr8:66887547 | C | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074-3318C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887547 | |||||||
| chr8:66887856 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1074-3009A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887856 | |||||||
| chr8:66887873 | CAG | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0071 a0001c0001t0001g0112 others(2): Show |
5 | HG00621.hp1 HG01081.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-2991_1074-299 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887873 | |||||||
| chr8:66887903 | T | C | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
5 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-2962T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887903 | |||||||
| chr8:66888111 | C | T | 17 | a0001c0001t0001g0111 a0001c0001t0002g0007 a0001c0001t0002g0009 others(14): Show |
20 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(17): Show |
intron_variant | MODIFIER | c.1074-2754C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888111 | |||||||
| chr8:66888112 | G | A | 2 | a0002c0009t0002g0154 a0002c0009t0002g0155 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1074-2753G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888112 | |||||||
| chr8:66888247 | AT | A | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1074-2611delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66888247 | ||||||
| chr8:66888389 | T | C | 1 | a0001c0001t0005g0026 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1074-2476T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888389 | |||||||
| chr8:66888430 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1074-2435T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888430 | |||||||
| chr8:66888742 | T | C | 13 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0023 others(10): Show |
14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074-2123T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888742 | |||||||
| chr8:66888821 | G | A | 21 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(18): Show |
24 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1074-2044G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888821 | |||||||
| chr8:66889075 | G | A | 1 | a0009c0010t0001g0082 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1074-1790G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889075 | |||||||
| chr8:66889379 | C | T | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1074-1486C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889379 | |||||||
| chr8:66889472 | C | T | 1 | a0001c0001t0001g0004 | 3 | HG00544.hp2 NA19011.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1074-1393C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889472 | |||||||
| chr8:66889549 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1074-1316G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889549 | |||||||
| chr8:66889591 | A | G | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1074-1274A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889591 | |||||||
| chr8:66889754 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1074-1111C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889754 | |||||||
| chr8:66889968 | A | G | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1074-897A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889968 | |||||||
| chr8:66890001 | A | AT | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
5 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-863dupT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66890001 | ||||||
| chr8:66890030 | C | G | 21 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(18): Show |
24 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1074-835C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66890030 | |||||||
| chr8:66890169 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1074-696C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66890169 | |||||||
| chr8:66890402 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1074-463C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66890402 | |||||||
| chr8:66890519 | G | C | 13 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0023 others(10): Show |
14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074-346G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66890519 | |||||||
| chr8:66890555 | C | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074-310C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66890555 | |||||||
| chr8:66891293 | T | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1279+223T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891293 | |||||||
| chr8:66891434 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0140 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1279+364A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891434 | |||||||
| chr8:66891504 | G | A | 16 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(13): Show |
19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1279+434G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891504 | |||||||
| chr8:66891518 | T | A | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1279+448T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891518 | |||||||
| chr8:66891720 | C | T | 1 | a0001c0001t0012g0108 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1279+650C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891720 | |||||||
| chr8:66891917 | T | C | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1279+847T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891917 | |||||||
| chr8:66891981 | C | T | 16 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(13): Show |
19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1279+911C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891981 | |||||||
| chr8:66891995 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1279+925G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891995 | |||||||
| chr8:66892260 | C | G | 21 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(18): Show |
24 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1279+1190C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66892260 | |||||||
| chr8:66892542 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1279+1472C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66892542 | |||||||
| chr8:66892581 | G | C | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+1511G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66892581 | |||||||
| chr8:66892815 | C | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1279+1745C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66892815 | |||||||
| chr8:66892956 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1279+1886T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66892956 | |||||||
| chr8:66893174 | T | G | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1279+2104T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66893174 | |||||||
| chr8:66893688 | A | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280-2482A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66893688 | |||||||
| chr8:66893851 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1280-2319G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66893851 | |||||||
| chr8:66893865 | TG | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(116): Show |
133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1280-2303delG | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 66893865 | ||||||
| chr8:66894221 | A | G | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1280-1949A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894221 | |||||||
| chr8:66894285 | A | C | 1 | a0005c0006t0001g0018 | 2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1280-1885A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894285 | |||||||
| chr8:66894374 | T | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280-1796T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894374 | |||||||
| chr8:66894405 | A | G | 2 | a0001c0001t0002g0176 a0001c0001t0002g0177 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1280-1765A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894405 | |||||||
| chr8:66894665 | G | A | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1280-1505G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894665 | |||||||
| chr8:66894714 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1280-1456C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894714 | |||||||
| chr8:66894830 | A | T | 1 | a0001c0001t0006g0064 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1280-1340A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894830 | |||||||
| chr8:66894914 | G | A | 1 | a0001c0001t0008g0012 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1280-1256G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894914 | |||||||
| chr8:66895014 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1280-1156C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66895014 | |||||||
| chr8:66895163 | C | T | 16 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(13): Show |
19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1280-1007C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66895163 | |||||||
| chr8:66895400 | C | CT | 5 | a0005c0006t0001g0018 a0005c0006t0001g0116 a0005c0006t0001g0117 others(2): Show |
6 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-754dupT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 66895400 | ||||||
| chr8:66895400 | C | CTT | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280-755_1280-754d others(4): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 66895400 | ||||||
| chr8:66895400 | CT | C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0098 a0001c0001t0001g0110 others(6): Show |
10 | HG01891.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1280-754delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 66895400 | ||||||
| chr8:66895462 | A | G | 1 | a0006c0005t0001g0042 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1280-708A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66895462 | |||||||
| chr8:66895944 | G | A | 42 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
46 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.1280-226G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66895944 | |||||||
| chr8:66896573 | T | A | 9 | a0001c0001t0002g0019 a0001c0001t0002g0171 a0001c0001t0002g0172 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1447-207T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 11/14 | chr8 | 66896573 | |||||||
| chr8:66896620 | A | T | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1447-160A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 11/14 | chr8 | 66896620 | |||||||
| chr8:66896774 | A | G | 1 | a0003c0003t0004g0105 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.1447-6A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 11/14 | chr8 | 66896774 | |||||||
| chr8:66897413 | AAAAAAAA others(1): Show |
A | 10 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(7): Show |
10 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1626+469_1626+476d others(10): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 66897413 | ||||||
| chr8:66897728 | C | A | 6 | a0005c0006t0001g0018 a0005c0006t0001g0115 a0005c0006t0001g0116 others(3): Show |
7 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1626+769C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66897728 | |||||||
| chr8:66897915 | T | C | 1 | a0004c0004t0003g0011 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1626+956T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66897915 | |||||||
| chr8:66898001 | C | T | 6 | a0001c0001t0002g0019 a0001c0001t0002g0171 a0001c0001t0002g0172 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1626+1042C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898001 | |||||||
| chr8:66898149 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1626+1190T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898149 | |||||||
| chr8:66898166 | C | T | 1 | a0004c0004t0003g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1626+1207C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898166 | |||||||
| chr8:66898342 | T | C | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1626+1383T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898342 | |||||||
| chr8:66898366 | C | T | 2 | a0008c0007t0001g0020 a0008c0007t0001g0021 |
2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1626+1407C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898366 | |||||||
| chr8:66898624 | C | CA | 6 | a0001c0001t0001g0085 a0001c0001t0001g0136 a0001c0001t0002g0143 others(3): Show |
6 | HG01106.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1626+1684dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 66898624 | ||||||
| chr8:66898624 | CA | C | 31 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0001c0001t0001g0104 others(28): Show |
32 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(29): Show |
intron_variant | MODIFIER | c.1626+1684delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 66898624 | ||||||
| chr8:66898737 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1626+1778G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898737 | |||||||
| chr8:66898752 | G | A | 13 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0023 others(10): Show |
14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1626+1793G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898752 | |||||||
| chr8:66898868 | A | G | 6 | a0001c0001t0002g0019 a0001c0001t0002g0171 a0001c0001t0002g0172 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1626+1909A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898868 | |||||||
| chr8:66899343 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1627-1863C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899343 | |||||||
| chr8:66899644 | C | T | 1 | a0001c0001t0008g0012 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1627-1562C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899644 | |||||||
| chr8:66899680 | T | C | 1 | a0004c0004t0003g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1627-1526T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899680 | |||||||
| chr8:66899710 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1627-1496A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899710 | |||||||
| chr8:66899791 | C | T | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1627-1415C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899791 | |||||||
| chr8:66899892 | C | T | 2 | a0002c0009t0002g0154 a0002c0009t0002g0155 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1627-1314C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899892 | |||||||
| chr8:66899920 | G | A | 1 | a0010c0014t0001g0087 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1627-1286G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899920 | |||||||
| chr8:66899965 | C | CA | 13 | a0001c0001t0008g0012 a0002c0002t0002g0153 a0002c0002t0002g0156 others(10): Show |
14 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627-1232dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 66899965 | ||||||
| chr8:66900089 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1627-1117C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900089 | |||||||
| chr8:66900163 | G | A | 1 | a0008c0007t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1627-1043G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900163 | |||||||
| chr8:66900164 | C | T | 1 | a0003c0003t0002g0005 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1627-1042C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900164 | |||||||
| chr8:66900298 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1627-908C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900298 | |||||||
| chr8:66900308 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1627-898C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900308 | |||||||
| chr8:66900335 | G | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0079 a0001c0001t0001g0084 others(2): Show |
7 | HG00642.hp1 HG01346.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1627-871G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900335 | |||||||
| chr8:66900336 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1627-870G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900336 | |||||||
| chr8:66900398 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1627-808A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900398 | |||||||
| chr8:66900457 | A | C | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1627-749A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900457 | |||||||
| chr8:66900667 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1627-539C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900667 | |||||||
| chr8:66900803 | G | C | 1 | a0001c0001t0002g0145 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1627-403G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900803 | |||||||
| chr8:66900857 | C | T | 1 | a0006c0005t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1627-349C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900857 | |||||||
| chr8:66901029 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1627-177A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66901029 | |||||||
| chr8:66901086 | C | T | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1627-120C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66901086 | |||||||
| chr8:66901155 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1627-51T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66901155 | |||||||
| chr8:66901398 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
196 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.1769+50A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66901398 | |||||||
| chr8:66901630 | T | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG00609.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1769+282T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66901630 | |||||||
| chr8:66901674 | G | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1769+326G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66901674 | |||||||
| chr8:66901833 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0114 |
2 | NA18957.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1769+485A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66901833 | |||||||
| chr8:66901944 | A | T | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1769+596A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66901944 | |||||||
| chr8:66902006 | G | T | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1769+658G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902006 | |||||||
| chr8:66902127 | A | AAGAACAG others(54): Show |
1 | a0001c0001t0001g0090 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1769+783_1769+843d others(63): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902127 | ||||||
| chr8:66902408 | G | C | 1 | a0001c0001t0008g0012 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1769+1060G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902408 | |||||||
| chr8:66902684 | T | C | 1 | a0001c0001t0016g0030 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1769+1336T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902684 | |||||||
| chr8:66902692 | C | CA | 20 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0092 others(17): Show |
22 | HG01346.hp2 HG01358.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1769+1364dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902692 | ||||||
| chr8:66902692 | C | CAA | 11 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0053 others(8): Show |
12 | HG00544.hp1 HG00741.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1769+1363_1769+136 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902692 | ||||||
| chr8:66902692 | C | CAAA | 6 | a0001c0001t0002g0019 a0001c0001t0002g0173 a0001c0001t0002g0175 others(3): Show |
6 | HG02109.hp1 HG02622.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769+1362_1769+136 others(7): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902692 | ||||||
| chr8:66902692 | C | CAAAA | 6 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0002g0024 others(3): Show |
6 | HG01981.hp1 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769+1361_1769+136 others(8): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902692 | ||||||
| chr8:66902692 | CAA | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0110 a0001c0001t0001g0167 others(10): Show |
17 | HG00099.hp1 HG01070.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1769+1363_1769+136 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902692 | ||||||
| chr8:66902705 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1769+1359_1769+137 others(18): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902705 | ||||||
| chr8:66902707 | AAAAAATA others(1): Show |
A | 7 | a0001c0001t0001g0004 a0002c0002t0002g0153 a0002c0002t0002g0156 others(4): Show |
7 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1769+1361_1769+136 others(12): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902707 | ||||||
| chr8:66902707 | AAAAAATA others(7): Show |
A | 2 | a0001c0001t0007g0147 a0001c0001t0007g0149 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1769+1361_1769+137 others(18): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902707 | ||||||
| chr8:66902709 | A | T | 13 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0111 others(10): Show |
13 | HG01074.hp1 HG02622.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1769+1361A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902709 | |||||||
| chr8:66902711 | A | AAAAAAAA others(16): Show |
1 | a0004c0004t0003g0038 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(27): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | ||||||
| chr8:66902711 | A | AAAAAAAA others(15): Show |
1 | a0004c0004t0003g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(26): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | ||||||
| chr8:66902711 | A | AAAAAAAA others(16): Show |
1 | a0004c0004t0003g0040 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(27): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | ||||||
| chr8:66902711 | A | AAAAAAAA others(15): Show |
1 | a0004c0004t0003g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(26): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | ||||||
| chr8:66902711 | A | AAAAAAAA others(12): Show |
1 | a0004c0004t0003g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(23): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | ||||||
| chr8:66902711 | A | AAAAAAAA others(13): Show |
1 | a0004c0004t0003g0011 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1769+1364_1769+136 others(24): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | ||||||
| chr8:66902711 | A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(14): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | ||||||
| chr8:66902711 | A | AATATAT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0061 others(3): Show |
7 | HG00642.hp1 HG01346.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1769+1389_1769+139 others(10): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | ||||||
| chr8:66902711 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0003 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1769+1385_1769+139 others(14): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | ||||||
| chr8:66902711 | A | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0049 others(34): Show |
40 | HG00544.hp2 HG00621.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1769+1363A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902711 | |||||||
| chr8:66902711 | AAT | A | 6 | a0001c0001t0001g0135 a0001c0001t0002g0009 a0003c0003t0004g0017 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769+1393_1769+139 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | ||||||
| chr8:66902712 | AT | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0093 others(3): Show |
6 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769+1365delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902712 | |||||||
| chr8:66902712 | ATAT | A | 3 | a0001c0001t0002g0009 a0005c0006t0001g0116 a0007c0008t0002g0035 |
3 | HG01081.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1769+1365_1769+136 others(7): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902712 | |||||||
| chr8:66902713 | T | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0057 others(51): Show |
58 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1769+1365T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902713 | |||||||
| chr8:66902715 | T | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0078 others(40): Show |
47 | HG00639.hp1 HG00735.hp2 HG01993.hp2 others(44): Show |
intron_variant | MODIFIER | c.1769+1367T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902715 | |||||||
| chr8:66902717 | T | A | 20 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0009 others(17): Show |
21 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.1769+1369T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902717 | |||||||
| chr8:66902719 | T | A | 9 | a0001c0001t0002g0009 a0001c0001t0002g0143 a0001c0001t0002g0144 others(6): Show |
9 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1769+1371T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902719 | |||||||
| chr8:66902721 | T | A | 6 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0004c0004t0003g0036 others(3): Show |
6 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769+1373T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902721 | |||||||
| chr8:66902723 | T | A | 3 | a0004c0004t0003g0036 a0004c0004t0003g0037 a0007c0008t0002g0035 |
3 | HG02717.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1769+1375T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902723 | |||||||
| chr8:66902725 | T | A | 1 | a0004c0004t0003g0037 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1769+1377T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902725 | |||||||
| chr8:66902739 | T | C | 1 | a0001c0001t0005g0032 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1769+1391T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902739 | |||||||
| chr8:66902741 | T | C | 20 | a0001c0001t0001g0099 a0001c0001t0002g0007 a0001c0001t0002g0009 others(17): Show |
23 | HG01255.hp1 HG02738.hp1 HG03017.hp1 others(20): Show |
intron_variant | MODIFIER | c.1769+1393T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902741 | |||||||
| chr8:66902834 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1769+1486A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902834 | |||||||
| chr8:66902859 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1769+1511C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902859 | |||||||
| chr8:66903120 | C | CA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0049 others(33): Show |
41 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1769+1786dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66903120 | ||||||
| chr8:66903186 | A | G | 1 | a0013c0012t0001g0138 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1769+1838A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903186 | |||||||
| chr8:66903329 | ATTTATAC others(8): Show |
A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0091 |
2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1770-1894_1770-188 others(19): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66903329 | ||||||
| chr8:66903346 | T | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0091 |
2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1770-1880T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903346 | |||||||
| chr8:66903501 | G | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1770-1725G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903501 | |||||||
| chr8:66903536 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0058 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1770-1690C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903536 | |||||||
| chr8:66903637 | G | C | 5 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1770-1589G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903637 | |||||||
| chr8:66903845 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1770-1381G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903845 | |||||||
| chr8:66904565 | T | TA | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1770-660dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66904565 | ||||||
| chr8:66904947 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1770-279C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66904947 | |||||||
| chr8:66905460 | T | A | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1879+125T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905460 | |||||||
| chr8:66905503 | T | C | 1 | a0004c0004t0003g0038 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1879+168T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905503 | |||||||
| chr8:66905788 | C | T | 1 | a0013c0012t0001g0138 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1879+453C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905788 | |||||||
| chr8:66905847 | G | A | 18 | a0001c0001t0001g0065 a0001c0001t0006g0013 a0001c0001t0006g0064 others(15): Show |
21 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1879+512G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905847 | |||||||
| chr8:66905918 | T | C | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1879+583T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905918 | |||||||
| chr8:66905927 | A | C | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+592A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905927 | |||||||
| chr8:66905973 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1879+638C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905973 | |||||||
| chr8:66906019 | AG | A | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1879+685delG | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906019 | |||||||
| chr8:66906020 | G | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+685G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906020 | |||||||
| chr8:66906054 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1879+719C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906054 | |||||||
| chr8:66906237 | G | A | 6 | a0001c0001t0002g0019 a0001c0001t0002g0171 a0001c0001t0002g0172 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1879+902G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906237 | |||||||
| chr8:66906784 | A | T | 13 | a0001c0001t0001g0141 a0001c0001t0007g0147 a0001c0001t0007g0149 others(10): Show |
13 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1879+1449A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906784 | |||||||
| chr8:66906787 | T | A | 1 | a0007c0008t0002g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1879+1452T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906787 | |||||||
| chr8:66907191 | G | A | 1 | a0011c0011t0010g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1879+1856G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907191 | |||||||
| chr8:66907313 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1879+1978G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907313 | |||||||
| chr8:66907423 | A | T | 1 | a0001c0001t0005g0044 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1879+2088A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907423 | |||||||
| chr8:66907604 | G | A | 13 | a0001c0001t0015g0169 a0002c0002t0002g0153 a0002c0002t0002g0156 others(10): Show |
13 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1879+2269G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907604 | |||||||
| chr8:66907644 | G | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG00733.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1879+2309G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907644 | |||||||
| chr8:66907869 | CT | C | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+2542delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66907869 | ||||||
| chr8:66907978 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1879+2643C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907978 | |||||||
| chr8:66908165 | G | A | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1879+2830G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908165 | |||||||
| chr8:66908251 | G | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+2916G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908251 | |||||||
| chr8:66908380 | C | A | 1 | a0004c0004t0003g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1879+3045C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908380 | |||||||
| chr8:66908409 | T | A | 1 | a0001c0001t0008g0012 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1879+3074T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908409 | |||||||
| chr8:66908523 | C | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+3188C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908523 | |||||||
| chr8:66908551 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1879+3216G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908551 | |||||||
| chr8:66909176 | C | T | 4 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0007c0008t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1879+3841C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909176 | |||||||
| chr8:66909429 | G | T | 1 | a0003c0003t0004g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1879+4094G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909429 | |||||||
| chr8:66909437 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1879+4102G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909437 | |||||||
| chr8:66909809 | G | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+4474G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909809 | |||||||
| chr8:66909821 | A | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0048 others(18): Show |
24 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1879+4486A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909821 | |||||||
| chr8:66909961 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1879+4626G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909961 | |||||||
| chr8:66910079 | G | A | 7 | a0003c0003t0004g0017 a0003c0003t0004g0101 a0003c0003t0004g0102 others(4): Show |
8 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1879+4744G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910079 | |||||||
| chr8:66910180 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1879+4845T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910180 | |||||||
| chr8:66910240 | T | C | 59 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(56): Show |
66 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.1879+4905T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910240 | |||||||
| chr8:66910247 | C | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+4912C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910247 | |||||||
| chr8:66910324 | T | A | 32 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(29): Show |
35 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.1879+4989T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910324 | |||||||
| chr8:66910325 | C | G | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1879+4990C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910325 | |||||||
| chr8:66910581 | G | C | 1 | a0001c0001t0006g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1879+5246G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910581 | |||||||
| chr8:66910666 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1879+5331G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910666 | |||||||
| chr8:66910867 | C | G | 2 | a0002c0002t0002g0160 a0002c0002t0002g0163 |
2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1879+5532C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910867 | |||||||
| chr8:66911498 | G | A | 8 | a0001c0001t0001g0124 a0004c0004t0003g0010 a0004c0004t0003g0011 others(5): Show |
10 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1879+6163G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66911498 | |||||||
| chr8:66911611 | A | ATCAGGAG others(1261): Show |
7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+6291_1879+629 others(1272): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66911611 | ||||||
| chr8:66911628 | A | C | 1 | a0013c0012t0001g0138 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1879+6293A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66911628 | |||||||
| chr8:66911754 | C | T | 26 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0023 others(23): Show |
27 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.1879+6419C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66911754 | |||||||
| chr8:66911771 | C | T | 16 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(13): Show |
19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1879+6436C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66911771 | |||||||
| chr8:66912028 | G | A | 7 | a0006c0005t0001g0041 a0006c0005t0001g0042 a0006c0005t0001g0059 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1879+6693G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912028 | |||||||
| chr8:66912237 | C | T | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-6766C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912237 | |||||||
| chr8:66912238 | G | A | 3 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 |
3 | HG02109.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1880-6765G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912238 | |||||||
| chr8:66912378 | C | T | 14 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0023 others(11): Show |
15 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1880-6625C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912378 | |||||||
| chr8:66912382 | G | C | 1 | a0003c0003t0004g0132 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1880-6621G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912382 | |||||||
| chr8:66912458 | G | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-6545G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912458 | |||||||
| chr8:66912592 | A | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0069 |
4 | HG01070.hp2 HG01255.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1880-6411A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912592 | |||||||
| chr8:66912898 | G | A | 16 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(13): Show |
19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880-6105G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912898 | |||||||
| chr8:66913688 | G | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-5315G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66913688 | |||||||
| chr8:66913731 | C | T | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1880-5272C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66913731 | |||||||
| chr8:66913833 | G | A | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1880-5170G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66913833 | |||||||
| chr8:66913915 | G | A | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1880-5088G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66913915 | |||||||
| chr8:66913962 | T | TA | 23 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0136 others(20): Show |
23 | HG00099.hp2 HG00741.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1880-5018dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66913962 | ||||||
| chr8:66913962 | T | TAA | 6 | a0001c0001t0008g0012 a0002c0002t0002g0157 a0002c0002t0002g0161 others(3): Show |
7 | HG00741.hp2 HG01978.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1880-5019_1880-501 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66913962 | ||||||
| chr8:66913962 | TA | T | 31 | a0001c0001t0001g0097 a0001c0001t0001g0100 a0001c0001t0001g0130 others(28): Show |
36 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1880-5018delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66913962 | ||||||
| chr8:66914076 | G | A | 1 | a0001c0001t0008g0012 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1880-4927G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914076 | |||||||
| chr8:66914122 | A | T | 1 | a0002c0009t0002g0154 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1880-4881A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914122 | |||||||
| chr8:66914177 | A | G | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1880-4826A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914177 | |||||||
| chr8:66914217 | A | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0071 others(3): Show |
8 | HG00544.hp2 HG00621.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1880-4786A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914217 | |||||||
| chr8:66914283 | C | CA | 16 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0090 others(13): Show |
19 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880-4699dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66914283 | ||||||
| chr8:66914283 | CA | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(68): Show |
76 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.1880-4699delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66914283 | ||||||
| chr8:66914283 | CAA | C | 7 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(4): Show |
8 | HG02258.hp1 HG02809.hp1 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.1880-4700_1880-469 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66914283 | ||||||
| chr8:66914283 | CAAA | C | 18 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(15): Show |
21 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1880-4701_1880-469 others(7): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66914283 | ||||||
| chr8:66914525 | G | C | 16 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(13): Show |
19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880-4478G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914525 | |||||||
| chr8:66914793 | G | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-4210G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914793 | |||||||
| chr8:66914834 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG00609.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1880-4169G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914834 | |||||||
| chr8:66914855 | G | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG00609.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1880-4148G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914855 | |||||||
| chr8:66914972 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(88): Show |
102 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(99): Show |
intron_variant | MODIFIER | c.1880-4031T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914972 | |||||||
| chr8:66915162 | T | TA | 16 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(13): Show |
19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880-3833dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66915162 | ||||||
| chr8:66915171 | T | A | 7 | a0004c0004t0003g0010 a0004c0004t0003g0011 a0004c0004t0003g0036 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-3832T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915171 | |||||||
| chr8:66915329 | G | A | 1 | a0002c0002t0018g0159 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1880-3674G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915329 | |||||||
| chr8:66915367 | G | A | 1 | a0011c0011t0010g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1880-3636G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915367 | |||||||
| chr8:66915451 | C | CA | 12 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0157 others(9): Show |
12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1880-3540dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66915451 | ||||||
| chr8:66915451 | CA | C | 16 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(13): Show |
19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880-3540delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66915451 | ||||||
| chr8:66915495 | TTA | T | 47 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(44): Show |
51 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(48): Show |
intron_variant | MODIFIER | c.1880-3502_1880-350 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66915495 | ||||||
| chr8:66915548 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1880-3455G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915548 | |||||||
| chr8:66915640 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1880-3363C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915640 | |||||||
| chr8:66915641 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG00609.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1880-3362G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915641 | |||||||
| chr8:66915750 | G | T | 2 | a0006c0005t0001g0059 a0006c0005t0001g0060 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1880-3253G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915750 | |||||||
| chr8:66915910 | G | GA | 58 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(55): Show |
65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1880-3091dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66915910 | ||||||
| chr8:66915970 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1880-3033T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915970 | |||||||
| chr8:66916161 | G | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG00280.hp1 HG01071.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1880-2842G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66916161 | |||||||
| chr8:66916186 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0071 others(3): Show |
8 | HG00544.hp2 HG00621.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1880-2817A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66916186 | |||||||
| chr8:66916545 | C | G | 36 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0025 others(33): Show |
39 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(36): Show |
intron_variant | MODIFIER | c.1880-2458C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66916545 | |||||||
| chr8:66917158 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1880-1845A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66917158 | |||||||
| chr8:66917194 | T | C | 14 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0023 others(11): Show |
15 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1880-1809T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66917194 | |||||||
| chr8:66917290 | C | T | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
5 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1880-1713C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66917290 | |||||||
| chr8:66917892 | T | C | 59 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0019 others(56): Show |
66 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.1880-1111T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66917892 | |||||||
| chr8:66918027 | A | G | 2 | a0002c0009t0002g0154 a0002c0009t0002g0155 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1880-976A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918027 | |||||||
| chr8:66918067 | TTTTG | T | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0017g0148 |
3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1880-932_1880-929d others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66918067 | ||||||
| chr8:66918222 | C | T | 3 | a0005c0006t0001g0018 a0005c0006t0001g0115 a0005c0006t0001g0119 |
4 | HG00099.hp1 HG01192.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1880-781C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918222 | |||||||
| chr8:66918271 | T | TTG | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0048 others(19): Show |
25 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1880-731_1880-730i others(4): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66918271 | ||||||
| chr8:66918800 | G | C | 1 | a0001c0001t0002g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1880-203G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918800 | |||||||
| chr8:66918844 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1880-159G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918844 | |||||||
| chr8:66918898 | T | G | 1 | a0001c0001t0015g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1880-105T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918898 | |||||||
| chr8:66918971 | G | T | 1 | a0004c0004t0003g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1880-32G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918971 |