Item | Value |
---|---|
geneid | 55388 |
ensemblid | ENSG00000065328.17 |
hgncid | 18043 |
symbol | MCM10 |
name | minichromosome maintenance 10 replication initiation factor |
refseq_nuc | NM_018518.5 |
refseq_prot | NP_060988.3 |
ensembl_nuc | ENST00000378714.8 |
ensembl_prot | ENSP00000367986.3 |
mane_status | MANE Select |
chr | chr10 |
start | 13161558 |
end | 13211110 |
strand | + |
ver | v1.2 |
region | chr10:13161558-13211110 |
region5000 | chr10:13156558-13216110 |
regionname0 | MCM10_chr10_13161558_13211110 |
regionname5000 | MCM10_chr10_13156558_13216110 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 874 | 342 | 81 | 58 | 156 | 10 | 35 | 124 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0002 | 0/0 | 874 | 40 | 1 | 9 | 18 | 6 | 6 | 9 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0003 | 0/0 | 874 | 9 | 0 | 2 | 4 | 1 | 2 | 3 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0004 | 0/0 | 874 | 9 | 0 | 8 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0005 | 0/0 | 874 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0006 | 0/0 | 874 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0007 | 0/0 | 874 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0008 | 0/0 | 874 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0009 | 0/0 | 874 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0010 | 0/0 | 874 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0011 | 0/0 | 874 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0012 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0013 | 0/0 | 874 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0014 | 0/0 | 874 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0015 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0016 | 0/0 | 874 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0017 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0018 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0019 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0020 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0021 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0022 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
a0023 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | MDEEE others(869): Show |
chr10 | 13156558 | 13216110 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2622 | 241 | 62 | 38 | 109 | 7 | 23 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0001c0002 | 0/0 | 2622 | 72 | 2 | 20 | 36 | 3 | 11 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0001c0004 | 0/0 | 2622 | 20 | 9 | 0 | 11 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0001c0008 | 0/0 | 2622 | 5 | 5 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0001c0012 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0001c0020 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0001c0030 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0002c0003 | 0/0 | 2622 | 38 | 1 | 7 | 18 | 6 | 6 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0002c0014 | 0/0 | 2622 | 2 | 0 | 2 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0003c0007 | 0/0 | 2622 | 5 | 0 | 2 | 0 | 1 | 2 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0003c0009 | 0/0 | 2622 | 4 | 0 | 0 | 4 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0004c0005 | 0/0 | 2622 | 9 | 0 | 8 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0005c0006 | 0/0 | 2622 | 6 | 5 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0005c0026 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0006c0010 | 0/0 | 2622 | 3 | 0 | 3 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0007c0015 | 0/0 | 2622 | 2 | 0 | 0 | 0 | 1 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0008c0016 | 0/0 | 2622 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0009c0011 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0010c0013 | 0/0 | 2622 | 2 | 0 | 0 | 0 | 0 | 2 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0011c0017 | 0/0 | 2622 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0012c0028 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0013c0025 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0014c0031 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0015c0019 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0016c0023 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0017c0021 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0018c0027 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0019c0024 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0020c0018 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0021c0022 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0022c0029 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 | ||
a0023c0032 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | ATGGA others(2617): Show |
chr10 | 13156558 | 13216110 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4549 | 96 | 26 | 8 | 52 | 1 | 8 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0002 | 0/1 | 4551 | 64 | 1 | 15 | 35 | 1 | 11 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0003 | 0/0 | 4550 | 31 | 14 | 4 | 7 | 5 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0004 | 0/0 | 4551 | 4 | 2 | 1 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0005 | 0/0 | 4552 | 19 | 0 | 8 | 9 | 0 | 2 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4547): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0006 | 0/0 | 4551 | 5 | 5 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0007 | 0/0 | 4551 | 8 | 8 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0008 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0010 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0011 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0013 | 0/0 | 4550 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0015 | 0/0 | 4549 | 2 | 2 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0016 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0018 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0020 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0023 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0025 | 0/0 | 4550 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0026 | 0/0 | 4551 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0001t0027 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0002t0001 | 0/0 | 4549 | 54 | 1 | 17 | 28 | 1 | 7 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0002t0004 | 0/0 | 4551 | 5 | 1 | 1 | 0 | 0 | 3 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0002t0005 | 0/0 | 4552 | 2 | 0 | 1 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4547): Show |
chr10 | 13156558 | 13216110 |
a0001c0002t0006 | 0/0 | 4551 | 4 | 0 | 0 | 3 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0002t0008 | 0/0 | 4549 | 4 | 0 | 0 | 4 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0002t0010 | 0/0 | 4549 | 2 | 0 | 1 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0002t0024 | 0/0 | 4550 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0001c0004t0001 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0004t0003 | 0/0 | 4550 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0001c0004t0004 | 0/0 | 4551 | 16 | 8 | 0 | 8 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0004t0014 | 0/0 | 4551 | 2 | 1 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0008t0007 | 0/0 | 4551 | 4 | 4 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0001c0008t0011 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0001c0012t0001 | 0/0 | 4549 | 2 | 2 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0001c0020t0003 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0001c0030t0003 | 0/0 | 4550 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0002c0003t0001 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0002c0003t0002 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0002c0003t0003 | 0/0 | 4550 | 22 | 0 | 2 | 11 | 3 | 6 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0002c0003t0005 | 0/0 | 4552 | 3 | 1 | 1 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4547): Show |
chr10 | 13156558 | 13216110 |
a0002c0003t0006 | 0/0 | 4551 | 4 | 0 | 0 | 4 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0002c0003t0009 | 0/0 | 4552 | 4 | 0 | 2 | 0 | 2 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4547): Show |
chr10 | 13156558 | 13216110 |
a0002c0003t0012 | 0/0 | 4549 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0002c0003t0019 | 0/0 | 4550 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0002c0014t0003 | 0/0 | 4550 | 2 | 0 | 2 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0003c0007t0003 | 0/0 | 4550 | 5 | 0 | 2 | 0 | 1 | 2 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0003c0009t0006 | 0/0 | 4551 | 4 | 0 | 0 | 4 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0004c0005t0002 | 0/0 | 4551 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0004c0005t0004 | 0/0 | 4551 | 6 | 0 | 6 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0004c0005t0005 | 0/0 | 4552 | 2 | 0 | 2 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4547): Show |
chr10 | 13156558 | 13216110 |
a0005c0006t0006 | 0/0 | 4551 | 2 | 2 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0005c0006t0007 | 0/0 | 4551 | 3 | 2 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0005c0006t0017 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0005c0026t0004 | 0/0 | 4551 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0006c0010t0002 | 0/0 | 4551 | 3 | 0 | 3 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0007c0015t0001 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0007c0015t0002 | 0/0 | 4551 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0008c0016t0002 | 0/0 | 4551 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0009c0011t0002 | 0/0 | 4551 | 2 | 2 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0010c0013t0003 | 0/0 | 4550 | 2 | 0 | 0 | 0 | 0 | 2 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0011c0017t0004 | 0/0 | 4551 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0012c0028t0003 | 0/0 | 4550 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0013c0025t0001 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0014c0031t0003 | 0/0 | 4550 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4545): Show |
chr10 | 13156558 | 13216110 |
a0015c0019t0021 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0016c0023t0001 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0017c0021t0001 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0018c0027t0022 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0019c0024t0004 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0020c0018t0004 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0021c0022t0001 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4544): Show |
chr10 | 13156558 | 13216110 |
a0022c0029t0004 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
a0023c0032t0004 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | GGAAT others(4546): Show |
chr10 | 13156558 | 13216110 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0334 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0002g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0003g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0005g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0006g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0006g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0006g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0007g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0010g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0011g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0013g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0015g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0016g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0018g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0020g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0023g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0025g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0026g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0001t0027g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0001g0386 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0004g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0006g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0006g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0008g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0008g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0008g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0008g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0010g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0010g0388 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0002t0024g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0004g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0014g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0004t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0008t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0008t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0008t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0008t0007g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0008t0011g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0012t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0012t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0020t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0001c0030t0003g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0005g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0006g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0006g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0006g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0009g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0009g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0009g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0009g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0012g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0012g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0003t0019g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0014t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0002c0014t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0003c0007t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0003c0007t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0003c0007t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0003c0007t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0003c0007t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0003c0009t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0003c0009t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0003c0009t0006g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0003c0009t0006g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0004c0005t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0004c0005t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0004c0005t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0004c0005t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0004c0005t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0004c0005t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0004c0005t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0004c0005t0005g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0004c0005t0005g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0005c0006t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0005c0006t0006g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0005c0006t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0005c0006t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0005c0006t0007g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0005c0006t0017g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0005c0026t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0006c0010t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0006c0010t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0006c0010t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0007c0015t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0007c0015t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0008c0016t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0008c0016t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0009c0011t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0010c0013t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0011c0017t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0011c0017t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0012c0028t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0013c0025t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0014c0031t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0015c0019t0021g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0016c0023t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0017c0021t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0018c0027t0022g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0019c0024t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0020c0018t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0021c0022t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0022c0029t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
a0023c0032t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0110 | EUR | GBR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0386 | EUR | GBR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00140 | hp1 | a0002 | c0003 | t0003 | g0165 | EUR | GBR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00140 | hp2 | a0002 | c0003 | t0005 | g0176 | EUR | GBR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00280 | hp1 | a0002 | c0003 | t0003 | g0310 | EUR | FIN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0128 | EUR | FIN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00323 | hp1 | a0002 | c0003 | t0003 | g0229 | EUR | FIN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00323 | hp2 | a0001 | c0002 | t0005 | g0111 | EUR | FIN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00408 | hp1 | a0002 | c0003 | t0003 | g0277 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00408 | hp2 | a0003 | c0009 | t0006 | g0219 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00423 | hp2 | a0002 | c0003 | t0006 | g0163 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00544 | hp2 | a0002 | c0003 | t0003 | g0285 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00558 | hp1 | a0001 | c0002 | t0008 | g0339 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00558 | hp2 | a0002 | c0003 | t0003 | g0275 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00597 | hp2 | a0002 | c0003 | t0003 | g0046 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00621 | hp2 | a0012 | c0028 | t0003 | g0337 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0231 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00639 | hp2 | a0001 | c0002 | t0005 | g0234 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0351 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00673 | hp1 | a0002 | c0003 | t0003 | g0284 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | CHS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00733 | hp2 | a0002 | c0003 | t0009 | g0385 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01069 | hp2 | a0003 | c0007 | t0003 | g0058 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01074 | hp1 | a0001 | c0002 | t0010 | g0349 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01074 | hp2 | a0002 | c0003 | t0003 | g0168 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01081 | hp1 | a0001 | c0001 | t0026 | g0054 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0173 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0327 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01106 | hp2 | a0005 | c0006 | t0007 | g0270 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01109 | hp2 | a0004 | c0005 | t0005 | g0344 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01167 | hp2 | a0002 | c0014 | t0003 | g0170 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01169 | hp1 | a0002 | c0014 | t0003 | g0169 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01169 | hp2 | a0004 | c0005 | t0005 | g0317 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0174 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01175 | hp2 | a0003 | c0007 | t0003 | g0052 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01243 | hp1 | a0013 | c0025 | t0001 | g0263 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01243 | hp2 | a0002 | c0003 | t0019 | g0047 | AMR | PUR | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01255 | hp2 | a0001 | c0002 | t0004 | g0129 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01256 | hp1 | a0005 | c0026 | t0004 | g0313 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01257 | hp1 | a0004 | c0005 | t0004 | g0345 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01346 | hp2 | a0002 | c0003 | t0005 | g0383 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01358 | hp2 | a0004 | c0005 | t0004 | g0133 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01433 | hp1 | a0014 | c0031 | t0003 | g0276 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01496 | hp1 | a0004 | c0005 | t0004 | g0203 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0324 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0308 | EUR | IBS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01515 | hp2 | a0007 | c0015 | t0001 | g0300 | EUR | IBS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01516 | hp1 | a0002 | c0003 | t0009 | g0108 | EUR | IBS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01516 | hp2 | a0003 | c0007 | t0003 | g0053 | EUR | IBS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01517 | hp1 | a0002 | c0003 | t0009 | g0107 | EUR | IBS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0309 | EUR | IBS | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01884 | hp1 | a0015 | c0019 | t0021 | g0064 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01891 | hp2 | a0001 | c0008 | t0007 | g0033 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01928 | hp2 | a0006 | c0010 | t0002 | g0023 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01934 | hp1 | a0004 | c0005 | t0004 | g0204 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0283 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0338 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02004 | hp1 | a0006 | c0010 | t0002 | g0319 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0331 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02055 | hp2 | a0001 | c0012 | t0001 | g0150 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0350 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02074 | hp1 | a0001 | c0002 | t0006 | g0018 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02083 | hp2 | a0008 | c0016 | t0002 | g0330 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02132 | hp2 | a0002 | c0003 | t0003 | g0166 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02145 | hp1 | a0001 | c0004 | t0004 | g0152 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0392 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02148 | hp1 | a0002 | c0003 | t0009 | g0387 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02148 | hp2 | a0004 | c0005 | t0004 | g0202 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02155 | hp1 | a0002 | c0003 | t0003 | g0167 | EAS | CDX | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02155 | hp2 | a0001 | c0002 | t0006 | g0018 | EAS | CDX | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CDX | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | CDX | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02257 | hp2 | a0001 | c0004 | t0004 | g0042 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0230 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02293 | hp2 | a0004 | c0005 | t0004 | g0132 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02300 | hp2 | a0006 | c0010 | t0002 | g0177 | AMR | PEL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | KHV | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02572 | hp1 | a0001 | c0008 | t0007 | g0262 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0394 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02602 | hp1 | a0016 | c0023 | t0001 | g0065 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02615 | hp1 | a0005 | c0006 | t0006 | g0369 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02615 | hp2 | a0017 | c0021 | t0001 | g0036 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02622 | hp1 | a0001 | c0020 | t0003 | g0347 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0367 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02630 | hp1 | a0001 | c0008 | t0007 | g0068 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02630 | hp2 | a0018 | c0027 | t0022 | g0393 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0243 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02698 | hp2 | a0002 | c0003 | t0003 | g0161 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02723 | hp2 | a0001 | c0004 | t0004 | g0272 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02738 | hp1 | a0002 | c0003 | t0003 | g0224 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0366 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02809 | hp2 | a0005 | c0006 | t0007 | g0040 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0371 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02886 | hp1 | a0001 | c0004 | t0004 | g0260 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02896 | hp2 | a0009 | c0011 | t0002 | g0006 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02897 | hp2 | a0009 | c0011 | t0002 | g0006 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02965 | hp2 | a0001 | c0001 | t0027 | g0156 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02976 | hp2 | a0001 | c0004 | t0004 | g0151 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0273 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0382 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03098 | hp2 | a0001 | c0004 | t0004 | g0039 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0223 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03139 | hp1 | a0001 | c0012 | t0001 | g0269 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0012 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03195 | hp1 | a0001 | c0001 | t0015 | g0012 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0084 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03225 | hp1 | a0005 | c0006 | t0006 | g0306 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03225 | hp2 | a0001 | c0004 | t0014 | g0157 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03239 | hp1 | a0002 | c0003 | t0003 | g0304 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03453 | hp2 | a0019 | c0024 | t0004 | g0256 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03486 | hp2 | a0001 | c0008 | t0011 | g0268 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03490 | hp1 | a0010 | c0013 | t0003 | g0026 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0368 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03492 | hp1 | a0010 | c0013 | t0003 | g0026 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03540 | hp1 | a0005 | c0006 | t0007 | g0155 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03579 | hp1 | a0020 | c0018 | t0004 | g0086 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0342 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0365 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0186 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | STU | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03688 | hp2 | a0007 | c0015 | t0002 | g0214 | SAS | STU | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0096 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0211 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0318 | SAS | BEB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03834 | hp1 | a0002 | c0003 | t0003 | g0145 | SAS | BEB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03927 | hp1 | a0001 | c0002 | t0006 | g0134 | SAS | BEB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03942 | hp1 | a0001 | c0002 | t0004 | g0312 | SAS | BEB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | STU | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG04184 | hp2 | a0003 | c0007 | t0003 | g0316 | SAS | BEB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | STU | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG04199 | hp2 | a0001 | c0002 | t0004 | g0144 | SAS | STU | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG04204 | hp1 | a0004 | c0005 | t0002 | g0346 | SAS | STU | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG04204 | hp2 | a0002 | c0003 | t0003 | g0245 | SAS | STU | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG04228 | hp2 | a0002 | c0003 | t0003 | g0185 | SAS | STU | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | YRI | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | CHB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18612 | hp2 | a0002 | c0003 | t0003 | g0307 | EAS | CHB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18906 | hp1 | a0001 | c0008 | t0007 | g0067 | AFR | YRI | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0038 | AFR | YRI | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0391 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18947 | hp1 | a0001 | c0004 | t0004 | g0323 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18948 | hp1 | a0002 | c0003 | t0006 | g0376 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18952 | hp2 | a0001 | c0001 | t0020 | g0192 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0379 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18959 | hp1 | a0008 | c0016 | t0002 | g0195 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18967 | hp1 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18968 | hp1 | a0001 | c0004 | t0004 | g0005 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18972 | hp2 | a0001 | c0001 | t0013 | g0059 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18973 | hp1 | a0002 | c0003 | t0006 | g0378 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18977 | hp1 | a0001 | c0001 | t0013 | g0340 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18977 | hp2 | a0021 | c0022 | t0001 | g0250 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18978 | hp2 | a0001 | c0001 | t0005 | g0362 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18980 | hp1 | a0002 | c0003 | t0003 | g0013 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18981 | hp1 | a0001 | c0002 | t0008 | g0020 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18985 | hp1 | a0001 | c0004 | t0004 | g0088 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18990 | hp1 | a0011 | c0017 | t0004 | g0246 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18991 | hp1 | a0001 | c0002 | t0024 | g0001 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18991 | hp2 | a0002 | c0003 | t0003 | g0184 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18992 | hp1 | a0001 | c0004 | t0001 | g0070 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18994 | hp1 | a0001 | c0002 | t0008 | g0325 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19000 | hp2 | a0001 | c0001 | t0016 | g0140 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0380 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19002 | hp2 | a0001 | c0001 | t0008 | g0092 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19003 | hp1 | a0002 | c0003 | t0006 | g0377 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19003 | hp2 | a0001 | c0004 | t0003 | g0181 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19005 | hp2 | a0022 | c0029 | t0004 | g0322 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19009 | hp2 | a0002 | c0003 | t0012 | g0153 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19010 | hp2 | a0001 | c0004 | t0004 | g0005 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | LWK | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0375 | AFR | LWK | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0373 | AFR | LWK | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0374 | AFR | LWK | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19056 | hp1 | a0023 | c0032 | t0004 | g0063 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19056 | hp2 | a0003 | c0009 | t0006 | g0363 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19058 | hp2 | a0002 | c0003 | t0012 | g0013 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0358 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19063 | hp2 | a0001 | c0004 | t0004 | g0071 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0381 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19068 | hp1 | a0001 | c0001 | t0025 | g0004 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19068 | hp2 | a0011 | c0017 | t0004 | g0098 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19074 | hp2 | a0001 | c0004 | t0004 | g0069 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19075 | hp2 | a0003 | c0009 | t0006 | g0364 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19077 | hp1 | a0001 | c0004 | t0004 | g0072 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19080 | hp1 | a0002 | c0003 | t0003 | g0328 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19080 | hp2 | a0001 | c0002 | t0006 | g0326 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19084 | hp1 | a0001 | c0002 | t0008 | g0241 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19084 | hp2 | a0002 | c0003 | t0002 | g0126 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19085 | hp1 | a0001 | c0004 | t0004 | g0100 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19087 | hp2 | a0003 | c0009 | t0006 | g0123 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0390 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19091 | hp1 | a0001 | c0004 | t0014 | g0099 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | YRI | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | YRI | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | ASW | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ASW | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | TSI | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA20752 | hp2 | a0001 | c0002 | t0010 | g0388 | EUR | TSI | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0162 | EUR | TSI | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA20905 | hp1 | a0003 | c0007 | t0003 | g0051 | SAS | GIH | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA20905 | hp2 | a0001 | c0030 | t0003 | g0354 | SAS | GIH | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01123 | hp1 | a0002 | c0003 | t0003 | g0228 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG01123 | hp2 | a0001 | c0001 | t0023 | g0361 | AMR | CLM | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02109 | hp1 | a0001 | c0004 | t0004 | g0222 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0207 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG06807 | hp1 | a0001 | c0004 | t0004 | g0372 | AFR | USA | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
HG06807 | hp2 | a0001 | c0001 | t0010 | g0384 | AFR | USA | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA20300 | hp1 | a0005 | c0006 | t0017 | g0206 | AFR | USA | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | USA | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA21309 | hp1 | a0002 | c0003 | t0005 | g0032 | AFR | LWK | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0334 | REF | REF | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0094 | REF | REF | MCM10_chr10_13156558_13216110 | MCM10 | chr10 | 13156558 | 13216110 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:13171036 | C | T | 2 | a0011 a0023 |
3 | NA18990.hp1 NA19056.hp1 NA19068.hp2 |
missense_variant | MODERATE | c.122C>T | p.Ala41Val | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/20 | 246/4549 | 122/2625 | 41/874 | chr10 | 13171036 | |||
chr10:13171117 | G | C | 1 | a0009 | 2 | HG02896.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.203G>C | p.Arg68Thr | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/20 | 327/4549 | 203/2625 | 68/874 | chr10 | 13171117 | |||
chr10:13171188 | G | T | 1 | a0014 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.274G>T | p.Ala92Ser | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/20 | 398/4549 | 274/2625 | 92/874 | chr10 | 13171188 | |||
chr10:13172427 | A | G | 1 | a0004 | 9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
missense_variant | MODERATE | c.401A>G | p.Lys134Arg | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 4/20 | 525/4549 | 401/2625 | 134/874 | chr10 | 13172427 | |||
chr10:13172715 | C | T | 1 | a0022 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.542C>T | p.Ala181Val | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/20 | 666/4549 | 542/2625 | 181/874 | chr10 | 13172715 | |||
chr10:13172753 | G | C | 1 | a0003 | 9 | HG00408.hp2 HG01069.hp2 HG01175.hp2 others(6): Show |
missense_variant | MODERATE | c.580G>C | p.Ala194Pro | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/20 | 704/4549 | 580/2625 | 194/874 | chr10 | 13172753 | |||
chr10:13175560 | C | G | 2 | a0008 a0012 |
3 | HG00621.hp2 HG02083.hp2 NA18959.hp1 |
missense_variant | MODERATE | c.643C>G | p.Gln215Glu | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/20 | 767/4549 | 643/2625 | 215/874 | chr10 | 13175560 | |||
chr10:13175630 | G | A | 1 | a0020 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.713G>A | p.Gly238Glu | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/20 | 837/4549 | 713/2625 | 238/874 | chr10 | 13175630 | |||
chr10:13180452 | G | A | 1 | a0015 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.775G>A | p.Val259Ile | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/20 | 899/4549 | 775/2625 | 259/874 | chr10 | 13180452 | |||
chr10:13182970 | G | A | 1 | a0006 | 3 | HG01928.hp2 HG02004.hp1 HG02300.hp2 |
missense_variant | MODERATE | c.968G>A | p.Arg323His | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/20 | 1092/4549 | 968/2625 | 323/874 | chr10 | 13182970 | |||
chr10:13186177 | T | C | 1 | a0017 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1112T>C | p.Ile371Thr | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/20 | 1236/4549 | 1112/2625 | 371/874 | chr10 | 13186177 | |||
chr10:13186228 | C | G | 1 | a0018 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1163C>G | p.Thr388Ser | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/20 | 1287/4549 | 1163/2625 | 388/874 | chr10 | 13186228 | |||
chr10:13188915 | C | T | 1 | a0007 | 2 | HG01515.hp2 HG03688.hp2 |
missense_variant | MODERATE | c.1250C>T | p.Ala417Val | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/20 | 1374/4549 | 1250/2625 | 417/874 | chr10 | 13188915 | |||
chr10:13188995 | C | T | 1 | a0019 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1330C>T | p.Arg444Cys | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/20 | 1454/4549 | 1330/2625 | 444/874 | chr10 | 13188995 | |||
chr10:13192356 | A | T | 2 | a0003 a0005 |
16 | HG00408.hp2 HG01069.hp2 HG01106.hp2 others(13): Show |
missense_variant | MODERATE | c.1618A>T | p.Thr540Ser | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 12/20 | 1742/4549 | 1618/2625 | 540/874 | chr10 | 13192356 | |||
chr10:13197651 | A | G | 4 | a0002 a0010 a0012 others(1): Show |
44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
missense_variant | MODERATE | c.2003A>G | p.Lys668Arg | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/20 | 2127/4549 | 2003/2625 | 668/874 | chr10 | 13197651 | |||
chr10:13198713 | G | A | 1 | a0010 | 2 | HG03490.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.2144G>A | p.Arg715Lys | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/20 | 2268/4549 | 2144/2625 | 715/874 | chr10 | 13198713 | |||
chr10:13204349 | C | T | 2 | a0011 a0013 |
3 | HG01243.hp1 NA18990.hp1 NA19068.hp2 |
missense_variant | MODERATE | c.2483C>T | p.Pro828Leu | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/20 | 2607/4549 | 2483/2625 | 828/874 | chr10 | 13204349 | |||
chr10:13209099 | G | A | 1 | a0016 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.2507G>A | p.Gly836Asp | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 19/20 | 2631/4549 | 2507/2625 | 836/874 | chr10 | 13209099 | |||
chr10:13209117 | G | A | 1 | a0021 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.2525G>A | p.Arg842Gln | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 19/20 | 2649/4549 | 2525/2625 | 842/874 | chr10 | 13209117 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:13171232 | C | G | 1 | a0001c0030 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.318C>G | p.Pro106Pro | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/20 | 442/4549 | 318/2625 | 106/874 | chr10 | 13171232 | |||
chr10:13175628 | T | G | 1 | a0020c0018 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.711T>G | p.Ser237Ser | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/20 | 835/4549 | 711/2625 | 237/874 | chr10 | 13175628 | |||
chr10:13175637 | G | T | 1 | a0020c0018 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.720G>T | p.Thr240Thr | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/20 | 844/4549 | 720/2625 | 240/874 | chr10 | 13175637 | |||
chr10:13180508 | T | C | 2 | a0001c0008 a0001c0020 |
6 | HG01891.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
synonymous_variant | LOW | c.831T>C | p.Ser277Ser | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/20 | 955/4549 | 831/2625 | 277/874 | chr10 | 13180508 | |||
chr10:13188934 | C | T | 2 | a0003c0007 a0005c0026 |
6 | HG01069.hp2 HG01175.hp2 HG01256.hp1 others(3): Show |
synonymous_variant | LOW | c.1269C>T | p.Ser423Ser | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/20 | 1393/4549 | 1269/2625 | 423/874 | chr10 | 13188934 | |||
chr10:13188950 | C | T | 6 | a0001c0002 a0001c0008 a0001c0030 others(3): Show |
90 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(87): Show |
synonymous_variant | LOW | c.1285C>T | p.Leu429Leu | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/20 | 1409/4549 | 1285/2625 | 429/874 | chr10 | 13188950 | |||
chr10:13195101 | C | T | 1 | a0002c0014 | 2 | HG01167.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.1806C>T | p.Pro602Pro | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/20 | 1930/4549 | 1806/2625 | 602/874 | chr10 | 13195101 | |||
chr10:13201456 | A | T | 1 | a0001c0012 | 2 | HG02055.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.2274A>T | p.Pro758Pro | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/20 | 2398/4549 | 2274/2625 | 758/874 | chr10 | 13201456 | |||
chr10:13204284 | T | C | 5 | a0001c0004 a0011c0017 a0019c0024 others(2): Show |
25 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(22): Show |
synonymous_variant | LOW | c.2418T>C | p.His806His | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/20 | 2542/4549 | 2418/2625 | 806/874 | chr10 | 13204284 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:13164169 | C | T | 3 | a0001c0001t0015 a0001c0001t0027 a0001c0004t0014 |
5 | HG02965.hp2 HG03139.hp2 HG03195.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-34C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/20 | chr10 | 13164169 | |||||||
chr10:13209785 | C | A | 2 | a0001c0001t0011 a0001c0008t0011 |
2 | HG02622.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*475C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 475 | chr10 | 13209785 | ||||||
chr10:13209808 | G | A | 1 | a0001c0001t0016 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*498G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 498 | chr10 | 13209808 | ||||||
chr10:13209867 | G | T | 1 | a0001c0001t0026 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*557G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 557 | chr10 | 13209867 | ||||||
chr10:13209911 | T | G | 6 | a0001c0001t0006 a0001c0002t0006 a0002c0003t0006 others(3): Show |
20 | HG00408.hp2 HG00423.hp2 HG02074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*601T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 601 | chr10 | 13209911 | ||||||
chr10:13209973 | T | G | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(47): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*663T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 663 | chr10 | 13209973 | ||||||
chr10:13209987 | G | C | 1 | a0002c0003t0012 | 2 | NA19009.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*677G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 677 | chr10 | 13209987 | ||||||
chr10:13209987 | G | GC | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(47): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*677_*678insC | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 678 | chr10 | 13209987 | ||||||
chr10:13209999 | A | C | 2 | a0001c0001t0008 a0001c0002t0008 |
5 | HG00558.hp1 NA18981.hp1 NA18994.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*689A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 689 | chr10 | 13209999 | ||||||
chr10:13210045 | A | AT | 7 | a0001c0001t0005 a0001c0001t0025 a0001c0002t0005 others(4): Show |
32 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*745dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 746 | INFO_REALIGN_3_PRIME | chr10 | 13210045 | |||||
chr10:13210055 | T | A | 1 | a0001c0001t0018 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*745T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 745 | chr10 | 13210055 | ||||||
chr10:13210064 | T | A | 1 | a0002c0003t0019 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*754T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 754 | chr10 | 13210064 | ||||||
chr10:13210120 | C | T | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*810C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 810 | chr10 | 13210120 | ||||||
chr10:13210200 | G | A | 1 | a0001c0001t0023 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*890G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 890 | chr10 | 13210200 | ||||||
chr10:13210309 | T | C | 14 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(11): Show |
93 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*999T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 999 | chr10 | 13210309 | ||||||
chr10:13210313 | C | CA | 38 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(35): Show |
184 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1019dupA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 1020 | INFO_REALIGN_3_PRIME | chr10 | 13210313 | |||||
chr10:13210387 | C | T | 1 | a0002c0003t0009 | 4 | HG00733.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1077C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 1077 | chr10 | 13210387 | ||||||
chr10:13210503 | T | A | 4 | a0001c0001t0007 a0001c0001t0027 a0001c0008t0007 others(1): Show |
16 | HG01106.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1193T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 1193 | chr10 | 13210503 | ||||||
chr10:13210598 | G | A | 2 | a0001c0001t0010 a0001c0002t0010 |
3 | HG01074.hp1 HG06807.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1288G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 1288 | chr10 | 13210598 | ||||||
chr10:13210832 | T | C | 14 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(11): Show |
93 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1522T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 20/20 | 1522 | chr10 | 13210832 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:13161627 | G | T | 2 | a0001c0001t0003g0394 a0018c0027t0022g0393 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-76+21G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13161627 | |||||||
chr10:13161663 | G | T | 1 | a0001c0001t0006g0392 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-76+57G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13161663 | |||||||
chr10:13161711 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0389 a0001c0001t0001g0390 others(2): Show |
6 | NA18943.hp2 NA18961.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.-76+105C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13161711 | |||||||
chr10:13161772 | A | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(271): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.-76+166A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13161772 | |||||||
chr10:13161831 | C | T | 6 | a0001c0001t0010g0384 a0001c0002t0001g0386 a0001c0002t0010g0388 others(3): Show |
6 | HG00099.hp2 HG00733.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-76+225C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13161831 | |||||||
chr10:13161834 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-76+228C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13161834 | |||||||
chr10:13161891 | TATTC | T | 118 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0146 others(115): Show |
135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-76+309_-76+312del others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr10 | 13161891 | ||||||
chr10:13161891 | TATTCATT others(5): Show |
T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0029 others(153): Show |
165 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.-76+301_-76+312del others(12): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr10 | 13161891 | ||||||
chr10:13162283 | AAG | A | 7 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0149 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-76+687_-76+688del others(2): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr10 | 13162283 | ||||||
chr10:13162413 | A | C | 1 | a0001c0001t0007g0382 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-76+807A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13162413 | |||||||
chr10:13162556 | G | A | 2 | a0001c0008t0007g0033 a0002c0003t0005g0032 |
2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-76+950G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13162556 | |||||||
chr10:13162704 | A | G | 2 | a0001c0002t0004g0144 a0002c0003t0003g0145 |
2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-76+1098A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13162704 | |||||||
chr10:13162905 | C | T | 6 | a0001c0001t0002g0379 a0001c0001t0002g0380 a0001c0002t0001g0381 others(3): Show |
6 | NA18948.hp1 NA18953.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.-75-1223C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13162905 | |||||||
chr10:13162941 | T | A | 2 | a0001c0001t0001g0244 a0001c0002t0004g0243 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-75-1187T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13162941 | |||||||
chr10:13162994 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-75-1134G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13162994 | |||||||
chr10:13163003 | C | T | 1 | a0001c0001t0005g0022 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-75-1125C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163003 | |||||||
chr10:13163006 | G | A | 7 | a0001c0001t0001g0249 a0001c0001t0001g0251 a0001c0001t0002g0247 others(4): Show |
7 | HG00609.hp1 HG01981.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.-75-1122G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163006 | |||||||
chr10:13163062 | G | T | 2 | a0001c0002t0004g0144 a0002c0003t0003g0145 |
2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-75-1066G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163062 | |||||||
chr10:13163074 | C | CA | 16 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0154 others(13): Show |
16 | HG02257.hp2 HG02258.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.-75-1040dupA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr10 | 13163074 | ||||||
chr10:13163074 | CA | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0375 a0001c0001t0003g0374 others(2): Show |
6 | HG01884.hp2 HG06807.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.-75-1040delA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr10 | 13163074 | ||||||
chr10:13163195 | C | T | 7 | a0001c0001t0001g0021 a0001c0002t0001g0020 a0001c0002t0001g0239 others(4): Show |
8 | NA18950.hp1 NA18954.hp2 NA18981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-75-933C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163195 | |||||||
chr10:13163270 | C | T | 1 | a0001c0001t0006g0371 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-75-858C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163270 | |||||||
chr10:13163281 | G | A | 1 | a0005c0006t0007g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-75-847G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163281 | |||||||
chr10:13163324 | G | C | 3 | a0001c0001t0001g0244 a0001c0002t0004g0243 a0019c0024t0004g0256 |
3 | HG02647.hp2 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-75-804G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163324 | |||||||
chr10:13163490 | A | G | 325 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(322): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.-75-638A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163490 | |||||||
chr10:13163592 | A | AGTGT | 74 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0029 others(71): Show |
80 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-75-536_-75-535ins others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163592 | |||||||
chr10:13163595 | C | CCACG | 74 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0029 others(71): Show |
80 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-75-533_-75-532ins others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163595 | |||||||
chr10:13163597 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0029 others(71): Show |
80 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-75-531T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163597 | |||||||
chr10:13163687 | T | TTG | 165 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(162): Show |
179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.-75-425_-75-424dup others(2): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr10 | 13163687 | ||||||
chr10:13163687 | TTG | T | 4 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0004g0257 others(1): Show |
4 | HG02257.hp1 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-75-425_-75-424del others(2): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr10 | 13163687 | ||||||
chr10:13163709 | T | C | 2 | a0001c0001t0003g0394 a0018c0027t0022g0393 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-75-419T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163709 | |||||||
chr10:13163712 | A | T | 1 | a0001c0004t0004g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-75-416A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163712 | |||||||
chr10:13163742 | G | T | 3 | a0001c0001t0001g0244 a0001c0002t0004g0243 a0019c0024t0004g0256 |
3 | HG02647.hp2 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-75-386G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163742 | |||||||
chr10:13163743 | C | A | 3 | a0001c0001t0001g0244 a0001c0002t0004g0243 a0019c0024t0004g0256 |
3 | HG02647.hp2 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-75-385C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163743 | |||||||
chr10:13163773 | C | A | 1 | a0001c0001t0003g0261 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-75-355C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163773 | |||||||
chr10:13163773 | C | G | 321 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(318): Show |
352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.-75-355C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163773 | |||||||
chr10:13163867 | C | T | 2 | a0001c0001t0001g0251 a0021c0022t0001g0250 |
2 | NA18977.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-75-261C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 1/19 | chr10 | 13163867 | |||||||
chr10:13164233 | A | T | 319 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(316): Show |
350 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.7+24A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13164233 | |||||||
chr10:13164296 | G | A | 3 | a0001c0001t0001g0244 a0001c0002t0004g0243 a0019c0024t0004g0256 |
3 | HG02647.hp2 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7+87G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13164296 | |||||||
chr10:13164336 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0003g0159 |
2 | HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.7+127T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13164336 | |||||||
chr10:13164401 | C | T | 95 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0030 others(92): Show |
102 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.7+192C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13164401 | |||||||
chr10:13164824 | C | T | 1 | a0001c0001t0005g0019 | 2 | HG00438.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.7+615C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13164824 | |||||||
chr10:13164971 | G | GT | 11 | a0001c0001t0001g0225 a0001c0001t0001g0370 a0001c0001t0003g0041 others(8): Show |
11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.7+769dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13164971 | ||||||
chr10:13164978 | T | A | 6 | a0001c0001t0002g0034 a0001c0001t0002g0253 a0001c0001t0003g0162 others(3): Show |
6 | HG01516.hp1 HG01517.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+769T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13164978 | |||||||
chr10:13165047 | A | T | 1 | a0001c0002t0001g0368 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.7+838A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165047 | |||||||
chr10:13165115 | T | C | 2 | a0001c0001t0002g0226 a0001c0001t0002g0227 |
2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.7+906T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165115 | |||||||
chr10:13165152 | T | A | 4 | a0001c0001t0001g0146 a0001c0001t0003g0045 a0001c0001t0003g0158 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+943T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165152 | |||||||
chr10:13165227 | T | C | 65 | a0001c0001t0001g0027 a0001c0001t0001g0056 a0001c0001t0001g0057 others(62): Show |
67 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.7+1018T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165227 | |||||||
chr10:13165238 | A | G | 1 | a0001c0001t0003g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.7+1029A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165238 | |||||||
chr10:13165277 | G | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(103): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.7+1068G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165277 | |||||||
chr10:13165311 | G | C | 1 | a0013c0025t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7+1102G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165311 | |||||||
chr10:13165487 | T | C | 2 | a0001c0001t0006g0373 a0001c0004t0004g0372 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7+1278T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165487 | |||||||
chr10:13165507 | G | C | 1 | a0013c0025t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7+1298G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165507 | |||||||
chr10:13165583 | A | C | 1 | a0002c0003t0003g0224 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.7+1374A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165583 | |||||||
chr10:13165647 | G | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0370 a0001c0001t0007g0223 |
3 | HG02976.hp1 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.7+1438G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165647 | |||||||
chr10:13165740 | T | C | 55 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0001t0001g0278 others(52): Show |
56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.7+1531T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165740 | |||||||
chr10:13165875 | G | GA | 19 | a0001c0001t0001g0030 a0001c0001t0001g0200 a0001c0001t0001g0375 others(16): Show |
20 | HG00609.hp1 HG01169.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.7+1683dupA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13165875 | ||||||
chr10:13165875 | G | GAA | 139 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(136): Show |
146 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.7+1682_7+1683dupAA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13165875 | ||||||
chr10:13165875 | G | GAAA | 7 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(4): Show |
9 | HG01070.hp2 HG01071.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+1681_7+1683dupAA others(1): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13165875 | ||||||
chr10:13165875 | GA | G | 32 | a0001c0001t0001g0031 a0001c0001t0001g0106 a0001c0001t0001g0143 others(29): Show |
34 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.7+1683delA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13165875 | ||||||
chr10:13165896 | G | GAAAAAGA others(315): Show |
4 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0305 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+1703_7+1704insGT others(320): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13165896 | ||||||
chr10:13165896 | G | GAAAAAGA others(316): Show |
3 | a0001c0004t0004g0151 a0001c0004t0004g0152 a0001c0004t0004g0222 |
3 | HG02109.hp1 HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.7+1703_7+1704insGT others(321): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13165896 | ||||||
chr10:13165896 | G | GAAAAAGA others(317): Show |
1 | a0001c0004t0014g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+1703_7+1704insGT others(322): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13165896 | ||||||
chr10:13165913 | A | G | 168 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(165): Show |
177 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.7+1704A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165913 | |||||||
chr10:13165930 | C | G | 1 | a0002c0003t0003g0310 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.7+1721C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165930 | |||||||
chr10:13165969 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0002g0205 |
2 | NA18982.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.7+1760G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13165969 | |||||||
chr10:13166041 | G | C | 2 | a0001c0001t0001g0106 a0001c0001t0005g0049 |
2 | HG02015.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.7+1832G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166041 | |||||||
chr10:13166063 | G | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(108): Show |
118 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.7+1854G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166063 | |||||||
chr10:13166284 | C | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(123): Show |
135 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.7+2075C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166284 | |||||||
chr10:13166288 | C | T | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+2079C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166288 | |||||||
chr10:13166308 | G | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(114): Show |
126 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.7+2099G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166308 | |||||||
chr10:13166362 | G | A | 1 | a0013c0025t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7+2153G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166362 | |||||||
chr10:13166474 | G | A | 156 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(153): Show |
165 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.7+2265G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166474 | |||||||
chr10:13166496 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.7+2287G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166496 | |||||||
chr10:13166496 | G | C | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+2287G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166496 | |||||||
chr10:13166599 | C | T | 2 | a0001c0002t0001g0119 a0001c0002t0001g0121 |
2 | NA18951.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.7+2390C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166599 | |||||||
chr10:13166635 | C | CA | 64 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0106 others(61): Show |
67 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.7+2441dupA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166635 | ||||||
chr10:13166635 | C | CAA | 51 | a0001c0001t0001g0122 a0001c0001t0001g0315 a0001c0001t0001g0329 others(48): Show |
52 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.7+2440_7+2441dupAA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166635 | ||||||
chr10:13166647 | A | AATACATA others(3): Show |
1 | a0001c0004t0004g0151 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.7+2439_7+2440insTA others(8): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166647 | ||||||
chr10:13166647 | A | AATACATA others(5): Show |
2 | a0001c0004t0004g0222 a0001c0004t0014g0157 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.7+2439_7+2440insTA others(10): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166647 | ||||||
chr10:13166647 | A | AATACATA others(13): Show |
1 | a0001c0001t0001g0305 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7+2439_7+2440insTA others(18): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166647 | ||||||
chr10:13166647 | A | ATACATAT others(4): Show |
1 | a0001c0001t0001g0271 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.7+2438_7+2439insTA others(9): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166647 | |||||||
chr10:13166647 | AAAATACA others(9): Show |
A | 1 | a0001c0001t0001g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7+2440_7+2455delAA others(14): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166647 | ||||||
chr10:13166649 | A | T | 7 | a0001c0001t0001g0271 a0001c0001t0001g0305 a0001c0001t0011g0367 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+2440A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166649 | |||||||
chr10:13166649 | AATAC | A | 18 | a0001c0001t0001g0259 a0001c0001t0001g0341 a0001c0001t0003g0055 others(15): Show |
18 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.7+2452_7+2455delCA others(2): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166649 | ||||||
chr10:13166649 | AATACATA others(1): Show |
A | 6 | a0001c0001t0001g0343 a0001c0001t0003g0041 a0001c0001t0003g0043 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+2448_7+2455delCA others(6): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166649 | ||||||
chr10:13166649 | AATACATA others(7): Show |
A | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+2444_7+2457delCA others(12): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166649 | ||||||
chr10:13166650 | ATAC | A | 3 | a0001c0001t0001g0266 a0001c0001t0006g0373 a0001c0004t0004g0372 |
3 | HG02559.hp2 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7+2442_7+2444delTA others(1): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166650 | |||||||
chr10:13166653 | C | CAT | 5 | a0001c0001t0001g0146 a0001c0001t0002g0201 a0001c0001t0002g0287 others(2): Show |
5 | HG01943.hp1 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+2446_7+2447dupTA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166653 | ||||||
chr10:13166653 | C | T | 7 | a0001c0001t0001g0271 a0001c0001t0001g0305 a0001c0001t0011g0367 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+2444C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166653 | |||||||
chr10:13166653 | CATACATA others(5): Show |
C | 2 | a0001c0001t0003g0083 a0001c0002t0004g0243 |
2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.7+2448_7+2459delCA others(10): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166653 | ||||||
chr10:13166653 | CATACATA others(15): Show |
C | 1 | a0001c0001t0002g0014 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.7+2448_7+2469delCA others(20): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166653 | ||||||
chr10:13166653 | CATACATA others(17): Show |
C | 3 | a0001c0001t0001g0074 a0001c0001t0002g0264 a0009c0011t0002g0006 |
4 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+2448_7+2471delCA others(22): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166653 | ||||||
chr10:13166655 | T | TATAC | 3 | a0001c0001t0003g0045 a0001c0001t0003g0158 a0008c0016t0002g0330 |
3 | HG02083.hp2 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7+2447_7+2448insTA others(2): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166655 | ||||||
chr10:13166655 | TAC | T | 102 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(99): Show |
108 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.7+2448_7+2449delCA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166655 | ||||||
chr10:13166657 | C | CATATATA others(3): Show |
1 | a0005c0006t0007g0270 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.7+2451_7+2452insTA others(8): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166657 | ||||||
chr10:13166657 | C | CATATATA others(5): Show |
3 | a0003c0009t0006g0123 a0003c0009t0006g0363 a0020c0018t0004g0086 |
3 | HG03579.hp1 NA19056.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.7+2451_7+2452insTA others(10): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166657 | ||||||
chr10:13166657 | C | CATATATA others(7): Show |
1 | a0003c0009t0006g0219 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.7+2451_7+2452insTA others(12): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166657 | ||||||
chr10:13166657 | C | CATATATA others(9): Show |
1 | a0003c0009t0006g0364 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.7+2451_7+2452insTA others(14): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166657 | ||||||
chr10:13166657 | C | T | 18 | a0001c0001t0001g0075 a0001c0001t0001g0105 a0001c0001t0001g0271 others(15): Show |
19 | HG01256.hp2 HG01258.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.7+2448C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166657 | |||||||
chr10:13166657 | CATACATA others(1): Show |
C | 3 | a0002c0003t0003g0165 a0002c0003t0003g0224 a0002c0003t0003g0229 |
3 | HG00140.hp1 HG00323.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.7+2452_7+2459delCA others(6): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166657 | ||||||
chr10:13166657 | CATACATA others(3): Show |
C | 43 | a0001c0001t0001g0122 a0001c0001t0001g0315 a0001c0001t0001g0329 others(40): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.7+2452_7+2461delCA others(8): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166657 | ||||||
chr10:13166657 | CATACATA others(13): Show |
C | 2 | a0001c0012t0001g0150 a0001c0012t0001g0269 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.7+2452_7+2471delCA others(18): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166657 | ||||||
chr10:13166659 | T | C | 7 | a0001c0001t0001g0075 a0001c0001t0001g0105 a0001c0001t0002g0016 others(4): Show |
8 | HG01256.hp2 HG01258.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+2450T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166659 | |||||||
chr10:13166659 | TAC | T | 18 | a0001c0001t0001g0115 a0001c0001t0001g0348 a0001c0004t0001g0070 others(15): Show |
19 | HG01069.hp2 HG01074.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.7+2452_7+2453delCA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166659 | ||||||
chr10:13166661 | C | CAT | 29 | a0001c0001t0001g0011 a0001c0001t0001g0106 a0001c0001t0001g0137 others(26): Show |
32 | HG00438.hp1 HG00735.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.7+2479_7+2480dupAT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166661 | ||||||
chr10:13166661 | C | CATAT | 15 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0021 others(12): Show |
15 | HG01074.hp1 HG01975.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.7+2477_7+2480dupAT others(2): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166661 | ||||||
chr10:13166661 | C | CATATATA others(3): Show |
1 | a0001c0001t0003g0394 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7+2471_7+2480dupAT others(8): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166661 | ||||||
chr10:13166661 | C | T | 56 | a0001c0001t0001g0075 a0001c0001t0001g0105 a0001c0001t0001g0146 others(53): Show |
57 | HG00408.hp2 HG00642.hp2 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.7+2452C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166661 | |||||||
chr10:13166665 | T | A | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+2456T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166665 | |||||||
chr10:13166667 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7+2458T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166667 | |||||||
chr10:13166669 | T | C | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+2460T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166669 | |||||||
chr10:13166683 | T | G | 8 | a0001c0001t0003g0055 a0001c0001t0003g0314 a0001c0001t0006g0114 others(5): Show |
8 | HG00642.hp2 HG01192.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+2474T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166683 | |||||||
chr10:13166685 | T | A | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+2476T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166685 | |||||||
chr10:13166687 | T | A | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+2478T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166687 | |||||||
chr10:13166687 | T | G | 30 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0266 others(27): Show |
30 | HG00642.hp2 HG01192.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.7+2478T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166687 | |||||||
chr10:13166688 | A | ATATATAT others(11): Show |
9 | a0001c0001t0001g0037 a0001c0001t0003g0149 a0001c0001t0007g0207 others(6): Show |
9 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+2480_7+2481insAT others(16): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166688 | ||||||
chr10:13166688 | A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0008t0007g0068 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+2480_7+2481insAT others(14): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166688 | ||||||
chr10:13166688 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0066 a0001c0008t0011g0268 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.7+2480_7+2481insAT others(12): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166688 | ||||||
chr10:13166688 | A | ATATATAT others(5): Show |
1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7+2480_7+2481insAT others(10): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13166688 | ||||||
chr10:13166688 | A | C | 1 | a0001c0001t0013g0340 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.7+2479A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166688 | |||||||
chr10:13166688 | A | G | 18 | a0001c0001t0001g0115 a0001c0001t0001g0348 a0001c0004t0001g0070 others(15): Show |
19 | HG01243.hp1 HG02257.hp2 HG02723.hp2 others(16): Show |
intron_variant | MODIFIER | c.7+2479A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166688 | |||||||
chr10:13166756 | C | T | 5 | a0002c0003t0003g0161 a0002c0003t0003g0168 a0002c0003t0019g0047 others(2): Show |
5 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+2547C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166756 | |||||||
chr10:13166771 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0375 a0005c0006t0007g0270 |
4 | HG01106.hp2 HG01884.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+2562C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166771 | |||||||
chr10:13166821 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.7+2612T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166821 | |||||||
chr10:13166912 | G | A | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+2703G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13166912 | |||||||
chr10:13167053 | C | T | 50 | a0001c0001t0001g0122 a0001c0001t0001g0315 a0001c0001t0001g0329 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.7+2844C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167053 | |||||||
chr10:13167074 | G | A | 2 | a0001c0001t0007g0076 a0005c0006t0006g0306 |
2 | HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.7+2865G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167074 | |||||||
chr10:13167147 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.7+2938T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167147 | |||||||
chr10:13167166 | A | C | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+2957A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167166 | |||||||
chr10:13167275 | A | C | 12 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0180 others(9): Show |
12 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.7+3066A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167275 | |||||||
chr10:13167287 | G | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0348 a0001c0004t0004g0039 others(1): Show |
4 | HG02886.hp2 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+3078G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167287 | |||||||
chr10:13167334 | T | C | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7+3125T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167334 | |||||||
chr10:13167465 | A | T | 1 | a0001c0002t0004g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.7+3256A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167465 | |||||||
chr10:13167545 | G | A | 3 | a0001c0008t0007g0067 a0001c0008t0007g0068 a0001c0008t0007g0262 |
3 | HG02572.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7+3336G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167545 | |||||||
chr10:13167585 | C | CG | 38 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0220 others(35): Show |
41 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.8-3329dupG | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13167585 | ||||||
chr10:13167585 | CG | C | 63 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0274 others(60): Show |
74 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.8-3329delG | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13167585 | ||||||
chr10:13167587 | G | GT | 31 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0266 others(28): Show |
31 | HG00642.hp2 HG01192.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.8-3335_8-3334insT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167587 | |||||||
chr10:13167675 | CAG | C | 20 | a0001c0001t0001g0115 a0001c0001t0001g0348 a0001c0001t0003g0083 others(17): Show |
21 | HG02257.hp2 HG02723.hp2 HG02886.hp1 others(18): Show |
intron_variant | MODIFIER | c.8-3242_8-3241delAG | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13167675 | ||||||
chr10:13167703 | A | C | 14 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(11): Show |
15 | HG02257.hp2 HG02723.hp2 HG03239.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-3219A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167703 | |||||||
chr10:13167747 | A | C | 1 | a0001c0002t0008g0339 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.8-3175A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167747 | |||||||
chr10:13167783 | G | A | 105 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(102): Show |
112 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.8-3139G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167783 | |||||||
chr10:13167804 | A | G | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-3118A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167804 | |||||||
chr10:13167832 | T | C | 339 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(336): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.8-3090T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167832 | |||||||
chr10:13167833 | G | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(118): Show |
130 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.8-3089G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167833 | |||||||
chr10:13167865 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.8-3057A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167865 | |||||||
chr10:13167902 | C | T | 4 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(1): Show |
6 | HG01070.hp2 HG01071.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-3020C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13167902 | |||||||
chr10:13168100 | C | T | 4 | a0001c0001t0002g0016 a0001c0001t0002g0085 a0001c0001t0002g0130 others(1): Show |
5 | HG01256.hp2 HG01258.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-2822C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168100 | |||||||
chr10:13168159 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.8-2763C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168159 | |||||||
chr10:13168175 | T | C | 204 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0037 others(201): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.8-2747T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168175 | |||||||
chr10:13168250 | C | T | 29 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0266 others(26): Show |
29 | HG00642.hp2 HG01192.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.8-2672C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168250 | |||||||
chr10:13168253 | T | C | 20 | a0001c0001t0001g0115 a0001c0001t0001g0160 a0001c0001t0001g0348 others(17): Show |
21 | HG02257.hp2 HG02723.hp2 HG02886.hp1 others(18): Show |
intron_variant | MODIFIER | c.8-2669T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168253 | |||||||
chr10:13168325 | G | T | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-2597G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168325 | |||||||
chr10:13168375 | C | G | 1 | a0001c0001t0007g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.8-2547C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168375 | |||||||
chr10:13168536 | C | T | 1 | a0001c0001t0026g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.8-2386C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168536 | |||||||
chr10:13168538 | GAT | G | 152 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(149): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.8-2381_8-2380delAT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13168538 | ||||||
chr10:13168636 | A | G | 1 | a0001c0001t0003g0149 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8-2286A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168636 | |||||||
chr10:13168649 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.8-2273G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168649 | |||||||
chr10:13168759 | A | C | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-2163A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13168759 | |||||||
chr10:13169075 | C | T | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-1847C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169075 | |||||||
chr10:13169098 | C | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0305 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1824C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169098 | |||||||
chr10:13169179 | C | T | 1 | a0001c0004t0004g0005 | 2 | NA18968.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.8-1743C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169179 | |||||||
chr10:13169192 | A | G | 2 | a0007c0015t0001g0300 a0007c0015t0002g0214 |
2 | HG01515.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.8-1730A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169192 | |||||||
chr10:13169239 | T | C | 1 | a0013c0025t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.8-1683T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169239 | |||||||
chr10:13169270 | G | A | 2 | a0002c0014t0003g0169 a0002c0014t0003g0170 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.8-1652G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169270 | |||||||
chr10:13169293 | C | T | 1 | a0007c0015t0002g0214 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.8-1629C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169293 | |||||||
chr10:13169328 | A | G | 1 | a0020c0018t0004g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.8-1594A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169328 | |||||||
chr10:13169533 | C | A | 4 | a0001c0001t0001g0027 a0001c0001t0002g0127 a0001c0001t0002g0189 others(1): Show |
5 | HG04184.hp1 NA18947.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-1389C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169533 | |||||||
chr10:13169549 | G | T | 51 | a0001c0001t0001g0122 a0001c0001t0001g0315 a0001c0001t0001g0329 others(48): Show |
52 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.8-1373G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169549 | |||||||
chr10:13169741 | T | G | 1 | a0001c0001t0001g0220 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.8-1181T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169741 | |||||||
chr10:13169835 | A | T | 13 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0002g0073 others(10): Show |
15 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-1087A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169835 | |||||||
chr10:13169948 | C | T | 6 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(3): Show |
8 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-974C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13169948 | |||||||
chr10:13170014 | A | G | 1 | a0008c0016t0002g0195 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.8-908A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170014 | |||||||
chr10:13170076 | A | C | 2 | a0001c0001t0001g0259 a0001c0001t0001g0341 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.8-846A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170076 | |||||||
chr10:13170363 | A | G | 15 | a0001c0001t0001g0037 a0001c0001t0001g0180 a0001c0001t0003g0149 others(12): Show |
15 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-559A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170363 | |||||||
chr10:13170365 | C | T | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-557C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170365 | |||||||
chr10:13170365 | CT | C | 56 | a0001c0001t0001g0122 a0001c0001t0001g0315 a0001c0001t0001g0329 others(53): Show |
57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.8-546delT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13170365 | ||||||
chr10:13170376 | T | A | 1 | a0005c0006t0007g0270 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.8-546T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170376 | |||||||
chr10:13170385 | A | G | 1 | a0011c0017t0004g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.8-537A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170385 | |||||||
chr10:13170397 | G | A | 30 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0266 others(27): Show |
30 | HG00642.hp2 HG01192.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.8-525G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170397 | |||||||
chr10:13170559 | C | T | 1 | a0002c0003t0003g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.8-363C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170559 | |||||||
chr10:13170603 | C | G | 4 | a0001c0001t0001g0037 a0001c0001t0003g0149 a0005c0006t0007g0040 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-319C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170603 | |||||||
chr10:13170682 | G | T | 4 | a0001c0001t0001g0106 a0001c0001t0005g0049 a0001c0001t0005g0186 others(1): Show |
4 | HG02015.hp2 HG02886.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-240G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170682 | |||||||
chr10:13170698 | G | GT | 10 | a0003c0007t0003g0051 a0003c0007t0003g0052 a0003c0007t0003g0053 others(7): Show |
10 | HG00408.hp2 HG01069.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-217dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 13170698 | ||||||
chr10:13170848 | A | T | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-74A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170848 | |||||||
chr10:13170884 | C | T | 267 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(264): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.8-38C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170884 | |||||||
chr10:13170915 | C | A | 19 | a0001c0001t0001g0115 a0001c0001t0001g0348 a0001c0004t0001g0070 others(16): Show |
20 | HG02257.hp2 HG02723.hp2 HG02886.hp1 others(17): Show |
splice_region_variant&intron_variant | LOW | c.8-7C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 2/19 | chr10 | 13170915 | |||||||
chr10:13171395 | A | G | 19 | a0001c0001t0001g0115 a0001c0001t0001g0348 a0001c0004t0001g0070 others(16): Show |
20 | HG02257.hp2 HG02723.hp2 HG02886.hp1 others(17): Show |
intron_variant | MODIFIER | c.349+132A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13171395 | |||||||
chr10:13171499 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.349+236T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13171499 | |||||||
chr10:13171670 | T | C | 1 | a0001c0001t0001g0021 | 2 | NA18950.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.349+407T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13171670 | |||||||
chr10:13171760 | A | C | 2 | a0001c0002t0001g0091 a0001c0002t0001g0103 |
2 | HG02040.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.349+497A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13171760 | |||||||
chr10:13171767 | A | AT | 11 | a0001c0002t0001g0183 a0001c0004t0004g0323 a0004c0005t0002g0346 others(8): Show |
11 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+517dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr10 | 13171767 | ||||||
chr10:13171783 | G | A | 52 | a0001c0001t0001g0122 a0001c0001t0001g0208 a0001c0001t0001g0315 others(49): Show |
53 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.349+520G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13171783 | |||||||
chr10:13171803 | C | T | 1 | a0001c0001t0003g0374 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.349+540C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13171803 | |||||||
chr10:13171810 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.349+547G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13171810 | |||||||
chr10:13171862 | T | C | 1 | a0001c0002t0001g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.350-514T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13171862 | |||||||
chr10:13171884 | C | T | 1 | a0001c0030t0003g0354 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.350-492C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13171884 | |||||||
chr10:13172056 | G | A | 1 | a0001c0002t0004g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.350-320G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13172056 | |||||||
chr10:13172077 | A | G | 16 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0180 others(13): Show |
16 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.350-299A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13172077 | |||||||
chr10:13172160 | T | C | 343 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(340): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.350-216T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13172160 | |||||||
chr10:13172322 | T | C | 3 | a0001c0001t0003g0055 a0001c0001t0003g0314 a0005c0026t0004g0313 |
3 | HG00642.hp2 HG01192.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.350-54T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 3/19 | chr10 | 13172322 | |||||||
chr10:13172506 | C | T | 1 | a0001c0002t0001g0381 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.454+26C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 4/19 | chr10 | 13172506 | |||||||
chr10:13172786 | G | A | 13 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0002g0073 others(10): Show |
15 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.592+21G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13172786 | |||||||
chr10:13172812 | A | G | 271 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(268): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.592+47A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13172812 | |||||||
chr10:13172878 | G | GAGAA | 178 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(175): Show |
187 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.592+120_592+123dup others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr10 | 13172878 | ||||||
chr10:13173038 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0003g0045 a0001c0001t0003g0158 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+273A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13173038 | |||||||
chr10:13173042 | C | G | 1 | a0001c0001t0003g0321 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.592+277C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13173042 | |||||||
chr10:13173106 | G | A | 31 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0266 others(28): Show |
31 | HG00642.hp2 HG01192.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.592+341G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13173106 | |||||||
chr10:13173211 | A | G | 3 | a0001c0008t0007g0067 a0001c0008t0007g0068 a0001c0008t0007g0262 |
3 | HG02572.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.592+446A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13173211 | |||||||
chr10:13173350 | T | C | 2 | a0001c0001t0006g0373 a0001c0004t0004g0372 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.592+585T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13173350 | |||||||
chr10:13173522 | T | G | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.592+757T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13173522 | |||||||
chr10:13173544 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.592+779G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13173544 | |||||||
chr10:13173822 | G | T | 1 | a0001c0001t0002g0303 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.592+1057G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13173822 | |||||||
chr10:13173915 | A | G | 2 | a0002c0003t0009g0107 a0002c0003t0009g0108 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.592+1150A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13173915 | |||||||
chr10:13173974 | A | G | 9 | a0004c0005t0002g0346 a0004c0005t0004g0132 a0004c0005t0004g0133 others(6): Show |
9 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.592+1209A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13173974 | |||||||
chr10:13174103 | C | T | 1 | a0001c0004t0004g0323 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.592+1338C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13174103 | |||||||
chr10:13174134 | A | AT | 85 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0037 others(82): Show |
99 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.593-1350dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr10 | 13174134 | ||||||
chr10:13174134 | A | ATT | 16 | a0001c0001t0001g0136 a0001c0001t0001g0251 a0001c0001t0001g0359 others(13): Show |
16 | HG00741.hp1 HG01928.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.593-1351_593-1350d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr10 | 13174134 | ||||||
chr10:13174134 | AT | A | 58 | a0001c0001t0001g0172 a0001c0001t0001g0190 a0001c0001t0001g0315 others(55): Show |
60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.593-1350delT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr10 | 13174134 | ||||||
chr10:13174134 | ATT | A | 102 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(99): Show |
108 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.593-1351_593-1350d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr10 | 13174134 | ||||||
chr10:13174134 | ATTT | A | 52 | a0001c0001t0001g0074 a0001c0001t0001g0106 a0001c0001t0001g0220 others(49): Show |
56 | HG00438.hp1 HG00642.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.593-1352_593-1350d others(5): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr10 | 13174134 | ||||||
chr10:13174436 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.593-1074T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13174436 | |||||||
chr10:13174493 | C | T | 2 | a0001c0012t0001g0150 a0001c0012t0001g0269 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.593-1017C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13174493 | |||||||
chr10:13174722 | G | A | 57 | a0001c0001t0001g0236 a0001c0001t0001g0274 a0001c0002t0001g0001 others(54): Show |
68 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.593-788G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13174722 | |||||||
chr10:13174784 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0278 |
2 | HG00735.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.593-726G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13174784 | |||||||
chr10:13174838 | G | A | 323 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(320): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.593-672G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13174838 | |||||||
chr10:13175063 | G | T | 15 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0180 others(12): Show |
15 | HG01109.hp1 HG01891.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.593-447G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13175063 | |||||||
chr10:13175088 | A | G | 1 | a0010c0013t0003g0026 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.593-422A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13175088 | |||||||
chr10:13175118 | C | G | 1 | a0001c0001t0003g0159 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.593-392C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13175118 | |||||||
chr10:13175203 | G | A | 13 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0002g0073 others(10): Show |
15 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.593-307G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13175203 | |||||||
chr10:13175332 | C | T | 30 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0266 others(27): Show |
30 | HG00642.hp2 HG01192.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.593-178C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13175332 | |||||||
chr10:13175457 | C | T | 7 | a0003c0007t0003g0058 a0003c0009t0006g0123 a0003c0009t0006g0219 others(4): Show |
7 | HG00408.hp2 HG01069.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-53C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 5/19 | chr10 | 13175457 | |||||||
chr10:13175780 | A | G | 1 | a0001c0002t0001g0182 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.764+99A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13175780 | |||||||
chr10:13175835 | C | T | 6 | a0003c0007t0003g0058 a0003c0009t0006g0123 a0003c0009t0006g0219 others(3): Show |
6 | HG00408.hp2 HG01069.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.764+154C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13175835 | |||||||
chr10:13175940 | A | G | 335 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(332): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.764+259A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13175940 | |||||||
chr10:13175951 | A | C | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.764+270A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13175951 | |||||||
chr10:13176400 | C | T | 6 | a0003c0007t0003g0058 a0003c0009t0006g0123 a0003c0009t0006g0219 others(3): Show |
6 | HG00408.hp2 HG01069.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.764+719C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13176400 | |||||||
chr10:13176415 | A | G | 1 | a0001c0012t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.764+734A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13176415 | |||||||
chr10:13176456 | T | C | 13 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0002g0073 others(10): Show |
15 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.764+775T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13176456 | |||||||
chr10:13176500 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.764+819T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13176500 | |||||||
chr10:13176964 | C | T | 1 | a0019c0024t0004g0256 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.764+1283C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13176964 | |||||||
chr10:13177018 | T | C | 15 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(12): Show |
16 | HG02257.hp2 HG02723.hp2 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.764+1337T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13177018 | |||||||
chr10:13177028 | T | A | 5 | a0001c0001t0003g0110 a0002c0003t0001g0327 a0002c0003t0005g0032 others(2): Show |
5 | HG00099.hp1 HG00140.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.764+1347T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13177028 | |||||||
chr10:13177056 | TG | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0180 a0005c0006t0006g0369 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.764+1376delG | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13177056 | |||||||
chr10:13177063 | A | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0180 a0005c0006t0006g0369 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.764+1382A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13177063 | |||||||
chr10:13177166 | A | G | 8 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0266 others(5): Show |
8 | HG02257.hp1 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.764+1485A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13177166 | |||||||
chr10:13177508 | C | CT | 78 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0074 others(75): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.764+1850dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 13177508 | ||||||
chr10:13177508 | CT | C | 61 | a0001c0001t0001g0087 a0001c0001t0001g0106 a0001c0001t0001g0215 others(58): Show |
64 | HG00438.hp1 HG00642.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.764+1850delT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 13177508 | ||||||
chr10:13177508 | CTT | C | 12 | a0001c0001t0005g0096 a0001c0002t0004g0243 a0001c0004t0004g0069 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.764+1849_764+1850d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 13177508 | ||||||
chr10:13177508 | CTTTTTTT others(2): Show |
C | 95 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(92): Show |
101 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.764+1842_764+1850d others(11): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 13177508 | ||||||
chr10:13177508 | CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0007g0076 a0001c0001t0007g0078 a0001c0001t0007g0331 others(2): Show |
5 | HG00558.hp1 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.764+1841_764+1850d others(12): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 13177508 | ||||||
chr10:13177726 | C | T | 1 | a0001c0002t0001g0299 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.764+2045C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13177726 | |||||||
chr10:13177770 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.764+2089G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13177770 | |||||||
chr10:13177849 | C | CA | 244 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(241): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.764+2182dupA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 13177849 | ||||||
chr10:13177849 | C | CAA | 12 | a0001c0008t0007g0067 a0001c0008t0007g0068 a0001c0008t0007g0262 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.764+2181_764+2182d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 13177849 | ||||||
chr10:13177862 | A | C | 12 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0002g0365 others(9): Show |
14 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.764+2181A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13177862 | |||||||
chr10:13177877 | T | A | 1 | a0001c0001t0002g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.764+2196T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13177877 | |||||||
chr10:13177998 | C | T | 3 | a0001c0008t0007g0067 a0001c0008t0007g0068 a0001c0008t0007g0262 |
3 | HG02572.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.764+2317C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13177998 | |||||||
chr10:13178143 | T | G | 86 | a0001c0001t0001g0074 a0001c0001t0001g0106 a0001c0001t0001g0122 others(83): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.765-2299T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13178143 | |||||||
chr10:13178328 | A | T | 1 | a0001c0001t0002g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.765-2114A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13178328 | |||||||
chr10:13178639 | T | C | 1 | a0001c0001t0003g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.765-1803T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13178639 | |||||||
chr10:13178640 | C | G | 268 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(265): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.765-1802C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13178640 | |||||||
chr10:13178762 | A | G | 1 | a0001c0001t0001g0027 | 2 | NA18947.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.765-1680A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13178762 | |||||||
chr10:13178767 | G | A | 1 | a0013c0025t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.765-1675G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13178767 | |||||||
chr10:13178779 | G | A | 5 | a0003c0007t0003g0058 a0003c0009t0006g0123 a0003c0009t0006g0219 others(2): Show |
5 | HG00408.hp2 HG01069.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.765-1663G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13178779 | |||||||
chr10:13178983 | C | T | 1 | a0001c0001t0002g0379 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.765-1459C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13178983 | |||||||
chr10:13179004 | T | C | 13 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(10): Show |
14 | HG02257.hp2 HG02723.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.765-1438T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13179004 | |||||||
chr10:13179227 | C | T | 3 | a0002c0003t0019g0047 a0002c0014t0003g0169 a0002c0014t0003g0170 |
3 | HG01167.hp2 HG01169.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.765-1215C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13179227 | |||||||
chr10:13179271 | C | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0305 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.765-1171C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13179271 | |||||||
chr10:13179389 | C | T | 1 | a0001c0001t0003g0298 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.765-1053C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13179389 | |||||||
chr10:13179681 | T | C | 12 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(9): Show |
14 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.765-761T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13179681 | |||||||
chr10:13179771 | C | T | 1 | a0001c0002t0001g0213 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.765-671C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13179771 | |||||||
chr10:13179831 | G | A | 1 | a0002c0003t0006g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.765-611G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13179831 | |||||||
chr10:13179894 | C | T | 3 | a0002c0003t0003g0165 a0002c0003t0003g0224 a0002c0003t0003g0229 |
3 | HG00140.hp1 HG00323.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.765-548C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13179894 | |||||||
chr10:13179912 | A | C | 12 | a0001c0002t0001g0210 a0001c0002t0004g0129 a0001c0002t0004g0312 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.765-530A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13179912 | |||||||
chr10:13180082 | C | T | 1 | a0001c0002t0001g0352 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.765-360C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13180082 | |||||||
chr10:13180118 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.765-324G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13180118 | |||||||
chr10:13180145 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.765-297G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13180145 | |||||||
chr10:13180171 | A | T | 4 | a0001c0001t0002g0196 a0001c0001t0002g0253 a0001c0001t0002g0289 others(1): Show |
4 | HG01361.hp2 HG01975.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.765-271A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13180171 | |||||||
chr10:13180175 | T | C | 318 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(315): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.765-267T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13180175 | |||||||
chr10:13180207 | C | T | 21 | a0001c0002t0001g0210 a0001c0002t0004g0129 a0001c0002t0004g0312 others(18): Show |
21 | HG00408.hp2 HG01069.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.765-235C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13180207 | |||||||
chr10:13180251 | TA | T | 60 | a0001c0001t0001g0074 a0001c0001t0001g0095 a0001c0001t0001g0160 others(57): Show |
63 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.765-177delA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 13180251 | ||||||
chr10:13180265 | A | G | 11 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(8): Show |
13 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.765-177A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13180265 | |||||||
chr10:13180389 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.765-53A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 6/19 | chr10 | 13180389 | |||||||
chr10:13180620 | A | T | 1 | a0001c0001t0002g0193 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.930+13A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13180620 | |||||||
chr10:13180793 | A | G | 3 | a0001c0001t0001g0180 a0001c0001t0001g0244 a0001c0001t0001g0370 |
3 | HG02723.hp1 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.930+186A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13180793 | |||||||
chr10:13180825 | C | G | 1 | a0001c0001t0001g0251 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.930+218C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13180825 | |||||||
chr10:13180925 | G | A | 5 | a0001c0008t0007g0033 a0001c0008t0007g0067 a0001c0008t0007g0068 others(2): Show |
5 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+318G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13180925 | |||||||
chr10:13181048 | G | A | 1 | a0001c0001t0005g0025 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.930+441G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13181048 | |||||||
chr10:13181107 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.930+500A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13181107 | |||||||
chr10:13181300 | A | G | 16 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(13): Show |
17 | HG02257.hp2 HG02723.hp2 NA18947.hp1 others(14): Show |
intron_variant | MODIFIER | c.930+693A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13181300 | |||||||
chr10:13181308 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(98): Show |
108 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.930+701T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13181308 | |||||||
chr10:13181414 | T | C | 25 | a0001c0001t0003g0083 a0001c0004t0001g0070 a0001c0004t0003g0181 others(22): Show |
26 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.930+807T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13181414 | |||||||
chr10:13181539 | G | A | 5 | a0004c0005t0004g0132 a0004c0005t0004g0133 a0004c0005t0004g0202 others(2): Show |
5 | HG01358.hp2 HG01496.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+932G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13181539 | |||||||
chr10:13181549 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.930+942A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13181549 | |||||||
chr10:13181823 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0305 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-1110G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13181823 | |||||||
chr10:13181851 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA18972.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.931-1082G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13181851 | |||||||
chr10:13181894 | C | A | 1 | a0020c0018t0004g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.931-1039C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13181894 | |||||||
chr10:13182115 | A | T | 3 | a0001c0001t0003g0083 a0001c0004t0004g0039 a0019c0024t0004g0256 |
3 | HG03098.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.931-818A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13182115 | |||||||
chr10:13182185 | A | T | 1 | a0001c0001t0002g0130 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.931-748A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13182185 | |||||||
chr10:13182211 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.931-722C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13182211 | |||||||
chr10:13182412 | T | G | 1 | a0001c0001t0002g0124 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.931-521T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13182412 | |||||||
chr10:13182419 | C | T | 1 | a0001c0001t0005g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.931-514C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13182419 | |||||||
chr10:13182486 | A | C | 2 | a0001c0001t0001g0311 a0001c0001t0005g0174 |
2 | HG01070.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.931-447A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13182486 | |||||||
chr10:13182528 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0348 |
2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.931-405A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13182528 | |||||||
chr10:13182756 | C | G | 5 | a0001c0001t0003g0041 a0001c0001t0003g0043 a0001c0001t0003g0261 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.931-177C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13182756 | |||||||
chr10:13182886 | G | T | 121 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(118): Show |
128 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.931-47G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 7/19 | chr10 | 13182886 | |||||||
chr10:13183119 | G | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(118): Show |
128 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1098+19G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13183119 | |||||||
chr10:13183198 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1098+98G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13183198 | |||||||
chr10:13183470 | T | C | 1 | a0001c0001t0003g0314 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1098+370T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13183470 | |||||||
chr10:13183511 | T | C | 1 | a0004c0005t0004g0345 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1098+411T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13183511 | |||||||
chr10:13183691 | C | CT | 11 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(8): Show |
13 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1098+602dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr10 | 13183691 | ||||||
chr10:13183728 | G | A | 115 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(112): Show |
121 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1098+628G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13183728 | |||||||
chr10:13183847 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1098+747G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13183847 | |||||||
chr10:13183922 | G | T | 1 | a0001c0004t0004g0152 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1098+822G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13183922 | |||||||
chr10:13183938 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1098+838A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13183938 | |||||||
chr10:13184024 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1098+924T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184024 | |||||||
chr10:13184050 | G | A | 2 | a0001c0012t0001g0150 a0001c0012t0001g0269 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+950G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184050 | |||||||
chr10:13184176 | A | G | 1 | a0001c0001t0002g0303 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1098+1076A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184176 | |||||||
chr10:13184204 | G | A | 3 | a0001c0001t0003g0083 a0001c0004t0004g0039 a0019c0024t0004g0256 |
3 | HG03098.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1098+1104G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184204 | |||||||
chr10:13184282 | C | T | 52 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(49): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1098+1182C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184282 | |||||||
chr10:13184300 | T | A | 5 | a0001c0001t0006g0114 a0001c0001t0006g0148 a0001c0001t0006g0371 others(2): Show |
5 | HG02145.hp2 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+1200T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184300 | |||||||
chr10:13184363 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1098+1263G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184363 | |||||||
chr10:13184461 | T | C | 4 | a0003c0009t0006g0123 a0003c0009t0006g0219 a0003c0009t0006g0363 others(1): Show |
4 | HG00408.hp2 NA19056.hp2 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+1361T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184461 | |||||||
chr10:13184476 | C | T | 2 | a0001c0001t0004g0318 a0014c0031t0003g0276 |
2 | HG01433.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1098+1376C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184476 | |||||||
chr10:13184829 | T | G | 335 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(332): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1099-1335T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184829 | |||||||
chr10:13184892 | T | G | 137 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(134): Show |
147 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1099-1272T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13184892 | |||||||
chr10:13185100 | C | G | 226 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(223): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1099-1064C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185100 | |||||||
chr10:13185205 | C | T | 1 | a0017c0021t0001g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1099-959C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185205 | |||||||
chr10:13185244 | C | G | 1 | a0001c0001t0003g0309 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1099-920C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185244 | |||||||
chr10:13185274 | G | A | 2 | a0001c0008t0007g0033 a0001c0008t0011g0268 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1099-890G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185274 | |||||||
chr10:13185293 | C | G | 1 | a0001c0001t0003g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1099-871C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185293 | |||||||
chr10:13185319 | A | G | 1 | a0001c0002t0001g0112 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1099-845A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185319 | |||||||
chr10:13185601 | T | C | 12 | a0001c0002t0001g0210 a0001c0002t0004g0129 a0001c0002t0004g0312 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1099-563T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185601 | |||||||
chr10:13185604 | G | T | 308 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(305): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1099-560G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185604 | |||||||
chr10:13185615 | G | A | 1 | a0005c0006t0006g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-549G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185615 | |||||||
chr10:13185634 | A | G | 2 | a0001c0004t0004g0088 a0001c0004t0004g0100 |
2 | NA18985.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1099-530A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185634 | |||||||
chr10:13185785 | C | T | 15 | a0003c0007t0003g0051 a0003c0007t0003g0052 a0003c0007t0003g0053 others(12): Show |
15 | HG00408.hp2 HG01069.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1099-379C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185785 | |||||||
chr10:13185862 | G | A | 1 | a0002c0003t0003g0228 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1099-302G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185862 | |||||||
chr10:13185907 | C | T | 1 | a0001c0001t0002g0391 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1099-257C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185907 | |||||||
chr10:13185936 | G | GT | 5 | a0001c0002t0001g0020 a0001c0002t0008g0020 a0001c0002t0008g0241 others(2): Show |
5 | HG00558.hp1 NA18981.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-222dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr10 | 13185936 | ||||||
chr10:13185990 | G | C | 1 | a0013c0025t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1099-174G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13185990 | |||||||
chr10:13186004 | C | T | 1 | a0001c0001t0016g0140 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1099-160C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13186004 | |||||||
chr10:13186066 | CCTT | C | 5 | a0001c0001t0006g0114 a0001c0001t0006g0148 a0001c0001t0006g0371 others(2): Show |
5 | HG02145.hp2 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-94_1099-92del others(3): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr10 | 13186066 | ||||||
chr10:13186106 | G | A | 1 | a0020c0018t0004g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1099-58G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 8/19 | chr10 | 13186106 | |||||||
chr10:13186622 | C | G | 1 | a0001c0001t0002g0060 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1215+342C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13186622 | |||||||
chr10:13186698 | G | A | 1 | a0015c0019t0021g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1215+418G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13186698 | |||||||
chr10:13186881 | A | G | 6 | a0001c0008t0007g0033 a0001c0008t0007g0067 a0001c0008t0007g0068 others(3): Show |
6 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+601A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13186881 | |||||||
chr10:13186882 | C | T | 60 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(57): Show |
63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.1215+602C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13186882 | |||||||
chr10:13186903 | A | C | 3 | a0001c0008t0007g0067 a0001c0008t0007g0068 a0001c0008t0007g0262 |
3 | HG02572.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1215+623A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13186903 | |||||||
chr10:13186939 | C | G | 1 | a0001c0001t0003g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1215+659C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13186939 | |||||||
chr10:13186994 | A | G | 3 | a0001c0001t0001g0259 a0001c0001t0001g0341 a0001c0001t0006g0373 |
3 | HG02922.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1215+714A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13186994 | |||||||
chr10:13187351 | T | TA | 3 | a0001c0001t0003g0113 a0001c0001t0003g0159 a0001c0001t0003g0374 |
3 | HG02818.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1215+1072dupA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 13187351 | ||||||
chr10:13187430 | G | A | 5 | a0001c0008t0007g0033 a0001c0008t0007g0067 a0001c0008t0007g0068 others(2): Show |
5 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215+1150G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13187430 | |||||||
chr10:13187478 | C | A | 60 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(57): Show |
63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.1215+1198C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13187478 | |||||||
chr10:13187479 | C | T | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1215+1199C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13187479 | |||||||
chr10:13187480 | C | A | 2 | a0001c0004t0004g0039 a0019c0024t0004g0256 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1215+1200C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13187480 | |||||||
chr10:13187873 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0255 a0001c0001t0002g0048 |
4 | NA18943.hp1 NA18968.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-1008G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13187873 | |||||||
chr10:13187918 | G | A | 1 | a0020c0018t0004g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1216-963G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13187918 | |||||||
chr10:13187920 | C | T | 1 | a0001c0002t0001g0232 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1216-961C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13187920 | |||||||
chr10:13188101 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1216-780C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13188101 | |||||||
chr10:13188471 | G | A | 1 | a0001c0002t0001g0213 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1216-410G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13188471 | |||||||
chr10:13188537 | TTATATTA others(14): Show |
T | 55 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(52): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1216-325_1216-305d others(23): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 13188537 | ||||||
chr10:13188661 | G | A | 5 | a0001c0001t0003g0041 a0001c0001t0003g0043 a0001c0001t0003g0261 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-220G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13188661 | |||||||
chr10:13188666 | T | G | 7 | a0001c0001t0006g0114 a0001c0001t0006g0148 a0001c0001t0006g0371 others(4): Show |
7 | HG02145.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1216-215T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13188666 | |||||||
chr10:13188782 | C | T | 2 | a0001c0012t0001g0150 a0001c0012t0001g0269 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1216-99C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13188782 | |||||||
chr10:13188792 | C | T | 2 | a0008c0016t0002g0195 a0008c0016t0002g0330 |
2 | HG02083.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1216-89C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13188792 | |||||||
chr10:13188837 | A | G | 118 | a0001c0001t0001g0074 a0001c0001t0001g0106 a0001c0001t0001g0220 others(115): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1216-44A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 9/19 | chr10 | 13188837 | |||||||
chr10:13189094 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1415+14G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13189094 | |||||||
chr10:13189194 | A | G | 183 | a0001c0001t0001g0074 a0001c0001t0001g0106 a0001c0001t0001g0220 others(180): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1415+114A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13189194 | |||||||
chr10:13189559 | G | C | 122 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0057 others(119): Show |
129 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1415+479G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13189559 | |||||||
chr10:13189812 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1415+732T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13189812 | |||||||
chr10:13189839 | G | A | 1 | a0001c0001t0005g0019 | 2 | HG00438.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1415+759G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13189839 | |||||||
chr10:13189939 | T | C | 6 | a0001c0001t0001g0311 a0001c0001t0005g0022 a0001c0001t0005g0173 others(3): Show |
7 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1415+859T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13189939 | |||||||
chr10:13190115 | T | C | 11 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(8): Show |
13 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1415+1035T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13190115 | |||||||
chr10:13190117 | C | CATT | 62 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0009 others(59): Show |
73 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1415+1040_1415+104 others(7): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr10 | 13190117 | ||||||
chr10:13190342 | A | T | 41 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0341 others(38): Show |
41 | HG00408.hp2 HG00642.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1416-957A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13190342 | |||||||
chr10:13190421 | C | T | 1 | a0020c0018t0004g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1416-878C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13190421 | |||||||
chr10:13190489 | G | A | 1 | a0001c0001t0018g0038 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1416-810G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13190489 | |||||||
chr10:13190527 | CA | C | 310 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(307): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1416-764delA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr10 | 13190527 | ||||||
chr10:13190538 | A | C | 123 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(120): Show |
130 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1416-761A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13190538 | |||||||
chr10:13190771 | TA | T | 11 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(8): Show |
13 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1416-524delA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr10 | 13190771 | ||||||
chr10:13190783 | ATATTGTT others(2): Show |
A | 11 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(8): Show |
13 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1416-511_1416-503d others(11): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr10 | 13190783 | ||||||
chr10:13190830 | TTAA | T | 55 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(52): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1416-467_1416-465d others(5): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr10 | 13190830 | ||||||
chr10:13190895 | A | G | 2 | a0001c0012t0001g0150 a0001c0012t0001g0269 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1416-404A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13190895 | |||||||
chr10:13191049 | A | T | 3 | a0001c0001t0003g0164 a0001c0001t0003g0308 a0001c0001t0003g0309 |
3 | HG00741.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1416-250A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 10/19 | chr10 | 13191049 | |||||||
chr10:13191471 | C | T | 122 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(119): Show |
129 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1516+72C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13191471 | |||||||
chr10:13191504 | G | T | 1 | a0001c0002t0006g0326 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1516+105G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13191504 | |||||||
chr10:13191562 | A | C | 3 | a0002c0003t0019g0047 a0002c0014t0003g0169 a0002c0014t0003g0170 |
3 | HG01167.hp2 HG01169.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1516+163A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13191562 | |||||||
chr10:13191563 | TAAGC | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(94): Show |
103 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1516+190_1516+193d others(6): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 13191563 | ||||||
chr10:13191563 | TAAGCAAG others(1): Show |
T | 3 | a0001c0001t0003g0113 a0001c0001t0003g0159 a0001c0001t0003g0374 |
3 | HG02818.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1516+186_1516+193d others(10): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 13191563 | ||||||
chr10:13191581 | A | T | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1516+182A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13191581 | |||||||
chr10:13191597 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0191 a0001c0001t0001g0332 |
3 | NA18939.hp2 NA19010.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1516+198T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13191597 | |||||||
chr10:13191683 | T | G | 1 | a0001c0001t0002g0196 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1516+284T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13191683 | |||||||
chr10:13191867 | T | C | 189 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1517-388T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13191867 | |||||||
chr10:13191902 | AAAATAAA others(3): Show |
A | 55 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(52): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1517-340_1517-331d others(12): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 13191902 | ||||||
chr10:13192018 | C | G | 1 | a0001c0002t0010g0388 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1517-237C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13192018 | |||||||
chr10:13192043 | A | G | 1 | a0001c0001t0001g0370 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1517-212A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13192043 | |||||||
chr10:13192051 | T | C | 2 | a0001c0001t0002g0333 a0001c0001t0002g0336 |
2 | HG00597.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1517-204T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13192051 | |||||||
chr10:13192132 | G | T | 2 | a0001c0004t0004g0039 a0019c0024t0004g0256 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1517-123G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 11/19 | chr10 | 13192132 | |||||||
chr10:13192390 | G | T | 1 | a0001c0004t0004g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1627+25G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 12/19 | chr10 | 13192390 | |||||||
chr10:13192693 | T | G | 2 | a0001c0001t0003g0055 a0001c0001t0003g0314 |
2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1745+125T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13192693 | |||||||
chr10:13192728 | G | A | 1 | a0001c0002t0004g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1745+160G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13192728 | |||||||
chr10:13192758 | C | T | 1 | a0001c0002t0001g0119 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1745+190C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13192758 | |||||||
chr10:13192760 | AC | A | 60 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(57): Show |
63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.1745+193delC | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13192760 | |||||||
chr10:13192764 | CA | C | 60 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(57): Show |
63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.1745+199delA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr10 | 13192764 | ||||||
chr10:13192966 | A | G | 1 | a0001c0001t0001g0021 | 2 | NA18950.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1745+398A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13192966 | |||||||
chr10:13193303 | T | TA | 49 | a0001c0001t0001g0066 a0001c0001t0001g0199 a0001c0001t0001g0258 others(46): Show |
49 | HG00408.hp2 HG00642.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1745+749dupA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr10 | 13193303 | ||||||
chr10:13193372 | C | T | 1 | a0002c0003t0003g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1745+804C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13193372 | |||||||
chr10:13193416 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0180 a0001c0001t0001g0244 others(1): Show |
4 | HG02258.hp1 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1745+848G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13193416 | |||||||
chr10:13193620 | C | A | 22 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(19): Show |
23 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1745+1052C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13193620 | |||||||
chr10:13193622 | A | C | 22 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(19): Show |
23 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1745+1054A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13193622 | |||||||
chr10:13193765 | A | G | 6 | a0001c0004t0004g0151 a0001c0004t0004g0152 a0001c0004t0004g0222 others(3): Show |
6 | HG02109.hp1 HG02145.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1745+1197A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13193765 | |||||||
chr10:13193920 | T | C | 5 | a0001c0001t0003g0041 a0001c0001t0003g0043 a0001c0001t0003g0261 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1746-1121T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13193920 | |||||||
chr10:13193998 | G | C | 1 | a0002c0003t0003g0285 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1746-1043G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13193998 | |||||||
chr10:13194027 | A | T | 61 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(58): Show |
64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1746-1014A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194027 | |||||||
chr10:13194049 | G | T | 1 | a0001c0001t0003g0233 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1746-992G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194049 | |||||||
chr10:13194056 | T | C | 122 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0061 others(119): Show |
129 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1746-985T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194056 | |||||||
chr10:13194080 | TGA | T | 61 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(58): Show |
64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1746-959_1746-958d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr10 | 13194080 | ||||||
chr10:13194140 | G | C | 1 | a0001c0001t0002g0201 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1746-901G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194140 | |||||||
chr10:13194182 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0199 a0001c0001t0001g0266 |
3 | HG01109.hp1 HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1746-859G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194182 | |||||||
chr10:13194194 | T | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(197): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1746-847T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194194 | |||||||
chr10:13194214 | A | G | 12 | a0001c0002t0001g0210 a0001c0002t0004g0129 a0001c0002t0004g0312 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1746-827A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194214 | |||||||
chr10:13194256 | G | A | 4 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(1): Show |
6 | HG01070.hp2 HG01071.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1746-785G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194256 | |||||||
chr10:13194306 | C | T | 1 | a0001c0001t0003g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1746-735C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194306 | |||||||
chr10:13194307 | G | A | 5 | a0004c0005t0004g0132 a0004c0005t0004g0133 a0004c0005t0004g0202 others(2): Show |
5 | HG01358.hp2 HG01496.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.1746-734G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194307 | |||||||
chr10:13194315 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0287 a0001c0001t0002g0290 |
4 | NA18941.hp2 NA18953.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1746-726A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194315 | |||||||
chr10:13194322 | C | T | 55 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(52): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1746-719C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194322 | |||||||
chr10:13194323 | A | G | 61 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(58): Show |
64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1746-718A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194323 | |||||||
chr10:13194409 | T | C | 2 | a0001c0002t0004g0144 a0001c0002t0004g0211 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1746-632T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194409 | |||||||
chr10:13194536 | ACT | A | 16 | a0003c0007t0003g0051 a0003c0007t0003g0052 a0003c0007t0003g0053 others(13): Show |
16 | HG00408.hp2 HG01069.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1746-502_1746-501d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr10 | 13194536 | ||||||
chr10:13194571 | A | T | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1746-470A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194571 | |||||||
chr10:13194882 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1746-159G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13194882 | |||||||
chr10:13195015 | G | A | 319 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(316): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1746-26G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 13/19 | chr10 | 13195015 | |||||||
chr10:13195286 | C | G | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1974+17C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13195286 | |||||||
chr10:13195435 | A | G | 41 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0341 others(38): Show |
41 | HG00408.hp2 HG00642.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1974+166A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13195435 | |||||||
chr10:13195466 | A | C | 1 | a0001c0002t0010g0388 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1974+197A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13195466 | |||||||
chr10:13195491 | T | G | 1 | a0001c0001t0001g0044 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1974+222T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13195491 | |||||||
chr10:13195497 | C | T | 1 | a0001c0001t0002g0014 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1974+228C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13195497 | |||||||
chr10:13195582 | G | GTTTA | 48 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0087 others(45): Show |
51 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1974+353_1974+356d others(6): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr10 | 13195582 | ||||||
chr10:13195582 | G | GTTTATTT others(1): Show |
30 | a0001c0001t0001g0030 a0001c0001t0001g0360 a0001c0001t0001g0375 others(27): Show |
32 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1974+349_1974+356d others(10): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr10 | 13195582 | ||||||
chr10:13195582 | G | GTTTATTT others(5): Show |
2 | a0001c0001t0027g0156 a0002c0003t0009g0387 |
2 | HG02148.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1974+345_1974+356d others(14): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr10 | 13195582 | ||||||
chr10:13195582 | GTTTA | G | 10 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(7): Show |
11 | HG00438.hp1 HG02015.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1974+353_1974+356d others(6): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr10 | 13195582 | ||||||
chr10:13195582 | GTTTATTT others(1): Show |
G | 46 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0341 others(43): Show |
46 | HG00408.hp2 HG00642.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.1974+349_1974+356d others(10): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr10 | 13195582 | ||||||
chr10:13195582 | GTTTATTT others(5): Show |
G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0278 |
2 | HG00735.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1974+345_1974+356d others(14): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr10 | 13195582 | ||||||
chr10:13195582 | GTTTATTT others(13): Show |
G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(198): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1974+337_1974+356d others(22): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr10 | 13195582 | ||||||
chr10:13195679 | C | T | 55 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(52): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1974+410C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13195679 | |||||||
chr10:13195752 | A | G | 2 | a0001c0008t0011g0268 a0001c0020t0003g0347 |
2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1974+483A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13195752 | |||||||
chr10:13195772 | G | A | 56 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(53): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1974+503G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13195772 | |||||||
chr10:13195968 | A | T | 1 | a0015c0019t0021g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1974+699A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13195968 | |||||||
chr10:13196074 | A | C | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1974+805A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196074 | |||||||
chr10:13196106 | C | A | 1 | a0001c0008t0011g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1974+837C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196106 | |||||||
chr10:13196204 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1974+935C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196204 | |||||||
chr10:13196329 | A | G | 24 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(21): Show |
25 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1974+1060A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196329 | |||||||
chr10:13196379 | C | A | 1 | a0001c0001t0002g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1974+1110C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196379 | |||||||
chr10:13196404 | T | A | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1974+1135T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196404 | |||||||
chr10:13196500 | GTTTA | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0075 others(96): Show |
106 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1975-1109_1975-110 others(8): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr10 | 13196500 | ||||||
chr10:13196636 | C | T | 41 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0341 others(38): Show |
41 | HG00408.hp2 HG00642.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1975-987C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196636 | |||||||
chr10:13196704 | G | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0305 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975-919G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196704 | |||||||
chr10:13196712 | C | T | 1 | a0001c0001t0003g0394 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1975-911C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196712 | |||||||
chr10:13196805 | G | A | 2 | a0001c0001t0007g0078 a0001c0001t0007g0331 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1975-818G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196805 | |||||||
chr10:13196808 | C | T | 56 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(53): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1975-815C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13196808 | |||||||
chr10:13196922 | C | CT | 99 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0101 others(96): Show |
112 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1975-694dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr10 | 13196922 | ||||||
chr10:13197045 | TC | T | 55 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(52): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1975-574delC | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr10 | 13197045 | ||||||
chr10:13197106 | C | T | 99 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0075 others(96): Show |
106 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1975-517C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13197106 | |||||||
chr10:13197152 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0101 others(72): Show |
87 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1975-471A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13197152 | |||||||
chr10:13197211 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0101 others(71): Show |
86 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1975-412T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13197211 | |||||||
chr10:13197489 | T | C | 55 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(52): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1975-134T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 14/19 | chr10 | 13197489 | |||||||
chr10:13197917 | A | AT | 70 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(67): Show |
78 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(75): Show |
intron_variant | MODIFIER | c.2119+166dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr10 | 13197917 | ||||||
chr10:13197917 | AT | A | 213 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0074 others(210): Show |
225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.2119+166delT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr10 | 13197917 | ||||||
chr10:13197917 | ATT | A | 26 | a0001c0001t0002g0060 a0001c0002t0004g0243 a0001c0004t0001g0070 others(23): Show |
27 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.2119+165_2119+166d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr10 | 13197917 | ||||||
chr10:13197917 | ATTT | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0101 others(71): Show |
86 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.2119+164_2119+166d others(5): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr10 | 13197917 | ||||||
chr10:13197938 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2119+171G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13197938 | |||||||
chr10:13198016 | G | A | 1 | a0001c0001t0003g0394 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2119+249G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198016 | |||||||
chr10:13198058 | G | A | 1 | a0001c0002t0001g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2119+291G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198058 | |||||||
chr10:13198061 | C | T | 11 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(8): Show |
13 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2119+294C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198061 | |||||||
chr10:13198130 | C | T | 176 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0075 others(173): Show |
185 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.2119+363C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198130 | |||||||
chr10:13198143 | A | C | 24 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(21): Show |
25 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.2119+376A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198143 | |||||||
chr10:13198154 | C | T | 1 | a0001c0001t0007g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2119+387C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198154 | |||||||
chr10:13198166 | C | A | 12 | a0001c0002t0001g0210 a0001c0002t0004g0129 a0001c0002t0004g0312 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.2119+399C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198166 | |||||||
chr10:13198219 | T | C | 1 | a0001c0001t0007g0076 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2119+452T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198219 | |||||||
chr10:13198240 | T | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0101 others(72): Show |
87 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.2120-449T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198240 | |||||||
chr10:13198407 | A | G | 17 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(14): Show |
19 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2120-282A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198407 | |||||||
chr10:13198456 | G | A | 2 | a0001c0004t0004g0039 a0019c0024t0004g0256 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2120-233G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198456 | |||||||
chr10:13198543 | T | C | 12 | a0001c0002t0001g0210 a0001c0002t0004g0129 a0001c0002t0004g0312 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.2120-146T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198543 | |||||||
chr10:13198562 | G | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0074 others(152): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2120-127G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 15/19 | chr10 | 13198562 | |||||||
chr10:13198887 | G | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0074 others(152): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2238+80G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13198887 | |||||||
chr10:13198964 | C | T | 1 | a0006c0010t0002g0177 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2238+157C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13198964 | |||||||
chr10:13199075 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2238+268T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13199075 | |||||||
chr10:13199096 | G | A | 1 | a0002c0003t0003g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2238+289G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13199096 | |||||||
chr10:13199145 | C | G | 1 | a0001c0002t0001g0089 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2238+338C>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13199145 | |||||||
chr10:13199156 | A | C | 56 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(53): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2238+349A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13199156 | |||||||
chr10:13199240 | T | C | 15 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0341 others(12): Show |
15 | HG00642.hp2 HG01192.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2238+433T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13199240 | |||||||
chr10:13199680 | A | T | 3 | a0001c0001t0003g0113 a0001c0001t0003g0159 a0001c0001t0003g0374 |
3 | HG02818.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2238+873A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13199680 | |||||||
chr10:13199814 | G | C | 23 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0341 others(20): Show |
23 | HG00642.hp2 HG01192.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.2238+1007G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13199814 | |||||||
chr10:13199957 | G | A | 325 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(322): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.2238+1150G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13199957 | |||||||
chr10:13199983 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0180 a0001c0001t0001g0244 others(1): Show |
4 | HG02258.hp1 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2238+1176T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13199983 | |||||||
chr10:13199986 | G | A | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2238+1179G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13199986 | |||||||
chr10:13200027 | C | A | 1 | a0001c0004t0014g0099 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2238+1220C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200027 | |||||||
chr10:13200173 | A | C | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2239-1248A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200173 | |||||||
chr10:13200287 | A | G | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2239-1134A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200287 | |||||||
chr10:13200296 | G | A | 1 | a0001c0001t0004g0318 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2239-1125G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200296 | |||||||
chr10:13200299 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0329 |
2 | HG02015.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2239-1122G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200299 | |||||||
chr10:13200364 | G | C | 1 | a0001c0002t0001g0381 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2239-1057G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200364 | |||||||
chr10:13200379 | C | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0101 others(71): Show |
86 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.2239-1042C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200379 | |||||||
chr10:13200413 | G | A | 41 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0341 others(38): Show |
41 | HG00408.hp2 HG00642.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.2239-1008G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200413 | |||||||
chr10:13200423 | A | G | 11 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(8): Show |
13 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2239-998A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200423 | |||||||
chr10:13200698 | C | T | 12 | a0001c0002t0001g0210 a0001c0002t0004g0129 a0001c0002t0004g0312 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.2239-723C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200698 | |||||||
chr10:13200785 | T | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0074 others(152): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2239-636T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13200785 | |||||||
chr10:13201106 | A | G | 1 | a0002c0003t0005g0383 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2239-315A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13201106 | |||||||
chr10:13201187 | T | C | 1 | a0001c0004t0004g0039 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2239-234T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13201187 | |||||||
chr10:13201216 | C | T | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2239-205C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13201216 | |||||||
chr10:13201333 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2239-88T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13201333 | |||||||
chr10:13201345 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0101 others(72): Show |
87 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.2239-76C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 16/19 | chr10 | 13201345 | |||||||
chr10:13201688 | C | T | 12 | a0001c0002t0001g0210 a0001c0002t0004g0129 a0001c0002t0004g0312 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.2352+154C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13201688 | |||||||
chr10:13201866 | G | A | 1 | a0013c0025t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2352+332G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13201866 | |||||||
chr10:13201898 | C | T | 326 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(323): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2352+364C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13201898 | |||||||
chr10:13202085 | G | A | 1 | a0001c0002t0005g0234 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2352+551G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13202085 | |||||||
chr10:13202086 | T | C | 326 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(323): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2352+552T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13202086 | |||||||
chr10:13202172 | A | G | 1 | a0002c0003t0003g0284 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2352+638A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13202172 | |||||||
chr10:13202177 | C | T | 1 | a0015c0019t0021g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2352+643C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13202177 | |||||||
chr10:13202214 | C | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0341 a0001c0001t0006g0373 |
3 | HG02922.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2352+680C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13202214 | |||||||
chr10:13202255 | G | T | 12 | a0001c0002t0001g0210 a0001c0002t0004g0129 a0001c0002t0004g0312 others(9): Show |
12 | HG01109.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.2352+721G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13202255 | |||||||
chr10:13202884 | G | A | 1 | a0001c0002t0001g0182 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2353-1335G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13202884 | |||||||
chr10:13202895 | A | G | 24 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(21): Show |
25 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.2353-1324A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13202895 | |||||||
chr10:13202909 | G | A | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(320): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2353-1310G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13202909 | |||||||
chr10:13202948 | G | A | 41 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0341 others(38): Show |
41 | HG00408.hp2 HG00642.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.2353-1271G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13202948 | |||||||
chr10:13203051 | G | T | 1 | a0001c0001t0001g0249 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2353-1168G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203051 | |||||||
chr10:13203143 | C | T | 25 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(22): Show |
26 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.2353-1076C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203143 | |||||||
chr10:13203183 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2353-1036G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203183 | |||||||
chr10:13203263 | G | A | 11 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(8): Show |
13 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2353-956G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203263 | |||||||
chr10:13203428 | C | T | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2353-791C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203428 | |||||||
chr10:13203559 | C | T | 3 | a0001c0008t0007g0067 a0001c0008t0007g0068 a0001c0008t0007g0262 |
3 | HG02572.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2353-660C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203559 | |||||||
chr10:13203686 | C | T | 11 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(8): Show |
13 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2353-533C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203686 | |||||||
chr10:13203753 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0101 others(72): Show |
87 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.2353-466A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203753 | |||||||
chr10:13203804 | AAG | A | 55 | a0001c0001t0001g0074 a0001c0001t0002g0014 a0001c0001t0002g0264 others(52): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.2353-412_2353-411d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr10 | 13203804 | ||||||
chr10:13203834 | A | C | 1 | a0001c0001t0003g0261 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2353-385A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203834 | |||||||
chr10:13203843 | C | T | 4 | a0001c0001t0002g0196 a0001c0001t0002g0253 a0001c0001t0002g0289 others(1): Show |
4 | HG01361.hp2 HG01975.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.2353-376C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203843 | |||||||
chr10:13203915 | G | A | 24 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(21): Show |
25 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.2353-304G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13203915 | |||||||
chr10:13204037 | A | AG | 25 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0341 others(22): Show |
25 | HG00642.hp2 HG01192.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.2353-179dupG | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr10 | 13204037 | ||||||
chr10:13204062 | A | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0075 others(98): Show |
108 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2353-157A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13204062 | |||||||
chr10:13204190 | C | T | 15 | a0001c0001t0001g0106 a0001c0001t0001g0220 a0001c0001t0001g0315 others(12): Show |
17 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2353-29C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 17/19 | chr10 | 13204190 | |||||||
chr10:13204414 | T | A | 1 | a0001c0001t0002g0253 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2498+50T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204414 | |||||||
chr10:13204415 | T | C | 1 | a0002c0003t0003g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2498+51T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204415 | |||||||
chr10:13204448 | C | A | 24 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(21): Show |
25 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.2498+84C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204448 | |||||||
chr10:13204448 | CG | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0305 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2498+85delG | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204448 | |||||||
chr10:13204450 | T | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0305 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2498+86T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204450 | |||||||
chr10:13204451 | T | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0305 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2498+87T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204451 | |||||||
chr10:13204611 | T | C | 45 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0341 others(42): Show |
45 | HG00408.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2498+247T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204611 | |||||||
chr10:13204727 | C | A | 5 | a0001c0001t0002g0034 a0001c0001t0003g0128 a0001c0001t0003g0162 others(2): Show |
5 | HG00280.hp2 HG01081.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2498+363C>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204727 | |||||||
chr10:13204768 | G | A | 1 | a0001c0002t0001g0366 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2498+404G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204768 | |||||||
chr10:13204945 | GT | G | 24 | a0001c0004t0001g0070 a0001c0004t0003g0181 a0001c0004t0004g0005 others(21): Show |
25 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.2498+583delT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204945 | ||||||
chr10:13204983 | CATGT | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0057 others(6): Show |
10 | HG00735.hp1 HG01106.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.2498+638_2498+641d others(6): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204983 | ||||||
chr10:13204983 | CATGTATG others(5): Show |
C | 5 | a0001c0002t0001g0112 a0001c0002t0001g0386 a0001c0002t0010g0388 others(2): Show |
5 | HG00099.hp2 HG01255.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.2498+630_2498+641d others(14): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204983 | ||||||
chr10:13204990 | GTATGTA | G | 3 | a0001c0004t0004g0071 a0001c0004t0004g0072 a0001c0004t0004g0100 |
3 | NA19063.hp2 NA19077.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2498+628_2498+633d others(8): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(3): Show |
G | 2 | a0011c0017t0004g0098 a0011c0017t0004g0246 |
2 | NA18990.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2498+628_2498+637d others(12): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(7): Show |
G | 8 | a0001c0001t0001g0106 a0001c0002t0001g0299 a0001c0002t0010g0349 others(5): Show |
9 | HG00673.hp2 HG01074.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.2498+630_2498+643d others(16): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(9): Show |
G | 2 | a0001c0002t0001g0090 a0001c0004t0004g0042 |
2 | HG01975.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2498+630_2498+645d others(18): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(11): Show |
G | 2 | a0001c0002t0001g0097 a0001c0002t0001g0216 |
2 | HG02165.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2498+630_2498+647d others(20): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(13): Show |
G | 6 | a0001c0001t0001g0356 a0001c0001t0002g0303 a0001c0001t0010g0384 others(3): Show |
6 | HG02027.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2498+630_2498+649d others(22): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(15): Show |
G | 9 | a0001c0001t0001g0279 a0001c0001t0001g0357 a0001c0001t0001g0359 others(6): Show |
9 | HG01346.hp1 HG01515.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.2498+630_2498+651d others(24): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(17): Show |
G | 16 | a0001c0001t0001g0075 a0001c0001t0001g0101 a0001c0001t0001g0251 others(13): Show |
16 | HG00558.hp1 HG01070.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.2498+630_2498+653d others(26): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(19): Show |
G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0077 others(21): Show |
26 | HG00621.hp1 HG00642.hp1 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.2498+630_2498+655d others(28): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(21): Show |
G | 12 | a0001c0002t0001g0002 a0001c0002t0001g0015 a0001c0002t0001g0028 others(9): Show |
17 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.2498+630_2498+657d others(30): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(31): Show |
G | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2498+630_2498+667d others(40): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(33): Show |
G | 1 | a0001c0001t0005g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2498+630_2498+669d others(42): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(35): Show |
G | 18 | a0001c0001t0001g0208 a0001c0001t0001g0315 a0001c0001t0005g0019 others(15): Show |
20 | HG00438.hp1 HG00639.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.2498+630_2498+671d others(44): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(37): Show |
G | 1 | a0004c0005t0005g0317 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2498+630_2498+673d others(46): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204990 | GTATGTAT others(39): Show |
G | 173 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0027 others(170): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2498+630_2498+675d others(48): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204990 | ||||||
chr10:13204992 | A | G | 14 | a0001c0001t0001g0074 a0001c0001t0001g0146 a0001c0001t0002g0014 others(11): Show |
16 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2498+628A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204992 | |||||||
chr10:13204994 | GTATGTAT others(3): Show |
G | 2 | a0001c0012t0001g0269 a0003c0009t0006g0219 |
2 | HG00408.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2498+634_2498+643d others(12): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204994 | ||||||
chr10:13204994 | GTATGTAT others(5): Show |
G | 2 | a0001c0001t0002g0014 a0001c0002t0004g0211 |
3 | HG01070.hp2 HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2498+634_2498+645d others(14): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204994 | ||||||
chr10:13204994 | GTATGTAT others(7): Show |
G | 6 | a0001c0002t0004g0129 a0004c0005t0004g0132 a0004c0005t0004g0202 others(3): Show |
7 | HG01255.hp2 HG01257.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2498+634_2498+647d others(16): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204994 | ||||||
chr10:13204994 | GTATGTAT others(9): Show |
G | 3 | a0004c0005t0002g0346 a0004c0005t0004g0203 a0021c0022t0001g0250 |
3 | HG01496.hp1 HG04204.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.2498+634_2498+649d others(18): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204994 | ||||||
chr10:13204994 | GTATGTAT others(11): Show |
G | 2 | a0001c0001t0001g0074 a0001c0001t0002g0264 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2498+634_2498+651d others(20): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204994 | ||||||
chr10:13204994 | GTATGTAT others(17): Show |
G | 6 | a0005c0006t0006g0306 a0005c0006t0006g0369 a0005c0006t0007g0040 others(3): Show |
6 | HG01106.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2498+634_2498+657d others(26): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204994 | ||||||
chr10:13204994 | GTATGTAT others(23): Show |
G | 4 | a0001c0001t0001g0146 a0001c0001t0003g0045 a0001c0001t0003g0158 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2498+634_2498+663d others(32): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204994 | ||||||
chr10:13204994 | GTATGTAT others(25): Show |
G | 4 | a0001c0008t0007g0067 a0001c0008t0007g0068 a0001c0008t0007g0262 others(1): Show |
4 | HG02572.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2498+634_2498+665d others(34): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204994 | ||||||
chr10:13204994 | GTATGTAT others(27): Show |
G | 1 | a0001c0002t0001g0210 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2498+634_2498+667d others(36): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204994 | ||||||
chr10:13204994 | GTATGTAT others(33): Show |
G | 1 | a0001c0012t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2498+634_2498+673d others(42): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204994 | ||||||
chr10:13204996 | A | G | 2 | a0001c0001t0011g0367 a0001c0008t0011g0268 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2498+632A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13204996 | |||||||
chr10:13204998 | G | GTA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0137 others(3): Show |
6 | HG01884.hp2 HG02015.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.2498+636_2498+637d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | G | GTATATAT others(5): Show |
1 | a0001c0001t0002g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2498+637_2498+638i others(14): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTA | G | 13 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0095 others(10): Show |
13 | HG00738.hp2 HG01123.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.2498+638_2498+643d others(8): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTAT others(1): Show |
G | 11 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0141 others(8): Show |
11 | HG01952.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2498+638_2498+645d others(10): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTAT others(3): Show |
G | 7 | a0001c0001t0001g0147 a0001c0001t0003g0041 a0001c0001t0003g0043 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2498+638_2498+647d others(12): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTAT others(5): Show |
G | 8 | a0001c0001t0001g0115 a0001c0001t0001g0180 a0001c0001t0001g0244 others(5): Show |
8 | HG01981.hp2 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2498+638_2498+649d others(14): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTAT others(7): Show |
G | 3 | a0001c0001t0001g0360 a0001c0001t0015g0012 a0001c0001t0018g0038 |
4 | HG02970.hp1 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2498+638_2498+651d others(16): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTAT others(11): Show |
G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0255 a0001c0001t0001g0305 others(2): Show |
5 | HG01243.hp1 HG02622.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.2498+638_2498+655d others(20): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTAT others(19): Show |
G | 2 | a0001c0001t0001g0021 a0015c0019t0021g0064 |
3 | HG01884.hp1 NA18950.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2498+638_2498+663d others(28): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTAT others(21): Show |
G | 1 | a0001c0001t0003g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2498+638_2498+665d others(30): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTAT others(25): Show |
G | 1 | a0001c0001t0001g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2498+638_2498+669d others(34): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTAT others(27): Show |
G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0266 |
2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2498+638_2498+671d others(36): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13204998 | GTATGTAT others(31): Show |
G | 1 | a0001c0001t0001g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2498+638_2498+675d others(40): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13204998 | ||||||
chr10:13205000 | ATG | A | 9 | a0001c0001t0001g0259 a0001c0001t0001g0343 a0001c0001t0003g0055 others(6): Show |
9 | HG00642.hp2 HG01192.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2498+638_2498+639d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13205000 | ||||||
chr10:13205002 | G | A | 12 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0087 others(9): Show |
13 | HG01884.hp2 HG02015.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2498+638G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205002 | |||||||
chr10:13205004 | A | G | 2 | a0001c0004t0003g0181 a0001c0004t0004g0069 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2498+640A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205004 | |||||||
chr10:13205006 | A | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0088 a0001c0004t0004g0323 others(2): Show |
6 | NA18947.hp1 NA18968.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.2498+642A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205006 | |||||||
chr10:13205008 | A | G | 3 | a0001c0001t0003g0149 a0001c0002t0004g0211 a0001c0004t0004g0042 |
3 | HG02109.hp2 HG02257.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2498+644A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205008 | |||||||
chr10:13205010 | A | G | 5 | a0001c0002t0004g0129 a0004c0005t0004g0132 a0004c0005t0004g0202 others(2): Show |
5 | HG01255.hp2 HG01257.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.2498+646A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205010 | |||||||
chr10:13205012 | A | G | 6 | a0001c0004t0004g0039 a0001c0004t0004g0272 a0001c0008t0011g0268 others(3): Show |
6 | HG01496.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2498+648A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205012 | |||||||
chr10:13205016 | A | G | 3 | a0001c0001t0001g0311 a0001c0004t0004g0151 a0001c0004t0004g0372 |
3 | HG01070.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2498+652A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205016 | |||||||
chr10:13205018 | A | G | 4 | a0001c0004t0004g0152 a0001c0004t0004g0222 a0001c0004t0004g0260 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2498+654A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205018 | |||||||
chr10:13205020 | A | G | 2 | a0001c0004t0001g0070 a0001c0004t0014g0157 |
2 | HG03225.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2498+656A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205020 | |||||||
chr10:13205030 | A | G | 2 | a0001c0002t0001g0210 a0018c0027t0022g0393 |
2 | HG01934.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2498+666A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205030 | |||||||
chr10:13205032 | A | G | 1 | a0001c0001t0005g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2498+668A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205032 | |||||||
chr10:13205034 | A | G | 18 | a0001c0001t0001g0208 a0001c0001t0001g0315 a0001c0001t0005g0019 others(15): Show |
20 | HG00438.hp1 HG00639.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.2498+670A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205034 | |||||||
chr10:13205036 | A | G | 1 | a0004c0005t0005g0317 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2498+672A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205036 | |||||||
chr10:13205038 | A | G | 173 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0027 others(170): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2498+674A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205038 | |||||||
chr10:13205054 | T | A | 1 | a0001c0001t0001g0238 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2498+690T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205054 | |||||||
chr10:13205098 | G | C | 4 | a0001c0001t0002g0081 a0001c0001t0005g0019 a0001c0001t0005g0049 others(1): Show |
5 | HG00438.hp1 HG02015.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.2498+734G>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205098 | |||||||
chr10:13205122 | C | T | 26 | a0001c0001t0001g0146 a0001c0001t0003g0045 a0001c0001t0003g0158 others(23): Show |
27 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.2498+758C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205122 | |||||||
chr10:13205155 | T | C | 11 | a0001c0001t0004g0338 a0001c0002t0001g0210 a0001c0002t0004g0129 others(8): Show |
11 | HG01255.hp2 HG01257.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.2498+791T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205155 | |||||||
chr10:13205160 | A | G | 11 | a0001c0001t0001g0160 a0001c0001t0001g0343 a0001c0001t0003g0041 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2498+796A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205160 | |||||||
chr10:13205195 | C | T | 23 | a0001c0004t0003g0181 a0001c0004t0004g0005 a0001c0004t0004g0039 others(20): Show |
24 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.2498+831C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205195 | |||||||
chr10:13205206 | T | C | 1 | a0001c0002t0001g0299 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2498+842T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205206 | |||||||
chr10:13205262 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2498+898G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205262 | |||||||
chr10:13205288 | T | C | 11 | a0003c0009t0006g0123 a0003c0009t0006g0219 a0003c0009t0006g0363 others(8): Show |
11 | HG00408.hp2 HG01106.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2498+924T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205288 | |||||||
chr10:13205305 | T | C | 6 | a0001c0001t0002g0034 a0001c0001t0002g0196 a0001c0001t0002g0253 others(3): Show |
6 | HG01361.hp2 HG01975.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2498+941T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205305 | |||||||
chr10:13205476 | T | G | 245 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0074 others(242): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.2498+1112T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205476 | |||||||
chr10:13205500 | A | G | 6 | a0001c0001t0006g0114 a0001c0001t0006g0148 a0001c0001t0006g0371 others(3): Show |
6 | HG02145.hp2 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2498+1136A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205500 | |||||||
chr10:13205571 | T | G | 1 | a0001c0001t0003g0149 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2498+1207T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205571 | |||||||
chr10:13205611 | A | G | 175 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0105 others(172): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.2498+1247A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205611 | |||||||
chr10:13205642 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2498+1278A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205642 | |||||||
chr10:13205742 | T | C | 15 | a0001c0001t0006g0114 a0001c0001t0006g0148 a0001c0001t0006g0371 others(12): Show |
16 | HG00408.hp2 HG02074.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.2498+1378T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205742 | |||||||
chr10:13205758 | G | A | 11 | a0001c0002t0001g0002 a0001c0002t0001g0015 a0001c0002t0001g0125 others(8): Show |
15 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.2498+1394G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205758 | |||||||
chr10:13205859 | C | T | 7 | a0001c0001t0003g0045 a0001c0001t0003g0158 a0001c0008t0007g0033 others(4): Show |
7 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2498+1495C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205859 | |||||||
chr10:13205893 | G | T | 5 | a0001c0004t0004g0151 a0001c0004t0004g0222 a0001c0004t0004g0260 others(2): Show |
5 | HG02109.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2498+1529G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205893 | |||||||
chr10:13205895 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0074 a0001c0001t0001g0180 others(3): Show |
6 | HG02258.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2498+1531C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205895 | |||||||
chr10:13205927 | C | T | 1 | a0002c0003t0003g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2498+1563C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13205927 | |||||||
chr10:13206028 | T | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0172 others(94): Show |
104 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.2498+1664T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13206028 | |||||||
chr10:13206091 | T | G | 26 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0022 others(23): Show |
30 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.2498+1727T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13206091 | |||||||
chr10:13206284 | A | G | 1 | a0001c0002t0010g0388 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2498+1920A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13206284 | |||||||
chr10:13206410 | G | T | 244 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0016 others(241): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.2498+2046G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13206410 | |||||||
chr10:13206639 | A | C | 164 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0016 others(161): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2498+2275A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13206639 | |||||||
chr10:13206682 | A | T | 3 | a0001c0004t0004g0042 a0001c0004t0004g0272 a0018c0027t0022g0393 |
3 | HG02257.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2498+2318A>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13206682 | |||||||
chr10:13206771 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2499-2320T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13206771 | |||||||
chr10:13206798 | C | CT | 173 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0016 others(170): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2499-2281dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13206798 | ||||||
chr10:13206798 | C | CTT | 6 | a0002c0003t0003g0310 a0003c0007t0003g0051 a0003c0007t0003g0052 others(3): Show |
6 | HG00280.hp1 HG01175.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2499-2282_2499-228 others(6): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13206798 | ||||||
chr10:13206885 | G | A | 1 | a0020c0018t0004g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2499-2206G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13206885 | |||||||
chr10:13207190 | T | C | 246 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0016 others(243): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.2499-1901T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207190 | |||||||
chr10:13207191 | G | A | 2 | a0002c0003t0003g0224 a0002c0003t0003g0229 |
2 | HG00323.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2499-1900G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207191 | |||||||
chr10:13207236 | G | T | 2 | a0001c0002t0001g0119 a0001c0002t0001g0121 |
2 | NA18951.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.2499-1855G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207236 | |||||||
chr10:13207347 | A | AT | 22 | a0001c0001t0004g0257 a0001c0001t0004g0265 a0001c0004t0003g0181 others(19): Show |
23 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.2499-1734dupT | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13207347 | ||||||
chr10:13207379 | G | T | 165 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0016 others(162): Show |
176 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2499-1712G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207379 | |||||||
chr10:13207386 | A | G | 40 | a0001c0001t0004g0338 a0001c0001t0005g0007 a0001c0001t0005g0019 others(37): Show |
44 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.2499-1705A>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207386 | |||||||
chr10:13207451 | G | A | 1 | a0015c0019t0021g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2499-1640G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207451 | |||||||
chr10:13207475 | C | T | 24 | a0001c0001t0004g0257 a0001c0001t0004g0265 a0001c0004t0003g0181 others(21): Show |
25 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.2499-1616C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207475 | |||||||
chr10:13207500 | G | T | 2 | a0001c0001t0011g0367 a0001c0008t0011g0268 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2499-1591G>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207500 | |||||||
chr10:13207546 | T | C | 1 | a0018c0027t0022g0393 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2499-1545T>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207546 | |||||||
chr10:13207577 | G | A | 2 | a0001c0001t0011g0367 a0001c0008t0011g0268 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2499-1514G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207577 | |||||||
chr10:13207652 | G | A | 26 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0022 others(23): Show |
30 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.2499-1439G>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207652 | |||||||
chr10:13207805 | T | A | 2 | a0001c0001t0011g0367 a0001c0008t0011g0268 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2499-1286T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207805 | |||||||
chr10:13207990 | TTCTC | T | 109 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0016 others(106): Show |
115 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.2499-1095_2499-109 others(8): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13207990 | ||||||
chr10:13207996 | C | T | 26 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0022 others(23): Show |
30 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.2499-1095C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13207996 | |||||||
chr10:13208090 | T | A | 2 | a0001c0001t0003g0128 a0002c0003t0003g0228 |
2 | HG00280.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2499-1001T>A | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13208090 | |||||||
chr10:13208090 | T | G | 225 | a0001c0001t0001g0236 a0001c0001t0002g0008 a0001c0001t0002g0014 others(222): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.2499-1001T>G | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13208090 | |||||||
chr10:13208133 | C | T | 17 | a0001c0001t0003g0045 a0001c0001t0003g0055 a0001c0001t0003g0062 others(14): Show |
17 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.2499-958C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13208133 | |||||||
chr10:13208409 | A | C | 26 | a0001c0001t0005g0007 a0001c0001t0005g0019 a0001c0001t0005g0022 others(23): Show |
30 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.2499-682A>C | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13208409 | |||||||
chr10:13208471 | C | T | 2 | a0001c0001t0002g0008 a0001c0001t0002g0379 |
3 | NA18953.hp2 NA18957.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2499-620C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13208471 | |||||||
chr10:13208566 | C | CA | 20 | a0001c0001t0001g0160 a0001c0001t0001g0343 a0001c0001t0006g0114 others(17): Show |
21 | HG00408.hp2 HG02074.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2499-509dupA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13208566 | ||||||
chr10:13208566 | C | CAA | 14 | a0001c0001t0002g0117 a0001c0001t0004g0338 a0001c0002t0004g0129 others(11): Show |
14 | HG01255.hp2 HG01257.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.2499-510_2499-509d others(4): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13208566 | ||||||
chr10:13208566 | C | CAAA | 161 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0016 others(158): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.2499-511_2499-509d others(5): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13208566 | ||||||
chr10:13208566 | CA | C | 23 | a0001c0001t0004g0257 a0001c0001t0004g0265 a0001c0002t0001g0119 others(20): Show |
24 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.2499-509delA | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13208566 | ||||||
chr10:13208566 | CAAAA | C | 25 | a0001c0001t0003g0041 a0001c0001t0003g0043 a0001c0001t0003g0045 others(22): Show |
25 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.2499-512_2499-509d others(6): Show |
MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 13208566 | ||||||
chr10:13208743 | C | T | 7 | a0001c0001t0001g0066 a0001c0001t0001g0146 a0001c0001t0001g0199 others(4): Show |
7 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2499-348C>T | MCM10 | ENSG00000065328.17 | transcript | ENST00000378714.8 | protein_coding | 18/19 | chr10 | 13208743 |