Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79258 |
| ensemblid | ENSG00000142606.16 |
| hgncid | 14668 |
| symbol | MMEL1 |
| name | membrane metalloendopeptidase like 1 |
| refseq_nuc | NM_033467.4 |
| refseq_prot | NP_258428.2 |
| ensembl_nuc | ENST00000378412.8 |
| ensembl_prot | ENSP00000367668.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 2590639 |
| end | 2633016 |
| strand | - |
| ver | v1.2 |
| region | chr1:2590639-2633016 |
| region5000 | chr1:2585639-2638016 |
| regionname0 | MMEL1_chr1_2590639_2633016 |
| regionname5000 | MMEL1_chr1_2585639_2638016 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 779 | 166 | 30 | 30 | 72 | 11 | 22 | 52 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0002 | 0/0 | 779 | 161 | 50 | 30 | 63 | 3 | 15 | 50 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0003 | 0/0 | 779 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0004 | 0/0 | 779 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0005 | 0/0 | 779 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0006 | 0/0 | 779 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0007 | 0/0 | 779 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0008 | 0/0 | 779 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0009 | 0/0 | 779 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0010 | 0/0 | 779 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0011 | 0/0 | 779 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0012 | 0/0 | 779 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| a0013 | 0/0 | 779 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | MGKSE others(774): Show |
chr1 | 2585639 | 2638016 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2337 | 160 | 29 | 29 | 68 | 11 | 22 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0001c0005 | 0/0 | 2337 | 3 | 1 | 1 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0001c0014 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0001c0021 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0001c0022 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0002c0002 | 0/0 | 2337 | 137 | 33 | 29 | 58 | 2 | 15 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0002c0003 | 0/0 | 2337 | 11 | 7 | 1 | 2 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0002c0004 | 0/0 | 2337 | 5 | 5 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0002c0008 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0002c0012 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0002c0016 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0002c0017 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0002c0018 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0002c0023 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0002c0025 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0003c0006 | 0/0 | 2337 | 3 | 0 | 2 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0004c0010 | 0/0 | 2337 | 2 | 1 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0005c0009 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0006c0007 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0007c0026 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0008c0024 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0009c0015 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0010c0013 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0011c0020 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0012c0011 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 | ||
| a0013c0019 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | ATGGG others(2332): Show |
chr1 | 2585639 | 2638016 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2879 | 88 | 27 | 16 | 24 | 6 | 14 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0001c0001t0002 | 0/0 | 2879 | 70 | 1 | 13 | 43 | 5 | 8 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0001c0001t0005 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0001c0001t0007 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0001c0005t0001 | 0/0 | 2879 | 3 | 1 | 1 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0001c0014t0002 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0001c0021t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0001c0022t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0002t0001 | 0/0 | 2879 | 85 | 33 | 17 | 31 | 1 | 3 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0002t0003 | 0/0 | 2879 | 52 | 0 | 12 | 27 | 1 | 12 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0003t0001 | 0/0 | 2879 | 10 | 7 | 1 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0003t0006 | 0/0 | 2879 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0004t0001 | 0/0 | 2879 | 5 | 5 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0008t0001 | 0/0 | 2879 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0012t0001 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0016t0001 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0017t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0018t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0023t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0002c0025t0003 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0003c0006t0001 | 0/0 | 2879 | 3 | 0 | 2 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0004c0010t0001 | 0/0 | 2879 | 2 | 1 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0005c0009t0004 | 0/0 | 2879 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0006c0007t0001 | 0/0 | 2879 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0007c0026t0002 | 0/0 | 2879 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0008c0024t0002 | 0/0 | 2879 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0009c0015t0003 | 0/0 | 2879 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0010c0013t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0011c0020t0001 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0012c0011t0001 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| a0013c0019t0001 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | AGGCA others(2874): Show |
chr1 | 2585639 | 2638016 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0001 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0005t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0005t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0014t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0021t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0001c0022t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0002 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0003 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0003t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0003t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0003t0006g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0004t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0008t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0008t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0012t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0016t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0017t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0018t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0023t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0002c0025t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0003c0006t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0003c0006t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0004c0010t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0004c0010t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0005c0009t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0005c0009t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0006c0007t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0007c0026t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0008c0024t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0009c0015t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0010c0013t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0011c0020t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0012c0011t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| a0013c0019t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0053 | EUR | GBR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00099 | hp2 | a0007 | c0026 | t0002 | g0242 | EUR | GBR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | GBR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00140 | hp2 | a0002 | c0003 | t0006 | g0127 | EUR | GBR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | FIN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00323 | hp1 | a0004 | c0010 | t0001 | g0234 | EUR | FIN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00438 | hp1 | a0002 | c0018 | t0001 | g0109 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00544 | hp1 | a0002 | c0002 | t0003 | g0107 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00597 | hp1 | a0002 | c0002 | t0003 | g0117 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00642 | hp1 | a0002 | c0002 | t0003 | g0010 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00733 | hp2 | a0002 | c0002 | t0003 | g0016 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00735 | hp2 | a0003 | c0006 | t0001 | g0024 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0049 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00741 | hp1 | a0008 | c0024 | t0002 | g0134 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01069 | hp1 | a0003 | c0006 | t0001 | g0024 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01074 | hp2 | a0002 | c0002 | t0003 | g0046 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01255 | hp1 | a0001 | c0005 | t0001 | g0059 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01255 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01346 | hp1 | a0009 | c0015 | t0003 | g0121 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01346 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0047 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01361 | hp2 | a0002 | c0002 | t0003 | g0083 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01433 | hp2 | a0002 | c0002 | t0003 | g0010 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01496 | hp2 | a0002 | c0002 | t0003 | g0010 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | IBS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0241 | EUR | IBS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0027 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01891 | hp1 | a0002 | c0016 | t0001 | g0033 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0099 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01978 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02040 | hp1 | a0002 | c0002 | t0003 | g0039 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02055 | hp1 | a0004 | c0010 | t0001 | g0239 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02055 | hp2 | a0002 | c0012 | t0001 | g0044 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02074 | hp1 | a0001 | c0014 | t0002 | g0115 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02080 | hp2 | a0010 | c0013 | t0001 | g0092 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0080 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CDX | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02280 | hp2 | a0002 | c0008 | t0001 | g0041 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0089 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02523 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02572 | hp2 | a0011 | c0020 | t0001 | g0266 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02615 | hp2 | a0002 | c0004 | t0001 | g0270 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0273 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02630 | hp2 | a0002 | c0004 | t0001 | g0269 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02647 | hp1 | a0012 | c0011 | t0001 | g0124 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02683 | hp2 | a0002 | c0002 | t0003 | g0045 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02698 | hp1 | a0002 | c0002 | t0003 | g0048 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02717 | hp1 | a0002 | c0004 | t0001 | g0278 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02723 | hp2 | a0002 | c0004 | t0001 | g0268 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0087 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02965 | hp2 | a0005 | c0009 | t0004 | g0133 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02976 | hp1 | a0013 | c0019 | t0001 | g0271 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0272 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0112 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03225 | hp2 | a0006 | c0007 | t0001 | g0028 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0113 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03453 | hp2 | a0006 | c0007 | t0001 | g0028 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0086 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0003 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0003 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03579 | hp1 | a0002 | c0003 | t0001 | g0274 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0094 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0002 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0016 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03831 | hp2 | a0002 | c0002 | t0003 | g0111 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03942 | hp1 | a0003 | c0006 | t0001 | g0155 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0003 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0002 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG04228 | hp2 | a0002 | c0002 | t0003 | g0101 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18612 | hp1 | a0002 | c0002 | t0003 | g0068 | EAS | CHB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | CHB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CHB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18906 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18906 | hp2 | a0002 | c0004 | t0001 | g0267 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18940 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18956 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18956 | hp2 | a0001 | c0021 | t0001 | g0157 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18963 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18969 | hp2 | a0002 | c0002 | t0003 | g0069 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18970 | hp1 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18974 | hp2 | a0002 | c0002 | t0003 | g0091 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18979 | hp2 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18984 | hp1 | a0002 | c0002 | t0003 | g0065 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0072 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18986 | hp2 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18990 | hp2 | a0002 | c0002 | t0003 | g0081 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18998 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18999 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19000 | hp1 | a0002 | c0002 | t0003 | g0105 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19003 | hp1 | a0002 | c0002 | t0003 | g0084 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0075 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19065 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19067 | hp2 | a0001 | c0005 | t0001 | g0078 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19070 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19079 | hp2 | a0002 | c0023 | t0001 | g0256 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19081 | hp2 | a0002 | c0002 | t0003 | g0082 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19087 | hp1 | a0002 | c0002 | t0003 | g0063 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19089 | hp2 | a0002 | c0017 | t0001 | g0125 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ASW | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | ASW | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0218 | EUR | TSI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | TSI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA20805 | hp2 | a0002 | c0002 | t0003 | g0120 | EUR | TSI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA20905 | hp1 | a0002 | c0002 | t0003 | g0100 | SAS | GIH | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | GIH | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0027 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02109 | hp1 | a0002 | c0025 | t0003 | g0223 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02559 | hp1 | a0005 | c0009 | t0004 | g0128 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG06807 | hp1 | a0002 | c0008 | t0001 | g0040 | AFR | USA | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | USA | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18955 | hp1 | a0001 | c0022 | t0001 | g0175 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | USA | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0263 | REF | REF | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:2591973 | C | T | 1 | a0008 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.2122G>A | p.Asp708Asn | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 22/24 | 2310/2879 | 2122/2340 | 708/779 | chr1 | 2591973 | |||
| chr1:2591992 | G | T | 1 | a0003 | 3 | HG00735.hp2 HG01069.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.2103C>A | p.Asp701Glu | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 22/24 | 2291/2879 | 2103/2340 | 701/779 | chr1 | 2591992 | |||
| chr1:2592689 | A | G | 1 | a0004 | 2 | HG00323.hp1 HG02055.hp1 |
missense_variant | MODERATE | c.2033T>C | p.Ile678Thr | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/24 | 2221/2879 | 2033/2340 | 678/779 | chr1 | 2592689 | |||
| chr1:2595307 | A | G | 8 | a0002 a0005 a0006 others(5): Show |
170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
missense_variant | MODERATE | c.1553T>C | p.Met518Thr | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/24 | 1741/2879 | 1553/2340 | 518/779 | chr1 | 2595307 | |||
| chr1:2603958 | C | G | 1 | a0009 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.967G>C | p.Glu323Gln | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/24 | 1155/2879 | 967/2340 | 323/779 | chr1 | 2603958 | |||
| chr1:2604193 | T | C | 1 | a0005 | 2 | HG02559.hp1 HG02965.hp2 |
missense_variant | MODERATE | c.905A>G | p.Gln302Arg | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/24 | 1093/2879 | 905/2340 | 302/779 | chr1 | 2604193 | |||
| chr1:2604278 | G | A | 1 | a0011 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.820C>T | p.Arg274Trp | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/24 | 1008/2879 | 820/2340 | 274/779 | chr1 | 2604278 | |||
| chr1:2606261 | C | T | 2 | a0006 a0013 |
3 | HG02976.hp1 HG03225.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.737G>A | p.Arg246Gln | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/24 | 925/2879 | 737/2340 | 246/779 | chr1 | 2606261 | |||
| chr1:2606280 | C | T | 1 | a0010 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.718G>A | p.Asp240Asn | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/24 | 906/2879 | 718/2340 | 240/779 | chr1 | 2606280 | |||
| chr1:2609389 | C | G | 1 | a0012 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.485G>C | p.Arg162Pro | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/24 | 673/2879 | 485/2340 | 162/779 | chr1 | 2609389 | |||
| chr1:2609829 | C | T | 1 | a0013 | 1 | HG02976.hp1 | missense_variant&splice_region_variant | MODERATE | c.295G>A | p.Ala99Thr | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 5/24 | 483/2879 | 295/2340 | 99/779 | chr1 | 2609829 | |||
| chr1:2612197 | C | A | 1 | a0007 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.162G>T | p.Gln54His | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/24 | 350/2879 | 162/2340 | 54/779 | chr1 | 2612197 | |||
| chr1:2629468 | C | G | 1 | a0006 | 2 | HG03225.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.17G>C | p.Gly6Ala | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/24 | 205/2879 | 17/2340 | 6/779 | chr1 | 2629468 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:2593833 | C | T | 1 | a0002c0008 | 2 | HG02280.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.1848G>A | p.Thr616Thr | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/24 | 2036/2879 | 1848/2340 | 616/779 | chr1 | 2593833 | |||
| chr1:2593842 | G | A | 1 | a0002c0017 | 1 | NA19089.hp2 | synonymous_variant | LOW | c.1839C>T | p.His613His | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/24 | 2027/2879 | 1839/2340 | 613/779 | chr1 | 2593842 | |||
| chr1:2596018 | C | T | 1 | a0001c0022 | 1 | NA18955.hp1 | synonymous_variant | LOW | c.1491G>A | p.Ala497Ala | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/24 | 1679/2879 | 1491/2340 | 497/779 | chr1 | 2596018 | |||
| chr1:2596033 | C | T | 1 | a0002c0016 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1476G>A | p.Glu492Glu | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/24 | 1664/2879 | 1476/2340 | 492/779 | chr1 | 2596033 | |||
| chr1:2604174 | C | A | 14 | a0001c0005 a0001c0021 a0002c0002 others(11): Show |
157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
synonymous_variant | LOW | c.924G>T | p.Val308Val | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/24 | 1112/2879 | 924/2340 | 308/779 | chr1 | 2604174 | |||
| chr1:2604240 | C | T | 1 | a0013c0019 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.858G>A | p.Thr286Thr | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/24 | 1046/2879 | 858/2340 | 286/779 | chr1 | 2604240 | |||
| chr1:2606362 | G | A | 6 | a0002c0004 a0002c0012 a0005c0009 others(3): Show |
12 | HG02055.hp2 HG02559.hp1 HG02572.hp2 others(9): Show |
synonymous_variant | LOW | c.636C>T | p.Leu212Leu | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/24 | 824/2879 | 636/2340 | 212/779 | chr1 | 2606362 | |||
| chr1:2607005 | C | T | 5 | a0002c0004 a0002c0012 a0006c0007 others(2): Show |
10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
synonymous_variant | LOW | c.600G>A | p.Pro200Pro | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/24 | 788/2879 | 600/2340 | 200/779 | chr1 | 2607005 | |||
| chr1:2609830 | A | G | 16 | a0001c0005 a0001c0014 a0001c0021 others(13): Show |
170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
splice_region_variant&synonymous_variant | LOW | c.294T>C | p.Ala98Ala | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 5/24 | 482/2879 | 294/2340 | 98/779 | chr1 | 2609830 | |||
| chr1:2629443 | G | A | 9 | a0001c0001 a0001c0021 a0001c0022 others(6): Show |
170 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(167): Show |
synonymous_variant | LOW | c.42C>T | p.Ala14Ala | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/24 | 230/2879 | 42/2340 | 14/779 | chr1 | 2629443 | |||
| chr1:2629464 | T | G | 15 | a0001c0001 a0001c0021 a0001c0022 others(12): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
synonymous_variant | LOW | c.21A>C | p.Pro7Pro | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/24 | 209/2879 | 21/2340 | 7/779 | chr1 | 2629464 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:2590765 | G | T | 3 | a0002c0002t0003 a0002c0025t0003 a0009c0015t0003 |
54 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*225C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 24/24 | 225 | chr1 | 2590765 | ||||||
| chr1:2590917 | G | A | 1 | a0002c0003t0006 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*73C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 24/24 | 73 | chr1 | 2590917 | ||||||
| chr1:2590931 | C | T | 1 | a0001c0001t0007 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*59G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 24/24 | 59 | chr1 | 2590931 | ||||||
| chr1:2590953 | G | A | 5 | a0001c0001t0002 a0001c0001t0007 a0001c0014t0002 others(2): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*37C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 24/24 | 37 | chr1 | 2590953 | ||||||
| chr1:2629500 | C | T | 1 | a0005c0009t0004 | 2 | HG02559.hp1 HG02965.hp2 |
5_prime_UTR_variant | MODIFIER | c.-16G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/24 | 16 | chr1 | 2629500 | ||||||
| chr1:2632905 | C | T | 1 | a0001c0001t0005 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/24 | 3421 | chr1 | 2632905 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:2591413 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2240+144G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 23/23 | chr1 | 2591413 | |||||||
| chr1:2591461 | T | C | 1 | a0010c0013t0001g0092 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2240+96A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 23/23 | chr1 | 2591461 | |||||||
| chr1:2591486 | T | C | 7 | a0002c0002t0001g0006 a0002c0002t0001g0038 a0002c0002t0001g0054 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2240+71A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 23/23 | chr1 | 2591486 | |||||||
| chr1:2591495 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2240+62G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 23/23 | chr1 | 2591495 | |||||||
| chr1:2591773 | G | C | 116 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(113): Show |
155 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.2164-140C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 22/23 | chr1 | 2591773 | |||||||
| chr1:2591905 | T | A | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2163+27A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 22/23 | chr1 | 2591905 | |||||||
| chr1:2591922 | C | T | 3 | a0002c0002t0001g0097 a0002c0002t0001g0098 a0002c0012t0001g0044 |
3 | HG02055.hp2 HG02056.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2163+10G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 22/23 | chr1 | 2591922 | |||||||
| chr1:2592031 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.2068-4G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592031 | |||||||
| chr1:2592221 | CG | C | 183 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0137 others(180): Show |
229 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2068-195delC | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592221 | |||||||
| chr1:2592224 | G | T | 1 | a0001c0001t0002g0218 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2068-197C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592224 | |||||||
| chr1:2592257 | C | G | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2068-230G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592257 | |||||||
| chr1:2592267 | C | T | 116 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(113): Show |
155 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.2068-240G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592267 | |||||||
| chr1:2592282 | C | T | 1 | a0005c0009t0004g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2068-255G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592282 | |||||||
| chr1:2592283 | GCCCCCTC others(17): Show |
G | 1 | a0005c0009t0004g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2068-280_2068-257d others(26): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592283 | |||||||
| chr1:2592284 | C | T | 118 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(115): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.2068-257G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592284 | |||||||
| chr1:2592305 | T | C | 9 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(6): Show |
13 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2068-278A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592305 | |||||||
| chr1:2592307 | C | CCCCCCTC others(41): Show |
5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2068-281_2068-280i others(50): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592307 | |||||||
| chr1:2592323 | C | T | 1 | a0005c0009t0004g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2068-296G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592323 | |||||||
| chr1:2592330 | GC | G | 110 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(107): Show |
149 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.2068-304delG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592330 | |||||||
| chr1:2592347 | A | G | 2 | a0002c0008t0001g0040 a0002c0008t0001g0041 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2067+308T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592347 | |||||||
| chr1:2592353 | ACGCCCCC others(200): Show |
A | 1 | a0002c0002t0001g0090 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2067+95_2067+301de others(1): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592353 | |||||||
| chr1:2592355 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2067+300C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592355 | |||||||
| chr1:2592356 | CCCCCTCC others(199): Show |
C | 2 | a0002c0002t0001g0057 a0002c0002t0003g0080 |
2 | HG02083.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2067+93_2067+298de others(1): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592356 | |||||||
| chr1:2592368 | C | A | 113 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(110): Show |
152 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2067+287G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592368 | |||||||
| chr1:2592369 | T | A | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+286A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592369 | |||||||
| chr1:2592371 | T | C | 115 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(112): Show |
155 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2067+284A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592371 | |||||||
| chr1:2592372 | G | A | 113 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(110): Show |
152 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2067+283C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592372 | |||||||
| chr1:2592375 | GGCACCCC others(37): Show |
G | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+236_2067+279d others(46): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592375 | |||||||
| chr1:2592378 | A | AC | 6 | a0001c0001t0001g0197 a0001c0001t0002g0030 a0001c0001t0002g0190 others(3): Show |
6 | HG00597.hp2 HG01099.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2067+276dupG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592378 | |||||||
| chr1:2592378 | ACCCCCTC others(223): Show |
A | 110 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(107): Show |
147 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.2067+47_2067+276de others(1): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592378 | |||||||
| chr1:2592379 | C | T | 47 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0137 others(44): Show |
50 | HG00544.hp2 HG00609.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2067+276G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592379 | |||||||
| chr1:2592379 | CCCCCTCC others(222): Show |
C | 5 | a0002c0002t0001g0055 a0002c0002t0003g0002 a0002c0002t0003g0003 others(2): Show |
5 | HG02080.hp2 HG03490.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.2067+47_2067+275de others(1): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592379 | |||||||
| chr1:2592415 | T | G | 8 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(5): Show |
11 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+240A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592415 | |||||||
| chr1:2592420 | T | A | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+235A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592420 | |||||||
| chr1:2592421 | G | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+234C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592421 | |||||||
| chr1:2592423 | C | T | 8 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(5): Show |
11 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+232G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592423 | |||||||
| chr1:2592424 | G | C | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+231C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592424 | |||||||
| chr1:2592424 | G | GC | 6 | a0001c0001t0002g0219 a0002c0003t0001g0014 a0002c0003t0001g0027 others(3): Show |
9 | HG01123.hp1 HG01192.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2067+230dupG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592424 | |||||||
| chr1:2592425 | CCCCCTCC others(84): Show |
C | 3 | a0002c0008t0001g0040 a0002c0008t0001g0041 a0005c0009t0004g0133 |
3 | HG02280.hp2 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2067+139_2067+229d others(93): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592425 | |||||||
| chr1:2592438 | C | A | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+217G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592438 | |||||||
| chr1:2592439 | A | G | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+216T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592439 | |||||||
| chr1:2592440 | T | C | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+215A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592440 | |||||||
| chr1:2592445 | A | ATG | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+209_2067+210i others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592445 | |||||||
| chr1:2592447 | G | C | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+208C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592447 | |||||||
| chr1:2592461 | C | A | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+194G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592461 | |||||||
| chr1:2592461 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.2067+194G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592461 | |||||||
| chr1:2592462 | G | A | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+193C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592462 | |||||||
| chr1:2592463 | T | C | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+192A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592463 | |||||||
| chr1:2592468 | G | A | 7 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(4): Show |
11 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+187C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592468 | |||||||
| chr1:2592468 | GCGCCCCC others(16): Show |
G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2067+164_2067+186d others(25): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592468 | |||||||
| chr1:2592469 | C | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+186G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592469 | |||||||
| chr1:2592470 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2067+185C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592470 | |||||||
| chr1:2592472 | CCCCTCCC others(37): Show |
C | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+139_2067+182d others(46): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592472 | |||||||
| chr1:2592484 | C | A | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+171G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592484 | |||||||
| chr1:2592491 | A | ATG | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+163_2067+164i others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592491 | |||||||
| chr1:2592493 | G | C | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+162C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592493 | |||||||
| chr1:2592508 | G | A | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+147C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592508 | |||||||
| chr1:2592509 | C | T | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+146G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592509 | |||||||
| chr1:2592530 | C | A | 3 | a0002c0008t0001g0040 a0002c0008t0001g0041 a0005c0009t0004g0133 |
3 | HG02280.hp2 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2067+125G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592530 | |||||||
| chr1:2592530 | C | T | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+125G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592530 | |||||||
| chr1:2592531 | G | A | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+124C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592531 | |||||||
| chr1:2592532 | C | T | 7 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(4): Show |
11 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+123G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592532 | |||||||
| chr1:2592537 | A | C | 1 | a0002c0003t0001g0273 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+118T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592537 | |||||||
| chr1:2592537 | A | G | 4 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(1): Show |
7 | HG01123.hp1 HG01884.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2067+118T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592537 | |||||||
| chr1:2592538 | T | A | 1 | a0002c0003t0001g0273 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+117A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592538 | |||||||
| chr1:2592538 | T | C | 6 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(3): Show |
10 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2067+117A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592538 | |||||||
| chr1:2592539 | G | A | 4 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(1): Show |
7 | HG01123.hp1 HG01884.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2067+116C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592539 | |||||||
| chr1:2592539 | G | C | 1 | a0002c0003t0001g0273 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+116C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592539 | |||||||
| chr1:2592554 | G | A | 3 | a0002c0008t0001g0040 a0002c0008t0001g0041 a0005c0009t0004g0133 |
3 | HG02280.hp2 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2067+101C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592554 | |||||||
| chr1:2592555 | T | C | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+100A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592555 | |||||||
| chr1:2592560 | G | A | 8 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(5): Show |
11 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+95C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592560 | |||||||
| chr1:2592561 | C | T | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+94G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592561 | |||||||
| chr1:2592575 | A | C | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+80T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592575 | |||||||
| chr1:2592576 | T | C | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+79A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592576 | |||||||
| chr1:2592576 | T | G | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+79A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592576 | |||||||
| chr1:2592578 | C | T | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+77G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592578 | |||||||
| chr1:2592579 | A | G | 4 | a0001c0001t0002g0244 a0001c0001t0002g0245 a0002c0008t0001g0040 others(1): Show |
4 | HG01168.hp2 HG02129.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2067+76T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592579 | |||||||
| chr1:2592583 | G | GT | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+71_2067+72ins others(1): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592583 | |||||||
| chr1:2592584 | C | G | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+71G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592584 | |||||||
| chr1:2592585 | A | AC | 11 | a0001c0001t0001g0141 a0001c0001t0001g0162 a0001c0001t0001g0196 others(8): Show |
11 | HG00597.hp2 HG00735.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+69dupG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592585 | |||||||
| chr1:2592585 | A | C | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+70T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592585 | |||||||
| chr1:2592585 | A | G | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+70T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592585 | |||||||
| chr1:2592585 | ACCCCCTC others(16): Show |
A | 6 | a0002c0002t0001g0057 a0002c0002t0001g0090 a0002c0002t0003g0080 others(3): Show |
6 | HG02083.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2067+47_2067+69del others(23): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592585 | |||||||
| chr1:2592598 | C | A | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+57G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592598 | |||||||
| chr1:2592599 | C | A | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+56G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592599 | |||||||
| chr1:2592599 | C | T | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+56G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592599 | |||||||
| chr1:2592602 | G | A | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+53C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592602 | |||||||
| chr1:2592606 | A | ATGCCCCC others(41): Show |
5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+48_2067+49ins others(48): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592606 | |||||||
| chr1:2592606 | A | G | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+49T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592606 | |||||||
| chr1:2592608 | G | A | 7 | a0001c0001t0002g0244 a0001c0001t0002g0245 a0002c0003t0001g0014 others(4): Show |
10 | HG01123.hp1 HG01168.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2067+47C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592608 | |||||||
| chr1:2592725 | G | A | 3 | a0002c0002t0001g0108 a0002c0008t0001g0040 a0002c0008t0001g0041 |
3 | HG02280.hp2 HG06807.hp1 NA18943.hp1 |
splice_region_variant&intron_variant | LOW | c.2002-5C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 20/23 | chr1 | 2592725 | |||||||
| chr1:2592766 | C | T | 116 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(113): Show |
155 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.2002-46G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 20/23 | chr1 | 2592766 | |||||||
| chr1:2592803 | C | T | 7 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(4): Show |
10 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2001+30G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 20/23 | chr1 | 2592803 | |||||||
| chr1:2593018 | T | C | 126 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(123): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1868-52A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593018 | |||||||
| chr1:2593046 | C | T | 65 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0009 others(62): Show |
88 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1868-80G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593046 | |||||||
| chr1:2593057 | C | T | 1 | a0002c0002t0001g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1868-91G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593057 | |||||||
| chr1:2593347 | G | A | 1 | a0005c0009t0004g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1868-381C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593347 | |||||||
| chr1:2593402 | C | T | 1 | a0002c0002t0001g0021 | 2 | HG01070.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1867+412G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593402 | |||||||
| chr1:2593456 | G | C | 54 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0009 others(51): Show |
74 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1867+358C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593456 | |||||||
| chr1:2593476 | G | T | 116 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(113): Show |
155 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1867+338C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593476 | |||||||
| chr1:2593504 | G | A | 126 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(123): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1867+310C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593504 | |||||||
| chr1:2593527 | C | T | 123 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(120): Show |
165 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.1867+287G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593527 | |||||||
| chr1:2593573 | G | A | 1 | a0002c0008t0001g0040 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1867+241C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593573 | |||||||
| chr1:2593631 | C | T | 3 | a0002c0003t0001g0023 a0002c0003t0006g0127 a0005c0009t0004g0133 |
4 | HG00140.hp2 HG02965.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1867+183G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593631 | |||||||
| chr1:2593713 | T | C | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1867+101A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593713 | |||||||
| chr1:2593725 | G | A | 7 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(4): Show |
10 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1867+89C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593725 | |||||||
| chr1:2593769 | C | T | 3 | a0002c0003t0001g0023 a0002c0003t0006g0127 a0005c0009t0004g0133 |
4 | HG00140.hp2 HG02965.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1867+45G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593769 | |||||||
| chr1:2594084 | C | T | 1 | a0001c0001t0002g0212 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1748-151G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 18/23 | chr1 | 2594084 | |||||||
| chr1:2594221 | G | A | 109 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(106): Show |
148 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1747+164C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 18/23 | chr1 | 2594221 | |||||||
| chr1:2594226 | T | C | 126 | a0001c0005t0001g0059 a0002c0002t0001g0004 a0002c0002t0001g0005 others(123): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1747+159A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 18/23 | chr1 | 2594226 | |||||||
| chr1:2594533 | G | T | 1 | a0002c0002t0001g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1689-90C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 17/23 | chr1 | 2594533 | |||||||
| chr1:2594569 | A | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0162 a0001c0001t0001g0164 others(1): Show |
4 | NA18956.hp2 NA18974.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689-126T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 17/23 | chr1 | 2594569 | |||||||
| chr1:2594752 | G | GC | 22 | a0001c0001t0001g0140 a0001c0001t0001g0146 a0001c0001t0001g0147 others(19): Show |
22 | HG00597.hp2 HG00741.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1688+37dupG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 17/23 | chr1 | 2594752 | |||||||
| chr1:2594761 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1688+29C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 17/23 | chr1 | 2594761 | |||||||
| chr1:2594897 | C | T | 4 | a0002c0002t0001g0038 a0002c0002t0001g0055 a0002c0002t0001g0060 others(1): Show |
4 | HG02922.hp1 HG03130.hp1 HG03225.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1585-4G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2594897 | |||||||
| chr1:2594913 | A | G | 1 | a0004c0010t0001g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1585-20T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2594913 | |||||||
| chr1:2595006 | G | A | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1585-113C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595006 | |||||||
| chr1:2595019 | TG | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1585-127delC | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595019 | |||||||
| chr1:2595084 | G | A | 2 | a0002c0002t0001g0042 a0002c0002t0001g0043 |
2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1585-191C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595084 | |||||||
| chr1:2595098 | C | T | 1 | a0005c0009t0004g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1584+178G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595098 | |||||||
| chr1:2595132 | G | A | 15 | a0002c0002t0001g0042 a0002c0002t0001g0043 a0002c0002t0003g0003 others(12): Show |
22 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1584+144C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595132 | |||||||
| chr1:2595182 | G | A | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1584+94C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595182 | |||||||
| chr1:2595236 | C | T | 1 | a0001c0001t0007g0216 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1584+40G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595236 | |||||||
| chr1:2595423 | G | A | 1 | a0001c0005t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1501-64C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595423 | |||||||
| chr1:2595497 | G | A | 2 | a0002c0008t0001g0040 a0002c0008t0001g0041 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1501-138C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595497 | |||||||
| chr1:2595741 | C | G | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1500+268G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595741 | |||||||
| chr1:2595805 | T | TGGTCCTG others(33): Show |
6 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1500+164_1500+203d others(42): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595805 | |||||||
| chr1:2595805 | TGGTCCTG others(33): Show |
T | 10 | a0001c0001t0001g0163 a0002c0003t0001g0014 a0002c0003t0001g0023 others(7): Show |
14 | HG00140.hp2 HG01106.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1500+164_1500+203d others(42): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595805 | |||||||
| chr1:2595864 | C | A | 1 | a0002c0003t0001g0273 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1500+145G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595864 | |||||||
| chr1:2595891 | T | C | 1 | a0002c0002t0001g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1500+118A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595891 | |||||||
| chr1:2595904 | C | T | 2 | a0002c0008t0001g0040 a0002c0008t0001g0041 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1500+105G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595904 | |||||||
| chr1:2595931 | G | A | 1 | a0002c0004t0001g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1500+78C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595931 | |||||||
| chr1:2596239 | A | G | 161 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(158): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1402-132T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 14/23 | chr1 | 2596239 | |||||||
| chr1:2596255 | C | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1402-148G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 14/23 | chr1 | 2596255 | |||||||
| chr1:2596391 | C | T | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1401+170G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 14/23 | chr1 | 2596391 | |||||||
| chr1:2596420 | C | T | 1 | a0001c0001t0005g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1401+141G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 14/23 | chr1 | 2596420 | |||||||
| chr1:2596462 | TG | T | 9 | a0002c0002t0003g0003 a0002c0002t0003g0010 a0002c0002t0003g0047 others(6): Show |
15 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1401+98delC | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 14/23 | chr1 | 2596462 | |||||||
| chr1:2596694 | T | C | 162 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(159): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
splice_region_variant&intron_variant | LOW | c.1273-5A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2596694 | |||||||
| chr1:2596705 | G | A | 1 | a0003c0006t0001g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1273-16C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2596705 | |||||||
| chr1:2596858 | G | A | 1 | a0001c0001t0002g0212 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1273-169C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2596858 | |||||||
| chr1:2596901 | C | A | 10 | a0002c0002t0003g0003 a0002c0002t0003g0010 a0002c0002t0003g0016 others(7): Show |
17 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1273-212G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2596901 | |||||||
| chr1:2597132 | TC | T | 2 | a0002c0002t0001g0011 a0012c0011t0001g0124 |
4 | HG01109.hp2 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273-444delG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597132 | |||||||
| chr1:2597240 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0251 |
2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1273-551G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597240 | |||||||
| chr1:2597243 | T | C | 159 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(156): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1273-554A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597243 | |||||||
| chr1:2597304 | C | G | 1 | a0002c0002t0001g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1273-615G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597304 | |||||||
| chr1:2597336 | C | A | 12 | a0002c0002t0003g0003 a0002c0002t0003g0010 a0002c0002t0003g0016 others(9): Show |
19 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1273-647G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597336 | |||||||
| chr1:2597494 | C | T | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | HG02055.hp2 HG02451.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1272+713G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597494 | |||||||
| chr1:2597513 | G | A | 1 | a0002c0002t0001g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1272+694C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597513 | |||||||
| chr1:2597560 | G | T | 151 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(148): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1272+647C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597560 | |||||||
| chr1:2597658 | T | C | 151 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(148): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1272+549A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597658 | |||||||
| chr1:2597718 | C | A | 4 | a0002c0002t0003g0063 a0002c0002t0003g0065 a0002c0002t0003g0079 others(1): Show |
4 | NA18970.hp1 NA18984.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272+489G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597718 | |||||||
| chr1:2597753 | A | G | 161 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(158): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1272+454T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597753 | |||||||
| chr1:2597829 | C | T | 1 | a0001c0001t0002g0217 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1272+378G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597829 | |||||||
| chr1:2597842 | G | A | 2 | a0001c0001t0002g0227 a0001c0001t0007g0216 |
2 | HG02080.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1272+365C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597842 | |||||||
| chr1:2597844 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1272+363C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597844 | |||||||
| chr1:2597921 | G | A | 151 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(148): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1272+286C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597921 | |||||||
| chr1:2597960 | G | T | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1272+247C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597960 | |||||||
| chr1:2597998 | C | T | 151 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(148): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1272+209G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597998 | |||||||
| chr1:2598078 | C | T | 1 | a0002c0002t0003g0079 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1272+129G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2598078 | |||||||
| chr1:2598113 | G | A | 14 | a0001c0001t0001g0137 a0001c0001t0001g0139 a0001c0001t0001g0140 others(11): Show |
14 | HG00735.hp1 HG01192.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1272+94C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2598113 | |||||||
| chr1:2598124 | G | A | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1272+83C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2598124 | |||||||
| chr1:2598806 | G | A | 1 | a0002c0002t0001g0067 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1042-16C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2598806 | |||||||
| chr1:2598820 | G | GGA | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1042-32_1042-31dup others(2): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2598820 | |||||||
| chr1:2598856 | T | C | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1042-66A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2598856 | |||||||
| chr1:2598902 | A | AG | 163 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(160): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1042-113dupC | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2598902 | |||||||
| chr1:2598972 | C | T | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1042-182G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2598972 | |||||||
| chr1:2599035 | A | G | 1 | a0001c0001t0007g0216 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1042-245T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599035 | |||||||
| chr1:2599119 | T | C | 160 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(157): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1042-329A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599119 | |||||||
| chr1:2599255 | G | A | 163 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(160): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1042-465C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599255 | |||||||
| chr1:2599455 | C | A | 1 | a0002c0002t0001g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1042-665G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599455 | |||||||
| chr1:2599723 | T | G | 1 | a0002c0017t0001g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1042-933A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599723 | |||||||
| chr1:2599772 | G | A | 1 | a0002c0003t0006g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1042-982C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599772 | |||||||
| chr1:2599856 | C | CAA | 17 | a0001c0001t0001g0132 a0001c0001t0001g0143 a0001c0001t0001g0148 others(14): Show |
20 | HG01106.hp1 HG01106.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1042-1068_1042-106 others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599856 | |||||||
| chr1:2599856 | C | CAAA | 137 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(134): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1042-1069_1042-106 others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599856 | |||||||
| chr1:2599933 | A | C | 160 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(157): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1042-1143T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599933 | |||||||
| chr1:2600028 | T | C | 160 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(157): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1042-1238A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600028 | |||||||
| chr1:2600066 | C | T | 151 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(148): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1042-1276G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600066 | |||||||
| chr1:2600075 | C | A | 160 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(157): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1042-1285G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600075 | |||||||
| chr1:2600297 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1042-1507C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600297 | |||||||
| chr1:2600334 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1042-1544T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600334 | |||||||
| chr1:2600536 | GAA | G | 9 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(6): Show |
13 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042-1748_1042-174 others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600536 | |||||||
| chr1:2600536 | GAAA | G | 151 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(148): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1042-1749_1042-174 others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600536 | |||||||
| chr1:2600539 | A | G | 9 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(6): Show |
13 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042-1749T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600539 | |||||||
| chr1:2600540 | A | G | 151 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(148): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1042-1750T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600540 | |||||||
| chr1:2600541 | A | G | 38 | a0001c0005t0001g0059 a0002c0002t0001g0005 a0002c0002t0001g0006 others(35): Show |
54 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1042-1751T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600541 | |||||||
| chr1:2600570 | G | T | 1 | a0002c0002t0001g0096 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1042-1780C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600570 | |||||||
| chr1:2600607 | G | A | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1042-1817C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600607 | |||||||
| chr1:2600642 | T | C | 1 | a0002c0002t0001g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1042-1852A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600642 | |||||||
| chr1:2600684 | T | TCAAACAA others(5): Show |
1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1042-1906_1042-189 others(16): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600684 | |||||||
| chr1:2600684 | TCAAACAA others(5): Show |
T | 160 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(157): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1042-1906_1042-189 others(16): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600684 | |||||||
| chr1:2600720 | C | CTGT | 160 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(157): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1042-1933_1042-193 others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600720 | |||||||
| chr1:2600977 | T | C | 163 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(160): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1042-2187A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600977 | |||||||
| chr1:2601001 | A | T | 1 | a0002c0017t0001g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1042-2211T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601001 | |||||||
| chr1:2601014 | C | CT | 163 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(160): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1042-2225dupA | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601014 | |||||||
| chr1:2601040 | A | T | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG02896.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1042-2250T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601040 | |||||||
| chr1:2601067 | G | A | 162 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(159): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1042-2277C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601067 | |||||||
| chr1:2601088 | G | A | 9 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(6): Show |
13 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042-2298C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601088 | |||||||
| chr1:2601185 | C | T | 160 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(157): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1042-2395G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601185 | |||||||
| chr1:2601222 | T | A | 1 | a0002c0008t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1042-2432A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601222 | |||||||
| chr1:2601348 | C | A | 1 | a0002c0002t0001g0089 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1041+2536G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601348 | |||||||
| chr1:2601460 | C | A | 161 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(158): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1041+2424G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601460 | |||||||
| chr1:2601582 | T | G | 1 | a0002c0017t0001g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1041+2302A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601582 | |||||||
| chr1:2601669 | C | T | 3 | a0002c0002t0001g0008 a0002c0002t0001g0051 a0002c0002t0001g0085 |
3 | NA18952.hp1 NA18960.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1041+2215G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601669 | |||||||
| chr1:2601726 | G | A | 9 | a0001c0001t0001g0156 a0002c0004t0001g0267 a0002c0004t0001g0268 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1041+2158C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601726 | |||||||
| chr1:2601786 | T | C | 1 | a0002c0002t0001g0090 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1041+2098A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601786 | |||||||
| chr1:2601811 | C | A | 117 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(114): Show |
156 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.1041+2073G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601811 | |||||||
| chr1:2601902 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1041+1982G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601902 | |||||||
| chr1:2601963 | CAG | C | 11 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(8): Show |
15 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1041+1919_1041+192 others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601963 | |||||||
| chr1:2602003 | CAGCAATT others(64): Show |
C | 1 | a0001c0021t0001g0157 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1041+1810_1041+188 others(75): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602003 | |||||||
| chr1:2602113 | A | C | 118 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(115): Show |
157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1041+1771T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602113 | |||||||
| chr1:2602115 | G | GTTCTTAG others(73): Show |
118 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(115): Show |
157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1041+1768_1041+176 others(84): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602115 | |||||||
| chr1:2602166 | G | A | 110 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(107): Show |
149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1041+1718C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602166 | |||||||
| chr1:2602257 | C | T | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1041+1627G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602257 | |||||||
| chr1:2602258 | G | A | 1 | a0005c0009t0004g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1041+1626C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602258 | |||||||
| chr1:2602267 | G | A | 118 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(115): Show |
157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1041+1617C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602267 | |||||||
| chr1:2602312 | G | GGGCGATT others(29): Show |
1 | a0002c0017t0001g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1041+1536_1041+157 others(40): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602312 | |||||||
| chr1:2602328 | C | T | 5 | a0002c0002t0001g0008 a0002c0002t0001g0051 a0002c0002t0001g0064 others(2): Show |
7 | NA18952.hp1 NA18955.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041+1556G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602328 | |||||||
| chr1:2602393 | G | A | 2 | a0004c0010t0001g0234 a0004c0010t0001g0239 |
2 | HG00323.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1041+1491C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602393 | |||||||
| chr1:2602648 | C | T | 110 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(107): Show |
149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1041+1236G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602648 | |||||||
| chr1:2602683 | C | T | 3 | a0001c0001t0002g0189 a0001c0001t0002g0206 a0001c0001t0002g0208 |
3 | HG01175.hp2 HG01256.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1041+1201G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602683 | |||||||
| chr1:2602738 | C | T | 7 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(4): Show |
7 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1146G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602738 | |||||||
| chr1:2602758 | T | C | 9 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(6): Show |
10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+1126A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602758 | |||||||
| chr1:2602808 | G | C | 11 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(8): Show |
15 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1041+1076C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602808 | |||||||
| chr1:2602866 | AGCTCATC others(19): Show |
A | 9 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(6): Show |
10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+992_1041+1017 others(29): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602866 | |||||||
| chr1:2602894 | T | A | 9 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(6): Show |
10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+990A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602894 | |||||||
| chr1:2602895 | GA | G | 9 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(6): Show |
10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+988delT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602895 | |||||||
| chr1:2602936 | G | A | 14 | a0002c0002t0001g0042 a0002c0002t0001g0043 a0002c0002t0003g0003 others(11): Show |
21 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1041+948C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602936 | |||||||
| chr1:2602947 | T | A | 7 | a0001c0005t0001g0059 a0002c0002t0001g0011 a0002c0002t0001g0022 others(4): Show |
10 | HG00642.hp2 HG01109.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1041+937A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602947 | |||||||
| chr1:2602948 | C | A | 7 | a0001c0005t0001g0059 a0002c0002t0001g0011 a0002c0002t0001g0022 others(4): Show |
10 | HG00642.hp2 HG01109.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1041+936G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602948 | |||||||
| chr1:2603033 | G | A | 2 | a0002c0002t0003g0084 a0002c0002t0003g0117 |
2 | HG00597.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1041+851C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603033 | |||||||
| chr1:2603289 | C | T | 9 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(6): Show |
10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+595G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603289 | |||||||
| chr1:2603362 | G | C | 118 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(115): Show |
157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1041+522C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603362 | |||||||
| chr1:2603513 | C | A | 1 | a0002c0002t0001g0020 | 2 | NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1041+371G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603513 | |||||||
| chr1:2603539 | G | A | 109 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(106): Show |
147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1041+345C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603539 | |||||||
| chr1:2603653 | ACT | A | 109 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(106): Show |
147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1041+229_1041+230d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603653 | |||||||
| chr1:2603763 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0162 a0001c0001t0001g0164 |
3 | NA18974.hp1 NA19056.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1041+121C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603763 | |||||||
| chr1:2603836 | C | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | HG02559.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+48G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603836 | |||||||
| chr1:2604001 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.952-28G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/23 | chr1 | 2604001 | |||||||
| chr1:2604057 | C | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
12 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.952-84G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/23 | chr1 | 2604057 | |||||||
| chr1:2604130 | C | A | 7 | a0002c0002t0001g0005 a0002c0002t0001g0032 a0002c0002t0001g0034 others(4): Show |
10 | HG01099.hp1 HG01261.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.951+17G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/23 | chr1 | 2604130 | |||||||
| chr1:2604318 | C | T | 1 | a0001c0005t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.817-37G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604318 | |||||||
| chr1:2604319 | A | G | 129 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(126): Show |
172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.817-38T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604319 | |||||||
| chr1:2604445 | C | T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG02109.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.817-164G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604445 | |||||||
| chr1:2604454 | C | T | 1 | a0002c0004t0001g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.817-173G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604454 | |||||||
| chr1:2604456 | C | T | 116 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(113): Show |
155 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.817-175G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604456 | |||||||
| chr1:2604482 | G | A | 9 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(6): Show |
10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-201C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604482 | |||||||
| chr1:2604563 | C | G | 118 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(115): Show |
157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.817-282G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604563 | |||||||
| chr1:2605117 | C | T | 1 | a0002c0002t0003g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.816+441G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2605117 | |||||||
| chr1:2605205 | G | A | 1 | a0001c0001t0002g0205 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.816+353C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2605205 | |||||||
| chr1:2605374 | C | A | 12 | a0002c0002t0003g0003 a0002c0002t0003g0010 a0002c0002t0003g0016 others(9): Show |
19 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.816+184G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2605374 | |||||||
| chr1:2605406 | C | T | 9 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(6): Show |
10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.816+152G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2605406 | |||||||
| chr1:2605459 | G | C | 2 | a0006c0007t0001g0028 a0013c0019t0001g0271 |
3 | HG02976.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.816+99C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2605459 | |||||||
| chr1:2605633 | C | T | 8 | a0001c0001t0001g0154 a0001c0001t0001g0250 a0001c0001t0001g0252 others(5): Show |
8 | HG00738.hp1 HG01515.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.751-10G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2605633 | |||||||
| chr1:2605656 | G | A | 117 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(114): Show |
158 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.751-33C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2605656 | |||||||
| chr1:2605727 | A | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.751-104T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2605727 | |||||||
| chr1:2605790 | C | T | 7 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(4): Show |
11 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.751-167G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2605790 | |||||||
| chr1:2605974 | C | T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG02109.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.750+274G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2605974 | |||||||
| chr1:2606025 | A | G | 130 | a0001c0001t0002g0207 a0001c0005t0001g0059 a0001c0005t0001g0078 others(127): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.750+223T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2606025 | |||||||
| chr1:2606104 | C | T | 1 | a0002c0002t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.750+144G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2606104 | |||||||
| chr1:2606399 | C | T | 109 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(106): Show |
147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.632-33G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606399 | |||||||
| chr1:2606550 | G | A | 1 | a0002c0002t0001g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.632-184C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606550 | |||||||
| chr1:2606566 | G | A | 2 | a0002c0008t0001g0040 a0002c0008t0001g0041 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.632-200C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606566 | |||||||
| chr1:2606570 | G | A | 1 | a0002c0002t0003g0094 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.632-204C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606570 | |||||||
| chr1:2606685 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.631+289G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606685 | |||||||
| chr1:2606770 | G | A | 109 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(106): Show |
147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.631+204C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606770 | |||||||
| chr1:2606828 | C | T | 1 | a0002c0003t0001g0272 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.631+146G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606828 | |||||||
| chr1:2606905 | A | G | 18 | a0002c0003t0001g0014 a0002c0003t0001g0023 a0002c0003t0001g0027 others(15): Show |
23 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.631+69T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606905 | |||||||
| chr1:2606910 | G | A | 109 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(106): Show |
147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.631+64C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606910 | |||||||
| chr1:2606941 | T | G | 1 | a0002c0002t0001g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.631+33A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606941 | |||||||
| chr1:2607081 | C | T | 2 | a0002c0008t0001g0040 a0002c0008t0001g0041 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.536-12G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607081 | |||||||
| chr1:2607136 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.536-67A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607136 | |||||||
| chr1:2607143 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.536-74C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607143 | |||||||
| chr1:2607196 | C | T | 1 | a0002c0002t0003g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.536-127G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607196 | |||||||
| chr1:2607267 | C | T | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.536-198G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607267 | |||||||
| chr1:2607299 | C | T | 10 | a0002c0002t0003g0003 a0002c0002t0003g0010 a0002c0002t0003g0016 others(7): Show |
17 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.536-230G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607299 | |||||||
| chr1:2607387 | C | T | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.536-318G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607387 | |||||||
| chr1:2607447 | G | T | 109 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(106): Show |
147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.536-378C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607447 | |||||||
| chr1:2607532 | C | T | 1 | a0002c0002t0001g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.536-463G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607532 | |||||||
| chr1:2607567 | T | C | 127 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(124): Show |
170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.536-498A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607567 | |||||||
| chr1:2607742 | C | T | 127 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(124): Show |
170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.536-673G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607742 | |||||||
| chr1:2607784 | C | T | 1 | a0002c0002t0003g0094 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.536-715G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607784 | |||||||
| chr1:2607790 | C | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.536-721G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607790 | |||||||
| chr1:2607830 | T | G | 1 | a0002c0003t0001g0023 | 2 | NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.536-761A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607830 | |||||||
| chr1:2607961 | T | C | 113 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(110): Show |
152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.536-892A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607961 | |||||||
| chr1:2608093 | A | G | 127 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(124): Show |
170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.536-1024T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608093 | |||||||
| chr1:2608116 | A | G | 127 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(124): Show |
170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.536-1047T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608116 | |||||||
| chr1:2608151 | C | T | 129 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(126): Show |
172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.536-1082G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608151 | |||||||
| chr1:2608164 | G | A | 111 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(108): Show |
149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.536-1095C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608164 | |||||||
| chr1:2608172 | C | T | 1 | a0002c0002t0001g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.536-1103G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608172 | |||||||
| chr1:2608220 | G | A | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.535+1119C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608220 | |||||||
| chr1:2608235 | C | A | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.535+1104G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608235 | |||||||
| chr1:2608357 | C | T | 111 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(108): Show |
149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.535+982G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608357 | |||||||
| chr1:2608389 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.535+950A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608389 | |||||||
| chr1:2608462 | A | C | 127 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(124): Show |
170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.535+877T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608462 | |||||||
| chr1:2608507 | CAT | C | 111 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(108): Show |
149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.535+830_535+831del others(2): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608507 | |||||||
| chr1:2608542 | CACAT | C | 111 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(108): Show |
149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.535+793_535+796del others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608542 | |||||||
| chr1:2608790 | G | A | 1 | a0002c0002t0003g0084 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.535+549C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608790 | |||||||
| chr1:2608823 | C | T | 129 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(126): Show |
172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.535+516G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608823 | |||||||
| chr1:2608838 | A | G | 1 | a0002c0002t0003g0075 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.535+501T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608838 | |||||||
| chr1:2608860 | T | C | 1 | a0001c0001t0002g0214 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.535+479A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608860 | |||||||
| chr1:2608904 | A | C | 129 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(126): Show |
172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.535+435T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608904 | |||||||
| chr1:2608906 | C | CACATAT | 184 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0137 others(181): Show |
230 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.535+427_535+432dup others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608906 | |||||||
| chr1:2608925 | G | A | 129 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(126): Show |
172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.535+414C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608925 | |||||||
| chr1:2608932 | C | A | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.535+407G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608932 | |||||||
| chr1:2609034 | T | TAC | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(9): Show |
12 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+303_535+304dup others(2): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | T | TACAC | 15 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0139 others(12): Show |
18 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.535+301_535+304dup others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | T | TACACAC | 14 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0147 others(11): Show |
14 | HG00544.hp2 HG00609.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.535+299_535+304dup others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0137 a0001c0001t0001g0169 |
2 | HG02109.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.535+295_535+304dup others(10): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | TAC | T | 26 | a0001c0001t0001g0025 a0001c0001t0001g0126 a0001c0001t0001g0138 others(23): Show |
29 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.535+303_535+304del others(2): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | TACAC | T | 50 | a0001c0001t0001g0168 a0001c0001t0001g0174 a0001c0001t0001g0182 others(47): Show |
65 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.535+301_535+304del others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | TACACAC | T | 5 | a0001c0001t0002g0015 a0001c0001t0002g0179 a0001c0001t0002g0206 others(2): Show |
6 | HG00140.hp1 HG00639.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.535+299_535+304del others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | TACACACA others(3): Show |
T | 3 | a0002c0002t0001g0088 a0002c0002t0001g0089 a0002c0003t0001g0023 |
4 | HG02273.hp2 HG02451.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+295_535+304del others(10): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | TACACACA others(5): Show |
T | 15 | a0001c0005t0001g0087 a0002c0002t0001g0004 a0002c0002t0001g0019 others(12): Show |
21 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.535+293_535+304del others(12): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | TACACACA others(7): Show |
T | 93 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0014t0002g0115 others(90): Show |
125 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.535+291_535+304del others(14): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | TACACACA others(9): Show |
T | 8 | a0002c0002t0001g0113 a0002c0003t0001g0014 a0002c0003t0001g0027 others(5): Show |
11 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.535+289_535+304del others(16): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | TACACACA others(11): Show |
T | 2 | a0002c0012t0001g0044 a0011c0020t0001g0266 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.535+287_535+304del others(18): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609034 | TACACACA others(13): Show |
T | 7 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(4): Show |
8 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+285_535+304del others(20): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | |||||||
| chr1:2609155 | T | G | 8 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(5): Show |
8 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.535+184A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609155 | |||||||
| chr1:2609203 | C | A | 1 | a0001c0001t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.535+136G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609203 | |||||||
| chr1:2609473 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.455-54C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 5/23 | chr1 | 2609473 | |||||||
| chr1:2609617 | G | A | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.454+53C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 5/23 | chr1 | 2609617 | |||||||
| chr1:2610117 | T | C | 2 | a0002c0002t0001g0018 a0002c0002t0001g0090 |
3 | HG02083.hp2 NA18951.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.293-286A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610117 | |||||||
| chr1:2610220 | T | A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0253 |
2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.293-389A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610220 | |||||||
| chr1:2610288 | C | T | 11 | a0001c0001t0001g0025 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
12 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-457G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610288 | |||||||
| chr1:2610365 | C | T | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.293-534G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610365 | |||||||
| chr1:2610502 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.293-671G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610502 | |||||||
| chr1:2610533 | G | C | 1 | a0002c0016t0001g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.293-702C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610533 | |||||||
| chr1:2610724 | A | AC | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+556dupG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610724 | |||||||
| chr1:2610936 | A | G | 3 | a0002c0002t0001g0022 a0002c0002t0001g0061 a0002c0002t0001g0103 |
4 | HG00642.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+345T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610936 | |||||||
| chr1:2611053 | T | G | 1 | a0002c0002t0003g0091 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.292+228A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2611053 | |||||||
| chr1:2611060 | C | T | 1 | a0002c0003t0001g0274 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.292+221G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2611060 | |||||||
| chr1:2611080 | G | A | 1 | a0010c0013t0001g0092 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.292+201C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2611080 | |||||||
| chr1:2611199 | C | T | 1 | a0002c0002t0001g0122 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.292+82G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2611199 | |||||||
| chr1:2611214 | A | G | 131 | a0001c0001t0001g0126 a0001c0001t0005g0029 a0001c0005t0001g0059 others(128): Show |
174 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.292+67T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2611214 | |||||||
| chr1:2611372 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.233-32C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611372 | |||||||
| chr1:2611415 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.233-75C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611415 | |||||||
| chr1:2611423 | TGGTGGGT others(46): Show |
T | 1 | a0002c0004t0001g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.233-136_233-84delC others(52): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611423 | |||||||
| chr1:2611444 | G | A | 1 | a0010c0013t0001g0092 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.233-104C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611444 | |||||||
| chr1:2611799 | C | T | 1 | a0002c0002t0001g0061 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.232+328G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611799 | |||||||
| chr1:2611862 | G | A | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.232+265C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611862 | |||||||
| chr1:2611931 | A | G | 1 | a0002c0002t0001g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.232+196T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611931 | |||||||
| chr1:2612072 | G | A | 2 | a0002c0002t0001g0053 a0002c0002t0001g0093 |
2 | HG00099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.232+55C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2612072 | |||||||
| chr1:2612352 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.155-148C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2612352 | |||||||
| chr1:2612379 | C | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0205 |
3 | NA19007.hp1 NA19079.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.155-175G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2612379 | |||||||
| chr1:2612436 | C | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.155-232G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2612436 | |||||||
| chr1:2612743 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.155-539C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2612743 | |||||||
| chr1:2613200 | C | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0205 |
3 | NA19007.hp1 NA19079.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.155-996G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613200 | |||||||
| chr1:2613201 | G | A | 108 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(105): Show |
146 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.155-997C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613201 | |||||||
| chr1:2613208 | G | A | 2 | a0002c0008t0001g0040 a0002c0008t0001g0041 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.155-1004C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613208 | |||||||
| chr1:2613567 | G | A | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.155-1363C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613567 | |||||||
| chr1:2613649 | C | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG00738.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.155-1445G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613649 | |||||||
| chr1:2613830 | G | C | 16 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(13): Show |
20 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-1626C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613830 | |||||||
| chr1:2613977 | G | A | 1 | a0002c0002t0001g0055 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.155-1773C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613977 | |||||||
| chr1:2614215 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.155-2011G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614215 | |||||||
| chr1:2614346 | C | T | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.155-2142G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614346 | |||||||
| chr1:2614394 | C | T | 16 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(13): Show |
20 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-2190G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614394 | |||||||
| chr1:2614650 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.155-2446G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614650 | |||||||
| chr1:2614790 | G | A | 111 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(108): Show |
149 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.155-2586C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614790 | |||||||
| chr1:2614852 | C | T | 11 | a0001c0001t0001g0250 a0001c0001t0001g0252 a0001c0001t0001g0253 others(8): Show |
11 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-2648G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614852 | |||||||
| chr1:2614904 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.155-2700G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614904 | |||||||
| chr1:2614906 | C | A | 2 | a0001c0001t0001g0193 a0002c0002t0003g0047 |
2 | HG01358.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.155-2702G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614906 | |||||||
| chr1:2615007 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.155-2803G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615007 | |||||||
| chr1:2615039 | A | C | 3 | a0002c0002t0001g0022 a0002c0002t0001g0061 a0002c0002t0001g0103 |
4 | HG00642.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-2835T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615039 | |||||||
| chr1:2615121 | T | C | 1 | a0002c0002t0001g0099 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.155-2917A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615121 | |||||||
| chr1:2615154 | G | A | 4 | a0002c0002t0001g0019 a0002c0002t0001g0052 a0002c0002t0001g0053 others(1): Show |
5 | HG00099.hp1 HG00639.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-2950C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615154 | |||||||
| chr1:2615322 | G | C | 1 | a0002c0002t0003g0072 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.155-3118C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615322 | |||||||
| chr1:2615369 | T | C | 1 | a0001c0001t0002g0229 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.155-3165A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615369 | |||||||
| chr1:2615568 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.155-3364C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615568 | |||||||
| chr1:2615712 | C | T | 1 | a0002c0002t0001g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.155-3508G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615712 | |||||||
| chr1:2615772 | G | A | 3 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0002g0131 |
3 | HG01256.hp1 HG02683.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.155-3568C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615772 | |||||||
| chr1:2615819 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.155-3615T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615819 | |||||||
| chr1:2615838 | A | T | 4 | a0002c0002t0001g0070 a0002c0002t0001g0073 a0002c0002t0001g0108 others(1): Show |
4 | NA18943.hp1 NA18982.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-3634T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615838 | |||||||
| chr1:2615855 | C | T | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.155-3651G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615855 | |||||||
| chr1:2616028 | C | T | 5 | a0002c0002t0001g0006 a0002c0002t0001g0054 a0002c0002t0001g0058 others(2): Show |
7 | HG01891.hp2 HG02886.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-3824G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616028 | |||||||
| chr1:2616121 | A | T | 1 | a0005c0009t0004g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.155-3917T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616121 | |||||||
| chr1:2616170 | A | G | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.155-3966T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616170 | |||||||
| chr1:2616342 | C | CA | 16 | a0001c0001t0002g0230 a0001c0005t0001g0059 a0002c0002t0001g0036 others(13): Show |
16 | HG00140.hp2 HG00741.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.155-4139dupT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616342 | |||||||
| chr1:2616342 | C | CAA | 97 | a0001c0005t0001g0078 a0001c0005t0001g0087 a0001c0014t0002g0115 others(94): Show |
135 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.155-4140_155-4139d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616342 | |||||||
| chr1:2616342 | C | CAAAA | 7 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(4): Show |
7 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-4142_155-4139d others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616342 | |||||||
| chr1:2616342 | C | CAAAAA | 6 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(3): Show |
9 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.155-4143_155-4139d others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616342 | |||||||
| chr1:2616342 | CA | C | 12 | a0001c0001t0001g0135 a0001c0001t0001g0166 a0001c0001t0001g0167 others(9): Show |
13 | HG00280.hp2 HG01070.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.155-4139delT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616342 | |||||||
| chr1:2616410 | C | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.155-4206G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616410 | |||||||
| chr1:2616522 | A | G | 1 | a0005c0009t0004g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.155-4318T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616522 | |||||||
| chr1:2616712 | A | C | 1 | a0002c0002t0003g0068 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.155-4508T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616712 | |||||||
| chr1:2616802 | C | T | 5 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG02723.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-4598G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616802 | |||||||
| chr1:2616849 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.155-4645G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616849 | |||||||
| chr1:2616910 | C | G | 1 | a0005c0009t0004g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.155-4706G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616910 | |||||||
| chr1:2616944 | T | G | 2 | a0002c0002t0001g0034 a0002c0002t0001g0035 |
2 | HG01261.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.155-4740A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616944 | |||||||
| chr1:2617228 | C | T | 1 | a0002c0002t0001g0096 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.155-5024G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617228 | |||||||
| chr1:2617234 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.155-5030G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617234 | |||||||
| chr1:2617238 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.155-5034A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617238 | |||||||
| chr1:2617299 | C | T | 2 | a0002c0002t0003g0045 a0002c0002t0003g0046 |
2 | HG01074.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.155-5095G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617299 | |||||||
| chr1:2617336 | A | G | 1 | a0002c0012t0001g0044 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.155-5132T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617336 | |||||||
| chr1:2617344 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.155-5140C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617344 | |||||||
| chr1:2617381 | C | T | 4 | a0002c0002t0001g0017 a0002c0002t0001g0038 a0002c0002t0001g0066 others(1): Show |
5 | HG02280.hp1 HG02647.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-5177G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617381 | |||||||
| chr1:2617382 | G | T | 5 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG02723.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-5178C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617382 | |||||||
| chr1:2617383 | C | T | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.155-5179G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617383 | |||||||
| chr1:2617413 | A | C | 128 | a0001c0005t0001g0078 a0001c0005t0001g0087 a0001c0014t0002g0115 others(125): Show |
171 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.155-5209T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617413 | |||||||
| chr1:2617413 | A | T | 1 | a0001c0005t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.155-5209T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617413 | |||||||
| chr1:2617426 | C | CA | 21 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0001t0001g0151 others(18): Show |
21 | HG00733.hp1 HG00738.hp1 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.155-5223dupT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617426 | |||||||
| chr1:2617426 | C | CAAAA | 5 | a0002c0003t0001g0027 a0002c0003t0001g0272 a0002c0003t0001g0273 others(2): Show |
6 | HG01123.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-5226_155-5223d others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617426 | |||||||
| chr1:2617426 | C | CAAAAA | 7 | a0002c0003t0001g0014 a0002c0003t0001g0274 a0002c0004t0001g0269 others(4): Show |
9 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-5227_155-5223d others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617426 | |||||||
| chr1:2617426 | CA | C | 99 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0143 others(96): Show |
135 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.155-5223delT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617426 | |||||||
| chr1:2617426 | CAA | C | 16 | a0001c0001t0001g0166 a0001c0001t0001g0172 a0002c0002t0001g0006 others(13): Show |
19 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.155-5224_155-5223d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617426 | |||||||
| chr1:2617460 | C | T | 1 | a0001c0001t0002g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.155-5256G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617460 | |||||||
| chr1:2617461 | G | A | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-5257C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617461 | |||||||
| chr1:2617650 | T | G | 16 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(13): Show |
20 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-5446A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617650 | |||||||
| chr1:2617710 | A | G | 16 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(13): Show |
20 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-5506T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617710 | |||||||
| chr1:2617714 | T | A | 1 | a0002c0002t0001g0020 | 2 | NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.155-5510A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617714 | |||||||
| chr1:2617802 | G | T | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.155-5598C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617802 | |||||||
| chr1:2618163 | G | A | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.155-5959C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618163 | |||||||
| chr1:2618178 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.155-5974A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618178 | |||||||
| chr1:2618322 | T | C | 1 | a0002c0002t0001g0021 | 2 | HG01070.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.155-6118A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618322 | |||||||
| chr1:2618681 | G | T | 1 | a0001c0001t0002g0202 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.155-6477C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618681 | |||||||
| chr1:2618812 | C | A | 1 | a0002c0002t0001g0095 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.155-6608G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618812 | |||||||
| chr1:2618904 | C | T | 2 | a0002c0008t0001g0040 a0002c0008t0001g0041 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.155-6700G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618904 | |||||||
| chr1:2619027 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.155-6823C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619027 | |||||||
| chr1:2619197 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.155-6993A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619197 | |||||||
| chr1:2619345 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.155-7141C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619345 | |||||||
| chr1:2619352 | A | G | 1 | a0002c0002t0003g0120 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.155-7148T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619352 | |||||||
| chr1:2619503 | C | T | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.155-7299G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619503 | |||||||
| chr1:2619526 | C | T | 16 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(13): Show |
20 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-7322G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619526 | |||||||
| chr1:2619612 | C | T | 1 | a0002c0002t0001g0106 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.155-7408G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619612 | |||||||
| chr1:2619614 | T | C | 129 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(126): Show |
172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.155-7410A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619614 | |||||||
| chr1:2619655 | CA | C | 132 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(129): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.155-7452delT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619655 | |||||||
| chr1:2619655 | CAA | C | 45 | a0001c0001t0001g0139 a0001c0001t0001g0167 a0001c0001t0001g0168 others(42): Show |
62 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.155-7453_155-7452d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619655 | |||||||
| chr1:2619655 | CAAA | C | 19 | a0001c0014t0002g0115 a0002c0002t0001g0032 a0002c0002t0001g0055 others(16): Show |
20 | HG00140.hp2 HG02055.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.155-7454_155-7452d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619655 | |||||||
| chr1:2619655 | CAAAA | C | 66 | a0001c0005t0001g0078 a0001c0005t0001g0087 a0002c0002t0001g0004 others(63): Show |
89 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.155-7455_155-7452d others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619655 | |||||||
| chr1:2619655 | CAAAAA | C | 4 | a0002c0002t0003g0007 a0002c0002t0003g0050 a0002c0002t0003g0063 others(1): Show |
6 | HG02523.hp2 NA18956.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-7456_155-7452d others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619655 | |||||||
| chr1:2619933 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.155-7729C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619933 | |||||||
| chr1:2619989 | T | C | 1 | a0002c0002t0001g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.155-7785A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619989 | |||||||
| chr1:2620014 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.155-7810C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620014 | |||||||
| chr1:2620221 | T | G | 109 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(106): Show |
147 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.155-8017A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620221 | |||||||
| chr1:2620346 | C | T | 46 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0137 others(43): Show |
49 | HG00544.hp2 HG00609.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.155-8142G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620346 | |||||||
| chr1:2620461 | G | A | 77 | a0001c0005t0001g0078 a0001c0005t0001g0087 a0002c0002t0001g0004 others(74): Show |
100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.155-8257C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620461 | |||||||
| chr1:2620632 | T | C | 129 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(126): Show |
172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.155-8428A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620632 | |||||||
| chr1:2620778 | G | GA | 142 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(139): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.154+8552dupT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620778 | |||||||
| chr1:2620778 | G | GAA | 110 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(107): Show |
148 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.154+8551_154+8552d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620778 | |||||||
| chr1:2620778 | G | GAAA | 9 | a0002c0002t0001g0096 a0002c0002t0001g0097 a0002c0002t0001g0098 others(6): Show |
9 | HG01975.hp2 HG02015.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+8550_154+8552d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620778 | |||||||
| chr1:2621383 | G | A | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+7948C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621383 | |||||||
| chr1:2621392 | A | G | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+7939T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621392 | |||||||
| chr1:2621572 | A | AT | 101 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(98): Show |
137 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.154+7758dupA | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621572 | |||||||
| chr1:2621572 | A | ATT | 8 | a0002c0002t0001g0005 a0002c0002t0001g0032 a0002c0002t0001g0034 others(5): Show |
11 | HG01099.hp1 HG01169.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.154+7757_154+7758d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621572 | |||||||
| chr1:2621626 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.154+7705G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621626 | |||||||
| chr1:2621644 | G | A | 129 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(126): Show |
172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.154+7687C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621644 | |||||||
| chr1:2621652 | C | T | 1 | a0002c0002t0001g0052 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.154+7679G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621652 | |||||||
| chr1:2621712 | C | T | 1 | a0002c0002t0001g0051 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.154+7619G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621712 | |||||||
| chr1:2621829 | T | C | 1 | a0002c0002t0001g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+7502A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621829 | |||||||
| chr1:2621943 | C | T | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+7388G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621943 | |||||||
| chr1:2622055 | G | A | 8 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(5): Show |
8 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+7276C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622055 | |||||||
| chr1:2622103 | TAGG | T | 121 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(118): Show |
164 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.154+7225_154+7227d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622103 | |||||||
| chr1:2622185 | T | C | 114 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(111): Show |
153 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.154+7146A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622185 | |||||||
| chr1:2622218 | C | T | 11 | a0001c0001t0001g0025 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
12 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.154+7113G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622218 | |||||||
| chr1:2622312 | C | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+7019G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622312 | |||||||
| chr1:2622319 | C | T | 129 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(126): Show |
172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.154+7012G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622319 | |||||||
| chr1:2622571 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.154+6760A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622571 | |||||||
| chr1:2622606 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.154+6725G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622606 | |||||||
| chr1:2622681 | T | G | 13 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0156 others(10): Show |
16 | HG00735.hp2 HG01069.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.154+6650A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622681 | |||||||
| chr1:2622747 | T | C | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+6584A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622747 | |||||||
| chr1:2622815 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
3 | HG02717.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.154+6516G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622815 | |||||||
| chr1:2622848 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.154+6483G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622848 | |||||||
| chr1:2622883 | CA | C | 21 | a0001c0001t0001g0132 a0001c0001t0001g0142 a0001c0001t0001g0143 others(18): Show |
21 | HG00597.hp2 HG01515.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.154+6447delT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622883 | |||||||
| chr1:2622883 | CAA | C | 9 | a0002c0002t0001g0112 a0002c0003t0001g0014 a0002c0003t0001g0023 others(6): Show |
13 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.154+6446_154+6447d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622883 | |||||||
| chr1:2622883 | CAAA | C | 11 | a0002c0002t0001g0022 a0002c0002t0001g0103 a0002c0002t0001g0104 others(8): Show |
12 | HG00438.hp1 HG00544.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.154+6445_154+6447d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622883 | |||||||
| chr1:2622883 | CAAAA | C | 100 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(97): Show |
138 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.154+6444_154+6447d others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622883 | |||||||
| chr1:2622905 | T | G | 119 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(116): Show |
161 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.154+6426A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622905 | |||||||
| chr1:2623124 | A | G | 112 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(109): Show |
151 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.154+6207T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623124 | |||||||
| chr1:2623164 | T | TA | 13 | a0001c0001t0001g0164 a0001c0001t0001g0265 a0001c0001t0002g0236 others(10): Show |
13 | HG00597.hp1 HG00738.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.154+6166dupT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623164 | |||||||
| chr1:2623275 | G | A | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+6056C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623275 | |||||||
| chr1:2623314 | A | C | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.154+6017T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623314 | |||||||
| chr1:2623506 | C | T | 1 | a0002c0002t0003g0050 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.154+5825G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623506 | |||||||
| chr1:2623690 | C | T | 10 | a0002c0002t0003g0003 a0002c0002t0003g0010 a0002c0002t0003g0016 others(7): Show |
17 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.154+5641G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623690 | |||||||
| chr1:2623810 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.154+5521G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623810 | |||||||
| chr1:2623859 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.154+5472G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623859 | |||||||
| chr1:2623875 | A | G | 1 | a0001c0001t0002g0186 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.154+5456T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623875 | |||||||
| chr1:2624025 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154+5306C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624025 | |||||||
| chr1:2624158 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.154+5173G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624158 | |||||||
| chr1:2624201 | T | A | 122 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(119): Show |
161 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.154+5130A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624201 | |||||||
| chr1:2624278 | G | A | 1 | a0011c0020t0001g0266 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.154+5053C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624278 | |||||||
| chr1:2624337 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG00735.hp1 HG01361.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.154+4994G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624337 | |||||||
| chr1:2624371 | A | G | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG02451.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+4960T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624371 | |||||||
| chr1:2624381 | C | T | 1 | a0002c0017t0001g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.154+4950G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624381 | |||||||
| chr1:2624572 | T | C | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+4759A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624572 | |||||||
| chr1:2624686 | C | T | 110 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(107): Show |
148 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.154+4645G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624686 | |||||||
| chr1:2624847 | C | T | 7 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+4484G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624847 | |||||||
| chr1:2624907 | C | T | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+4424G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624907 | |||||||
| chr1:2624948 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.154+4383C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624948 | |||||||
| chr1:2625090 | A | G | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+4241T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625090 | |||||||
| chr1:2625109 | C | T | 113 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(110): Show |
152 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.154+4222G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625109 | |||||||
| chr1:2625268 | G | C | 1 | a0001c0001t0002g0240 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.154+4063C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625268 | |||||||
| chr1:2625270 | G | A | 113 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(110): Show |
152 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.154+4061C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625270 | |||||||
| chr1:2625318 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154+4013G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625318 | |||||||
| chr1:2625327 | G | T | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+4004C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625327 | |||||||
| chr1:2625328 | A | T | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+4003T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625328 | |||||||
| chr1:2625469 | C | T | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+3862G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625469 | |||||||
| chr1:2625548 | G | A | 2 | a0001c0001t0002g0241 a0007c0026t0002g0242 |
2 | HG00099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.154+3783C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625548 | |||||||
| chr1:2625752 | C | T | 164 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(161): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.154+3579G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625752 | |||||||
| chr1:2625837 | T | C | 1 | a0001c0001t0002g0015 | 2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.154+3494A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625837 | |||||||
| chr1:2625872 | C | A | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+3459G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625872 | |||||||
| chr1:2625937 | G | GGAA | 148 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(145): Show |
170 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.154+3391_154+3393d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625937 | |||||||
| chr1:2626092 | C | T | 164 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(161): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.154+3239G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626092 | |||||||
| chr1:2626215 | T | C | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.154+3116A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626215 | |||||||
| chr1:2626217 | G | A | 1 | a0001c0001t0002g0243 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.154+3114C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626217 | |||||||
| chr1:2626608 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.154+2723G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626608 | |||||||
| chr1:2626770 | C | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+2561G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626770 | |||||||
| chr1:2626771 | G | A | 2 | a0002c0002t0001g0011 a0012c0011t0001g0124 |
4 | HG01109.hp2 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+2560C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626771 | |||||||
| chr1:2626869 | A | C | 164 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(161): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.154+2462T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626869 | |||||||
| chr1:2627178 | G | C | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG02109.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.154+2153C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627178 | |||||||
| chr1:2627179 | T | TTC | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG02109.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.154+2151_154+2152i others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627179 | |||||||
| chr1:2627180 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG02109.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.154+2151C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627180 | |||||||
| chr1:2627255 | C | T | 2 | a0002c0012t0001g0044 a0005c0009t0004g0133 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.154+2076G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627255 | |||||||
| chr1:2627256 | G | A | 1 | a0002c0003t0001g0274 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.154+2075C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627256 | |||||||
| chr1:2627257 | C | A | 2 | a0002c0008t0001g0040 a0002c0008t0001g0041 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.154+2074G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627257 | |||||||
| chr1:2627301 | C | T | 165 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(162): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.154+2030G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627301 | |||||||
| chr1:2627444 | T | C | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+1887A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627444 | |||||||
| chr1:2627747 | A | G | 2 | a0002c0002t0001g0042 a0002c0002t0001g0043 |
2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.154+1584T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627747 | |||||||
| chr1:2627834 | C | A | 1 | a0002c0004t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.154+1497G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627834 | |||||||
| chr1:2627984 | G | A | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+1347C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627984 | |||||||
| chr1:2628064 | G | A | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+1267C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628064 | |||||||
| chr1:2628150 | T | G | 165 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(162): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.154+1181A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628150 | |||||||
| chr1:2628167 | C | T | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+1164G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628167 | |||||||
| chr1:2628191 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.154+1140C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628191 | |||||||
| chr1:2628295 | G | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.154+1036C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628295 | |||||||
| chr1:2628299 | C | A | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+1032G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628299 | |||||||
| chr1:2628459 | T | A | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.154+872A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628459 | |||||||
| chr1:2628461 | C | A | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+870G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628461 | |||||||
| chr1:2628548 | G | C | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+783C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628548 | |||||||
| chr1:2628659 | G | C | 1 | a0001c0001t0001g0246 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.154+672C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628659 | |||||||
| chr1:2628679 | TGGGGGCG others(23): Show |
T | 2 | a0002c0008t0001g0040 a0002c0008t0001g0041 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.154+622_154+651del others(30): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628679 | |||||||
| chr1:2628915 | C | A | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+416G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628915 | |||||||
| chr1:2628957 | G | A | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.154+374C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628957 | |||||||
| chr1:2629028 | CGGCGGAG others(5): Show |
C | 7 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+291_154+302del others(12): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2629028 | |||||||
| chr1:2629176 | C | T | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+155G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2629176 | |||||||
| chr1:2629296 | A | G | 166 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(163): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.154+35T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2629296 | |||||||
| chr1:2629536 | C | CAGGGGAG | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-37-22_-37-16dupCT others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629536 | |||||||
| chr1:2629580 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-37-59C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629580 | |||||||
| chr1:2629820 | GCCC | G | 165 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(162): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-37-302_-37-300del others(3): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629820 | |||||||
| chr1:2629828 | C | A | 3 | a0002c0002t0003g0010 a0002c0002t0003g0120 a0009c0015t0003g0121 |
5 | HG00642.hp1 HG01346.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-307G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629828 | |||||||
| chr1:2629828 | C | G | 1 | a0002c0002t0001g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-37-307G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629828 | |||||||
| chr1:2629829 | C | A | 1 | a0002c0002t0001g0122 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-37-308G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629829 | |||||||
| chr1:2629847 | T | G | 165 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(162): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-37-326A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629847 | |||||||
| chr1:2629938 | G | A | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-37-417C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629938 | |||||||
| chr1:2630051 | G | A | 1 | a0002c0002t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-37-530C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630051 | |||||||
| chr1:2630125 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-37-604G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630125 | |||||||
| chr1:2630136 | T | A | 5 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(2): Show |
5 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-615A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630136 | |||||||
| chr1:2630313 | TGA | T | 7 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-794_-37-793del others(2): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630313 | |||||||
| chr1:2630408 | G | T | 7 | a0002c0002t0001g0005 a0002c0002t0001g0032 a0002c0002t0001g0034 others(4): Show |
10 | HG01099.hp1 HG01261.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-37-887C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630408 | |||||||
| chr1:2630449 | TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0005g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-37-942_-37-929del others(14): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630449 | |||||||
| chr1:2630455 | T | C | 1 | a0002c0012t0001g0044 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-37-934A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630455 | |||||||
| chr1:2630477 | TGTGTGTG others(3): Show |
T | 7 | a0002c0004t0001g0267 a0002c0004t0001g0268 a0002c0004t0001g0269 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-966_-37-957del others(10): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630477 | |||||||
| chr1:2630516 | G | C | 1 | a0001c0001t0001g0248 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-37-995C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630516 | |||||||
| chr1:2630541 | GTC | G | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-1022_-37-1021d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630541 | |||||||
| chr1:2630546 | C | T | 1 | a0002c0003t0001g0023 | 2 | NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-37-1025G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630546 | |||||||
| chr1:2630570 | TGTGA | T | 9 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
9 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-1053_-37-1050d others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630570 | |||||||
| chr1:2630586 | CGT | C | 92 | a0001c0001t0001g0025 a0001c0001t0001g0126 a0001c0001t0001g0135 others(89): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-37-1067_-37-1066d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630586 | |||||||
| chr1:2630587 | G | C | 1 | a0002c0002t0001g0122 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-37-1066C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630587 | |||||||
| chr1:2630638 | C | T | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-37-1117G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630638 | |||||||
| chr1:2630696 | CGTG | C | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-1178_-37-1176d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630696 | |||||||
| chr1:2630730 | C | T | 151 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(148): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-37-1209G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630730 | |||||||
| chr1:2630746 | CAT | C | 2 | a0002c0002t0001g0011 a0012c0011t0001g0124 |
4 | HG01109.hp2 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-1227_-37-1226d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630746 | |||||||
| chr1:2630777 | CGT | C | 17 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(14): Show |
18 | HG00544.hp2 HG00609.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-37-1258_-37-1257d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630777 | |||||||
| chr1:2630835 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.-37-1314G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630835 | |||||||
| chr1:2630861 | C | G | 1 | a0002c0004t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-37-1340G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630861 | |||||||
| chr1:2631020 | T | C | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-1499A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631020 | |||||||
| chr1:2631328 | T | G | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-38+1538A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631328 | |||||||
| chr1:2631523 | C | T | 1 | a0005c0009t0004g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+1343G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631523 | |||||||
| chr1:2631557 | G | C | 5 | a0002c0003t0001g0014 a0002c0003t0001g0027 a0002c0003t0001g0272 others(2): Show |
8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-38+1309C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631557 | |||||||
| chr1:2631659 | C | T | 1 | a0002c0002t0001g0031 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-38+1207G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631659 | |||||||
| chr1:2631663 | C | T | 1 | a0008c0024t0002g0134 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-38+1203G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631663 | |||||||
| chr1:2631698 | G | A | 1 | a0002c0017t0001g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-38+1168C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631698 | |||||||
| chr1:2631811 | G | T | 148 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(145): Show |
170 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-38+1055C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631811 | |||||||
| chr1:2631823 | C | T | 2 | a0005c0009t0004g0128 a0005c0009t0004g0133 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-38+1043G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631823 | |||||||
| chr1:2632100 | C | T | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-38+766G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632100 | |||||||
| chr1:2632197 | C | G | 1 | a0001c0001t0001g0132 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-38+669G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632197 | |||||||
| chr1:2632398 | G | A | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG02896.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+468C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632398 | |||||||
| chr1:2632408 | T | C | 1 | a0002c0004t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-38+458A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632408 | |||||||
| chr1:2632462 | T | C | 1 | a0002c0003t0006g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-38+404A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632462 | |||||||
| chr1:2632528 | C | T | 3 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0002g0131 |
3 | HG01256.hp1 HG02683.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-38+338G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632528 | |||||||
| chr1:2632530 | C | T | 1 | a0005c0009t0004g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+336G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632530 | |||||||
| chr1:2632533 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+333G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632533 | |||||||
| chr1:2632535 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+331G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632535 | |||||||
| chr1:2632536 | A | T | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+330T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632536 | |||||||
| chr1:2632539 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+327G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632539 | |||||||
| chr1:2632540 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+326T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632540 | |||||||
| chr1:2632542 | A | C | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+324T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632542 | |||||||
| chr1:2632544 | T | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+322A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632544 | |||||||
| chr1:2632545 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+321T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632545 | |||||||
| chr1:2632547 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+319T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632547 | |||||||
| chr1:2632550 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+316G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632550 | |||||||
| chr1:2632551 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+315G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632551 | |||||||
| chr1:2632557 | A | G | 2 | a0002c0003t0001g0023 a0002c0003t0006g0127 |
3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-38+309T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632557 | |||||||
| chr1:2632562 | G | C | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+304C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632562 | |||||||
| chr1:2632564 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+302G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632564 | |||||||
| chr1:2632568 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+298A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632568 | |||||||
| chr1:2632573 | G | A | 110 | a0001c0005t0001g0059 a0001c0005t0001g0078 a0001c0005t0001g0087 others(107): Show |
145 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-38+293C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632573 | |||||||
| chr1:2632575 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+291C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632575 | |||||||
| chr1:2632577 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+289G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632577 | |||||||
| chr1:2632580 | G | T | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+286C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632580 | |||||||
| chr1:2632588 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+278A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632588 | |||||||
| chr1:2632591 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+275G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632591 | |||||||
| chr1:2632592 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+274A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632592 | |||||||
| chr1:2632601 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+265C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632601 | |||||||
| chr1:2632604 | G | T | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+262C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632604 | |||||||
| chr1:2632605 | G | GATTGATC others(4): Show |
1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+260_-38+261ins others(11): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632605 | |||||||
| chr1:2632608 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+258G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632608 | |||||||
| chr1:2632614 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+252G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632614 | |||||||
| chr1:2632618 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+248G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632618 | |||||||
| chr1:2632624 | A | C | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+242T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632624 | |||||||
| chr1:2632625 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+241G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632625 | |||||||
| chr1:2632626 | A | T | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+240T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632626 | |||||||
| chr1:2632633 | G | T | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+233C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632633 | |||||||
| chr1:2632635 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+231G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632635 | |||||||
| chr1:2632638 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+228A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632638 | |||||||
| chr1:2632648 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+218A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632648 | |||||||
| chr1:2632655 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+211C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632655 | |||||||
| chr1:2632662 | A | C | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+204T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632662 | |||||||
| chr1:2632664 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+202G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632664 | |||||||
| chr1:2632672 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+194A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632672 | |||||||
| chr1:2632680 | GATAAACC others(3): Show |
G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+176_-38+185del others(10): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632680 | |||||||
| chr1:2632708 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+158A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632708 | |||||||
| chr1:2632710 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+156G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632710 | |||||||
| chr1:2632711 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+155G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632711 | |||||||
| chr1:2632714 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+152C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632714 | |||||||
| chr1:2632716 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+150G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632716 | |||||||
| chr1:2632717 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+149T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632717 | |||||||
| chr1:2632718 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+148G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632718 | |||||||
| chr1:2632719 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-38+147T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632719 | |||||||
| chr1:2632724 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+142T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632724 | |||||||
| chr1:2632725 | G | C | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+141C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632725 | |||||||
| chr1:2632726 | A | C | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+140T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632726 | |||||||
| chr1:2632739 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+127G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632739 | |||||||
| chr1:2632744 | T | C | 163 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0126 others(160): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.-38+122A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632744 | |||||||
| chr1:2632751 | C | T | 1 | a0001c0001t0002g0015 | 2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.-38+115G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632751 | |||||||
| chr1:2632840 | G | A | 1 | a0006c0007t0001g0028 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-38+26C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632840 |