Item | Value |
---|---|
geneid | 254394 |
ensemblid | ENSG00000111877.18 |
hgncid | 21484 |
symbol | MCM9 |
name | minichromosome maintenance 9 homologous recombination repair factor |
refseq_nuc | NM_017696.3 |
refseq_prot | NP_060166.2 |
ensembl_nuc | ENST00000619706.5 |
ensembl_prot | ENSP00000480469.1 |
mane_status | MANE Select |
chr | chr6 |
start | 118813455 |
end | 118935159 |
strand | - |
ver | v1.2 |
region | chr6:118813455-118935159 |
region5000 | chr6:118808455-118940159 |
regionname0 | MCM9_chr6_118813455_118935159 |
regionname5000 | MCM9_chr6_118808455_118940159 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1143 | 272 | 74 | 46 | 113 | 14 | 24 | 81 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0002 | 0/0 | 1143 | 28 | 3 | 8 | 8 | 3 | 6 | 7 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0003 | 0/0 | 1143 | 13 | 0 | 4 | 9 | 0 | 0 | 6 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0004 | 0/0 | 1143 | 9 | 0 | 7 | 0 | 1 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0005 | 0/0 | 1143 | 6 | 0 | 2 | 2 | 0 | 2 | 2 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0006 | 0/0 | 1143 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0007 | 0/0 | 1143 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0008 | 0/0 | 1143 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0009 | 1/0 | 1143 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0010 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0011 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0012 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0013 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0014 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0015 | 0/0 | 1143 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0016 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0017 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0018 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0019 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | MKSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
a0020 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | MNSDQ others(1138): Show |
chr6 | 118808455 | 118940159 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3429 | 212 | 59 | 41 | 75 | 14 | 22 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0001c0002 | 0/0 | 3429 | 51 | 9 | 4 | 36 | 0 | 2 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0001c0005 | 0/0 | 3429 | 7 | 6 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0001c0016 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0001c0017 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0002c0003 | 0/0 | 3429 | 28 | 3 | 8 | 8 | 3 | 6 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0003c0004 | 0/0 | 3429 | 13 | 0 | 4 | 9 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0004c0006 | 0/0 | 3429 | 7 | 0 | 5 | 0 | 1 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0004c0009 | 0/0 | 3429 | 2 | 0 | 2 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0005c0007 | 0/0 | 3429 | 6 | 0 | 2 | 2 | 0 | 2 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0006c0008 | 0/0 | 3429 | 3 | 2 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0007c0010 | 0/0 | 3429 | 2 | 2 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0007c0026 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0008c0011 | 0/0 | 3429 | 2 | 2 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0009c0024 | 1/0 | 3429 | 1 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0010c0025 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0011c0015 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0012c0020 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0013c0018 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0014c0019 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0015c0022 | 0/0 | 3429 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0016c0023 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0017c0013 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0018c0014 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0019c0012 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 | ||
a0020c0021 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATGAA others(3424): Show |
chr6 | 118808455 | 118940159 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5219 | 132 | 17 | 18 | 73 | 8 | 16 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0001t0002 | 0/0 | 5219 | 26 | 22 | 2 | 1 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0001t0004 | 0/1 | 5219 | 39 | 8 | 20 | 0 | 5 | 5 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0001t0006 | 0/0 | 5219 | 4 | 4 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0001t0007 | 0/0 | 5218 | 4 | 4 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0001c0001t0008 | 0/0 | 5218 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0001c0001t0009 | 0/0 | 5218 | 3 | 3 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0001c0001t0014 | 0/0 | 5219 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0001t0020 | 0/0 | 5219 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0001t0021 | 0/0 | 5219 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0002t0003 | 0/0 | 5218 | 47 | 9 | 4 | 32 | 0 | 2 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0001c0002t0012 | 0/0 | 5218 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0001c0002t0017 | 0/0 | 5219 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0002t0018 | 0/0 | 5219 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0002t0019 | 0/0 | 5218 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0001c0005t0002 | 0/0 | 5219 | 6 | 5 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0005t0010 | 0/0 | 5219 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0001c0016t0003 | 0/0 | 5218 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0001c0017t0001 | 0/0 | 5219 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0002c0003t0001 | 0/0 | 5219 | 4 | 0 | 1 | 1 | 2 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0002c0003t0002 | 0/0 | 5219 | 22 | 1 | 7 | 7 | 1 | 6 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0002c0003t0011 | 0/0 | 5219 | 2 | 2 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0003c0004t0002 | 0/0 | 5219 | 13 | 0 | 4 | 9 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0004c0006t0002 | 0/0 | 5219 | 7 | 0 | 5 | 0 | 1 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0004c0009t0002 | 0/0 | 5219 | 2 | 0 | 2 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0005c0007t0005 | 0/0 | 5218 | 6 | 0 | 2 | 2 | 0 | 2 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0006c0008t0002 | 0/0 | 5219 | 3 | 2 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0007c0010t0008 | 0/0 | 5218 | 2 | 2 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0007c0026t0008 | 0/0 | 5218 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0008c0011t0001 | 0/0 | 5219 | 2 | 2 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0009c0024t0010 | 1/0 | 5219 | 1 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0010c0025t0013 | 0/0 | 5219 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0011c0015t0015 | 0/0 | 5218 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0012c0020t0016 | 0/0 | 5218 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0013c0018t0002 | 0/0 | 5219 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0014c0019t0002 | 0/0 | 5219 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0015c0022t0001 | 0/0 | 5219 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0016c0023t0001 | 0/0 | 5219 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
a0017c0013t0003 | 0/0 | 5218 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0018c0014t0003 | 0/0 | 5218 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0019c0012t0003 | 0/0 | 5218 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5213): Show |
chr6 | 118808455 | 118940159 |
a0020c0021t0002 | 0/0 | 5219 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | ATCCG others(5214): Show |
chr6 | 118808455 | 118940159 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0014g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0020g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0001t0021g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0012g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0017g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0018g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0002t0019g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0005t0002g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0005t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0005t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0005t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0005t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0005t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0016t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0001c0017t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0002c0003t0011g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0003c0004t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0004c0006t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0004c0006t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0004c0006t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0004c0006t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0004c0006t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0004c0006t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0004c0006t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0004c0009t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0004c0009t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0005c0007t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0005c0007t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0005c0007t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0005c0007t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0005c0007t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0005c0007t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0006c0008t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0006c0008t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0006c0008t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0007c0010t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0007c0010t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0007c0026t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0008c0011t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0008c0011t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0009c0024t0010g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0010c0025t0013g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0011c0015t0015g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0012c0020t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0013c0018t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0014c0019t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0015c0022t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0016c0023t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0017c0013t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0018c0014t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0019c0012t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
a0020c0021t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00099 | hp2 | a0004 | c0006 | t0002 | g0043 | EUR | GBR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0193 | EUR | GBR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0172 | EUR | FIN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | FIN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0196 | EUR | FIN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | FIN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00408 | hp1 | a0001 | c0002 | t0012 | g0015 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00423 | hp1 | a0003 | c0004 | t0002 | g0029 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00597 | hp1 | a0002 | c0003 | t0002 | g0070 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00609 | hp1 | a0001 | c0002 | t0018 | g0127 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00639 | hp1 | a0001 | c0005 | t0002 | g0003 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0289 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0194 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00642 | hp2 | a0006 | c0008 | t0002 | g0095 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00733 | hp1 | a0004 | c0006 | t0002 | g0034 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0207 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00735 | hp1 | a0003 | c0004 | t0002 | g0026 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00735 | hp2 | a0002 | c0003 | t0002 | g0082 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0206 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG00741 | hp2 | a0003 | c0004 | t0002 | g0030 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01069 | hp1 | a0001 | c0002 | t0003 | g0009 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01069 | hp2 | a0004 | c0009 | t0002 | g0031 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01071 | hp1 | a0001 | c0002 | t0003 | g0112 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01071 | hp2 | a0004 | c0009 | t0002 | g0032 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01081 | hp2 | a0002 | c0003 | t0002 | g0067 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0198 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01106 | hp2 | a0004 | c0006 | t0002 | g0050 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01167 | hp1 | a0005 | c0007 | t0005 | g0064 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0286 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01168 | hp2 | a0004 | c0006 | t0002 | g0035 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01169 | hp1 | a0004 | c0006 | t0002 | g0036 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01169 | hp2 | a0005 | c0007 | t0005 | g0063 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0317 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0106 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0285 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01243 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01255 | hp1 | a0001 | c0001 | t0021 | g0323 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01258 | hp1 | a0002 | c0003 | t0002 | g0076 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0288 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01261 | hp2 | a0002 | c0003 | t0002 | g0066 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01346 | hp1 | a0004 | c0006 | t0002 | g0033 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01346 | hp2 | a0002 | c0003 | t0002 | g0071 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01358 | hp2 | a0002 | c0003 | t0002 | g0068 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0316 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0200 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | IBS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0287 | EUR | IBS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0249 | EUR | IBS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01517 | hp1 | a0002 | c0003 | t0001 | g0248 | EUR | IBS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0114 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01884 | hp2 | a0007 | c0010 | t0008 | g0190 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01891 | hp2 | a0010 | c0025 | t0013 | g0017 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01928 | hp1 | a0002 | c0003 | t0002 | g0075 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0210 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01975 | hp2 | a0003 | c0004 | t0002 | g0025 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01978 | hp1 | a0003 | c0004 | t0002 | g0023 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0202 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02071 | hp2 | a0001 | c0002 | t0003 | g0123 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02080 | hp2 | a0001 | c0016 | t0003 | g0111 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02129 | hp1 | a0003 | c0004 | t0002 | g0079 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02135 | hp2 | a0001 | c0002 | t0003 | g0124 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0161 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02155 | hp1 | a0003 | c0004 | t0002 | g0024 | EAS | CDX | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02258 | hp1 | a0008 | c0011 | t0001 | g0183 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02258 | hp2 | a0006 | c0008 | t0002 | g0088 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0201 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0125 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0192 | AMR | PEL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02451 | hp1 | a0001 | c0005 | t0002 | g0021 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0128 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02572 | hp1 | a0011 | c0015 | t0015 | g0151 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02622 | hp1 | a0001 | c0002 | t0003 | g0140 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02683 | hp1 | a0005 | c0007 | t0005 | g0061 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02717 | hp1 | a0001 | c0005 | t0002 | g0020 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02717 | hp2 | a0012 | c0020 | t0016 | g0158 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02723 | hp1 | a0001 | c0005 | t0002 | g0019 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02818 | hp1 | a0013 | c0018 | t0002 | g0085 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02897 | hp2 | a0001 | c0005 | t0010 | g0022 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0160 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02965 | hp2 | a0007 | c0026 | t0008 | g0167 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03017 | hp1 | a0005 | c0007 | t0005 | g0062 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0159 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0110 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0141 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03195 | hp2 | a0001 | c0005 | t0002 | g0003 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03225 | hp1 | a0001 | c0002 | t0003 | g0119 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03453 | hp1 | a0014 | c0019 | t0002 | g0042 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03486 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03486 | hp2 | a0007 | c0010 | t0008 | g0191 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03490 | hp1 | a0002 | c0003 | t0002 | g0005 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03490 | hp2 | a0001 | c0002 | t0003 | g0129 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0203 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03492 | hp2 | a0002 | c0003 | t0002 | g0005 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03516 | hp1 | a0002 | c0003 | t0011 | g0092 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03540 | hp2 | a0008 | c0011 | t0001 | g0182 | AFR | GWD | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03654 | hp2 | a0002 | c0003 | t0002 | g0059 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0290 | SAS | STU | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03704 | hp1 | a0015 | c0022 | t0001 | g0226 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03704 | hp2 | a0004 | c0006 | t0002 | g0037 | SAS | PJL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03831 | hp1 | a0002 | c0003 | t0002 | g0072 | SAS | BEB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | BEB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03834 | hp1 | a0002 | c0003 | t0002 | g0077 | SAS | BEB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG04115 | hp1 | a0001 | c0001 | t0020 | g0272 | SAS | STU | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0163 | SAS | STU | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG04204 | hp1 | a0001 | c0002 | t0003 | g0134 | SAS | STU | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG04228 | hp1 | a0002 | c0003 | t0002 | g0073 | SAS | STU | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | STU | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18612 | hp2 | a0001 | c0002 | t0019 | g0162 | EAS | CHB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0157 | EAS | CHB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | YRI | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | YRI | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18939 | hp1 | a0001 | c0002 | t0003 | g0150 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18940 | hp2 | a0001 | c0002 | t0003 | g0115 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18943 | hp2 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0144 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18948 | hp1 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18948 | hp2 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18949 | hp1 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18950 | hp1 | a0016 | c0023 | t0001 | g0244 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18951 | hp1 | a0001 | c0002 | t0003 | g0130 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18952 | hp2 | a0017 | c0013 | t0003 | g0139 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18954 | hp1 | a0001 | c0002 | t0003 | g0152 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18964 | hp2 | a0001 | c0002 | t0003 | g0131 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18967 | hp1 | a0018 | c0014 | t0003 | g0153 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18968 | hp2 | a0019 | c0012 | t0003 | g0113 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18971 | hp1 | a0005 | c0007 | t0005 | g0065 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18975 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18977 | hp2 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18978 | hp1 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18980 | hp1 | a0003 | c0004 | t0002 | g0028 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18985 | hp1 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18986 | hp2 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18987 | hp2 | a0005 | c0007 | t0005 | g0060 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18989 | hp2 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0126 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18991 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18995 | hp2 | a0003 | c0004 | t0002 | g0004 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18998 | hp2 | a0003 | c0004 | t0002 | g0056 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18999 | hp2 | a0002 | c0003 | t0002 | g0080 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19000 | hp1 | a0002 | c0003 | t0002 | g0096 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19000 | hp2 | a0001 | c0002 | t0017 | g0116 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19002 | hp2 | a0001 | c0002 | t0003 | g0118 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19004 | hp2 | a0001 | c0002 | t0003 | g0132 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19005 | hp1 | a0001 | c0002 | t0003 | g0145 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19007 | hp1 | a0001 | c0002 | t0003 | g0148 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19011 | hp1 | a0001 | c0017 | t0001 | g0252 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19012 | hp1 | a0001 | c0002 | t0003 | g0155 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19030 | hp1 | a0002 | c0003 | t0011 | g0093 | AFR | LWK | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19030 | hp2 | a0001 | c0002 | t0003 | g0149 | AFR | LWK | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19055 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0133 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19060 | hp1 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19060 | hp2 | a0003 | c0004 | t0002 | g0004 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19066 | hp2 | a0002 | c0003 | t0002 | g0091 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19077 | hp1 | a0003 | c0004 | t0002 | g0027 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19078 | hp1 | a0002 | c0003 | t0001 | g0168 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19079 | hp2 | a0002 | c0003 | t0002 | g0081 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19082 | hp1 | a0001 | c0002 | t0003 | g0147 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19083 | hp2 | a0002 | c0003 | t0002 | g0090 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19084 | hp1 | a0002 | c0003 | t0002 | g0089 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19085 | hp2 | a0001 | c0002 | t0003 | g0138 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA19091 | hp2 | a0003 | c0004 | t0002 | g0055 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA20129 | hp1 | a0002 | c0003 | t0002 | g0078 | AFR | ASW | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0051 | AFR | ASW | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0164 | EUR | TSI | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0308 | EUR | TSI | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA20805 | hp2 | a0002 | c0003 | t0002 | g0083 | EUR | TSI | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | GIH | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | GIH | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01123 | hp1 | a0002 | c0003 | t0001 | g0265 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0197 | AMR | CLM | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02486 | hp2 | a0006 | c0008 | t0002 | g0094 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02559 | hp1 | a0001 | c0005 | t0002 | g0018 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0142 | AFR | MSL | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | USA | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | USA | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | USA | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA20300 | hp2 | a0020 | c0021 | t0002 | g0044 | AFR | USA | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA21309 | hp1 | a0001 | c0002 | t0003 | g0120 | AFR | LWK | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
NA21309 | hp2 | a0001 | c0001 | t0014 | g0097 | AFR | LWK | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0171 | REF | REF | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
homoSapiens | grch38p0 | a0009 | c0024 | t0010 | g0074 | REF | REF | MCM9_chr6_118808455_118940159 | MCM9 | chr6 | 118808455 | 118940159 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:118814839 | C | T | 1 | a0011 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.3417G>A | p.Met1139Ile | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 3835/5219 | 3417/3432 | 1139/1143 | chr6 | 118814839 | |||
chr6:118815033 | G | A | 1 | a0007 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.3223C>T | p.Pro1075Ser | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 3641/5219 | 3223/3432 | 1075/1143 | chr6 | 118815033 | |||
chr6:118815116 | C | G | 1 | a0014 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.3140G>C | p.Ser1047Thr | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 3558/5219 | 3140/3432 | 1047/1143 | chr6 | 118815116 | |||
chr6:118815438 | G | T | 1 | a0020 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2818C>A | p.His940Asn | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 3236/5219 | 2818/3432 | 940/1143 | chr6 | 118815438 | |||
chr6:118815563 | G | A | 1 | a0005 | 6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
missense_variant | MODERATE | c.2693C>T | p.Ser898Phe | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 3111/5219 | 2693/3432 | 898/1143 | chr6 | 118815563 | |||
chr6:118815596 | A | C | 2 | a0002 a0013 |
29 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(26): Show |
missense_variant | MODERATE | c.2660T>G | p.Met887Arg | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 3078/5219 | 2660/3432 | 887/1143 | chr6 | 118815596 | |||
chr6:118815808 | T | G | 1 | a0012 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2448A>C | p.Glu816Asp | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 2866/5219 | 2448/3432 | 816/1143 | chr6 | 118815808 | |||
chr6:118815848 | G | A | 2 | a0004 a0020 |
10 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(7): Show |
missense_variant | MODERATE | c.2408C>T | p.Pro803Leu | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 2826/5219 | 2408/3432 | 803/1143 | chr6 | 118815848 | |||
chr6:118815984 | T | C | 1 | a0006 | 3 | HG00642.hp2 HG02258.hp2 HG02486.hp2 |
missense_variant | MODERATE | c.2272A>G | p.Thr758Ala | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 2690/5219 | 2272/3432 | 758/1143 | chr6 | 118815984 | |||
chr6:118816282 | C | A | 1 | a0015 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.1974G>T | p.Gln658His | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 2392/5219 | 1974/3432 | 658/1143 | chr6 | 118816282 | |||
chr6:118826255 | G | C | 1 | a0016 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.1853C>G | p.Thr618Ser | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/14 | 2271/5219 | 1853/3432 | 618/1143 | chr6 | 118826255 | |||
chr6:118827986 | C | G | 18 | a0001 a0003 a0004 others(15): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
missense_variant | MODERATE | c.1673G>C | p.Cys558Ser | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/14 | 2091/5219 | 1673/3432 | 558/1143 | chr6 | 118827986 | |||
chr6:118828046 | A | G | 1 | a0018 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.1613T>C | p.Leu538Pro | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/14 | 2031/5219 | 1613/3432 | 538/1143 | chr6 | 118828046 | |||
chr6:118829055 | T | A | 1 | a0003 | 13 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
missense_variant | MODERATE | c.1521A>T | p.Glu507Asp | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/14 | 1939/5219 | 1521/3432 | 507/1143 | chr6 | 118829055 | |||
chr6:118829108 | G | C | 1 | a0010 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1468C>G | p.Leu490Val | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/14 | 1886/5219 | 1468/3432 | 490/1143 | chr6 | 118829108 | |||
chr6:118829246 | C | G | 1 | a0017 | 1 | NA18952.hp2 | missense_variant | MODERATE | c.1330G>C | p.Val444Leu | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/14 | 1748/5219 | 1330/3432 | 444/1143 | chr6 | 118829246 | |||
chr6:118924035 | T | C | 1 | a0008 | 2 | HG02258.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.397A>G | p.Thr133Ala | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/14 | 815/5219 | 397/3432 | 133/1143 | chr6 | 118924035 | |||
chr6:118931718 | A | C | 1 | a0019 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.6T>G | p.Asn2Lys | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/14 | 424/5219 | 6/3432 | 2/1143 | chr6 | 118931718 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:118815547 | T | C | 1 | a0001c0016 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.2709A>G | p.Glu903Glu | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 3127/5219 | 2709/3432 | 903/1143 | chr6 | 118815547 | |||
chr6:118816186 | T | C | 1 | a0007c0026 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.2070A>G | p.Ser690Ser | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 2488/5219 | 2070/3432 | 690/1143 | chr6 | 118816186 | |||
chr6:118917688 | C | T | 1 | a0001c0017 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.777G>A | p.Val259Val | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/14 | 1195/5219 | 777/3432 | 259/1143 | chr6 | 118917688 | |||
chr6:118917715 | G | A | 2 | a0007c0010 a0007c0026 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.750C>T | p.Pro250Pro | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/14 | 1168/5219 | 750/3432 | 250/1143 | chr6 | 118917715 | |||
chr6:118917739 | C | T | 1 | a0004c0009 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.726G>A | p.Gly242Gly | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/14 | 1144/5219 | 726/3432 | 242/1143 | chr6 | 118917739 | |||
chr6:118923859 | C | T | 6 | a0001c0002 a0001c0016 a0011c0015 others(3): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
synonymous_variant | LOW | c.573G>A | p.Ser191Ser | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/14 | 991/5219 | 573/3432 | 191/1143 | chr6 | 118923859 | |||
chr6:118931511 | A | G | 1 | a0001c0005 | 7 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
synonymous_variant | LOW | c.213T>C | p.Ser71Ser | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/14 | 631/5219 | 213/3432 | 71/1143 | chr6 | 118931511 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:118813505 | C | T | 1 | a0001c0001t0020 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 1319 | chr6 | 118813505 | ||||||
chr6:118813544 | G | A | 1 | a0001c0001t0021 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1280C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 1280 | chr6 | 118813544 | ||||||
chr6:118813693 | A | G | 1 | a0011c0015t0015 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1131T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 1131 | chr6 | 118813693 | ||||||
chr6:118813737 | A | T | 1 | a0002c0003t0011 | 2 | HG03516.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1087T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 1087 | chr6 | 118813737 | ||||||
chr6:118813772 | T | C | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(37): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*1052A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 1052 | chr6 | 118813772 | ||||||
chr6:118813930 | G | A | 1 | a0012c0020t0016 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*894C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 894 | chr6 | 118813930 | ||||||
chr6:118814108 | G | A | 1 | a0012c0020t0016 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 716 | chr6 | 118814108 | ||||||
chr6:118814109 | C | A | 1 | a0012c0020t0016 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*715G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 715 | chr6 | 118814109 | ||||||
chr6:118814247 | C | T | 9 | a0001c0002t0003 a0001c0002t0012 a0001c0002t0017 others(6): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*577G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 577 | chr6 | 118814247 | ||||||
chr6:118814263 | A | T | 1 | a0001c0001t0004 | 38 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*561T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 561 | chr6 | 118814263 | ||||||
chr6:118814390 | CA | C | 15 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0009 others(12): Show |
72 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*433delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 433 | chr6 | 118814390 | ||||||
chr6:118814695 | G | A | 1 | a0010c0025t0013 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 129 | chr6 | 118814695 | ||||||
chr6:118814759 | T | C | 1 | a0001c0001t0006 | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*65A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 14/14 | 65 | chr6 | 118814759 | ||||||
chr6:118932703 | T | A | 1 | a0001c0001t0014 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/14 | 980 | chr6 | 118932703 | ||||||
chr6:118932704 | C | T | 1 | a0001c0001t0014 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-113G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/14 | 981 | chr6 | 118932704 | ||||||
chr6:118932705 | T | C | 1 | a0001c0001t0014 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-114A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/14 | 982 | chr6 | 118932705 | ||||||
chr6:118934914 | A | G | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(9): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
5_prime_UTR_variant | MODIFIER | c.-173T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/14 | 3191 | chr6 | 118934914 | ||||||
chr6:118934917 | G | A | 12 | a0001c0001t0007 a0001c0002t0003 a0001c0002t0012 others(9): Show |
61 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-176C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/14 | 3194 | chr6 | 118934917 | ||||||
chr6:118935000 | A | G | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(9): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
5_prime_UTR_variant | MODIFIER | c.-259T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/14 | 3277 | chr6 | 118935000 | ||||||
chr6:118935001 | G | A | 1 | a0001c0001t0009 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-260C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/14 | 3278 | chr6 | 118935001 | ||||||
chr6:118935008 | C | G | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(9): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
5_prime_UTR_variant | MODIFIER | c.-267G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/14 | 3285 | chr6 | 118935008 | ||||||
chr6:118935063 | G | A | 1 | a0001c0002t0019 | 1 | NA18612.hp2 | 5_prime_UTR_variant | MODIFIER | c.-322C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/14 | 3340 | chr6 | 118935063 | ||||||
chr6:118935067 | G | C | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(9): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
5_prime_UTR_variant | MODIFIER | c.-326C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/14 | 3344 | chr6 | 118935067 | ||||||
chr6:118935136 | C | G | 1 | a0001c0002t0012 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-395G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/14 | 3413 | chr6 | 118935136 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:118816351 | C | A | 2 | a0001c0001t0001g0229 a0001c0002t0018g0127 |
2 | HG00609.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1962-57G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118816351 | |||||||
chr6:118816467 | A | G | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1962-173T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118816467 | |||||||
chr6:118816495 | A | C | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1962-201T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118816495 | |||||||
chr6:118816588 | CATTT | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1962-298_1962-295d others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118816588 | |||||||
chr6:118816655 | C | G | 1 | a0001c0001t0004g0205 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1962-361G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118816655 | |||||||
chr6:118816691 | T | C | 1 | a0002c0003t0002g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1962-397A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118816691 | |||||||
chr6:118816765 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1962-471C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118816765 | |||||||
chr6:118816845 | G | GT | 30 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0214 others(27): Show |
30 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.1962-552dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118816845 | |||||||
chr6:118816880 | G | A | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1962-586C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118816880 | |||||||
chr6:118817343 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1962-1049C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817343 | |||||||
chr6:118817358 | A | C | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(310): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1962-1064T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817358 | |||||||
chr6:118817461 | T | C | 51 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(48): Show |
54 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.1962-1167A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817461 | |||||||
chr6:118817504 | T | A | 3 | a0001c0001t0002g0016 a0001c0001t0002g0069 a0001c0001t0014g0097 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1962-1210A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817504 | |||||||
chr6:118817549 | T | C | 2 | a0007c0010t0008g0190 a0007c0010t0008g0191 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1962-1255A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817549 | |||||||
chr6:118817554 | A | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1962-1260T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817554 | |||||||
chr6:118817600 | C | T | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1962-1306G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817600 | |||||||
chr6:118817601 | G | A | 3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1962-1307C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817601 | |||||||
chr6:118817619 | A | T | 12 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(9): Show |
13 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1962-1325T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817619 | |||||||
chr6:118817709 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1962-1415C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817709 | |||||||
chr6:118817774 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1962-1480T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817774 | |||||||
chr6:118817776 | T | A | 1 | a0001c0002t0003g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1962-1482A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817776 | |||||||
chr6:118817956 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1962-1662A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118817956 | |||||||
chr6:118818078 | T | C | 5 | a0001c0002t0003g0007 a0001c0002t0003g0117 a0001c0002t0003g0118 others(2): Show |
6 | NA18954.hp1 NA18967.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1962-1784A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118818078 | |||||||
chr6:118818084 | T | A | 38 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.1962-1790A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118818084 | |||||||
chr6:118818115 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1962-1821A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118818115 | |||||||
chr6:118818128 | T | C | 1 | a0015c0022t0001g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1962-1834A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118818128 | |||||||
chr6:118818226 | T | A | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1962-1932A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118818226 | |||||||
chr6:118818400 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1962-2106C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118818400 | |||||||
chr6:118818559 | C | T | 2 | a0002c0003t0001g0248 a0002c0003t0001g0249 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1962-2265G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118818559 | |||||||
chr6:118818695 | T | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1962-2401A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118818695 | |||||||
chr6:118818838 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(325): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1962-2544A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118818838 | |||||||
chr6:118818855 | G | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0241 |
2 | HG02523.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1962-2561C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118818855 | |||||||
chr6:118819068 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1962-2774C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819068 | |||||||
chr6:118819088 | CT | C | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1962-2795delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819088 | |||||||
chr6:118819330 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(112): Show |
123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1962-3036C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819330 | |||||||
chr6:118819338 | G | C | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1962-3044C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819338 | |||||||
chr6:118819419 | C | T | 1 | a0015c0022t0001g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1962-3125G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819419 | |||||||
chr6:118819420 | G | A | 1 | a0001c0002t0003g0128 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1962-3126C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819420 | |||||||
chr6:118819445 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1962-3151G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819445 | |||||||
chr6:118819469 | C | G | 5 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0303 others(2): Show |
5 | NA18612.hp1 NA18947.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1962-3175G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819469 | |||||||
chr6:118819493 | T | C | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1962-3199A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819493 | |||||||
chr6:118819500 | T | A | 1 | a0003c0004t0002g0023 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1962-3206A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819500 | |||||||
chr6:118819964 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1962-3670C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819964 | |||||||
chr6:118819978 | A | AT | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1962-3685dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819978 | |||||||
chr6:118819986 | A | C | 1 | a0015c0022t0001g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1962-3692T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118819986 | |||||||
chr6:118820029 | T | C | 1 | a0001c0001t0001g0012 | 2 | HG00609.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1962-3735A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820029 | |||||||
chr6:118820073 | C | G | 2 | a0001c0001t0001g0300 a0001c0001t0002g0084 |
2 | NA18989.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1962-3779G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820073 | |||||||
chr6:118820231 | T | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1962-3937A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820231 | |||||||
chr6:118820310 | T | C | 9 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1962-4016A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820310 | |||||||
chr6:118820338 | T | C | 5 | a0003c0004t0002g0023 a0003c0004t0002g0025 a0003c0004t0002g0026 others(2): Show |
5 | HG00735.hp1 HG01975.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1962-4044A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820338 | |||||||
chr6:118820352 | T | C | 1 | a0001c0002t0003g0106 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1962-4058A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820352 | |||||||
chr6:118820499 | A | T | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1962-4205T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820499 | |||||||
chr6:118820792 | GA | G | 9 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1962-4499delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820792 | |||||||
chr6:118820833 | T | C | 4 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1962-4539A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820833 | |||||||
chr6:118820902 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1962-4608A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820902 | |||||||
chr6:118820985 | C | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(320): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1962-4691G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118820985 | |||||||
chr6:118821101 | T | C | 30 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0214 others(27): Show |
30 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.1962-4807A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118821101 | |||||||
chr6:118821122 | C | T | 5 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0303 others(2): Show |
5 | NA18612.hp1 NA18947.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1962-4828G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118821122 | |||||||
chr6:118821213 | T | C | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1962-4919A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118821213 | |||||||
chr6:118821214 | A | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(255): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1962-4920T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118821214 | |||||||
chr6:118821222 | C | T | 1 | a0003c0004t0002g0026 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1961+4925G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118821222 | |||||||
chr6:118821492 | G | A | 2 | a0001c0001t0002g0057 a0012c0020t0016g0158 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1961+4655C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118821492 | |||||||
chr6:118821824 | A | G | 4 | a0002c0003t0001g0168 a0002c0003t0002g0080 a0002c0003t0002g0081 others(1): Show |
4 | NA18999.hp2 NA19000.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1961+4323T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118821824 | |||||||
chr6:118821872 | T | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1961+4275A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118821872 | |||||||
chr6:118821903 | G | A | 12 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1961+4244C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118821903 | |||||||
chr6:118821955 | C | T | 1 | a0001c0002t0003g0141 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1961+4192G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118821955 | |||||||
chr6:118822142 | A | C | 7 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1961+4005T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822142 | |||||||
chr6:118822251 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1961+3896C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822251 | |||||||
chr6:118822386 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(151): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1961+3761A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822386 | |||||||
chr6:118822448 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1961+3699C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822448 | |||||||
chr6:118822510 | C | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0263 |
2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1961+3637G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822510 | |||||||
chr6:118822637 | G | A | 1 | a0001c0002t0003g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1961+3510C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822637 | |||||||
chr6:118822740 | C | G | 1 | a0001c0001t0002g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1961+3407G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822740 | |||||||
chr6:118822856 | C | T | 7 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1961+3291G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822856 | |||||||
chr6:118822857 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1961+3290C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822857 | |||||||
chr6:118822865 | G | A | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1961+3282C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822865 | |||||||
chr6:118822944 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1961+3203G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822944 | |||||||
chr6:118822971 | C | T | 1 | a0003c0004t0002g0024 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1961+3176G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118822971 | |||||||
chr6:118823126 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1961+3021G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118823126 | |||||||
chr6:118823230 | G | A | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1961+2917C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118823230 | |||||||
chr6:118823324 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1961+2823A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118823324 | |||||||
chr6:118823357 | G | A | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1961+2790C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118823357 | |||||||
chr6:118823357 | G | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02257.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1961+2790C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118823357 | |||||||
chr6:118823408 | T | C | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1961+2739A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118823408 | |||||||
chr6:118823477 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1961+2670C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118823477 | |||||||
chr6:118823560 | A | G | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1961+2587T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118823560 | |||||||
chr6:118823688 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1961+2459C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118823688 | |||||||
chr6:118823790 | T | C | 1 | a0002c0003t0002g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1961+2357A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118823790 | |||||||
chr6:118824035 | CTT | C | 7 | a0001c0001t0004g0186 a0001c0001t0004g0195 a0001c0001t0004g0197 others(4): Show |
7 | HG01106.hp1 HG01123.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1961+2110_1961+211 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTT | C | 13 | a0001c0001t0004g0010 a0001c0001t0004g0172 a0001c0001t0004g0184 others(10): Show |
14 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1961+2109_1961+211 others(7): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTTT | C | 19 | a0001c0001t0001g0169 a0001c0001t0004g0163 a0001c0001t0004g0164 others(16): Show |
19 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.1961+2108_1961+211 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTTTT | C | 14 | a0001c0001t0001g0260 a0001c0001t0002g0105 a0003c0004t0002g0004 others(11): Show |
15 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1961+2107_1961+211 others(9): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTTTTT | C | 50 | a0001c0001t0001g0166 a0001c0001t0001g0212 a0001c0001t0001g0216 others(47): Show |
50 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1961+2106_1961+211 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTTTTTT | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(124): Show |
135 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1961+2105_1961+211 others(11): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0007g0107 a0001c0001t0007g0109 a0001c0001t0007g0110 others(3): Show |
6 | HG00597.hp1 HG01884.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1961+2103_1961+211 others(13): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0002g0006 a0001c0001t0002g0086 a0002c0003t0001g0168 others(1): Show |
5 | HG00741.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1961+2102_1961+211 others(14): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTTTTTT others(4): Show |
C | 30 | a0001c0001t0002g0016 a0001c0001t0002g0069 a0001c0001t0002g0087 others(27): Show |
31 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1961+2101_1961+211 others(15): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(2): Show |
5 | HG02145.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1961+2098_1961+211 others(18): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTTTTTT others(8): Show |
C | 39 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(36): Show |
42 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1961+2097_1961+211 others(19): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824035 | CTTTTTTT others(9): Show |
C | 3 | a0001c0002t0003g0129 a0001c0002t0003g0137 a0001c0002t0003g0144 |
3 | HG03490.hp2 NA18947.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1961+2096_1961+211 others(20): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824035 | |||||||
chr6:118824061 | T | C | 2 | a0001c0002t0003g0120 a0001c0002t0003g0149 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1961+2086A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824061 | |||||||
chr6:118824070 | T | A | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1961+2077A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824070 | |||||||
chr6:118824070 | T | C | 12 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(9): Show |
13 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1961+2077A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824070 | |||||||
chr6:118824144 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1961+2003G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824144 | |||||||
chr6:118824316 | G | A | 7 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1961+1831C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824316 | |||||||
chr6:118824345 | C | CTTTTTTT others(4): Show |
7 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1961+1801_1961+180 others(15): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824345 | |||||||
chr6:118824345 | C | CTTTTTTT others(5): Show |
14 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1961+1801_1961+180 others(16): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824345 | |||||||
chr6:118824345 | C | CTTTTTTT others(6): Show |
47 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(44): Show |
50 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.1961+1801_1961+180 others(17): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824345 | |||||||
chr6:118824434 | G | A | 1 | a0001c0002t0003g0008 | 2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1961+1713C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824434 | |||||||
chr6:118824811 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1961+1336G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824811 | |||||||
chr6:118824833 | T | C | 13 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(10): Show |
14 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1961+1314A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118824833 | |||||||
chr6:118825110 | A | C | 1 | a0001c0001t0001g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1961+1037T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825110 | |||||||
chr6:118825222 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1961+925T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825222 | |||||||
chr6:118825269 | G | A | 12 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(9): Show |
13 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1961+878C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825269 | |||||||
chr6:118825334 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1961+813G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825334 | |||||||
chr6:118825482 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1961+665A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825482 | |||||||
chr6:118825581 | A | G | 1 | a0002c0003t0002g0067 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1961+566T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825581 | |||||||
chr6:118825621 | C | T | 1 | a0004c0006t0002g0050 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1961+526G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825621 | |||||||
chr6:118825842 | C | G | 6 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(3): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1961+305G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825842 | |||||||
chr6:118825882 | C | G | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1961+265G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825882 | |||||||
chr6:118825888 | T | C | 3 | a0002c0003t0002g0089 a0002c0003t0002g0090 a0002c0003t0002g0091 |
3 | NA19066.hp2 NA19083.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1961+259A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825888 | |||||||
chr6:118825902 | C | T | 2 | a0001c0001t0009g0159 a0001c0001t0009g0160 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1961+245G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825902 | |||||||
chr6:118825943 | G | A | 1 | a0001c0001t0004g0210 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1961+204C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 13/13 | chr6 | 118825943 | |||||||
chr6:118826371 | C | T | 1 | a0001c0002t0003g0148 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1816-79G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 12/13 | chr6 | 118826371 | |||||||
chr6:118826525 | A | T | 1 | a0001c0001t0001g0305 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1816-233T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 12/13 | chr6 | 118826525 | |||||||
chr6:118826654 | T | C | 1 | a0001c0001t0004g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1815+128A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 12/13 | chr6 | 118826654 | |||||||
chr6:118826735 | G | C | 2 | a0005c0007t0005g0061 a0005c0007t0005g0062 |
2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1815+47C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 12/13 | chr6 | 118826735 | |||||||
chr6:118826987 | T | A | 3 | a0001c0001t0002g0016 a0001c0001t0002g0069 a0001c0001t0014g0097 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1733-123A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/13 | chr6 | 118826987 | |||||||
chr6:118827027 | A | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1733-163T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/13 | chr6 | 118827027 | |||||||
chr6:118827117 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1733-253C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/13 | chr6 | 118827117 | |||||||
chr6:118827259 | A | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1733-395T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/13 | chr6 | 118827259 | |||||||
chr6:118827537 | C | T | 9 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1732+390G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/13 | chr6 | 118827537 | |||||||
chr6:118827696 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1732+231G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/13 | chr6 | 118827696 | |||||||
chr6:118827791 | G | A | 1 | a0001c0001t0001g0014 | 2 | NA18952.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1732+136C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/13 | chr6 | 118827791 | |||||||
chr6:118827886 | G | A | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1732+41C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/13 | chr6 | 118827886 | |||||||
chr6:118827914 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1732+13C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 11/13 | chr6 | 118827914 | |||||||
chr6:118828382 | A | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(320): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1529-252T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118828382 | |||||||
chr6:118828390 | A | AT | 13 | a0001c0001t0002g0054 a0003c0004t0002g0004 a0003c0004t0002g0023 others(10): Show |
14 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1529-261dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118828390 | |||||||
chr6:118828410 | G | T | 1 | a0002c0003t0002g0075 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1529-280C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118828410 | |||||||
chr6:118828437 | G | A | 51 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(48): Show |
54 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.1529-307C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118828437 | |||||||
chr6:118828702 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1528+346T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118828702 | |||||||
chr6:118828752 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1528+296T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118828752 | |||||||
chr6:118828763 | G | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1528+285C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118828763 | |||||||
chr6:118828764 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1528+284T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118828764 | |||||||
chr6:118828933 | T | C | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1528+115A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118828933 | |||||||
chr6:118828996 | A | G | 1 | a0002c0003t0002g0091 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1528+52T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118828996 | |||||||
chr6:118829044 | G | A | 1 | a0001c0001t0004g0204 | 1 | HG01255.hp2 | splice_region_variant&intron_variant | LOW | c.1528+4C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 10/13 | chr6 | 118829044 | |||||||
chr6:118829411 | C | A | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326-161G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118829411 | |||||||
chr6:118829461 | A | G | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1326-211T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118829461 | |||||||
chr6:118829519 | T | C | 6 | a0001c0002t0003g0122 a0001c0002t0003g0130 a0001c0002t0003g0131 others(3): Show |
6 | HG02080.hp2 NA18939.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-269A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118829519 | |||||||
chr6:118829623 | G | T | 1 | a0008c0011t0001g0182 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1326-373C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118829623 | |||||||
chr6:118829650 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1326-400A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118829650 | |||||||
chr6:118829760 | G | T | 1 | a0001c0002t0003g0112 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1326-510C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118829760 | |||||||
chr6:118829768 | G | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-518C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118829768 | |||||||
chr6:118829815 | A | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-565T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118829815 | |||||||
chr6:118829868 | GAAAC | G | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1326-622_1326-619d others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118829868 | |||||||
chr6:118830009 | A | G | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1326-759T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118830009 | |||||||
chr6:118830279 | T | C | 3 | a0006c0008t0002g0088 a0006c0008t0002g0094 a0006c0008t0002g0095 |
3 | HG00642.hp2 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1326-1029A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118830279 | |||||||
chr6:118830312 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1326-1062A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118830312 | |||||||
chr6:118830665 | A | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(35): Show |
43 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.1326-1415T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118830665 | |||||||
chr6:118831153 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(268): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.1326-1903T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831153 | |||||||
chr6:118831198 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-1948G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831198 | |||||||
chr6:118831315 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1326-2065C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831315 | |||||||
chr6:118831340 | C | CA | 49 | a0001c0001t0002g0049 a0001c0001t0002g0054 a0001c0001t0007g0107 others(46): Show |
52 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1326-2091dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831340 | |||||||
chr6:118831340 | C | CAA | 15 | a0001c0002t0003g0131 a0001c0002t0003g0144 a0001c0002t0017g0116 others(12): Show |
16 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1326-2092_1326-209 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831340 | |||||||
chr6:118831340 | CA | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(130): Show |
141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1326-2091delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831340 | |||||||
chr6:118831381 | A | G | 3 | a0001c0002t0003g0137 a0001c0002t0003g0138 a0001c0002t0003g0156 |
3 | NA18986.hp2 NA19055.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1326-2131T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831381 | |||||||
chr6:118831510 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1326-2260T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831510 | |||||||
chr6:118831624 | TA | T | 70 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(67): Show |
73 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.1326-2375delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831624 | |||||||
chr6:118831689 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-2439A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831689 | |||||||
chr6:118831692 | A | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-2442T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831692 | |||||||
chr6:118831726 | A | G | 59 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(56): Show |
62 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.1326-2476T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831726 | |||||||
chr6:118831803 | C | T | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-2553G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118831803 | |||||||
chr6:118832004 | C | T | 8 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(5): Show |
8 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1326-2754G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832004 | |||||||
chr6:118832043 | C | G | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(321): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1326-2793G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832043 | |||||||
chr6:118832052 | C | T | 10 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(7): Show |
10 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1326-2802G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832052 | |||||||
chr6:118832219 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1326-2969G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832219 | |||||||
chr6:118832309 | C | T | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-3059G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832309 | |||||||
chr6:118832369 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1326-3119A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832369 | |||||||
chr6:118832472 | C | T | 29 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(26): Show |
29 | HG00408.hp1 HG00639.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1326-3222G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832472 | |||||||
chr6:118832484 | A | G | 1 | a0001c0002t0017g0116 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1326-3234T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832484 | |||||||
chr6:118832558 | G | A | 1 | a0006c0008t0002g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1326-3308C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832558 | |||||||
chr6:118832664 | A | G | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1326-3414T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832664 | |||||||
chr6:118832673 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0260 |
2 | HG01261.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1326-3423C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832673 | |||||||
chr6:118832786 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1326-3536G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832786 | |||||||
chr6:118832787 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1326-3537C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118832787 | |||||||
chr6:118833040 | T | C | 3 | a0001c0001t0002g0016 a0001c0001t0002g0069 a0001c0001t0014g0097 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1326-3790A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833040 | |||||||
chr6:118833050 | T | C | 1 | a0003c0004t0002g0079 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1326-3800A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833050 | |||||||
chr6:118833143 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-3893C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833143 | |||||||
chr6:118833154 | C | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(311): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1326-3904G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833154 | |||||||
chr6:118833161 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1326-3911G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833161 | |||||||
chr6:118833183 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(161): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1326-3933G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833183 | |||||||
chr6:118833197 | T | C | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-3947A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833197 | |||||||
chr6:118833267 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-4017T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833267 | |||||||
chr6:118833401 | T | C | 38 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.1326-4151A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833401 | |||||||
chr6:118833407 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-4157G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833407 | |||||||
chr6:118833437 | A | G | 3 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0058 |
3 | HG02109.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1326-4187T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833437 | |||||||
chr6:118833509 | G | C | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-4259C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833509 | |||||||
chr6:118833533 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-4283G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833533 | |||||||
chr6:118833804 | A | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1326-4554T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833804 | |||||||
chr6:118833827 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1326-4577C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833827 | |||||||
chr6:118833861 | A | C | 26 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(23): Show |
26 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1326-4611T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833861 | |||||||
chr6:118833952 | G | T | 1 | a0001c0001t0001g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1326-4702C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118833952 | |||||||
chr6:118834033 | C | A | 1 | a0001c0001t0001g0300 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1326-4783G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834033 | |||||||
chr6:118834094 | A | G | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1326-4844T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834094 | |||||||
chr6:118834143 | T | C | 1 | a0005c0007t0005g0065 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1326-4893A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834143 | |||||||
chr6:118834174 | C | T | 2 | a0003c0004t0002g0027 a0003c0004t0002g0028 |
2 | NA18980.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1326-4924G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834174 | |||||||
chr6:118834196 | T | A | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-4946A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834196 | |||||||
chr6:118834322 | C | T | 3 | a0006c0008t0002g0088 a0006c0008t0002g0094 a0006c0008t0002g0095 |
3 | HG00642.hp2 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1326-5072G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834322 | |||||||
chr6:118834329 | ATG | A | 35 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0069 others(32): Show |
37 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1326-5081_1326-508 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834329 | |||||||
chr6:118834376 | A | G | 59 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(56): Show |
62 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.1326-5126T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834376 | |||||||
chr6:118834408 | G | A | 1 | a0007c0010t0008g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1326-5158C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834408 | |||||||
chr6:118834431 | G | A | 1 | a0015c0022t0001g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1326-5181C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834431 | |||||||
chr6:118834526 | CCTGA | C | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326-5280_1326-527 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834526 | |||||||
chr6:118834661 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-5411T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834661 | |||||||
chr6:118834700 | G | T | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1326-5450C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834700 | |||||||
chr6:118834819 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1326-5569A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834819 | |||||||
chr6:118834891 | C | T | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-5641G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834891 | |||||||
chr6:118834914 | A | G | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1326-5664T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834914 | |||||||
chr6:118834959 | T | G | 4 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(1): Show |
5 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1326-5709A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118834959 | |||||||
chr6:118835030 | G | T | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326-5780C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118835030 | |||||||
chr6:118835044 | T | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1326-5794A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118835044 | |||||||
chr6:118835071 | A | T | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1326-5821T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118835071 | |||||||
chr6:118835145 | G | A | 12 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(9): Show |
13 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1326-5895C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118835145 | |||||||
chr6:118835200 | T | C | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1326-5950A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118835200 | |||||||
chr6:118835412 | T | C | 1 | a0001c0002t0003g0141 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1326-6162A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118835412 | |||||||
chr6:118835520 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1326-6270A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118835520 | |||||||
chr6:118835893 | G | A | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1326-6643C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118835893 | |||||||
chr6:118835971 | A | T | 2 | a0008c0011t0001g0182 a0008c0011t0001g0183 |
2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1326-6721T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118835971 | |||||||
chr6:118835984 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0314 |
2 | HG01361.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1326-6734A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118835984 | |||||||
chr6:118836108 | A | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-6858T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118836108 | |||||||
chr6:118836224 | T | A | 1 | a0001c0002t0003g0112 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1326-6974A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118836224 | |||||||
chr6:118836231 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-6981C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118836231 | |||||||
chr6:118836354 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-7104C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118836354 | |||||||
chr6:118836497 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0236 |
2 | HG01934.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1326-7247G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118836497 | |||||||
chr6:118836623 | T | G | 3 | a0004c0006t0002g0034 a0004c0009t0002g0031 a0004c0009t0002g0032 |
3 | HG00733.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1326-7373A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118836623 | |||||||
chr6:118836746 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1326-7496T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118836746 | |||||||
chr6:118836761 | A | C | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1326-7511T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118836761 | |||||||
chr6:118836826 | G | C | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1326-7576C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118836826 | |||||||
chr6:118837066 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1326-7816G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837066 | |||||||
chr6:118837145 | A | C | 4 | a0003c0004t0002g0004 a0003c0004t0002g0030 a0003c0004t0002g0055 others(1): Show |
5 | HG00741.hp2 NA18995.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-7895T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837145 | |||||||
chr6:118837229 | CTGTT | C | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-7983_1326-798 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837229 | |||||||
chr6:118837253 | T | G | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1326-8003A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837253 | |||||||
chr6:118837451 | T | C | 7 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1326-8201A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837451 | |||||||
chr6:118837552 | C | T | 5 | a0001c0001t0004g0184 a0001c0001t0004g0186 a0001c0001t0004g0187 others(2): Show |
5 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-8302G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837552 | |||||||
chr6:118837561 | T | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-8311A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837561 | |||||||
chr6:118837636 | C | CT | 5 | a0001c0001t0004g0184 a0001c0001t0004g0186 a0001c0001t0004g0187 others(2): Show |
5 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-8387dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837636 | |||||||
chr6:118837760 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-8510G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837760 | |||||||
chr6:118837887 | T | C | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1326-8637A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837887 | |||||||
chr6:118837890 | G | A | 59 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(56): Show |
62 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.1326-8640C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118837890 | |||||||
chr6:118838050 | G | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-8800C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838050 | |||||||
chr6:118838159 | C | CT | 69 | a0001c0001t0001g0229 a0001c0001t0001g0266 a0001c0001t0001g0293 others(66): Show |
72 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.1326-8910dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838159 | |||||||
chr6:118838183 | C | T | 1 | a0002c0003t0002g0076 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1326-8933G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838183 | |||||||
chr6:118838192 | A | T | 1 | a0001c0002t0003g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1326-8942T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838192 | |||||||
chr6:118838210 | T | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-8960A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838210 | |||||||
chr6:118838318 | A | G | 1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1326-9068T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838318 | |||||||
chr6:118838319 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(117): Show |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1326-9069G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838319 | |||||||
chr6:118838320 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-9070C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838320 | |||||||
chr6:118838418 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-9168A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838418 | |||||||
chr6:118838454 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0319 |
2 | HG00558.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1326-9204G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838454 | |||||||
chr6:118838464 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1326-9214C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838464 | |||||||
chr6:118838503 | G | A | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-9253C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838503 | |||||||
chr6:118838630 | C | G | 1 | a0001c0001t0002g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1326-9380G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838630 | |||||||
chr6:118838656 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1326-9406G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838656 | |||||||
chr6:118838664 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1326-9414C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838664 | |||||||
chr6:118838671 | G | A | 2 | a0002c0003t0002g0072 a0002c0003t0002g0073 |
2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1326-9421C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838671 | |||||||
chr6:118838752 | C | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(320): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1326-9502G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838752 | |||||||
chr6:118838796 | C | T | 9 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1326-9546G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838796 | |||||||
chr6:118838835 | G | A | 27 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(24): Show |
27 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1326-9585C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838835 | |||||||
chr6:118838987 | T | C | 7 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(4): Show |
7 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1326-9737A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118838987 | |||||||
chr6:118839069 | G | A | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-9819C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839069 | |||||||
chr6:118839272 | G | A | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1326-10022C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839272 | |||||||
chr6:118839299 | C | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-10049G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839299 | |||||||
chr6:118839328 | C | T | 70 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(67): Show |
73 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1326-10078G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839328 | |||||||
chr6:118839452 | C | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1326-10202G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839452 | |||||||
chr6:118839607 | A | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(311): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1326-10357T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839607 | |||||||
chr6:118839735 | G | C | 1 | a0001c0001t0004g0290 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1326-10485C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839735 | |||||||
chr6:118839815 | C | G | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-10565G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839815 | |||||||
chr6:118839870 | G | T | 1 | a0003c0004t0002g0056 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1326-10620C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839870 | |||||||
chr6:118839877 | C | G | 1 | a0003c0004t0002g0056 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1326-10627G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839877 | |||||||
chr6:118839879 | C | T | 1 | a0004c0006t0002g0037 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1326-10629G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839879 | |||||||
chr6:118839997 | T | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1326-10747A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118839997 | |||||||
chr6:118840078 | C | T | 1 | a0001c0002t0019g0162 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1326-10828G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840078 | |||||||
chr6:118840166 | G | T | 26 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(23): Show |
26 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1326-10916C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840166 | |||||||
chr6:118840169 | A | AT | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(266): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1326-10920dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840169 | |||||||
chr6:118840174 | T | A | 1 | a0004c0006t0002g0050 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1326-10924A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840174 | |||||||
chr6:118840358 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-11108A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840358 | |||||||
chr6:118840548 | G | T | 328 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(325): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1326-11298C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840548 | |||||||
chr6:118840628 | A | T | 2 | a0008c0011t0001g0182 a0008c0011t0001g0183 |
2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1326-11378T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840628 | |||||||
chr6:118840634 | C | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0222 a0001c0001t0001g0223 |
4 | NA18939.hp2 NA19009.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-11384G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840634 | |||||||
chr6:118840660 | T | C | 1 | a0001c0001t0020g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1326-11410A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840660 | |||||||
chr6:118840738 | C | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-11488G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840738 | |||||||
chr6:118840739 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1326-11489G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840739 | |||||||
chr6:118840741 | CCT | C | 49 | a0001c0001t0004g0197 a0001c0001t0004g0284 a0001c0002t0003g0007 others(46): Show |
52 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1326-11493_1326-11 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840741 | |||||||
chr6:118840742 | CT | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(241): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1326-11493delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840742 | |||||||
chr6:118840743 | T | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0254 a0001c0001t0001g0320 others(12): Show |
15 | HG00597.hp1 HG00642.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1326-11493A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840743 | |||||||
chr6:118840774 | G | A | 35 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0069 others(32): Show |
37 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1326-11524C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840774 | |||||||
chr6:118840905 | T | C | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1326-11655A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840905 | |||||||
chr6:118840948 | T | C | 1 | a0002c0003t0011g0092 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1326-11698A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118840948 | |||||||
chr6:118841317 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-12067C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841317 | |||||||
chr6:118841319 | A | C | 69 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(66): Show |
72 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.1326-12069T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841319 | |||||||
chr6:118841369 | C | T | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1326-12119G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841369 | |||||||
chr6:118841419 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-12169G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841419 | |||||||
chr6:118841516 | G | A | 2 | a0007c0010t0008g0190 a0007c0010t0008g0191 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1326-12266C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841516 | |||||||
chr6:118841529 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1326-12279T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841529 | |||||||
chr6:118841568 | G | A | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326-12318C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841568 | |||||||
chr6:118841706 | C | T | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1326-12456G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841706 | |||||||
chr6:118841824 | A | C | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1326-12574T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841824 | |||||||
chr6:118841835 | C | CT | 15 | a0001c0001t0001g0177 a0001c0001t0001g0332 a0001c0002t0003g0008 others(12): Show |
16 | HG00642.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1326-12586dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841835 | |||||||
chr6:118841835 | C | CTT | 43 | a0001c0002t0003g0007 a0001c0002t0003g0009 a0001c0002t0003g0106 others(40): Show |
45 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1326-12587_1326-12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841835 | |||||||
chr6:118841835 | CT | C | 9 | a0001c0001t0001g0247 a0001c0001t0001g0297 a0001c0001t0004g0285 others(6): Show |
9 | HG00558.hp1 HG01168.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1326-12586delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841835 | |||||||
chr6:118841890 | A | C | 7 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(4): Show |
7 | HG00558.hp2 HG00597.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1326-12640T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841890 | |||||||
chr6:118841896 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1326-12646C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841896 | |||||||
chr6:118841923 | C | G | 1 | a0001c0001t0001g0293 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1326-12673G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118841923 | |||||||
chr6:118842108 | C | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-12858G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842108 | |||||||
chr6:118842115 | G | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-12865C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842115 | |||||||
chr6:118842122 | C | T | 4 | a0002c0003t0001g0168 a0002c0003t0002g0080 a0002c0003t0002g0081 others(1): Show |
4 | NA18999.hp2 NA19000.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-12872G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842122 | |||||||
chr6:118842194 | T | C | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1326-12944A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842194 | |||||||
chr6:118842224 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-12974C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842224 | |||||||
chr6:118842477 | C | G | 1 | a0002c0003t0002g0072 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1326-13227G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842477 | |||||||
chr6:118842673 | C | T | 2 | a0001c0001t0009g0159 a0001c0001t0009g0160 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1326-13423G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842673 | |||||||
chr6:118842685 | A | G | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1326-13435T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842685 | |||||||
chr6:118842712 | G | A | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1326-13462C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842712 | |||||||
chr6:118842746 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1326-13496G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842746 | |||||||
chr6:118842955 | TAAAG | T | 26 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(23): Show |
26 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1325+13412_1325+13 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118842955 | |||||||
chr6:118843061 | G | A | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+13310C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843061 | |||||||
chr6:118843261 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+13110A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843261 | |||||||
chr6:118843343 | C | G | 4 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(1): Show |
5 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325+13028G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843343 | |||||||
chr6:118843354 | T | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(320): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1325+13017A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843354 | |||||||
chr6:118843357 | A | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(320): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1325+13014T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843357 | |||||||
chr6:118843431 | C | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+12940G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843431 | |||||||
chr6:118843449 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1325+12922G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843449 | |||||||
chr6:118843484 | C | T | 1 | a0001c0001t0004g0198 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1325+12887G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843484 | |||||||
chr6:118843542 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+12829A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843542 | |||||||
chr6:118843550 | C | T | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1325+12821G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843550 | |||||||
chr6:118843581 | T | C | 4 | a0001c0001t0001g0256 a0007c0010t0008g0190 a0007c0010t0008g0191 others(1): Show |
4 | HG00621.hp2 HG01884.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325+12790A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843581 | |||||||
chr6:118843610 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+12761A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843610 | |||||||
chr6:118843641 | C | CATATATA others(45): Show |
1 | a0001c0005t0010g0022 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1325+12729_1325+12 others(58): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843641 | |||||||
chr6:118843641 | C | CATATATA others(47): Show |
4 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(1): Show |
5 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325+12729_1325+12 others(60): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843641 | |||||||
chr6:118843641 | C | CATATATA others(83): Show |
1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+12729_1325+12 others(96): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843641 | |||||||
chr6:118843642 | A | ATATATAT others(39): Show |
3 | a0001c0001t0001g0318 a0001c0001t0001g0322 a0001c0001t0021g0323 |
3 | HG00558.hp2 HG00597.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1325+12728_1325+12 others(52): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843642 | |||||||
chr6:118843642 | A | ATATATAT others(41): Show |
2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG02027.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1325+12728_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843642 | |||||||
chr6:118843642 | A | ATATATAT others(43): Show |
2 | a0001c0001t0001g0298 a0001c0001t0008g0170 |
2 | NA18948.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1325+12728_1325+12 others(56): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843642 | |||||||
chr6:118843642 | A | ATATATAT others(41): Show |
1 | a0001c0001t0001g0012 | 2 | HG00609.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1325+12728_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843642 | |||||||
chr6:118843642 | A | ATATATAT others(45): Show |
1 | a0001c0005t0002g0020 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1325+12728_1325+12 others(58): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843642 | |||||||
chr6:118843644 | A | ATATATAT others(67): Show |
1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1325+12726_1325+12 others(80): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(41): Show |
1 | a0001c0001t0001g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1325+12726_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(35): Show |
1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1325+12726_1325+12 others(48): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(37): Show |
4 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0002g0084 others(1): Show |
4 | HG02615.hp2 NA18968.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+12726_1325+12 others(50): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(37): Show |
9 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0293 others(6): Show |
9 | HG02257.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1325+12726_1325+12 others(50): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(39): Show |
117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(114): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1325+12726_1325+12 others(52): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(83): Show |
1 | a0001c0001t0004g0184 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1325+12726_1325+12 others(96): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(69): Show |
3 | a0001c0001t0004g0186 a0001c0001t0004g0187 a0001c0001t0004g0189 |
3 | HG03041.hp2 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1325+12726_1325+12 others(82): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(41): Show |
1 | a0008c0011t0001g0182 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1325+12726_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(43): Show |
1 | a0001c0001t0001g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1325+12726_1325+12 others(56): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(37): Show |
3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02809.hp2 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1325+12726_1325+12 others(50): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0230 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1325+12726_1325+12 others(30): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(39): Show |
2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1325+12726_1325+12 others(52): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(41): Show |
18 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0240 others(15): Show |
18 | HG00423.hp2 HG00558.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1325+12726_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(43): Show |
2 | a0001c0001t0002g0016 a0001c0001t0014g0097 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1325+12726_1325+12 others(56): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(47): Show |
1 | a0001c0001t0002g0069 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1325+12726_1325+12 others(60): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843644 | A | ATATATAT others(41): Show |
1 | a0001c0001t0004g0205 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1325+12726_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843644 | |||||||
chr6:118843646 | A | ATATATAT others(33): Show |
18 | a0002c0003t0002g0005 a0002c0003t0002g0059 a0002c0003t0002g0066 others(15): Show |
19 | HG00735.hp2 HG01258.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1325+12724_1325+12 others(46): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843646 | |||||||
chr6:118843646 | A | ATATATAT others(61): Show |
1 | a0002c0003t0001g0168 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1325+12724_1325+12 others(74): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843646 | |||||||
chr6:118843646 | A | ATATATAT others(35): Show |
5 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0006c0008t0002g0088 others(2): Show |
5 | HG00642.hp2 HG00741.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1325+12724_1325+12 others(48): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843646 | |||||||
chr6:118843646 | A | ATATATAT others(35): Show |
2 | a0001c0001t0002g0006 a0002c0003t0002g0070 |
3 | HG00597.hp1 HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1325+12724_1325+12 others(48): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843646 | |||||||
chr6:118843646 | A | ATATATAT others(39): Show |
1 | a0013c0018t0002g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1325+12724_1325+12 others(52): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843646 | |||||||
chr6:118843646 | A | ATATATAT others(41): Show |
1 | a0001c0001t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1325+12724_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843646 | |||||||
chr6:118843648 | A | ATATATAT others(77): Show |
5 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325+12722_1325+12 others(90): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843648 | |||||||
chr6:118843648 | A | ATATATAT others(79): Show |
1 | a0005c0007t0005g0065 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1325+12722_1325+12 others(92): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843648 | |||||||
chr6:118843648 | A | ATATATAT others(63): Show |
3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1325+12722_1325+12 others(76): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843648 | |||||||
chr6:118843652 | ATATGTG | A | 2 | a0001c0002t0003g0009 a0001c0002t0003g0112 |
3 | HG01069.hp1 HG01071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1325+12713_1325+12 others(12): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843652 | |||||||
chr6:118843654 | A | ATACACAC others(43): Show |
5 | a0001c0001t0002g0057 a0001c0001t0002g0102 a0001c0001t0002g0103 others(2): Show |
5 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325+12716_1325+12 others(56): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAC others(37): Show |
1 | a0003c0004t0002g0023 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1325+12716_1325+12 others(50): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAC others(41): Show |
1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1325+12716_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAC others(41): Show |
11 | a0003c0004t0002g0004 a0003c0004t0002g0024 a0003c0004t0002g0025 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1325+12716_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAC others(43): Show |
9 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0004c0006t0002g0034 others(6): Show |
9 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1325+12716_1325+12 others(56): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAC others(41): Show |
1 | a0004c0006t0002g0050 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1325+12716_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAC others(45): Show |
2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1325+12716_1325+12 others(58): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAC others(39): Show |
1 | a0001c0001t0002g0045 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1325+12716_1325+12 others(52): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAC others(41): Show |
4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+12716_1325+12 others(54): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAT others(65): Show |
4 | a0002c0003t0002g0067 a0002c0003t0002g0072 a0002c0003t0002g0073 others(1): Show |
4 | HG01081.hp2 HG03831.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+12716_1325+12 others(78): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAT others(45): Show |
3 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0058 |
3 | HG02109.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1325+12716_1325+12 others(58): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAT others(45): Show |
2 | a0004c0006t0002g0033 a0004c0006t0002g0043 |
2 | HG00099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1325+12716_1325+12 others(58): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAT others(71): Show |
1 | a0001c0001t0004g0209 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1325+12716_1325+12 others(84): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843654 | A | ATATATAT others(47): Show |
1 | a0001c0001t0006g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325+12716_1325+12 others(60): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843654 | |||||||
chr6:118843655 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+12716A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843655 | |||||||
chr6:118843655 | T | TACAC | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+12715_1325+12 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843655 | |||||||
chr6:118843655 | T | TACACACA others(1): Show |
3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1325+12715_1325+12 others(14): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843655 | |||||||
chr6:118843655 | T | TATACACG others(9): Show |
3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1325+12715_1325+12 others(22): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843655 | |||||||
chr6:118843655 | T | TATATATA others(3): Show |
1 | a0001c0002t0003g0156 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1325+12715_1325+12 others(16): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843655 | |||||||
chr6:118843656 | G | A | 87 | a0001c0001t0001g0302 a0001c0001t0002g0006 a0001c0001t0002g0086 others(84): Show |
91 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.1325+12715C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843656 | |||||||
chr6:118843658 | G | A | 86 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(83): Show |
88 | HG00099.hp2 HG00408.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.1325+12713C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843658 | |||||||
chr6:118843660 | A | G | 28 | a0001c0001t0001g0302 a0001c0001t0002g0006 a0001c0001t0002g0086 others(25): Show |
30 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1325+12711T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843660 | |||||||
chr6:118843661 | T | C | 25 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0114 others(22): Show |
27 | HG01243.hp2 HG01884.hp1 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.1325+12710A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843661 | |||||||
chr6:118843662 | A | ACACG | 21 | a0001c0002t0003g0106 a0001c0002t0003g0115 a0001c0002t0003g0121 others(18): Show |
21 | HG00408.hp1 HG01192.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.1325+12708_1325+12 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843662 | |||||||
chr6:118843662 | A | ACG | 20 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0114 others(17): Show |
22 | HG01243.hp2 HG01884.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.1325+12708_1325+12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843662 | |||||||
chr6:118843663 | T | C | 6 | a0001c0002t0003g0120 a0001c0002t0003g0140 a0001c0002t0003g0149 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+12708A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843663 | |||||||
chr6:118843664 | A | G | 46 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0106 others(43): Show |
48 | HG00408.hp1 HG01192.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.1325+12707T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843664 | |||||||
chr6:118843666 | A | G | 6 | a0001c0002t0003g0120 a0001c0002t0003g0140 a0001c0002t0003g0149 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+12705T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843666 | |||||||
chr6:118843667 | T | C | 2 | a0001c0002t0003g0009 a0001c0002t0003g0112 |
3 | HG01069.hp1 HG01071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1325+12704A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843667 | |||||||
chr6:118843668 | A | ACG | 13 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(10): Show |
14 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1325+12702_1325+12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843668 | |||||||
chr6:118843669 | T | C | 4 | a0001c0002t0003g0009 a0001c0002t0003g0112 a0001c0002t0003g0123 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1325+12702A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843669 | |||||||
chr6:118843670 | G | A | 55 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(52): Show |
57 | HG00408.hp1 HG01192.hp1 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.1325+12701C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843670 | |||||||
chr6:118843670 | GTATGTA | G | 2 | a0001c0002t0003g0009 a0001c0002t0003g0112 |
3 | HG01069.hp1 HG01071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1325+12695_1325+12 others(12): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843670 | |||||||
chr6:118843671 | T | C | 42 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0106 others(39): Show |
44 | HG00408.hp1 HG01192.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1325+12700A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843671 | |||||||
chr6:118843672 | A | G | 46 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0106 others(43): Show |
48 | HG00408.hp1 HG01192.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.1325+12699T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843672 | |||||||
chr6:118843673 | T | C | 7 | a0001c0002t0003g0120 a0001c0002t0003g0140 a0001c0002t0003g0149 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325+12698A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843673 | |||||||
chr6:118843673 | T | TATATAC | 3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1325+12697_1325+12 others(12): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843673 | |||||||
chr6:118843674 | G | A | 10 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1325+12697C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843674 | |||||||
chr6:118843676 | A | ATG | 3 | a0001c0001t0004g0186 a0001c0001t0004g0187 a0001c0001t0004g0189 |
3 | HG03041.hp2 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1325+12694_1325+12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843676 | |||||||
chr6:118843676 | A | G | 9 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1325+12695T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843676 | |||||||
chr6:118843678 | A | G | 2 | a0001c0002t0003g0009 a0001c0002t0003g0112 |
3 | HG01069.hp1 HG01071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1325+12693T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843678 | |||||||
chr6:118843684 | A | ATG | 3 | a0001c0001t0001g0318 a0001c0001t0001g0322 a0001c0001t0021g0323 |
3 | HG00558.hp2 HG00597.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1325+12685_1325+12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843684 | |||||||
chr6:118843684 | A | ATGTATGT others(5): Show |
1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1325+12686_1325+12 others(18): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843684 | |||||||
chr6:118843684 | A | G | 2 | a0001c0002t0003g0123 a0017c0013t0003g0139 |
2 | HG02071.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1325+12687T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843684 | |||||||
chr6:118843684 | ATG | A | 7 | a0001c0001t0004g0209 a0001c0002t0003g0156 a0002c0003t0002g0096 others(4): Show |
7 | HG02683.hp1 HG02895.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1325+12685_1325+12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843684 | |||||||
chr6:118843685 | T | C | 3 | a0001c0002t0003g0009 a0001c0002t0003g0112 a0012c0020t0016g0158 |
4 | HG01069.hp1 HG01071.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+12686A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843685 | |||||||
chr6:118843686 | G | A | 18 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(15): Show |
18 | HG01891.hp1 HG02071.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1325+12685C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843686 | |||||||
chr6:118843686 | G | GTATATAT others(3): Show |
2 | a0005c0007t0005g0063 a0005c0007t0005g0064 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1325+12684_1325+12 others(16): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843686 | |||||||
chr6:118843686 | GTGTA | G | 3 | a0002c0003t0002g0067 a0002c0003t0002g0072 a0002c0003t0002g0073 |
3 | HG01081.hp2 HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1325+12681_1325+12 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843686 | |||||||
chr6:118843688 | G | A | 48 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(45): Show |
50 | HG00408.hp1 HG01192.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.1325+12683C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843688 | |||||||
chr6:118843688 | G | GTA | 22 | a0001c0001t0001g0298 a0001c0001t0001g0320 a0001c0001t0001g0321 others(19): Show |
22 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1325+12681_1325+12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843688 | |||||||
chr6:118843688 | G | GTGTGTGT others(5): Show |
2 | a0007c0010t0008g0190 a0007c0010t0008g0191 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1325+12682_1325+12 others(18): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843688 | |||||||
chr6:118843688 | GTA | G | 30 | a0001c0001t0002g0006 a0001c0001t0002g0086 a0001c0001t0002g0087 others(27): Show |
32 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1325+12681_1325+12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843688 | |||||||
chr6:118843688 | GTATA | G | 7 | a0001c0001t0002g0057 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1325+12679_1325+12 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843688 | |||||||
chr6:118843690 | A | G | 8 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(5): Show |
9 | HG00639.hp1 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1325+12681T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843690 | |||||||
chr6:118843692 | A | G | 3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1325+12679T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843692 | |||||||
chr6:118843694 | A | G | 2 | a0007c0010t0008g0190 a0007c0010t0008g0191 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1325+12677T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843694 | |||||||
chr6:118843696 | A | ATATGTAT others(1): Show |
3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1325+12674_1325+12 others(14): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843696 | |||||||
chr6:118843696 | A | G | 1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1325+12675T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843696 | |||||||
chr6:118843704 | G | A | 56 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(53): Show |
58 | HG00408.hp1 HG01192.hp1 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.1325+12667C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843704 | |||||||
chr6:118843706 | A | ATGTGTGT others(3): Show |
4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+12664_1325+12 others(16): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843706 | |||||||
chr6:118843708 | G | A | 8 | a0001c0002t0003g0009 a0001c0002t0003g0112 a0001c0002t0003g0156 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1325+12663C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843708 | |||||||
chr6:118843710 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1325+12661T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843710 | |||||||
chr6:118843712 | A | G | 5 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(2): Show |
5 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325+12659T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843712 | |||||||
chr6:118843720 | G | A | 57 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(54): Show |
59 | HG00408.hp1 HG01192.hp1 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.1325+12651C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843720 | |||||||
chr6:118843720 | G | GTA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(145): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1325+12649_1325+12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843720 | |||||||
chr6:118843720 | G | GTATA | 12 | a0001c0001t0001g0166 a0001c0001t0001g0225 a0001c0001t0001g0234 others(9): Show |
12 | HG00733.hp2 HG01168.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1325+12647_1325+12 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843720 | |||||||
chr6:118843720 | G | GTATATAT others(25): Show |
1 | a0001c0001t0004g0184 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1325+12650_1325+12 others(38): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843720 | |||||||
chr6:118843720 | G | GTGTA | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0010c0025t0013g0017 |
3 | HG01891.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1325+12650_1325+12 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843720 | |||||||
chr6:118843720 | GTA | G | 3 | a0001c0002t0003g0009 a0001c0002t0003g0112 a0001c0002t0003g0156 |
4 | HG01069.hp1 HG01071.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+12649_1325+12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843720 | |||||||
chr6:118843722 | A | ATG | 47 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0106 others(44): Show |
49 | HG00408.hp1 HG01192.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.1325+12648_1325+12 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843722 | |||||||
chr6:118843722 | A | G | 53 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(50): Show |
54 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.1325+12649T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843722 | |||||||
chr6:118843724 | A | G | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+12647T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843724 | |||||||
chr6:118843726 | A | G | 51 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(48): Show |
54 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.1325+12645T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843726 | |||||||
chr6:118843728 | A | G | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1325+12643T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843728 | |||||||
chr6:118843730 | A | G | 51 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(48): Show |
54 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.1325+12641T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843730 | |||||||
chr6:118843737 | T | TA | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+12633dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843737 | |||||||
chr6:118843740 | A | G | 59 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(56): Show |
62 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.1325+12631T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843740 | |||||||
chr6:118843747 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+12624T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843747 | |||||||
chr6:118843785 | C | T | 5 | a0001c0001t0001g0275 a0001c0001t0001g0278 a0001c0001t0001g0280 others(2): Show |
5 | HG01081.hp1 HG01167.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325+12586G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843785 | |||||||
chr6:118843886 | AGAAAGCA others(4828): Show |
A | 7 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(4): Show |
7 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325+7650_1325+124 others(5): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843886 | |||||||
chr6:118843960 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+12411G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118843960 | |||||||
chr6:118844016 | A | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+12355T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844016 | |||||||
chr6:118844151 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0314 |
2 | HG01361.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1325+12220C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844151 | |||||||
chr6:118844195 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+12176A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844195 | |||||||
chr6:118844350 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1325+12021C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844350 | |||||||
chr6:118844545 | CA | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0243 a0001c0001t0001g0255 others(10): Show |
13 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325+11825delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844545 | |||||||
chr6:118844583 | A | G | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0214 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325+11788T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844583 | |||||||
chr6:118844614 | T | C | 1 | a0001c0001t0001g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1325+11757A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844614 | |||||||
chr6:118844712 | CT | C | 59 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(56): Show |
62 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.1325+11658delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844712 | |||||||
chr6:118844737 | G | A | 44 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(41): Show |
47 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1325+11634C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844737 | |||||||
chr6:118844827 | C | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0250 |
2 | HG00544.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1325+11544G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844827 | |||||||
chr6:118844828 | G | A | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+11543C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844828 | |||||||
chr6:118844877 | A | G | 59 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(56): Show |
62 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.1325+11494T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844877 | |||||||
chr6:118844886 | T | C | 3 | a0001c0001t0002g0016 a0001c0001t0002g0069 a0001c0001t0014g0097 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1325+11485A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118844886 | |||||||
chr6:118845000 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(192): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1325+11371A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845000 | |||||||
chr6:118845031 | G | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(314): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1325+11340C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845031 | |||||||
chr6:118845044 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+11327C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845044 | |||||||
chr6:118845109 | G | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+11262C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845109 | |||||||
chr6:118845175 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+11196G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845175 | |||||||
chr6:118845262 | G | A | 2 | a0001c0001t0001g0318 a0001c0001t0001g0322 |
2 | HG00558.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.1325+11109C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845262 | |||||||
chr6:118845327 | C | A | 1 | a0001c0001t0002g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1325+11044G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845327 | |||||||
chr6:118845364 | C | T | 3 | a0001c0002t0003g0137 a0001c0002t0003g0138 a0001c0002t0003g0156 |
3 | NA18986.hp2 NA19055.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1325+11007G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845364 | |||||||
chr6:118845511 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+10860C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845511 | |||||||
chr6:118845733 | T | C | 3 | a0001c0001t0004g0163 a0001c0001t0004g0164 a0001c0001t0004g0198 |
3 | HG01099.hp1 HG04115.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1325+10638A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845733 | |||||||
chr6:118845782 | C | G | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1325+10589G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845782 | |||||||
chr6:118845954 | C | T | 59 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(56): Show |
62 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.1325+10417G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845954 | |||||||
chr6:118845990 | T | A | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | HG00741.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1325+10381A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118845990 | |||||||
chr6:118846096 | AATAAT | A | 12 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(9): Show |
13 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325+10270_1325+10 others(11): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846096 | |||||||
chr6:118846179 | A | C | 12 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(9): Show |
13 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325+10192T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846179 | |||||||
chr6:118846189 | A | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+10182T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846189 | |||||||
chr6:118846448 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+9923C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846448 | |||||||
chr6:118846451 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1325+9920C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846451 | |||||||
chr6:118846519 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1325+9852A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846519 | |||||||
chr6:118846586 | C | T | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325+9785G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846586 | |||||||
chr6:118846595 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1325+9776A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846595 | |||||||
chr6:118846622 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1325+9749G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846622 | |||||||
chr6:118846786 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(201): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1325+9585C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846786 | |||||||
chr6:118846890 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1325+9481T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118846890 | |||||||
chr6:118847198 | G | A | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
5 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1325+9173C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118847198 | |||||||
chr6:118847422 | C | CA | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(141): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1325+8948dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118847422 | |||||||
chr6:118847422 | C | CAA | 55 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0259 others(52): Show |
57 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.1325+8947_1325+894 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118847422 | |||||||
chr6:118847422 | CA | C | 51 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(48): Show |
52 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1325+8948delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118847422 | |||||||
chr6:118847438 | AAAG | A | 6 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(3): Show |
6 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+8930_1325+893 others(7): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118847438 | |||||||
chr6:118847439 | AAG | A | 49 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(46): Show |
52 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1325+8930_1325+893 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118847439 | |||||||
chr6:118847607 | T | C | 52 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(49): Show |
53 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1325+8764A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118847607 | |||||||
chr6:118847996 | G | A | 3 | a0006c0008t0002g0088 a0006c0008t0002g0094 a0006c0008t0002g0095 |
3 | HG00642.hp2 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1325+8375C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118847996 | |||||||
chr6:118848121 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1325+8250G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848121 | |||||||
chr6:118848135 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1325+8236A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848135 | |||||||
chr6:118848458 | C | T | 31 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1325+7913G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848458 | |||||||
chr6:118848477 | T | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1325+7894A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848477 | |||||||
chr6:118848526 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+7845G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848526 | |||||||
chr6:118848584 | T | C | 1 | a0001c0001t0004g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1325+7787A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848584 | |||||||
chr6:118848615 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+7756G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848615 | |||||||
chr6:118848663 | C | G | 38 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0069 others(35): Show |
40 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1325+7708G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848663 | |||||||
chr6:118848664 | C | T | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1325+7707G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848664 | |||||||
chr6:118848716 | G | A | 3 | a0001c0002t0003g0137 a0001c0002t0003g0138 a0001c0002t0003g0156 |
3 | NA18986.hp2 NA19055.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1325+7655C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848716 | |||||||
chr6:118848909 | A | G | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+7462T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848909 | |||||||
chr6:118848915 | T | G | 7 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(4): Show |
7 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325+7456A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848915 | |||||||
chr6:118848917 | GTTTCCAA others(2882): Show |
G | 7 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(4): Show |
7 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325+4565_1325+745 others(4): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848917 | |||||||
chr6:118848984 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1325+7387A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118848984 | |||||||
chr6:118849179 | T | A | 1 | a0001c0001t0001g0304 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1325+7192A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118849179 | |||||||
chr6:118849420 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1325+6951A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118849420 | |||||||
chr6:118849431 | T | TTG | 15 | a0001c0001t0001g0228 a0001c0001t0001g0274 a0001c0001t0009g0159 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1325+6938_1325+693 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118849431 | |||||||
chr6:118849431 | TTG | T | 75 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(72): Show |
79 | HG00408.hp1 HG00735.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.1325+6938_1325+693 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118849431 | |||||||
chr6:118849446 | T | A | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+6925A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118849446 | |||||||
chr6:118849453 | G | A | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+6918C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118849453 | |||||||
chr6:118849492 | T | G | 1 | a0002c0003t0002g0071 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1325+6879A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118849492 | |||||||
chr6:118849917 | C | T | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(313): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1325+6454G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118849917 | |||||||
chr6:118850026 | T | C | 7 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(4): Show |
7 | HG00639.hp2 HG01168.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325+6345A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850026 | |||||||
chr6:118850034 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(261): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1325+6337C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850034 | |||||||
chr6:118850239 | C | A | 3 | a0001c0001t0004g0200 a0001c0001t0004g0201 a0001c0001t0004g0205 |
3 | HG01433.hp1 HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1325+6132G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850239 | |||||||
chr6:118850249 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(225): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1325+6122A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850249 | |||||||
chr6:118850259 | G | GT | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(201): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1325+6111dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850259 | |||||||
chr6:118850363 | T | C | 26 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(23): Show |
26 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1325+6008A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850363 | |||||||
chr6:118850389 | G | C | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325+5982C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850389 | |||||||
chr6:118850621 | TGAAGG | T | 4 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(1): Show |
5 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325+5745_1325+574 others(9): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850621 | |||||||
chr6:118850674 | G | A | 2 | a0001c0001t0004g0172 a0001c0001t0004g0207 |
2 | HG00280.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1325+5697C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850674 | |||||||
chr6:118850703 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(201): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1325+5668A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850703 | |||||||
chr6:118850719 | C | T | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1325+5652G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850719 | |||||||
chr6:118850720 | G | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(201): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1325+5651C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850720 | |||||||
chr6:118850726 | G | T | 1 | a0001c0001t0002g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1325+5645C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850726 | |||||||
chr6:118850772 | G | T | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(314): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1325+5599C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850772 | |||||||
chr6:118850957 | T | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1325+5414A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850957 | |||||||
chr6:118850964 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1325+5407C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118850964 | |||||||
chr6:118851011 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+5360C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118851011 | |||||||
chr6:118851087 | C | T | 1 | a0001c0001t0014g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1325+5284G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118851087 | |||||||
chr6:118851114 | C | T | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1325+5257G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118851114 | |||||||
chr6:118851185 | A | T | 1 | a0001c0002t0003g0009 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1325+5186T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118851185 | |||||||
chr6:118851386 | G | C | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1325+4985C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118851386 | |||||||
chr6:118851562 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1325+4809A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118851562 | |||||||
chr6:118851707 | T | G | 26 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(23): Show |
26 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1325+4664A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118851707 | |||||||
chr6:118851853 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1325+4518G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118851853 | |||||||
chr6:118852005 | G | A | 1 | a0001c0002t0018g0127 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1325+4366C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852005 | |||||||
chr6:118852062 | A | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325+4309T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852062 | |||||||
chr6:118852111 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+4260G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852111 | |||||||
chr6:118852181 | A | T | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1325+4190T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852181 | |||||||
chr6:118852187 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+4184G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852187 | |||||||
chr6:118852236 | C | T | 2 | a0005c0007t0005g0063 a0005c0007t0005g0064 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1325+4135G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852236 | |||||||
chr6:118852244 | G | A | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+4127C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852244 | |||||||
chr6:118852261 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+4110G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852261 | |||||||
chr6:118852324 | T | C | 1 | a0017c0013t0003g0139 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1325+4047A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852324 | |||||||
chr6:118852479 | A | G | 7 | a0001c0002t0003g0114 a0001c0002t0003g0119 a0001c0002t0003g0120 others(4): Show |
7 | HG01884.hp1 HG02622.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1325+3892T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852479 | |||||||
chr6:118852491 | G | A | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+3880C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852491 | |||||||
chr6:118852506 | C | T | 1 | a0003c0004t0002g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1325+3865G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852506 | |||||||
chr6:118852534 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+3837G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852534 | |||||||
chr6:118852600 | C | T | 3 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0058 |
3 | HG02109.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1325+3771G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852600 | |||||||
chr6:118852736 | C | T | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1325+3635G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852736 | |||||||
chr6:118852872 | A | G | 7 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(4): Show |
7 | HG00558.hp2 HG00597.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1325+3499T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118852872 | |||||||
chr6:118853002 | G | A | 1 | a0001c0002t0003g0112 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1325+3369C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853002 | |||||||
chr6:118853010 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1325+3361A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853010 | |||||||
chr6:118853129 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1325+3242C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853129 | |||||||
chr6:118853316 | T | C | 7 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(4): Show |
7 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325+3055A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853316 | |||||||
chr6:118853437 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+2934G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853437 | |||||||
chr6:118853446 | A | AT | 7 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0303 others(4): Show |
7 | HG03654.hp2 NA18612.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.1325+2924dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853446 | |||||||
chr6:118853493 | T | C | 26 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(23): Show |
26 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1325+2878A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853493 | |||||||
chr6:118853676 | G | A | 54 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(51): Show |
57 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1325+2695C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853676 | |||||||
chr6:118853679 | C | T | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+2692G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853679 | |||||||
chr6:118853723 | C | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02257.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1325+2648G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853723 | |||||||
chr6:118853916 | T | C | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1325+2455A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853916 | |||||||
chr6:118853976 | A | C | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+2395T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118853976 | |||||||
chr6:118854265 | T | C | 1 | a0001c0001t0002g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1325+2106A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118854265 | |||||||
chr6:118854334 | T | C | 2 | a0001c0001t0009g0159 a0001c0001t0009g0160 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1325+2037A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118854334 | |||||||
chr6:118854339 | C | T | 4 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+2032G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118854339 | |||||||
chr6:118854441 | CT | C | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+1929delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118854441 | |||||||
chr6:118854865 | T | C | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1325+1506A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118854865 | |||||||
chr6:118854990 | A | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+1381T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118854990 | |||||||
chr6:118855047 | T | C | 38 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.1325+1324A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118855047 | |||||||
chr6:118855048 | G | A | 1 | a0001c0001t0004g0164 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1325+1323C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118855048 | |||||||
chr6:118855083 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1325+1288G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118855083 | |||||||
chr6:118855164 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1325+1207T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118855164 | |||||||
chr6:118855219 | T | C | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1325+1152A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118855219 | |||||||
chr6:118855452 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0247 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1325+919C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118855452 | |||||||
chr6:118855475 | T | C | 26 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(23): Show |
26 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1325+896A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118855475 | |||||||
chr6:118855964 | G | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(268): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.1325+407C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118855964 | |||||||
chr6:118856043 | T | C | 1 | a0002c0003t0002g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1325+328A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118856043 | |||||||
chr6:118856061 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1325+310T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118856061 | |||||||
chr6:118856317 | T | A | 5 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0303 others(2): Show |
5 | NA18612.hp1 NA18947.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1325+54A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118856317 | |||||||
chr6:118856317 | T | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(194): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1325+54A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118856317 | |||||||
chr6:118856329 | A | C | 1 | a0001c0001t0009g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1325+42T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 9/13 | chr6 | 118856329 | |||||||
chr6:118856569 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-24G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118856569 | |||||||
chr6:118856612 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-67G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118856612 | |||||||
chr6:118856711 | T | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-166A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118856711 | |||||||
chr6:118856735 | T | C | 4 | a0003c0004t0002g0004 a0003c0004t0002g0030 a0003c0004t0002g0055 others(1): Show |
5 | HG00741.hp2 NA18995.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151-190A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118856735 | |||||||
chr6:118856872 | T | A | 70 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(67): Show |
73 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1151-327A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118856872 | |||||||
chr6:118857094 | T | C | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-549A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857094 | |||||||
chr6:118857198 | A | T | 2 | a0007c0010t0008g0190 a0007c0010t0008g0191 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-653T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857198 | |||||||
chr6:118857203 | G | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-658C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857203 | |||||||
chr6:118857365 | G | A | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-820C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857365 | |||||||
chr6:118857610 | T | C | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1151-1065A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857610 | |||||||
chr6:118857626 | C | CA | 19 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0208 others(16): Show |
22 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1151-1082dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857626 | |||||||
chr6:118857626 | CA | C | 23 | a0001c0001t0001g0173 a0001c0001t0001g0225 a0001c0001t0001g0229 others(20): Show |
23 | HG01255.hp1 HG01496.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1151-1082delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857626 | |||||||
chr6:118857626 | CAA | C | 56 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(53): Show |
59 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.1151-1083_1151-108 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857626 | |||||||
chr6:118857626 | CAAAAAAA | C | 34 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0069 others(31): Show |
36 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1151-1088_1151-108 others(11): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857626 | |||||||
chr6:118857661 | AGTTACAA others(12): Show |
A | 1 | a0001c0002t0003g0141 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1151-1135_1151-111 others(23): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857661 | |||||||
chr6:118857783 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1151-1238A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857783 | |||||||
chr6:118857818 | C | A | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1151-1273G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857818 | |||||||
chr6:118857893 | C | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(208): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1151-1348G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857893 | |||||||
chr6:118857907 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1151-1362A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857907 | |||||||
chr6:118857916 | C | T | 13 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(10): Show |
14 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1151-1371G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118857916 | |||||||
chr6:118858114 | A | C | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-1569T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858114 | |||||||
chr6:118858232 | G | A | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1151-1687C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858232 | |||||||
chr6:118858265 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1151-1720G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858265 | |||||||
chr6:118858345 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1151-1800G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858345 | |||||||
chr6:118858385 | TA | T | 57 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(54): Show |
60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.1151-1841delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858385 | |||||||
chr6:118858388 | T | C | 57 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(54): Show |
60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.1151-1843A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858388 | |||||||
chr6:118858418 | A | G | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1151-1873T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858418 | |||||||
chr6:118858564 | A | C | 1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1151-2019T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858564 | |||||||
chr6:118858599 | G | C | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-2054C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858599 | |||||||
chr6:118858707 | T | C | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-2162A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858707 | |||||||
chr6:118858739 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-2194T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858739 | |||||||
chr6:118858782 | C | T | 1 | a0001c0001t0001g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1151-2237G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858782 | |||||||
chr6:118858831 | C | CT | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1151-2287dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858831 | |||||||
chr6:118858836 | T | C | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-2291A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858836 | |||||||
chr6:118858909 | T | A | 1 | a0001c0001t0001g0283 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1151-2364A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858909 | |||||||
chr6:118858924 | G | A | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-2379C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118858924 | |||||||
chr6:118859000 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1151-2455A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118859000 | |||||||
chr6:118859057 | G | T | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-2512C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118859057 | |||||||
chr6:118859064 | A | G | 2 | a0001c0001t0001g0253 a0001c0017t0001g0252 |
2 | NA19004.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1151-2519T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118859064 | |||||||
chr6:118859093 | A | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0258 |
2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1151-2548T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118859093 | |||||||
chr6:118859169 | T | C | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-2624A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118859169 | |||||||
chr6:118859354 | T | C | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1151-2809A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118859354 | |||||||
chr6:118859443 | A | G | 1 | a0001c0001t0002g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1151-2898T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118859443 | |||||||
chr6:118859922 | G | A | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-3377C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118859922 | |||||||
chr6:118859962 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(117): Show |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1151-3417C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118859962 | |||||||
chr6:118860138 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1151-3593G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118860138 | |||||||
chr6:118860215 | T | C | 51 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(48): Show |
54 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.1151-3670A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118860215 | |||||||
chr6:118860509 | C | T | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1151-3964G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118860509 | |||||||
chr6:118860709 | C | A | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1151-4164G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118860709 | |||||||
chr6:118860876 | G | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-4331C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118860876 | |||||||
chr6:118860944 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1151-4399C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118860944 | |||||||
chr6:118860996 | G | A | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-4451C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118860996 | |||||||
chr6:118861015 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1151-4470G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861015 | |||||||
chr6:118861023 | A | G | 1 | a0001c0001t0006g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1151-4478T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861023 | |||||||
chr6:118861049 | G | A | 57 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(54): Show |
60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.1151-4504C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861049 | |||||||
chr6:118861125 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(268): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.1151-4580A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861125 | |||||||
chr6:118861133 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-4588G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861133 | |||||||
chr6:118861207 | G | A | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-4662C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861207 | |||||||
chr6:118861252 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1151-4707C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861252 | |||||||
chr6:118861394 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1151-4849G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861394 | |||||||
chr6:118861445 | G | C | 2 | a0001c0001t0004g0203 a0012c0020t0016g0158 |
2 | HG02717.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1151-4900C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861445 | |||||||
chr6:118861575 | G | A | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1151-5030C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861575 | |||||||
chr6:118861609 | A | C | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1151-5064T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861609 | |||||||
chr6:118861674 | A | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(301): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1151-5129T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861674 | |||||||
chr6:118861736 | C | T | 33 | a0001c0001t0002g0006 a0001c0001t0002g0086 a0001c0001t0002g0087 others(30): Show |
35 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1151-5191G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861736 | |||||||
chr6:118861915 | A | G | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-5370T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861915 | |||||||
chr6:118861979 | C | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0176 a0001c0001t0001g0208 others(10): Show |
14 | HG00544.hp1 HG02523.hp2 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.1151-5434G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861979 | |||||||
chr6:118861984 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1151-5439G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861984 | |||||||
chr6:118861985 | G | A | 57 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(54): Show |
60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.1151-5440C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118861985 | |||||||
chr6:118862323 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1151-5778C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862323 | |||||||
chr6:118862326 | C | T | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-5781G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862326 | |||||||
chr6:118862340 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1151-5795G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862340 | |||||||
chr6:118862403 | T | C | 3 | a0001c0001t0002g0016 a0001c0001t0002g0069 a0001c0001t0014g0097 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1151-5858A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862403 | |||||||
chr6:118862413 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1151-5868A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862413 | |||||||
chr6:118862505 | T | C | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1151-5960A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862505 | |||||||
chr6:118862710 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-6165G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862710 | |||||||
chr6:118862724 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(208): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1151-6179A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862724 | |||||||
chr6:118862734 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1151-6189C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862734 | |||||||
chr6:118862912 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(157): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1151-6367T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862912 | |||||||
chr6:118862950 | T | G | 1 | a0001c0001t0006g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1151-6405A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118862950 | |||||||
chr6:118863228 | A | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-6683T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118863228 | |||||||
chr6:118863359 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-6814G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118863359 | |||||||
chr6:118863401 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1151-6856G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118863401 | |||||||
chr6:118863551 | C | A | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1151-7006G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118863551 | |||||||
chr6:118863743 | A | G | 3 | a0001c0002t0003g0137 a0001c0002t0003g0138 a0001c0002t0003g0156 |
3 | NA18986.hp2 NA19055.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1151-7198T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118863743 | |||||||
chr6:118863790 | A | C | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1151-7245T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118863790 | |||||||
chr6:118863934 | C | A | 1 | a0001c0001t0004g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1151-7389G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118863934 | |||||||
chr6:118863971 | A | T | 4 | a0002c0003t0001g0168 a0002c0003t0002g0080 a0002c0003t0002g0081 others(1): Show |
4 | NA18999.hp2 NA19000.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-7426T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118863971 | |||||||
chr6:118864007 | T | TA | 18 | a0001c0001t0002g0054 a0001c0001t0009g0159 a0001c0001t0009g0160 others(15): Show |
19 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1151-7463dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864007 | |||||||
chr6:118864201 | C | G | 37 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0069 others(34): Show |
39 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1151-7656G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864201 | |||||||
chr6:118864239 | C | T | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-7694G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864239 | |||||||
chr6:118864340 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(155): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1151-7795G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864340 | |||||||
chr6:118864449 | C | T | 6 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(3): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-7904G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864449 | |||||||
chr6:118864491 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-7946G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864491 | |||||||
chr6:118864496 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1151-7951G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864496 | |||||||
chr6:118864513 | C | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-7968G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864513 | |||||||
chr6:118864534 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(298): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.1151-7989G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864534 | |||||||
chr6:118864551 | A | G | 6 | a0004c0006t0002g0033 a0004c0006t0002g0035 a0004c0006t0002g0036 others(3): Show |
6 | HG00099.hp2 HG01106.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1151-8006T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864551 | |||||||
chr6:118864809 | T | C | 1 | a0002c0003t0002g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1151-8264A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864809 | |||||||
chr6:118864953 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-8408G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118864953 | |||||||
chr6:118865030 | G | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-8485C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865030 | |||||||
chr6:118865139 | C | T | 1 | a0004c0006t0002g0033 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1151-8594G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865139 | |||||||
chr6:118865295 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-8750T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865295 | |||||||
chr6:118865410 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(208): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1151-8865A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865410 | |||||||
chr6:118865453 | T | A | 1 | a0001c0001t0002g0045 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1151-8908A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865453 | |||||||
chr6:118865481 | C | T | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1151-8936G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865481 | |||||||
chr6:118865640 | C | T | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1151-9095G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865640 | |||||||
chr6:118865850 | GA | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(208): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1151-9306delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865850 | |||||||
chr6:118865861 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1151-9316C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865861 | |||||||
chr6:118865876 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1151-9331C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865876 | |||||||
chr6:118865993 | A | T | 1 | a0013c0018t0002g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1151-9448T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118865993 | |||||||
chr6:118866061 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-9516G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118866061 | |||||||
chr6:118866090 | C | T | 7 | a0001c0001t0001g0217 a0001c0001t0001g0227 a0001c0001t0001g0229 others(4): Show |
7 | HG00438.hp1 HG00609.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-9545G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118866090 | |||||||
chr6:118866711 | C | T | 2 | a0001c0001t0001g0321 a0001c0001t0008g0170 |
2 | NA18948.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1151-10166G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118866711 | |||||||
chr6:118866846 | A | G | 1 | a0001c0001t0004g0206 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1151-10301T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118866846 | |||||||
chr6:118867165 | C | CA | 15 | a0001c0001t0001g0216 a0001c0001t0001g0277 a0001c0001t0002g0049 others(12): Show |
15 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1151-10621dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867165 | |||||||
chr6:118867306 | A | G | 9 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1151-10761T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867306 | |||||||
chr6:118867424 | T | C | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1151-10879A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867424 | |||||||
chr6:118867516 | C | A | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1151-10971G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867516 | |||||||
chr6:118867591 | A | G | 9 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1151-11046T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867591 | |||||||
chr6:118867639 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-11094T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867639 | |||||||
chr6:118867648 | G | A | 1 | a0004c0006t0002g0034 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1151-11103C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867648 | |||||||
chr6:118867738 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(208): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1151-11193G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867738 | |||||||
chr6:118867774 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(208): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1151-11229A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867774 | |||||||
chr6:118867878 | T | C | 51 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(48): Show |
54 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.1151-11333A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867878 | |||||||
chr6:118867879 | C | CT | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-11335dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867879 | |||||||
chr6:118867879 | C | CTT | 7 | a0002c0003t0002g0077 a0005c0007t0005g0060 a0005c0007t0005g0061 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-11336_1151-11 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867879 | |||||||
chr6:118867879 | C | CTTT | 156 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(153): Show |
163 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1151-11337_1151-11 others(9): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867879 | |||||||
chr6:118867879 | C | CTTTT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0165 others(45): Show |
52 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1151-11338_1151-11 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867879 | |||||||
chr6:118867885 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(267): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1151-11340G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118867885 | |||||||
chr6:118868126 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1151-11581G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868126 | |||||||
chr6:118868139 | T | A | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-11594A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868139 | |||||||
chr6:118868260 | A | T | 1 | a0001c0002t0003g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1151-11715T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868260 | |||||||
chr6:118868297 | G | A | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1151-11752C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868297 | |||||||
chr6:118868423 | A | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(208): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1151-11878T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868423 | |||||||
chr6:118868441 | G | T | 2 | a0001c0001t0009g0159 a0001c0001t0009g0160 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1151-11896C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868441 | |||||||
chr6:118868583 | A | C | 3 | a0004c0006t0002g0035 a0004c0006t0002g0036 a0004c0006t0002g0037 |
3 | HG01168.hp2 HG01169.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1151-12038T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868583 | |||||||
chr6:118868584 | C | A | 1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1151-12039G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868584 | |||||||
chr6:118868611 | G | A | 1 | a0001c0001t0004g0290 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1151-12066C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868611 | |||||||
chr6:118868727 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(208): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1151-12182G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868727 | |||||||
chr6:118868814 | T | C | 56 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(53): Show |
59 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.1151-12269A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118868814 | |||||||
chr6:118869161 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-12616G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869161 | |||||||
chr6:118869353 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1151-12808A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869353 | |||||||
chr6:118869496 | G | A | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1151-12951C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869496 | |||||||
chr6:118869599 | C | CA | 14 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1151-13055dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869599 | |||||||
chr6:118869599 | C | CAAAAAA | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(92): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1151-13060_1151-13 others(12): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869599 | |||||||
chr6:118869599 | C | CAAAAAAA | 99 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(96): Show |
103 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1151-13061_1151-13 others(13): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869599 | |||||||
chr6:118869599 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0235 others(5): Show |
8 | HG01243.hp1 HG01934.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1151-13062_1151-13 others(14): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869599 | |||||||
chr6:118869599 | CA | C | 52 | a0001c0001t0002g0041 a0001c0001t0006g0051 a0001c0002t0003g0007 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1151-13055delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869599 | |||||||
chr6:118869599 | CAAA | C | 8 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(5): Show |
8 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1151-13057_1151-13 others(9): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869599 | |||||||
chr6:118869761 | T | C | 57 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(54): Show |
60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.1151-13216A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869761 | |||||||
chr6:118869792 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1151-13247C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869792 | |||||||
chr6:118869833 | A | G | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1151-13288T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869833 | |||||||
chr6:118869889 | C | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-13344G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869889 | |||||||
chr6:118869912 | C | T | 3 | a0001c0001t0001g0298 a0001c0001t0001g0321 a0001c0001t0008g0170 |
3 | NA18948.hp1 NA19009.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1151-13367G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869912 | |||||||
chr6:118869932 | A | G | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0214 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1151-13387T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869932 | |||||||
chr6:118869948 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-13403C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118869948 | |||||||
chr6:118870237 | G | A | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-13692C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118870237 | |||||||
chr6:118870316 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0307 |
2 | HG00438.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1151-13771C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118870316 | |||||||
chr6:118870422 | GT | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(241): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.1151-13878delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118870422 | |||||||
chr6:118870422 | GTT | G | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-13879_1151-13 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118870422 | |||||||
chr6:118870801 | G | T | 1 | a0001c0002t0003g0117 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1151-14256C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118870801 | |||||||
chr6:118870920 | C | A | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-14375G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118870920 | |||||||
chr6:118870966 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1151-14421A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118870966 | |||||||
chr6:118871084 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1151-14539G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118871084 | |||||||
chr6:118871173 | T | G | 1 | a0002c0003t0002g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1151-14628A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118871173 | |||||||
chr6:118871201 | T | C | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1151-14656A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118871201 | |||||||
chr6:118871314 | T | G | 7 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(4): Show |
7 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-14769A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118871314 | |||||||
chr6:118871451 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1151-14906G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118871451 | |||||||
chr6:118871605 | T | C | 1 | a0001c0001t0001g0313 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1151-15060A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118871605 | |||||||
chr6:118871875 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1151-15330G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118871875 | |||||||
chr6:118871912 | AAAAC | A | 7 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-15371_1151-15 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118871912 | |||||||
chr6:118871938 | C | T | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1151-15393G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118871938 | |||||||
chr6:118872028 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-15483T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872028 | |||||||
chr6:118872040 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-15495C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872040 | |||||||
chr6:118872045 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1151-15500G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872045 | |||||||
chr6:118872134 | G | A | 1 | a0001c0001t0007g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1151-15589C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872134 | |||||||
chr6:118872180 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-15635C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872180 | |||||||
chr6:118872188 | G | T | 1 | a0001c0001t0002g0006 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1151-15643C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872188 | |||||||
chr6:118872232 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1151-15687A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872232 | |||||||
chr6:118872243 | C | A | 1 | a0001c0001t0001g0257 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1151-15698G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872243 | |||||||
chr6:118872318 | C | CAA | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(206): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1151-15775_1151-15 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872318 | |||||||
chr6:118872337 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(213): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1151-15792C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872337 | |||||||
chr6:118872487 | C | G | 3 | a0001c0001t0002g0016 a0001c0001t0002g0069 a0001c0001t0014g0097 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1151-15942G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872487 | |||||||
chr6:118872641 | G | A | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1151-16096C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872641 | |||||||
chr6:118872794 | A | G | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1151-16249T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872794 | |||||||
chr6:118872799 | A | C | 2 | a0001c0001t0001g0297 a0001c0001t0001g0319 |
2 | HG00558.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1151-16254T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872799 | |||||||
chr6:118872936 | A | T | 2 | a0001c0005t0002g0020 a0001c0005t0010g0022 |
2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1151-16391T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872936 | |||||||
chr6:118872941 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-16396T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872941 | |||||||
chr6:118872959 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-16414C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118872959 | |||||||
chr6:118873048 | T | G | 1 | a0013c0018t0002g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1151-16503A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873048 | |||||||
chr6:118873064 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1151-16519G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873064 | |||||||
chr6:118873101 | G | C | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-16556C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873101 | |||||||
chr6:118873128 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-16583G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873128 | |||||||
chr6:118873165 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1151-16620C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873165 | |||||||
chr6:118873214 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-16669T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873214 | |||||||
chr6:118873215 | AAGGGAAA others(6): Show |
A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-16683_1151-16 others(19): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873215 | |||||||
chr6:118873323 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-16778C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873323 | |||||||
chr6:118873381 | G | A | 9 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1151-16836C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873381 | |||||||
chr6:118873476 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-16931G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873476 | |||||||
chr6:118873549 | T | C | 1 | a0001c0001t0004g0206 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1151-17004A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873549 | |||||||
chr6:118873883 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-17338A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873883 | |||||||
chr6:118873994 | C | T | 1 | a0001c0002t0003g0141 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1151-17449G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118873994 | |||||||
chr6:118874032 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1151-17487A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874032 | |||||||
chr6:118874036 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-17491A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874036 | |||||||
chr6:118874053 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1151-17508T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874053 | |||||||
chr6:118874165 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1151-17620C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874165 | |||||||
chr6:118874287 | T | A | 2 | a0003c0004t0002g0027 a0003c0004t0002g0028 |
2 | NA18980.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1151-17742A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874287 | |||||||
chr6:118874302 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-17757A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874302 | |||||||
chr6:118874392 | A | C | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1151-17847T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874392 | |||||||
chr6:118874622 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(34): Show |
42 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1151-18077C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874622 | |||||||
chr6:118874656 | G | A | 13 | a0001c0001t0002g0054 a0003c0004t0002g0004 a0003c0004t0002g0023 others(10): Show |
14 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1151-18111C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874656 | |||||||
chr6:118874728 | A | T | 1 | a0001c0002t0003g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1151-18183T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874728 | |||||||
chr6:118874818 | T | C | 53 | a0001c0001t0002g0054 a0001c0002t0003g0007 a0001c0002t0003g0008 others(50): Show |
56 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.1151-18273A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874818 | |||||||
chr6:118874912 | G | A | 7 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-18367C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874912 | |||||||
chr6:118874931 | T | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-18386A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118874931 | |||||||
chr6:118875028 | G | A | 1 | a0005c0007t0005g0065 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1151-18483C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875028 | |||||||
chr6:118875090 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-18545C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875090 | |||||||
chr6:118875091 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(274): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1151-18546A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875091 | |||||||
chr6:118875223 | T | C | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02809.hp2 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1151-18678A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875223 | |||||||
chr6:118875255 | T | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-18710A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875255 | |||||||
chr6:118875334 | C | T | 2 | a0001c0002t0003g0120 a0001c0002t0003g0149 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1151-18789G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875334 | |||||||
chr6:118875361 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-18816G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875361 | |||||||
chr6:118875365 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1151-18820C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875365 | |||||||
chr6:118875382 | T | C | 3 | a0001c0002t0003g0137 a0001c0002t0003g0138 a0001c0002t0003g0156 |
3 | NA18986.hp2 NA19055.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1151-18837A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875382 | |||||||
chr6:118875482 | C | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(275): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1151-18937G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875482 | |||||||
chr6:118875495 | G | T | 1 | a0001c0002t0003g0008 | 2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1151-18950C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875495 | |||||||
chr6:118875513 | A | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-18968T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875513 | |||||||
chr6:118875546 | G | A | 1 | a0003c0004t0002g0024 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1151-19001C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875546 | |||||||
chr6:118875640 | A | T | 1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1151-19095T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875640 | |||||||
chr6:118875658 | AAAT | A | 26 | a0001c0001t0002g0054 a0001c0001t0002g0057 a0001c0001t0002g0099 others(23): Show |
27 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1151-19116_1151-19 others(9): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875658 | |||||||
chr6:118875658 | AAATAAT | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(274): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1151-19119_1151-19 others(12): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875658 | |||||||
chr6:118875662 | A | T | 1 | a0001c0001t0001g0266 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1151-19117T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875662 | |||||||
chr6:118875664 | T | A | 1 | a0001c0001t0001g0266 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1151-19119A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875664 | |||||||
chr6:118875710 | G | T | 1 | a0001c0001t0001g0012 | 2 | HG00609.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1151-19165C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875710 | |||||||
chr6:118875775 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-19230A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875775 | |||||||
chr6:118875870 | T | G | 13 | a0001c0001t0002g0054 a0003c0004t0002g0004 a0003c0004t0002g0023 others(10): Show |
14 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1151-19325A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875870 | |||||||
chr6:118875874 | C | T | 1 | a0002c0003t0002g0071 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1151-19329G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875874 | |||||||
chr6:118875911 | G | A | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1151-19366C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118875911 | |||||||
chr6:118876117 | G | C | 1 | a0001c0001t0001g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1151-19572C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118876117 | |||||||
chr6:118876220 | T | A | 8 | a0001c0001t0004g0010 a0001c0001t0004g0195 a0001c0001t0004g0196 others(5): Show |
9 | HG00323.hp1 HG01106.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1151-19675A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118876220 | |||||||
chr6:118876223 | AAGGGAAA others(1): Show |
A | 56 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(53): Show |
59 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.1151-19686_1151-19 others(14): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118876223 | |||||||
chr6:118876798 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-20253C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118876798 | |||||||
chr6:118876981 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1151-20436A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118876981 | |||||||
chr6:118877041 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-20496C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877041 | |||||||
chr6:118877055 | C | A | 1 | a0001c0001t0001g0251 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1151-20510G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877055 | |||||||
chr6:118877075 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0314 |
2 | HG01361.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1151-20530C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877075 | |||||||
chr6:118877079 | C | T | 1 | a0003c0004t0002g0004 | 2 | NA18995.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1151-20534G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877079 | |||||||
chr6:118877083 | A | G | 1 | a0001c0002t0003g0148 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1151-20538T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877083 | |||||||
chr6:118877150 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-20605G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877150 | |||||||
chr6:118877311 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-20766A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877311 | |||||||
chr6:118877345 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-20800C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877345 | |||||||
chr6:118877362 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1151-20817G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877362 | |||||||
chr6:118877557 | G | C | 3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1151-21012C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877557 | |||||||
chr6:118877564 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1151-21019T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877564 | |||||||
chr6:118877571 | G | C | 1 | a0002c0003t0002g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1151-21026C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877571 | |||||||
chr6:118877625 | A | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-21080T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877625 | |||||||
chr6:118877627 | G | C | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1151-21082C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877627 | |||||||
chr6:118877645 | A | G | 11 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1151-21100T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877645 | |||||||
chr6:118877669 | T | C | 1 | a0001c0001t0004g0193 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1151-21124A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877669 | |||||||
chr6:118877741 | G | A | 51 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(48): Show |
54 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.1151-21196C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877741 | |||||||
chr6:118877778 | T | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-21233A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877778 | |||||||
chr6:118877802 | C | T | 5 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0303 others(2): Show |
5 | NA18612.hp1 NA18947.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151-21257G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877802 | |||||||
chr6:118877826 | T | C | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-21281A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877826 | |||||||
chr6:118877844 | G | A | 4 | a0001c0001t0001g0302 a0007c0010t0008g0190 a0007c0010t0008g0191 others(1): Show |
4 | HG01884.hp2 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1151-21299C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118877844 | |||||||
chr6:118878148 | C | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0269 a0001c0001t0001g0309 |
3 | NA18949.hp2 NA18977.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1151-21603G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118878148 | |||||||
chr6:118878153 | C | A | 1 | a0001c0001t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1151-21608G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118878153 | |||||||
chr6:118878277 | G | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1151-21732C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118878277 | |||||||
chr6:118878614 | T | C | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1151-22069A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118878614 | |||||||
chr6:118878690 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-22145A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118878690 | |||||||
chr6:118878740 | A | G | 1 | a0005c0007t0005g0060 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1151-22195T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118878740 | |||||||
chr6:118878786 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-22241C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118878786 | |||||||
chr6:118878787 | T | C | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1151-22242A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118878787 | |||||||
chr6:118878866 | G | A | 57 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(54): Show |
60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.1151-22321C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118878866 | |||||||
chr6:118878925 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-22380T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118878925 | |||||||
chr6:118879021 | A | G | 3 | a0004c0006t0002g0035 a0004c0006t0002g0036 a0004c0006t0002g0037 |
3 | HG01168.hp2 HG01169.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1151-22476T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879021 | |||||||
chr6:118879031 | G | GTC | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-22487_1151-22 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879031 | |||||||
chr6:118879032 | G | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-22487C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879032 | |||||||
chr6:118879033 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-22488C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879033 | |||||||
chr6:118879034 | C | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-22489G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879034 | |||||||
chr6:118879037 | C | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-22492G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879037 | |||||||
chr6:118879039 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-22494C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879039 | |||||||
chr6:118879136 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1151-22591A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879136 | |||||||
chr6:118879215 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1151-22670G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879215 | |||||||
chr6:118879248 | GA | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(181): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1151-22704delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879248 | |||||||
chr6:118879248 | GAA | G | 96 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0069 others(93): Show |
102 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1151-22705_1151-22 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879248 | |||||||
chr6:118879251 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-22706T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879251 | |||||||
chr6:118879254 | A | G | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1151-22709T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879254 | |||||||
chr6:118879371 | AAAACAGA others(7): Show |
A | 57 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(54): Show |
60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.1151-22840_1151-22 others(20): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879371 | |||||||
chr6:118879681 | G | C | 7 | a0002c0003t0002g0082 a0005c0007t0005g0060 a0005c0007t0005g0061 others(4): Show |
7 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-23136C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879681 | |||||||
chr6:118879685 | G | A | 1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1151-23140C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879685 | |||||||
chr6:118879732 | TA | T | 22 | a0001c0001t0002g0054 a0001c0005t0002g0003 a0001c0005t0002g0018 others(19): Show |
24 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1151-23188delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879732 | |||||||
chr6:118879744 | A | C | 1 | a0001c0001t0001g0321 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1151-23199T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879744 | |||||||
chr6:118879764 | C | T | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1151-23219G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879764 | |||||||
chr6:118879835 | G | C | 3 | a0001c0002t0003g0137 a0001c0002t0003g0138 a0001c0002t0003g0156 |
3 | NA18986.hp2 NA19055.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1151-23290C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879835 | |||||||
chr6:118879905 | G | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-23360C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118879905 | |||||||
chr6:118880023 | G | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(270): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1151-23478C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880023 | |||||||
chr6:118880051 | C | A | 2 | a0002c0003t0002g0072 a0002c0003t0002g0073 |
2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1151-23506G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880051 | |||||||
chr6:118880051 | C | CA | 9 | a0001c0001t0002g0039 a0001c0001t0004g0164 a0001c0001t0004g0189 others(6): Show |
9 | HG00099.hp2 HG01346.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1151-23507dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880051 | |||||||
chr6:118880089 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-23544T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880089 | |||||||
chr6:118880171 | T | TA | 15 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(12): Show |
15 | HG01081.hp1 HG01167.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1151-23627dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880171 | |||||||
chr6:118880193 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1151-23648G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880193 | |||||||
chr6:118880250 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1151-23705T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880250 | |||||||
chr6:118880329 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1151-23784C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880329 | |||||||
chr6:118880409 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1151-23864T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880409 | |||||||
chr6:118880654 | A | G | 1 | a0003c0004t0002g0024 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1151-24109T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880654 | |||||||
chr6:118880886 | C | T | 1 | a0001c0002t0003g0123 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1151-24341G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880886 | |||||||
chr6:118880945 | T | A | 1 | a0001c0001t0004g0210 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1151-24400A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118880945 | |||||||
chr6:118881063 | C | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(269): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1151-24518G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118881063 | |||||||
chr6:118881188 | A | T | 57 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(54): Show |
60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.1151-24643T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118881188 | |||||||
chr6:118881224 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-24679C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118881224 | |||||||
chr6:118881278 | C | T | 6 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(3): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-24733G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118881278 | |||||||
chr6:118881406 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-24861A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118881406 | |||||||
chr6:118881539 | T | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-24994A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118881539 | |||||||
chr6:118881568 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0307 |
2 | HG00438.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1151-25023G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118881568 | |||||||
chr6:118881706 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1151-25161T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118881706 | |||||||
chr6:118881805 | T | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-25260A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118881805 | |||||||
chr6:118881986 | G | A | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1151-25441C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118881986 | |||||||
chr6:118882006 | C | T | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1151-25461G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882006 | |||||||
chr6:118882014 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-25469C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882014 | |||||||
chr6:118882077 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-25532G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882077 | |||||||
chr6:118882111 | C | G | 27 | a0001c0001t0002g0084 a0002c0003t0001g0168 a0002c0003t0002g0005 others(24): Show |
28 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.1151-25566G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882111 | |||||||
chr6:118882334 | T | C | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1151-25789A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882334 | |||||||
chr6:118882511 | T | C | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1151-25966A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882511 | |||||||
chr6:118882519 | A | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-25974T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882519 | |||||||
chr6:118882715 | TAC | T | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-26172_1151-26 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882715 | |||||||
chr6:118882717 | C | T | 1 | a0001c0001t0004g0290 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1151-26172G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882717 | |||||||
chr6:118882794 | T | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(301): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1151-26249A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882794 | |||||||
chr6:118882830 | T | TA | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(36): Show |
44 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1151-26286dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882830 | |||||||
chr6:118882838 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-26293T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882838 | |||||||
chr6:118882861 | G | A | 1 | a0001c0002t0012g0015 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1151-26316C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882861 | |||||||
chr6:118882904 | A | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA18951.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1151-26359T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882904 | |||||||
chr6:118882940 | A | G | 328 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(325): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1151-26395T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118882940 | |||||||
chr6:118883021 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1151-26476A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883021 | |||||||
chr6:118883069 | C | CA | 86 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(83): Show |
90 | HG00408.hp1 HG00639.hp1 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.1151-26525dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883069 | |||||||
chr6:118883069 | C | CAA | 7 | a0001c0001t0002g0057 a0001c0001t0006g0051 a0001c0001t0006g0052 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-26526_1151-26 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883069 | |||||||
chr6:118883069 | CAAAAAAA others(3): Show |
C | 11 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1151-26534_1151-26 others(16): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883069 | |||||||
chr6:118883140 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-26595C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883140 | |||||||
chr6:118883241 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1151-26696T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883241 | |||||||
chr6:118883267 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-26722A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883267 | |||||||
chr6:118883309 | A | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-26764T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883309 | |||||||
chr6:118883384 | C | G | 6 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(3): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-26839G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883384 | |||||||
chr6:118883405 | G | A | 1 | a0019c0012t0003g0113 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1151-26860C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883405 | |||||||
chr6:118883460 | AC | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1151-26916delG | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883460 | |||||||
chr6:118883465 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(270): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1151-26920C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883465 | |||||||
chr6:118883697 | G | GA | 60 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(57): Show |
63 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-27153dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883697 | |||||||
chr6:118883852 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-27307T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883852 | |||||||
chr6:118883883 | T | C | 2 | a0003c0004t0002g0027 a0003c0004t0002g0028 |
2 | NA18980.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1151-27338A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883883 | |||||||
chr6:118883895 | T | G | 1 | a0001c0001t0002g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1151-27350A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118883895 | |||||||
chr6:118884080 | T | C | 1 | a0002c0003t0002g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1151-27535A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118884080 | |||||||
chr6:118884297 | T | A | 1 | a0001c0001t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1150+27353A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118884297 | |||||||
chr6:118884906 | A | G | 11 | a0001c0001t0001g0178 a0001c0001t0001g0259 a0001c0001t0001g0261 others(8): Show |
11 | HG00423.hp2 HG02027.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1150+26744T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118884906 | |||||||
chr6:118884963 | G | A | 6 | a0001c0002t0003g0121 a0001c0002t0003g0126 a0001c0002t0003g0143 others(3): Show |
6 | NA18943.hp2 NA18952.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150+26687C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118884963 | |||||||
chr6:118885012 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(269): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1150+26638A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118885012 | |||||||
chr6:118885013 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1150+26637C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118885013 | |||||||
chr6:118885353 | T | G | 3 | a0001c0001t0004g0200 a0001c0001t0004g0201 a0001c0001t0004g0205 |
3 | HG01433.hp1 HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1150+26297A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118885353 | |||||||
chr6:118885355 | A | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(301): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1150+26295T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118885355 | |||||||
chr6:118885377 | G | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | NA18951.hp2 NA18967.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1150+26273C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118885377 | |||||||
chr6:118885658 | A | G | 1 | a0001c0001t0004g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1150+25992T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118885658 | |||||||
chr6:118885787 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1150+25863T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118885787 | |||||||
chr6:118885804 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1150+25846G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118885804 | |||||||
chr6:118885847 | GAC | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+25801_1150+25 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118885847 | |||||||
chr6:118885896 | G | C | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150+25754C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118885896 | |||||||
chr6:118886037 | G | A | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+25613C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118886037 | |||||||
chr6:118886037 | G | C | 1 | a0001c0001t0004g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1150+25613C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118886037 | |||||||
chr6:118886055 | CA | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(295): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1150+25594delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118886055 | |||||||
chr6:118886195 | C | T | 1 | a0001c0002t0003g0106 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1150+25455G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118886195 | |||||||
chr6:118886296 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+25354T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118886296 | |||||||
chr6:118886458 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1150+25192A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118886458 | |||||||
chr6:118886522 | C | CA | 10 | a0001c0001t0001g0264 a0001c0001t0001g0269 a0001c0001t0001g0309 others(7): Show |
10 | HG01884.hp2 HG02965.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150+25127dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118886522 | |||||||
chr6:118886570 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+25080A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118886570 | |||||||
chr6:118886843 | T | C | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA18951.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1150+24807A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118886843 | |||||||
chr6:118886925 | A | T | 1 | a0001c0001t0004g0193 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1150+24725T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118886925 | |||||||
chr6:118887012 | A | T | 6 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(3): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150+24638T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887012 | |||||||
chr6:118887033 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1150+24617A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887033 | |||||||
chr6:118887042 | A | G | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1150+24608T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887042 | |||||||
chr6:118887044 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(163): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1150+24606G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887044 | |||||||
chr6:118887049 | T | C | 2 | a0002c0003t0001g0248 a0002c0003t0001g0249 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1150+24601A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887049 | |||||||
chr6:118887112 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+24538C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887112 | |||||||
chr6:118887126 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+24524C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887126 | |||||||
chr6:118887598 | C | G | 3 | a0004c0006t0002g0035 a0004c0006t0002g0036 a0004c0006t0002g0037 |
3 | HG01168.hp2 HG01169.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1150+24052G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887598 | |||||||
chr6:118887637 | A | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1150+24013T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887637 | |||||||
chr6:118887737 | G | T | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1150+23913C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887737 | |||||||
chr6:118887760 | G | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1150+23890C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887760 | |||||||
chr6:118887861 | G | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1150+23789C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887861 | |||||||
chr6:118887896 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1150+23754G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887896 | |||||||
chr6:118887953 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+23697T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887953 | |||||||
chr6:118887997 | T | C | 6 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(3): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150+23653A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118887997 | |||||||
chr6:118888041 | A | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+23609T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888041 | |||||||
chr6:118888214 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1150+23436A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888214 | |||||||
chr6:118888343 | C | T | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0214 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+23307G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888343 | |||||||
chr6:118888344 | G | A | 54 | a0001c0001t0002g0006 a0001c0001t0002g0086 a0001c0001t0002g0087 others(51): Show |
58 | HG00408.hp1 HG00741.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.1150+23306C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888344 | |||||||
chr6:118888379 | C | T | 1 | a0004c0006t0002g0034 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1150+23271G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888379 | |||||||
chr6:118888419 | A | C | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+23231T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888419 | |||||||
chr6:118888486 | A | AAAACAAA others(5): Show |
2 | a0007c0010t0008g0190 a0007c0010t0008g0191 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+23152_1150+23 others(18): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888486 | |||||||
chr6:118888486 | AAAACAAA others(5): Show |
A | 1 | a0003c0004t0002g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1150+23152_1150+23 others(18): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888486 | |||||||
chr6:118888544 | A | G | 1 | a0003c0004t0002g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1150+23106T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888544 | |||||||
chr6:118888644 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1150+23006T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888644 | |||||||
chr6:118888673 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+22977G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888673 | |||||||
chr6:118888804 | C | T | 1 | a0001c0002t0003g0126 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1150+22846G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888804 | |||||||
chr6:118888851 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1150+22799A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888851 | |||||||
chr6:118888961 | T | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+22689A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118888961 | |||||||
chr6:118889002 | T | C | 1 | a0005c0007t0005g0065 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1150+22648A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889002 | |||||||
chr6:118889108 | A | T | 1 | a0001c0001t0002g0041 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1150+22542T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889108 | |||||||
chr6:118889326 | GC | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+22323delG | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889326 | |||||||
chr6:118889328 | C | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+22322G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889328 | |||||||
chr6:118889346 | C | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+22304G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889346 | |||||||
chr6:118889410 | G | A | 1 | a0001c0002t0003g0117 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1150+22240C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889410 | |||||||
chr6:118889752 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0165 a0001c0001t0001g0258 others(5): Show |
10 | HG00323.hp2 HG00738.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150+21898G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889752 | |||||||
chr6:118889875 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+21775G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889875 | |||||||
chr6:118889888 | G | T | 1 | a0001c0002t0003g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1150+21762C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889888 | |||||||
chr6:118889895 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1150+21755T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889895 | |||||||
chr6:118889919 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1150+21731G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889919 | |||||||
chr6:118889972 | C | T | 1 | a0001c0001t0004g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1150+21678G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889972 | |||||||
chr6:118889994 | T | C | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | HG00741.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1150+21656A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118889994 | |||||||
chr6:118890084 | G | T | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.1150+21566C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118890084 | |||||||
chr6:118890122 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1150+21528G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118890122 | |||||||
chr6:118890309 | GTAC | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+21338_1150+21 others(9): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118890309 | |||||||
chr6:118890372 | A | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+21278T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118890372 | |||||||
chr6:118890382 | A | T | 1 | a0001c0001t0001g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1150+21268T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118890382 | |||||||
chr6:118890426 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+21224A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118890426 | |||||||
chr6:118890515 | C | T | 2 | a0001c0001t0004g0192 a0001c0001t0004g0202 |
2 | HG01981.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1150+21135G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118890515 | |||||||
chr6:118890900 | C | T | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1150+20750G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118890900 | |||||||
chr6:118890901 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+20749C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118890901 | |||||||
chr6:118890984 | A | G | 58 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(55): Show |
61 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.1150+20666T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118890984 | |||||||
chr6:118891009 | G | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(301): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1150+20641C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891009 | |||||||
chr6:118891024 | A | C | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1150+20626T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891024 | |||||||
chr6:118891142 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1150+20508T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891142 | |||||||
chr6:118891159 | G | A | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+20491C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891159 | |||||||
chr6:118891194 | T | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+20456A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891194 | |||||||
chr6:118891355 | G | A | 1 | a0001c0001t0021g0323 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1150+20295C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891355 | |||||||
chr6:118891396 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+20254T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891396 | |||||||
chr6:118891462 | T | C | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1150+20188A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891462 | |||||||
chr6:118891594 | T | C | 11 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150+20056A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891594 | |||||||
chr6:118891717 | T | C | 2 | a0005c0007t0005g0063 a0005c0007t0005g0064 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1150+19933A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891717 | |||||||
chr6:118891721 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+19929C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891721 | |||||||
chr6:118891727 | A | G | 1 | a0002c0003t0002g0075 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1150+19923T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891727 | |||||||
chr6:118891929 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+19721A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891929 | |||||||
chr6:118891986 | G | A | 54 | a0001c0001t0001g0230 a0001c0002t0003g0007 a0001c0002t0003g0008 others(51): Show |
57 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.1150+19664C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118891986 | |||||||
chr6:118892092 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+19558A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118892092 | |||||||
chr6:118892109 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+19541G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118892109 | |||||||
chr6:118892129 | T | C | 3 | a0006c0008t0002g0088 a0006c0008t0002g0094 a0006c0008t0002g0095 |
3 | HG00642.hp2 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1150+19521A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118892129 | |||||||
chr6:118892625 | T | C | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1150+19025A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118892625 | |||||||
chr6:118892938 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0165 a0001c0001t0001g0258 others(5): Show |
10 | HG00323.hp2 HG00738.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150+18712C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118892938 | |||||||
chr6:118892987 | A | G | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150+18663T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118892987 | |||||||
chr6:118893187 | CG | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0255 others(1): Show |
7 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+18462delC | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893187 | |||||||
chr6:118893222 | T | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+18428A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893222 | |||||||
chr6:118893237 | G | A | 9 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1150+18413C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893237 | |||||||
chr6:118893305 | T | C | 5 | a0001c0002t0003g0007 a0001c0002t0003g0117 a0001c0002t0003g0118 others(2): Show |
6 | NA18954.hp1 NA18967.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+18345A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893305 | |||||||
chr6:118893360 | A | G | 11 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150+18290T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893360 | |||||||
chr6:118893374 | C | T | 2 | a0004c0006t0002g0033 a0004c0006t0002g0043 |
2 | HG00099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1150+18276G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893374 | |||||||
chr6:118893401 | C | T | 1 | a0002c0003t0002g0070 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1150+18249G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893401 | |||||||
chr6:118893497 | G | C | 2 | a0005c0007t0005g0063 a0005c0007t0005g0064 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1150+18153C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893497 | |||||||
chr6:118893533 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+18117C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893533 | |||||||
chr6:118893666 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1150+17984T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893666 | |||||||
chr6:118893715 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1150+17935T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893715 | |||||||
chr6:118893730 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+17920G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893730 | |||||||
chr6:118893766 | C | G | 1 | a0001c0002t0003g0124 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1150+17884G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893766 | |||||||
chr6:118893845 | C | CA | 9 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1150+17804dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893845 | |||||||
chr6:118893847 | A | AAAC | 52 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(49): Show |
55 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.1150+17802_1150+17 others(9): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893847 | |||||||
chr6:118893855 | A | AC | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(198): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1150+17794_1150+17 others(7): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893855 | |||||||
chr6:118893891 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+17759A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893891 | |||||||
chr6:118893922 | T | TCCCGCCG others(12): Show |
51 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(48): Show |
54 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.1150+17709_1150+17 others(25): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893922 | |||||||
chr6:118893931 | A | AGCCACGC others(50): Show |
1 | a0001c0002t0003g0123 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1150+17718_1150+17 others(63): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893931 | |||||||
chr6:118893931 | A | AGCCACGC others(31): Show |
1 | a0001c0002t0003g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1150+17718_1150+17 others(44): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893931 | |||||||
chr6:118893940 | T | TCCCCGCC others(10): Show |
1 | a0001c0001t0001g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1150+17693_1150+17 others(23): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118893940 | |||||||
chr6:118894053 | A | G | 10 | a0001c0001t0004g0163 a0001c0001t0004g0164 a0001c0001t0004g0198 others(7): Show |
10 | HG00639.hp2 HG01099.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150+17597T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894053 | |||||||
chr6:118894238 | A | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(118): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1150+17412T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894238 | |||||||
chr6:118894325 | G | A | 2 | a0001c0001t0001g0300 a0002c0003t0001g0168 |
2 | NA18989.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1150+17325C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894325 | |||||||
chr6:118894343 | A | G | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150+17307T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894343 | |||||||
chr6:118894542 | G | A | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+17108C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894542 | |||||||
chr6:118894558 | G | A | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+17092C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894558 | |||||||
chr6:118894600 | C | G | 1 | a0001c0001t0002g0047 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1150+17050G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894600 | |||||||
chr6:118894637 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1150+17013C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894637 | |||||||
chr6:118894637 | G | T | 38 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.1150+17013C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894637 | |||||||
chr6:118894649 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1150+17001C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894649 | |||||||
chr6:118894738 | C | G | 69 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(66): Show |
72 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1150+16912G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894738 | |||||||
chr6:118894744 | TGAGCGGA others(1): Show |
T | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+16898_1150+16 others(14): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894744 | |||||||
chr6:118894801 | G | T | 1 | a0001c0001t0002g0045 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1150+16849C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894801 | |||||||
chr6:118894859 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1150+16791C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894859 | |||||||
chr6:118894893 | C | G | 36 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0069 others(33): Show |
38 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1150+16757G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894893 | |||||||
chr6:118894980 | AGCGACCC others(2): Show |
A | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+16661_1150+16 others(15): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894980 | |||||||
chr6:118894994 | A | T | 1 | a0001c0001t0004g0202 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1150+16656T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118894994 | |||||||
chr6:118895559 | CA | C | 58 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(55): Show |
61 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.1150+16090delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118895559 | |||||||
chr6:118895565 | C | T | 11 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150+16085G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118895565 | |||||||
chr6:118895646 | TAATA | T | 7 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(4): Show |
7 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+16000_1150+16 others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118895646 | |||||||
chr6:118895672 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150+15978T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118895672 | |||||||
chr6:118895818 | G | C | 61 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(58): Show |
64 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.1150+15832C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118895818 | |||||||
chr6:118895877 | T | C | 2 | a0001c0001t0009g0159 a0001c0001t0009g0160 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1150+15773A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118895877 | |||||||
chr6:118895910 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(163): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1150+15740T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118895910 | |||||||
chr6:118895992 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+15658C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118895992 | |||||||
chr6:118896041 | G | GT | 36 | a0001c0001t0001g0230 a0001c0001t0001g0300 a0001c0001t0002g0006 others(33): Show |
38 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1150+15608dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896041 | |||||||
chr6:118896041 | GT | G | 68 | a0001c0001t0001g0241 a0001c0001t0001g0319 a0001c0001t0002g0099 others(65): Show |
71 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.1150+15608delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896041 | |||||||
chr6:118896041 | GTT | G | 12 | a0001c0001t0002g0101 a0001c0001t0009g0159 a0001c0001t0009g0160 others(9): Show |
12 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1150+15607_1150+15 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896041 | |||||||
chr6:118896043 | T | G | 1 | a0001c0001t0002g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1150+15607A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896043 | |||||||
chr6:118896046 | T | G | 6 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(3): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150+15604A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896046 | |||||||
chr6:118896194 | A | G | 2 | a0001c0001t0001g0254 a0001c0001t0001g0260 |
2 | HG01261.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1150+15456T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896194 | |||||||
chr6:118896210 | A | G | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+15440T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896210 | |||||||
chr6:118896391 | C | CAA | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+15257_1150+15 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896391 | |||||||
chr6:118896469 | C | T | 1 | a0001c0002t0003g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1150+15181G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896469 | |||||||
chr6:118896500 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1150+15150C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896500 | |||||||
chr6:118896510 | T | C | 11 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150+15140A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896510 | |||||||
chr6:118896559 | A | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+15091T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896559 | |||||||
chr6:118896609 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+15041G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896609 | |||||||
chr6:118896632 | A | G | 1 | a0002c0003t0011g0092 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1150+15018T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896632 | |||||||
chr6:118896775 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(163): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1150+14875C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896775 | |||||||
chr6:118896786 | T | G | 1 | a0001c0001t0001g0332 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1150+14864A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896786 | |||||||
chr6:118896836 | AT | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(175): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1150+14813delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896836 | |||||||
chr6:118896932 | G | A | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+14718C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118896932 | |||||||
chr6:118897046 | C | T | 1 | a0001c0002t0003g0115 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150+14604G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897046 | |||||||
chr6:118897194 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+14456G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897194 | |||||||
chr6:118897211 | A | C | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1150+14439T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897211 | |||||||
chr6:118897291 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1150+14359C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897291 | |||||||
chr6:118897305 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(270): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1150+14345A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897305 | |||||||
chr6:118897339 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1150+14311C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897339 | |||||||
chr6:118897442 | T | TTA | 8 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1150+14206_1150+14 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897442 | |||||||
chr6:118897442 | TTA | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+14206_1150+14 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897442 | |||||||
chr6:118897461 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+14189T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897461 | |||||||
chr6:118897645 | C | A | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1150+14005G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897645 | |||||||
chr6:118897785 | C | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | HG00741.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1150+13865G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897785 | |||||||
chr6:118897837 | AC | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+13812delG | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897837 | |||||||
chr6:118897841 | C | A | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+13809G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897841 | |||||||
chr6:118897906 | A | G | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1150+13744T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897906 | |||||||
chr6:118897933 | A | T | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+13717T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897933 | |||||||
chr6:118897976 | C | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+13674G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118897976 | |||||||
chr6:118898080 | A | G | 58 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(55): Show |
61 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.1150+13570T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898080 | |||||||
chr6:118898285 | T | C | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1150+13365A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898285 | |||||||
chr6:118898425 | A | AT | 16 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0174 others(13): Show |
17 | HG00099.hp1 HG01891.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1150+13224dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898425 | |||||||
chr6:118898425 | AT | A | 62 | a0001c0001t0001g0280 a0001c0001t0001g0298 a0001c0001t0001g0318 others(59): Show |
64 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1150+13224delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898425 | |||||||
chr6:118898442 | T | C | 1 | a0014c0019t0002g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1150+13208A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898442 | |||||||
chr6:118898545 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1150+13105G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898545 | |||||||
chr6:118898556 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1150+13094G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898556 | |||||||
chr6:118898648 | C | G | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1150+13002G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898648 | |||||||
chr6:118898686 | G | A | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150+12964C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898686 | |||||||
chr6:118898698 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1150+12952C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898698 | |||||||
chr6:118898773 | C | G | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+12877G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898773 | |||||||
chr6:118898830 | C | T | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+12820G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898830 | |||||||
chr6:118898926 | T | C | 7 | a0001c0002t0003g0114 a0001c0002t0003g0119 a0001c0002t0003g0120 others(4): Show |
7 | HG01884.hp1 HG02622.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150+12724A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898926 | |||||||
chr6:118898959 | AG | A | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+12690delC | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118898959 | |||||||
chr6:118899102 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1150+12548G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899102 | |||||||
chr6:118899238 | T | C | 4 | a0001c0001t0002g0006 a0001c0001t0002g0086 a0001c0001t0002g0087 others(1): Show |
5 | HG00741.hp1 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150+12412A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899238 | |||||||
chr6:118899308 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+12342T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899308 | |||||||
chr6:118899363 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+12287A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899363 | |||||||
chr6:118899374 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+12276A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899374 | |||||||
chr6:118899409 | T | TG | 5 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0303 others(2): Show |
5 | NA18612.hp1 NA18947.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150+12240dupC | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899409 | |||||||
chr6:118899466 | G | A | 1 | a0001c0001t0007g0108 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1150+12184C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899466 | |||||||
chr6:118899469 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150+12181C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899469 | |||||||
chr6:118899492 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1150+12158G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899492 | |||||||
chr6:118899583 | T | C | 70 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(67): Show |
73 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.1150+12067A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899583 | |||||||
chr6:118899598 | A | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150+12052T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899598 | |||||||
chr6:118899690 | A | G | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+11960T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899690 | |||||||
chr6:118899706 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1150+11944G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899706 | |||||||
chr6:118899842 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+11808C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899842 | |||||||
chr6:118899862 | C | T | 7 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(4): Show |
7 | HG00639.hp2 HG01168.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+11788G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118899862 | |||||||
chr6:118900025 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+11625G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118900025 | |||||||
chr6:118900165 | CAG | C | 7 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(4): Show |
7 | HG00639.hp2 HG01168.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+11483_1150+11 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118900165 | |||||||
chr6:118900616 | T | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+11034A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118900616 | |||||||
chr6:118901115 | A | C | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1150+10535T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118901115 | |||||||
chr6:118901165 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1150+10485A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118901165 | |||||||
chr6:118901266 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1150+10384C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118901266 | |||||||
chr6:118901374 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1150+10276A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118901374 | |||||||
chr6:118901463 | TA | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+10186delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118901463 | |||||||
chr6:118901472 | T | A | 1 | a0011c0015t0015g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150+10178A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118901472 | |||||||
chr6:118901637 | A | G | 1 | a0001c0002t0003g0115 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150+10013T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118901637 | |||||||
chr6:118901853 | T | C | 2 | a0001c0001t0004g0172 a0001c0001t0004g0207 |
2 | HG00280.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1150+9797A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118901853 | |||||||
chr6:118901893 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+9757T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118901893 | |||||||
chr6:118902012 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+9638G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118902012 | |||||||
chr6:118902220 | G | A | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+9430C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118902220 | |||||||
chr6:118902316 | TA | T | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+9333delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118902316 | |||||||
chr6:118902443 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+9207G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118902443 | |||||||
chr6:118902448 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+9202G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118902448 | |||||||
chr6:118902507 | G | C | 12 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150+9143C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118902507 | |||||||
chr6:118902528 | C | CT | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(256): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1150+9121dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118902528 | |||||||
chr6:118902528 | C | CTT | 15 | a0001c0001t0001g0243 a0001c0001t0001g0276 a0001c0001t0002g0099 others(12): Show |
15 | HG00280.hp2 HG01069.hp2 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.1150+9120_1150+912 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118902528 | |||||||
chr6:118902580 | T | C | 1 | a0001c0001t0007g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1150+9070A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118902580 | |||||||
chr6:118902834 | A | G | 61 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(58): Show |
64 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.1150+8816T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118902834 | |||||||
chr6:118903059 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0306 |
2 | HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1150+8591A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903059 | |||||||
chr6:118903081 | T | G | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+8569A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903081 | |||||||
chr6:118903086 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1150+8564T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903086 | |||||||
chr6:118903110 | G | T | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+8540C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903110 | |||||||
chr6:118903120 | CAG | C | 9 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1150+8528_1150+852 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903120 | |||||||
chr6:118903251 | T | G | 26 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(23): Show |
26 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1150+8399A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903251 | |||||||
chr6:118903329 | C | T | 1 | a0013c0018t0002g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1150+8321G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903329 | |||||||
chr6:118903443 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0086 a0001c0001t0002g0087 |
4 | HG00741.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+8207G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903443 | |||||||
chr6:118903543 | A | G | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+8107T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903543 | |||||||
chr6:118903575 | A | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150+8075T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903575 | |||||||
chr6:118903602 | C | T | 1 | a0002c0003t0002g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1150+8048G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903602 | |||||||
chr6:118903743 | G | A | 61 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(58): Show |
64 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.1150+7907C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903743 | |||||||
chr6:118903750 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
6 | HG00323.hp2 HG00738.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150+7900A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903750 | |||||||
chr6:118903762 | GT | G | 4 | a0001c0001t0001g0214 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG02809.hp2 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+7887delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903762 | |||||||
chr6:118903853 | C | T | 1 | a0001c0005t0002g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1150+7797G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903853 | |||||||
chr6:118903854 | T | A | 1 | a0001c0005t0002g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1150+7796A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903854 | |||||||
chr6:118903856 | G | T | 1 | a0001c0005t0002g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1150+7794C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903856 | |||||||
chr6:118903857 | G | C | 1 | a0001c0005t0002g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1150+7793C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903857 | |||||||
chr6:118903858 | A | C | 1 | a0001c0005t0002g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1150+7792T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903858 | |||||||
chr6:118903867 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1150+7783C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903867 | |||||||
chr6:118903877 | G | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0307 |
2 | HG00438.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1150+7773C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903877 | |||||||
chr6:118903888 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+7762C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903888 | |||||||
chr6:118903979 | G | T | 11 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150+7671C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903979 | |||||||
chr6:118903991 | AC | A | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1150+7658delG | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118903991 | |||||||
chr6:118904100 | A | AG | 128 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0001g0320 others(125): Show |
133 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1150+7549dupC | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904100 | |||||||
chr6:118904219 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+7431T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904219 | |||||||
chr6:118904266 | A | G | 61 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(58): Show |
64 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.1150+7384T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904266 | |||||||
chr6:118904292 | C | CACTAGGT others(76): Show |
1 | a0001c0002t0003g0152 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1150+7275_1150+735 others(87): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904292 | |||||||
chr6:118904392 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1150+7258A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904392 | |||||||
chr6:118904418 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1150+7232A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904418 | |||||||
chr6:118904449 | C | T | 1 | a0001c0005t0002g0018 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1150+7201G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904449 | |||||||
chr6:118904468 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1150+7182G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904468 | |||||||
chr6:118904566 | C | T | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+7084G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904566 | |||||||
chr6:118904589 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+7061C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904589 | |||||||
chr6:118904590 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1150+7060G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904590 | |||||||
chr6:118904626 | C | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02257.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1150+7024G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904626 | |||||||
chr6:118904985 | C | G | 61 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(58): Show |
64 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.1150+6665G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118904985 | |||||||
chr6:118905272 | C | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+6378G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118905272 | |||||||
chr6:118905317 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+6333C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118905317 | |||||||
chr6:118905335 | C | T | 11 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150+6315G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118905335 | |||||||
chr6:118905368 | CT | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(291): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1150+6281delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118905368 | |||||||
chr6:118905567 | G | T | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1150+6083C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118905567 | |||||||
chr6:118905568 | T | G | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1150+6082A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118905568 | |||||||
chr6:118905908 | C | T | 1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1150+5742G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118905908 | |||||||
chr6:118906060 | T | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+5590A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118906060 | |||||||
chr6:118906246 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1150+5404A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118906246 | |||||||
chr6:118906534 | T | A | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | HG00741.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1150+5116A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118906534 | |||||||
chr6:118907013 | C | A | 1 | a0001c0001t0009g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1150+4637G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118907013 | |||||||
chr6:118907179 | T | G | 1 | a0001c0002t0003g0144 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1150+4471A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118907179 | |||||||
chr6:118907219 | G | C | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+4431C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118907219 | |||||||
chr6:118907261 | TACTTA | T | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+4384_1150+438 others(9): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118907261 | |||||||
chr6:118907682 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1150+3968C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118907682 | |||||||
chr6:118907691 | T | C | 2 | a0002c0003t0002g0091 a0012c0020t0016g0158 |
2 | HG02717.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1150+3959A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118907691 | |||||||
chr6:118907908 | G | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+3742C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118907908 | |||||||
chr6:118907974 | T | C | 2 | a0007c0010t0008g0190 a0007c0010t0008g0191 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+3676A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118907974 | |||||||
chr6:118908084 | T | C | 1 | a0001c0002t0003g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1150+3566A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118908084 | |||||||
chr6:118908184 | A | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+3466T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118908184 | |||||||
chr6:118908355 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1150+3295C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118908355 | |||||||
chr6:118908397 | C | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(291): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1150+3253G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118908397 | |||||||
chr6:118908409 | T | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+3241A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118908409 | |||||||
chr6:118908418 | T | C | 1 | a0003c0004t0002g0079 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1150+3232A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118908418 | |||||||
chr6:118908559 | ATTTTCAC others(5): Show |
A | 1 | a0001c0002t0003g0148 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1150+3079_1150+309 others(16): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118908559 | |||||||
chr6:118908675 | A | G | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+2975T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118908675 | |||||||
chr6:118908835 | CA | C | 7 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 others(4): Show |
7 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+2814delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118908835 | |||||||
chr6:118909065 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1150+2585G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909065 | |||||||
chr6:118909284 | T | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1150+2366A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909284 | |||||||
chr6:118909333 | G | T | 70 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(67): Show |
73 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.1150+2317C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909333 | |||||||
chr6:118909350 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0255 others(1): Show |
7 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+2300T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909350 | |||||||
chr6:118909464 | CG | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+2185delC | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909464 | |||||||
chr6:118909482 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150+2168T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909482 | |||||||
chr6:118909664 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1150+1986G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909664 | |||||||
chr6:118909718 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1150+1932C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909718 | |||||||
chr6:118909750 | A | T | 51 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(48): Show |
53 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1150+1900T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909750 | |||||||
chr6:118909843 | G | A | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1150+1807C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909843 | |||||||
chr6:118909865 | C | G | 1 | a0001c0001t0001g0274 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1150+1785G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909865 | |||||||
chr6:118909866 | C | G | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1150+1784G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909866 | |||||||
chr6:118909887 | C | T | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1150+1763G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118909887 | |||||||
chr6:118910116 | CA | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(191): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1150+1533delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910116 | |||||||
chr6:118910116 | CAA | C | 18 | a0001c0001t0001g0245 a0001c0001t0002g0057 a0001c0001t0002g0099 others(15): Show |
18 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1150+1532_1150+153 others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910116 | |||||||
chr6:118910116 | CAAAA | C | 15 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(12): Show |
15 | HG01081.hp1 HG01167.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1150+1530_1150+153 others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910116 | |||||||
chr6:118910136 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150+1514C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910136 | |||||||
chr6:118910141 | C | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150+1509G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910141 | |||||||
chr6:118910214 | T | C | 38 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.1150+1436A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910214 | |||||||
chr6:118910217 | G | T | 1 | a0003c0004t0002g0079 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1150+1433C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910217 | |||||||
chr6:118910218 | T | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0224 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1150+1432A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910218 | |||||||
chr6:118910300 | C | G | 1 | a0001c0001t0001g0293 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1150+1350G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910300 | |||||||
chr6:118910334 | G | A | 1 | a0002c0003t0002g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1150+1316C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910334 | |||||||
chr6:118910368 | G | A | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1150+1282C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910368 | |||||||
chr6:118910456 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | NA18964.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1150+1194A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910456 | |||||||
chr6:118910522 | A | G | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+1128T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910522 | |||||||
chr6:118910699 | A | T | 1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1150+951T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910699 | |||||||
chr6:118910750 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1150+900G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910750 | |||||||
chr6:118910803 | T | C | 112 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(109): Show |
117 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1150+847A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118910803 | |||||||
chr6:118911215 | CCCTA | C | 3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1150+431_1150+434d others(6): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118911215 | |||||||
chr6:118911290 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+360T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118911290 | |||||||
chr6:118911302 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150+348G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118911302 | |||||||
chr6:118911329 | T | C | 1 | a0002c0003t0002g0078 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1150+321A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118911329 | |||||||
chr6:118911332 | T | C | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150+318A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118911332 | |||||||
chr6:118911376 | C | T | 1 | a0001c0005t0010g0022 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1150+274G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118911376 | |||||||
chr6:118911509 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+141A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118911509 | |||||||
chr6:118911557 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+93A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118911557 | |||||||
chr6:118911634 | T | C | 7 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+16A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 8/13 | chr6 | 118911634 | |||||||
chr6:118911907 | C | T | 61 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(58): Show |
64 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.1031-138G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118911907 | |||||||
chr6:118912046 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1031-277G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912046 | |||||||
chr6:118912315 | A | C | 19 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(16): Show |
19 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1031-546T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912315 | |||||||
chr6:118912397 | G | A | 6 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(3): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1031-628C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912397 | |||||||
chr6:118912415 | T | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0250 |
2 | HG00544.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1031-646A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912415 | |||||||
chr6:118912580 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(291): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1030+715C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912580 | |||||||
chr6:118912592 | C | G | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1030+703G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912592 | |||||||
chr6:118912619 | C | T | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1030+676G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912619 | |||||||
chr6:118912706 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1030+589C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912706 | |||||||
chr6:118912851 | A | G | 1 | a0001c0001t0004g0184 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1030+444T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912851 | |||||||
chr6:118912888 | G | A | 1 | a0001c0002t0003g0155 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1030+407C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912888 | |||||||
chr6:118912963 | A | G | 1 | a0001c0001t0004g0287 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1030+332T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118912963 | |||||||
chr6:118913072 | A | G | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG01168.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1030+223T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118913072 | |||||||
chr6:118913075 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1030+220G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118913075 | |||||||
chr6:118913077 | A | T | 1 | a0001c0001t0002g0086 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1030+218T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118913077 | |||||||
chr6:118913122 | T | C | 3 | a0006c0008t0002g0088 a0006c0008t0002g0094 a0006c0008t0002g0095 |
3 | HG00642.hp2 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1030+173A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118913122 | |||||||
chr6:118913287 | G | A | 1 | a0001c0002t0003g0145 | 1 | NA19005.hp1 | splice_region_variant&intron_variant | LOW | c.1030+8C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 7/13 | chr6 | 118913287 | |||||||
chr6:118913523 | T | C | 51 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(48): Show |
53 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.905-103A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118913523 | |||||||
chr6:118913534 | G | A | 61 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(58): Show |
64 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.905-114C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118913534 | |||||||
chr6:118913635 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.905-215A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118913635 | |||||||
chr6:118913661 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.905-241C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118913661 | |||||||
chr6:118913681 | C | T | 1 | a0003c0004t0002g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.905-261G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118913681 | |||||||
chr6:118913756 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.905-336G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118913756 | |||||||
chr6:118913757 | G | A | 1 | a0002c0003t0002g0091 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905-337C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118913757 | |||||||
chr6:118913923 | G | A | 1 | a0016c0023t0001g0244 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.905-503C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118913923 | |||||||
chr6:118913948 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.905-528T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118913948 | |||||||
chr6:118914003 | A | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.905-583T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914003 | |||||||
chr6:118914162 | A | G | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-742T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914162 | |||||||
chr6:118914164 | G | C | 58 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(55): Show |
61 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.905-744C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914164 | |||||||
chr6:118914272 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.905-852A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914272 | |||||||
chr6:118914309 | A | G | 2 | a0005c0007t0005g0063 a0005c0007t0005g0064 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.905-889T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914309 | |||||||
chr6:118914330 | G | A | 2 | a0006c0008t0002g0094 a0006c0008t0002g0095 |
2 | HG00642.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.905-910C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914330 | |||||||
chr6:118914398 | C | T | 1 | a0002c0003t0002g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.905-978G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914398 | |||||||
chr6:118914399 | G | A | 1 | a0001c0001t0009g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.905-979C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914399 | |||||||
chr6:118914475 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.905-1055A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914475 | |||||||
chr6:118914485 | G | A | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-1065C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914485 | |||||||
chr6:118914534 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1114C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914534 | |||||||
chr6:118914637 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.905-1217G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914637 | |||||||
chr6:118914889 | A | C | 1 | a0018c0014t0003g0153 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.905-1469T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914889 | |||||||
chr6:118914998 | T | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-1578A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118914998 | |||||||
chr6:118915109 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.905-1689G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118915109 | |||||||
chr6:118915288 | T | C | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.905-1868A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118915288 | |||||||
chr6:118915428 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.905-2008C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118915428 | |||||||
chr6:118915582 | C | T | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+1979G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118915582 | |||||||
chr6:118915737 | T | C | 11 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.904+1824A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118915737 | |||||||
chr6:118915825 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.904+1736A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118915825 | |||||||
chr6:118915895 | C | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.904+1666G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118915895 | |||||||
chr6:118915909 | A | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+1652T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118915909 | |||||||
chr6:118915977 | A | C | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.904+1584T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118915977 | |||||||
chr6:118916110 | T | G | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.904+1451A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916110 | |||||||
chr6:118916170 | T | C | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.904+1391A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916170 | |||||||
chr6:118916176 | A | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02257.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.904+1385T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916176 | |||||||
chr6:118916332 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.904+1229C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916332 | |||||||
chr6:118916367 | C | A | 1 | a0003c0004t0002g0079 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.904+1194G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916367 | |||||||
chr6:118916367 | CA | C | 7 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.904+1193delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916367 | |||||||
chr6:118916369 | A | C | 60 | a0001c0001t0001g0326 a0001c0001t0007g0107 a0001c0001t0007g0108 others(57): Show |
63 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.904+1192T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916369 | |||||||
chr6:118916371 | A | C | 2 | a0001c0002t0003g0120 a0001c0002t0003g0149 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.904+1190T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916371 | |||||||
chr6:118916432 | C | CATT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0169 a0001c0001t0001g0218 others(21): Show |
28 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.904+1126_904+1128d others(5): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916432 | |||||||
chr6:118916432 | C | CATTATT | 14 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(11): Show |
14 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.904+1123_904+1128d others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916432 | |||||||
chr6:118916432 | C | CCTT | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.904+1128_904+1129i others(5): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916432 | |||||||
chr6:118916432 | CATT | C | 38 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0175 others(35): Show |
40 | HG00438.hp2 HG00597.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.904+1126_904+1128d others(5): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916432 | |||||||
chr6:118916432 | CATTATT | C | 8 | a0001c0001t0001g0208 a0001c0001t0001g0223 a0001c0001t0001g0250 others(5): Show |
8 | HG00544.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+1123_904+1128d others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916432 | |||||||
chr6:118916432 | CATTATTA others(5): Show |
C | 9 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(6): Show |
9 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.904+1117_904+1128d others(14): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916432 | |||||||
chr6:118916432 | CATTATTA others(8): Show |
C | 100 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(97): Show |
105 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.904+1114_904+1128d others(17): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916432 | |||||||
chr6:118916445 | A | C | 9 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(6): Show |
9 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.904+1116T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916445 | |||||||
chr6:118916448 | A | C | 100 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(97): Show |
105 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.904+1113T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916448 | |||||||
chr6:118916491 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.904+1070G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916491 | |||||||
chr6:118916605 | CACGCCAC others(36): Show |
C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.904+913_904+955del others(43): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916605 | |||||||
chr6:118916705 | T | C | 2 | a0001c0002t0003g0106 a0001c0002t0003g0148 |
2 | HG01192.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.904+856A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916705 | |||||||
chr6:118916887 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.904+674C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118916887 | |||||||
chr6:118917007 | T | A | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+554A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118917007 | |||||||
chr6:118917025 | A | C | 1 | a0001c0002t0003g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.904+536T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118917025 | |||||||
chr6:118917052 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.904+509A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118917052 | |||||||
chr6:118917175 | A | T | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+386T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118917175 | |||||||
chr6:118917299 | ACT | A | 9 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.904+260_904+261del others(2): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 6/13 | chr6 | 118917299 | |||||||
chr6:118917782 | A | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.704-21T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118917782 | |||||||
chr6:118918058 | A | C | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0214 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-297T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918058 | |||||||
chr6:118918143 | G | A | 31 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.704-382C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918143 | |||||||
chr6:118918215 | T | G | 1 | a0001c0001t0004g0206 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.704-454A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918215 | |||||||
chr6:118918323 | A | G | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704-562T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918323 | |||||||
chr6:118918334 | C | T | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.704-573G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918334 | |||||||
chr6:118918373 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.704-612C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918373 | |||||||
chr6:118918397 | C | T | 58 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(55): Show |
61 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.704-636G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918397 | |||||||
chr6:118918408 | G | A | 6 | a0001c0005t0002g0003 a0001c0005t0002g0018 a0001c0005t0002g0019 others(3): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-647C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918408 | |||||||
chr6:118918751 | G | C | 1 | a0001c0001t0001g0283 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.704-990C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918751 | |||||||
chr6:118918910 | G | A | 1 | a0001c0001t0004g0290 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.704-1149C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918910 | |||||||
chr6:118918954 | C | T | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-1193G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118918954 | |||||||
chr6:118919024 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0224 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.704-1263G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919024 | |||||||
chr6:118919061 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(170): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.704-1300T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919061 | |||||||
chr6:118919342 | C | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0222 a0001c0001t0001g0223 |
4 | NA18939.hp2 NA19009.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-1581G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919342 | |||||||
chr6:118919381 | A | G | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.704-1620T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919381 | |||||||
chr6:118919394 | T | C | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.704-1633A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919394 | |||||||
chr6:118919472 | C | CTGCATTT others(4): Show |
4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-1712_704-1711i others(13): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919472 | |||||||
chr6:118919473 | G | A | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-1712C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919473 | |||||||
chr6:118919570 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.704-1809A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919570 | |||||||
chr6:118919674 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.704-1913A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919674 | |||||||
chr6:118919688 | C | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(291): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.704-1927G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919688 | |||||||
chr6:118919763 | A | G | 31 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.704-2002T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919763 | |||||||
chr6:118919962 | T | C | 2 | a0001c0001t0004g0163 a0001c0001t0004g0164 |
2 | HG04115.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.703+2043A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118919962 | |||||||
chr6:118920144 | G | C | 1 | a0001c0002t0019g0162 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.703+1861C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920144 | |||||||
chr6:118920303 | C | T | 5 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(2): Show |
5 | HG02258.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+1702G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920303 | |||||||
chr6:118920426 | C | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.703+1579G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920426 | |||||||
chr6:118920477 | T | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.703+1528A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920477 | |||||||
chr6:118920525 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.703+1480C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920525 | |||||||
chr6:118920587 | C | T | 121 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(118): Show |
126 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.703+1418G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920587 | |||||||
chr6:118920669 | C | G | 19 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(16): Show |
19 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.703+1336G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920669 | |||||||
chr6:118920695 | C | G | 121 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(118): Show |
126 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.703+1310G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920695 | |||||||
chr6:118920747 | C | T | 7 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+1258G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920747 | |||||||
chr6:118920797 | G | T | 1 | a0001c0001t0007g0108 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.703+1208C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920797 | |||||||
chr6:118920817 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703+1188G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920817 | |||||||
chr6:118920865 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.703+1140G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118920865 | |||||||
chr6:118921242 | T | C | 1 | a0007c0010t0008g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.703+763A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118921242 | |||||||
chr6:118921254 | CTAAT | C | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+747_703+750del others(4): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118921254 | |||||||
chr6:118921367 | G | T | 1 | a0001c0001t0004g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.703+638C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118921367 | |||||||
chr6:118921717 | G | C | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+288C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118921717 | |||||||
chr6:118921745 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.703+260G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118921745 | |||||||
chr6:118921907 | T | C | 58 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(55): Show |
61 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.703+98A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118921907 | |||||||
chr6:118921937 | A | G | 51 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(48): Show |
53 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.703+68T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 5/13 | chr6 | 118921937 | |||||||
chr6:118922212 | G | T | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.622-126C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118922212 | |||||||
chr6:118922324 | G | A | 11 | a0003c0004t0002g0004 a0003c0004t0002g0023 a0003c0004t0002g0024 others(8): Show |
12 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.622-238C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118922324 | |||||||
chr6:118922340 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.622-254C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118922340 | |||||||
chr6:118922429 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.622-343C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118922429 | |||||||
chr6:118922879 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.622-793T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118922879 | |||||||
chr6:118922892 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.622-806G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118922892 | |||||||
chr6:118922931 | C | A | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.622-845G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118922931 | |||||||
chr6:118923029 | C | A | 1 | a0002c0003t0002g0091 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.621+782G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923029 | |||||||
chr6:118923029 | C | CA | 37 | a0001c0001t0001g0166 a0001c0001t0001g0213 a0001c0001t0001g0251 others(34): Show |
39 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.621+781dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923029 | |||||||
chr6:118923029 | CA | C | 56 | a0001c0001t0001g0253 a0001c0001t0001g0275 a0001c0001t0001g0325 others(53): Show |
59 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.621+781delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923029 | |||||||
chr6:118923029 | CAAAA | C | 7 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+778_621+781del others(4): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923029 | |||||||
chr6:118923045 | A | C | 1 | a0013c0018t0002g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.621+766T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923045 | |||||||
chr6:118923060 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.621+751T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923060 | |||||||
chr6:118923101 | C | A | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.621+710G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923101 | |||||||
chr6:118923200 | C | G | 4 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+611G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923200 | |||||||
chr6:118923259 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.621+552G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923259 | |||||||
chr6:118923268 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(35): Show |
43 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.621+543A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923268 | |||||||
chr6:118923285 | A | AT | 113 | a0001c0001t0001g0166 a0001c0001t0001g0173 a0001c0001t0001g0174 others(110): Show |
117 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.621+525dupA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923285 | |||||||
chr6:118923285 | A | ATT | 7 | a0001c0002t0003g0007 a0001c0002t0003g0115 a0001c0002t0003g0117 others(4): Show |
8 | NA18940.hp2 NA18954.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.621+524_621+525dup others(2): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923285 | |||||||
chr6:118923299 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.621+512A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923299 | |||||||
chr6:118923315 | G | A | 58 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(55): Show |
61 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.621+496C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923315 | |||||||
chr6:118923320 | G | A | 1 | a0001c0001t0021g0323 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.621+491C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923320 | |||||||
chr6:118923343 | G | A | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.621+468C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923343 | |||||||
chr6:118923424 | A | G | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.621+387T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923424 | |||||||
chr6:118923615 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.621+196A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923615 | |||||||
chr6:118923680 | G | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(302): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.621+131C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 4/13 | chr6 | 118923680 | |||||||
chr6:118924227 | CA | C | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.305-101delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118924227 | |||||||
chr6:118924327 | GT | G | 5 | a0001c0001t0001g0315 a0001c0001t0007g0107 a0001c0001t0007g0108 others(2): Show |
5 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-201delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118924327 | |||||||
chr6:118924474 | T | A | 1 | a0001c0001t0002g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.305-347A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118924474 | |||||||
chr6:118924474 | T | C | 2 | a0001c0001t0004g0172 a0001c0001t0004g0207 |
2 | HG00280.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.305-347A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118924474 | |||||||
chr6:118924540 | G | A | 2 | a0001c0002t0003g0009 a0001c0002t0003g0112 |
3 | HG01069.hp1 HG01071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.305-413C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118924540 | |||||||
chr6:118924579 | G | C | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.305-452C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118924579 | |||||||
chr6:118924816 | G | A | 38 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.305-689C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118924816 | |||||||
chr6:118924823 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-696G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118924823 | |||||||
chr6:118924965 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.305-838T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118924965 | |||||||
chr6:118925036 | C | T | 1 | a0001c0001t0007g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.305-909G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118925036 | |||||||
chr6:118925153 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(291): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.305-1026A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118925153 | |||||||
chr6:118925250 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-1123G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118925250 | |||||||
chr6:118925392 | A | G | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.305-1265T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118925392 | |||||||
chr6:118925567 | G | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-1440C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118925567 | |||||||
chr6:118925754 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-1627C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118925754 | |||||||
chr6:118925795 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(295): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.305-1668T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118925795 | |||||||
chr6:118925905 | T | A | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.305-1778A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118925905 | |||||||
chr6:118926025 | A | G | 1 | a0019c0012t0003g0113 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.305-1898T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926025 | |||||||
chr6:118926037 | A | C | 1 | a0001c0001t0002g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.305-1910T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926037 | |||||||
chr6:118926082 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.305-1955T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926082 | |||||||
chr6:118926401 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-2274A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926401 | |||||||
chr6:118926435 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.305-2308A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926435 | |||||||
chr6:118926569 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(125): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.305-2442A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926569 | |||||||
chr6:118926634 | A | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-2507T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926634 | |||||||
chr6:118926766 | A | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-2639T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926766 | |||||||
chr6:118926797 | GAGT | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-2673_305-2671d others(5): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926797 | |||||||
chr6:118926839 | T | A | 4 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 others(1): Show |
4 | HG01884.hp2 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-2712A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926839 | |||||||
chr6:118926884 | C | G | 1 | a0001c0002t0003g0112 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.305-2757G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118926884 | |||||||
chr6:118927023 | A | G | 8 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-2896T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927023 | |||||||
chr6:118927075 | C | A | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.305-2948G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927075 | |||||||
chr6:118927086 | C | A | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.305-2959G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927086 | |||||||
chr6:118927213 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-3086C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927213 | |||||||
chr6:118927370 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.305-3243C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927370 | |||||||
chr6:118927453 | T | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-3326A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927453 | |||||||
chr6:118927546 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-3419T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927546 | |||||||
chr6:118927581 | G | C | 1 | a0005c0007t0005g0065 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.305-3454C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927581 | |||||||
chr6:118927620 | C | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-3493G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927620 | |||||||
chr6:118927634 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.305-3507C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927634 | |||||||
chr6:118927704 | C | G | 1 | a0001c0001t0001g0320 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.305-3577G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927704 | |||||||
chr6:118927810 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+3610A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927810 | |||||||
chr6:118927855 | T | C | 1 | a0020c0021t0002g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.304+3565A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118927855 | |||||||
chr6:118928021 | G | A | 19 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(16): Show |
19 | HG01081.hp1 HG01167.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.304+3399C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928021 | |||||||
chr6:118928186 | G | A | 1 | a0001c0001t0009g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.304+3234C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928186 | |||||||
chr6:118928268 | G | A | 3 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 |
3 | HG02055.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.304+3152C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928268 | |||||||
chr6:118928283 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.304+3137G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928283 | |||||||
chr6:118928291 | AT | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+3128delA | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928291 | |||||||
chr6:118928304 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+3116C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928304 | |||||||
chr6:118928392 | C | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+3028G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928392 | |||||||
chr6:118928397 | T | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+3023A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928397 | |||||||
chr6:118928476 | T | C | 1 | a0003c0004t0002g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.304+2944A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928476 | |||||||
chr6:118928610 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.304+2810C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928610 | |||||||
chr6:118928697 | A | T | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+2723T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928697 | |||||||
chr6:118928926 | A | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+2494T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928926 | |||||||
chr6:118928942 | G | A | 38 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.304+2478C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118928942 | |||||||
chr6:118929124 | G | A | 1 | a0001c0001t0004g0209 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.304+2296C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929124 | |||||||
chr6:118929144 | C | A | 2 | a0005c0007t0005g0063 a0005c0007t0005g0064 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.304+2276G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929144 | |||||||
chr6:118929164 | G | C | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+2256C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929164 | |||||||
chr6:118929172 | A | G | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.304+2248T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929172 | |||||||
chr6:118929258 | A | C | 1 | a0002c0003t0002g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.304+2162T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929258 | |||||||
chr6:118929312 | A | G | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+2108T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929312 | |||||||
chr6:118929432 | CCTAGCAA others(3): Show |
C | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.304+1978_304+1987d others(12): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929432 | |||||||
chr6:118929452 | G | A | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.304+1968C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929452 | |||||||
chr6:118929501 | A | C | 2 | a0002c0003t0002g0066 a0002c0003t0002g0067 |
2 | HG01081.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.304+1919T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929501 | |||||||
chr6:118929740 | G | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+1680C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929740 | |||||||
chr6:118929773 | T | A | 3 | a0007c0010t0008g0190 a0007c0010t0008g0191 a0007c0026t0008g0167 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.304+1647A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929773 | |||||||
chr6:118929826 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.304+1594T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929826 | |||||||
chr6:118929864 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.304+1556T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118929864 | |||||||
chr6:118930103 | A | ATTTTAT | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.304+1316_304+1317i others(8): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930103 | |||||||
chr6:118930142 | G | A | 31 | a0001c0001t0001g0169 a0001c0001t0004g0010 a0001c0001t0004g0163 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.304+1278C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930142 | |||||||
chr6:118930149 | T | C | 4 | a0001c0001t0009g0161 a0002c0003t0002g0089 a0002c0003t0002g0090 others(1): Show |
4 | HG02145.hp1 NA19066.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+1271A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930149 | |||||||
chr6:118930173 | C | T | 50 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(47): Show |
52 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.304+1247G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930173 | |||||||
chr6:118930180 | G | A | 58 | a0001c0001t0007g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(55): Show |
61 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.304+1240C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930180 | |||||||
chr6:118930212 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02257.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.304+1208T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930212 | |||||||
chr6:118930256 | G | A | 12 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0100 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.304+1164C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930256 | |||||||
chr6:118930259 | C | T | 1 | a0001c0002t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.304+1161G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930259 | |||||||
chr6:118930267 | T | C | 1 | a0005c0007t0005g0065 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.304+1153A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930267 | |||||||
chr6:118930314 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.304+1106C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930314 | |||||||
chr6:118930358 | C | T | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.304+1062G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930358 | |||||||
chr6:118930363 | T | C | 2 | a0002c0003t0011g0092 a0002c0003t0011g0093 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.304+1057A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930363 | |||||||
chr6:118930392 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.304+1028C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930392 | |||||||
chr6:118930402 | G | A | 1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.304+1018C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930402 | |||||||
chr6:118930541 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.304+879G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930541 | |||||||
chr6:118930715 | G | A | 1 | a0004c0006t0002g0050 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.304+705C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930715 | |||||||
chr6:118930741 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.304+679G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930741 | |||||||
chr6:118930806 | G | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.304+614C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930806 | |||||||
chr6:118930841 | A | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(172): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.304+579T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930841 | |||||||
chr6:118930842 | A | T | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.304+578T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930842 | |||||||
chr6:118930863 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.304+557C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930863 | |||||||
chr6:118930875 | C | A | 3 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.304+545G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930875 | |||||||
chr6:118930946 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.304+474T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930946 | |||||||
chr6:118930973 | A | T | 1 | a0001c0001t0014g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.304+447T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118930973 | |||||||
chr6:118931073 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.304+347G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118931073 | |||||||
chr6:118931163 | C | G | 1 | a0001c0002t0019g0162 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.304+257G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118931163 | |||||||
chr6:118931200 | C | T | 1 | a0007c0026t0008g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.304+220G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118931200 | |||||||
chr6:118931235 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.304+185T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118931235 | |||||||
chr6:118931399 | T | C | 2 | a0006c0008t0002g0094 a0006c0008t0002g0095 |
2 | HG00642.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.304+21A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 3/13 | chr6 | 118931399 | |||||||
chr6:118931978 | C | T | 18 | a0001c0001t0002g0054 a0001c0005t0002g0003 a0001c0005t0002g0018 others(15): Show |
20 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-240G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/13 | chr6 | 118931978 | |||||||
chr6:118932070 | C | A | 1 | a0001c0001t0014g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-15-332G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/13 | chr6 | 118932070 | |||||||
chr6:118932071 | G | A | 65 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(62): Show |
68 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.-15-333C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/13 | chr6 | 118932071 | |||||||
chr6:118932086 | T | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-15-348A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/13 | chr6 | 118932086 | |||||||
chr6:118932105 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-15-367G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/13 | chr6 | 118932105 | |||||||
chr6:118932193 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-16+414C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/13 | chr6 | 118932193 | |||||||
chr6:118932252 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-16+355C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/13 | chr6 | 118932252 | |||||||
chr6:118932434 | T | C | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG00558.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-16+173A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/13 | chr6 | 118932434 | |||||||
chr6:118932516 | T | C | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+91A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/13 | chr6 | 118932516 | |||||||
chr6:118932517 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-16+90C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 2/13 | chr6 | 118932517 | |||||||
chr6:118932809 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-149-69T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118932809 | |||||||
chr6:118932811 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-149-71T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118932811 | |||||||
chr6:118932812 | A | T | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-149-72T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118932812 | |||||||
chr6:118932813 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-149-73C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118932813 | |||||||
chr6:118932814 | T | G | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-149-74A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118932814 | |||||||
chr6:118932818 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-149-78T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118932818 | |||||||
chr6:118932863 | T | A | 1 | a0001c0001t0014g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-149-123A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118932863 | |||||||
chr6:118932902 | C | T | 1 | a0001c0002t0003g0112 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-149-162G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118932902 | |||||||
chr6:118932991 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(226): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.-149-251A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118932991 | |||||||
chr6:118933027 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-149-287A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933027 | |||||||
chr6:118933085 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-149-345T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933085 | |||||||
chr6:118933208 | A | G | 65 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(62): Show |
68 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.-149-468T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933208 | |||||||
chr6:118933214 | T | C | 1 | a0001c0002t0003g0152 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-149-474A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933214 | |||||||
chr6:118933218 | G | T | 1 | a0001c0016t0003g0111 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-149-478C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933218 | |||||||
chr6:118933221 | CG | C | 7 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149-482delC | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933221 | |||||||
chr6:118933271 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-531T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933271 | |||||||
chr6:118933274 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-534A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933274 | |||||||
chr6:118933292 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-149-552C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933292 | |||||||
chr6:118933296 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-556C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933296 | |||||||
chr6:118933303 | T | C | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0001g0326 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149-563A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933303 | |||||||
chr6:118933307 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-567C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933307 | |||||||
chr6:118933316 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-576C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933316 | |||||||
chr6:118933323 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-583A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933323 | |||||||
chr6:118933341 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-601T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933341 | |||||||
chr6:118933348 | C | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-608G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933348 | |||||||
chr6:118933362 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-622A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933362 | |||||||
chr6:118933363 | G | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-623C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933363 | |||||||
chr6:118933375 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-635T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933375 | |||||||
chr6:118933378 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-638A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933378 | |||||||
chr6:118933384 | A | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-644T>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933384 | |||||||
chr6:118933399 | A | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-659T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933399 | |||||||
chr6:118933429 | C | G | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-689G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933429 | |||||||
chr6:118933430 | C | T | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-149-690G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933430 | |||||||
chr6:118933481 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-149-741C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933481 | |||||||
chr6:118933504 | CA | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(168): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-149-765delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933504 | |||||||
chr6:118933665 | T | G | 4 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0053 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-925A>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933665 | |||||||
chr6:118933683 | G | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | NA18964.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-149-943C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933683 | |||||||
chr6:118933723 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-149-983G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933723 | |||||||
chr6:118933732 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-149-992G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933732 | |||||||
chr6:118933757 | G | A | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.-149-1017C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933757 | |||||||
chr6:118933764 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-149-1024A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933764 | |||||||
chr6:118933794 | T | C | 7 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0320 others(4): Show |
7 | HG00558.hp1 HG00597.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-1054A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933794 | |||||||
chr6:118933838 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-150+1053T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933838 | |||||||
chr6:118933964 | C | CA | 12 | a0001c0001t0002g0054 a0001c0001t0002g0057 a0001c0001t0006g0058 others(9): Show |
12 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-150+926dupT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933964 | |||||||
chr6:118933964 | C | CAAAAAAA others(1): Show |
42 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(39): Show |
43 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.-150+919_-150+926d others(10): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933964 | |||||||
chr6:118933964 | C | CAAAAAAA others(2): Show |
96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(93): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-150+918_-150+926d others(11): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933964 | |||||||
chr6:118933964 | C | CAAAAAAA others(3): Show |
27 | a0001c0001t0001g0165 a0001c0001t0001g0299 a0001c0001t0001g0300 others(24): Show |
27 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.-150+917_-150+926d others(12): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933964 | |||||||
chr6:118933964 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0326 others(3): Show |
6 | HG02723.hp2 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+916_-150+926d others(13): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933964 | |||||||
chr6:118933964 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0330 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-150+915_-150+926d others(14): Show |
MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933964 | |||||||
chr6:118933964 | CA | C | 22 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(19): Show |
23 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-150+926delT | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933964 | |||||||
chr6:118933966 | A | C | 6 | a0005c0007t0005g0060 a0005c0007t0005g0061 a0005c0007t0005g0062 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+925T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118933966 | |||||||
chr6:118934011 | G | A | 1 | a0001c0002t0003g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-150+880C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934011 | |||||||
chr6:118934057 | T | A | 1 | a0001c0001t0014g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-150+834A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934057 | |||||||
chr6:118934096 | A | C | 7 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+795T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934096 | |||||||
chr6:118934103 | C | G | 1 | a0010c0025t0013g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-150+788G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934103 | |||||||
chr6:118934140 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-150+751A>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934140 | |||||||
chr6:118934144 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-150+747C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934144 | |||||||
chr6:118934145 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-150+746G>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934145 | |||||||
chr6:118934182 | T | C | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-150+709A>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934182 | |||||||
chr6:118934283 | G | C | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG02027.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-150+608C>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934283 | |||||||
chr6:118934292 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-150+599C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934292 | |||||||
chr6:118934311 | AG | A | 53 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(50): Show |
56 | HG00408.hp1 HG00609.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.-150+579delC | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934311 | |||||||
chr6:118934324 | A | C | 1 | a0002c0003t0002g0059 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-150+567T>G | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934324 | |||||||
chr6:118934326 | C | T | 44 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(41): Show |
46 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-150+565G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934326 | |||||||
chr6:118934576 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-150+315G>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934576 | |||||||
chr6:118934615 | G | T | 1 | a0001c0002t0003g0106 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-150+276C>A | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934615 | |||||||
chr6:118934636 | C | A | 1 | a0012c0020t0016g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-150+255G>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934636 | |||||||
chr6:118934683 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-150+208T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934683 | |||||||
chr6:118934737 | A | G | 2 | a0001c0001t0004g0163 a0001c0001t0004g0164 |
2 | HG04115.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-150+154T>C | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934737 | |||||||
chr6:118934870 | G | A | 7 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+21C>T | MCM9 | ENSG00000111877.18 | transcript | ENST00000619706.5 | protein_coding | 1/13 | chr6 | 118934870 |