Item | Value |
---|---|
geneid | 84515 |
ensemblid | ENSG00000125885.13 |
hgncid | 16147 |
symbol | MCM8 |
name | minichromosome maintenance 8 homologous recombination repair factor |
refseq_nuc | NM_032485.6 |
refseq_prot | NP_115874.3 |
ensembl_nuc | ENST00000610722.4 |
ensembl_prot | ENSP00000478141.1 |
mane_status | MANE Select |
chr | chr20 |
start | 5950652 |
end | 5998977 |
strand | + |
ver | v1.2 |
region | chr20:5950652-5998977 |
region5000 | chr20:5945652-6003977 |
regionname0 | MCM8_chr20_5950652_5998977 |
regionname5000 | MCM8_chr20_5945652_6003977 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 840 | 173 | 28 | 39 | 78 | 10 | 16 | 56 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0002 | 0/0 | 840 | 92 | 39 | 10 | 27 | 3 | 13 | 19 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0003 | 0/0 | 840 | 48 | 1 | 0 | 45 | 0 | 2 | 39 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0004 | 0/0 | 840 | 22 | 12 | 8 | 0 | 1 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0005 | 0/0 | 840 | 8 | 0 | 6 | 0 | 1 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0006 | 0/0 | 840 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0007 | 0/0 | 840 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0008 | 0/0 | 840 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0009 | 0/0 | 840 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0010 | 0/0 | 840 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0011 | 0/0 | 840 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0012 | 0/0 | 840 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0013 | 0/0 | 840 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0014 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0015 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0016 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
a0017 | 0/0 | 840 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | MNGEY others(835): Show |
chr20 | 5945652 | 6003977 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2520 | 161 | 27 | 33 | 78 | 9 | 13 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0001c0006 | 0/0 | 2520 | 4 | 1 | 2 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0001c0008 | 0/0 | 2520 | 4 | 0 | 3 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0001c0012 | 0/1 | 2520 | 3 | 0 | 1 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0001c0022 | 0/0 | 2520 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0002c0002 | 0/0 | 2520 | 92 | 39 | 10 | 27 | 3 | 13 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0003c0003 | 0/0 | 2520 | 43 | 1 | 0 | 40 | 0 | 2 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0003c0007 | 0/0 | 2520 | 4 | 0 | 0 | 4 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0003c0020 | 0/0 | 2520 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0004c0004 | 0/0 | 2520 | 21 | 11 | 8 | 0 | 1 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0004c0024 | 0/0 | 2520 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0005c0005 | 0/0 | 2520 | 8 | 0 | 6 | 0 | 1 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0006c0010 | 0/0 | 2520 | 3 | 3 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0007c0013 | 0/0 | 2520 | 3 | 3 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0008c0009 | 0/0 | 2520 | 3 | 3 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0009c0011 | 0/0 | 2520 | 3 | 3 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0010c0016 | 0/0 | 2520 | 2 | 0 | 0 | 0 | 0 | 2 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0011c0014 | 0/0 | 2520 | 2 | 0 | 0 | 0 | 0 | 2 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0012c0015 | 0/0 | 2520 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0013c0018 | 0/0 | 2520 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0014c0021 | 0/0 | 2520 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0015c0023 | 0/0 | 2520 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0016c0019 | 0/0 | 2520 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 | ||
a0017c0017 | 0/0 | 2520 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | ATGAA others(2515): Show |
chr20 | 5945652 | 6003977 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7487 | 75 | 7 | 15 | 45 | 3 | 5 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0003 | 1/0 | 7486 | 18 | 6 | 6 | 0 | 2 | 3 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0006 | 0/0 | 7486 | 11 | 1 | 1 | 8 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0010 | 0/0 | 7486 | 6 | 0 | 1 | 5 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0012 | 0/0 | 7487 | 5 | 5 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0013 | 0/0 | 7487 | 3 | 3 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0018 | 0/0 | 7487 | 3 | 0 | 3 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0021 | 0/0 | 7487 | 3 | 0 | 0 | 3 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0025 | 0/0 | 7485 | 2 | 0 | 1 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7480): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0026 | 0/0 | 7487 | 3 | 0 | 1 | 0 | 2 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0031 | 0/0 | 7483 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7478): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0034 | 0/0 | 7487 | 2 | 0 | 0 | 0 | 0 | 2 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0035 | 0/0 | 7487 | 2 | 0 | 1 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0036 | 0/0 | 7487 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0044 | 0/0 | 7487 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0049 | 0/0 | 7488 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0051 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0054 | 0/0 | 7487 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0057 | 0/0 | 7482 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7477): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0066 | 0/0 | 7488 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0067 | 0/0 | 7487 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0068 | 0/0 | 7487 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0069 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0070 | 0/0 | 7488 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0071 | 0/0 | 7487 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0072 | 0/0 | 7486 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0074 | 0/0 | 7487 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0075 | 0/0 | 7487 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0082 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0084 | 0/0 | 7486 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0085 | 0/0 | 7486 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0093 | 0/0 | 7485 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7480): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0094 | 0/0 | 7485 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7480): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0095 | 0/0 | 7484 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7479): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0096 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0097 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0001t0098 | 0/0 | 7486 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0006t0006 | 0/0 | 7486 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0006t0023 | 0/0 | 7486 | 3 | 1 | 2 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0008t0030 | 0/0 | 7486 | 2 | 0 | 2 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0008t0055 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0008t0056 | 0/0 | 7485 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7480): Show |
chr20 | 5945652 | 6003977 |
a0001c0012t0001 | 0/0 | 7487 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0001c0012t0010 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0001c0012t0062 | 0/1 | 7489 | 1 | 0 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0001c0022t0019 | 0/0 | 7485 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7480): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0002 | 0/0 | 7489 | 30 | 13 | 2 | 12 | 1 | 2 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0005 | 0/0 | 7489 | 18 | 5 | 0 | 5 | 0 | 8 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0009 | 0/0 | 7488 | 6 | 3 | 0 | 3 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0011 | 0/0 | 7489 | 5 | 2 | 2 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0015 | 0/0 | 7488 | 4 | 2 | 1 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0016 | 0/0 | 7490 | 3 | 3 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7485): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0024 | 0/0 | 7488 | 3 | 0 | 1 | 1 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0027 | 0/0 | 7484 | 3 | 2 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7479): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0028 | 0/0 | 7488 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0029 | 0/0 | 7489 | 2 | 1 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0046 | 0/0 | 7489 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0047 | 0/0 | 7489 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0048 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0050 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0052 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0053 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0063 | 0/0 | 7489 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0064 | 0/0 | 7488 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0073 | 0/0 | 7488 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0076 | 0/0 | 7488 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0077 | 0/0 | 7489 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0078 | 0/0 | 7489 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0079 | 0/0 | 7487 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0080 | 0/0 | 7487 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0092 | 0/0 | 7487 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0002c0002t0099 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0004 | 0/0 | 7482 | 18 | 0 | 0 | 18 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7477): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0008 | 0/0 | 7472 | 9 | 0 | 0 | 9 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7467): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0032 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7473): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0033 | 0/0 | 7476 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7471): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0040 | 0/0 | 7481 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7476): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0043 | 0/0 | 7481 | 2 | 0 | 0 | 1 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7476): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0058 | 0/0 | 7477 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7472): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0059 | 0/0 | 7472 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7467): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0060 | 0/0 | 7470 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7465): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0061 | 0/0 | 7468 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7463): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0081 | 0/0 | 7482 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7477): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0086 | 0/0 | 7482 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7477): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0087 | 0/0 | 7486 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0089 | 0/0 | 7481 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7476): Show |
chr20 | 5945652 | 6003977 |
a0003c0003t0090 | 0/0 | 7482 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7477): Show |
chr20 | 5945652 | 6003977 |
a0003c0007t0004 | 0/0 | 7482 | 4 | 0 | 0 | 4 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7477): Show |
chr20 | 5945652 | 6003977 |
a0003c0020t0032 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7473): Show |
chr20 | 5945652 | 6003977 |
a0004c0004t0007 | 0/0 | 7486 | 10 | 0 | 8 | 0 | 1 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0004c0004t0014 | 0/0 | 7486 | 4 | 4 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0004c0004t0022 | 0/0 | 7486 | 3 | 3 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0004c0004t0037 | 0/0 | 7486 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0004c0004t0065 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0004c0004t0088 | 0/0 | 7485 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7480): Show |
chr20 | 5945652 | 6003977 |
a0004c0024t0083 | 0/0 | 7486 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0005c0005t0003 | 0/0 | 7486 | 7 | 0 | 5 | 0 | 1 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0005c0005t0025 | 0/0 | 7485 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7480): Show |
chr20 | 5945652 | 6003977 |
a0006c0010t0020 | 0/0 | 7488 | 3 | 3 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0007c0013t0039 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0007c0013t0042 | 0/0 | 7486 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0008c0009t0017 | 0/0 | 7487 | 3 | 3 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0009c0011t0041 | 0/0 | 7486 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0009c0011t0091 | 0/0 | 7485 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7480): Show |
chr20 | 5945652 | 6003977 |
a0010c0016t0019 | 0/0 | 7485 | 2 | 0 | 0 | 0 | 0 | 2 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7480): Show |
chr20 | 5945652 | 6003977 |
a0011c0014t0002 | 0/0 | 7489 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7484): Show |
chr20 | 5945652 | 6003977 |
a0011c0014t0009 | 0/0 | 7488 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0012c0015t0038 | 0/0 | 7487 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0013c0018t0001 | 0/0 | 7487 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0014c0021t0045 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
a0015c0023t0039 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7483): Show |
chr20 | 5945652 | 6003977 |
a0016c0019t0013 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7482): Show |
chr20 | 5945652 | 6003977 |
a0017c0017t0006 | 0/0 | 7486 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | CTTTG others(7481): Show |
chr20 | 5945652 | 6003977 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 24 | 2 | 4 | 16 | 0 | 2 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0004 | 1/0 | 3 | 0 | 1 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0006g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0006g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0010g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0010g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0010g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0010g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0012g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0012g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0012g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0013g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0013g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0018g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0018g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0018g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0021g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0021g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0025g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0025g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0026g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0031g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0034g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0034g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0035g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0035g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0036g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0036g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0044g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0044g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0049g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0051g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0054g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0057g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0066g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0067g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0068g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0069g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0070g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0071g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0072g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0074g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0075g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0082g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0084g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0085g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0093g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0094g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0095g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0096g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0097g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0001t0098g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0006t0006g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0006t0023g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0006t0023g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0006t0023g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0008t0030g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0008t0030g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0008t0055g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0008t0056g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0012t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0012t0010g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0012t0062g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0001c0022t0019g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0006 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0009g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0009g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0011g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0011g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0011g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0015g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0015g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0015g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0016g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0016g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0024g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0024g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0024g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0027g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0028g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0028g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0029g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0029g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0046g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0047g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0048g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0050g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0052g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0053g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0063g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0064g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0073g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0076g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0077g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0078g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0079g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0080g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0092g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0002c0002t0099g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0004g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0004g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0004g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0004g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0008g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0008g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0008g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0032g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0033g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0033g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0040g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0043g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0043g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0058g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0059g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0060g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0061g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0081g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0086g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0087g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0089g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0003t0090g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0007t0004g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0007t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0007t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0003c0020t0032g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0007g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0007g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0007g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0007g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0007g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0014g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0014g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0014g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0022g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0022g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0037g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0065g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0004t0088g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0004c0024t0083g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0005c0005t0003g0004 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0005c0005t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0005c0005t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0005c0005t0025g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0006c0010t0020g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0006c0010t0020g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0006c0010t0020g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0007c0013t0039g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0007c0013t0042g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0007c0013t0042g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0008c0009t0017g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0008c0009t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0009c0011t0041g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0009c0011t0091g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0010c0016t0019g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0010c0016t0019g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0011c0014t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0011c0014t0009g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0012c0015t0038g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0012c0015t0038g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0013c0018t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0014c0021t0045g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0015c0023t0039g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0016c0019t0013g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
a0017c0017t0006g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0013 | c0018 | t0001 | g0104 | EUR | GBR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00099 | hp2 | a0001 | c0001 | t0026 | g0003 | EUR | GBR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0125 | EUR | GBR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0187 | EUR | FIN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00323 | hp2 | a0004 | c0004 | t0007 | g0134 | EUR | FIN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00408 | hp2 | a0003 | c0003 | t0033 | g0213 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00423 | hp1 | a0001 | c0001 | t0098 | g0085 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00438 | hp1 | a0001 | c0001 | t0085 | g0116 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00544 | hp1 | a0001 | c0001 | t0072 | g0001 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00544 | hp2 | a0003 | c0003 | t0004 | g0018 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00558 | hp1 | a0003 | c0003 | t0008 | g0208 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00558 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00597 | hp1 | a0001 | c0001 | t0074 | g0005 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00597 | hp2 | a0003 | c0003 | t0004 | g0002 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00609 | hp1 | a0002 | c0002 | t0080 | g0145 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0027 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00621 | hp2 | a0002 | c0002 | t0029 | g0014 | EAS | CHS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00642 | hp1 | a0004 | c0004 | t0007 | g0114 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00735 | hp1 | a0002 | c0002 | t0011 | g0224 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00735 | hp2 | a0001 | c0001 | t0018 | g0011 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0181 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01070 | hp1 | a0001 | c0001 | t0051 | g0149 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01070 | hp2 | a0005 | c0005 | t0025 | g0035 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01071 | hp1 | a0002 | c0002 | t0063 | g0006 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01071 | hp2 | a0005 | c0005 | t0003 | g0004 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01074 | hp1 | a0001 | c0001 | t0067 | g0001 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01074 | hp2 | a0001 | c0008 | t0030 | g0234 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01081 | hp1 | a0005 | c0005 | t0003 | g0004 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01081 | hp2 | a0001 | c0008 | t0030 | g0235 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01099 | hp1 | a0001 | c0001 | t0035 | g0102 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01099 | hp2 | a0002 | c0002 | t0024 | g0037 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01109 | hp1 | a0005 | c0005 | t0003 | g0004 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01109 | hp2 | a0014 | c0021 | t0045 | g0230 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01167 | hp1 | a0001 | c0001 | t0018 | g0162 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01167 | hp2 | a0001 | c0001 | t0025 | g0126 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01168 | hp2 | a0005 | c0005 | t0003 | g0035 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0201 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01175 | hp2 | a0001 | c0001 | t0026 | g0003 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01243 | hp2 | a0002 | c0002 | t0027 | g0016 | AMR | PUR | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01255 | hp2 | a0001 | c0008 | t0055 | g0049 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01256 | hp1 | a0001 | c0006 | t0023 | g0086 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01256 | hp2 | a0001 | c0001 | t0010 | g0100 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01257 | hp1 | a0004 | c0004 | t0007 | g0136 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01257 | hp2 | a0001 | c0001 | t0066 | g0007 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01258 | hp1 | a0001 | c0006 | t0023 | g0087 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01261 | hp2 | a0001 | c0001 | t0082 | g0003 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01346 | hp1 | a0001 | c0001 | t0018 | g0161 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01346 | hp2 | a0004 | c0004 | t0007 | g0053 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01496 | hp2 | a0002 | c0002 | t0073 | g0159 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01515 | hp2 | a0001 | c0001 | t0095 | g0010 | EUR | IBS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01516 | hp1 | a0001 | c0008 | t0056 | g0049 | EUR | IBS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01516 | hp2 | a0002 | c0002 | t0015 | g0225 | EUR | IBS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01517 | hp1 | a0002 | c0002 | t0079 | g0019 | EUR | IBS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | IBS | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01884 | hp1 | a0004 | c0004 | t0037 | g0031 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01884 | hp2 | a0006 | c0010 | t0020 | g0207 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01891 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01891 | hp2 | a0001 | c0006 | t0023 | g0026 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01928 | hp2 | a0002 | c0002 | t0015 | g0223 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01934 | hp2 | a0004 | c0004 | t0007 | g0052 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01943 | hp1 | a0001 | c0012 | t0010 | g0058 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01943 | hp2 | a0004 | c0004 | t0007 | g0135 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01952 | hp1 | a0002 | c0002 | t0064 | g0019 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01978 | hp2 | a0004 | c0004 | t0007 | g0036 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01981 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01993 | hp1 | a0002 | c0002 | t0011 | g0019 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01993 | hp2 | a0004 | c0004 | t0007 | g0131 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02055 | hp1 | a0001 | c0001 | t0069 | g0229 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02055 | hp2 | a0004 | c0004 | t0022 | g0025 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02056 | hp1 | a0001 | c0001 | t0070 | g0078 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02056 | hp2 | a0001 | c0001 | t0084 | g0115 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02074 | hp1 | a0003 | c0003 | t0081 | g0043 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02083 | hp2 | a0002 | c0002 | t0047 | g0188 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02145 | hp1 | a0002 | c0002 | t0016 | g0164 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0096 | EAS | CDX | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02257 | hp1 | a0001 | c0001 | t0013 | g0048 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02258 | hp1 | a0002 | c0002 | t0029 | g0013 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0202 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02273 | hp1 | a0004 | c0004 | t0007 | g0036 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02280 | hp1 | a0002 | c0002 | t0053 | g0175 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02280 | hp2 | a0001 | c0001 | t0013 | g0048 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02451 | hp1 | a0004 | c0024 | t0083 | g0110 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02451 | hp2 | a0004 | c0004 | t0088 | g0132 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02523 | hp1 | a0002 | c0002 | t0076 | g0150 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02572 | hp1 | a0002 | c0002 | t0028 | g0173 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02572 | hp2 | a0004 | c0004 | t0022 | g0112 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02602 | hp1 | a0001 | c0001 | t0035 | g0105 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02602 | hp2 | a0010 | c0016 | t0019 | g0231 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02615 | hp1 | a0001 | c0001 | t0012 | g0088 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02615 | hp2 | a0002 | c0002 | t0016 | g0166 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02622 | hp2 | a0007 | c0013 | t0042 | g0139 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02630 | hp1 | a0008 | c0009 | t0017 | g0169 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02630 | hp2 | a0004 | c0004 | t0014 | g0030 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02647 | hp1 | a0002 | c0002 | t0050 | g0174 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0167 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02683 | hp1 | a0002 | c0002 | t0011 | g0040 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02683 | hp2 | a0002 | c0002 | t0005 | g0180 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02698 | hp2 | a0002 | c0002 | t0005 | g0158 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02717 | hp1 | a0002 | c0002 | t0009 | g0015 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0051 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02723 | hp1 | a0001 | c0001 | t0012 | g0089 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0182 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02735 | hp1 | a0005 | c0005 | t0003 | g0004 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02735 | hp2 | a0002 | c0002 | t0005 | g0153 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02738 | hp1 | a0001 | c0012 | t0001 | g0075 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02738 | hp2 | a0002 | c0002 | t0005 | g0156 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0183 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02818 | hp2 | a0001 | c0001 | t0096 | g0178 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02886 | hp2 | a0006 | c0010 | t0020 | g0147 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02895 | hp2 | a0002 | c0002 | t0016 | g0163 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0171 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02896 | hp2 | a0002 | c0002 | t0002 | g0165 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0172 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02922 | hp2 | a0008 | c0009 | t0017 | g0038 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02965 | hp1 | a0004 | c0004 | t0014 | g0054 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02965 | hp2 | a0002 | c0002 | t0052 | g0168 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02970 | hp1 | a0002 | c0002 | t0099 | g0130 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02970 | hp2 | a0015 | c0023 | t0039 | g0142 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03017 | hp2 | a0010 | c0016 | t0019 | g0233 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0190 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03130 | hp1 | a0002 | c0002 | t0011 | g0184 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03130 | hp2 | a0004 | c0004 | t0014 | g0030 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03139 | hp1 | a0009 | c0011 | t0091 | g0238 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03139 | hp2 | a0008 | c0009 | t0017 | g0038 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0090 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03195 | hp2 | a0002 | c0002 | t0005 | g0013 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03209 | hp1 | a0002 | c0002 | t0027 | g0016 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03209 | hp2 | a0006 | c0010 | t0020 | g0148 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03225 | hp1 | a0001 | c0001 | t0012 | g0055 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03225 | hp2 | a0016 | c0019 | t0013 | g0227 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03453 | hp1 | a0001 | c0001 | t0097 | g0186 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03453 | hp2 | a0004 | c0004 | t0022 | g0025 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03486 | hp1 | a0009 | c0011 | t0041 | g0050 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0228 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03491 | hp1 | a0011 | c0014 | t0009 | g0205 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03516 | hp1 | a0004 | c0004 | t0014 | g0113 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03516 | hp2 | a0007 | c0013 | t0042 | g0140 | AFR | ESN | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03540 | hp1 | a0002 | c0002 | t0027 | g0016 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03540 | hp2 | a0002 | c0002 | t0015 | g0039 | AFR | GWD | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03579 | hp1 | a0002 | c0002 | t0009 | g0015 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03579 | hp2 | a0002 | c0002 | t0005 | g0151 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03669 | hp1 | a0002 | c0002 | t0005 | g0006 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03669 | hp2 | a0001 | c0006 | t0006 | g0026 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03704 | hp1 | a0001 | c0001 | t0049 | g0011 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03704 | hp2 | a0002 | c0002 | t0024 | g0006 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03710 | hp1 | a0002 | c0002 | t0005 | g0014 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03834 | hp1 | a0002 | c0002 | t0005 | g0154 | SAS | BEB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03834 | hp2 | a0003 | c0003 | t0043 | g0210 | SAS | BEB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03927 | hp1 | a0017 | c0017 | t0006 | g0091 | SAS | BEB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0199 | SAS | BEB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03942 | hp1 | a0003 | c0003 | t0090 | g0216 | SAS | BEB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03942 | hp2 | a0011 | c0014 | t0002 | g0206 | SAS | BEB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG04115 | hp1 | a0002 | c0002 | t0077 | g0160 | SAS | STU | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | STU | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0189 | SAS | BEB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG04184 | hp2 | a0001 | c0001 | t0034 | g0119 | SAS | BEB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0117 | SAS | STU | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG04199 | hp2 | a0002 | c0002 | t0005 | g0037 | SAS | STU | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG04228 | hp1 | a0001 | c0001 | t0034 | g0032 | SAS | STU | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | STU | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18522 | hp1 | a0002 | c0002 | t0015 | g0039 | AFR | YRI | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18522 | hp2 | a0002 | c0002 | t0005 | g0006 | AFR | YRI | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18612 | hp1 | a0001 | c0001 | t0010 | g0082 | EAS | CHB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18612 | hp2 | a0003 | c0003 | t0004 | g0002 | EAS | CHB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18747 | hp2 | a0002 | c0002 | t0005 | g0157 | EAS | CHB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | YRI | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18906 | hp2 | a0007 | c0013 | t0039 | g0141 | AFR | YRI | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18939 | hp2 | a0003 | c0003 | t0033 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18940 | hp1 | a0001 | c0001 | t0006 | g0095 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18941 | hp1 | a0003 | c0003 | t0008 | g0222 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18942 | hp1 | a0003 | c0007 | t0004 | g0212 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18942 | hp2 | a0001 | c0001 | t0075 | g0003 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18944 | hp1 | a0001 | c0001 | t0036 | g0060 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18944 | hp2 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18946 | hp2 | a0002 | c0002 | t0024 | g0014 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18947 | hp2 | a0003 | c0003 | t0004 | g0219 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18948 | hp2 | a0003 | c0003 | t0008 | g0047 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18949 | hp2 | a0003 | c0003 | t0004 | g0220 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18952 | hp1 | a0012 | c0015 | t0038 | g0237 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18952 | hp2 | a0003 | c0003 | t0004 | g0218 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18953 | hp1 | a0003 | c0020 | t0032 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18953 | hp2 | a0001 | c0001 | t0031 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18954 | hp1 | a0003 | c0003 | t0040 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18957 | hp1 | a0012 | c0015 | t0038 | g0236 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18957 | hp2 | a0001 | c0001 | t0093 | g0097 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18963 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18964 | hp1 | a0003 | c0003 | t0043 | g0044 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18965 | hp2 | a0002 | c0002 | t0092 | g0012 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18969 | hp1 | a0003 | c0007 | t0004 | g0045 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18972 | hp1 | a0003 | c0003 | t0004 | g0046 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18973 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18974 | hp2 | a0003 | c0003 | t0004 | g0008 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18977 | hp2 | a0001 | c0001 | t0021 | g0005 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18979 | hp1 | a0002 | c0002 | t0005 | g0155 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18979 | hp2 | a0001 | c0001 | t0031 | g0070 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18980 | hp1 | a0001 | c0001 | t0036 | g0074 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18980 | hp2 | a0003 | c0003 | t0008 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18982 | hp1 | a0002 | c0002 | t0009 | g0197 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18982 | hp2 | a0001 | c0001 | t0068 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18983 | hp1 | a0003 | c0003 | t0004 | g0046 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18984 | hp1 | a0001 | c0001 | t0010 | g0022 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18986 | hp2 | a0003 | c0007 | t0004 | g0215 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18987 | hp1 | a0001 | c0001 | t0010 | g0021 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18987 | hp2 | a0003 | c0003 | t0089 | g0211 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18989 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18990 | hp2 | a0003 | c0003 | t0004 | g0018 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18992 | hp1 | a0003 | c0003 | t0058 | g0217 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18992 | hp2 | a0002 | c0002 | t0005 | g0152 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18998 | hp1 | a0003 | c0003 | t0008 | g0043 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18998 | hp2 | a0002 | c0002 | t0046 | g0200 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA18999 | hp2 | a0003 | c0003 | t0004 | g0018 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19006 | hp2 | a0003 | c0003 | t0008 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19009 | hp1 | a0003 | c0003 | t0004 | g0221 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19010 | hp1 | a0003 | c0003 | t0032 | g0214 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19011 | hp1 | a0003 | c0003 | t0008 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19011 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19012 | hp2 | a0003 | c0003 | t0008 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | LWK | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19030 | hp2 | a0002 | c0002 | t0078 | g0013 | AFR | LWK | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19043 | hp1 | a0009 | c0011 | t0041 | g0050 | AFR | LWK | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19043 | hp2 | a0003 | c0003 | t0087 | g0209 | AFR | LWK | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19054 | hp1 | a0003 | c0003 | t0008 | g0047 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19056 | hp1 | a0003 | c0003 | t0061 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19057 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19057 | hp2 | a0001 | c0001 | t0094 | g0092 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19058 | hp1 | a0003 | c0003 | t0086 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19058 | hp2 | a0001 | c0001 | t0054 | g0022 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19062 | hp1 | a0003 | c0003 | t0040 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19062 | hp2 | a0001 | c0001 | t0071 | g0068 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19063 | hp1 | a0002 | c0002 | t0005 | g0012 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19063 | hp2 | a0001 | c0001 | t0057 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19065 | hp2 | a0003 | c0003 | t0059 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19066 | hp2 | a0003 | c0003 | t0004 | g0044 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19067 | hp1 | a0002 | c0002 | t0009 | g0042 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19070 | hp2 | a0003 | c0003 | t0004 | g0008 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19079 | hp1 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19081 | hp2 | a0002 | c0002 | t0009 | g0041 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19084 | hp1 | a0003 | c0007 | t0004 | g0045 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19085 | hp1 | a0002 | c0002 | t0005 | g0012 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19085 | hp2 | a0003 | c0003 | t0004 | g0008 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19087 | hp1 | a0003 | c0003 | t0060 | g0002 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19087 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19088 | hp1 | a0003 | c0003 | t0004 | g0008 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA20129 | hp1 | a0002 | c0002 | t0005 | g0006 | AFR | ASW | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA20129 | hp2 | a0001 | c0001 | t0044 | g0177 | AFR | ASW | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA20752 | hp1 | a0001 | c0001 | t0026 | g0003 | EUR | TSI | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA20752 | hp2 | a0005 | c0005 | t0003 | g0004 | EUR | TSI | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA20805 | hp2 | a0001 | c0001 | t0025 | g0129 | EUR | TSI | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA20905 | hp1 | a0004 | c0004 | t0007 | g0133 | SAS | GIH | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA20905 | hp2 | a0001 | c0022 | t0019 | g0232 | SAS | GIH | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01123 | hp1 | a0005 | c0005 | t0003 | g0124 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02109 | hp1 | a0002 | c0002 | t0048 | g0176 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02486 | hp1 | a0002 | c0002 | t0009 | g0170 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02486 | hp2 | a0001 | c0001 | t0044 | g0185 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02559 | hp1 | a0004 | c0004 | t0065 | g0111 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ACB | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03471 | hp1 | a0002 | c0002 | t0028 | g0146 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG03471 | hp2 | a0002 | c0002 | t0005 | g0179 | AFR | MSL | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG06807 | hp1 | a0002 | c0002 | t0011 | g0204 | AFR | USA | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | USA | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | USA | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA21309 | hp1 | a0004 | c0004 | t0037 | g0031 | AFR | LWK | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
homoSapiens | chm13v2 | a0001 | c0012 | t0062 | g0076 | REF | REF | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0004 | REF | REF | MCM8_chr20_5945652_6003977 | MCM8 | chr20 | 5945652 | 6003977 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:5951023 | A | T | 1 | a0001 | 1 | HG00423.hp1 | splice_region_variant | LOW | c.-6A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/19 | chr20 | 5951023 | |||||||
chr20:5952149 | G | A | 1 | a0017 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.134G>A | p.Gly45Glu | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 2/19 | 511/7486 | 134/2523 | 45/840 | chr20 | 5952149 | |||
chr20:5952462 | C | A | 3 | a0002 a0008 a0011 |
97 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(94): Show |
missense_variant | MODERATE | c.187C>A | p.Gln63Lys | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/19 | 564/7486 | 187/2523 | 63/840 | chr20 | 5952462 | |||
chr20:5952484 | A | G | 1 | a0010 | 2 | HG02602.hp2 HG03017.hp2 |
missense_variant | MODERATE | c.209A>G | p.Asp70Gly | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/19 | 586/7486 | 209/2523 | 70/840 | chr20 | 5952484 | |||
chr20:5954657 | A | C | 1 | a0004 | 22 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(19): Show |
missense_variant | MODERATE | c.303A>C | p.Lys101Asn | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/19 | 680/7486 | 303/2523 | 101/840 | chr20 | 5954657 | |||
chr20:5954679 | T | G | 1 | a0006 | 3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.325T>G | p.Leu109Val | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/19 | 702/7486 | 325/2523 | 109/840 | chr20 | 5954679 | |||
chr20:5955179 | A | G | 1 | a0011 | 2 | HG03491.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.414A>G | p.Ile138Met | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/19 | 791/7486 | 414/2523 | 138/840 | chr20 | 5955179 | |||
chr20:5955186 | A | G | 1 | a0012 | 2 | NA18952.hp1 NA18957.hp1 |
missense_variant | MODERATE | c.421A>G | p.Ile141Val | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/19 | 798/7486 | 421/2523 | 141/840 | chr20 | 5955186 | |||
chr20:5955229 | G | A | 2 | a0009 a0012 |
5 | HG03139.hp1 HG03486.hp1 NA18952.hp1 others(2): Show |
missense_variant | MODERATE | c.464G>A | p.Cys155Tyr | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/19 | 841/7486 | 464/2523 | 155/840 | chr20 | 5955229 | |||
chr20:5957187 | A | G | 4 | a0007 a0009 a0012 others(1): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
missense_variant | MODERATE | c.548A>G | p.Asn183Ser | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/19 | 925/7486 | 548/2523 | 183/840 | chr20 | 5957187 | |||
chr20:5963310 | G | C | 1 | a0003 | 48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
missense_variant | MODERATE | c.826G>C | p.Ala276Pro | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/19 | 1203/7486 | 826/2523 | 276/840 | chr20 | 5963310 | |||
chr20:5967581 | G | A | 1 | a0005 | 8 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(5): Show |
missense_variant | MODERATE | c.1021G>A | p.Glu341Lys | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 9/19 | 1398/7486 | 1021/2523 | 341/840 | chr20 | 5967581 | |||
chr20:5967896 | G | A | 1 | a0003 | 48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
missense_variant | MODERATE | c.1094G>A | p.Ser365Asn | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/19 | 1471/7486 | 1094/2523 | 365/840 | chr20 | 5967896 | |||
chr20:5973165 | A | G | 1 | a0016 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1364A>G | p.Asp455Gly | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/19 | 1741/7486 | 1364/2523 | 455/840 | chr20 | 5973165 | |||
chr20:5977962 | T | G | 1 | a0015 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1482T>G | p.Asp494Glu | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/19 | 1859/7486 | 1482/2523 | 494/840 | chr20 | 5977962 | |||
chr20:5986117 | A | G | 1 | a0013 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.2149A>G | p.Ile717Val | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/19 | 2526/7486 | 2149/2523 | 717/840 | chr20 | 5986117 | |||
chr20:5993619 | A | G | 2 | a0004 a0008 |
25 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(22): Show |
missense_variant | MODERATE | c.2354A>G | p.Asn785Ser | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 18/19 | 2731/7486 | 2354/2523 | 785/840 | chr20 | 5993619 | |||
chr20:5993694 | A | G | 1 | a0014 | 1 | HG01109.hp2 | missense_variant&splice_region_variant | MODERATE | c.2429A>G | p.Gln810Arg | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 18/19 | 2806/7486 | 2429/2523 | 810/840 | chr20 | 5993694 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:5958568 | A | C | 11 | a0001c0008 a0001c0022 a0003c0003 others(8): Show |
65 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(62): Show |
synonymous_variant | LOW | c.631A>C | p.Arg211Arg | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/19 | 1008/7486 | 631/2523 | 211/840 | chr20 | 5958568 | |||
chr20:5963339 | G | A | 2 | a0004c0024 a0008c0009 |
4 | HG02451.hp1 HG02630.hp1 HG02922.hp2 others(1): Show |
synonymous_variant | LOW | c.855G>A | p.Thr285Thr | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/19 | 1232/7486 | 855/2523 | 285/840 | chr20 | 5963339 | |||
chr20:5967514 | T | C | 1 | a0014c0021 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.954T>C | p.Asp318Asp | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 9/19 | 1331/7486 | 954/2523 | 318/840 | chr20 | 5967514 | |||
chr20:5967535 | G | A | 1 | a0003c0007 | 4 | NA18942.hp1 NA18969.hp1 NA18986.hp2 others(1): Show |
synonymous_variant | LOW | c.975G>A | p.Pro325Pro | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 9/19 | 1352/7486 | 975/2523 | 325/840 | chr20 | 5967535 | |||
chr20:5967894 | T | C | 1 | a0001c0012 | 2 | HG01943.hp1 HG02738.hp1 |
synonymous_variant | LOW | c.1092T>C | p.Asn364Asn | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/19 | 1469/7486 | 1092/2523 | 364/840 | chr20 | 5967894 | |||
chr20:5973106 | C | T | 2 | a0001c0022 a0010c0016 |
3 | HG02602.hp2 HG03017.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.1305C>T | p.Tyr435Tyr | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/19 | 1682/7486 | 1305/2523 | 435/840 | chr20 | 5973106 | |||
chr20:5973169 | A | G | 1 | a0001c0006 | 4 | HG01256.hp1 HG01258.hp1 HG01891.hp2 others(1): Show |
synonymous_variant | LOW | c.1368A>G | p.Pro456Pro | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/19 | 1745/7486 | 1368/2523 | 456/840 | chr20 | 5973169 | |||
chr20:5973187 | A | G | 10 | a0001c0008 a0001c0022 a0003c0003 others(7): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
synonymous_variant | LOW | c.1386A>G | p.Gln462Gln | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/19 | 1763/7486 | 1386/2523 | 462/840 | chr20 | 5973187 | |||
chr20:5993602 | T | C | 1 | a0003c0020 | 1 | NA18953.hp1 | synonymous_variant | LOW | c.2337T>C | p.Phe779Phe | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 18/19 | 2714/7486 | 2337/2523 | 779/840 | chr20 | 5993602 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:5950728 | T | C | 1 | a0014c0021t0045 | 1 | HG01109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-301T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/19 | 1288 | chr20 | 5950728 | ||||||
chr20:5950750 | A | G | 1 | a0002c0002t0027 | 3 | HG01243.hp2 HG03209.hp1 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-279A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/19 | 1266 | chr20 | 5950750 | ||||||
chr20:5950824 | G | T | 1 | a0002c0002t0099 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-205G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/19 | 1192 | chr20 | 5950824 | ||||||
chr20:5950827 | G | A | 18 | a0001c0001t0018 a0001c0001t0049 a0001c0001t0051 others(15): Show |
62 | HG00323.hp1 HG00621.hp2 HG00735.hp2 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-202G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/19 | 1189 | chr20 | 5950827 | ||||||
chr20:5950854 | T | C | 1 | a0001c0001t0054 | 1 | NA19058.hp2 | 5_prime_UTR_variant | MODIFIER | c.-175T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/19 | 1162 | chr20 | 5950854 | ||||||
chr20:5950929 | G | C | 5 | a0001c0008t0030 a0001c0008t0055 a0001c0008t0056 others(2): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-100G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/19 | 1087 | chr20 | 5950929 | ||||||
chr20:5950931 | A | G | 5 | a0001c0008t0030 a0001c0008t0055 a0001c0008t0056 others(2): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-98A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/19 | 1085 | chr20 | 5950931 | ||||||
chr20:5950958 | C | G | 2 | a0001c0022t0019 a0010c0016t0019 |
3 | HG02602.hp2 HG03017.hp2 NA20905.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-71C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/19 | chr20 | 5950958 | |||||||
chr20:5994466 | CACAG | C | 4 | a0001c0001t0031 a0001c0001t0057 a0003c0003t0032 others(1): Show |
5 | NA18953.hp1 NA18953.hp2 NA18979.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*87_*90delGACA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 87 | INFO_REALIGN_3_PRIME | chr20 | 5994466 | |||||
chr20:5994474 | GACAGAC | G | 2 | a0003c0003t0033 a0003c0003t0058 |
3 | HG00408.hp2 NA18939.hp2 NA18992.hp1 |
3_prime_UTR_variant | MODIFIER | c.*87_*92delGACACA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 87 | INFO_REALIGN_3_PRIME | chr20 | 5994474 | |||||
chr20:5994474 | GACAGACA others(3): Show |
G | 2 | a0003c0003t0008 a0003c0003t0059 |
10 | HG00558.hp1 NA18941.hp1 NA18948.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*87_*96delGACACACA others(2): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 87 | INFO_REALIGN_3_PRIME | chr20 | 5994474 | |||||
chr20:5994474 | GACAGACA others(5): Show |
G | 1 | a0003c0003t0060 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87_*98delGACACACA others(4): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 87 | INFO_REALIGN_3_PRIME | chr20 | 5994474 | |||||
chr20:5994474 | GACAGACA others(7): Show |
G | 1 | a0003c0003t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87_*100delGACACAC others(7): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 87 | INFO_REALIGN_3_PRIME | chr20 | 5994474 | |||||
chr20:5994478 | G | GAC | 34 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0010 others(31): Show |
84 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*131_*132dupCA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 133 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994478 | G | GACAC | 17 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0026 others(14): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*129_*132dupCACA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 133 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994478 | G | GACACAC | 8 | a0001c0001t0001 a0001c0001t0026 a0001c0001t0034 others(5): Show |
17 | HG00738.hp1 HG00738.hp2 HG01106.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*127_*132dupCACACA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 133 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994478 | G | GACACACA others(3): Show |
1 | a0002c0002t0016 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*123_*132dupCACACA others(4): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 133 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994478 | G | GACACACA others(13): Show |
1 | a0002c0002t0016 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113_*132dupCACACA others(14): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 133 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994478 | GAC | G | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(20): Show |
47 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*131_*132delCA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 131 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994478 | GACAC | G | 10 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(7): Show |
18 | HG00438.hp1 HG00438.hp2 HG01167.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*129_*132delCACA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 129 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994478 | GACACACA others(1): Show |
G | 3 | a0001c0022t0019 a0003c0003t0004 a0010c0016t0019 |
7 | HG02602.hp2 HG03017.hp2 NA18974.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*125_*132delCACACA others(2): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 125 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994478 | GACACACA others(3): Show |
G | 12 | a0002c0002t0002 a0003c0003t0004 a0003c0003t0040 others(9): Show |
31 | HG00544.hp2 HG00597.hp2 HG02074.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*123_*132delCACACA others(4): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 123 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994478 | GACACACA others(5): Show |
G | 4 | a0006c0010t0020 a0009c0011t0041 a0009c0011t0091 others(1): Show |
6 | HG01884.hp2 HG03139.hp1 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*121_*132delCACACA others(6): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 121 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994478 | GACACACA others(7): Show |
G | 2 | a0007c0013t0039 a0015c0023t0039 |
2 | HG02970.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*119_*132delCACACA others(8): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 119 | INFO_REALIGN_3_PRIME | chr20 | 5994478 | |||||
chr20:5994543 | A | G | 1 | a0001c0001t0026 | 3 | HG00099.hp2 HG01175.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*152A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 152 | chr20 | 5994543 | ||||||
chr20:5994658 | G | A | 1 | a0002c0002t0063 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*267G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 267 | chr20 | 5994658 | ||||||
chr20:5994732 | C | T | 3 | a0001c0001t0044 a0001c0001t0096 a0001c0001t0097 |
4 | HG02486.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*341C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 341 | chr20 | 5994732 | ||||||
chr20:5994733 | T | TA | 2 | a0001c0001t0044 a0001c0001t0096 |
3 | HG02486.hp2 HG02818.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*342_*343insA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 343 | chr20 | 5994733 | ||||||
chr20:5994734 | T | A | 2 | a0001c0001t0044 a0001c0001t0096 |
3 | HG02486.hp2 HG02818.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*343T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 343 | chr20 | 5994734 | ||||||
chr20:5994734 | T | TA | 47 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0013 others(44): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*361dupA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 362 | INFO_REALIGN_3_PRIME | chr20 | 5994734 | |||||
chr20:5994734 | TA | T | 11 | a0001c0001t0025 a0001c0001t0093 a0001c0001t0094 others(8): Show |
15 | HG01070.hp2 HG01099.hp2 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*361delA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 361 | INFO_REALIGN_3_PRIME | chr20 | 5994734 | |||||
chr20:5994952 | T | G | 1 | a0001c0001t0034 | 2 | HG04184.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*561T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 561 | chr20 | 5994952 | ||||||
chr20:5995185 | A | G | 1 | a0001c0001t0075 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*794A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 794 | chr20 | 5995185 | ||||||
chr20:5995234 | C | G | 1 | a0007c0013t0042 | 2 | HG02622.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*843C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 843 | chr20 | 5995234 | ||||||
chr20:5995333 | T | C | 26 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0009 others(23): Show |
92 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*942T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 942 | chr20 | 5995333 | ||||||
chr20:5995395 | A | G | 1 | a0001c0008t0055 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1004A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1004 | chr20 | 5995395 | ||||||
chr20:5995421 | A | G | 1 | a0001c0001t0074 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1030A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1030 | chr20 | 5995421 | ||||||
chr20:5995464 | C | A | 1 | a0004c0004t0007 | 10 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1073C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1073 | chr20 | 5995464 | ||||||
chr20:5995518 | C | T | 1 | a0002c0002t0073 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1127C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1127 | chr20 | 5995518 | ||||||
chr20:5995655 | T | A | 1 | a0014c0021t0045 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1264T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1264 | chr20 | 5995655 | ||||||
chr20:5995795 | A | T | 6 | a0007c0013t0039 a0007c0013t0042 a0009c0011t0041 others(3): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1404A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1404 | chr20 | 5995795 | ||||||
chr20:5995827 | C | T | 1 | a0004c0004t0037 | 2 | HG01884.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1436C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1436 | chr20 | 5995827 | ||||||
chr20:5995896 | A | G | 1 | a0003c0003t0090 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1505A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1505 | chr20 | 5995896 | ||||||
chr20:5995990 | A | C | 1 | a0001c0006t0023 | 3 | HG01256.hp1 HG01258.hp1 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1599A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1599 | chr20 | 5995990 | ||||||
chr20:5996005 | G | A | 1 | a0003c0003t0081 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1614G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1614 | chr20 | 5996005 | ||||||
chr20:5996228 | T | A | 2 | a0001c0001t0035 a0001c0001t0082 |
3 | HG01099.hp1 HG01261.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1837T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1837 | chr20 | 5996228 | ||||||
chr20:5996279 | G | GA | 23 | a0001c0001t0044 a0001c0001t0049 a0001c0001t0066 others(20): Show |
71 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1902dupA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1903 | INFO_REALIGN_3_PRIME | chr20 | 5996279 | |||||
chr20:5996279 | G | GAA | 10 | a0002c0002t0005 a0002c0002t0016 a0002c0002t0024 others(7): Show |
32 | HG00621.hp2 HG01071.hp1 HG01099.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1901_*1902dupAA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1903 | INFO_REALIGN_3_PRIME | chr20 | 5996279 | |||||
chr20:5996279 | GA | G | 11 | a0001c0001t0072 a0001c0001t0095 a0003c0003t0040 others(8): Show |
27 | HG00323.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1902delA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1902 | INFO_REALIGN_3_PRIME | chr20 | 5996279 | |||||
chr20:5996294 | T | A | 1 | a0002c0002t0079 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1903T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1903 | chr20 | 5996294 | ||||||
chr20:5996328 | G | A | 28 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0009 others(25): Show |
94 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1937G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 1937 | chr20 | 5996328 | ||||||
chr20:5996404 | C | T | 28 | a0001c0008t0030 a0001c0008t0055 a0001c0008t0056 others(25): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2013C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2013 | chr20 | 5996404 | ||||||
chr20:5996408 | A | G | 1 | a0001c0001t0094 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2017A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2017 | chr20 | 5996408 | ||||||
chr20:5996464 | C | T | 1 | a0003c0003t0087 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2073C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2073 | chr20 | 5996464 | ||||||
chr20:5996497 | C | T | 1 | a0001c0001t0085 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2106C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2106 | chr20 | 5996497 | ||||||
chr20:5996507 | C | T | 1 | a0002c0002t0047 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2116C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2116 | chr20 | 5996507 | ||||||
chr20:5996520 | CTAAA | C | 16 | a0003c0003t0004 a0003c0003t0008 a0003c0003t0032 others(13): Show |
47 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2133_*2136delATAA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2133 | INFO_REALIGN_3_PRIME | chr20 | 5996520 | |||||
chr20:5996543 | G | GA | 28 | a0001c0008t0030 a0001c0008t0055 a0001c0008t0056 others(25): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2160dupA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2161 | INFO_REALIGN_3_PRIME | chr20 | 5996543 | |||||
chr20:5996620 | TAGAC | T | 1 | a0002c0002t0027 | 3 | HG01243.hp2 HG03209.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2233_*2236delCAGA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2233 | INFO_REALIGN_3_PRIME | chr20 | 5996620 | |||||
chr20:5996672 | C | T | 1 | a0001c0001t0071 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2281C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2281 | chr20 | 5996672 | ||||||
chr20:5996687 | T | C | 5 | a0001c0008t0030 a0001c0008t0055 a0001c0008t0056 others(2): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2296T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2296 | chr20 | 5996687 | ||||||
chr20:5996737 | A | T | 1 | a0004c0004t0014 | 4 | HG02630.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2346A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2346 | chr20 | 5996737 | ||||||
chr20:5997002 | GT | G | 5 | a0001c0008t0030 a0001c0008t0055 a0001c0008t0056 others(2): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2614delT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2614 | INFO_REALIGN_3_PRIME | chr20 | 5997002 | |||||
chr20:5997033 | C | T | 28 | a0001c0008t0030 a0001c0008t0055 a0001c0008t0056 others(25): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2642C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2642 | chr20 | 5997033 | ||||||
chr20:5997169 | T | G | 1 | a0001c0001t0067 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2778T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2778 | chr20 | 5997169 | ||||||
chr20:5997174 | T | G | 1 | a0007c0013t0042 | 2 | HG02622.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2783T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2783 | chr20 | 5997174 | ||||||
chr20:5997185 | C | CT | 24 | a0001c0001t0070 a0002c0002t0002 a0002c0002t0005 others(21): Show |
89 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2810dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2811 | INFO_REALIGN_3_PRIME | chr20 | 5997185 | |||||
chr20:5997185 | CT | C | 27 | a0001c0001t0044 a0001c0001t0097 a0001c0008t0030 others(24): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2810delT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2810 | INFO_REALIGN_3_PRIME | chr20 | 5997185 | |||||
chr20:5997245 | C | T | 22 | a0001c0008t0030 a0001c0008t0055 a0001c0008t0056 others(19): Show |
55 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2854C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2854 | chr20 | 5997245 | ||||||
chr20:5997294 | C | T | 1 | a0001c0001t0069 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2903C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2903 | chr20 | 5997294 | ||||||
chr20:5997331 | T | C | 1 | a0003c0003t0087 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2940T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2940 | chr20 | 5997331 | ||||||
chr20:5997383 | T | C | 2 | a0004c0024t0083 a0008c0009t0017 |
4 | HG02451.hp1 HG02630.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2992T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 2992 | chr20 | 5997383 | ||||||
chr20:5997407 | C | T | 9 | a0002c0002t0005 a0002c0002t0024 a0002c0002t0029 others(6): Show |
29 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3016C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3016 | chr20 | 5997407 | ||||||
chr20:5997448 | C | T | 2 | a0001c0001t0036 a0001c0001t0075 |
3 | NA18942.hp2 NA18944.hp1 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3057C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3057 | chr20 | 5997448 | ||||||
chr20:5997482 | A | G | 1 | a0003c0003t0087 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3091A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3091 | chr20 | 5997482 | ||||||
chr20:5997495 | C | T | 61 | a0001c0001t0044 a0001c0001t0096 a0001c0001t0097 others(58): Show |
166 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*3104C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3104 | chr20 | 5997495 | ||||||
chr20:5997607 | A | C | 1 | a0002c0002t0046 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3216A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3216 | chr20 | 5997607 | ||||||
chr20:5997792 | A | C | 25 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0018 others(22): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*3401A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3401 | chr20 | 5997792 | ||||||
chr20:5998000 | C | T | 6 | a0007c0013t0039 a0007c0013t0042 a0009c0011t0041 others(3): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3609C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3609 | chr20 | 5998000 | ||||||
chr20:5998092 | C | G | 1 | a0003c0003t0059 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3701C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3701 | chr20 | 5998092 | ||||||
chr20:5998102 | T | C | 1 | a0001c0001t0084 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3711T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3711 | chr20 | 5998102 | ||||||
chr20:5998188 | G | A | 4 | a0003c0003t0032 a0003c0003t0033 a0003c0003t0058 others(1): Show |
5 | HG00408.hp2 NA18939.hp2 NA18953.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3797G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3797 | chr20 | 5998188 | ||||||
chr20:5998297 | C | G | 2 | a0003c0003t0086 a0003c0003t0089 |
2 | NA18987.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3906C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 3906 | chr20 | 5998297 | ||||||
chr20:5998411 | T | C | 1 | a0001c0001t0068 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4020T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 4020 | chr20 | 5998411 | ||||||
chr20:5998470 | G | C | 1 | a0002c0002t0099 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4079G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 4079 | chr20 | 5998470 | ||||||
chr20:5998487 | C | T | 17 | a0003c0003t0004 a0003c0003t0008 a0003c0003t0032 others(14): Show |
48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*4096C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 4096 | chr20 | 5998487 | ||||||
chr20:5998488 | G | A | 1 | a0001c0001t0021 | 3 | NA18973.hp2 NA18977.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4097G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 4097 | chr20 | 5998488 | ||||||
chr20:5998498 | C | T | 1 | a0002c0002t0078 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4107C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 4107 | chr20 | 5998498 | ||||||
chr20:5998601 | T | C | 1 | a0002c0002t0077 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4210T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 4210 | chr20 | 5998601 | ||||||
chr20:5998605 | G | T | 1 | a0004c0004t0065 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4214G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 4214 | chr20 | 5998605 | ||||||
chr20:5998890 | A | G | 3 | a0001c0008t0030 a0001c0008t0055 a0001c0008t0056 |
4 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4499A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 4499 | chr20 | 5998890 | ||||||
chr20:5998969 | T | A | 104 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(101): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
3_prime_UTR_variant | MODIFIER | c.*4578T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 19/19 | 4578 | chr20 | 5998969 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:5951045 | G | A | 1 | a0001c0001t0012g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-6+22G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | chr20 | 5951045 | |||||||
chr20:5951097 | T | C | 1 | a0001c0001t0001g0020 | 2 | HG01168.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-6+74T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | chr20 | 5951097 | |||||||
chr20:5951170 | G | A | 2 | a0004c0004t0007g0052 a0004c0004t0007g0053 |
2 | HG01346.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-6+147G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | chr20 | 5951170 | |||||||
chr20:5951179 | G | A | 1 | a0004c0004t0014g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-6+156G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | chr20 | 5951179 | |||||||
chr20:5951436 | C | T | 12 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(9): Show |
13 | HG01074.hp2 HG01081.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6+413C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | chr20 | 5951436 | |||||||
chr20:5951441 | A | G | 5 | a0001c0001t0006g0226 a0001c0001t0013g0048 a0001c0001t0013g0228 others(2): Show |
6 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6+418A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | chr20 | 5951441 | |||||||
chr20:5951458 | C | CT | 144 | a0001c0001t0001g0011 a0001c0001t0018g0011 a0001c0001t0018g0161 others(141): Show |
170 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.-6+437dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr20 | 5951458 | ||||||
chr20:5951544 | A | G | 132 | a0001c0001t0001g0011 a0001c0001t0018g0011 a0001c0001t0018g0161 others(129): Show |
157 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.-5-467A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | chr20 | 5951544 | |||||||
chr20:5951900 | G | T | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-111G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | chr20 | 5951900 | |||||||
chr20:5951958 | G | A | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-5-53G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | chr20 | 5951958 | |||||||
chr20:5952004 | C | T | 6 | a0002c0002t0011g0019 a0002c0002t0011g0224 a0002c0002t0015g0223 others(3): Show |
6 | HG00735.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.-5-7C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 1/18 | chr20 | 5952004 | |||||||
chr20:5952200 | T | TAATG | 42 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(39): Show |
58 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.148+39_148+40insTG others(2): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr20 | 5952200 | ||||||
chr20:5952216 | G | A | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.148+53G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 2/18 | chr20 | 5952216 | |||||||
chr20:5952294 | T | C | 1 | a0002c0002t0002g0143 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.149-130T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 2/18 | chr20 | 5952294 | |||||||
chr20:5952386 | ACT | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-35_149-34delCT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr20 | 5952386 | ||||||
chr20:5952533 | G | A | 1 | a0002c0002t0002g0144 | 1 | NA18972.hp2 | splice_region_variant&intron_variant | LOW | c.253+5G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5952533 | |||||||
chr20:5952688 | T | G | 1 | a0002c0002t0080g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.253+160T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5952688 | |||||||
chr20:5952706 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.253+178A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5952706 | |||||||
chr20:5952734 | C | T | 1 | a0006c0010t0020g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.253+206C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5952734 | |||||||
chr20:5952808 | A | T | 34 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(31): Show |
49 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.253+280A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5952808 | |||||||
chr20:5952889 | A | G | 34 | a0002c0002t0002g0040 a0002c0002t0002g0041 a0002c0002t0002g0042 others(31): Show |
34 | HG00323.hp1 HG00735.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.253+361A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5952889 | |||||||
chr20:5953071 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.253+543A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953071 | |||||||
chr20:5953167 | C | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.253+639C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953167 | |||||||
chr20:5953238 | T | C | 1 | a0010c0016t0019g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.253+710T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953238 | |||||||
chr20:5953392 | T | G | 1 | a0002c0002t0002g0143 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.253+864T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953392 | |||||||
chr20:5953438 | G | GGT | 10 | a0003c0003t0008g0047 a0003c0003t0008g0222 a0004c0004t0007g0036 others(7): Show |
12 | HG00323.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.253+942_253+943dup others(2): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr20 | 5953438 | ||||||
chr20:5953438 | G | GGTGTGT | 4 | a0007c0013t0039g0141 a0012c0015t0038g0236 a0012c0015t0038g0237 others(1): Show |
4 | HG02970.hp2 NA18906.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+938_253+943dup others(6): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr20 | 5953438 | ||||||
chr20:5953438 | G | GGTGTGTG others(3): Show |
1 | a0009c0011t0041g0050 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.253+934_253+943dup others(10): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr20 | 5953438 | ||||||
chr20:5953438 | G | GGTGTGTG others(13): Show |
1 | a0009c0011t0091g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.253+924_253+943dup others(20): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr20 | 5953438 | ||||||
chr20:5953438 | GGT | G | 127 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0029 others(124): Show |
153 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.253+942_253+943del others(2): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr20 | 5953438 | ||||||
chr20:5953438 | GGTGT | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(75): Show |
113 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.253+940_253+943del others(4): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr20 | 5953438 | ||||||
chr20:5953438 | GGTGTGTG others(5): Show |
G | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.253+932_253+943del others(12): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr20 | 5953438 | ||||||
chr20:5953438 | GGTGTGTG others(7): Show |
G | 1 | a0001c0001t0012g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.253+930_253+943del others(14): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr20 | 5953438 | ||||||
chr20:5953440 | T | G | 2 | a0004c0004t0014g0030 a0004c0004t0014g0113 |
3 | HG02630.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.253+912T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953440 | |||||||
chr20:5953442 | T | G | 2 | a0002c0002t0028g0146 a0003c0003t0008g0208 |
2 | HG00558.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.253+914T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953442 | |||||||
chr20:5953459 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.253+931G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953459 | |||||||
chr20:5953533 | G | A | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.253+1005G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953533 | |||||||
chr20:5953536 | C | T | 2 | a0001c0001t0044g0185 a0001c0001t0097g0186 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.253+1008C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953536 | |||||||
chr20:5953592 | G | C | 16 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(13): Show |
20 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.254-1016G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953592 | |||||||
chr20:5953598 | C | T | 1 | a0003c0003t0004g0220 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.254-1010C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953598 | |||||||
chr20:5953663 | C | T | 18 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(15): Show |
22 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.254-945C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953663 | |||||||
chr20:5953673 | C | T | 90 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(87): Show |
100 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.254-935C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953673 | |||||||
chr20:5953675 | G | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-933G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953675 | |||||||
chr20:5953715 | C | T | 1 | a0002c0002t0002g0143 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.254-893C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953715 | |||||||
chr20:5953719 | C | T | 34 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(31): Show |
49 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.254-889C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953719 | |||||||
chr20:5953731 | C | T | 2 | a0002c0002t0011g0184 a0002c0002t0015g0039 |
3 | HG03130.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.254-877C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953731 | |||||||
chr20:5953734 | A | G | 1 | a0002c0002t0077g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.254-874A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953734 | |||||||
chr20:5953762 | C | T | 1 | a0001c0001t0069g0229 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.254-846C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953762 | |||||||
chr20:5953763 | G | A | 1 | a0001c0001t0098g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.254-845G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953763 | |||||||
chr20:5953778 | C | CT | 101 | a0001c0001t0001g0084 a0001c0001t0044g0177 a0001c0001t0044g0185 others(98): Show |
111 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.254-819dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr20 | 5953778 | ||||||
chr20:5953778 | CT | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-819delT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr20 | 5953778 | ||||||
chr20:5953797 | C | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-811C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953797 | |||||||
chr20:5953804 | T | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-804T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953804 | |||||||
chr20:5953841 | T | C | 2 | a0004c0004t0065g0111 a0004c0024t0083g0110 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.254-767T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953841 | |||||||
chr20:5953867 | G | A | 26 | a0002c0002t0005g0006 a0002c0002t0005g0012 a0002c0002t0005g0013 others(23): Show |
29 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.254-741G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953867 | |||||||
chr20:5953905 | C | T | 4 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(1): Show |
4 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.254-703C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953905 | |||||||
chr20:5953920 | A | G | 59 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(56): Show |
66 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.254-688A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953920 | |||||||
chr20:5953937 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-671A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953937 | |||||||
chr20:5953961 | G | A | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.254-647G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5953961 | |||||||
chr20:5954225 | T | C | 4 | a0001c0006t0006g0026 a0001c0006t0023g0026 a0001c0006t0023g0086 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.254-383T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5954225 | |||||||
chr20:5954309 | T | C | 1 | a0001c0022t0019g0232 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.254-299T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5954309 | |||||||
chr20:5954443 | G | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-165G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5954443 | |||||||
chr20:5954458 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-150A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5954458 | |||||||
chr20:5954476 | T | C | 2 | a0007c0013t0042g0139 a0007c0013t0042g0140 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.254-132T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5954476 | |||||||
chr20:5954518 | C | T | 1 | a0002c0002t0028g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.254-90C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5954518 | |||||||
chr20:5954592 | A | G | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.254-16A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 3/18 | chr20 | 5954592 | |||||||
chr20:5954738 | A | G | 1 | a0002c0002t0048g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.336+48A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/18 | chr20 | 5954738 | |||||||
chr20:5954739 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(256): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.336+49T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/18 | chr20 | 5954739 | |||||||
chr20:5954740 | G | C | 1 | a0002c0002t0053g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.336+50G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/18 | chr20 | 5954740 | |||||||
chr20:5954745 | C | T | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.336+55C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/18 | chr20 | 5954745 | |||||||
chr20:5954803 | C | T | 90 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(87): Show |
100 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.336+113C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/18 | chr20 | 5954803 | |||||||
chr20:5954839 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.336+149A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/18 | chr20 | 5954839 | |||||||
chr20:5954854 | C | G | 2 | a0002c0002t0028g0173 a0002c0002t0050g0174 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.336+164C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/18 | chr20 | 5954854 | |||||||
chr20:5954876 | G | A | 1 | a0001c0001t0006g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.336+186G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/18 | chr20 | 5954876 | |||||||
chr20:5954995 | C | T | 1 | a0001c0001t0010g0082 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.337-107C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/18 | chr20 | 5954995 | |||||||
chr20:5955038 | G | T | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.337-64G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 4/18 | chr20 | 5955038 | |||||||
chr20:5955476 | C | T | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+225C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5955476 | |||||||
chr20:5955489 | GGAT | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+239_486+241del others(3): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5955489 | |||||||
chr20:5955583 | G | A | 2 | a0007c0013t0042g0139 a0007c0013t0042g0140 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.486+332G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5955583 | |||||||
chr20:5955662 | G | A | 1 | a0003c0003t0043g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.486+411G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5955662 | |||||||
chr20:5955673 | T | C | 1 | a0001c0001t0003g0121 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.486+422T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5955673 | |||||||
chr20:5955689 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(257): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.486+438G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5955689 | |||||||
chr20:5955740 | A | G | 33 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(30): Show |
48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.486+489A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5955740 | |||||||
chr20:5955742 | A | G | 1 | a0002c0002t0002g0203 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.486+491A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5955742 | |||||||
chr20:5955848 | C | T | 1 | a0002c0002t0005g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.486+597C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5955848 | |||||||
chr20:5955968 | G | A | 18 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(15): Show |
22 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.486+717G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5955968 | |||||||
chr20:5956018 | T | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+767T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956018 | |||||||
chr20:5956083 | C | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+832C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956083 | |||||||
chr20:5956287 | C | T | 2 | a0004c0004t0065g0111 a0004c0024t0083g0110 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.487-839C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956287 | |||||||
chr20:5956504 | C | A | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-622C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956504 | |||||||
chr20:5956529 | G | T | 59 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(56): Show |
66 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.487-597G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956529 | |||||||
chr20:5956545 | T | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-581T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956545 | |||||||
chr20:5956592 | C | T | 2 | a0002c0002t0073g0159 a0002c0002t0099g0130 |
2 | HG01496.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.487-534C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956592 | |||||||
chr20:5956645 | T | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-481T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956645 | |||||||
chr20:5956652 | C | G | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-474C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956652 | |||||||
chr20:5956683 | T | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-443T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956683 | |||||||
chr20:5956693 | G | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-433G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956693 | |||||||
chr20:5956701 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-425A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956701 | |||||||
chr20:5956772 | G | A | 1 | a0002c0002t0002g0189 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.487-354G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956772 | |||||||
chr20:5956777 | G | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-349G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956777 | |||||||
chr20:5956789 | A | G | 4 | a0009c0011t0041g0050 a0009c0011t0091g0238 a0012c0015t0038g0236 others(1): Show |
5 | HG03139.hp1 HG03486.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-337A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956789 | |||||||
chr20:5956805 | AT | A | 6 | a0001c0001t0001g0056 a0001c0008t0030g0234 a0001c0008t0030g0235 others(3): Show |
6 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-308delT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr20 | 5956805 | ||||||
chr20:5956855 | G | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-271G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5956855 | |||||||
chr20:5957039 | A | G | 2 | a0002c0002t0002g0171 a0002c0002t0002g0172 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.487-87A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5957039 | |||||||
chr20:5957052 | T | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-74T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5957052 | |||||||
chr20:5957073 | A | G | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-53A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 5/18 | chr20 | 5957073 | |||||||
chr20:5957295 | A | G | 1 | a0002c0002t0099g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.590+66A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5957295 | |||||||
chr20:5957296 | C | T | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.590+67C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5957296 | |||||||
chr20:5957354 | A | G | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.590+125A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5957354 | |||||||
chr20:5957364 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.590+135A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5957364 | |||||||
chr20:5957395 | A | G | 2 | a0002c0002t0009g0170 a0002c0002t0050g0174 |
2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.590+166A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5957395 | |||||||
chr20:5957450 | T | G | 5 | a0001c0001t0012g0051 a0001c0001t0012g0055 a0001c0001t0012g0088 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.590+221T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5957450 | |||||||
chr20:5957561 | G | A | 139 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(136): Show |
165 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.590+332G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5957561 | |||||||
chr20:5957566 | G | C | 32 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(29): Show |
47 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.590+337G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5957566 | |||||||
chr20:5957597 | C | T | 1 | a0009c0011t0091g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.590+368C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5957597 | |||||||
chr20:5957665 | T | C | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.590+436T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5957665 | |||||||
chr20:5958004 | A | AT | 59 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(56): Show |
66 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.591-521dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr20 | 5958004 | ||||||
chr20:5958008 | C | T | 157 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(154): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.591-520C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958008 | |||||||
chr20:5958030 | A | G | 2 | a0001c0001t0013g0228 a0001c0001t0069g0229 |
2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.591-498A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958030 | |||||||
chr20:5958104 | G | A | 33 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(30): Show |
48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.591-424G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958104 | |||||||
chr20:5958142 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.591-386A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958142 | |||||||
chr20:5958166 | C | T | 1 | a0007c0013t0042g0140 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.591-362C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958166 | |||||||
chr20:5958247 | T | A | 16 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(13): Show |
20 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.591-281T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958247 | |||||||
chr20:5958250 | T | C | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.591-278T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958250 | |||||||
chr20:5958261 | C | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.591-267C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958261 | |||||||
chr20:5958294 | G | A | 2 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.591-234G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958294 | |||||||
chr20:5958339 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.591-189A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958339 | |||||||
chr20:5958347 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.591-181A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958347 | |||||||
chr20:5958363 | A | T | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.591-165A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958363 | |||||||
chr20:5958375 | C | G | 1 | a0001c0001t0001g0081 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.591-153C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958375 | |||||||
chr20:5958437 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.591-91A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958437 | |||||||
chr20:5958448 | C | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.591-80C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 6/18 | chr20 | 5958448 | |||||||
chr20:5958807 | C | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+81C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5958807 | |||||||
chr20:5958847 | C | T | 2 | a0004c0004t0022g0025 a0004c0004t0037g0031 |
4 | HG01884.hp1 HG02055.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+121C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5958847 | |||||||
chr20:5958871 | C | A | 1 | a0002c0002t0002g0165 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.789+145C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5958871 | |||||||
chr20:5958943 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.789+217C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5958943 | |||||||
chr20:5958992 | G | GT | 85 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(82): Show |
95 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.789+272dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5958992 | ||||||
chr20:5959003 | A | C | 87 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(84): Show |
97 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.789+277A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959003 | |||||||
chr20:5959058 | C | T | 2 | a0002c0002t0002g0182 a0002c0002t0002g0183 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.789+332C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959058 | |||||||
chr20:5959081 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+355A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959081 | |||||||
chr20:5959093 | C | T | 1 | a0001c0001t0025g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.789+367C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959093 | |||||||
chr20:5959125 | T | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+399T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959125 | |||||||
chr20:5959139 | G | GT | 49 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(46): Show |
65 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.789+419dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5959139 | ||||||
chr20:5959206 | TG | T | 34 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(31): Show |
49 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.789+481delG | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959206 | |||||||
chr20:5959253 | TTTTAGCT others(9): Show |
T | 1 | a0017c0017t0006g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.789+528_789+543del others(16): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959253 | |||||||
chr20:5959301 | T | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+575T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959301 | |||||||
chr20:5959336 | T | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+610T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959336 | |||||||
chr20:5959458 | C | T | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+732C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959458 | |||||||
chr20:5959514 | A | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+788A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959514 | |||||||
chr20:5959538 | G | T | 2 | a0003c0003t0004g0018 a0003c0003t0004g0219 |
4 | HG00544.hp2 NA18947.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+812G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959538 | |||||||
chr20:5959539 | A | G | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.789+813A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959539 | |||||||
chr20:5959632 | G | A | 19 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(16): Show |
21 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.789+906G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959632 | |||||||
chr20:5959659 | T | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+933T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959659 | |||||||
chr20:5959661 | A | G | 32 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(29): Show |
47 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.789+935A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959661 | |||||||
chr20:5959690 | C | CT | 5 | a0001c0001t0001g0009 a0001c0001t0001g0079 a0001c0001t0001g0107 others(2): Show |
7 | HG00140.hp1 HG01070.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.789+990dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5959690 | ||||||
chr20:5959690 | CT | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(95): Show |
134 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.789+990delT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5959690 | ||||||
chr20:5959690 | CTT | C | 55 | a0001c0001t0001g0118 a0001c0001t0094g0092 a0001c0006t0023g0086 others(52): Show |
73 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.789+989_789+990del others(2): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5959690 | ||||||
chr20:5959690 | CTTT | C | 89 | a0001c0022t0019g0232 a0002c0002t0002g0015 a0002c0002t0002g0017 others(86): Show |
101 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.789+988_789+990del others(3): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5959690 | ||||||
chr20:5959690 | CTTTTTTT others(9): Show |
C | 2 | a0007c0013t0042g0139 a0007c0013t0042g0140 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.789+975_789+990del others(16): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5959690 | ||||||
chr20:5959729 | C | T | 3 | a0004c0004t0007g0114 a0004c0004t0007g0135 a0004c0004t0007g0136 |
3 | HG00642.hp1 HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.789+1003C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959729 | |||||||
chr20:5959736 | T | C | 1 | a0001c0001t0003g0083 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.789+1010T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959736 | |||||||
chr20:5959910 | G | T | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.789+1184G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959910 | |||||||
chr20:5959925 | C | G | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.789+1199C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959925 | |||||||
chr20:5959932 | G | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+1206G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959932 | |||||||
chr20:5959939 | C | T | 2 | a0007c0013t0042g0139 a0007c0013t0042g0140 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.789+1213C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5959939 | |||||||
chr20:5960028 | T | C | 52 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(49): Show |
69 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.789+1302T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5960028 | |||||||
chr20:5960030 | G | A | 1 | a0002c0002t0073g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.789+1304G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5960030 | |||||||
chr20:5960037 | A | G | 5 | a0001c0001t0012g0051 a0001c0001t0012g0055 a0001c0001t0012g0088 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+1311A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5960037 | |||||||
chr20:5960285 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+1559A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5960285 | |||||||
chr20:5960424 | G | A | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.789+1698G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5960424 | |||||||
chr20:5960509 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+1783A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5960509 | |||||||
chr20:5960713 | A | T | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.789+1987A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5960713 | |||||||
chr20:5960785 | A | G | 2 | a0012c0015t0038g0236 a0012c0015t0038g0237 |
2 | NA18952.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.789+2059A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5960785 | |||||||
chr20:5960808 | G | A | 3 | a0001c0022t0019g0232 a0010c0016t0019g0231 a0010c0016t0019g0233 |
3 | HG02602.hp2 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.789+2082G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5960808 | |||||||
chr20:5960827 | C | T | 1 | a0001c0001t0018g0162 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.789+2101C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5960827 | |||||||
chr20:5960944 | CATAA | C | 32 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(29): Show |
47 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.789+2227_789+2230d others(6): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5960944 | ||||||
chr20:5961029 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.790-2245A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5961029 | |||||||
chr20:5961275 | A | T | 1 | a0004c0004t0007g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.790-1999A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5961275 | |||||||
chr20:5961332 | C | T | 1 | a0001c0001t0003g0121 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.790-1942C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5961332 | |||||||
chr20:5961353 | C | A | 94 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(91): Show |
105 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.790-1921C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5961353 | |||||||
chr20:5961370 | T | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.790-1904T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5961370 | |||||||
chr20:5961414 | T | C | 2 | a0007c0013t0039g0141 a0015c0023t0039g0142 |
2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.790-1860T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5961414 | |||||||
chr20:5961511 | C | T | 4 | a0002c0002t0005g0037 a0002c0002t0005g0156 a0002c0002t0005g0158 others(1): Show |
4 | HG01099.hp2 HG02698.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-1763C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5961511 | |||||||
chr20:5961561 | G | A | 87 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(84): Show |
97 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.790-1713G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5961561 | |||||||
chr20:5961988 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.790-1286G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5961988 | |||||||
chr20:5962052 | T | C | 1 | a0001c0001t0013g0228 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.790-1222T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5962052 | |||||||
chr20:5962060 | T | C | 8 | a0001c0001t0025g0129 a0001c0008t0030g0234 a0001c0008t0030g0235 others(5): Show |
8 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.790-1214T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5962060 | |||||||
chr20:5962264 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.790-1010C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5962264 | |||||||
chr20:5962309 | C | A | 161 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(158): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.790-965C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5962309 | |||||||
chr20:5962341 | AGCCTTCA others(322): Show |
A | 161 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(158): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.790-919_790-591del | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5962341 | ||||||
chr20:5962352 | C | CT | 29 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(26): Show |
40 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.790-889dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5962352 | ||||||
chr20:5962352 | C | CTT | 35 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(32): Show |
46 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.790-890_790-889dup others(2): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5962352 | ||||||
chr20:5962352 | C | CTTT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0023 others(5): Show |
10 | HG00735.hp2 HG01099.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.790-891_790-889dup others(3): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5962352 | ||||||
chr20:5962352 | C | CTTTT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0064 others(3): Show |
6 | HG01255.hp1 NA19000.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.790-892_790-889dup others(4): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5962352 | ||||||
chr20:5962352 | CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0012g0051 a0001c0001t0012g0055 a0001c0001t0012g0088 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-899_790-889del others(11): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5962352 | ||||||
chr20:5962352 | CTTTTTTT others(6): Show |
C | 19 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(16): Show |
21 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.790-901_790-889del others(13): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5962352 | ||||||
chr20:5962352 | CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0031g0001 a0001c0001t0031g0070 a0001c0001t0057g0001 |
3 | NA18953.hp2 NA18979.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.790-904_790-889del others(16): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5962352 | ||||||
chr20:5962352 | CTTTTTTT others(14): Show |
C | 3 | a0001c0001t0001g0003 a0001c0001t0034g0032 a0001c0001t0034g0119 |
3 | HG03654.hp2 HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.790-909_790-889del others(21): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr20 | 5962352 | ||||||
chr20:5962535 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.790-739C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5962535 | |||||||
chr20:5962871 | G | C | 1 | a0016c0019t0013g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.790-403G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5962871 | |||||||
chr20:5963003 | A | G | 161 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(158): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.790-271A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5963003 | |||||||
chr20:5963047 | C | A | 157 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(154): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.790-227C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 7/18 | chr20 | 5963047 | |||||||
chr20:5963439 | A | T | 2 | a0001c0001t0003g0128 a0001c0001t0025g0129 |
2 | HG00639.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.875+80A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5963439 | |||||||
chr20:5963525 | C | CT | 5 | a0001c0001t0001g0024 a0001c0001t0003g0127 a0001c0001t0006g0117 others(2): Show |
6 | HG00621.hp1 HG02027.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+187dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr20 | 5963525 | ||||||
chr20:5963525 | CT | C | 126 | a0001c0001t0001g0080 a0001c0006t0023g0086 a0002c0002t0002g0015 others(123): Show |
151 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.875+187delT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr20 | 5963525 | ||||||
chr20:5963609 | A | G | 83 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(80): Show |
92 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.875+250A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5963609 | |||||||
chr20:5963672 | C | T | 2 | a0002c0002t0011g0184 a0002c0002t0015g0039 |
3 | HG03130.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.875+313C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5963672 | |||||||
chr20:5963767 | A | G | 1 | a0001c0001t0025g0126 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.875+408A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5963767 | |||||||
chr20:5963811 | C | T | 2 | a0008c0009t0017g0038 a0008c0009t0017g0169 |
3 | HG02630.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.875+452C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5963811 | |||||||
chr20:5963825 | C | T | 1 | a0001c0001t0093g0097 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.875+466C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5963825 | |||||||
chr20:5964119 | CT | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(166): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.875+777delT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr20 | 5964119 | ||||||
chr20:5964119 | CTTTTT | C | 86 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(83): Show |
95 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.875+773_875+777del others(5): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr20 | 5964119 | ||||||
chr20:5964144 | A | G | 19 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(16): Show |
21 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.875+785A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5964144 | |||||||
chr20:5964241 | G | A | 4 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.875+882G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5964241 | |||||||
chr20:5964285 | G | A | 2 | a0007c0013t0039g0141 a0015c0023t0039g0142 |
2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.875+926G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5964285 | |||||||
chr20:5964455 | G | A | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.875+1096G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5964455 | |||||||
chr20:5964502 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.875+1143A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5964502 | |||||||
chr20:5964609 | A | G | 1 | a0001c0001t0031g0070 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.875+1250A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5964609 | |||||||
chr20:5964643 | C | A | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.875+1284C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5964643 | |||||||
chr20:5964677 | T | C | 1 | a0001c0012t0010g0058 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.875+1318T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5964677 | |||||||
chr20:5964740 | G | T | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.875+1381G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5964740 | |||||||
chr20:5964991 | A | G | 4 | a0002c0002t0005g0014 a0002c0002t0005g0157 a0002c0002t0024g0014 others(1): Show |
4 | HG00621.hp2 HG03710.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+1632A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5964991 | |||||||
chr20:5965462 | G | C | 32 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(29): Show |
47 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.876-1974G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5965462 | |||||||
chr20:5965662 | T | C | 3 | a0002c0002t0002g0015 a0002c0002t0009g0015 a0002c0002t0053g0175 |
4 | HG02280.hp1 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-1774T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5965662 | |||||||
chr20:5965768 | TTTTACTT others(12): Show |
T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.876-1667_876-1649d others(21): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5965768 | |||||||
chr20:5966350 | T | C | 1 | a0002c0002t0076g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.876-1086T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5966350 | |||||||
chr20:5966363 | A | G | 25 | a0002c0002t0005g0006 a0002c0002t0005g0012 a0002c0002t0005g0013 others(22): Show |
28 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.876-1073A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5966363 | |||||||
chr20:5966610 | G | A | 1 | a0002c0002t0005g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.876-826G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5966610 | |||||||
chr20:5966653 | G | A | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.876-783G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5966653 | |||||||
chr20:5966663 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0077 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.876-773T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5966663 | |||||||
chr20:5966729 | ATG | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.876-703_876-702del others(2): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr20 | 5966729 | ||||||
chr20:5966793 | C | T | 33 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(30): Show |
48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.876-643C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5966793 | |||||||
chr20:5966962 | G | A | 18 | a0001c0001t0044g0177 a0001c0001t0096g0178 a0004c0004t0007g0036 others(15): Show |
22 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.876-474G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5966962 | |||||||
chr20:5967063 | A | G | 3 | a0003c0007t0004g0045 a0003c0007t0004g0212 a0003c0007t0004g0215 |
4 | NA18942.hp1 NA18969.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-373A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5967063 | |||||||
chr20:5967073 | T | C | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-363T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5967073 | |||||||
chr20:5967111 | A | G | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-325A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5967111 | |||||||
chr20:5967116 | G | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.876-320G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5967116 | |||||||
chr20:5967186 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.876-250C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5967186 | |||||||
chr20:5967299 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.876-137T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5967299 | |||||||
chr20:5967373 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.876-63T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5967373 | |||||||
chr20:5967411 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG00741.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.876-25A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 8/18 | chr20 | 5967411 | |||||||
chr20:5967607 | A | G | 1 | a0004c0004t0065g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1027+20A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 9/18 | chr20 | 5967607 | |||||||
chr20:5967664 | A | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1027+77A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 9/18 | chr20 | 5967664 | |||||||
chr20:5967775 | CATT | C | 85 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(82): Show |
94 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1028-54_1028-52del others(3): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 9/18 | chr20 | 5967775 | |||||||
chr20:5967784 | G | A | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1028-46G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 9/18 | chr20 | 5967784 | |||||||
chr20:5967794 | A | C | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1028-36A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 9/18 | chr20 | 5967794 | |||||||
chr20:5968235 | A | C | 1 | a0001c0001t0010g0082 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1223+210A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5968235 | |||||||
chr20:5968342 | C | T | 3 | a0001c0001t0003g0033 a0001c0001t0003g0128 a0001c0001t0025g0129 |
4 | HG00639.hp2 HG00642.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1223+317C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5968342 | |||||||
chr20:5968606 | A | G | 1 | a0001c0001t0025g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1223+581A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5968606 | |||||||
chr20:5968620 | A | G | 4 | a0004c0004t0065g0111 a0004c0024t0083g0110 a0008c0009t0017g0038 others(1): Show |
5 | HG02451.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1223+595A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5968620 | |||||||
chr20:5968622 | A | T | 1 | a0002c0002t0076g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1223+597A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5968622 | |||||||
chr20:5968736 | G | C | 4 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(1): Show |
4 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223+711G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5968736 | |||||||
chr20:5968888 | G | A | 19 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(16): Show |
21 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1223+863G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5968888 | |||||||
chr20:5968925 | G | A | 32 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(29): Show |
47 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1223+900G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5968925 | |||||||
chr20:5969334 | G | C | 1 | a0002c0002t0076g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1223+1309G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5969334 | |||||||
chr20:5969335 | T | G | 1 | a0002c0002t0076g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1223+1310T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5969335 | |||||||
chr20:5969336 | A | T | 1 | a0002c0002t0076g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1223+1311A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5969336 | |||||||
chr20:5969400 | G | A | 1 | a0001c0001t0013g0048 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1223+1375G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5969400 | |||||||
chr20:5969427 | A | G | 3 | a0002c0002t0005g0013 a0002c0002t0029g0013 a0002c0002t0078g0013 |
3 | HG02258.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1223+1402A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5969427 | |||||||
chr20:5969593 | C | CA | 32 | a0001c0001t0001g0024 a0001c0001t0001g0084 a0001c0001t0006g0027 others(29): Show |
34 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1223+1585dupA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr20 | 5969593 | ||||||
chr20:5969593 | CA | C | 85 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(82): Show |
94 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1223+1585delA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr20 | 5969593 | ||||||
chr20:5969599 | A | C | 1 | a0002c0002t0076g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1223+1574A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5969599 | |||||||
chr20:5969741 | T | G | 1 | a0002c0002t0076g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1223+1716T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5969741 | |||||||
chr20:5969750 | A | T | 1 | a0002c0002t0076g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1223+1725A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5969750 | |||||||
chr20:5970008 | C | T | 1 | a0001c0001t0035g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1223+1983C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970008 | |||||||
chr20:5970214 | T | C | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1224-1793T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970214 | |||||||
chr20:5970292 | T | C | 2 | a0002c0002t0002g0171 a0002c0002t0002g0172 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1224-1715T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970292 | |||||||
chr20:5970337 | T | C | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1224-1670T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970337 | |||||||
chr20:5970404 | A | G | 1 | a0013c0018t0001g0104 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1224-1603A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970404 | |||||||
chr20:5970551 | G | A | 1 | a0001c0001t0018g0162 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1224-1456G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970551 | |||||||
chr20:5970579 | G | T | 5 | a0001c0001t0012g0051 a0001c0001t0012g0055 a0001c0001t0012g0088 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1224-1428G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970579 | |||||||
chr20:5970619 | A | C | 4 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(1): Show |
4 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224-1388A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970619 | |||||||
chr20:5970630 | G | A | 2 | a0001c0001t0036g0060 a0001c0001t0036g0074 |
2 | NA18944.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1224-1377G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970630 | |||||||
chr20:5970805 | T | C | 48 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(45): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1224-1202T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970805 | |||||||
chr20:5970835 | G | T | 1 | a0002c0002t0002g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1224-1172G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970835 | |||||||
chr20:5970942 | A | G | 49 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(46): Show |
65 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1224-1065A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5970942 | |||||||
chr20:5971114 | A | G | 20 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(17): Show |
25 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1224-893A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971114 | |||||||
chr20:5971190 | A | G | 1 | a0002c0002t0076g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1224-817A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971190 | |||||||
chr20:5971265 | A | G | 11 | a0002c0002t0002g0017 a0002c0002t0002g0167 a0002c0002t0002g0171 others(8): Show |
13 | HG00741.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1224-742A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971265 | |||||||
chr20:5971278 | A | C | 32 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(29): Show |
47 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1224-729A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971278 | |||||||
chr20:5971320 | G | T | 85 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(82): Show |
94 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1224-687G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971320 | |||||||
chr20:5971663 | C | T | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1224-344C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971663 | |||||||
chr20:5971677 | T | C | 1 | a0001c0001t0006g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1224-330T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971677 | |||||||
chr20:5971801 | C | G | 1 | a0001c0001t0001g0069 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1224-206C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971801 | |||||||
chr20:5971811 | A | T | 1 | a0001c0001t0001g0029 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1224-196A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971811 | |||||||
chr20:5971829 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1224-178T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971829 | |||||||
chr20:5971976 | T | C | 4 | a0002c0002t0002g0017 a0002c0002t0002g0181 a0002c0002t0016g0166 others(1): Show |
6 | HG00741.hp2 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1224-31T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971976 | |||||||
chr20:5971998 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1224-9G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 10/18 | chr20 | 5971998 | |||||||
chr20:5972188 | T | C | 1 | a0001c0001t0006g0093 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1254+151T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 11/18 | chr20 | 5972188 | |||||||
chr20:5972311 | C | T | 5 | a0001c0001t0012g0051 a0001c0001t0012g0055 a0001c0001t0012g0088 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+274C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 11/18 | chr20 | 5972311 | |||||||
chr20:5972423 | G | A | 2 | a0007c0013t0042g0139 a0007c0013t0042g0140 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1254+386G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 11/18 | chr20 | 5972423 | |||||||
chr20:5972453 | C | T | 1 | a0003c0003t0004g0218 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1254+416C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 11/18 | chr20 | 5972453 | |||||||
chr20:5972494 | G | A | 1 | a0001c0001t0003g0122 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1254+457G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 11/18 | chr20 | 5972494 | |||||||
chr20:5972614 | G | T | 1 | a0001c0001t0003g0034 | 2 | HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1255-442G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 11/18 | chr20 | 5972614 | |||||||
chr20:5972790 | C | T | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1255-266C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 11/18 | chr20 | 5972790 | |||||||
chr20:5972791 | G | A | 1 | a0002c0002t0002g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1255-265G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 11/18 | chr20 | 5972791 | |||||||
chr20:5972869 | A | G | 1 | a0002c0002t0005g0154 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1255-187A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 11/18 | chr20 | 5972869 | |||||||
chr20:5972973 | A | G | 20 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(17): Show |
25 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1255-83A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 11/18 | chr20 | 5972973 | |||||||
chr20:5973313 | G | A | 1 | a0002c0002t0016g0163 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1395+117G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973313 | |||||||
chr20:5973510 | T | C | 3 | a0001c0022t0019g0232 a0010c0016t0019g0231 a0010c0016t0019g0233 |
3 | HG02602.hp2 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1395+314T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973510 | |||||||
chr20:5973556 | C | T | 24 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(21): Show |
26 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.1395+360C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973556 | |||||||
chr20:5973662 | C | T | 1 | a0001c0001t0003g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1395+466C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973662 | |||||||
chr20:5973694 | G | A | 1 | a0004c0004t0022g0025 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1395+498G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973694 | |||||||
chr20:5973739 | C | T | 1 | a0001c0001t0006g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1395+543C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973739 | |||||||
chr20:5973741 | G | T | 1 | a0001c0001t0003g0121 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1395+545G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973741 | |||||||
chr20:5973835 | A | G | 2 | a0009c0011t0041g0050 a0009c0011t0091g0238 |
3 | HG03139.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1395+639A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973835 | |||||||
chr20:5973914 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1395+718C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973914 | |||||||
chr20:5973934 | T | C | 48 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(45): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1395+738T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973934 | |||||||
chr20:5973964 | G | A | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1395+768G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5973964 | |||||||
chr20:5974061 | T | G | 2 | a0004c0004t0022g0025 a0004c0004t0037g0031 |
4 | HG01884.hp1 HG02055.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+865T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974061 | |||||||
chr20:5974261 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1395+1065G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974261 | |||||||
chr20:5974346 | C | T | 5 | a0001c0001t0012g0051 a0001c0001t0012g0055 a0001c0001t0012g0088 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+1150C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974346 | |||||||
chr20:5974456 | C | T | 3 | a0001c0022t0019g0232 a0010c0016t0019g0231 a0010c0016t0019g0233 |
3 | HG02602.hp2 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1395+1260C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974456 | |||||||
chr20:5974542 | A | G | 16 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(13): Show |
20 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1395+1346A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974542 | |||||||
chr20:5974548 | T | G | 1 | a0001c0001t0010g0100 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1395+1352T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974548 | |||||||
chr20:5974559 | C | G | 1 | a0002c0002t0002g0181 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1395+1363C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974559 | |||||||
chr20:5974614 | C | G | 4 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395+1418C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974614 | |||||||
chr20:5974672 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0120 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1395+1476C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974672 | |||||||
chr20:5974696 | A | C | 3 | a0004c0004t0014g0030 a0004c0004t0014g0054 a0004c0004t0014g0113 |
4 | HG02630.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+1500A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974696 | |||||||
chr20:5974886 | A | T | 2 | a0009c0011t0041g0050 a0009c0011t0091g0238 |
3 | HG03139.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1395+1690A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974886 | |||||||
chr20:5974996 | C | T | 20 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(17): Show |
25 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1395+1800C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974996 | |||||||
chr20:5974997 | G | A | 16 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(13): Show |
20 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1395+1801G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5974997 | |||||||
chr20:5975027 | G | A | 1 | a0004c0004t0014g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1395+1831G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975027 | |||||||
chr20:5975070 | G | C | 4 | a0004c0004t0065g0111 a0004c0024t0083g0110 a0008c0009t0017g0038 others(1): Show |
5 | HG02451.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+1874G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975070 | |||||||
chr20:5975240 | T | C | 4 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(1): Show |
4 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+2044T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975240 | |||||||
chr20:5975259 | TA | T | 16 | a0001c0001t0001g0073 a0001c0001t0001g0103 a0001c0001t0010g0022 others(13): Show |
16 | HG00323.hp1 HG00741.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1395+2078delA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr20 | 5975259 | ||||||
chr20:5975497 | CT | C | 147 | a0001c0001t0003g0108 a0001c0001t0044g0177 a0001c0001t0044g0185 others(144): Show |
176 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1395+2318delT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr20 | 5975497 | ||||||
chr20:5975520 | G | A | 85 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(82): Show |
94 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1395+2324G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975520 | |||||||
chr20:5975536 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1395+2340G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975536 | |||||||
chr20:5975592 | G | A | 1 | a0001c0001t0084g0115 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1396-2284G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975592 | |||||||
chr20:5975718 | C | G | 3 | a0002c0002t0005g0013 a0002c0002t0029g0013 a0002c0002t0078g0013 |
3 | HG02258.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1396-2158C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975718 | |||||||
chr20:5975738 | C | T | 33 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(30): Show |
48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1396-2138C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975738 | |||||||
chr20:5975743 | G | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0137 others(3): Show |
8 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1396-2133G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975743 | |||||||
chr20:5975788 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0101 |
2 | NA18990.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1396-2088G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975788 | |||||||
chr20:5975795 | C | CT | 7 | a0001c0001t0001g0069 a0001c0001t0001g0138 a0001c0001t0012g0051 others(4): Show |
7 | HG01981.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396-2068dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr20 | 5975795 | ||||||
chr20:5975837 | C | G | 4 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(1): Show |
4 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-2039C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5975837 | |||||||
chr20:5976139 | A | T | 33 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(30): Show |
48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1396-1737A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5976139 | |||||||
chr20:5976141 | A | C | 4 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 others(1): Show |
4 | HG01109.hp2 HG01884.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1735A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5976141 | |||||||
chr20:5976155 | G | A | 4 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-1721G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5976155 | |||||||
chr20:5976398 | A | G | 48 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(45): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1396-1478A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5976398 | |||||||
chr20:5976523 | A | G | 2 | a0002c0002t0011g0184 a0002c0002t0015g0039 |
3 | HG03130.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1396-1353A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5976523 | |||||||
chr20:5976592 | C | T | 2 | a0001c0012t0001g0075 a0001c0012t0010g0058 |
2 | HG01943.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1396-1284C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5976592 | |||||||
chr20:5976801 | T | A | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1396-1075T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5976801 | |||||||
chr20:5976828 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1396-1048G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5976828 | |||||||
chr20:5976930 | C | T | 2 | a0003c0003t0087g0209 a0014c0021t0045g0230 |
2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1396-946C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5976930 | |||||||
chr20:5977075 | T | C | 2 | a0002c0002t0002g0165 a0002c0002t0052g0168 |
2 | HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1396-801T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977075 | |||||||
chr20:5977164 | G | C | 1 | a0002c0002t0002g0165 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1396-712G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977164 | |||||||
chr20:5977205 | C | T | 1 | a0017c0017t0006g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1396-671C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977205 | |||||||
chr20:5977211 | C | T | 1 | a0001c0001t0012g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1396-665C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977211 | |||||||
chr20:5977338 | G | C | 1 | a0003c0003t0033g0213 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1396-538G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977338 | |||||||
chr20:5977341 | C | T | 54 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(51): Show |
60 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1396-535C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977341 | |||||||
chr20:5977359 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1396-517G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977359 | |||||||
chr20:5977445 | G | A | 14 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(11): Show |
16 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1396-431G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977445 | |||||||
chr20:5977506 | C | T | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1396-370C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977506 | |||||||
chr20:5977508 | T | C | 4 | a0004c0004t0065g0111 a0004c0024t0083g0110 a0008c0009t0017g0038 others(1): Show |
5 | HG02451.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-368T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977508 | |||||||
chr20:5977539 | T | C | 2 | a0012c0015t0038g0236 a0012c0015t0038g0237 |
2 | NA18952.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1396-337T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977539 | |||||||
chr20:5977553 | G | A | 1 | a0001c0001t0018g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1396-323G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977553 | |||||||
chr20:5977587 | T | G | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1396-289T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977587 | |||||||
chr20:5977700 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1396-176T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977700 | |||||||
chr20:5977737 | T | A | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1396-139T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977737 | |||||||
chr20:5977801 | G | A | 1 | a0003c0003t0004g0008 | 4 | NA18974.hp2 NA19070.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-75G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 12/18 | chr20 | 5977801 | |||||||
chr20:5978292 | TC | T | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1537+278delC | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr20 | 5978292 | ||||||
chr20:5978314 | T | C | 161 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(158): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.1537+297T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978314 | |||||||
chr20:5978318 | T | G | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1537+301T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978318 | |||||||
chr20:5978325 | AT | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.1537+316delT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr20 | 5978325 | ||||||
chr20:5978383 | G | A | 1 | a0002c0002t0002g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1537+366G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978383 | |||||||
chr20:5978417 | A | G | 32 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(29): Show |
47 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1537+400A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978417 | |||||||
chr20:5978452 | G | A | 3 | a0006c0010t0020g0147 a0007c0013t0039g0141 a0015c0023t0039g0142 |
3 | HG02886.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1537+435G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978452 | |||||||
chr20:5978465 | A | C | 1 | a0002c0002t0002g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1537+448A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978465 | |||||||
chr20:5978562 | C | T | 4 | a0001c0001t0013g0048 a0001c0001t0013g0228 a0001c0001t0069g0229 others(1): Show |
5 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1537+545C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978562 | |||||||
chr20:5978598 | C | CT | 19 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(16): Show |
21 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1537+582dupT | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr20 | 5978598 | ||||||
chr20:5978619 | A | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1537+602A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978619 | |||||||
chr20:5978688 | G | A | 1 | a0013c0018t0001g0104 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1537+671G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978688 | |||||||
chr20:5978706 | C | T | 19 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(16): Show |
21 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1537+689C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978706 | |||||||
chr20:5978707 | G | A | 3 | a0001c0022t0019g0232 a0010c0016t0019g0231 a0010c0016t0019g0233 |
3 | HG02602.hp2 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1537+690G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978707 | |||||||
chr20:5978777 | T | C | 48 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(45): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1537+760T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978777 | |||||||
chr20:5978797 | A | G | 1 | a0001c0001t0035g0102 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1537+780A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978797 | |||||||
chr20:5978808 | A | G | 4 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(1): Show |
4 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537+791A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978808 | |||||||
chr20:5978887 | C | T | 4 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537+870C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5978887 | |||||||
chr20:5979004 | C | G | 2 | a0012c0015t0038g0236 a0012c0015t0038g0237 |
2 | NA18952.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1537+987C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5979004 | |||||||
chr20:5979051 | G | A | 1 | a0005c0005t0003g0124 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1537+1034G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5979051 | |||||||
chr20:5979186 | C | G | 89 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(86): Show |
98 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.1537+1169C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5979186 | |||||||
chr20:5979355 | C | T | 33 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(30): Show |
48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1537+1338C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5979355 | |||||||
chr20:5979446 | A | G | 19 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(16): Show |
21 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1537+1429A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5979446 | |||||||
chr20:5979595 | T | G | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1537+1578T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5979595 | |||||||
chr20:5979708 | T | C | 4 | a0009c0011t0041g0050 a0009c0011t0091g0238 a0012c0015t0038g0236 others(1): Show |
5 | HG03139.hp1 HG03486.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1537+1691T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5979708 | |||||||
chr20:5979847 | C | T | 1 | a0006c0010t0020g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1537+1830C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5979847 | |||||||
chr20:5979852 | C | T | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1537+1835C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5979852 | |||||||
chr20:5980045 | T | C | 161 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(158): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.1537+2028T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5980045 | |||||||
chr20:5980138 | G | A | 2 | a0002c0002t0002g0017 a0002c0002t0002g0181 |
4 | HG00741.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537+2121G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5980138 | |||||||
chr20:5980154 | C | T | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1537+2137C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5980154 | |||||||
chr20:5980593 | T | A | 3 | a0001c0022t0019g0232 a0010c0016t0019g0231 a0010c0016t0019g0233 |
3 | HG02602.hp2 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1538-2377T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5980593 | |||||||
chr20:5980812 | T | C | 141 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(138): Show |
166 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.1538-2158T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5980812 | |||||||
chr20:5980835 | G | A | 20 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(17): Show |
25 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1538-2135G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5980835 | |||||||
chr20:5980873 | CA | C | 127 | a0001c0001t0001g0061 a0001c0001t0003g0108 a0001c0001t0006g0096 others(124): Show |
151 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.1538-2078delA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr20 | 5980873 | ||||||
chr20:5980873 | CAA | C | 10 | a0002c0002t0002g0203 a0002c0002t0009g0197 a0003c0003t0008g0222 others(7): Show |
11 | HG02970.hp2 HG03139.hp1 HG03486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1538-2079_1538-207 others(6): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr20 | 5980873 | ||||||
chr20:5980910 | T | C | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1538-2060T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5980910 | |||||||
chr20:5980947 | T | C | 16 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(13): Show |
20 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1538-2023T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5980947 | |||||||
chr20:5980978 | A | G | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1538-1992A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5980978 | |||||||
chr20:5981026 | G | T | 1 | a0001c0001t0044g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1538-1944G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981026 | |||||||
chr20:5981027 | GACAA | G | 10 | a0001c0001t0003g0010 a0001c0001t0095g0010 a0007c0013t0039g0141 others(7): Show |
12 | HG01243.hp1 HG01515.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1538-1931_1538-192 others(8): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr20 | 5981027 | ||||||
chr20:5981029 | C | A | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1538-1941C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981029 | |||||||
chr20:5981030 | A | G | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1538-1940A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981030 | |||||||
chr20:5981031 | A | G | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1538-1939A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981031 | |||||||
chr20:5981070 | G | A | 4 | a0003c0003t0058g0217 a0004c0004t0014g0030 a0004c0004t0014g0054 others(1): Show |
5 | HG02630.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1538-1900G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981070 | |||||||
chr20:5981107 | A | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(257): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1538-1863A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981107 | |||||||
chr20:5981257 | A | G | 1 | a0001c0012t0001g0075 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1538-1713A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981257 | |||||||
chr20:5981267 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(257): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1538-1703G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981267 | |||||||
chr20:5981300 | A | G | 3 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 |
3 | HG01884.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1538-1670A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981300 | |||||||
chr20:5981313 | C | G | 48 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(45): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1538-1657C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981313 | |||||||
chr20:5981387 | CAGGCTA | C | 33 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(30): Show |
48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1538-1581_1538-157 others(10): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr20 | 5981387 | ||||||
chr20:5981423 | G | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1538-1547G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981423 | |||||||
chr20:5981689 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1538-1281G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981689 | |||||||
chr20:5981739 | A | G | 1 | a0002c0002t0002g0187 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1538-1231A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981739 | |||||||
chr20:5981858 | G | C | 3 | a0002c0002t0002g0191 a0002c0002t0002g0192 a0002c0002t0002g0198 |
3 | NA18967.hp2 NA18973.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1538-1112G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981858 | |||||||
chr20:5981879 | A | G | 1 | a0003c0003t0032g0214 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1538-1091A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5981879 | |||||||
chr20:5981997 | TA | T | 4 | a0009c0011t0041g0050 a0009c0011t0091g0238 a0012c0015t0038g0236 others(1): Show |
5 | HG03139.hp1 HG03486.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1538-971delA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr20 | 5981997 | ||||||
chr20:5982115 | G | A | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1538-855G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5982115 | |||||||
chr20:5982164 | C | T | 5 | a0002c0002t0002g0041 a0002c0002t0002g0144 a0002c0002t0002g0195 others(2): Show |
5 | NA18969.hp2 NA18972.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1538-806C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5982164 | |||||||
chr20:5982256 | T | C | 1 | a0001c0001t0006g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1538-714T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5982256 | |||||||
chr20:5982268 | C | T | 1 | a0002c0002t0099g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1538-702C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5982268 | |||||||
chr20:5982541 | C | T | 5 | a0001c0001t0012g0051 a0001c0001t0012g0055 a0001c0001t0012g0088 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1538-429C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5982541 | |||||||
chr20:5982739 | T | C | 48 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(45): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1538-231T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5982739 | |||||||
chr20:5982768 | C | T | 1 | a0002c0002t0028g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1538-202C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5982768 | |||||||
chr20:5982770 | A | G | 6 | a0002c0002t0011g0019 a0002c0002t0011g0224 a0002c0002t0015g0223 others(3): Show |
6 | HG00735.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1538-200A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5982770 | |||||||
chr20:5982801 | G | A | 4 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(1): Show |
4 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1538-169G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5982801 | |||||||
chr20:5982940 | T | G | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1538-30T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 13/18 | chr20 | 5982940 | |||||||
chr20:5983198 | T | C | 2 | a0007c0013t0042g0139 a0007c0013t0042g0140 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1733+33T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983198 | |||||||
chr20:5983237 | C | T | 4 | a0004c0004t0065g0111 a0004c0024t0083g0110 a0008c0009t0017g0038 others(1): Show |
5 | HG02451.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1733+72C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983237 | |||||||
chr20:5983246 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG01168.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1733+81A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983246 | |||||||
chr20:5983401 | T | A | 1 | a0003c0003t0090g0216 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1733+236T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983401 | |||||||
chr20:5983426 | C | T | 4 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(1): Show |
4 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733+261C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983426 | |||||||
chr20:5983573 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1733+408G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983573 | |||||||
chr20:5983594 | G | A | 1 | a0002c0002t0002g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1733+429G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983594 | |||||||
chr20:5983644 | G | T | 2 | a0002c0002t0005g0153 a0002c0002t0005g0180 |
2 | HG02683.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1733+479G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983644 | |||||||
chr20:5983699 | C | CA | 30 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(27): Show |
44 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1733+544dupA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr20 | 5983699 | ||||||
chr20:5983755 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1733+590A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983755 | |||||||
chr20:5983844 | A | G | 4 | a0002c0002t0005g0014 a0002c0002t0005g0157 a0002c0002t0024g0014 others(1): Show |
4 | HG00621.hp2 HG03710.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733+679A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983844 | |||||||
chr20:5983848 | A | C | 2 | a0007c0013t0039g0141 a0015c0023t0039g0142 |
2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1733+683A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983848 | |||||||
chr20:5983858 | C | T | 4 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1733+693C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983858 | |||||||
chr20:5983904 | T | C | 1 | a0002c0002t0099g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1733+739T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5983904 | |||||||
chr20:5984085 | C | T | 1 | a0013c0018t0001g0104 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1734-696C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5984085 | |||||||
chr20:5984266 | C | A | 1 | a0002c0002t0050g0174 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1734-515C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5984266 | |||||||
chr20:5984518 | G | A | 1 | a0003c0003t0004g0218 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1734-263G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5984518 | |||||||
chr20:5984742 | A | T | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1734-39A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5984742 | |||||||
chr20:5984760 | T | C | 3 | a0001c0022t0019g0232 a0010c0016t0019g0231 a0010c0016t0019g0233 |
3 | HG02602.hp2 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1734-21T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 14/18 | chr20 | 5984760 | |||||||
chr20:5985085 | A | T | 85 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(82): Show |
94 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1953+85A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985085 | |||||||
chr20:5985111 | T | C | 6 | a0002c0002t0002g0015 a0002c0002t0009g0015 a0002c0002t0009g0170 others(3): Show |
9 | HG01243.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1953+111T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985111 | |||||||
chr20:5985135 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG00741.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1953+135C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985135 | |||||||
chr20:5985150 | A | G | 19 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(16): Show |
21 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1953+150A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985150 | |||||||
chr20:5985349 | C | A | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1953+349C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985349 | |||||||
chr20:5985441 | C | CA | 28 | a0001c0001t0001g0069 a0001c0001t0003g0123 a0001c0001t0003g0127 others(25): Show |
30 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1953+458dupA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr20 | 5985441 | ||||||
chr20:5985441 | CA | C | 121 | a0001c0001t0003g0083 a0001c0001t0044g0177 a0001c0001t0044g0185 others(118): Show |
136 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(133): Show |
intron_variant | MODIFIER | c.1953+458delA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr20 | 5985441 | ||||||
chr20:5985441 | CAA | C | 36 | a0002c0002t0002g0172 a0002c0002t0002g0196 a0002c0002t0005g0152 others(33): Show |
51 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1953+457_1953+458d others(4): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr20 | 5985441 | ||||||
chr20:5985592 | C | T | 4 | a0006c0010t0020g0147 a0006c0010t0020g0148 a0006c0010t0020g0207 others(1): Show |
4 | HG01109.hp2 HG01884.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1954-330C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985592 | |||||||
chr20:5985601 | A | G | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1954-321A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985601 | |||||||
chr20:5985651 | T | G | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1954-271T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985651 | |||||||
chr20:5985692 | C | T | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1954-230C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985692 | |||||||
chr20:5985733 | A | G | 1 | a0002c0002t0080g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1954-189A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985733 | |||||||
chr20:5985837 | C | T | 1 | a0001c0022t0019g0232 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1954-85C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 15/18 | chr20 | 5985837 | |||||||
chr20:5986290 | T | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0010g0021 |
3 | NA18941.hp2 NA18987.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2163+159T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/18 | chr20 | 5986290 | |||||||
chr20:5986354 | ACTTTT | A | 5 | a0002c0002t0002g0017 a0002c0002t0002g0181 a0002c0002t0016g0166 others(2): Show |
7 | HG00741.hp2 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2163+229_2163+233d others(7): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr20 | 5986354 | ||||||
chr20:5986496 | T | G | 1 | a0002c0002t0015g0223 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2163+365T>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/18 | chr20 | 5986496 | |||||||
chr20:5986750 | T | C | 1 | a0001c0001t0006g0095 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2164-532T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/18 | chr20 | 5986750 | |||||||
chr20:5986769 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2164-513G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/18 | chr20 | 5986769 | |||||||
chr20:5986924 | C | G | 1 | a0003c0003t0090g0216 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2164-358C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/18 | chr20 | 5986924 | |||||||
chr20:5987046 | C | G | 4 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164-236C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/18 | chr20 | 5987046 | |||||||
chr20:5987098 | T | A | 161 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(158): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.2164-184T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/18 | chr20 | 5987098 | |||||||
chr20:5987107 | G | A | 1 | a0002c0002t0005g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2164-175G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/18 | chr20 | 5987107 | |||||||
chr20:5987200 | C | T | 1 | a0002c0002t0002g0189 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2164-82C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 16/18 | chr20 | 5987200 | |||||||
chr20:5987728 | T | A | 8 | a0004c0004t0065g0111 a0004c0024t0083g0110 a0006c0010t0020g0147 others(5): Show |
9 | HG01109.hp2 HG01884.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2240+370T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5987728 | |||||||
chr20:5987905 | C | A | 4 | a0009c0011t0041g0050 a0009c0011t0091g0238 a0012c0015t0038g0236 others(1): Show |
5 | HG03139.hp1 HG03486.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2240+547C>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5987905 | |||||||
chr20:5987913 | C | T | 93 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(90): Show |
102 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.2240+555C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5987913 | |||||||
chr20:5988025 | G | T | 33 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(30): Show |
48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.2240+667G>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5988025 | |||||||
chr20:5988091 | G | A | 48 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(45): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2240+733G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5988091 | |||||||
chr20:5988120 | A | T | 2 | a0007c0013t0042g0139 a0007c0013t0042g0140 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2240+762A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5988120 | |||||||
chr20:5988162 | A | G | 3 | a0001c0022t0019g0232 a0010c0016t0019g0231 a0010c0016t0019g0233 |
3 | HG02602.hp2 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2240+804A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5988162 | |||||||
chr20:5988318 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(257): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.2240+960T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5988318 | |||||||
chr20:5988461 | C | CA | 48 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(45): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2240+1115dupA | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr20 | 5988461 | ||||||
chr20:5988521 | G | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2240+1163G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5988521 | |||||||
chr20:5988713 | G | A | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2240+1355G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5988713 | |||||||
chr20:5988812 | A | G | 9 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(6): Show |
10 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2240+1454A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5988812 | |||||||
chr20:5988836 | C | T | 2 | a0001c0006t0023g0086 a0001c0006t0023g0087 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2240+1478C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5988836 | |||||||
chr20:5988848 | ACCAGGTG others(7): Show |
A | 5 | a0001c0001t0006g0117 a0001c0008t0030g0234 a0001c0008t0030g0235 others(2): Show |
5 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.2240+1509_2240+152 others(18): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr20 | 5988848 | ||||||
chr20:5989120 | C | CTTTTTTT others(1): Show |
32 | a0002c0002t0002g0143 a0002c0002t0005g0153 a0003c0003t0004g0002 others(29): Show |
47 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.2240+1771_2240+177 others(12): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr20 | 5989120 | ||||||
chr20:5989120 | C | CTTTTTTT others(2): Show |
68 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0040 others(65): Show |
76 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2240+1770_2240+177 others(13): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr20 | 5989120 | ||||||
chr20:5989120 | C | CTTTTTTT others(3): Show |
38 | a0001c0001t0044g0177 a0001c0001t0096g0178 a0001c0001t0097g0186 others(35): Show |
43 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.2240+1769_2240+177 others(14): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr20 | 5989120 | ||||||
chr20:5989120 | C | CTTTTTTT others(4): Show |
13 | a0001c0001t0044g0185 a0002c0002t0011g0184 a0004c0004t0014g0113 others(10): Show |
14 | HG01109.hp2 HG01884.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2240+1768_2240+177 others(15): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr20 | 5989120 | ||||||
chr20:5989120 | C | CTTTTTTT others(5): Show |
6 | a0001c0022t0019g0232 a0004c0024t0083g0110 a0008c0009t0017g0038 others(3): Show |
7 | HG02451.hp1 HG02602.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2240+1767_2240+177 others(16): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr20 | 5989120 | ||||||
chr20:5989120 | C | CTTTTTTT others(6): Show |
2 | a0001c0008t0055g0049 a0001c0008t0056g0049 |
2 | HG01255.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2240+1766_2240+177 others(17): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr20 | 5989120 | ||||||
chr20:5989120 | C | CTTTTTTT others(7): Show |
2 | a0001c0008t0030g0234 a0001c0008t0030g0235 |
2 | HG01074.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2240+1765_2240+177 others(18): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr20 | 5989120 | ||||||
chr20:5989208 | C | G | 4 | a0009c0011t0041g0050 a0009c0011t0091g0238 a0012c0015t0038g0236 others(1): Show |
5 | HG03139.hp1 HG03486.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2240+1850C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5989208 | |||||||
chr20:5989246 | A | T | 1 | a0012c0015t0038g0237 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2240+1888A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5989246 | |||||||
chr20:5989303 | A | G | 3 | a0002c0002t0002g0189 a0011c0014t0002g0206 a0011c0014t0009g0205 |
3 | HG03491.hp1 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2240+1945A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5989303 | |||||||
chr20:5989407 | C | T | 19 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(16): Show |
21 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.2240+2049C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5989407 | |||||||
chr20:5989488 | C | T | 1 | a0003c0003t0032g0214 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2240+2130C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5989488 | |||||||
chr20:5989489 | A | G | 48 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(45): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2240+2131A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5989489 | |||||||
chr20:5989491 | A | G | 3 | a0001c0001t0006g0028 a0001c0001t0006g0093 a0001c0001t0006g0095 |
4 | NA18940.hp1 NA18977.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.2240+2133A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5989491 | |||||||
chr20:5989572 | C | T | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2240+2214C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5989572 | |||||||
chr20:5989792 | G | C | 161 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(158): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.2240+2434G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5989792 | |||||||
chr20:5990034 | T | A | 2 | a0002c0002t0016g0163 a0002c0002t0016g0164 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2240+2676T>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990034 | |||||||
chr20:5990104 | A | G | 161 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(158): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.2240+2746A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990104 | |||||||
chr20:5990177 | C | T | 2 | a0007c0013t0042g0139 a0007c0013t0042g0140 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2240+2819C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990177 | |||||||
chr20:5990179 | A | G | 1 | a0001c0001t0012g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2240+2821A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990179 | |||||||
chr20:5990326 | G | C | 48 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(45): Show |
64 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2240+2968G>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990326 | |||||||
chr20:5990368 | C | T | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2240+3010C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990368 | |||||||
chr20:5990420 | C | T | 11 | a0002c0002t0002g0017 a0002c0002t0002g0167 a0002c0002t0002g0171 others(8): Show |
13 | HG00741.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2240+3062C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990420 | |||||||
chr20:5990491 | C | G | 1 | a0002c0002t0073g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2241-3015C>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990491 | |||||||
chr20:5990520 | A | G | 1 | a0001c0001t0035g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2241-2986A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990520 | |||||||
chr20:5990704 | T | C | 1 | a0007c0013t0039g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2241-2802T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990704 | |||||||
chr20:5990776 | A | T | 1 | a0014c0021t0045g0230 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2241-2730A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5990776 | |||||||
chr20:5991617 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2241-1889T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5991617 | |||||||
chr20:5991801 | T | C | 2 | a0001c0001t0003g0128 a0001c0001t0025g0129 |
2 | HG00639.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2241-1705T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5991801 | |||||||
chr20:5991876 | TC | T | 31 | a0002c0002t0002g0040 a0002c0002t0002g0041 a0002c0002t0002g0042 others(28): Show |
31 | HG00323.hp1 HG00735.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.2241-1629delC | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5991876 | |||||||
chr20:5991886 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2241-1620C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5991886 | |||||||
chr20:5991948 | T | C | 161 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(158): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.2241-1558T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5991948 | |||||||
chr20:5992082 | C | T | 8 | a0007c0013t0039g0141 a0007c0013t0042g0139 a0007c0013t0042g0140 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2241-1424C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992082 | |||||||
chr20:5992129 | T | C | 1 | a0001c0001t0093g0097 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2241-1377T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992129 | |||||||
chr20:5992402 | C | T | 9 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(6): Show |
10 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2241-1104C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992402 | |||||||
chr20:5992500 | C | T | 16 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(13): Show |
20 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.2241-1006C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992500 | |||||||
chr20:5992543 | A | G | 19 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0093 others(16): Show |
21 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.2241-963A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992543 | |||||||
chr20:5992624 | C | T | 4 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(1): Show |
5 | HG01346.hp2 HG01934.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241-882C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992624 | |||||||
chr20:5992749 | A | G | 1 | a0002c0002t0002g0189 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2241-757A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992749 | |||||||
chr20:5992865 | G | A | 33 | a0003c0003t0004g0002 a0003c0003t0004g0008 a0003c0003t0004g0018 others(30): Show |
48 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.2241-641G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992865 | |||||||
chr20:5992882 | G | A | 97 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(94): Show |
107 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.2241-624G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992882 | |||||||
chr20:5992917 | A | G | 4 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2241-589A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992917 | |||||||
chr20:5992959 | C | T | 1 | a0003c0003t0087g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2241-547C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992959 | |||||||
chr20:5992960 | G | A | 1 | a0002c0002t0047g0188 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2241-546G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5992960 | |||||||
chr20:5993042 | A | C | 1 | a0002c0002t0028g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2241-464A>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5993042 | |||||||
chr20:5993147 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(261): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.2241-359G>A | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5993147 | |||||||
chr20:5993183 | A | G | 3 | a0001c0022t0019g0232 a0010c0016t0019g0231 a0010c0016t0019g0233 |
3 | HG02602.hp2 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2241-323A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 17/18 | chr20 | 5993183 | |||||||
chr20:5993699 | T | C | 1 | a0009c0011t0091g0238 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.2430+4T>C | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 18/18 | chr20 | 5993699 | |||||||
chr20:5993853 | C | T | 1 | a0002c0002t0099g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2430+158C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 18/18 | chr20 | 5993853 | |||||||
chr20:5994042 | A | T | 7 | a0001c0008t0030g0234 a0001c0008t0030g0235 a0001c0008t0055g0049 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.2431-257A>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 18/18 | chr20 | 5994042 | |||||||
chr20:5994055 | T | TTTTG | 161 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(158): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.2431-241_2431-240i others(6): Show |
MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr20 | 5994055 | ||||||
chr20:5994128 | C | T | 4 | a0001c0001t0044g0177 a0001c0001t0044g0185 a0001c0001t0096g0178 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2431-171C>T | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 18/18 | chr20 | 5994128 | |||||||
chr20:5994250 | A | G | 9 | a0004c0004t0007g0036 a0004c0004t0007g0052 a0004c0004t0007g0053 others(6): Show |
10 | HG00323.hp2 HG00642.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2431-49A>G | MCM8 | ENSG00000125885.13 | transcript | ENST00000610722.4 | protein_coding | 18/18 | chr20 | 5994250 |